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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
2 | INTRODUCTION | 1 | 33 | [
"B33"
] | 17,483,513 | pmid-11044999 | (C) Complementation of doxycycline (2βΞΌgβmlβ1) -induced growth phenotypes was tested on SGal-uracil plates [YCp33Supex2-CDC33 (YCp-CDC33) and YCp33Supex2-TIF4631 (YCp-TIF4631)], or on SD-uracil plates [pRS316-TIF11 (pRS-TIF11) and pRS316-FUN12 (pRS-FUN12)]. | [
"33"
] | 257 | 6,400 | 0 | false | (C) Complementation of doxycycline (2 ΞΌg mlβ1) -induced growth phenotypes was tested on SGal-uracil plates, or on SD-uracil plates [pRS316-TIF11 (pRS-TIF11) and pRS316-FUN12 (pRS-FUN12)]. | [
"YCp33Supex2-CDC33 (YCp-CDC33) and YCp33Supex2-TIF4631 (YCp-TIF4631)"
] | (C) Complementation of doxycycline (2 ΞΌg mlβ1) -induced growth phenotypes was tested on SGal-uracil plates, or on SD-uracil plates. | false | false | true | true | false | 1,052 |
3 | INTRODUCTION | 1 | 16β20 | [
"B16 B17 B18 B19 B20",
"B21 B22 B23",
"B19",
"B20",
"B24"
] | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | The functioning of living cells depends on the coordinated action of many molecular processes, including translation. | [
"16β20",
"21β23",
"19",
"20",
"24"
] | 117 | 6,401 | 0 | false | The functioning of living cells depends on the coordinated action of many molecular processes, including translation. | [] | The functioning of living cells depends on the coordinated action of many molecular processes, including translation. | true | true | true | true | true | 1,053 |
3 | INTRODUCTION | 1 | 16β20 | [
"B16 B17 B18 B19 B20",
"B21 B22 B23",
"B19",
"B20",
"B24"
] | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | However, thinking on the rate control of processes such as translation has been influenced by the expectation that control is usually determined by a single rate-limiting step. | [
"16β20",
"21β23",
"19",
"20",
"24"
] | 176 | 6,402 | 0 | false | However, thinking on the rate control of processes such as translation has been influenced by the expectation that control is usually determined by a single rate-limiting step. | [] | However, thinking on the rate control of processes such as translation has been influenced by the expectation that control is usually determined by a single rate-limiting step. | true | true | true | true | true | 1,053 |
3 | INTRODUCTION | 1 | 16β20 | [
"B16 B17 B18 B19 B20",
"B21 B22 B23",
"B19",
"B20",
"B24"
] | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | For example, it has frequently been suggested or assumed that eIF4E acts as a rate-limiting factor in translation initiation (16β20). | [
"16β20",
"21β23",
"19",
"20",
"24"
] | 133 | 6,403 | 1 | false | For example, it has frequently been suggested or assumed that eIF4E acts as a rate-limiting factor in translation initiation. | [
"16β20"
] | For example, it has frequently been suggested or assumed that eIF4E acts as a rate-limiting factor in translation initiation. | true | true | true | true | true | 1,053 |
3 | INTRODUCTION | 1 | 21β23 | [
"B16 B17 B18 B19 B20",
"B21 B22 B23",
"B19",
"B20",
"B24"
] | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | This approach to posttranscriptional gene expression probably derives from early models of metabolic control, widely disseminated in biochemistry teaching texts (21β23), in which it has been assumed that one enzyme-catalysed step would be responsible for rate control through each pathway. | [
"16β20",
"21β23",
"19",
"20",
"24"
] | 289 | 6,404 | 1 | false | This approach to posttranscriptional gene expression probably derives from early models of metabolic control, widely disseminated in biochemistry teaching texts, in which it has been assumed that one enzyme-catalysed step would be responsible for rate control through each pathway. | [
"21β23"
] | This approach to posttranscriptional gene expression probably derives from early models of metabolic control, widely disseminated in biochemistry teaching texts, in which it has been assumed that one enzyme-catalysed step would be responsible for rate control through each pathway. | true | true | true | true | true | 1,053 |
3 | INTRODUCTION | 1 | 16β20 | [
"B16 B17 B18 B19 B20",
"B21 B22 B23",
"B19",
"B20",
"B24"
] | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | On the other hand, uncertainty about the role of eIF4E in rate control has been created by contrasting observations of the effects of artificially enhanced eIF4E synthesis in primary cell cultures as opposed to cell lines (19,20,24). | [
"16β20",
"21β23",
"19",
"20",
"24"
] | 233 | 6,405 | 0 | false | On the other hand, uncertainty about the role of eIF4E in rate control has been created by contrasting observations of the effects of artificially enhanced eIF4E synthesis in primary cell cultures as opposed to cell lines. | [
"19,20,24"
] | On the other hand, uncertainty about the role of eIF4E in rate control has been created by contrasting observations of the effects of artificially enhanced eIF4E synthesis in primary cell cultures as opposed to cell lines. | true | true | true | true | true | 1,053 |
4 | INTRODUCTION | 0 | null | null | 17,483,513 | null | Up to now, translation has not been subjected to detailed quantitative control analysis, and therefore the mode of control in the translation initiation pathway could not be precisely elucidated. | null | 195 | 6,406 | 0 | false | null | null | Up to now, translation has not been subjected to detailed quantitative control analysis, and therefore the mode of control in the translation initiation pathway could not be precisely elucidated. | true | true | true | true | true | 1,054 |
4 | INTRODUCTION | 0 | null | null | 17,483,513 | null | In this article, we address the issue of rate control in the translation initiation pathway using genetic titration combined with control analysis of eIF synthesis rates in vivo. | null | 178 | 6,407 | 0 | false | null | null | In this article, we address the issue of rate control in the translation initiation pathway using genetic titration combined with control analysis of eIF synthesis rates in vivo. | true | true | true | true | true | 1,054 |
4 | INTRODUCTION | 0 | null | null | 17,483,513 | null | We have chosen to perform this work in S. cerevisiae, the eukaryotic organism with the best-defined translation system as well as the eukaryotic organism of choice for attempts to achieve comprehensive characterization of metabolic and genetic pathways in the coming years. | null | 273 | 6,408 | 0 | false | null | null | We have chosen to perform this work in S. cerevisiae, the eukaryotic organism with the best-defined translation system as well as the eukaryotic organism of choice for attempts to achieve comprehensive characterization of metabolic and genetic pathways in the coming years. | true | true | true | true | true | 1,054 |
4 | INTRODUCTION | 0 | null | null | 17,483,513 | null | Studies of this relatively simple eukaryote are far more readily integrated into coherent models of rate control than are the largely qualitative results derived from the diversity of dissimilar higher eukaryotic systems under study. | null | 233 | 6,409 | 0 | false | null | null | Studies of this relatively simple eukaryote are far more readily integrated into coherent models of rate control than are the largely qualitative results derived from the diversity of dissimilar higher eukaryotic systems under study. | true | true | true | true | true | 1,054 |
4 | INTRODUCTION | 0 | null | null | 17,483,513 | null | In our study, we find that control follows a distributed model in which all steps investigated contribute to the determination of overall rate, albeit to differing degrees. | null | 172 | 6,410 | 0 | false | null | null | In our study, we find that control follows a distributed model in which all steps investigated contribute to the determination of overall rate, albeit to differing degrees. | true | true | true | true | true | 1,054 |
4 | INTRODUCTION | 0 | null | null | 17,483,513 | null | The approach taken here has broad relevance for research on gene expression. | null | 76 | 6,411 | 0 | false | null | null | The approach taken here has broad relevance for research on gene expression. | true | true | true | true | true | 1,054 |
