paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
22 | INTRODUCTION | 1 | 7 | [
"B7"
] | 17,483,517 | pmid-15466295 | The underlying algorithm for the Gibbs Centroid Sampler and the Gibbs Recursive Sampler is a forward–backward algorithm (7). | [
"7"
] | 124 | 9,100 | 1 | false | The underlying algorithm for the Gibbs Centroid Sampler and the Gibbs Recursive Sampler is a forward–backward algorithm. | [
"7"
] | The underlying algorithm for the Gibbs Centroid Sampler and the Gibbs Recursive Sampler is a forward–backward algorithm. | true | true | true | true | true | 1,452 |
22 | INTRODUCTION | 1 | 7 | [
"B7"
] | 17,483,517 | pmid-15466295 | The forward step is the most compute intensive part of the algorithm, with runtime increasing as the square of the length of the individual sequences; thus, the most important factor affecting runtime is the length of the individual sequences. | [
"7"
] | 243 | 9,101 | 0 | false | The forward step is the most compute intensive part of the algorithm, with runtime increasing as the square of the length of the individual sequences; thus, the most important factor affecting runtime is the length of the individual sequences. | [] | The forward step is the most compute intensive part of the algorithm, with runtime increasing as the square of the length of the individual sequences; thus, the most important factor affecting runtime is the length of the individual sequences. | true | true | true | true | true | 1,452 |
22 | INTRODUCTION | 1 | 7 | [
"B7"
] | 17,483,517 | pmid-15466295 | Other parameters, such as the number of sequences, the number of motif models, the number of seeds and the number of iterations, affect the runtime linearly. | [
"7"
] | 157 | 9,102 | 0 | false | Other parameters, such as the number of sequences, the number of motif models, the number of seeds and the number of iterations, affect the runtime linearly. | [] | Other parameters, such as the number of sequences, the number of motif models, the number of seeds and the number of iterations, affect the runtime linearly. | true | true | true | true | true | 1,452 |
22 | INTRODUCTION | 1 | 7 | [
"B7"
] | 17,483,517 | pmid-15466295 | Therefore, due to the increased number of iterations for burn-in and sampling, the runtime of the centroid sampler is somewhat greater than that of the Gibbs Recursive Sampler. | [
"7"
] | 176 | 9,103 | 0 | false | Therefore, due to the increased number of iterations for burn-in and sampling, the runtime of the centroid sampler is somewhat greater than that of the Gibbs Recursive Sampler. | [] | Therefore, due to the increased number of iterations for burn-in and sampling, the runtime of the centroid sampler is somewhat greater than that of the Gibbs Recursive Sampler. | true | true | true | true | true | 1,452 |
22 | INTRODUCTION | 1 | 7 | [
"B7"
] | 17,483,517 | pmid-15466295 | Additional parameters, such as the use of palindromic or direct repeat models, while not directly affecting the runtime of the centroid sampler, greatly improve its ability to discover realistic TFBS by taking into account the biological characteristics of the system under study. | [
"7"
] | 280 | 9,104 | 0 | false | Additional parameters, such as the use of palindromic or direct repeat models, while not directly affecting the runtime of the centroid sampler, greatly improve its ability to discover realistic TFBS by taking into account the biological characteristics of the system under study. | [] | Additional parameters, such as the use of palindromic or direct repeat models, while not directly affecting the runtime of the centroid sampler, greatly improve its ability to discover realistic TFBS by taking into account the biological characteristics of the system under study. | true | true | true | true | true | 1,452 |
22 | INTRODUCTION | 1 | 7 | [
"B7"
] | 17,483,517 | pmid-15466295 | The program lists the total execution time for the program as the last line of the output. | [
"7"
] | 90 | 9,105 | 0 | false | The program lists the total execution time for the program as the last line of the output. | [] | The program lists the total execution time for the program as the last line of the output. | true | true | true | true | true | 1,452 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | The Gibbs Sampler Web site contains tutorials for prokaryotic phylogenetic footprinting (http://bayesweb.wadsworth.org/web_help.PF.html) and for analysis of prokaryotic co-expression data from microarray and promoter fusion experiments (http://bayesweb.wadsworth.org/web_help_text.CE.html). | [
"5",
"6",
"8",
"18"
] | 290 | 9,106 | 0 | false | The Gibbs Sampler Web site contains tutorials for prokaryotic phylogenetic footprinting (http://bayesweb.wadsworth.org/web_help.PF.html) and for analysis of prokaryotic co-expression data from microarray and promoter fusion experiments (http://bayesweb.wadsworth.org/web_help_text.CE.html). | [] | The Gibbs Sampler Web site contains tutorials for prokaryotic phylogenetic footprinting (http://bayesweb.wadsworth.org/web_help.PF.html) and for analysis of prokaryotic co-expression data from microarray and promoter fusion experiments (http://bayesweb.wadsworth.org/web_help_text.CE.html). | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | Links to these pages are provided on the main Gibbs entry pages. | [
"5",
"6",
"8",
"18"
] | 64 | 9,107 | 0 | false | Links to these pages are provided on the main Gibbs entry pages. | [] | Links to these pages are provided on the main Gibbs entry pages. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | The tutorials provide guidance to users for all the sampling modes available (site, motif, recursive and centroid), and for both the Gibbs Sampler web server and the stand-alone version of Gibbs. | [
"5",
"6",
"8",
"18"
] | 195 | 9,108 | 0 | false | The tutorials provide guidance to users for all the sampling modes available (site, motif, recursive and centroid), and for both the Gibbs Sampler web server and the stand-alone version of Gibbs. | [] | The tutorials provide guidance to users for all the sampling modes available (site, motif, recursive and centroid), and for both the Gibbs Sampler web server and the stand-alone version of Gibbs. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | Specifically, the Gibbs Sampler offers a large array of options, some of which are used to model-specific aspects of biological sequences, while others are meant to control details of how the sampling is done. | [
"5",
"6",
"8",
"18"
] | 209 | 9,109 | 0 | false | Specifically, the Gibbs Sampler offers a large array of options, some of which are used to model-specific aspects of biological sequences, while others are meant to control details of how the sampling is done. | [] | Specifically, the Gibbs Sampler offers a large array of options, some of which are used to model-specific aspects of biological sequences, while others are meant to control details of how the sampling is done. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | The tutorials focus on the options that are useful in modeling the biology of transcription regulation. | [
"5",
"6",
"8",
"18"
] | 103 | 9,110 | 0 | false | The tutorials focus on the options that are useful in modeling the biology of transcription regulation. | [] | The tutorials focus on the options that are useful in modeling the biology of transcription regulation. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | The particular examples presented in the tutorials are drawn from the studies presented in (5,6,8,18). | [
"5",
"6",
"8",
"18"
] | 102 | 9,111 | 0 | false | The particular examples presented in the tutorials are drawn from the studies presented in. | [
"5,6,8,18"
] | The particular examples presented in the tutorials are drawn from the studies presented in. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | Each tutorial gives the command line used to run the analysis, a description of each parameter and why its particular value was chosen, and a link that will automatically run the data on the Gibbs Web site with the Gibbs Centroid Sampler or with the Gibbs Recursive Sampler. | [
"5",
"6",
"8",
"18"
