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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | There are other approaches to predicting non-coding RNA. | null | 56 | 9,300 | 0 | false | null | null | There are other approaches to predicting non-coding RNA. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | One commonly used method is sequence alignment, e.g. | null | 52 | 9,301 | 0 | false | null | null | One commonly used method is sequence alignment, e.g. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | BLAST (3), Paralign (20) or FASTA (21). | null | 39 | 9,302 | 0 | false | null | null | BLAST (3), Paralign (20) or FASTA (21). | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | Another is based on structure-sensitive Stochastic Context Free Grammars (SCFG) (22) which form the basis of the tRNA prediction program tRNAscan-SE (23) and of Infernal (24), which is used when creating RFAM. | null | 209 | 9,303 | 0 | false | null | null | Another is based on structure-sensitive Stochastic Context Free Grammars (SCFG) (22) which form the basis of the tRNA prediction program tRNAscan-SE (23) and of Infernal (24), which is used when creating RFAM. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | While the sequence alignment methods are very fast, they are not particularly suited for prediction of non-coding RNA (1). | null | 122 | 9,304 | 0 | false | null | null | While the sequence alignment methods are very fast, they are not particularly suited for prediction of non-coding RNA (1). | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | Infernal, however, has a general worst case running time of order O(MN3) , which is prohibitive. | null | 96 | 9,305 | 0 | false | null | null | Infernal, however, has a general worst case running time of order O(MN3) , which is prohibitive. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | The RFAM database (17,18), which includes 5S and the 5β² domain of 16S, uses BLAST to pre-screen genome sequences, followed by Infernal; despite a more efficient approach than the general SCFG, it does not analyze the entire 16S. | null | 228 | 9,306 | 0 | false | null | null | The RFAM database (17,18), which includes 5S and the 5β² domain of 16S, uses BLAST to pre-screen genome sequences, followed by Infernal; despite a more efficient approach than the general SCFG, it does not analyze the entire 16S. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | A search for 5S in a 1 Mbp genome using Infernal took 4 hours 45 minutes: almost 1000 times as much as the 16 seconds used by RNAmmer for the much larger 16S model. | null | 164 | 9,307 | 0 | false | null | null | A search for 5S in a 1 Mbp genome using Infernal took 4 hours 45 minutes: almost 1000 times as much as the 16 seconds used by RNAmmer for the much larger 16S model. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | A time-saving approach to SCFGs could be to use the RaveNna (25) package which can convert an RFAM SCFG to an HMM. | null | 114 | 9,308 | 0 | false | null | null | A time-saving approach to SCFGs could be to use the RaveNna (25) package which can convert an RFAM SCFG to an HMM. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | This drastically reduces the running time; however, its usefulness would be limited since no models for the larger rRNAs are available. | null | 135 | 9,309 | 0 | false | null | null | This drastically reduces the running time; however, its usefulness would be limited since no models for the larger rRNAs are available. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | Another factor is that the 5S found by RaveNna (26) which were not already in RFAM were all in organellar sequences, sequences not analyzed by RNAmmer. | null | 151 | 9,310 | 0 | false | null | null | Another factor is that the 5S found by RaveNna (26) which were not already in RFAM were all in organellar sequences, sequences not analyzed by RNAmmer. | true | true | true | true | true | 1,481 |
8 | DISCUSSION | 0 | null | null | 17,452,365 | null | For further comparisons and comments on these different methods, we refer to (1). | null | 81 | 9,311 | 0 | false | null | null | For further comparisons and comments on these different methods, we refer to (1). | true | true | true | true | true | 1,481 |
9 | DISCUSSION | 0 | null | null | 17,452,365 | null | The RNAmmer program is available as a traditional HTML-based prediction server at http://www.cbs.dtu.dk/services/RNAmmer as well as through a SOAP-based web service. | null | 165 | 9,312 | 0 | false | null | null | The RNAmmer program is available as a traditional HTML-based prediction server at http://www.cbs.dtu.dk/services/RNAmmer as well as through a SOAP-based web service. | true | true | true | true | true | 1,482 |
9 | DISCUSSION | 0 | null | null | 17,452,365 | null | It is also available for download through the same site. | null | 56 | 9,313 | 0 | false | null | null | It is also available for download through the same site. | true | true | true | true | true | 1,482 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2 B3 B4",
"B5",
"B6",
"B7 B8 B9",
"B10",
"B11",
"B12"
] | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | RNA interference (RNAi) is induced by double-stranded RNA (dsRNA) and results in gene silencing through sequence-specific degradation of the target RNA (1). | [
"1",
"2β4",
"5",
"6",
"7β9",
"10",
"11",
"12"
] | 156 | 9,314 | 1 | false | RNA interference (RNAi) is induced by double-stranded RNA (dsRNA) and results in gene silencing through sequence-specific degradation of the target RNA. | [