0 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-215319|NA|pmid-11106749|pmid-15659338|pmid-15931189|pmid-9841679 | This study has provided the first set of component control coefficients for eukaryotic translation initiation, and thus the first quantitative framework for defining how the components of this pathway collectively contribute to its overall control. | null | 248 | 6,412 | 0 | false | null | null | This study has provided the first set of component control coefficients for eukaryotic translation initiation, and thus the first quantitative framework for defining how the components of this pathway collectively contribute to its overall control. | true | true | true | true | true | 1,055 |
0 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-215319|NA|pmid-11106749|pmid-15659338|pmid-15931189|pmid-9841679 | The procedure utilized here could be applied to all of the macromolecular assembly pathways based on intermolecular interactions and different conformational states, thus building up an increasingly accurate picture of control across the network of intracellular interactions that are involved in gene expression. | null | 313 | 6,413 | 0 | false | null | null | The procedure utilized here could be applied to all of the macromolecular assembly pathways based on intermolecular interactions and different conformational states, thus building up an increasingly accurate picture of control across the network of intracellular interactions that are involved in gene expression. | true | true | true | true | true | 1,055 |
0 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-215319|NA|pmid-11106749|pmid-15659338|pmid-15931189|pmid-9841679 | Establishing this common quantitative framework for representation and modelling of the control and regulation of gene expression should be generally useful. | null | 157 | 6,414 | 0 | false | null | null | Establishing this common quantitative framework for representation and modelling of the control and regulation of gene expression should be generally useful. | true | true | true | true | true | 1,055 |
1 | DISCUSSION | 1 | 6 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | Our study illustrates how quantitative control data provide important insight into the workings of a complex biological system. | [
"6",
"41",
"16β18"
] | 127 | 6,415 | 0 | false | Our study illustrates how quantitative control data provide important insight into the workings of a complex biological system. | [] | Our study illustrates how quantitative control data provide important insight into the workings of a complex biological system. | true | true | true | true | true | 1,056 |
1 | DISCUSSION | 1 | 6 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | The data show that rate control is distributed over different steps (and different eIFs) in the initiation pathway. | [
"6",
"41",
"16β18"
] | 115 | 6,416 | 0 | false | The data show that rate control is distributed over different steps (and different eIFs) in the initiation pathway. | [] | The data show that rate control is distributed over different steps (and different eIFs) in the initiation pathway. | true | true | true | true | true | 1,056 |
1 | DISCUSSION | 1 | 6 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | It was noted previously that distributed rate control could be an inevitable consequence of the action of evolutionary βforcesβ on a pathway of this type (6). | [
"6",
"41",
"16β18"
] | 158 | 6,417 | 1 | false | It was noted previously that distributed rate control could be an inevitable consequence of the action of evolutionary βforcesβ on a pathway of this type. | [
"6"
] | It was noted previously that distributed rate control could be an inevitable consequence of the action of evolutionary βforcesβ on a pathway of this type. | true | true | true | true | true | 1,056 |
1 | DISCUSSION | 1 | 6 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | An additional outcome is that there is no simple relationship between intracellular eIF concentration and a factor's contribution to control of the system. | [
"6",
"41",
"16β18"
] | 155 | 6,418 | 0 | false | An additional outcome is that there is no simple relationship between intracellular eIF concentration and a factor's contribution to control of the system. | [] | An additional outcome is that there is no simple relationship between intracellular eIF concentration and a factor's contribution to control of the system. | true | true | true | true | true | 1,056 |
1 | DISCUSSION | 1 | 41 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | Thus, eIF4E is significantly more abundant in yeast cells than are eIF1A and eIF4G (41), yet its CJ value is far from proportionately smaller than those of these other two factors. | [
"6",
"41",
"16β18"
] | 180 | 6,419 | 1 | false | Thus, eIF4E is significantly more abundant in yeast cells than are eIF1A and eIF4G, yet its CJ value is far from proportionately smaller than those of these other two factors. | [
"41"
] | Thus, eIF4E is significantly more abundant in yeast cells than are eIF1A and eIF4G, yet its CJ value is far from proportionately smaller than those of these other two factors. | true | true | true | true | true | 1,056 |
1 | DISCUSSION | 1 | 6 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | In other words, it is unwise to base any judgments of likely control strength of a component of such a pathway on intracellular abundance alone. | [
"6",
"41",
"16β18"
] | 144 | 6,420 | 0 | false | In other words, it is unwise to base any judgments of likely control strength of a component of such a pathway on intracellular abundance alone. | [] | In other words, it is unwise to base any judgments of likely control strength of a component of such a pathway on intracellular abundance alone. | true | true | true | true | true | 1,056 |
1 | DISCUSSION | 1 | 16β18 | [
"B6",
"B41",
"B16 B17 B18"
] | 17,483,513 | pmid-10364246|NA|pmid-15164008|pmid-15240832|NA|pmid-9732867|pmid-15145951|pmid-11018020|pmid-10364246|pmid-11018020|pmid-11387228|pmid-12861028|pmid-11044999|pmid-9841679|pmid-12406227|pmid-2122455|pmid-14607835|pmid-9935150 | This consideration is also relevant to any models of disease caused by mutationally induced deficiencies in eIF function (16β18), since the quantitative data presented here show that we need to abandon the assumption that any particular eIF commands full control over the rate of the overall pathway under any particular... | [
"6",
"41",
"16β18"
] | 339 | 6,421 | 1 | false | This consideration is also relevant to any models of disease caused by mutationally induced deficiencies in eIF function, since the quantitative data presented here show that we need to abandon the assumption that any particular eIF commands full control over the rate of the overall pathway under any particular set of ... | [
"16β18"
] | This consideration is also relevant to any models of disease caused by mutationally induced deficiencies in eIF function, since the quantitative data presented here show that we need to abandon the assumption that any particular eIF commands full control over the rate of the overall pathway under any particular set of ... | true | true | true | true | true | 1,056 |
2 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-11044999 | It is of course essential to remember in a study of this type that at least eIF1A and eIF4G may act at more than one site on the initiation pathway, and thus that each CJ value for these proteins represents the sum of multi-site action. | null | 236 | 6,422 | 0 | false | null | null | It is of course essential to remember in a study of this type that at least eIF1A and eIF4G may act at more than one site on the initiation pathway, and thus that each CJ value for these proteins represents the sum of multi-site action. | true | true | true | true | true | 1,057 |
2 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-11044999 | This does not detract from the usefulness of these values as quantitative indicators of factor-centric control as manifested by the system under the defined conditions, but does mean that any mechanistic interpretation must take the multi-site functions into account. | null | 267 | 6,423 | 0 | false | null | null | This does not detract from the usefulness of these values as quantitative indicators of factor-centric control as manifested by the system under the defined conditions, but does mean that any mechanistic interpretation must take the multi-site functions into account. | true | true | true | true | true | 1,057 |