] | 274 | 9,112 | 0 | false | Each tutorial gives the command line used to run the analysis, a description of each parameter and why its particular value was chosen, and a link that will automatically run the data on the Gibbs Web site with the Gibbs Centroid Sampler or with the Gibbs Recursive Sampler. | [] | Each tutorial gives the command line used to run the analysis, a description of each parameter and why its particular value was chosen, and a link that will automatically run the data on the Gibbs Web site with the Gibbs Centroid Sampler or with the Gibbs Recursive Sampler. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | The data from the examples can also be downloaded to be run with the stand-alone version. | [
"5",
"6",
"8",
"18"
] | 89 | 9,113 | 0 | false | The data from the examples can also be downloaded to be run with the stand-alone version. | [] | The data from the examples can also be downloaded to be run with the stand-alone version. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | It is important to note that Gibbs sampling is a stochastic process, and thus results run from the links may differ slightly from the examples. | [
"5",
"6",
"8",
"18"
] | 143 | 9,114 | 0 | false | It is important to note that Gibbs sampling is a stochastic process, and thus results run from the links may differ slightly from the examples. | [] | It is important to note that Gibbs sampling is a stochastic process, and thus results run from the links may differ slightly from the examples. | true | true | true | true | true | 1,453 |
23 | INTRODUCTION | 1 | 5 | [
"B5",
"B6",
"B8",
"B18"
] | 17,483,517 | pmid-11160901|pmid-12368244|pmid-12933881|pmid-11416222 | In addition, although the examples in these interactive tutorials use prokaryotic sequence data, the principles described and the reasoning behind how to choose parameters are species-independent; all sampling modes, including the Gibbs Centroid Sampler, can be readily applied to the analysis of eukaryotic sequences. | [
"5",
"6",
"8",
"18"
] | 318 | 9,115 | 0 | false | In addition, although the examples in these interactive tutorials use prokaryotic sequence data, the principles described and the reasoning behind how to choose parameters are species-independent; all sampling modes, including the Gibbs Centroid Sampler, can be readily applied to the analysis of eukaryotic sequences. | [] | In addition, although the examples in these interactive tutorials use prokaryotic sequence data, the principles described and the reasoning behind how to choose parameters are species-independent; all sampling modes, including the Gibbs Centroid Sampler, can be readily applied to the analysis of eukaryotic sequences. | true | true | true | true | true | 1,453 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | The tutorials, besides presenting detailed examples of the use of the Gibbs software, provide insights into the interpretation of, and biological reasoning behind, the computational experiments. | [
"2",
"18",
"2",
"3"
] | 194 | 9,116 | 0 | false | The tutorials, besides presenting detailed examples of the use of the Gibbs software, provide insights into the interpretation of, and biological reasoning behind, the computational experiments. | [] | The tutorials, besides presenting detailed examples of the use of the Gibbs software, provide insights into the interpretation of, and biological reasoning behind, the computational experiments. | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | The tutorial examples illustrate how solutions from MAP-based samplers sometimes include low probability sites in the solution. | [
"2",
"18",
"2",
"3"
] | 127 | 9,117 | 0 | false | The tutorial examples illustrate how solutions from MAP-based samplers sometimes include low probability sites in the solution. | [] | The tutorial examples illustrate how solutions from MAP-based samplers sometimes include low probability sites in the solution. | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | These sites increase the MAP slightly but may be false positive predictions. | [
"2",
"18",
"2",
"3"
] | 76 | 9,118 | 0 | false | These sites increase the MAP slightly but may be false positive predictions. | [] | These sites increase the MAP slightly but may be false positive predictions. | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | The centroid sampler avoids these low probability predictions and is thus less likely to make false positive predictions (2). | [
"2",
"18",
"2",
"3"
] | 125 | 9,119 | 1 | false | The centroid sampler avoids these low probability predictions and is thus less likely to make false positive predictions. | [
"2"
] | The centroid sampler avoids these low probability predictions and is thus less likely to make false positive predictions. | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 18 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | This is illustrated in the tutorial example, ‘Co-expression data from a microarray study of M. tuberculosis genes’, where the data comes from microarray results (18) that report a set of co-expressed genes, a subset of which are likely co-regulated by a common transcription factor. | [
"2",
"18",
"2",
"3"
] | 282 | 9,120 | 1 | false | This is illustrated in the tutorial example, ‘Co-expression data from a microarray study of M. tuberculosis genes’, where the data comes from microarray results that report a set of co-expressed genes, a subset of which are likely co-regulated by a common transcription factor. | [
"18"
] | This is illustrated in the tutorial example, ‘Co-expression data from a microarray study of M. tuberculosis genes’, where the data comes from microarray results that report a set of co-expressed genes, a subset of which are likely co-regulated by a common transcription factor. | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | When the Gibbs Recursive Sampler is used on the upstream sequences from these co-expressed genes, the results include several sites with low probability in the MAP solution, whereas the Gibbs Centroid Sampler avoids these low probability sites. | [
"2",
"18",
"2",
"3"
] | 244 | 9,121 | 0 | false | When the Gibbs Recursive Sampler is used on the upstream sequences from these co-expressed genes, the results include several sites with low probability in the MAP solution, whereas the Gibbs Centroid Sampler avoids these low probability sites. | [] | When the Gibbs Recursive Sampler is used on the upstream sequences from these co-expressed genes, the results include several sites with low probability in the MAP solution, whereas the Gibbs Centroid Sampler avoids these low probability sites. | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | The fully Bayesian sampling process that is performed by the Gibbs Centroid Sampler is more robust at eliminating these likely false-positive predictions (2) than the process employed in previous versions of the sampler, where, once a MAP solution was found, the sampler was allowed (as an option) to sample among high p... | [
"2",
"18",
"2",
"3"
] | 397 | 9,122 | 1 | false | The fully Bayesian sampling process that is performed by the Gibbs Centroid Sampler is more robust at eliminating these likely false-positive predictions than the process employed in previous versions of the sampler, where, once a MAP solution was found, the sampler was allowed (as an option) to sample among high proba... | [
"2"
] | The fully Bayesian sampling process that is performed by the Gibbs Centroid Sampler is more robust at eliminating these likely false-positive predictions than the process employed in previous versions of the sampler, where, once a MAP solution was found, the sampler was allowed (as an option) to sample among high proba... | true | true | true | true | true | 1,454 |
24 | INTRODUCTION | 1 | 3 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | the frequency solution) (3). | [
"2",
"18",
"2",
"3"
] | 28 | 9,123 | 1 | false | the frequency solution). | [
"3"
] | the frequency solution). | false | true | true | true | false | 1,454 |
24 | INTRODUCTION | 1 | 2 | [
"B2",
"B18",
"B2",
"B3"
] | 17,483,517 | NA|pmid-11416222|NA|pmid-12824370 | Since we began using centroid estimates, we have discovered that the inclusion of steps that even partially increase focus on MAP (or near MAP) solutions have a detrimental impact on the correct identification of sites. | [
"2",
"18",
"2",
"3"