"1"
] | RNA interference (RNAi) is induced by double-stranded RNA (dsRNA) and results in gene silencing through sequence-specific degradation of the target RNA. | true | true | true | true | true | 1,483 |
0 | INTRODUCTION | 1 | 2β4 | [
"B1",
"B2 B3 B4",
"B5",
"B6",
"B7 B8 B9",
"B10",
"B11",
"B12"
] | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | RNAi provides plants and animals a defense mechanism against viruses (2β4) and retrotransposons (5,6). | [
"1",
"2β4",
"5",
"6",
"7β9",
"10",
"11",
"12"
] | 102 | 9,315 | 1 | false | RNAi provides plants and animals a defense mechanism against viruses and retrotransposons. | [
"2β4",
"5,6"
] | RNAi provides plants and animals a defense mechanism against viruses and retrotransposons. | true | true | true | true | true | 1,483 |
0 | INTRODUCTION | 1 | 7β9 | [
"B1",
"B2 B3 B4",
"B5",
"B6",
"B7 B8 B9",
"B10",
"B11",
"B12"
] | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | The ribonuclease Dicer processes the long dsRNA replication intermediates into small interfering RNAs (siRNAs) of βΌ22 nucleotides (nt) (7β9). | [
"1",
"2β4",
"5",
"6",
"7β9",
"10",
"11",
"12"
] | 141 | 9,316 | 1 | false | The ribonuclease Dicer processes the long dsRNA replication intermediates into small interfering RNAs (siRNAs) of βΌ22 nucleotides (nt). | [
"7β9"
] | The ribonuclease Dicer processes the long dsRNA replication intermediates into small interfering RNAs (siRNAs) of βΌ22 nucleotides (nt). | true | true | true | true | true | 1,483 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2 B3 B4",
"B5",
"B6",
"B7 B8 B9",
"B10",
"B11",
"B12"
] | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | These siRNAs are incorporated into the RNA-induced silencing complex (RISC) that finds complementary RNA sequences, resulting in cleavage of the target RNA (10,11). | [
"1",
"2β4",
"5",
"6",
"7β9",
"10",
"11",
"12"
] | 164 | 9,317 | 0 | false | These siRNAs are incorporated into the RNA-induced silencing complex (RISC) that finds complementary RNA sequences, resulting in cleavage of the target RNA. | [
"10,11"
] | These siRNAs are incorporated into the RNA-induced silencing complex (RISC) that finds complementary RNA sequences, resulting in cleavage of the target RNA. | true | true | true | true | true | 1,483 |
0 | INTRODUCTION | 1 | 12 | [
"B1",
"B2 B3 B4",
"B5",
"B6",
"B7 B8 B9",
"B10",
"B11",
"B12"
] | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | The central catalytic component of RISC is an Argonaute protein, which contains the signature domains PAZ and PIWI responsible for binding the siRNA strand (12). | [
"1",
"2β4",
"5",
"6",
"7β9",
"10",
"11",
"12"
] | 161 | 9,318 | 1 | false | The central catalytic component of RISC is an Argonaute protein, which contains the signature domains PAZ and PIWI responsible for binding the siRNA strand. | [
"12"
] | The central catalytic component of RISC is an Argonaute protein, which contains the signature domains PAZ and PIWI responsible for binding the siRNA strand. | true | true | true | true | true | 1,483 |
1 | INTRODUCTION | 1 | 13β15 | [
"B13 B14 B15",
"B16",
"B17",
"B18",
"B19",
"B20",
"B19",
"B21 B22 B23"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | Transfection of synthetic siRNAs into cells or intracellular expression of short hairpin RNAs (shRNAs), which are processed into siRNA duplexes by Dicer, are powerful tools to suppress gene expression (13β15). | [
"13β15",
"16",
"17",
"18",
"19",
"20",
"19",
"21β23"
] | 209 | 9,319 | 1 | false | Transfection of synthetic siRNAs into cells or intracellular expression of short hairpin RNAs (shRNAs), which are processed into siRNA duplexes by Dicer, are powerful tools to suppress gene expression. | [
"13β15"
] | Transfection of synthetic siRNAs into cells or intracellular expression of short hairpin RNAs (shRNAs), which are processed into siRNA duplexes by Dicer, are powerful tools to suppress gene expression. | true | true | true | true | true | 1,484 |
1 | INTRODUCTION | 1 | 16 | [
"B13 B14 B15",
"B16",
"B17",
"B18",
"B19",
"B20",
"B19",
"B21 B22 B23"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | Randomly selected siRNAs against a target show a large variation in their efficacy (16). | [
"13β15",
"16",
"17",
"18",
"19",
"20",
"19",
"21β23"
] | 88 | 9,320 | 1 | false | Randomly selected siRNAs against a target show a large variation in their efficacy. | [
"16"
] | Randomly selected siRNAs against a target show a large variation in their efficacy. | true | true | true | true | true | 1,484 |
1 | INTRODUCTION | 1 | 13β15 | [
"B13 B14 B15",
"B16",
"B17",
"B18",
"B19",
"B20",
"B19",
"B21 B22 B23"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | Empirical rules on siRNA duplex features have been reported and improve design of effective siRNAs. | [
"13β15",
"16",
"17",
"18",
"19",
"20",
"19",
"21β23"
] | 99 | 9,321 | 0 | false | Empirical rules on siRNA duplex features have been reported and improve design of effective siRNAs. | [] | Empirical rules on siRNA duplex features have been reported and improve design of effective siRNAs. | true | true | true | true | true | 1,484 |
1 | INTRODUCTION | 1 | 13β15 | [
"B13 B14 B15",
"B16",
"B17",
"B18",
"B19",
"B20",
"B19",
"B21 B22 B23"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | The asymmetry rule for siRNA duplex ends requires that the 5β² end of the antisense strand forms a less stable end with its complement than the 5β² end of the sense strand (17,18). | [
"13β15",