2 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-11044999 | In this context, for example, it is remarkable that despite being involved in several steps on the initiation pathway, eIF1A manifests a CJ value that is only 16% greater than that of eIF4E, a factor that is thought to have a single site of action on the pathway. | null | 263 | 6,424 | 0 | false | null | null | In this context, for example, it is remarkable that despite being involved in several steps on the initiation pathway, eIF1A manifests a CJ value that is only 16% greater than that of eIF4E, a factor that is thought to have a single site of action on the pathway. | true | true | true | true | true | 1,057 |
3 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | In relation to potential targets for regulation of translation initiation, it is notable that the comparable CJ values of three of the eIFs studied in this work make them all potentially effective sites for targeting regulation. | null | 228 | 6,425 | 0 | false | null | null | In relation to potential targets for regulation of translation initiation, it is notable that the comparable CJ values of three of the eIFs studied in this work make them all potentially effective sites for targeting regulation. | true | true | true | true | true | 1,058 |
3 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | Thus, the observation of distributed control in the translation initiation pathway also tells us not to assume that regulation is likely only to be effective if targeted to one or two of the characterized eIFs. | null | 210 | 6,426 | 0 | false | null | null | Thus, the observation of distributed control in the translation initiation pathway also tells us not to assume that regulation is likely only to be effective if targeted to one or two of the characterized eIFs. | true | true | true | true | true | 1,058 |
3 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | Finally, the current study sets the stage for comprehensive rate control analysis of this, and other, eukaryotic gene expression pathways. | null | 138 | 6,427 | 0 | false | null | null | Finally, the current study sets the stage for comprehensive rate control analysis of this, and other, eukaryotic gene expression pathways. | true | true | true | true | true | 1,058 |
3 | DISCUSSION | 0 | null | null | 17,483,513 | pmid-2122455|pmid-14607835|pmid-9935150|pmid-2348862|pmid-1396596|NA|NA|NA|pmid-2348862|pmid-1396596|pmid-16982686 | This will ultimately lead to the discovery of new general control principles that guide such systems. | null | 101 | 6,428 | 0 | false | null | null | This will ultimately lead to the discovery of new general control principles that guide such systems. | true | true | true | true | true | 1,058 |
0 | INTRODUCTION | 1 | 1 | [
"b1"
] | 17,145,716 | pmid-7574500 | SELEX (Systematic Evolution of Ligands by Exponential Enrichment) (1) is a combinatorial chemistry methodology based on oligonucleotide libraries which are screened for high-affinity binding to a given target. | [
"1"
] | 209 | 6,429 | 1 | false | SELEX (Systematic Evolution of Ligands by Exponential Enrichment) is a combinatorial chemistry methodology based on oligonucleotide libraries which are screened for high-affinity binding to a given target. | [
"1"
] | SELEX (Systematic Evolution of Ligands by Exponential Enrichment) is a combinatorial chemistry methodology based on oligonucleotide libraries which are screened for high-affinity binding to a given target. | true | true | true | true | true | 1,059 |
0 | INTRODUCTION | 1 | 1 | [
"b1"
] | 17,145,716 | pmid-7574500 | High-affinity ligands can be isolated from the library using iterative rounds affinity-based enrichment, alternating with oligonucleotide amplification. | [
"1"
] | 152 | 6,430 | 0 | false | High-affinity ligands can be isolated from the library using iterative rounds affinity-based enrichment, alternating with oligonucleotide amplification. | [] | High-affinity ligands can be isolated from the library using iterative rounds affinity-based enrichment, alternating with oligonucleotide amplification. | true | true | true | true | true | 1,059 |
0 | INTRODUCTION | 1 | 1 | [
"b1"
] | 17,145,716 | pmid-7574500 | Ligands obtained using this methodology have often been referred to as aptamers. | [
"1"
] | 80 | 6,431 | 0 | false | Ligands obtained using this methodology have often been referred to as aptamers. | [] | Ligands obtained using this methodology have often been referred to as aptamers. | true | true | true | true | true | 1,059 |
1 | INTRODUCTION | 1 | 2 | [
"b2",
"b3",
"b4",
"b5",
"b6",
"b7"
] | 17,145,716 | pmid-1741036|NA|pmid-8298130|pmid-8448147|pmid-8475124|pmid-8407909 | In 1992, Block et al. | [
"2",
"3",
"4",
"5",
"6",
"7"
] | 21 | 6,432 | 0 | false | In 1992, Block et al. | [] | In 1992, Block et al. | true | true | true | true | true | 1,060 |
1 | INTRODUCTION | 1 | 2 | [
"b2",
"b3",
"b4",
"b5",
"b6",
"b7"
] | 17,145,716 | pmid-1741036|NA|pmid-8298130|pmid-8448147|pmid-8475124|pmid-8407909 | (2) screened a pool of βΌ1013 synthetic oligonucleotides for their interaction with thrombin, which is a serine protease with multiple functions in hemostasis whose roles in coronary heart disease and other thrombotic disorders have promoted efforts toward the identification of specific inhibitors. | [
"2",
"3",
"4",
"5",
"6",
"7"
] | 298 | 6,433 | 1 | false | screened a pool of βΌ1013 synthetic oligonucleotides for their interaction with thrombin, which is a serine protease with multiple functions in hemostasis whose roles in coronary heart disease and other thrombotic disorders have promoted efforts toward the identification of specific inhibitors. | [
"2"
] | screened a pool of βΌ1013 synthetic oligonucleotides for their interaction with thrombin, which is a serine protease with multiple functions in hemostasis whose roles in coronary heart disease and other thrombotic disorders have promoted efforts toward the identification of specific inhibitors. | false | true | true | true | false | 1,060 |
1 | INTRODUCTION | 1 | 2 | [
"b2",
"b3",
"b4",
"b5",
"b6",
"b7"
] | 17,145,716 | pmid-1741036|NA|pmid-8298130|pmid-8448147|pmid-8475124|pmid-8407909 | This study led to the identification of a consensus DNA 15mer, namely 5β²GGTTGGTGTGGTTGG3β² (TBA: thrombin binding aptamer), which was found to be a potent inhibitor of thrombin with an EC50 of 20 nM in a fibrinogen clotting assay (3,4). | [
"2",
"3",
"4",
"5",
"6",
"7"
] | 235 | 6,434 | 0 | false | This study led to the identification of a consensus DNA 15mer, namely 5β²GGTTGGTGTGGTTGG3β² (TBA: thrombin binding aptamer), which was found to be a potent inhibitor of thrombin with an EC50 of 20 nM in a fibrinogen clotting assay. | [
"3,4"
] | This study led to the identification of a consensus DNA 15mer, namely 5β²GGTTGGTGTGGTTGG3β² (TBA: thrombin binding aptamer), which was found to be a potent inhibitor of thrombin with an EC50 of 20 nM in a fibrinogen clotting assay. | true | true | true | true | true | 1,060 |
1 | INTRODUCTION | 1 | 2 | [
"b2",
"b3",
"b4",
"b5",
"b6",
"b7"
] | 17,145,716 | pmid-1741036|NA|pmid-8298130|pmid-8448147|pmid-8475124|pmid-8407909 | The 3D structure of TBA was solved using NMR techniques (5,6). | [
"2",
"3",
"4",
"5",
"6",
"7"
] | 62 | 6,435 | 0 | false | The 3D structure of TBA was solved using NMR techniques. | [
"5,6"
] | The 3D structure of TBA was solved using NMR techniques. | true | true | true | true | true | 1,060 |
1 | INTRODUCTION | 1 | 2 | [
"b2",
"b3",
"b4",
"b5",
"b6",
"b7"
] | 17,145,716 | pmid-1741036|NA|pmid-8298130|pmid-8448147|pmid-8475124|pmid-8407909 | As Figure 1 shows, TBA is characterized by a chair-like structure consisting of two G-tetrads connected by two TT loops and a single TGT loop. | [
"2",
"3",
"4",
"5",
"6",
"7"
] | 142 | 6,436 | 0 | false | As Figure 1 shows, TBA is characterized by a chair-like structure consisting of two G-tetrads connected by two TT loops and a single TGT loop. | [] | As Figure 1 shows, TBA is characterized by a chair-like structure consisting of two G-tetrads connected by two TT loops and a single TGT loop. | true | true | true | true | true | 1,060 |
1 | INTRODUCTION | 1 | 7 | [
"b2",
"b3",
"b4",
"b5",
"b6",
"b7"
] | 17,145,716 | pmid-1741036|NA|pmid-8298130|pmid-8448147|pmid-8475124|pmid-8407909 | As suggested by others (7), TBA binds at the anion exosite I of thrombin in a conformation little changed from that of the unbound species. | [
"2",
"3",
"4",
"5",
"6",
"7"
] | 139 | 6,437 | 1 | false | As suggested by others, TBA binds at the anion exosite I of thrombin in a conformation little changed from that of the unbound species. | [
"7"
] | As suggested by others, TBA binds at the anion exosite I of thrombin in a conformation little changed from that of the unbound species. | true | true | true | true | true | 1,060 |