] | 219 | 9,124 | 0 | false | Since we began using centroid estimates, we have discovered that the inclusion of steps that even partially increase focus on MAP (or near MAP) solutions have a detrimental impact on the correct identification of sites. | [] | Since we began using centroid estimates, we have discovered that the inclusion of steps that even partially increase focus on MAP (or near MAP) solutions have a detrimental impact on the correct identification of sites. | true | true | true | true | true | 1,454 |
25 | INTRODUCTION | 0 | null | null | 17,483,517 | null | The Gibbs Centroid Sampler can be used for the analysis of amino-acid sequences. | null | 80 | 9,125 | 0 | false | null | null | The Gibbs Centroid Sampler can be used for the analysis of amino-acid sequences. | true | true | true | true | true | 1,455 |
25 | INTRODUCTION | 0 | null | null | 17,483,517 | null | The link from the main Gibbs Web site page leads to a page allowing the entry of amino-acid sequences. | null | 102 | 9,126 | 0 | false | null | null | The link from the main Gibbs Web site page leads to a page allowing the entry of amino-acid sequences. | true | true | true | true | true | 1,455 |
25 | INTRODUCTION | 0 | null | null | 17,483,517 | null | The Web site also contains a link to an online user guide, which describes the various parameters and their input formats, has detailed descriptions of the output and lists possible error messages and their causes. | null | 214 | 9,127 | 0 | false | null | null | The Web site also contains a link to an online user guide, which describes the various parameters and their input formats, has detailed descriptions of the output and lists possible error messages and their causes. | true | true | true | true | true | 1,455 |
25 | INTRODUCTION | 0 | null | null | 17,483,517 | null | The Gibbs Sampler Web site allows a maximum of 1000 sequences of no longer than 10,000 nucleotides in length. | null | 109 | 9,128 | 0 | false | null | null | The Gibbs Sampler Web site allows a maximum of 1000 sequences of no longer than 10,000 nucleotides in length. | true | true | true | true | true | 1,455 |
25 | INTRODUCTION | 0 | null | null | 17,483,517 | null | Users with larger datasets are directed to use the stand-alone version of the Gibbs Sampler. | null | 92 | 9,129 | 0 | false | null | null | Users with larger datasets are directed to use the stand-alone version of the Gibbs Sampler. | true | true | true | true | true | 1,455 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B1",
"B6",
"B7"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The tumor suppressor protein p53 is a sequence-specific DNA-binding transcription factor that regulates the cell cycle checkpoint pathway in response to DNA damage (1). | [
"1",
"2",
"3",
"4",
"5",
"1",
"6",
"7"
] | 168 | 9,130 | 1 | false | The tumor suppressor protein p53 is a sequence-specific DNA-binding transcription factor that regulates the cell cycle checkpoint pathway in response to DNA damage. | [
"1"
] | The tumor suppressor protein p53 is a sequence-specific DNA-binding transcription factor that regulates the cell cycle checkpoint pathway in response to DNA damage. | true | true | true | true | true | 1,456 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B1",
"B6",
"B7"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The p53 gene is the most frequent target for genetic alterations in cancer, with mutations occurring in ∼50% of all human tumors (2,3). | [
"1",
"2",
"3",
"4",
"5",
"1",
"6",
"7"
] | 135 | 9,131 | 0 | false | The p53 gene is the most frequent target for genetic alterations in cancer, with mutations occurring in ∼50% of all human tumors. | [
"2,3"
] | The p53 gene is the most frequent target for genetic alterations in cancer, with mutations occurring in ∼50% of all human tumors. | true | true | true | true | true | 1,456 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B1",
"B6",
"B7"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The tumor suppressor functions of p53 are directly linked to its ability to control the expression of gene products implicated in cell cycle arrest and apoptosis (4,5). | [
"1",
"2",
"3",
"4",
"5",
"1",
"6",
"7"
] | 168 | 9,132 | 0 | false | The tumor suppressor functions of p53 are directly linked to its ability to control the expression of gene products implicated in cell cycle arrest and apoptosis. | [
"4,5"
] | The tumor suppressor functions of p53 are directly linked to its ability to control the expression of gene products implicated in cell cycle arrest and apoptosis. | true | true | true | true | true | 1,456 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B1",
"B6",
"B7"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | p53 binds as a tetramer to specific response elements located in the transcriptional control regions of p53 target genes, which initiates the recruitment of other transcriptional co-regulators to assemble a transcriptional complex that initiates RNA synthesis (1,6). | [
"1",
"2",
"3",
"4",
"5",
"1",
"6",
"7"
] | 266 | 9,133 | 0 | false | p53 binds as a tetramer to specific response elements located in the transcriptional control regions of p53 target genes, which initiates the recruitment of other transcriptional co-regulators to assemble a transcriptional complex that initiates RNA synthesis. | [
"1,6"
] | p53 binds as a tetramer to specific response elements located in the transcriptional control regions of p53 target genes, which initiates the recruitment of other transcriptional co-regulators to assemble a transcriptional complex that initiates RNA synthesis. | false | true | true | true | false | 1,456 |
0 | INTRODUCTION | 1 | 7 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B1",
"B6",
"B7"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | A broad spectrum of p53 downstream target genes have been identified to be controlled by p53 in a positive or negative manner (7). | [
"1",
"2",
"3",
"4",
"5",
"1",
"6",
"7"
] | 130 | 9,134 | 1 | false | A broad spectrum of p53 downstream target genes have been identified to be controlled by p53 in a positive or negative manner. | [
"7"
] | A broad spectrum of p53 downstream target genes have been identified to be controlled by p53 in a positive or negative manner. | true | true | true | true | true | 1,456 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B1",
"B6",
"B7"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The fact that a variety of pathways are mediated by these p53 target genes demonstrates the role of p53 as an integrator of diverse cellular signals. | [
"1",
"2",
"3",
"4",
"5",
"1",
"6",
"7"
] | 149 | 9,135 | 0 | false | The fact that a variety of pathways are mediated by these p53 target genes demonstrates the role of p53 as an integrator of diverse cellular signals. | [] | The fact that a variety of pathways are mediated by these p53 target genes demonstrates the role of p53 as an integrator of diverse cellular signals. | true | true | true | true | true | 1,456 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B8",
"B9"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | The p53 protein contains two N-terminal activation domains, a DNA-binding domain, and a C-terminal oligomerization domain (1). | [
"1",
"8",
"9"
] | 126 | 9,136 | 1 | false | The p53 protein contains two N-terminal activation domains, a DNA-binding domain, and a C-terminal oligomerization domain. | [
"1"
] | The p53 protein contains two N-terminal activation domains, a DNA-binding domain, and a C-terminal oligomerization domain. | true | true | true | true | true | 1,457 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B8",
"B9"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | The critical step for p53-mediated transcriptional activation is facilitated by the ability of p53 to simultaneously bind to specific DNA sequences and recruit CBP/p300 and other transcriptional co-regulators to p53-responsive promoters. | [
"1",
"8",
"9"
] | 237 | 9,137 | 0 | false | The critical step for p53-mediated transcriptional activation is facilitated by the ability of p53 to simultaneously bind to specific DNA sequences and recruit CBP/p300 and other transcriptional co-regulators to p53-responsive promoters. | [] | The critical step for p53-mediated transcriptional activation is facilitated by the ability of p53 to simultaneously bind to specific DNA sequences and recruit CBP/p300 and other transcriptional co-regulators to p53-responsive promoters. | true | true | true | true | true | 1,457 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B8",
