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 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | This phenomenon may be attributed to NO-caused impaired nuclear import of APE1 that helped in preventing the already exported APE1 from reimporting into nucleus. | [
"51"
] | 161 | 10,100 | 0 | false | This phenomenon may be attributed to NO-caused impaired nuclear import of APE1 that helped in preventing the already exported APE1 from reimporting into nucleus. | [] | This phenomenon may be attributed to NO-caused impaired nuclear import of APE1 that helped in preventing the already exported APE1 from reimporting into nucleus. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | Different from the APE1-overexpressed cell system, the nuclear-cytosolic shuttling of APE1 may be interfered by some of its binding proteins at normal physiological conditions. | [
"51"
] | 176 | 10,101 | 0 | false | Different from the APE1-overexpressed cell system, the nuclear-cytosolic shuttling of APE1 may be interfered by some of its binding proteins at normal physiological conditions. | [] | Different from the APE1-overexpressed cell system, the nuclear-cytosolic shuttling of APE1 may be interfered by some of its binding proteins at normal physiological conditions. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | It is possible that the protein–protein interactions can repress export of APE1 from nucleus to cytosol. | [
"51"
] | 104 | 10,102 | 0 | false | It is possible that the protein–protein interactions can repress export of APE1 from nucleus to cytosol. | [] | It is possible that the protein–protein interactions can repress export of APE1 from nucleus to cytosol. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | HDAC2 and p50 proteins may act as such intra-nuclear gatekeepers for their ability to antagonize NO-induced APE1 trafficking (Figure 7). | [
"51"
] | 136 | 10,103 | 0 | false | HDAC2 and p50 proteins may act as such intra-nuclear gatekeepers for their ability to antagonize NO-induced APE1 trafficking (Figure 7). | [] | HDAC2 and p50 proteins may act as such intra-nuclear gatekeepers for their ability to antagonize NO-induced APE1 trafficking (Figure 7). | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | The differential intra-nuclear levels of APE1-binding proteins may partly contribute to the cell-type-specific phenomena in APE1 nuclear export. | [
"51"
] | 144 | 10,104 | 0 | false | The differential intra-nuclear levels of APE1-binding proteins may partly contribute to the cell-type-specific phenomena in APE1 nuclear export. | [] | The differential intra-nuclear levels of APE1-binding proteins may partly contribute to the cell-type-specific phenomena in APE1 nuclear export. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | Therefore, the NO-caused APE1 cytosolic translocation may be a complicated process, simultaneously involved in S-nitrosation of Cys93 and Cys310 leading to “NES” exposure, interaction of APE1 with other nuclear proteins and defect in importin nuclear import pathway. | [
"51"
] | 266 | 10,105 | 0 | false | Therefore, the NO-caused APE1 cytosolic translocation may be a complicated process, simultaneously involved in S-nitrosation of Cys93 and Cys310 leading to “NES” exposure, interaction of APE1 with other nuclear proteins and defect in importin nuclear import pathway. | [] | Therefore, the NO-caused APE1 cytosolic translocation may be a complicated process, simultaneously involved in S-nitrosation of Cys93 and Cys310 leading to “NES” exposure, interaction of APE1 with other nuclear proteins and defect in importin nuclear import pathway. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | Figure 8.A model for nuclear-cytosolic translocation of APE1 in response to NO stimulation. | [
"51"
] | 91 | 10,106 | 0 | false | Figure 8.A model for nuclear-cytosolic translocation of APE1 in response to NO stimulation. | [] | Figure 8.A model for nuclear-cytosolic translocation of APE1 in response to NO stimulation. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | APE1 carries an importin-dependent NLS at the N-terminal end (not shown). | [
"51"
] | 73 | 10,107 | 0 | false | APE1 carries an importin-dependent NLS at the N-terminal end (not shown). | [] | APE1 carries an importin-dependent NLS at the N-terminal end (not shown). | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | Two antiparellel beta-strands (B1 and B2) in close proximity to C93 and C310 are masked in the internal structure. | [
"51"
] | 114 | 10,108 | 0 | false | Two antiparellel beta-strands (B1 and B2) in close proximity to C93 and C310 are masked in the internal structure. | [] | Two antiparellel beta-strands in close proximity to C93 and C310 are masked in the internal structure. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | In rested cells, APE1 resides in the nucleus due to the existence of NLS. | [
"51"
] | 73 | 10,109 | 0 | false | In rested cells, APE1 resides in the nucleus due to the existence of NLS. | [] | In rested cells, APE1 resides in the nucleus due to the existence of NLS. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | Upon nitrosative stress, S-nitrosation of C93 and C310 contributes to unmasking of the B1 and/or B2 by changing conformation, which may facilitate the nuclear export of APE1 in a CRM1-independet manner (perhaps mediated by an unknown transport protein). | [
"51"
] | 253 | 10,110 | 0 | false | Upon nitrosative stress, S-nitrosation of C93 and C310 contributes to unmasking of the B1 and/or B2 by changing conformation, which may facilitate the nuclear export of APE1 in a CRM1-independet manner (perhaps mediated by an unknown transport protein). | [] | Upon nitrosative stress, S-nitrosation of C93 and C310 contributes to unmasking of the B1 and/or B2 by changing conformation, which may facilitate the nuclear export of APE1 in a CRM1-independet manner (perhaps mediated by an unknown transport protein). | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | At the same time, importin-dependent nuclear import pathway is repressed by NO insult, which may prevent the already exported cytosolic APE1 from re-import into the nucleus. | [
"51"
] | 173 | 10,111 | 0 | false | At the same time, importin-dependent nuclear import pathway is repressed by NO insult, which may prevent the already exported cytosolic APE1 from re-import into the nucleus. | [] | At the same time, importin-dependent nuclear import pathway is repressed by NO insult, which may prevent the already exported cytosolic APE1 from re-import into the nucleus. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | However, once the intracellular environment becomes reductive (e.g. | [
"51"
] | 67 | 10,112 | 0 | false | However, once the intracellular environment becomes reductive (e.g. | [] | However, once the intracellular environment becomes reductive (e.g. | true | true | true | true | true | 1,613 |
2 | DISCUSSION | 1 | 51 | [
"B51"