2 | INTRODUCTION | 1 | 8 | [
"b8",
"b10",
"b9",
"b10",
"b11"
] | 17,145,716 | NA|pmid-9784097|pmid-9632356|pmid-9784097|NA | In order to improve the properties of TBA, a number of researches (8β10) have been devoted to its structureβactivity relationship to post-SELEX modifications. | [
"8",
"10",
"9",
"10",
"11"
] | 158 | 6,438 | 0 | false | In order to improve the properties of TBA, a number of researches have been devoted to its structureβactivity relationship to post-SELEX modifications. | [
"8β10"
] | In order to improve the properties of TBA, a number of researches have been devoted to its structureβactivity relationship to post-SELEX modifications. | true | true | true | true | true | 1,061 |
2 | INTRODUCTION | 1 | 8 | [
"b8",
"b10",
"b9",
"b10",
"b11"
] | 17,145,716 | NA|pmid-9784097|pmid-9632356|pmid-9784097|NA | For example, He et al. | [
"8",
"10",
"9",
"10",
"11"
] | 22 | 6,439 | 0 | false | For example, He et al. | [] | For example, He et al. | true | true | true | true | true | 1,061 |
2 | INTRODUCTION | 1 | 9 | [
"b8",
"b10",
"b9",
"b10",
"b11"
] | 17,145,716 | NA|pmid-9784097|pmid-9632356|pmid-9784097|NA | (9) synthesized numerous TBA analogues containing modified guanosine carrying several substituents at 8 position or at the exocyclic amino group. | [
"8",
"10",
"9",
"10",
"11"
] | 145 | 6,440 | 1 | false | synthesized numerous TBA analogues containing modified guanosine carrying several substituents at 8 position or at the exocyclic amino group. | [
"9"
] | synthesized numerous TBA analogues containing modified guanosine carrying several substituents at 8 position or at the exocyclic amino group. | false | true | true | true | false | 1,061 |
2 | INTRODUCTION | 1 | 10 | [
"b8",
"b10",
"b9",
"b10",
"b11"
] | 17,145,716 | NA|pmid-9784097|pmid-9632356|pmid-9784097|NA | In a different paper (10), the same authors reported the synthesis and the thrombin inhibiting properties of several TBA-based oligonucleotides containing neutral formacetal linkages. | [
"8",
"10",
"9",
"10",
"11"
] | 183 | 6,441 | 1 | false | In a different paper, the same authors reported the synthesis and the thrombin inhibiting properties of several TBA-based oligonucleotides containing neutral formacetal linkages. | [
"10"
] | In a different paper, the same authors reported the synthesis and the thrombin inhibiting properties of several TBA-based oligonucleotides containing neutral formacetal linkages. | true | true | true | true | true | 1,061 |
2 | INTRODUCTION | 1 | 11 | [
"b8",
"b10",
"b9",
"b10",
"b11"
] | 17,145,716 | NA|pmid-9784097|pmid-9632356|pmid-9784097|NA | However, although TBA was the first aptamer to be discovered, no studies dealing with the effects of introduction of sites of polarity inversion have been reported yet, even if such interesting backbone alteration has already been utilized in another aptamer, namely Macugen (11) (pegaptanib sodium), that has been recen... | [
"8",
"10",
"9",
"10",
"11"
] | 413 | 6,442 | 1 | false | However, although TBA was the first aptamer to be discovered, no studies dealing with the effects of introduction of sites of polarity inversion have been reported yet, even if such interesting backbone alteration has already been utilized in another aptamer, namely Macugen (pegaptanib sodium), that has been recently a... | [
"11"
] | However, although TBA was the first aptamer to be discovered, no studies dealing with the effects of introduction of sites of polarity inversion have been reported yet, even if such interesting backbone alteration has already been utilized in another aptamer, namely Macugen (pegaptanib sodium), that has been recently a... | true | true | true | true | true | 1,061 |
3 | INTRODUCTION | 1 | 1 | [
"b1"
] | 17,145,716 | pmid-7574500 | In this frame, we have undertaken a study whose aim is to use a biologically driven approach in order to improve the knowledge of the interactions between thrombin and TBA that are critical for the biological activity. | [
"1"
] | 218 | 6,443 | 0 | false | In this frame, we have undertaken a study whose aim is to use a biologically driven approach in order to improve the knowledge of the interactions between thrombin and TBA that are critical for the biological activity. | [] | In this frame, we have undertaken a study whose aim is to use a biologically driven approach in order to improve the knowledge of the interactions between thrombin and TBA that are critical for the biological activity. | true | true | true | true | true | 1,062 |
3 | INTRODUCTION | 1 | 1 | [
"b1"
] | 17,145,716 | pmid-7574500 | Particularly, we have designed and synthesized a TBA-based oligodeoxynucleotide containing a 5β²β5β² site of polarity inversion, namely 3β²GGT5β²-5β²TGGTGTGGTTGG3β² (1). | [
"1"
] | 163 | 6,444 | 1 | false | Particularly, we have designed and synthesized a TBA-based oligodeoxynucleotide containing a 5β²β5β² site of polarity inversion, namely 3β²GGT5β²-5β²TGGTGTGGTTGG3β². | [
"1"
] | Particularly, we have designed and synthesized a TBA-based oligodeoxynucleotide containing a 5β²β5β² site of polarity inversion, namely 3β²GGT5β²-5β²TGGTGTGGTTGG3β². | true | true | true | true | true | 1,062 |
3 | INTRODUCTION | 1 | 1 | [
"b1"
] | 17,145,716 | pmid-7574500 | In this article, we report a detailed structural study, along with thermal stability analysis and a structureβactivity relationship of this new modified TBA. | [
"1"
] | 157 | 6,445 | 0 | false | In this article, we report a detailed structural study, along with thermal stability analysis and a structureβactivity relationship of this new modified TBA. | [] | In this article, we report a detailed structural study, along with thermal stability analysis and a structureβactivity relationship of this new modified TBA. | true | true | true | true | true | 1,062 |
0 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | Advanced genetics and metabolic engineering require reliable conditional gene control. | null | 86 | 6,446 | 0 | false | null | null | Advanced genetics and metabolic engineering require reliable conditional gene control. | true | true | true | true | true | 1,063 |
0 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | Unfortunately, gene disruption techniques remain difficult, applicable to a restricted set of species and strains and are particularly problematic in cases where the target gene is growth critical. | null | 197 | 6,447 | 0 | false | null | null | Unfortunately, gene disruption techniques remain difficult, applicable to a restricted set of species and strains and are particularly problematic in cases where the target gene is growth critical. | true | true | true | true | true | 1,063 |
0 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | In many eukaryotic systems, antisense and RNAi-mediated gene silencing is popular, whereas in bacteria RNAi mechanisms are absent and antisense technology is less developed and applied. | null | 185 | 6,448 | 0 | false | null | null | In many eukaryotic systems, antisense and RNAi-mediated gene silencing is popular, whereas in bacteria RNAi mechanisms are absent and antisense technology is less developed and applied. | true | true | true | true | true | 1,063 |
1 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b8",
"b9",
"b10",
"b11",
"b5",
"b9",
"b11",
"b7",
"b12",
"b13",
"b14",
"b15",
"b16"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Expressed antisense RNAs (asRNAs) appear to be suitable for conditional gene silencing in diverse bacteria (1,2) and for large scale applications. | [
"1",
"2",
"3",
"8",
"9",
"10",
"11",
"5",
"9",
"11",
"7",
"12",
"13",
"14",
"15",
"16"
] | 146 | 6,449 | 0 | false | Expressed antisense RNAs (asRNAs) appear to be suitable for conditional gene silencing in diverse bacteria and for large scale applications. | [
"1,2"
] | Expressed antisense RNAs (asRNAs) appear to be suitable for conditional gene silencing in diverse bacteria and for large scale applications. | true | true | true | true | true | 1,064 |
1 | INTRODUCTION | 1 | 11 | [
"b1",
"b2",
"b3",
"b8",
"b9",
"b10",
"b11",
"b5",
"b9",
"b11",
"b7",
"b12",
"b13",
"b14",
"b15",
"b16"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Indeed, asRNA can repress translation in diverse bacteria (3β8), and library screens have revealed effective antisense transcripts and putative new essential genes (9,10) and inhibitors (11). | [
"1",
"2",
"3",
"8",
"9",
"10",
"11",
"5",
"9",
"11",
"7",
"12",
"13",
"14",
"15",
"16"