"B9"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | CBP/p300 recruitment appears to concomitantly bring the general transcription machinery, including TFIIB and TBP, and RNA polymerase II to the target promoters (8,9). | [
"1",
"8",
"9"
] | 166 | 9,138 | 0 | false | CBP/p300 recruitment appears to concomitantly bring the general transcription machinery, including TFIIB and TBP, and RNA polymerase II to the target promoters. | [
"8,9"
] | CBP/p300 recruitment appears to concomitantly bring the general transcription machinery, including TFIIB and TBP, and RNA polymerase II to the target promoters. | true | true | true | true | true | 1,457 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B8",
"B9"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | Although a wealth of information exists concerning p53, it is unclear about the actual mechanism by which this critical tumor suppressor protein directly interacts with its target genes and co-regulators to mediate its transcriptional activity. | [
"1",
"8",
"9"
] | 244 | 9,139 | 0 | false | Although a wealth of information exists concerning p53, it is unclear about the actual mechanism by which this critical tumor suppressor protein directly interacts with its target genes and co-regulators to mediate its transcriptional activity. | [] | Although a wealth of information exists concerning p53, it is unclear about the actual mechanism by which this critical tumor suppressor protein directly interacts with its target genes and co-regulators to mediate its transcriptional activity. | true | true | true | true | true | 1,457 |
2 | INTRODUCTION | 1 | 10 | [
"B10",
"B11 B12 B13",
"B14",
"B15",
"B16",
"B17 B18 B19 B20 B21 B22 B23",
"B24",
"B25"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | The PIAS proteins (protein inhibitor of activated STAT) were first identified as transcriptional co-regulators of the JAK-STAT pathway (10). | [
"10",
"11–13",
"14",
"15",
"16",
"17–23",
"24",
"25"
] | 140 | 9,140 | 1 | false | The PIAS proteins (protein inhibitor of activated STAT) were first identified as transcriptional co-regulators of the JAK-STAT pathway. | [
"10"
] | The PIAS proteins (protein inhibitor of activated STAT) were first identified as transcriptional co-regulators of the JAK-STAT pathway. | true | true | true | true | true | 1,458 |
2 | INTRODUCTION | 1 | 11–13 | [
"B10",
"B11 B12 B13",
"B14",
"B15",
"B16",
"B17 B18 B19 B20 B21 B22 B23",
"B24",
"B25"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | PIAS1 and PIAS3 can inhibit the activity of STAT1 and STAT3, respectively (11–13). | [
"10",
"11–13",
"14",
"15",
"16",
"17–23",
"24",
"25"
] | 82 | 9,141 | 1 | false | PIAS1 and PIAS3 can inhibit the activity of STAT1 and STAT3, respectively. | [
"11–13"
] | PIAS1 and PIAS3 can inhibit the activity of STAT1 and STAT3, respectively. | true | true | true | true | true | 1,458 |
2 | INTRODUCTION | 1 | 10 | [
"B10",
"B11 B12 B13",
"B14",
"B15",
"B16",
"B17 B18 B19 B20 B21 B22 B23",
"B24",
"B25"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Recent studies imply that the PIAS proteins may play a role in chromatin modulation through sumoylation (14,15). | [
"10",
"11–13",
"14",
"15",
"16",
"17–23",
"24",
"25"
] | 112 | 9,142 | 0 | false | Recent studies imply that the PIAS proteins may play a role in chromatin modulation through sumoylation. | [
"14,15"
] | Recent studies imply that the PIAS proteins may play a role in chromatin modulation through sumoylation. | true | true | true | true | true | 1,458 |
2 | INTRODUCTION | 1 | 16 | [
"B10",
"B11 B12 B13",
"B14",
"B15",
"B16",
"B17 B18 B19 B20 B21 B22 B23",
"B24",
"B25"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Sequence analysis indicates that the SUMO E3 ligase RING domain shares significant homology with the Miz domain of PIAS proteins (16). | [
"10",
"11–13",
"14",
"15",
"16",
"17–23",
"24",
"25"
] | 134 | 9,143 | 1 | false | Sequence analysis indicates that the SUMO E3 ligase RING domain shares significant homology with the Miz domain of PIAS proteins. | [
"16"
] | Sequence analysis indicates that the SUMO E3 ligase RING domain shares significant homology with the Miz domain of PIAS proteins. | true | true | true | true | true | 1,458 |
2 | INTRODUCTION | 1 | 17–23 | [
"B10",
"B11 B12 B13",
"B14",
"B15",
"B16",
"B17 B18 B19 B20 B21 B22 B23",
"B24",
"B25"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Several PIAS proteins, such as PIASxα, xβ, 1 and 3, have been shown to interact with SUMO-1 and Ubc9 to sumoylate a variety of transcriptional factors and other regulatory proteins (17–23). | [
"10",
"11–13",
"14",
"15",
"16",
"17–23",
"24",
"25"
] | 189 | 9,144 | 1 | false | Several PIAS proteins, such as PIASxα, xβ, 1 and 3, have been shown to interact with SUMO-1 and Ubc9 to sumoylate a variety of transcriptional factors and other regulatory proteins. | [
"17–23"
] | Several PIAS proteins, such as PIASxα, xβ, 1 and 3, have been shown to interact with SUMO-1 and Ubc9 to sumoylate a variety of transcriptional factors and other regulatory proteins. | true | true | true | true | true | 1,458 |
2 | INTRODUCTION | 1 | 10 | [
"B10",
"B11 B12 B13",
"B14",
"B15",
"B16",
"B17 B18 B19 B20 B21 B22 B23",
"B24",
"B25"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Particularly, it has been shown that the transcriptional activity of p53 can be regulated by PIAS through sumoylation (24,25). | [
"10",
"11–13",
"14",
"15",
"16",
"17–23",
"24",
"25"
] | 126 | 9,145 | 0 | false | Particularly, it has been shown that the transcriptional activity of p53 can be regulated by PIAS through sumoylation. | [
"24,25"
] | Particularly, it has been shown that the transcriptional activity of p53 can be regulated by PIAS through sumoylation. | true | true | true | true | true | 1,458 |
3 | INTRODUCTION | 1 | 26 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | hZimp10 and hZimp7, also named zmiz1 and zmiz2, respectively, are novel PIAS-like proteins that share a ring finger domain, termed Miz (msx-interacting zinc finger), with other PIAS proteins (26,27). | [
"26",
"27",
"15",
"28"
] | 199 | 9,146 | 0 | false | hZimp10 and hZimp7, also named zmiz1 and zmiz2, respectively, are novel PIAS-like proteins that share a ring finger domain, termed Miz (msx-interacting zinc finger), with other PIAS proteins. | [
"26,27"
] | hZimp10 and hZimp7, also named zmiz1 and zmiz2, respectively, are novel PIAS-like proteins that share a ring finger domain, termed Miz (msx-interacting zinc finger), with other PIAS proteins. | false | true | true | true | false | 1,459 |
3 | INTRODUCTION | 1 | 15 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | This domain has been shown to be important for PIAS-target protein interactions and post-translational modifications (15). | [
"26",
"27",
"15",
"28"
] | 122 | 9,147 | 1 | false | This domain has been shown to be important for PIAS-target protein interactions and post-translational modifications. | [
"15"
] | This domain has been shown to be important for PIAS-target protein interactions and post-translational modifications. | true | true | true | true | true | 1,459 |
3 | INTRODUCTION | 1 | 28 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | A novel Drosophila gene, termed tonalli (tna), appears to be the ortholog of hZimp7 and 10 (28). | [
"26",
"27",
"15",
"28"
] | 96 | 9,148 | 1 | false | A novel Drosophila gene, termed tonalli (tna), appears to be the ortholog of hZimp7 and 10. | [
"28"
] | A novel Drosophila gene, termed tonalli (tna), appears to be the ortholog of hZimp7 and 10. | true | true | true | true | true | 1,459 |
3 | INTRODUCTION | 1 | 26 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | The protein encoded by tna genetically interacts with the SWI2/SNF2 and Mediator complexes, implying a potential role for the hZimp proteins in transcription. | [
"26",
"27",
"15",
"28"
] | 158 | 9,149 | 0 | false | The protein encoded by tna genetically interacts with the SWI2/SNF2 and Mediator complexes, implying a potential role for the hZimp proteins in transcription. | [] | The protein encoded by tna genetically interacts with the SWI2/SNF2 and Mediator complexes, implying a potential role for the hZimp proteins in transcription. | true | true | true | true | true | 1,459 |