] | 17,403,694 | pmid-9628873 | the increased reducing molecules such as DTT), both NO-elicited S-nitrosation of APE1 and NO-caused repression of importin can be abrogated; thus, the inducible nuclear export of APE1 by NO could be prevented or reversed. | [
"51"
] | 221 | 10,113 | 0 | false | the increased reducing molecules such as DTT), both NO-elicited S-nitrosation of APE1 and NO-caused repression of importin can be abrogated; thus, the inducible nuclear export of APE1 by NO could be prevented or reversed. | [] | the increased reducing molecules such as DTT), both NO-elicited S-nitrosation of APE1 and NO-caused repression of importin can be abrogated; thus, the inducible nuclear export of APE1 by NO could be prevented or reversed. | false | true | true | true | false | 1,613 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | A model for nuclear-cytosolic translocation of APE1 in response to NO stimulation. | null | 82 | 10,114 | 0 | false | null | null | A model for nuclear-cytosolic translocation of APE1 in response to NO stimulation. | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | APE1 carries an importin-dependent NLS at the N-terminal end (not shown). | null | 73 | 10,115 | 0 | false | null | null | APE1 carries an importin-dependent NLS at the N-terminal end (not shown). | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | Two antiparellel beta-strands (B1 and B2) in close proximity to C93 and C310 are masked in the internal structure. | null | 114 | 10,116 | 0 | false | null | null | Two antiparellel beta-strands (B1 and B2) in close proximity to C93 and C310 are masked in the internal structure. | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | In rested cells, APE1 resides in the nucleus due to the existence of NLS. | null | 73 | 10,117 | 0 | false | null | null | In rested cells, APE1 resides in the nucleus due to the existence of NLS. | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | Upon nitrosative stress, S-nitrosation of C93 and C310 contributes to unmasking of the B1 and/or B2 by changing conformation, which may facilitate the nuclear export of APE1 in a CRM1-independet manner (perhaps mediated by an unknown transport protein). | null | 253 | 10,118 | 0 | false | null | null | Upon nitrosative stress, S-nitrosation of C93 and C310 contributes to unmasking of the B1 and/or B2 by changing conformation, which may facilitate the nuclear export of APE1 in a CRM1-independet manner (perhaps mediated by an unknown transport protein). | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | At the same time, importin-dependent nuclear import pathway is repressed by NO insult, which may prevent the already exported cytosolic APE1 from re-import into the nucleus. | null | 173 | 10,119 | 0 | false | null | null | At the same time, importin-dependent nuclear import pathway is repressed by NO insult, which may prevent the already exported cytosolic APE1 from re-import into the nucleus. | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | However, once the intracellular environment becomes reductive (e.g. | null | 67 | 10,120 | 0 | false | null | null | However, once the intracellular environment becomes reductive (e.g. | true | true | true | true | true | 1,614 |
3 | DISCUSSION | 0 | null | null | 17,403,694 | null | the increased reducing molecules such as DTT), both NO-elicited S-nitrosation of APE1 and NO-caused repression of importin can be abrogated; thus, the inducible nuclear export of APE1 by NO could be prevented or reversed. | null | 221 | 10,121 | 0 | false | null | null | the increased reducing molecules such as DTT), both NO-elicited S-nitrosation of APE1 and NO-caused repression of importin can be abrogated; thus, the inducible nuclear export of APE1 by NO could be prevented or reversed. | false | true | true | true | false | 1,614 |
4 | DISCUSSION | 1 | 14 | [
"B14"
] | 17,403,694 | pmid-11554453 | In summary, we have reported here that nitric oxide controlled the nuclear export of APE1 through S-nitrosation of Cysteines 93 and 310, which described a novel link between the nitrosative stress and DNA repair/transcriptional regulation system. | [
"14"
] | 246 | 10,122 | 0 | false | In summary, we have reported here that nitric oxide controlled the nuclear export of APE1 through S-nitrosation of Cysteines 93 and 310, which described a novel link between the nitrosative stress and DNA repair/transcriptional regulation system. | [] | In summary, we have reported here that nitric oxide controlled the nuclear export of APE1 through S-nitrosation of Cysteines 93 and 310, which described a novel link between the nitrosative stress and DNA repair/transcriptional regulation system. | true | true | true | true | true | 1,615 |
4 | DISCUSSION | 1 | 14 | [
"B14"
] | 17,403,694 | pmid-11554453 | It has been reported that redox modification of Cys310 of APE1 can repress its AP endonuclease activity (14). | [
"14"
] | 109 | 10,123 | 1 | false | It has been reported that redox modification of Cys310 of APE1 can repress its AP endonuclease activity. | [
"14"
] | It has been reported that redox modification of Cys310 of APE1 can repress its AP endonuclease activity. | true | true | true | true | true | 1,615 |
4 | DISCUSSION | 1 | 14 | [
"B14"
] | 17,403,694 | pmid-11554453 | Thus, it is reasonable to expect that NO may exert influence on APE1 DNA repair function through nitrosation of this site. | [
"14"
] | 122 | 10,124 | 0 | false | Thus, it is reasonable to expect that NO may exert influence on APE1 DNA repair function through nitrosation of this site. | [] | Thus, it is reasonable to expect that NO may exert influence on APE1 DNA repair function through nitrosation of this site. | true | true | true | true | true | 1,615 |
4 | DISCUSSION | 1 | 14 | [
"B14"
] | 17,403,694 | pmid-11554453 | Unraveling the detailed mechanism by which S-nitrosation of APE1 controlled its nuclear export (such as whether a vehicle protein is required for the translocation) and revealing whether S-nitrosation of APE1 can affect its other biological functions present an exciting and relevant challenge for future research. | [
"14"
] | 314 | 10,125 | 0 | false | Unraveling the detailed mechanism by which S-nitrosation of APE1 controlled its nuclear export (such as whether a vehicle protein is required for the translocation) and revealing whether S-nitrosation of APE1 can affect its other biological functions present an exciting and relevant challenge for future research. | [] | Unraveling the detailed mechanism by which S-nitrosation of APE1 controlled its nuclear export (such as whether a vehicle protein is required for the translocation) and revealing whether S-nitrosation of APE1 can affect its other biological functions present an exciting and relevant challenge for future research. | true | true | true | true | true | 1,615 |
4 | DISCUSSION | 1 | 14 | [
"B14"