] | 191 | 6,450 | 1 | false | Indeed, asRNA can repress translation in diverse bacteria, and library screens have revealed effective antisense transcripts and putative new essential genes and inhibitors. | [
"3β8",
"9,10",
"11"
] | Indeed, asRNA can repress translation in diverse bacteria, and library screens have revealed effective antisense transcripts and putative new essential genes and inhibitors. | true | true | true | true | true | 1,064 |
1 | INTRODUCTION | 1 | 13 | [
"b1",
"b2",
"b3",
"b8",
"b9",
"b10",
"b11",
"b5",
"b9",
"b11",
"b7",
"b12",
"b13",
"b14",
"b15",
"b16"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | The expressed asRNA method may be more efficient in Gram-positive bacteria such as Staphylococcus aureus (5,9β11) and Clostridium acetobutylicum (7,12) relative to Gram-negative bacteria, such as Escherichia coli, but reports of mixed results (13) suggest that design improvements are needed. | [
"1",
"2",
"3",
"8",
"9",
"10",
"11",
"5",
"9",
"11",
"7",
"12",
"13",
"14",
"15",
"16"
] | 292 | 6,451 | 1 | false | The expressed asRNA method may be more efficient in Gram-positive bacteria such as Staphylococcus aureus and Clostridium acetobutylicum relative to Gram-negative bacteria, such as Escherichia coli, but reports of mixed results suggest that design improvements are needed. | [
"5,9β11",
"7,12",
"13"
] | The expressed asRNA method may be more efficient in Gram-positive bacteria such as Staphylococcus aureus and Clostridium acetobutylicum relative to Gram-negative bacteria, such as Escherichia coli, but reports of mixed results suggest that design improvements are needed. | true | true | true | true | true | 1,064 |
1 | INTRODUCTION | 1 | 14 | [
"b1",
"b2",
"b3",
"b8",
"b9",
"b10",
"b11",
"b5",
"b9",
"b11",
"b7",
"b12",
"b13",
"b14",
"b15",
"b16"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Also, bacteria have endogenous asRNA regulators (14) and cell permeable modified antisense agents are efficient inhibitors (15,16). | [
"1",
"2",
"3",
"8",
"9",
"10",
"11",
"5",
"9",
"11",
"7",
"12",
"13",
"14",
"15",
"16"
] | 131 | 6,452 | 1 | false | Also, bacteria have endogenous asRNA regulators and cell permeable modified antisense agents are efficient inhibitors. | [
"14",
"15,16"
] | Also, bacteria have endogenous asRNA regulators and cell permeable modified antisense agents are efficient inhibitors. | true | true | true | true | true | 1,064 |
1 | INTRODUCTION | 1 | 1 | [
"b1",
"b2",
"b3",
"b8",
"b9",
"b10",
"b11",
"b5",
"b9",
"b11",
"b7",
"b12",
"b13",
"b14",
"b15",
"b16"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Therefore, achieving improved antisense silencing in E.coli appears to be largely a technical challenge. | [
"1",
"2",
"3",
"8",
"9",
"10",
"11",
"5",
"9",
"11",
"7",
"12",
"13",
"14",
"15",
"16"
] | 104 | 6,453 | 0 | false | Therefore, achieving improved antisense silencing in E.coli appears to be largely a technical challenge. | [] | Therefore, achieving improved antisense silencing in E.coli appears to be largely a technical challenge. | true | true | true | true | true | 1,064 |
2 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-14633993|pmid-9367744 | Here we found that a simple paired-termini (PT) design stabilizes asRNA cassettes and enhances conditional gene silencing in E.coli. | null | 132 | 6,454 | 0 | false | null | null | Here we found that a simple paired-termini (PT) design stabilizes asRNA cassettes and enhances conditional gene silencing in E.coli. | true | true | true | true | true | 1,065 |
2 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-14633993|pmid-9367744 | Two well-characterized and tractable genes were targeted using a range of design variants. | null | 90 | 6,455 | 0 | false | null | null | Two well-characterized and tractable genes were targeted using a range of design variants. | true | true | true | true | true | 1,065 |
2 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-14633993|pmid-9367744 | The results show that PTasRNAs are stabilized, accumulate following induction and provide reliable gene inhibition that is sufficient to alter growth phenotypes. | null | 161 | 6,456 | 0 | false | null | null | The results show that PTasRNAs are stabilized, accumulate following induction and provide reliable gene inhibition that is sufficient to alter growth phenotypes. | true | true | true | true | true | 1,065 |
2 | INTRODUCTION | 0 | null | null | 17,062,631 | pmid-14633993|pmid-9367744 | The approach is compatible with comprehensive forward and reverse RNA-level genetics of both essential and non-essential bacterial genes and there are potential applications in pharmaceutical discovery and metabolic engineering. | null | 228 | 6,457 | 0 | false | null | null | The approach is compatible with comprehensive forward and reverse RNA-level genetics of both essential and non-essential bacterial genes and there are potential applications in pharmaceutical discovery and metabolic engineering. | true | true | true | true | true | 1,065 |
0 | DISCUSSION | 1 | 2 | [
"b2",
"b6",
"b4",
"b39"
] | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | PT asRNAs provide improved gene silencing tools for E.coli. | [
"2",
"6",
"4",
"39"
] | 59 | 6,458 | 0 | false | PT asRNAs provide improved gene silencing tools for E.coli. | [] | PT asRNAs provide improved gene silencing tools for E.coli. | true | true | true | true | true | 1,066 |
0 | DISCUSSION | 1 | 4 | [
"b2",
"b6",
"b4",
"b39"
] | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | Bacterial RNAs are typically short lived, and there is evidence that half-life is an important factor in asRNA efficacy (2,6) and that a molar excess of asRNAs (and ribozymes) is required for efficient inhibition (4). | [
"2",
"6",
"4",
"39"
] | 217 | 6,459 | 1 | false | Bacterial RNAs are typically short lived, and there is evidence that half-life is an important factor in asRNA efficacy and that a molar excess of asRNAs (and ribozymes) is required for efficient inhibition. | [
"2,6",
"4"
] | Bacterial RNAs are typically short lived, and there is evidence that half-life is an important factor in asRNA efficacy and that a molar excess of asRNAs (and ribozymes) is required for efficient inhibition. | true | true | true | true | true | 1,066 |
0 | DISCUSSION | 1 | 2 | [
"b2",
"b6",
"b4",
"b39"
] | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | An excess relative abundance should enable asRNAs to efficiently out-compete ribosomes at target RNAs. | [
"2",
"6",
"4",
"39"
] | 102 | 6,460 | 0 | false | An excess relative abundance should enable asRNAs to efficiently out-compete ribosomes at target RNAs. | [] | An excess relative abundance should enable asRNAs to efficiently out-compete ribosomes at target RNAs. | true | true | true | true | true | 1,066 |
0 | DISCUSSION | 1 | 2 | [
"b2",
"b6",
"b4",
"b39"
] | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | Therefore, the improved efficacy of PTasRNAs appears to be due to improved stability, which raises asRNA abundance. | [
"2",
"6",
"4",
"39"
] | 115 | 6,461 | 0 | false | Therefore, the improved efficacy of PTasRNAs appears to be due to improved stability, which raises asRNA abundance. | [] | Therefore, the improved efficacy of PTasRNAs appears to be due to improved stability, which raises asRNA abundance. | true | true | true | true | true | 1,066 |
0 | DISCUSSION | 1 | 2 | [
"b2",
"b6",
"b4",
"b39"
] | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | Also, it is possible that termini pairing aids target recognition by constraining the folded RNA. | [
"2",
"6",
"4",
"39"
] | 97 | 6,462 | 0 | false | Also, it is possible that termini pairing aids target recognition by constraining the folded RNA. | [] | Also, it is possible that termini pairing aids target recognition by constraining the folded RNA. | true | true | true | true | true | 1,066 |
0 | DISCUSSION | 1 | 39 | [
"b2",
"b6",
"b4",
"b39"
] | 17,062,631 | pmid-9241234|pmid-11258619|pmid-9131620|pmid-12975324 | Finally, following mRNA recognition, PTasRNAs may trigger intrinsic decay mechanisms (39), which are apparently independent of RNase III, but may involve RNase E, or other RNases. | [
"2",
"6",
"4",
"39"
] | 179 | 6,463 | 1 | false | Finally, following mRNA recognition, PTasRNAs may trigger intrinsic decay mechanisms, which are apparently independent of RNase III, but may involve RNase E, or other RNases. | [
"39"