3 | INTRODUCTION | 1 | 26 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | To further explore their roles in transcription, we performed a yeast two-hybrid screen to seek out potential interacting proteins of hZimp7 and 10. | [
"26",
"27",
"15",
"28"
] | 148 | 9,150 | 0 | false | To further explore their roles in transcription, we performed a yeast two-hybrid screen to seek out potential interacting proteins of hZimp7 and 10. | [] | To further explore their roles in transcription, we performed a yeast two-hybrid screen to seek out potential interacting proteins of hZimp7 and 10. | true | true | true | true | true | 1,459 |
3 | INTRODUCTION | 1 | 26 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Intriguingly, p53 was identified in the screen. | [
"26",
"27",
"15",
"28"
] | 47 | 9,151 | 0 | false | Intriguingly, p53 was identified in the screen. | [] | Intriguingly, p53 was identified in the screen. | true | true | true | true | true | 1,459 |
3 | INTRODUCTION | 1 | 26 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Using different in vitro and in vivo approaches, we demonstrated that hZimp10 physically interacts with the p53 protein, and through the interaction hZimp10 augments p53-mediated transcription. | [
"26",
"27",
"15",
"28"
] | 193 | 9,152 | 0 | false | Using different in vitro and in vivo approaches, we demonstrated that hZimp10 physically interacts with the p53 protein, and through the interaction hZimp10 augments p53-mediated transcription. | [] | Using different in vitro and in vivo approaches, we demonstrated that hZimp10 physically interacts with the p53 protein, and through the interaction hZimp10 augments p53-mediated transcription. | true | true | true | true | true | 1,459 |
3 | INTRODUCTION | 1 | 26 | [
"B26",
"B27",
"B15",
"B28"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | These data elucidate a link between hZimp10 and p53 and demonstrate that hZimp10 is a transcriptional co-regulator of p53. | [
"26",
"27",
"15",
"28"
] | 122 | 9,153 | 0 | false | These data elucidate a link between hZimp10 and p53 and demonstrate that hZimp10 is a transcriptional co-regulator of p53. | [] | These data elucidate a link between hZimp10 and p53 and demonstrate that hZimp10 is a transcriptional co-regulator of p53. | true | true | true | true | true | 1,459 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The p53 tumor suppressor is a DNA sequence-specific transcriptional factor that is mutated in ∼50% of human tumors (3). | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 119 | 9,154 | 1 | false | The p53 tumor suppressor is a DNA sequence-specific transcriptional factor that is mutated in ∼50% of human tumors. | [
"3"
] | The p53 tumor suppressor is a DNA sequence-specific transcriptional factor that is mutated in ∼50% of human tumors. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | In response to a variety of cellular signals, perhaps the most well studied is its DNA damage function. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 103 | 9,155 | 0 | false | In response to a variety of cellular signals, perhaps the most well studied is its DNA damage function. | [] | In response to a variety of cellular signals, perhaps the most well studied is its DNA damage function. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | p53 regulates the transcription of numerous genes involved in different cellular processes, including cell cycle arrest and cell death. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 135 | 9,156 | 0 | false | p53 regulates the transcription of numerous genes involved in different cellular processes, including cell cycle arrest and cell death. | [] | p53 regulates the transcription of numerous genes involved in different cellular processes, including cell cycle arrest and cell death. | false | true | true | true | false | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | Like other transcriptional factors, the transcriptional activity of p53 is largely dependent on its ability to recognize and bind specific DNA sequences and to recruit other necessary transcriptional co-regulators. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 214 | 9,157 | 0 | false | Like other transcriptional factors, the transcriptional activity of p53 is largely dependent on its ability to recognize and bind specific DNA sequences and to recruit other necessary transcriptional co-regulators. | [] | Like other transcriptional factors, the transcriptional activity of p53 is largely dependent on its ability to recognize and bind specific DNA sequences and to recruit other necessary transcriptional co-regulators. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | In recent years, numerous transcription co-regulators have been shown to either directly or indirectly interact with p53 to modulate its transcriptional activity. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 162 | 9,158 | 0 | false | In recent years, numerous transcription co-regulators have been shown to either directly or indirectly interact with p53 to modulate its transcriptional activity. | [] | In recent years, numerous transcription co-regulators have been shown to either directly or indirectly interact with p53 to modulate its transcriptional activity. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | For instance, physical and functional interactions between p53, p300 and HAT proteins have been well documented (48,49). | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 120 | 9,159 | 0 | false | For instance, physical and functional interactions between p53, p300 and HAT proteins have been well documented. | [
"48,49"
] | For instance, physical and functional interactions between p53, p300 and HAT proteins have been well documented. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 50 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The involvement of PRMT1 and CARM1 methyltransferases has also been demonstrated in previous studies (50). | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 106 | 9,160 | 1 | false | The involvement of PRMT1 and CARM1 methyltransferases has also been demonstrated in previous studies. | [
"50"
] | The involvement of PRMT1 and CARM1 methyltransferases has also been demonstrated in previous studies. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 51 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | Importantly, p53 has been shown to facilitate formation of a preinitiation complex via direct interactions with the components of the general transcription complex (51). | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 169 | 9,161 | 1 | false | Importantly, p53 has been shown to facilitate formation of a preinitiation complex via direct interactions with the components of the general transcription complex. | [
"51"
] | Importantly, p53 has been shown to facilitate formation of a preinitiation complex via direct interactions with the components of the general transcription complex. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 26 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The experiments reported here demonstrate a specific protein–protein interaction between p53 and hZimp10, a novel PIAS-like protein (26). | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 137 | 9,162 | 1 | false | The experiments reported here demonstrate a specific protein–protein interaction between p53 and hZimp10, a novel PIAS-like protein. | [
"26"