] | 17,403,694 | pmid-11554453 | Since NO and APE1 are connected to tumorigenesis and neurodegenerative diseases, the present findings will reasonably improve our understanding of how nitrosative stress leads to DNA damaging at the DNA-repair level and have the potential to yield therapeutic strategies to fight these diseases. | [
"14"
] | 295 | 10,126 | 0 | false | Since NO and APE1 are connected to tumorigenesis and neurodegenerative diseases, the present findings will reasonably improve our understanding of how nitrosative stress leads to DNA damaging at the DNA-repair level and have the potential to yield therapeutic strategies to fight these diseases. | [] | Since NO and APE1 are connected to tumorigenesis and neurodegenerative diseases, the present findings will reasonably improve our understanding of how nitrosative stress leads to DNA damaging at the DNA-repair level and have the potential to yield therapeutic strategies to fight these diseases. | true | true | true | true | true | 1,615 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | Opioid receptors (µ, δ and κ) mediate the diverse functions of endogenous opioid peptides and the opioid alkaloids such as morphine, including analgesia, reward, autonomic reflexes, and endocrine/immune regulation (1–3). | [
"1–3",
"4",
"5",
"6",
"7"
] | 220 | 10,127 | 1 | false | Opioid receptors (µ, δ and κ) mediate the diverse functions of endogenous opioid peptides and the opioid alkaloids such as morphine, including analgesia, reward, autonomic reflexes, and endocrine/immune regulation. | [
"1–3"
] | Opioid receptors (µ, δ and κ) mediate the diverse functions of endogenous opioid peptides and the opioid alkaloids such as morphine, including analgesia, reward, autonomic reflexes, and endocrine/immune regulation. | true | true | true | true | true | 1,616 |
0 | INTRODUCTION | 1 | 4 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | The mu opioid receptor (MOR) is considered to be the main site of action for morphine (4). | [
"1–3",
"4",
"5",
"6",
"7"
] | 90 | 10,128 | 1 | false | The mu opioid receptor (MOR) is considered to be the main site of action for morphine. | [
"4"
] | The mu opioid receptor (MOR) is considered to be the main site of action for morphine. | true | true | true | true | true | 1,616 |
0 | INTRODUCTION | 1 | 5 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | Many studies, including those with receptor knockout mice, have indicated that the responses to opiate agonists are dependent on the receptor level (5). | [
"1–3",
"4",
"5",
"6",
"7"
] | 152 | 10,129 | 1 | false | Many studies, including those with receptor knockout mice, have indicated that the responses to opiate agonists are dependent on the receptor level. | [
"5"
] | Many studies, including those with receptor knockout mice, have indicated that the responses to opiate agonists are dependent on the receptor level. | true | true | true | true | true | 1,616 |
0 | INTRODUCTION | 1 | 6 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | MOR is first detected in rat brain at embryonic day 14 (E14) (6) followed by a slight decline during the first week of postnatal development, then increasing to peak levels 2 weeks later (7). | [
"1–3",
"4",
"5",
"6",
"7"
] | 191 | 10,130 | 1 | false | MOR is first detected in rat brain at embryonic day 14 followed by a slight decline during the first week of postnatal development, then increasing to peak levels 2 weeks later. | [
"E14",
"6",
"7"
] | MOR is first detected in rat brain at embryonic day 14 followed by a slight decline during the first week of postnatal development, then increasing to peak levels 2 weeks later. | true | true | true | true | true | 1,616 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6",
"B7"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | The overall mechanisms involved in such spatial and temporal regulations of MOR have not yet been elucidated. | [
"1–3",
"4",
"5",
"6",
"7"
] | 109 | 10,131 | 0 | false | The overall mechanisms involved in such spatial and temporal regulations of MOR have not yet been elucidated. | [] | The overall mechanisms involved in such spatial and temporal regulations of MOR have not yet been elucidated. | true | true | true | true | true | 1,616 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Generally, transcriptional control is mediated by transcription factors, RNA polymerase and a series of cis-acting elements located in the gene sequences. | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 154 | 10,132 | 0 | false | Generally, transcriptional control is mediated by transcription factors, RNA polymerase and a series of cis-acting elements located in the gene sequences. | [] | Generally, transcriptional control is mediated by transcription factors, RNA polymerase and a series of cis-acting elements located in the gene sequences. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Such promoters, enhancers, silencers and locus-control elements are organized in a modular structure and regulate the production of pre-mRNA molecules (8). | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 155 | 10,133 | 1 | false | Such promoters, enhancers, silencers and locus-control elements are organized in a modular structure and regulate the production of pre-mRNA molecules. | [
"8"
] | Such promoters, enhancers, silencers and locus-control elements are organized in a modular structure and regulate the production of pre-mRNA molecules. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Opioid receptor expression can be regulated by multiple mechanisms, including transcriptional and post-transcriptional events (9,10). | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 133 | 10,134 | 0 | false | Opioid receptor expression can be regulated by multiple mechanisms, including transcriptional and post-transcriptional events. | [
"9,10"
] | Opioid receptor expression can be regulated by multiple mechanisms, including transcriptional and post-transcriptional events. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 11 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Our laboratory and others have demonstrated that MOR promoter activity is regulated by many enhancer elements and their related transcriptional factors such as SOX, SP1, AP2, NF-κB, PU.1, and NRSE (11). | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 202 | 10,135 | 1 | false | Our laboratory and others have demonstrated that MOR promoter activity is regulated by many enhancer elements and their related transcriptional factors such as SOX, SP1, AP2, NF-κB, PU.1, and NRSE. | [
"11"
] | Our laboratory and others have demonstrated that MOR promoter activity is regulated by many enhancer elements and their related transcriptional factors such as SOX, SP1, AP2, NF-κB, PU.1, and NRSE. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Post-transcriptional regulation occurs at the level of mRNA or protein. | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 71 | 10,136 | 0 | false | Post-transcriptional regulation occurs at the level of mRNA or protein. | [] | Post-transcriptional regulation occurs at the level of mRNA or protein. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Such regulation could be due to mRNA stability, differences in translation efficiency or mRNA transport, and covalent modification of receptor molecules (10,12–14). | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 164 | 10,137 | 0 | false | Such regulation could be due to mRNA stability, differences in translation efficiency or mRNA transport, and covalent modification of receptor molecules. | [