] | Finally, following mRNA recognition, PTasRNAs may trigger intrinsic decay mechanisms, which are apparently independent of RNase III, but may involve RNase E, or other RNases. | true | true | true | true | true | 1,066 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | PTasRNAs are effective, yet we suspect that further improvements are possible. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 78 | 6,464 | 0 | false | PTasRNAs are effective, yet we suspect that further improvements are possible. | [] | PTasRNAs are effective, yet we suspect that further improvements are possible. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | For example, target site position and length issues are not well addressed here, nor in the literature, although it is clear that target selection is an important factor. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 170 | 6,465 | 0 | false | For example, target site position and length issues are not well addressed here, nor in the literature, although it is clear that target selection is an important factor. | [] | For example, target site position and length issues are not well addressed here, nor in the literature, although it is clear that target selection is an important factor. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 11 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Most natural asRNAs target the translation initiation region (40,41), and we suspect that this region is a reasonable choice for most genes, but other susceptible regions exist (11). | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 182 | 6,466 | 1 | false | Most natural asRNAs target the translation initiation region, and we suspect that this region is a reasonable choice for most genes, but other susceptible regions exist. | [
"40,41",
"11"
] | Most natural asRNAs target the translation initiation region, and we suspect that this region is a reasonable choice for most genes, but other susceptible regions exist. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 6 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Successful asRNA cassettes as short as 12mer have been reported (6); however, in the absence of knowledge about target accessibility, we favor larger antisense cassettes, which are more likely to contain structures that efficiently seed hybridization. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 251 | 6,467 | 1 | false | Successful asRNA cassettes as short as 12mer have been reported ; however, in the absence of knowledge about target accessibility, we favor larger antisense cassettes, which are more likely to contain structures that efficiently seed hybridization. | [
"6"
] | Successful asRNA cassettes as short as 12mer have been reported ; however, in the absence of knowledge about target accessibility, we favor larger antisense cassettes, which are more likely to contain structures that efficiently seed hybridization. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Indeed, we found that the inhibition efficiency of a 147 base cassette exceeded that of a 29 base cassette (Figure 2C). | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 119 | 6,468 | 0 | false | Indeed, we found that the inhibition efficiency of a 147 base cassette exceeded that of a 29 base cassette (Figure 2C). | [] | Indeed, we found that the inhibition efficiency of a 147 base cassette exceeded that of a 29 base cassette (Figure 2C). | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Further comparisons are needed on this issue, and target accessibility prediction tools (12,42) may be helpful. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 111 | 6,469 | 0 | false | Further comparisons are needed on this issue, and target accessibility prediction tools may be helpful. | [
"12,42"
] | Further comparisons are needed on this issue, and target accessibility prediction tools may be helpful. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Also, recAβ strains showed more stable inhibition (data not shown) and we observed improved results in solid media relative to liquid media, possibly due to plasmid stability problems in liquid culture. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 202 | 6,470 | 0 | false | Also, recAβ strains showed more stable inhibition (data not shown) and we observed improved results in solid media relative to liquid media, possibly due to plasmid stability problems in liquid culture. | [] | Also, recAβ strains showed more stable inhibition (data not shown) and we observed improved results in solid media relative to liquid media, possibly due to plasmid stability problems in liquid culture. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 43 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Plasmid stability is a common problem, and plasmids containing growth inhibitory sequences and long inverted repeats may be unstable (43). | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 138 | 6,471 | 1 | false | Plasmid stability is a common problem, and plasmids containing growth inhibitory sequences and long inverted repeats may be unstable. | [
"43"
] | Plasmid stability is a common problem, and plasmids containing growth inhibitory sequences and long inverted repeats may be unstable. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Therefore, PT length should be the minimum that provides asRNA stability without compromising plasmid stability. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 112 | 6,472 | 0 | false | Therefore, PT length should be the minimum that provides asRNA stability without compromising plasmid stability. | [] | Therefore, PT length should be the minimum that provides asRNA stability without compromising plasmid stability. | true | true | true | true | true | 1,067 |
1 | DISCUSSION | 1 | 40 | [
"b40",
"b41",
"b11",
"b6",
"b12",
"b42",
"b43"
] | 17,062,631 | pmid-12057690|pmid-9241234|pmid-12889024|pmid-10849423|pmid-11567142|pmid-11952893|pmid-16436705|pmid-14987762|pmid-11567142|pmid-16436705|pmid-10049845|pmid-12618456|pmid-12047936|pmid-11931231|pmid-16870773|pmid-11283595|pmid-15914490|pmid-12827275|pmid-16436705|pmid-11258619|pmid-12618456|pmid-15215366|pmid-3302612 | Therefore, while the PT design proved effective against all genes and in all strains tested, it is clear that plasmid stability requires attention. | [
"40",
"41",
"11",
"6",
"12",
"42",
"43"
] | 147 | 6,473 | 0 | false | Therefore, while the PT design proved effective against all genes and in all strains tested, it is clear that plasmid stability requires attention. | [] | Therefore, while the PT design proved effective against all genes and in all strains tested, it is clear that plasmid stability requires attention. | true | true | true | true | true | 1,067 |
2 | DISCUSSION | 1 | 44 | [
"b44",
"b45"
] | 17,062,631 | pmid-14633993|pmid-9367744 | The effects of PTasRNAs may reflect the action of certain natural RNAs. | [
"44",
"45"
] | 71 | 6,474 | 0 | false | The effects of PTasRNAs may reflect the action of certain natural RNAs. | [] | The effects of PTasRNAs may reflect the action of certain natural RNAs. | true | true | true | true | true | 1,068 |
2 | DISCUSSION | 1 | 44 | [
"b44",
"b45"
] | 17,062,631 | pmid-14633993|pmid-9367744 | For example, natural asRNAs are also stabilized by paired sequences, and in the case of the FinP natural asRNA, stability and target interaction is promoted by the RNA chaperone FinO recognition of paired sequences (44). | [
"44",
"45"
] | 220 | 6,475 | 1 | false | For example, natural asRNAs are also stabilized by paired sequences, and in the case of the FinP natural asRNA, stability and target interaction is promoted by the RNA chaperone FinO recognition of paired sequences. | [
"44"
] | For example, natural asRNAs are also stabilized by paired sequences, and in the case of the FinP natural asRNA, stability and target interaction is promoted by the RNA chaperone FinO recognition of paired sequences. | true | true | true | true | true | 1,068 |
2 | DISCUSSION | 1 | 45 | [
"b44",
"b45"
] | 17,062,631 | pmid-14633993|pmid-9367744 | Also, the R1 plasmid encoded Hok toxin mRNA is processed into a stable isoform with perfectly matched PT (45). | [
"44",
"45"
] | 110 | 6,476 | 1 | false | Also, the R1 plasmid encoded Hok toxin mRNA is processed into a stable isoform with perfectly matched PT. | [
"45"
] | Also, the R1 plasmid encoded Hok toxin mRNA is processed into a stable isoform with perfectly matched PT. | true | true | true | true | true | 1,068 |
2 | DISCUSSION | 1 | 44 | [
"b44",
"b45"
] | 17,062,631 | pmid-14633993|pmid-9367744 | Therefore, PTasRNA effects may reflect endogenous mechanisms for stabilizing RNA and promoting interactions. | [
"44",
"45"