] | The experiments reported here demonstrate a specific protein–protein interaction between p53 and hZimp10, a novel PIAS-like protein. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | The interaction was first identified by a modified yeast two-hybrid screen. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 75 | 9,163 | 0 | false | The interaction was first identified by a modified yeast two-hybrid screen. | [] | The interaction was first identified by a modified yeast two-hybrid screen. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | Using GST pull-down and immunoprecipitation assays, we then show that p53 binds to hZimp10 both in vitro and in intact cells. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 125 | 9,164 | 0 | false | Using GST pull-down and immunoprecipitation assays, we then show that p53 binds to hZimp10 both in vitro and in intact cells. | [] | Using GST pull-down and immunoprecipitation assays, we then show that p53 binds to hZimp10 both in vitro and in intact cells. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | Moreover, immunofluorescence assays demonstrated that p53 co-localizes with hZimp10 within cell nuclei. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 103 | 9,165 | 0 | false | Moreover, immunofluorescence assays demonstrated that p53 co-localizes with hZimp10 within cell nuclei. | [] | Moreover, immunofluorescence assays demonstrated that p53 co-localizes with hZimp10 within cell nuclei. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | Furthermore, analysis of the interaction by ChIP (chromatin immunoprecipitation assay) on the promoter of the p21 gene, a downstream target of p53, showed that hZimp10 is involved in the p53-mediated transcriptional complex. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 224 | 9,166 | 0 | false | Furthermore, analysis of the interaction by ChIP (chromatin immunoprecipitation assay) on the promoter of the p21 gene, a downstream target of p53, showed that hZimp10 is involved in the p53-mediated transcriptional complex. | [] | Furthermore, analysis of the interaction by ChIP (chromatin immunoprecipitation assay) on the promoter of the p21 gene, a downstream target of p53, showed that hZimp10 is involved in the p53-mediated transcriptional complex. | true | true | true | true | true | 1,460 |
0 | DISCUSSION | 1 | 3 | [
"B3",
"B48",
"B49",
"B50",
"B51",
"B26"
] | 17,584,785 | pmid-8654922|pmid-3025664|pmid-8123467|pmid-12775760|pmid-7568035|pmid-8654922|pmid-9039259|pmid-10783169|pmid-8123467|pmid-15156177|pmid-15153330|pmid-15186775|pmid-8754830|pmid-14609956 | Taken together, these multiple lines of evidence clearly indicate that p53 and hZimp10 can specifically interact in a biologically relevant manner. | [
"3",
"48",
"49",
"50",
"51",
"26"
] | 147 | 9,167 | 0 | false | Taken together, these multiple lines of evidence clearly indicate that p53 and hZimp10 can specifically interact in a biologically relevant manner. | [] | Taken together, these multiple lines of evidence clearly indicate that p53 and hZimp10 can specifically interact in a biologically relevant manner. | true | true | true | true | true | 1,460 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | To search for the biological consequence of the interaction between p53 and hZimp10, we performed a series of experiments to assess the effect of hZimp10 on p53-mediated transcription. | [
"26",
"26",
"34"
] | 184 | 9,168 | 0 | false | To search for the biological consequence of the interaction between p53 and hZimp10, we performed a series of experiments to assess the effect of hZimp10 on p53-mediated transcription. | [] | To search for the biological consequence of the interaction between p53 and hZimp10, we performed a series of experiments to assess the effect of hZimp10 on p53-mediated transcription. | true | true | true | true | true | 1,461 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | As shown in this article, hZimp10 acts as a transcriptional co-activator to augment p53-mediated transcription. | [
"26",
"26",
"34"
] | 111 | 9,169 | 0 | false | As shown in this article, hZimp10 acts as a transcriptional co-activator to augment p53-mediated transcription. | [] | As shown in this article, hZimp10 acts as a transcriptional co-activator to augment p53-mediated transcription. | true | true | true | true | true | 1,461 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | We observed that expression of exogenous hZimp10 or knockdown of endogenous hZimp10 affects p53-mediated transcription on both the p21 and Mdm2 promoters. | [
"26",
"26",
"34"
] | 154 | 9,170 | 0 | false | We observed that expression of exogenous hZimp10 or knockdown of endogenous hZimp10 affects p53-mediated transcription on both the p21 and Mdm2 promoters. | [] | We observed that expression of exogenous hZimp10 or knockdown of endogenous hZimp10 affects p53-mediated transcription on both the p21 and Mdm2 promoters. | true | true | true | true | true | 1,461 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | Introducing exogenous hZimp10 into MCF7 cells also augments endogenous p53-mediated transcription by increasing p21 transcript levels. | [
"26",
"26",
"34"
] | 134 | 9,171 | 0 | false | Introducing exogenous hZimp10 into MCF7 cells also augments endogenous p53-mediated transcription by increasing p21 transcript levels. | [] | Introducing exogenous hZimp10 into MCF7 cells also augments endogenous p53-mediated transcription by increasing p21 transcript levels. | true | true | true | true | true | 1,461 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | Interestingly, hZimp10 consistently up-regulates p53-mediated transcriptional activity in all cell contexts examined to date. | [
"26",
"26",
"34"
] | 125 | 9,172 | 0 | false | Interestingly, hZimp10 consistently up-regulates p53-mediated transcriptional activity in all cell contexts examined to date. | [] | Interestingly, hZimp10 consistently up-regulates p53-mediated transcriptional activity in all cell contexts examined to date. | true | true | true | true | true | 1,461 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | This result is consistent with the observation that hZimp10 harbors a strong intrinsic transactivation domain within its C-terminus (26). | [
"26",
"26",
"34"
] | 137 | 9,173 | 1 | false | This result is consistent with the observation that hZimp10 harbors a strong intrinsic transactivation domain within its C-terminus. | [
"26"
] | This result is consistent with the observation that hZimp10 harbors a strong intrinsic transactivation domain within its C-terminus. | true | true | true | true | true | 1,461 |
1 | DISCUSSION | 1 | 26 | [
"B26",
"B26",
"B34"
] | 17,584,785 | pmid-8654922|pmid-15171255|pmid-11782467|pmid-14609956|pmid-14609956|pmid-16777850 | It appears that through this domain hZimp10 can act as a transcriptional co-activator to augment p53-mediated transcription, which is consistent with previous observations showing that hZimp10 functions as a transcriptional co-activator of the androgen receptor and Smad3 (26,34). | [
"26",
"26",
"34"
] | 280 | 9,174 | 0 | false | It appears that through this domain hZimp10 can act as a transcriptional co-activator to augment p53-mediated transcription, which is consistent with previous observations showing that hZimp10 functions as a transcriptional co-activator of the androgen receptor and Smad3. | [
"26,34"
] | It appears that through this domain hZimp10 can act as a transcriptional co-activator to augment p53-mediated transcription, which is consistent with previous observations showing that hZimp10 functions as a transcriptional co-activator of the androgen receptor and Smad3. | true | true | true | true | true | 1,461 |
2 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | It has been shown that the transcriptional activity of p53 can be regulated by multiple post-translational modifications, including phosphorylation, ubiquitination and acetylation (52). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 185 | 9,175 | 1 | false | It has been shown that the transcriptional activity of p53 can be regulated by multiple post-translational modifications, including phosphorylation, ubiquitination and acetylation. | [
"52"
] | It has been shown that the transcriptional activity of p53 can be regulated by multiple post-translational modifications, including phosphorylation, ubiquitination and acetylation. | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | In addition, p53 can also be covalently modified by sumoylation, which is mainly regulated through SUMO-1 (Small Ubiquitin-related Modifier 1) (53,54). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 151 | 9,176 | 0 | false | In addition, p53 can also be covalently modified by sumoylation, which is mainly regulated through SUMO-1 (Small Ubiquitin-related Modifier 1). | [
"53,54"