"10,12–14"
] | Such regulation could be due to mRNA stability, differences in translation efficiency or mRNA transport, and covalent modification of receptor molecules. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 15 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Our recent studies indicated that the 3′-untranslated region (UTR) of MOR mRNA could affect the overall transcript's activity (15). | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 131 | 10,138 | 1 | false | Our recent studies indicated that the 3′-untranslated region (UTR) of MOR mRNA could affect the overall transcript's activity. | [
"15"
] | Our recent studies indicated that the 3′-untranslated region (UTR) of MOR mRNA could affect the overall transcript's activity. | true | true | true | true | true | 1,617 |
1 | INTRODUCTION | 1 | 8 | [
"B8",
"B9",
"B10",
"B11",
"B10",
"B12 B13 B14",
"B15"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | Thus, posttranscriptional regulation of the MOR gene could have an important role in the spatial and temporal expression of the receptor proteins. | [
"8",
"9",
"10",
"11",
"10",
"12–14",
"15"
] | 146 | 10,139 | 0 | false | Thus, posttranscriptional regulation of the MOR gene could have an important role in the spatial and temporal expression of the receptor proteins. | [] | Thus, posttranscriptional regulation of the MOR gene could have an important role in the spatial and temporal expression of the receptor proteins. | true | true | true | true | true | 1,617 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | Recently, it has become increasingly clear that the 5′-UTR of eukaryotic mRNA is a key site of multiple forms of post-transcriptional regulation of gene expression, especially those containing | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 192 | 10,140 | 0 | false | Recently, it has become increasingly clear that the 5′-UTR of eukaryotic mRNA is a key site of multiple forms of post-transcriptional regulation of gene expression, especially those containing | [] | Recently, it has become increasingly clear that the 5′-UTR of eukaryotic mRNA is a key site of multiple forms of post-transcriptional regulation of gene expression, especially those containing | true | true | false | true | false | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | at least one AUG codon (uAUG) upstream of the main open reading frame (ORF) (16–19). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 84 | 10,141 | 1 | false | at least one AUG codon (uAUG) upstream of the main open reading frame (ORF). | [
"16–19"
] | at least one AUG codon (uAUG) upstream of the main open reading frame (ORF). | false | true | true | true | false | 1,618 |
2 | INTRODUCTION | 1 | 20–22 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | It is postulated that, in eukaryotic cells, most translation proceeds according to the ribosome scanning model (20–22), and initiates predominantly by a cap-binding/scanning mechanism (23). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 189 | 10,142 | 1 | false | It is postulated that, in eukaryotic cells, most translation proceeds according to the ribosome scanning model, and initiates predominantly by a cap-binding/scanning mechanism. | [
"20–22",
"23"
] | It is postulated that, in eukaryotic cells, most translation proceeds according to the ribosome scanning model, and initiates predominantly by a cap-binding/scanning mechanism. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The scanning model predicts that an uAUG codon will interfere with translation of a downstream main ORF. | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 104 | 10,143 | 0 | false | The scanning model predicts that an uAUG codon will interfere with translation of a downstream main ORF. | [] | The scanning model predicts that an uAUG codon will interfere with translation of a downstream main ORF. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 24 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | However, the scanning complex may bypass such uAUG codons by ‘leaky scanning’ if the surrounding nucleotide context is suboptimal or very close to the 5′ cap region of the mRNA (24). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 182 | 10,144 | 1 | false | However, the scanning complex may bypass such uAUG codons by ‘leaky scanning’ if the surrounding nucleotide context is suboptimal or very close to the 5′ cap region of the mRNA. | [
"24"
] | However, the scanning complex may bypass such uAUG codons by ‘leaky scanning’ if the surrounding nucleotide context is suboptimal or very close to the 5′ cap region of the mRNA. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The 43S pre-initiation complex binds to the 5′-cap region and then migrates progressively 5′ to 3′ until it recognizes an AUG start codon. | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 138 | 10,145 | 0 | false | The 43S pre-initiation complex binds to the 5′-cap region and then migrates progressively 5′ to 3′ until it recognizes an AUG start codon. | [] | The 43S pre-initiation complex binds to the 5′-cap region and then migrates progressively 5′ to 3′ until it recognizes an AUG start codon. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 20 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The resulting complex is joined by the large subunit to form a complete ribosome, and polypeptide synthesis begins (20). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 120 | 10,146 | 1 | false | The resulting complex is joined by the large subunit to form a complete ribosome, and polypeptide synthesis begins. | [
"20"
] | The resulting complex is joined by the large subunit to form a complete ribosome, and polypeptide synthesis begins. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | Ribosomes reaching the main AUG of these mRNAs do so mainly via context-dependent leaky scanning and/or reinitiation mechanisms, although it is widely believed that these are inefficient mechanisms (24,25). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 206 | 10,147 | 0 | false | Ribosomes reaching the main AUG of these mRNAs do so mainly via context-dependent leaky scanning and/or reinitiation mechanisms, although it is widely believed that these are inefficient mechanisms. | [
"24,25"