] | 108 | 6,477 | 0 | false | Therefore, PTasRNA effects may reflect endogenous mechanisms for stabilizing RNA and promoting interactions. | [] | Therefore, PTasRNA effects may reflect endogenous mechanisms for stabilizing RNA and promoting interactions. | true | true | true | true | true | 1,068 |
3 | DISCUSSION | 1 | 46 | [
"b46",
"b11",
"b40",
"b47",
"b48",
"b49"
] | 17,062,631 | pmid-16496020|pmid-16436705|pmid-15914490|pmid-16710421|pmid-11976303|pmid-12794188 | The PTasRNA design provides a framework to optimize and apply asRNA gene silencing in many applications. | [
"46",
"11",
"40",
"47",
"48",
"49"
] | 104 | 6,478 | 0 | false | The PTasRNA design provides a framework to optimize and apply asRNA gene silencing in many applications. | [] | The PTasRNA design provides a framework to optimize and apply asRNA gene silencing in many applications. | true | true | true | true | true | 1,069 |
3 | DISCUSSION | 1 | 46 | [
"b46",
"b11",
"b40",
"b47",
"b48",
"b49"
] | 17,062,631 | pmid-16496020|pmid-16436705|pmid-15914490|pmid-16710421|pmid-11976303|pmid-12794188 | Forward and reverse RNA level genetics can be considered (46), and there are potential applications in pharmaceutical discovery and metabolic engineering. | [
"46",
"11",
"40",
"47",
"48",
"49"
] | 154 | 6,479 | 1 | false | Forward and reverse RNA level genetics can be considered, and there are potential applications in pharmaceutical discovery and metabolic engineering. | [
"46"
] | Forward and reverse RNA level genetics can be considered, and there are potential applications in pharmaceutical discovery and metabolic engineering. | true | true | true | true | true | 1,069 |
3 | DISCUSSION | 1 | 46 | [
"b46",
"b11",
"b40",
"b47",
"b48",
"b49"
] | 17,062,631 | pmid-16496020|pmid-16436705|pmid-15914490|pmid-16710421|pmid-11976303|pmid-12794188 | For example, improved conditional redirection of metabolic flux could enhance metabolic engineering, and here we show that ackA asRNA induction in mid-growth phase increases heterologous gene expression. | [
"46",
"11",
"40",
"47",
"48",
"49"
] | 203 | 6,480 | 0 | false | For example, improved conditional redirection of metabolic flux could enhance metabolic engineering, and here we show that ackA asRNA induction in mid-growth phase increases heterologous gene expression. | [] | For example, improved conditional redirection of metabolic flux could enhance metabolic engineering, and here we show that ackA asRNA induction in mid-growth phase increases heterologous gene expression. | true | true | true | true | true | 1,069 |
3 | DISCUSSION | 1 | 47 | [
"b46",
"b11",
"b40",
"b47",
"b48",
"b49"
] | 17,062,631 | pmid-16496020|pmid-16436705|pmid-15914490|pmid-16710421|pmid-11976303|pmid-12794188 | Also, silencing of essential genes can aid discovery of much needed new antimicrobials (11,40), as demonstrated recently with the discovery of platensimycin (47), and here we show improved drug target silencing and inhibitor sensitization. | [
"46",
"11",
"40",
"47",
"48",
"49"
] | 239 | 6,481 | 1 | false | Also, silencing of essential genes can aid discovery of much needed new antimicrobials, as demonstrated recently with the discovery of platensimycin, and here we show improved drug target silencing and inhibitor sensitization. | [
"11,40",
"47"
] | Also, silencing of essential genes can aid discovery of much needed new antimicrobials, as demonstrated recently with the discovery of platensimycin, and here we show improved drug target silencing and inhibitor sensitization. | true | true | true | true | true | 1,069 |
3 | DISCUSSION | 1 | 46 | [
"b46",
"b11",
"b40",
"b47",
"b48",
"b49"
] | 17,062,631 | pmid-16496020|pmid-16436705|pmid-15914490|pmid-16710421|pmid-11976303|pmid-12794188 | Finally, for applications in other bacterial species, interspecies differences in asRNA and RNase activities (48,49) should be considered, but we suspect that the PT design and information about the stability and abundance of asRNAs will enable improved silencing. | [
"46",
"11",
"40",
"47",
"48",
"49"
] | 264 | 6,482 | 0 | false | Finally, for applications in other bacterial species, interspecies differences in asRNA and RNase activities should be considered, but we suspect that the PT design and information about the stability and abundance of asRNAs will enable improved silencing. | [
"48,49"
] | Finally, for applications in other bacterial species, interspecies differences in asRNA and RNase activities should be considered, but we suspect that the PT design and information about the stability and abundance of asRNAs will enable improved silencing. | true | true | true | true | true | 1,069 |
0 | INTRODUCTION | 1 | 1β4 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8 B9 B10"
] | 17,251,194 | pmid-11733745|pmid-15539566|pmid-16141072|pmid-16651366|pmid-15372042|pmid-14744438|pmid-15211354|pmid-16751776|pmid-16751777|pmid-16882976|pmid-1594442|pmid-10429245 | The completion of the genome projects of human and other model organisms provides us with an initial step towards deep understanding of various biological processes. | [
"1β4",
"5β7",
"8β10"
] | 165 | 6,483 | 0 | false | The completion of the genome projects of human and other model organisms provides us with an initial step towards deep understanding of various biological processes. | [] | The completion of the genome projects of human and other model organisms provides us with an initial step towards deep understanding of various biological processes. | true | true | true | true | true | 1,070 |
0 | INTRODUCTION | 1 | 1β4 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8 B9 B10"
] | 17,251,194 | pmid-11733745|pmid-15539566|pmid-16141072|pmid-16651366|pmid-15372042|pmid-14744438|pmid-15211354|pmid-16751776|pmid-16751777|pmid-16882976|pmid-1594442|pmid-10429245 | One of the striking findings from genome analyses is the presence of diverse classes of transcripts which do not encode protein products, the non-coding RNAs (ncRNAs) (1β4). | [
"1β4",
"5β7",
"8β10"
] | 173 | 6,484 | 1 | false | One of the striking findings from genome analyses is the presence of diverse classes of transcripts which do not encode protein products, the non-coding RNAs (ncRNAs). | [
"1β4"
] | One of the striking findings from genome analyses is the presence of diverse classes of transcripts which do not encode protein products, the non-coding RNAs (ncRNAs). | true | true | true | true | true | 1,070 |
0 | INTRODUCTION | 1 | 1β4 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8 B9 B10"
] | 17,251,194 | pmid-11733745|pmid-15539566|pmid-16141072|pmid-16651366|pmid-15372042|pmid-14744438|pmid-15211354|pmid-16751776|pmid-16751777|pmid-16882976|pmid-1594442|pmid-10429245 | In addition to classical ncRNAs, such as tRNA, rRNA, snRNA and snoRNA, newly identified ncRNAs include microRNAs (miRNAs), endogenous small interfering RNAs (siRNAs), natural anti-sense transcripts and mRNA-like ncRNAs. | [
"1β4",
"5β7",
"8β10"
] | 219 | 6,485 | 0 | false | In addition to classical ncRNAs, such as tRNA, rRNA, snRNA and snoRNA, newly identified ncRNAs include microRNAs (miRNAs), endogenous small interfering RNAs (siRNAs), natural anti-sense transcripts and mRNA-like ncRNAs. | [] | In addition to classical ncRNAs, such as tRNA, rRNA, snRNA and snoRNA, newly identified ncRNAs include microRNAs (miRNAs), endogenous small interfering RNAs (siRNAs), natural anti-sense transcripts and mRNA-like ncRNAs. | true | true | true | true | true | 1,070 |
0 | INTRODUCTION | 1 | 5β7 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8 B9 B10"
] | 17,251,194 | pmid-11733745|pmid-15539566|pmid-16141072|pmid-16651366|pmid-15372042|pmid-14744438|pmid-15211354|pmid-16751776|pmid-16751777|pmid-16882976|pmid-1594442|pmid-10429245 | The miRNAs, a class of well characterized small RNAs found in both plants and animals, are involved primarily in development and cell differentiation and function as negative regulators of gene expression through translational repression and/or mRNA cleavage by a mechanism similar to RNA interference (RNAi) (5β7). | [
"1β4",
"5β7",
"8β10"
] | 315 | 6,486 | 1 | false | The miRNAs, a class of well characterized small RNAs found in both plants and animals, are involved primarily in development and cell differentiation and function as negative regulators of gene expression through translational repression and/or mRNA cleavage by a mechanism similar to RNA interference (RNAi). | [
"5β7"