] | In addition, p53 can also be covalently modified by sumoylation, which is mainly regulated through SUMO-1 (Small Ubiquitin-related Modifier 1). | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Recent studies have shown that PIAS proteins can bind to, sumoylate, and influence the activity of p53 (22,25). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 111 | 9,177 | 0 | false | Recent studies have shown that PIAS proteins can bind to, sumoylate, and influence the activity of p53. | [
"22,25"
] | Recent studies have shown that PIAS proteins can bind to, sumoylate, and influence the activity of p53. | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 24 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | In particular, PIAS1 and PIASxβ act as E3 ligases to enhance sumoylation of p53 in vivo and in vitro (24). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 106 | 9,178 | 1 | false | In particular, PIAS1 and PIASxβ act as E3 ligases to enhance sumoylation of p53 in vivo and in vitro. | [
"24"
] | In particular, PIAS1 and PIASxβ act as E3 ligases to enhance sumoylation of p53 in vivo and in vitro. | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 22 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Although it has been shown that PIAS proteins negatively regulate the transcriptional activity of p53 through sumoylation, recent data indicated that PIAS1 and PIAS3 may function as activators of p53-dependent gene expression (22). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 231 | 9,179 | 1 | false | Although it has been shown that PIAS proteins negatively regulate the transcriptional activity of p53 through sumoylation, recent data indicated that PIAS1 and PIAS3 may function as activators of p53-dependent gene expression. | [
"22"
] | Although it has been shown that PIAS proteins negatively regulate the transcriptional activity of p53 through sumoylation, recent data indicated that PIAS1 and PIAS3 may function as activators of p53-dependent gene expression. | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | Previously, we have shown that Zimp10 co-localizes with the AR and SUMO-1 at replication foci and enhances AR sumoylation. | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 122 | 9,180 | 0 | false | Previously, we have shown that Zimp10 co-localizes with the AR and SUMO-1 at replication foci and enhances AR sumoylation. | [] | Previously, we have shown that Zimp10 co-localizes with the AR and SUMO-1 at replication foci and enhances AR sumoylation. | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | However, the mechanism for hZimp10-mediated enhancement of p53 activity appears to be through a sumoylation-independent pathway because over-expression of hZimp10 and SUMO-1 in HEK293 cells showed no effect on sumoylation of the p53 protein (Supplementary Data). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 262 | 9,181 | 0 | false | However, the mechanism for hZimp10-mediated enhancement of p53 activity appears to be through a sumoylation-independent pathway because over-expression of hZimp10 and SUMO-1 in HEK293 cells showed no effect on sumoylation of the p53 protein (Supplementary Data). | [] | However, the mechanism for hZimp10-mediated enhancement of p53 activity appears to be through a sumoylation-independent pathway because over-expression of hZimp10 and SUMO-1 in HEK293 cells showed no effect on sumoylation of the p53 protein (Supplementary Data). | true | true | true | true | true | 1,462 |
2 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B22",
"B25",
"B24",
"B22"
] | 17,584,785 | pmid-10851063|pmid-9388184|pmid-9724754|pmid-10628744|pmid-14701874|pmid-14685683|pmid-11595179|pmid-11731472|pmid-11117529|pmid-12077349|pmid-12060666|pmid-11893729|pmid-11788578|pmid-12177000|pmid-11583632|pmid-11867732|pmid-10618704|pmid-11124955|pmid-10562558|pmid-11788578|pmid-11867732|pmid-11583632|pmid-11788578 | In addition, our results indicate that the hZimp10-mediated enhancement of p53 activity may be at least partially Miz domain-independent because the strongest interaction was observed with a hZimp10 region containing only a portion of the Miz sequence (Figure 2A). | [
"52",
"53",
"54",
"22",
"25",
"24",
"22"
] | 264 | 9,182 | 0 | false | In addition, our results indicate that the hZimp10-mediated enhancement of p53 activity may be at least partially Miz domain-independent because the strongest interaction was observed with a hZimp10 region containing only a portion of the Miz sequence (Figure 2A). | [] | In addition, our results indicate that the hZimp10-mediated enhancement of p53 activity may be at least partially Miz domain-independent because the strongest interaction was observed with a hZimp10 region containing only a portion of the Miz sequence. | true | true | true | true | true | 1,462 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Recently, we have demonstrated that both hZimp7 and hZimp10 enhance the transcriptional activity of several transcriptional factors (26,27,34,44). | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 146 | 9,183 | 0 | false | Recently, we have demonstrated that both hZimp7 and hZimp10 enhance the transcriptional activity of several transcriptional factors. | [
"26,27,34,44"
] | Recently, we have demonstrated that both hZimp7 and hZimp10 enhance the transcriptional activity of several transcriptional factors. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | However, the precise mechanism(s) for these Zimp proteins in transcriptional regulation still remains unclear. | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 110 | 9,184 | 0 | false | However, the precise mechanism(s) for these Zimp proteins in transcriptional regulation still remains unclear. | [] | However, the precise mechanism(s) for these Zimp proteins in transcriptional regulation still remains unclear. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Our previous data showing that hZimp10 co-localizes with newly synthesized DNA at replication foci throughout S phase suggest that hZimp10 may play an important role in both chromatin assembly and maintenance of chromatin (26). | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 227 | 9,185 | 1 | false | Our previous data showing that hZimp10 co-localizes with newly synthesized DNA at replication foci throughout S phase suggest that hZimp10 may play an important role in both chromatin assembly and maintenance of chromatin. | [
"26"
] | Our previous data showing that hZimp10 co-localizes with newly synthesized DNA at replication foci throughout S phase suggest that hZimp10 may play an important role in both chromatin assembly and maintenance of chromatin. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 28 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Intriguingly, a homolog of human Zimp proteins, termed tonalli (tna), has been identified in Drosophila and was shown to genetically interact with SWI2/SNF2 and the Mediator complexes in complementation studies (28). | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 216 | 9,186 | 1 | false | Intriguingly, a homolog of human Zimp proteins, termed tonalli (tna), has been identified in Drosophila and was shown to genetically interact with SWI2/SNF2 and the Mediator complexes in complementation studies. | [
"28"
] | Intriguingly, a homolog of human Zimp proteins, termed tonalli (tna), has been identified in Drosophila and was shown to genetically interact with SWI2/SNF2 and the Mediator complexes in complementation studies. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | In addition, we have shown previously that the C-terminal proline-rich domains of hZimp7 and 10 possess significant intrinsic transcriptional activity (26,27), and through these domains, the Zimp proteins can enhance transcription both in trans and in cis. | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 256 | 9,187 | 0 | false | In addition, we have shown previously that the C-terminal proline-rich domains of hZimp7 and 10 possess significant intrinsic transcriptional activity, and through these domains, the Zimp proteins can enhance transcription both in trans and in cis. | [
"26,27"