] | Ribosomes reaching the main AUG of these mRNAs do so mainly via context-dependent leaky scanning and/or reinitiation mechanisms, although it is widely believed that these are inefficient mechanisms. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The context-dependent leaky scanning mechanism accounts for the observation that some 40S subunits will fail to initiate at AUG codons with a less than optimal context and continue scanning along the 5′-UTR. | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 207 | 10,148 | 0 | false | The context-dependent leaky scanning mechanism accounts for the observation that some 40S subunits will fail to initiate at AUG codons with a less than optimal context and continue scanning along the 5′-UTR. | [] | The context-dependent leaky scanning mechanism accounts for the observation that some 40S subunits will fail to initiate at AUG codons with a less than optimal context and continue scanning along the 5′-UTR. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 26 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The most efficient context for initiation of protein translation is known as the Kozak sequence (GCCRCCAUGG), which was identified initially as a consensus sequence in vertebrate mRNA (26). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 189 | 10,149 | 1 | false | The most efficient context for initiation of protein translation is known as the Kozak sequence (GCCRCCAUGG), which was identified initially as a consensus sequence in vertebrate mRNA. | [
"26"
] | The most efficient context for initiation of protein translation is known as the Kozak sequence (GCCRCCAUGG), which was identified initially as a consensus sequence in vertebrate mRNA. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The reinitiation mechanism describes the ability of 40S subunits to continue to scan and initiate at a downstream main AUG codon after translating a small independent uORF. | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 172 | 10,150 | 0 | false | The reinitiation mechanism describes the ability of 40S subunits to continue to scan and initiate at a downstream main AUG codon after translating a small independent uORF. | [] | The reinitiation mechanism describes the ability of 40S subunits to continue to scan and initiate at a downstream main AUG codon after translating a small independent uORF. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | Reinitiation is considered to be a rare event. | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 46 | 10,151 | 0 | false | Reinitiation is considered to be a rare event. | [] | Reinitiation is considered to be a rare event. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 24 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | Although the incidence of this mechanism may be much greater, only a few mRNAs with uORFs have been examined (24). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 114 | 10,152 | 1 | false | Although the incidence of this mechanism may be much greater, only a few mRNAs with uORFs have been examined. | [
"24"
] | Although the incidence of this mechanism may be much greater, only a few mRNAs with uORFs have been examined. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 26 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | These uAUGs or uORFs are features of at least a few percent of the mRNAs in yeast, plants and mammals (26), and can be important players in negative translational control. | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 171 | 10,153 | 1 | false | These uAUGs or uORFs are features of at least a few percent of the mRNAs in yeast, plants and mammals, and can be important players in negative translational control. | [
"26"
] | These uAUGs or uORFs are features of at least a few percent of the mRNAs in yeast, plants and mammals, and can be important players in negative translational control. | true | true | true | true | true | 1,618 |
2 | INTRODUCTION | 1 | 16–19 | [
"B16 B17 B18 B19",
"B20 B21 B22",
"B23",
"B24",
"B20",
"B24",
"B25",
"B26",
"B24",
"B26",
"B16",
"B27"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | However, in some cases, the upstream regulatory sequences stimulated translation of the major ORF (16,27). | [
"16–19",
"20–22",
"23",
"24",
"20",
"24",
"25",
"26",
"24",
"26",
"16",
"27"
] | 106 | 10,154 | 0 | false | However, in some cases, the upstream regulatory sequences stimulated translation of the major ORF. | [
"16,27"
] | However, in some cases, the upstream regulatory sequences stimulated translation of the major ORF. | true | true | true | true | true | 1,618 |
3 | INTRODUCTION | 0 | null | null | 17,284,463 | null | Within the 5′-UTR region of the mouse MOR gene, between the basal proximal promoter at nucleotides −445 to −240 and the AUG of the main ORF, three uORFs with variable lengths are identified. | null | 190 | 10,155 | 0 | false | null | null | Within the 5′-UTR region of the mouse MOR gene, between the basal proximal promoter at nucleotides −445 to −240 and the AUG of the main ORF, three uORFs with variable lengths are identified. | true | true | true | true | true | 1,619 |
3 | INTRODUCTION | 0 | null | null | 17,284,463 | null | Whether these uORFs can regulate the translation of the MOR transcripts was examined in this study. | null | 99 | 10,156 | 0 | false | null | null | Whether these uORFs can regulate the translation of the MOR transcripts was examined in this study. | true | true | true | true | true | 1,619 |
3 | INTRODUCTION | 0 | null | null | 17,284,463 | null | The uAUG-directed initiation and uORF-peptide-dependent regulations of the MOR transcript's translation were examined by mutational analyses of the uAUGs and internal sequences. | null | 177 | 10,157 | 0 | false | null | null | The uAUG-directed initiation and uORF-peptide-dependent regulations of the MOR transcript's translation were examined by mutational analyses of the uAUGs and internal sequences. | true | true | true | true | true | 1,619 |
3 | INTRODUCTION | 0 | null | null | 17,284,463 | null | We demonstrate that the translation of the MOR transcript is negatively regulated by these uORFs, and that such down-regulation is mediated via ribosome leaky scanning mechanism. | null | 178 | 10,158 | 0 | false | null | null | We demonstrate that the translation of the MOR transcript is negatively regulated by these uORFs, and that such down-regulation is mediated via ribosome leaky scanning mechanism. | true | true | true | true | true | 1,619 |
3 | INTRODUCTION | 0 | null | null | 17,284,463 | null | The initiation of peptide syntheses at these uAUGs of the MOR transcript provides a novel mechanism for the regulation of expression of the mouse MOR gene product. | null | 163 | 10,159 | 0 | false | null | null | The initiation of peptide syntheses at these uAUGs of the MOR transcript provides a novel mechanism for the regulation of expression of the mouse MOR gene product. | true | true | true | true | true | 1,619 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | The distribution of opioid receptors and the expression patterns of their mRNAs have been extensively examined (39,40). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 119 | 10,160 | 0 | false | The distribution of opioid receptors and the expression patterns of their mRNAs have been extensively examined. | [