] | The miRNAs, a class of well characterized small RNAs found in both plants and animals, are involved primarily in development and cell differentiation and function as negative regulators of gene expression through translational repression and/or mRNA cleavage by a mechanism similar to RNA interference (RNAi). | true | true | true | true | true | 1,070 |
0 | INTRODUCTION | 1 | 8β10 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8 B9 B10"
] | 17,251,194 | pmid-11733745|pmid-15539566|pmid-16141072|pmid-16651366|pmid-15372042|pmid-14744438|pmid-15211354|pmid-16751776|pmid-16751777|pmid-16882976|pmid-1594442|pmid-10429245 | Recently, germline-specific small RNAs were identified as another class of ncRNAs (8β10). | [
"1β4",
"5β7",
"8β10"
] | 89 | 6,487 | 1 | false | Recently, germline-specific small RNAs were identified as another class of ncRNAs. | [
"8β10"
] | Recently, germline-specific small RNAs were identified as another class of ncRNAs. | true | true | true | true | true | 1,070 |
0 | INTRODUCTION | 1 | 1β4 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8 B9 B10"
] | 17,251,194 | pmid-11733745|pmid-15539566|pmid-16141072|pmid-16651366|pmid-15372042|pmid-14744438|pmid-15211354|pmid-16751776|pmid-16751777|pmid-16882976|pmid-1594442|pmid-10429245 | Understanding the mechanisms by which ncRNAs function as regulatory elements will reveal a global picture of cellular and molecular networks connecting the transcriptome, proteome, interactome and epigenetics of the cell. | [
"1β4",
"5β7",
"8β10"
] | 221 | 6,488 | 0 | false | Understanding the mechanisms by which ncRNAs function as regulatory elements will reveal a global picture of cellular and molecular networks connecting the transcriptome, proteome, interactome and epigenetics of the cell. | [] | Understanding the mechanisms by which ncRNAs function as regulatory elements will reveal a global picture of cellular and molecular networks connecting the transcriptome, proteome, interactome and epigenetics of the cell. | true | true | true | true | true | 1,070 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | Post-transcriptional maturation of RNA molecules includes various processing events, such as capping, splicing, polyadenylation, modification, editing, 5β²- and/or 3β²-end processing, which take place in a spatiotemporal sequence. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 228 | 6,489 | 0 | false | Post-transcriptional maturation of RNA molecules includes various processing events, such as capping, splicing, polyadenylation, modification, editing, 5β²- and/or 3β²-end processing, which take place in a spatiotemporal sequence. | [] | Post-transcriptional maturation of RNA molecules includes various processing events, such as capping, splicing, polyadenylation, modification, editing, 5β²- and/or 3β²-end processing, which take place in a spatiotemporal sequence. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | According to studies of classical ncRNAs, various post-transcriptional processing events are important for correct folding, interaction and assembly with proteins, and determination of subcellular localization, so as to execute the proper functions of the RNAs. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 261 | 6,490 | 0 | false | According to studies of classical ncRNAs, various post-transcriptional processing events are important for correct folding, interaction and assembly with proteins, and determination of subcellular localization, so as to execute the proper functions of the RNAs. | [] | According to studies of classical ncRNAs, various post-transcriptional processing events are important for correct folding, interaction and assembly with proteins, and determination of subcellular localization, so as to execute the proper functions of the RNAs. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | Additionally, RNA modification (or editing) is a characteristic structural feature of ncRNAs. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 93 | 6,491 | 0 | false | Additionally, RNA modification (or editing) is a characteristic structural feature of ncRNAs. | [] | Additionally, RNA modification (or editing) is a characteristic structural feature of ncRNAs. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | To date, more than 100 different RNA modifications have been reported in many RNA molecules from all types of living organisms (11). | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 132 | 6,492 | 1 | false | To date, more than 100 different RNA modifications have been reported in many RNA molecules from all types of living organisms. | [
"11"
] | To date, more than 100 different RNA modifications have been reported in many RNA molecules from all types of living organisms. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | Most of these modifications have been found in abundant RNA molecules that have been isolated and analyzed, such as tRNAs, rRNAs or UsnRNAs. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 140 | 6,493 | 0 | false | Most of these modifications have been found in abundant RNA molecules that have been isolated and analyzed, such as tRNAs, rRNAs or UsnRNAs. | [] | Most of these modifications have been found in abundant RNA molecules that have been isolated and analyzed, such as tRNAs, rRNAs or UsnRNAs. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | However, it has been reported that even miRNAs are modified. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 60 | 6,494 | 0 | false | However, it has been reported that even miRNAs are modified. | [] | However, it has been reported that even miRNAs are modified. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 14 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | Plant miRNAs display 2β²-O-methylation of the 3β²-end nucleoside (12,13), which is required for normal miRNA maturation (14). | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 123 | 6,495 | 1 | false | Plant miRNAs display 2β²-O-methylation of the 3β²-end nucleoside, which is required for normal miRNA maturation. | [
"12,13",
"14"
] | Plant miRNAs display 2β²-O-methylation of the 3β²-end nucleoside, which is required for normal miRNA maturation. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 15 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | A recent study revealed that drosophila rasiRNA contains an unidentified modification of the 3β²-end (15). | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 105 | 6,496 | 1 | false | A recent study revealed that drosophila rasiRNA contains an unidentified modification of the 3β²-end. | [
"15"
] | A recent study revealed that drosophila rasiRNA contains an unidentified modification of the 3β²-end. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 16β18 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | A fraction of mammalian miRNAs (βΌ6%) contain inosine (I) which is produced in pre-miRNAs by A-to-I editing (16β18). | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 115 | 6,497 | 1 | false | A fraction of mammalian miRNAs (βΌ6%) contain inosine (I) which is produced in pre-miRNAs by A-to-I editing. | [
"16β18"
] | A fraction of mammalian miRNAs contain inosine (I) which is produced in pre-miRNAs by A-to-I editing. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | These observations indicate that RNA modifications are general and ubiquitous events during RNA maturation. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 107 | 6,498 | 0 | false | These observations indicate that RNA modifications are general and ubiquitous events during RNA maturation. | [] | These observations indicate that RNA modifications are general and ubiquitous events during RNA maturation. | true | true | true | true | true | 1,071 |
1 | INTRODUCTION | 1 | 11 | [
"B11",
"B12",
"B13",
"B14",
"B15",
"B16 B17 B18"
] | 17,251,194 | pmid-9847178|pmid-15705854|pmid-16449203|pmid-16111943|pmid-16809489|pmid-16594986|pmid-16369484|pmid-15272117|pmid-16683135 | Cellular RNAs can be detected by various hybridization-based techniques, including Northern hybridization, microarray technology and reverse transcription (RT)-PCR. | [
"11",
"12",
"13",
"14",
"15",
"16β18"
] | 164 | 6,499 | 0 | false | Cellular RNAs can be detected by various hybridization-based techniques, including Northern hybridization, microarray technology and reverse transcription (RT)-PCR. | [] | Cellular RNAs can be detected by various hybridization-based techniques, including Northern hybridization, microarray technology and reverse transcription (RT)-PCR. | true | true | true | true | true | 1,071 |
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