"16",
"17",
"18",
"19",
"20",
"19",
"21β23"
] | 178 | 9,322 | 0 | false | The asymmetry rule for siRNA duplex ends requires that the 5β² end of the antisense strand forms a less stable end with its complement than the 5β² end of the sense strand. | [
"17,18"
] | The asymmetry rule for siRNA duplex ends requires that the 5β² end of the antisense strand forms a less stable end with its complement than the 5β² end of the sense strand. | true | true | true | true | true | 1,484 |
1 | INTRODUCTION | 1 | 13β15 | [
"B13 B14 B15",
"B16",
"B17",
"B18",
"B19",
"B20",
"B19",
"B21 B22 B23"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | Related to this rule is the described requirement of high A/U content at the 5β² end of the antisense strand and high G/C at the 5β² end of the sense strand (19,20). | [
"13β15",
"16",
"17",
"18",
"19",
"20",
"19",
"21β23"
] | 163 | 9,323 | 0 | false | Related to this rule is the described requirement of high A/U content at the 5β² end of the antisense strand and high G/C at the 5β² end of the sense strand. | [
"19,20"
] | Related to this rule is the described requirement of high A/U content at the 5β² end of the antisense strand and high G/C at the 5β² end of the sense strand. | true | true | true | true | true | 1,484 |
1 | INTRODUCTION | 1 | 13β15 | [
"B13 B14 B15",
"B16",
"B17",
"B18",
"B19",
"B20",
"B19",
"B21 B22 B23"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | In addition, a number of position-specific nucleotides, an unstructured guide-RNA, and an accessible target site have been reported to positively effect siRNA efficiency (19,21β23). | [
"13β15",
"16",
"17",
"18",
"19",
"20",
"19",
"21β23"
] | 181 | 9,324 | 0 | false | In addition, a number of position-specific nucleotides, an unstructured guide-RNA, and an accessible target site have been reported to positively effect siRNA efficiency. | [
"19,21β23"
] | In addition, a number of position-specific nucleotides, an unstructured guide-RNA, and an accessible target site have been reported to positively effect siRNA efficiency. | true | true | true | true | true | 1,484 |
2 | INTRODUCTION | 1 | 24 | [
"B24",
"B25 B26 B27 B28",
"B29 B30 B31 B32 B33 B34",
"B31",
"B35",
"B36",
"B34",
"B37"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | RNAi can be used as a therapeutic strategy against human pathogenic viruses such as HIV-1 (24). | [
"24",
"25β28",
"29β34",
"31",
"35",
"36",
"34",
"37"
] | 95 | 9,325 | 1 | false | RNAi can be used as a therapeutic strategy against human pathogenic viruses such as HIV-1. | [
"24"
] | RNAi can be used as a therapeutic strategy against human pathogenic viruses such as HIV-1. | true | true | true | true | true | 1,485 |
2 | INTRODUCTION | 1 | 25β28 | [
"B24",
"B25 B26 B27 B28",
"B29 B30 B31 B32 B33 B34",
"B31",
"B35",
"B36",
"B34",
"B37"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | HIV-1 replication can be inhibited transiently by transfection of synthetic siRNAs targeting viral RNA sequences or cellular co-factors (25β28). | [
"24",
"25β28",
"29β34",
"31",
"35",
"36",
"34",
"37"
] | 144 | 9,326 | 1 | false | HIV-1 replication can be inhibited transiently by transfection of synthetic siRNAs targeting viral RNA sequences or cellular co-factors. | [
"25β28"
] | HIV-1 replication can be inhibited transiently by transfection of synthetic siRNAs targeting viral RNA sequences or cellular co-factors. | true | true | true | true | true | 1,485 |
2 | INTRODUCTION | 1 | 29β34 | [
"B24",
"B25 B26 B27 B28",
"B29 B30 B31 B32 B33 B34",
"B31",
"B35",
"B36",
"B34",
"B37"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | Furthermore, long-term inhibition of HIV-1 replication has been demonstrated in transduced cell lines stably expressing antiviral siRNAs or shRNAs (29β34). | [
"24",
"25β28",
"29β34",
"31",
"35",
"36",
"34",
"37"
] | 155 | 9,327 | 1 | false | Furthermore, long-term inhibition of HIV-1 replication has been demonstrated in transduced cell lines stably expressing antiviral siRNAs or shRNAs. | [
"29β34"
] | Furthermore, long-term inhibition of HIV-1 replication has been demonstrated in transduced cell lines stably expressing antiviral siRNAs or shRNAs. | true | true | true | true | true | 1,485 |
2 | INTRODUCTION | 1 | 24 | [
"B24",
"B25 B26 B27 B28",
"B29 B30 B31 B32 B33 B34",
"B31",
"B35",
"B36",
"B34",
"B37"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | However, HIV-1 escape variants with nucleotide substitutions or deletions in the siRNA target sequence do emerge after prolonged culturing (31,35,36). | [
"24",
"25β28",
"29β34",
"31",
"35",
"36",
"34",
"37"
] | 150 | 9,328 | 0 | false | However, HIV-1 escape variants with nucleotide substitutions or deletions in the siRNA target sequence do emerge after prolonged culturing. | [
"31,35,36"
] | However, HIV-1 escape variants with nucleotide substitutions or deletions in the siRNA target sequence do emerge after prolonged culturing. | true | true | true | true | true | 1,485 |
2 | INTRODUCTION | 1 | 24 | [
"B24",
"B25 B26 B27 B28",
"B29 B30 B31 B32 B33 B34",
"B31",
"B35",
"B36",
"B34",
"B37"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | The emergence of RNAi-resistant variants may be blocked by a combination-shRNA therapy, which simultaneously targets multiple conserved viral RNA sequences (34,37). | [
"24",
"25β28",
"29β34",
"31",
"35",
"36",
"34",
"37"
] | 164 | 9,329 | 0 | false | The emergence of RNAi-resistant variants may be blocked by a combination-shRNA therapy, which simultaneously targets multiple conserved viral RNA sequences. | [