"39,40"
] | The distribution of opioid receptors and the expression patterns of their mRNAs have been extensively examined. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 10 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | Opioid receptor proteins are also regulated by variations in the mRNA sequences (10). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 85 | 10,161 | 1 | false | Opioid receptor proteins are also regulated by variations in the mRNA sequences. | [
"10"
] | Opioid receptor proteins are also regulated by variations in the mRNA sequences. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | These mRNA variants differ mainly in the 5′- or 3′-UTR regions. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 63 | 10,162 | 0 | false | These mRNA variants differ mainly in the 5′- or 3′-UTR regions. | [] | These mRNA variants differ mainly in the 5′- or 3′-UTR regions. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 11 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | As such, regulation of opioid receptor expression involves not only transcriptional control at the DNA level, but also posttranscriptional control at the RNA level (11). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 169 | 10,163 | 1 | false | As such, regulation of opioid receptor expression involves not only transcriptional control at the DNA level, but also posttranscriptional control at the RNA level. | [
"11"
] | As such, regulation of opioid receptor expression involves not only transcriptional control at the DNA level, but also posttranscriptional control at the RNA level. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | We have characterized a novel regulatory mechanism of mouse MOR expression mediated by uAUG/uORF in this study. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 111 | 10,164 | 0 | false | We have characterized a novel regulatory mechanism of mouse MOR expression mediated by uAUG/uORF in this study. | [] | We have characterized a novel regulatory mechanism of mouse MOR expression mediated by uAUG/uORF in this study. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | The 301-bp extension of the mouse MOR 5′-UTR region includes the major MOR mRNA transcription sequence (derived from the proximal MOR promoter), and contains three uORFs. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 170 | 10,165 | 0 | false | The 301-bp extension of the mouse MOR 5′-UTR region includes the major MOR mRNA transcription sequence (derived from the proximal MOR promoter), and contains three uORFs. | [] | The 301-bp extension of the mouse MOR 5′-UTR region includes the major MOR mRNA transcription sequence (derived from the proximal MOR promoter), and contains three uORFs. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | These uORFs use the same termination codon (Figure 1). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 54 | 10,166 | 0 | false | These uORFs use the same termination codon (Figure 1). | [] | These uORFs use the same termination codon (Figure 1). | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | In most well-characterized examples of regulatory uORFs, mutation of the uAUG codon alters protein expression without affecting mRNA abundance. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 143 | 10,167 | 0 | false | In most well-characterized examples of regulatory uORFs, mutation of the uAUG codon alters protein expression without affecting mRNA abundance. | [] | In most well-characterized examples of regulatory uORFs, mutation of the uAUG codon alters protein expression without affecting mRNA abundance. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | However, uORFs do not always inhibit translation; cases have been described in which uORFs stimulated expression of downstream ORFs (41,42). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 140 | 10,168 | 0 | false | However, uORFs do not always inhibit translation; cases have been described in which uORFs stimulated expression of downstream ORFs. | [
"41,42"
] | However, uORFs do not always inhibit translation; cases have been described in which uORFs stimulated expression of downstream ORFs. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 16 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | If removal of uAUGs alters mRNA levels, then the AUG nucleotides may alter transcription or RNA stability, independent of translation of the uORF (16). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 151 | 10,169 | 1 | false | If removal of uAUGs alters mRNA levels, then the AUG nucleotides may alter transcription or RNA stability, independent of translation of the uORF. | [
"16"
] | If removal of uAUGs alters mRNA levels, then the AUG nucleotides may alter transcription or RNA stability, independent of translation of the uORF. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | We found that the presence of the uORF region suppressed translation without changing MOR transcription levels. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 111 | 10,170 | 0 | false | We found that the presence of the uORF region suppressed translation without changing MOR transcription levels. | [] | We found that the presence of the uORF region suppressed translation without changing MOR transcription levels. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | This was due to three uAUGs present in the region from nucleotides −301 to +1 bp in the MOR 5′-UTR. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 99 | 10,171 | 0 | false | This was due to three uAUGs present in the region from nucleotides −301 to +1 bp in the MOR 5′-UTR. | [] | This was due to three uAUGs present in the region from nucleotides −301 to +1 bp in the MOR 5′-UTR. | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 23 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | As uORF mechanisms usually function in a cap-dependent manner (23), we investigated this well-characterized regulatory mechanism by using capped and uncapped transcripts for in vitro translation (Figure 1E and F). | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 213 | 10,172 | 1 | false | As uORF mechanisms usually function in a cap-dependent manner, we investigated this well-characterized regulatory mechanism by using capped and uncapped transcripts for in vitro translation (Figure 1E and F). | [
"23"
] | As uORF mechanisms usually function in a cap-dependent manner, we investigated this well-characterized regulatory mechanism by using capped and uncapped transcripts for in vitro translation (Figure 1E and F). | true | true | true | true | true | 1,620 |
0 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B10",
"B11",
"B41",
"B42",
"B16",
"B23"