] | In addition, we have shown previously that the C-terminal proline-rich domains of hZimp7 and 10 possess significant intrinsic transcriptional activity, and through these domains, the Zimp proteins can enhance transcription both in trans and in cis. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | The finding that hZimp10 augments p53-mediated transcription is consistent with our previous studies showing that hZimp10 functions as a transcriptional co-activator of the androgen receptor and Smad3/Smad4 (26,34). | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 215 | 9,188 | 0 | false | The finding that hZimp10 augments p53-mediated transcription is consistent with our previous studies showing that hZimp10 functions as a transcriptional co-activator of the androgen receptor and Smad3/Smad4. | [
"26,34"
] | The finding that hZimp10 augments p53-mediated transcription is consistent with our previous studies showing that hZimp10 functions as a transcriptional co-activator of the androgen receptor and Smad3/Smad4. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Interestingly, the C-terminal proline-rich region is not found in other PIAS or PIAS-like proteins, suggesting that the Miz domain family may consist of distinct groups of proteins that contain unique structures and play distinct roles in regulating transcription and other cellular processes. | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 293 | 9,189 | 0 | false | Interestingly, the C-terminal proline-rich region is not found in other PIAS or PIAS-like proteins, suggesting that the Miz domain family may consist of distinct groups of proteins that contain unique structures and play distinct roles in regulating transcription and other cellular processes. | [] | Interestingly, the C-terminal proline-rich region is not found in other PIAS or PIAS-like proteins, suggesting that the Miz domain family may consist of distinct groups of proteins that contain unique structures and play distinct roles in regulating transcription and other cellular processes. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 26 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Therefore, it is conceivable that although hZimp10 and other PIAS proteins interact with p53 physically, they may regulate the function of p53 through different mechanisms. | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 172 | 9,190 | 0 | false | Therefore, it is conceivable that although hZimp10 and other PIAS proteins interact with p53 physically, they may regulate the function of p53 through different mechanisms. | [] | Therefore, it is conceivable that although hZimp10 and other PIAS proteins interact with p53 physically, they may regulate the function of p53 through different mechanisms. | true | true | true | true | true | 1,463 |
3 | DISCUSSION | 1 | 25 | [
"B26",
"B27",
"B34",
"B44",
"B26",
"B28",
"B26",
"B27",
"B26",
"B34",
"B25"
] | 17,584,785 | pmid-14609956|pmid-16051670|pmid-14685683|pmid-12466201|pmid-14609956|pmid-16051670|pmid-16777850|pmid-16862223|pmid-14609956|pmid-12466201|pmid-14609956|pmid-16051670|pmid-14609956|pmid-16777850|pmid-11867732 | Indeed, this is in agreement with our results suggesting that the Miz domain is generally dispensable for the hZimp10–p53 interaction while published reports suggest that the Miz domain is important for PIAS–p53 interactions (25). | [
"26",
"27",
"34",
"44",
"26",
"28",
"26",
"27",
"26",
"34",
"25"
] | 230 | 9,191 | 1 | false | Indeed, this is in agreement with our results suggesting that the Miz domain is generally dispensable for the hZimp10–p53 interaction while published reports suggest that the Miz domain is important for PIAS–p53 interactions. | [
"25"
] | Indeed, this is in agreement with our results suggesting that the Miz domain is generally dispensable for the hZimp10–p53 interaction while published reports suggest that the Miz domain is important for PIAS–p53 interactions. | true | true | true | true | true | 1,463 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | hZimp7 and hZimp10 share significant sequence similarity, particularly within their C-terminal regions (27). | [
"27",
"26",
"27"
] | 108 | 9,192 | 1 | false | hZimp7 and hZimp10 share significant sequence similarity, particularly within their C-terminal regions. | [
"27"
] | hZimp7 and hZimp10 share significant sequence similarity, particularly within their C-terminal regions. | false | true | true | true | false | 1,464 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | Both proteins contain an intrinsic transactivation domain and function as transcriptional co-activators (26,27). | [
"27",
"26",
"27"
] | 112 | 9,193 | 0 | false | Both proteins contain an intrinsic transactivation domain and function as transcriptional co-activators. | [
"26,27"
] | Both proteins contain an intrinsic transactivation domain and function as transcriptional co-activators. | true | true | true | true | true | 1,464 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | These two Zimp proteins show different tissue distribution profiles, which may suggest unique roles for these proteins in regulating different target genes. | [
"27",
"26",
"27"
] | 156 | 9,194 | 0 | false | These two Zimp proteins show different tissue distribution profiles, which may suggest unique roles for these proteins in regulating different target genes. | [] | These two Zimp proteins show different tissue distribution profiles, which may suggest unique roles for these proteins in regulating different target genes. | true | true | true | true | true | 1,464 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | Our recent data showing that disruption of the Zimp10 gene in mice results in embryonic lethality at approximately E10.5 suggest that hZimp7 and 10 are not functionally redundant. | [
"27",
"26",
"27"
] | 179 | 9,195 | 0 | false | Our recent data showing that disruption of the Zimp10 gene in mice results in embryonic lethality at approximately E10.5 suggest that hZimp7 and 10 are not functionally redundant. | [] | Our recent data showing that disruption of the Zimp10 gene in mice results in embryonic lethality at approximately E10.5 suggest that hZimp7 and 10 are not functionally redundant. | true | true | true | true | true | 1,464 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | In this study, even though we observed that hZimp7 interacts with p53 in a yeast two-hybrid assay, it showed no interaction between the two intact proteins in immunoprecipitation assays (see Supplementary Data). | [
"27",
"26",
"27"
] | 211 | 9,196 | 0 | false | In this study, even though we observed that hZimp7 interacts with p53 in a yeast two-hybrid assay, it showed no interaction between the two intact proteins in immunoprecipitation assays (see Supplementary Data). | [] | In this study, even though we observed that hZimp7 interacts with p53 in a yeast two-hybrid assay, it showed no interaction between the two intact proteins in immunoprecipitation assays (see Supplementary Data). | true | true | true | true | true | 1,464 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | In addition, we only observed a very weak effect of hZimp7 on p53-mediated transcription. | [
"27",
"26",
"27"
] | 89 | 9,197 | 0 | false | In addition, we only observed a very weak effect of hZimp7 on p53-mediated transcription. | [] | In addition, we only observed a very weak effect of hZimp7 on p53-mediated transcription. | true | true | true | true | true | 1,464 |
4 | DISCUSSION | 1 | 27 | [
"B27",
"B26",
"B27"
] | 17,584,785 | pmid-16051670|pmid-14609956|pmid-16051670 | These data suggest that hZimp7 and hZimp10 proteins, although structurally similar, likely play a different role in p53-mediated transcription. | [
"27",
"26",
"27"
] | 143 | 9,198 | 0 | false | These data suggest that hZimp7 and hZimp10 proteins, although structurally similar, likely play a different role in p53-mediated transcription. | [] | These data suggest that hZimp7 and hZimp10 proteins, although structurally similar, likely play a different role in p53-mediated transcription. | true | true | true | true | true | 1,464 |
5 | DISCUSSION | 0 | null | null | 17,584,785 | null | In this study, we also assessed the interaction between hZimp10 and p53 in Zimp10 null cells. | null | 93 | 9,199 | 0 | false | null | null | In this study, we also assessed the interaction between hZimp10 and p53 in Zimp10 null cells. | true | true | true | true | true | 1,465 |
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