"34,37"
] | The emergence of RNAi-resistant variants may be blocked by a combination-shRNA therapy, which simultaneously targets multiple conserved viral RNA sequences. | true | true | true | true | true | 1,485 |
3 | INTRODUCTION | 1 | 36 | [
"B36",
"B59",
"B38"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | We demonstrated that HIV-1 can also become resistant against RNAi by placing the target sequence in a stable RNA structure, which prevents binding of the siRNA (36). | [
"36",
"59",
"38"
] | 165 | 9,330 | 1 | false | We demonstrated that HIV-1 can also become resistant against RNAi by placing the target sequence in a stable RNA structure, which prevents binding of the siRNA. | [
"36"
] | We demonstrated that HIV-1 can also become resistant against RNAi by placing the target sequence in a stable RNA structure, which prevents binding of the siRNA. | true | true | true | true | true | 1,486 |
3 | INTRODUCTION | 1 | 59 | [
"B36",
"B59",
"B38"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | We also suggested that such structure-based target occlusion occurs in the RNA genomes of lentiviral vectors with a shRNA-cassette (59). | [
"36",
"59",
"38"
] | 136 | 9,331 | 1 | false | We also suggested that such structure-based target occlusion occurs in the RNA genomes of lentiviral vectors with a shRNA-cassette. | [
"59"
] | We also suggested that such structure-based target occlusion occurs in the RNA genomes of lentiviral vectors with a shRNA-cassette. | true | true | true | true | true | 1,486 |
3 | INTRODUCTION | 1 | 36 | [
"B36",
"B59",
"B38"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | By inserting these cassettes, the target sequence will automatically be present in the vector genome, and self-targeting by the shRNA should reduce the lentiviral production level. | [
"36",
"59",
"38"
] | 180 | 9,332 | 0 | false | By inserting these cassettes, the target sequence will automatically be present in the vector genome, and self-targeting by the shRNA should reduce the lentiviral production level. | [] | By inserting these cassettes, the target sequence will automatically be present in the vector genome, and self-targeting by the shRNA should reduce the lentiviral production level. | true | true | true | true | true | 1,486 |
3 | INTRODUCTION | 1 | 36 | [
"B36",
"B59",
"B38"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | However, since the target sequence in the genome is also located in this perfect shRNA hairpin, it is protected against RNAi, ensuring a normal vector titer. | [
"36",
"59",
"38"
] | 157 | 9,333 | 0 | false | However, since the target sequence in the genome is also located in this perfect shRNA hairpin, it is protected against RNAi, ensuring a normal vector titer. | [] | However, since the target sequence in the genome is also located in this perfect shRNA hairpin, it is protected against RNAi, ensuring a normal vector titer. | true | true | true | true | true | 1,486 |
3 | INTRODUCTION | 1 | 38 | [
"B36",
"B59",
"B38"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | Indeed, when the target in the lentiviral genome is unstructured, the titer is significantly reduced by the shRNA (38). | [
"36",
"59",
"38"
] | 119 | 9,334 | 1 | false | Indeed, when the target in the lentiviral genome is unstructured, the titer is significantly reduced by the shRNA. | [
"38"
] | Indeed, when the target in the lentiviral genome is unstructured, the titer is significantly reduced by the shRNA. | true | true | true | true | true | 1,486 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | The inhibitory effect of target RNA structure on RNAi efficiency has been described in several studies (23,39,40). | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 114 | 9,335 | 0 | false | The inhibitory effect of target RNA structure on RNAi efficiency has been described in several studies. | [
"23,39,40"
] | The inhibitory effect of target RNA structure on RNAi efficiency has been described in several studies. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | These studies compared the efficiency of different siRNAs on a fixed target, and found a correlation between target availability and RNAi efficiency. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 149 | 9,336 | 0 | false | These studies compared the efficiency of different siRNAs on a fixed target, and found a correlation between target availability and RNAi efficiency. | [] | These studies compared the efficiency of different siRNAs on a fixed target, and found a correlation between target availability and RNAi efficiency. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Schubert et al. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 15 | 9,337 | 0 | false | Schubert et al. | [] | Schubert et al. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 41 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | suggested that the local free energy of base pairing in the target region determines RNAi efficiency (41). | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 106 | 9,338 | 1 | false | suggested that the local free energy of base pairing in the target region determines RNAi efficiency. | [
"41"