] | 17,284,463 | pmid-8719033|NA|pmid-9437729|NA|pmid-9555078|pmid-9864069|pmid-10836142|NA|NA|pmid-14977578|pmid-15464146|pmid-11106749|pmid-10747993|pmid-11073965|pmid-10395892 | We determined that mouse MOR containing uORFs do indeed function in a cap-dependent manner. | [
"39",
"40",
"10",
"11",
"41",
"42",
"16",
"23"
] | 91 | 10,173 | 0 | false | We determined that mouse MOR containing uORFs do indeed function in a cap-dependent manner. | [] | We determined that mouse MOR containing uORFs do indeed function in a cap-dependent manner. | true | true | true | true | true | 1,620 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | The initiation efficiencies of each uAUG are important features of the codons in MOR 5′-UTR leaky scanning models (43,44). | [
"43",
"44"
] | 122 | 10,174 | 0 | false | The initiation efficiencies of each uAUG are important features of the codons in MOR 5′-UTR leaky scanning models. | [
"43,44"
] | The initiation efficiencies of each uAUG are important features of the codons in MOR 5′-UTR leaky scanning models. | true | true | true | true | true | 1,621 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | The relative strengths of the initiation codons were tested by in vitro translation (Figure 2). | [
"43",
"44"
] | 95 | 10,175 | 0 | false | The relative strengths of the initiation codons were tested by in vitro translation (Figure 2). | [] | The relative strengths of the initiation codons were tested by in vitro translation (Figure 2). | true | true | true | true | true | 1,621 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | The uAUG#1 had a very weak initiation context, while uAUG#2 had a slightly stronger initiation context. | [
"43",
"44"
] | 103 | 10,176 | 0 | false | The uAUG#1 had a very weak initiation context, while uAUG#2 had a slightly stronger initiation context. | [] | The uAUG#1 had a very weak initiation context, while uAUG#2 had a slightly stronger initiation context. | true | true | true | true | true | 1,621 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | The uAUG#3 had the strongest initiation context. | [
"43",
"44"
] | 48 | 10,177 | 0 | false | The uAUG#3 had the strongest initiation context. | [] | The uAUG#3 had the strongest initiation context. | true | true | true | true | true | 1,621 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | This likely facilitates higher levels of leaky scanning, enabling peptide synthesis from the uAUG#3 initiation codon on the MOR 5′-UTR. | [
"43",
"44"
] | 135 | 10,178 | 0 | false | This likely facilitates higher levels of leaky scanning, enabling peptide synthesis from the uAUG#3 initiation codon on the MOR 5′-UTR. | [] | This likely facilitates higher levels of leaky scanning, enabling peptide synthesis from the uAUG#3 initiation codon on the MOR 5′-UTR. | true | true | true | true | true | 1,621 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | When the sequence was mutated at all three uAUGs [uAUG(−)], only peptide products initiated from the main uAUG were produced. | [
"43",
"44"
] | 125 | 10,179 | 0 | false | When the sequence was mutated at all three uAUGs [uAUG(−)], only peptide products initiated from the main uAUG were produced. | [] | When the sequence was mutated at all three uAUGs [uAUG(−)], only peptide products initiated from the main uAUG were produced. | true | true | true | true | true | 1,621 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B44"
] | 17,284,463 | NA|pmid-11786311|pmid-14977578|pmid-15464146|pmid-14977578|pmid-10216946|pmid-11283722|pmid-11416182|pmid-15879516|pmid-7687304|pmid-1566578 | These results indicate that all three uAUGs can effectively be initiated and produce peptides, and that uORFs can negatively regulate downstream MOR ORF initiation. | [
"43",
"44"
] | 164 | 10,180 | 0 | false | These results indicate that all three uAUGs can effectively be initiated and produce peptides, and that uORFs can negatively regulate downstream MOR ORF initiation. | [] | These results indicate that all three uAUGs can effectively be initiated and produce peptides, and that uORFs can negatively regulate downstream MOR ORF initiation. | true | true | true | true | true | 1,621 |
2 | DISCUSSION | 1 | 45 | [
"B45",
"B46"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | We also performed FACS analyses and receptor binding assays to examine cell surface expression of the receptor (45,46). | [
"45",
"46"
] | 119 | 10,181 | 0 | false | We also performed FACS analyses and receptor binding assays to examine cell surface expression of the receptor. | [
"45,46"
] | We also performed FACS analyses and receptor binding assays to examine cell surface expression of the receptor. | true | true | true | true | true | 1,622 |
2 | DISCUSSION | 1 | 45 | [
"B45",
"B46"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | The results confirmed that these uORFs mediated down-regulation of MOR expression. | [
"45",
"46"
] | 82 | 10,182 | 0 | false | The results confirmed that these uORFs mediated down-regulation of MOR expression. | [] | The results confirmed that these uORFs mediated down-regulation of MOR expression. | true | true | true | true | true | 1,622 |
2 | DISCUSSION | 1 | 45 | [
"B45",
"B46"
] | 17,284,463 | pmid-11073965|pmid-11718907|pmid-11164040|pmid-14990743|pmid-12435632|pmid-681367|pmid-2645293|pmid-10395892|pmid-12799445|pmid-12435632|pmid-12799445|pmid-12459250|pmid-1955461|pmid-12799445|pmid-1955461|pmid-11073965|pmid-12890013|pmid-15657030|pmid-12851402 | Indeed, the presence of the uORFs decreased expression by up to 3.5-fold relative to samples lacking the uORFs (Figure 3). | [
"45",
"46"
] | 122 | 10,183 | 0 | false | Indeed, the presence of the uORFs decreased expression by up to 3.5-fold relative to samples lacking the uORFs (Figure 3). | [] | Indeed, the presence of the uORFs decreased expression by up to 3.5-fold relative to samples lacking the uORFs (Figure 3). | true | true | true | true | true | 1,622 |
3 | DISCUSSION | 0 | null | null | 17,284,463 | null | We further confirmed the context-dependent initiation activity of each uAUG by mutation. | null | 88 | 10,184 | 0 | false | null | null | We further confirmed the context-dependent initiation activity of each uAUG by mutation. | true | true | true | true | true | 1,623 |
3 | DISCUSSION | 0 | null | null | 17,284,463 | null | Translation initiation strength was most efficient in the third uAUG (Figure 4B). | null | 81 | 10,185 | 0 | false | null | null | Translation initiation strength was most efficient in the third uAUG (Figure 4B). | true | true | true | true | true | 1,623 |
3 | DISCUSSION | 0 | null | null | 17,284,463 | null | If the uAUGs reside in a non-optimal context, the scanning ribosomal complex may bypass possible starting AUGs by leaky scanning. | null | 129 | 10,186 | 0 | false | null | null | If the uAUGs reside in a non-optimal context, the scanning ribosomal complex may bypass possible starting AUGs by leaky scanning. | true | true | true | true | true | 1,623 |