] | suggested that the local free energy of base pairing in the target region determines RNAi efficiency. | false | true | true | true | false | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Ideally, one should test this concept by a mutational analysis of one target instead of comparing different siRNAs with intrinsically different RNAi efficacies. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 160 | 9,339 | 0 | false | Ideally, one should test this concept by a mutational analysis of one target instead of comparing different siRNAs with intrinsically different RNAi efficacies. | [] | Ideally, one should test this concept by a mutational analysis of one target instead of comparing different siRNAs with intrinsically different RNAi efficacies. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | In this scenario, mutations that affect the RNA structure should not affect the target sequence itself, such that the same siRNA inhibitor can be used. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 151 | 9,340 | 0 | false | In this scenario, mutations that affect the RNA structure should not affect the target sequence itself, such that the same siRNA inhibitor can be used. | [] | In this scenario, mutations that affect the RNA structure should not affect the target sequence itself, such that the same siRNA inhibitor can be used. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | In this study, we set out to determine the exact hairpin stability at which RNAi suppression occurs by systematically destabilizing a 21-base pair (bp) hairpin structure that occludes the complete target sequence. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 213 | 9,341 | 0 | false | In this study, we set out to determine the exact hairpin stability at which RNAi suppression occurs by systematically destabilizing a 21-base pair (bp) hairpin structure that occludes the complete target sequence. | [] | In this study, we set out to determine the exact hairpin stability at which RNAi suppression occurs by systematically destabilizing a 21-base pair (bp) hairpin structure that occludes the complete target sequence. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | We monitored the effects on siRNA binding in vitro and RNAi efficiency in vivo. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 79 | 9,342 | 0 | false | We monitored the effects on siRNA binding in vitro and RNAi efficiency in vivo. | [] | We monitored the effects on siRNA binding in vitro and RNAi efficiency in vivo. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | The 3β² end of the mRNA target sequence is initially recognized by bases 2β5 of the antisense/guide strand siRNA, therefore named the βseedβ sequence (42,43). | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 157 | 9,343 | 0 | false | The 3β² end of the mRNA target sequence is initially recognized by bases 2β5 of the antisense/guide strand siRNA, therefore named the βseedβ sequence. | [
"42,43"
] | The 3β² end of the mRNA target sequence is initially recognized by bases 2β5 of the antisense/guide strand siRNA, therefore named the βseedβ sequence. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Thus, one may expect a more prominent effect of an accessible target 3β² end, which primed us to address positional effects when destabilizing the target hairpin. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 161 | 9,344 | 0 | false | Thus, one may expect a more prominent effect of an accessible target 3β² end, which primed us to address positional effects when destabilizing the target hairpin. | [] | Thus, one may expect a more prominent effect of an accessible target 3β² end, which primed us to address positional effects when destabilizing the target hairpin. | true | true | true | true | true | 1,487 |
4 | INTRODUCTION | 1 | 23 | [
"B23",
"B39",
"B40",
"B41",
"B42",
"B43"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | The results demonstrate a clear correlation between the overall stability of the target hairpin and RNAi efficiency, but positional effects were also apparent. | [
"23",
"39",
"40",
"41",
"42",
"43"
] | 159 | 9,345 | 0 | false | The results demonstrate a clear correlation between the overall stability of the target hairpin and RNAi efficiency, but positional effects were also apparent. | [] | The results demonstrate a clear correlation between the overall stability of the target hairpin and RNAi efficiency, but positional effects were also apparent. | true | true | true | true | true | 1,487 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | It has been proposed that RNAi efficiency is influenced by the local RNA structure of the targeted sequence. | null | 108 | 9,346 | 0 | false | null | null | It has been proposed that RNAi efficiency is influenced by the local RNA structure of the targeted sequence. | true | true | true | true | true | 1,488 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | We investigated this phenomenon in detail by placement of the target sequence in a perfect hairpin structure (ΞG = β36.6βkcal/mol), which indeed resisted RNAi. | null | 159 | 9,347 | 0 | false | null | null | We investigated this phenomenon in detail by placement of the target sequence in a perfect hairpin structure (ΞG = β36.6βkcal/mol), which indeed resisted RNAi. | true | true | true | true | true | 1,488 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | Subsequently we destabilized this tight target structure resulting in a gradual exposure of the target sequence. | null | 112 | 9,348 | 0 | false | null | null | Subsequently we destabilized this tight target structure resulting in a gradual exposure of the target sequence. | true | true | true | true | true | 1,488 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | Destabilization of the hairpin structure has little effect on RNAi activity until a threshold is reached (ΞG β β30βkcal/mol). | null | 125 | 9,349 | 0 | false | null | null | Destabilization of the hairpin structure has little effect on RNAi activity until a threshold is reached (ΞG β β30βkcal/mol). | true | true | true | true | true | 1,488 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | Beyond this threshold we demonstrate an inverse correlation between hairpin stability and RNAi-mediated inhibition. | null | 115 | 9,350 | 0 | false | null | null | Beyond this threshold we demonstrate an inverse correlation between hairpin stability and RNAi-mediated inhibition. | true | true | true | true | true | 1,488 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | Maximal RNAi efficiency was observed with hairpins of ΞG β₯ β15βkcal/mol. | null | 72 | 9,351 | 0 | false | null | null | Maximal RNAi efficiency was observed with hairpins of ΞG β₯ β15βkcal/mol. | true | true | true | true | true | 1,488 |
0 | DISCUSSION | 0 | null | null | 17,576,691 | pmid-9486653|pmid-11423650|pmid-11459066|pmid-16554838|pmid-15817569|pmid-10535732|pmid-11157775|pmid-10749213|pmid-10778853|pmid-11253050|pmid-12230974|pmid-16009129 | In vitro binding experiments suggested that the increase of RNAi-mediated inhibition is due to efficient siRNA binding to the destabilized target RNA hairpins. | null | 159 | 9,352 | 0 | false | null | null | In vitro binding experiments suggested that the increase of RNAi-mediated inhibition is due to efficient siRNA binding to the destabilized target RNA hairpins. | true | true | true | true | true | 1,488 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | When we introduced position-specific mutations in the target hairpin, we observed RNAi efficiencies that deviate from this trend. | [
"43",
"46",
"47",
"48",
"36"
] | 129 | 9,353 | 0 | false | When we introduced position-specific mutations in the target hairpin, we observed RNAi efficiencies that deviate from this trend. | [] | When we introduced position-specific mutations in the target hairpin, we observed RNAi efficiencies that deviate from this trend. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | Hairpins with an opened 5β² end or central part of the target sequence show less RNAi activity than predicted based on their overall stability. | [
"43",
"46",
"47",
"48",
"36"
] | 142 | 9,354 | 0 | false | Hairpins with an opened 5β² end or central part of the target sequence show less RNAi activity than predicted based on their overall stability. | [] | Hairpins with an opened 5β² end or central part of the target sequence show less RNAi activity than predicted based on their overall stability. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | In contrast, hairpins with an opened 3β² end are more susceptible to RNAi than expected. | [
"43",
"46",
"47",
"48",
"36"
] | 87 | 9,355 | 0 | false | In contrast, hairpins with an opened 3β² end are more susceptible to RNAi than expected. | [] | In contrast, hairpins with an opened 3β² end are more susceptible to RNAi than expected. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | These results are consistent with the current notion that the 3β² region of the target is initially recognized and bound by the RISC/siRNA complex (43). | [
"43",
"46",
"47",
"48",
"36"
] | 151 | 9,356 | 1 | false | These results are consistent with the current notion that the 3β² region of the target is initially recognized and bound by the RISC/siRNA complex. | [
"43"
] | These results are consistent with the current notion that the 3β² region of the target is initially recognized and bound by the RISC/siRNA complex. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | This model is supported by structural data on RISC bound to the siRNA strand. | [
"43",
"46",
"47",
"48",
"36"
] | 77 | 9,357 | 0 | false | This model is supported by structural data on RISC bound to the siRNA strand. | [] | This model is supported by structural data on RISC bound to the siRNA strand. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 46 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | The 3β² end of the siRNA is recognized and bound in a pocket by the PAZ domain of the Argonaute protein (46). | [
"43",
"46",
"47",
"48",
"36"
] | 108 | 9,358 | 1 | false | The 3β² end of the siRNA is recognized and bound in a pocket by the PAZ domain of the Argonaute protein. | [
"46"
] | The 3β² end of the siRNA is recognized and bound in a pocket by the PAZ domain of the Argonaute protein. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | The 5β² end of the siRNA is anchored at the PIWI domain of Argonaute and these 5β² nucleotides are readily accessible for base pairing to complementary 3β² nucleotides of the target RNA (47,48). | [
"43",
"46",
"47",
"48",
"36"
] | 191 | 9,359 | 0 | false | The 5β² end of the siRNA is anchored at the PIWI domain of Argonaute and these 5β² nucleotides are readily accessible for base pairing to complementary 3β² nucleotides of the target RNA. | [
"47,48"
] | The 5β² end of the siRNA is anchored at the PIWI domain of Argonaute and these 5β² nucleotides are readily accessible for base pairing to complementary 3β² nucleotides of the target RNA. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 43 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | The importance of the target 3β² end was also revealed in experiments that selected for viruses that resist RNAi-mediated inhibition. | [
"43",
"46",
"47",
"48",
"36"