3 | DISCUSSION | 0 | null | null | 17,284,463 | null | Transient transfection results suggest that the inhibition of the main AUG imposed by one of the uORF (uAUG#3) was greater than that produced by the other uORFs (uAUG#1 or uAUG#2). | null | 180 | 10,187 | 0 | false | null | null | Transient transfection results suggest that the inhibition of the main AUG imposed by one of the uORF (uAUG#3) was greater than that produced by the other uORFs (uAUG#1 or uAUG#2). | true | true | true | true | true | 1,623 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | Moreover, some peptides produced by translation of uORFs have been reported to interact with the ribosome, further diminishing the efficiency of protein translation (47,48). | [
"47",
"48",
"49",
"50",
"51"
] | 173 | 10,188 | 0 | false | Moreover, some peptides produced by translation of uORFs have been reported to interact with the ribosome, further diminishing the efficiency of protein translation. | [
"47,48"
] | Moreover, some peptides produced by translation of uORFs have been reported to interact with the ribosome, further diminishing the efficiency of protein translation. | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | In contrast, regulation of yeast GCN4 translation by nutrient levels was independent of the peptide sequences encoded by its uORFs (49,50). | [
"47",
"48",
"49",
"50",
"51"
] | 139 | 10,189 | 0 | false | In contrast, regulation of yeast GCN4 translation by nutrient levels was independent of the peptide sequences encoded by its uORFs. | [
"49,50"
] | In contrast, regulation of yeast GCN4 translation by nutrient levels was independent of the peptide sequences encoded by its uORFs. | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | Our current study showed that introduction of stop codon constructs (+S), thereby changing the sequence of peptide encoded by the uORF, exhibited changes similar to those seen in the translation of the downstream cistron (Figure 5B). | [
"47",
"48",
"49",
"50",
"51"
] | 233 | 10,190 | 0 | false | Our current study showed that introduction of stop codon constructs (+S), thereby changing the sequence of peptide encoded by the uORF, exhibited changes similar to those seen in the translation of the downstream cistron (Figure 5B). | [] | Our current study showed that introduction of stop codon constructs (+S), thereby changing the sequence of peptide encoded by the uORF, exhibited changes similar to those seen in the translation of the downstream cistron (Figure 5B). | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | Furthermore, mutating the uAUGs while also introducing the stop codon (M + S) caused a marked increase in the translation of the downstream cistron (Figure 5D). | [
"47",
"48",
"49",
"50",
"51"
] | 160 | 10,191 | 0 | false | Furthermore, mutating the uAUGs while also introducing the stop codon (M + S) caused a marked increase in the translation of the downstream cistron (Figure 5D). | [] | Furthermore, mutating the uAUGs while also introducing the stop codon (M + S) caused a marked increase in the translation of the downstream cistron (Figure 5D). | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | These data show that regulation of the MOR uORF is independent of the peptide sequence of the uORF. | [
"47",
"48",
"49",
"50",
"51"
] | 99 | 10,192 | 0 | false | These data show that regulation of the MOR uORF is independent of the peptide sequence of the uORF. | [] | These data show that regulation of the MOR uORF is independent of the peptide sequence of the uORF. | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | Thus, the inhibitory effect of the uORF during MOR translation is a protein-independent mechanism. | [
"47",
"48",
"49",
"50",
"51"
] | 98 | 10,193 | 0 | false | Thus, the inhibitory effect of the uORF during MOR translation is a protein-independent mechanism. | [] | Thus, the inhibitory effect of the uORF during MOR translation is a protein-independent mechanism. | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 47 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | Although the mechanisms involved in explaining the inhibitory effects of the uORF peptide on translation are not understood, several models could be proposed. | [
"47",
"48",
"49",
"50",
"51"
] | 158 | 10,194 | 0 | false | Although the mechanisms involved in explaining the inhibitory effects of the uORF peptide on translation are not understood, several models could be proposed. | [] | Although the mechanisms involved in explaining the inhibitory effects of the uORF peptide on translation are not understood, several models could be proposed. | true | true | true | true | true | 1,624 |
4 | DISCUSSION | 1 | 51 | [
"B47",
"B48",
"B49",
"B50",
"B51"
] | 17,284,463 | pmid-11328869|pmid-12228716|NA|pmid-11707416|pmid-8308019 | For example, the peptide of the uORF could be synthesized and have the ability to inhibit translation only at high concentrations in the local microenvironment (51). | [
"47",
"48",
"49",
"50",
"51"
] | 165 | 10,195 | 1 | false | For example, the peptide of the uORF could be synthesized and have the ability to inhibit translation only at high concentrations in the local microenvironment. | [
"51"
] | For example, the peptide of the uORF could be synthesized and have the ability to inhibit translation only at high concentrations in the local microenvironment. | true | true | true | true | true | 1,624 |
5 | DISCUSSION | 0 | null | null | 17,284,463 | null | As shown in Figure 6, differences in LUC levels were detected between constructs with different uAUG contexts. | null | 110 | 10,196 | 0 | false | null | null | As shown in Figure 6, differences in LUC levels were detected between constructs with different uAUG contexts. | true | true | true | true | true | 1,625 |
5 | DISCUSSION | 0 | null | null | 17,284,463 | null | This indicates that ribosomes initiating at the main AUG must have scanned the uAUGs, especially when these uAUGs contain strong or adequate contexts. | null | 150 | 10,197 | 0 | false | null | null | This indicates that ribosomes initiating at the main AUG must have scanned the uAUGs, especially when these uAUGs contain strong or adequate contexts. | true | true | true | true | true | 1,625 |
5 | DISCUSSION | 0 | null | null | 17,284,463 | null | Leaky scanning is an extension of the scanning model and suggests that an AUG might be bypassed by scanning ribosomes if it resides in a suboptimal context. | null | 156 | 10,198 | 0 | false | null | null | Leaky scanning is an extension of the scanning model and suggests that an AUG might be bypassed by scanning ribosomes if it resides in a suboptimal context. | true | true | true | true | true | 1,625 |
5 | DISCUSSION | 0 | null | null | 17,284,463 | null | This mechanism could only occur by context-dependent leaky scanning. | null | 68 | 10,199 | 0 | false | null | null | This mechanism could only occur by context-dependent leaky scanning. | true | true | true | true | true | 1,625 |
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