] | 132 | 9,360 | 0 | false | The importance of the target 3β² end was also revealed in experiments that selected for viruses that resist RNAi-mediated inhibition. | [] | The importance of the target 3β² end was also revealed in experiments that selected for viruses that resist RNAi-mediated inhibition. | true | true | true | true | true | 1,489 |
1 | DISCUSSION | 1 | 36 | [
"B43",
"B46",
"B47",
"B48",
"B36"
] | 17,576,691 | pmid-11910072|pmid-11373684|pmid-11981566|pmid-11937629|pmid-14567918|pmid-14567917|pmid-14758366|pmid-14769950|pmid-14758366|pmid-16258545|pmid-12604614|pmid-12888501|pmid-15170178|pmid-15156196|pmid-15800629|pmid-15800628|pmid-15687388 | We described a unique HIV-1 escape variant that acquired a mutation outside the 19-nt target, which forces the RNA into an alternative structure that occludes the 3β² end of the target (36). | [
"43",
"46",
"47",
"48",
"36"
] | 189 | 9,361 | 1 | false | We described a unique HIV-1 escape variant that acquired a mutation outside the 19-nt target, which forces the RNA into an alternative structure that occludes the 3β² end of the target. | [
"36"
] | We described a unique HIV-1 escape variant that acquired a mutation outside the 19-nt target, which forces the RNA into an alternative structure that occludes the 3β² end of the target. | true | true | true | true | true | 1,489 |
2 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | Besides the in vivo RNAi measurements, we also tested the different RNA targets for their ability to interact with the siRNA in vitro. | [
"49"
] | 134 | 9,362 | 0 | false | Besides the in vivo RNAi measurements, we also tested the different RNA targets for their ability to interact with the siRNA in vitro. | [] | Besides the in vivo RNAi measurements, we also tested the different RNA targets for their ability to interact with the siRNA in vitro. | true | true | true | true | true | 1,490 |
2 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | The overall ΞG effect of stable target hairpins is confirmed in this simplified in vitro setting, demonstrating that RNAi resistance is due to the inability of the siRNA to interact with the base-paired stem of the hairpin. | [
"49"
] | 223 | 9,363 | 0 | false | The overall ΞG effect of stable target hairpins is confirmed in this simplified in vitro setting, demonstrating that RNAi resistance is due to the inability of the siRNA to interact with the base-paired stem of the hairpin. | [] | The overall ΞG effect of stable target hairpins is confirmed in this simplified in vitro setting, demonstrating that RNAi resistance is due to the inability of the siRNA to interact with the base-paired stem of the hairpin. | true | true | true | true | true | 1,490 |
2 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | We realize that the siRNA does not act by itself in vivo as it is part of RISC, of which the helicase activity may affect local structure in the target RNA (49). | [
"49"
] | 161 | 9,364 | 1 | false | We realize that the siRNA does not act by itself in vivo as it is part of RISC, of which the helicase activity may affect local structure in the target RNA. | [
"49"
] | We realize that the siRNA does not act by itself in vivo as it is part of RISC, of which the helicase activity may affect local structure in the target RNA. | true | true | true | true | true | 1,490 |
2 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | In fact, we observed an interesting discrepancy between the in vivo and in vitro results for the 5β²/center/3β²-destabilized hairpins. | [
"49"
] | 132 | 9,365 | 0 | false | In fact, we observed an interesting discrepancy between the in vivo and in vitro results for the 5β²/center/3β²-destabilized hairpins. | [] | In fact, we observed an interesting discrepancy between the in vivo and in vitro results for the 5β²/center/3β²-destabilized hairpins. | true | true | true | true | true | 1,490 |
2 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | We observed that an accessible 3β² target is key for RNAi activity, but this effect was not seen in vitro. | [
"49"
] | 105 | 9,366 | 0 | false | We observed that an accessible 3β² target is key for RNAi activity, but this effect was not seen in vitro. | [] | We observed that an accessible 3β² target is key for RNAi activity, but this effect was not seen in vitro. | true | true | true | true | true | 1,490 |
2 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,576,691 | NA|pmid-12186906|pmid-12087358|pmid-11981565|pmid-12042777|pmid-12842429|pmid-15006606|pmid-14963165|pmid-14581533|pmid-15831707|pmid-16959541|pmid-14963165|pmid-14557638|pmid-15687388|pmid-16959541|pmid-15195925|pmid-11701122 | This result may indicate an important contribution of RISC in the siRNA-target RNA annealing step. | [
"49"
] | 98 | 9,367 | 0 | false | This result may indicate an important contribution of RISC in the siRNA-target RNA annealing step. | [] | This result may indicate an important contribution of RISC in the siRNA-target RNA annealing step. | true | true | true | true | true | 1,490 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | Thus, target RNA structure is an important factor when selecting a suitable target sequence, as it can have a negative effect on RNAi efficiency. | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 145 | 9,368 | 0 | false | Thus, target RNA structure is an important factor when selecting a suitable target sequence, as it can have a negative effect on RNAi efficiency. | [] | Thus, target RNA structure is an important factor when selecting a suitable target sequence, as it can have a negative effect on RNAi efficiency. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | For instance, it has been shown that the TAR hairpin of the HIV-1 genome is an unsuitable target because of its tight structure (31,40,50). | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 139 | 9,369 | 0 | false | For instance, it has been shown that the TAR hairpin of the HIV-1 genome is an unsuitable target because of its tight structure. | [
"31,40,50"
] | For instance, it has been shown that the TAR hairpin of the HIV-1 genome is an unsuitable target because of its tight structure. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | On the other hand, it is obvious that an accessible sequence does not automatically make a good siRNA target (31), as the matching siRNA may not meet the criteria of an effective siRNA (51). | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 190 | 9,370 | 1 | false | On the other hand, it is obvious that an accessible sequence does not automatically make a good siRNA target, as the matching siRNA may not meet the criteria of an effective siRNA. | [
"31",
"51"
] | On the other hand, it is obvious that an accessible sequence does not automatically make a good siRNA target, as the matching siRNA may not meet the criteria of an effective siRNA. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 39 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | It has been proposed to include a calculation of the amount of hydrogen bonds within the target sequence as a parameter for efficient target sequences (39). | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 156 | 9,371 | 1 | false | It has been proposed to include a calculation of the amount of hydrogen bonds within the target sequence as a parameter for efficient target sequences. | [
"39"
] | It has been proposed to include a calculation of the amount of hydrogen bonds within the target sequence as a parameter for efficient target sequences. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | We provide a ΞG threshold at which an hairpin RNA structure becomes inaccessible, and we differentiate between different target positions. | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 138 | 9,372 | 0 | false | We provide a ΞG threshold at which an hairpin RNA structure becomes inaccessible, and we differentiate between different target positions. | [] | We provide a ΞG threshold at which an hairpin RNA structure becomes inaccessible, and we differentiate between different target positions. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 36 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | When designing antiviral siRNAs one may also consider ways to obstruct viral escape via folding of an alternative target RNA structure (36). | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 140 | 9,373 | 1 | false | When designing antiviral siRNAs one may also consider ways to obstruct viral escape via folding of an alternative target RNA structure. | [
"36"
] | When designing antiviral siRNAs one may also consider ways to obstruct viral escape via folding of an alternative target RNA structure. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | The local RNA region should be screened for the absence of alternative foldings that occlude the 3β² end of the target and that can be selected by one or two mutations. | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 167 | 9,374 | 0 | false | The local RNA region should be screened for the absence of alternative foldings that occlude the 3β² end of the target and that can be selected by one or two mutations. | [] | The local RNA region should be screened for the absence of alternative foldings that occlude the 3β² end of the target and that can be selected by one or two mutations. | true | true | true | true | true | 1,491 |
3 | DISCUSSION | 1 | 31 | [
"B31",
"B40",
"B50",
"B31",
"B51",
"B39",
"B36"
] | 17,576,691 | pmid-15687388|NA|pmid-16948865|pmid-14963165|pmid-14762201|pmid-15852021|pmid-14963165|pmid-15143318|pmid-15110788|pmid-15687388 | If not available, the genetic threshold for structure-based escape might prove too high, even for a fast evolving virus like HIV-1. | [
"31",
"40",
"50",
"31",
"51",
"39",
"36"
] | 131 | 9,375 | 0 | false | If not available, the genetic threshold for structure-based escape might prove too high, even for a fast evolving virus like HIV-1. | [] | If not available, the genetic threshold for structure-based escape might prove too high, even for a fast evolving virus like HIV-1. | true | true | true | true | true | 1,491 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | RNA structure-mediated resistance against RNAi is in fact beneficial when expressing highly structured shRNAs or miRNAs in cells. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 129 | 9,376 | 0 | false | RNA structure-mediated resistance against RNAi is in fact beneficial when expressing highly structured shRNAs or miRNAs in cells. | [] | RNA structure-mediated resistance against RNAi is in fact beneficial when expressing highly structured shRNAs or miRNAs in cells. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | For instance, the incorporation of shRNA cassettes in a lentiviral vector is potentially problematic, because the shRNA will target the viral RNA genome during vector production, thus reducing the titer. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 203 | 9,377 | 0 | false | For instance, the incorporation of shRNA cassettes in a lentiviral vector is potentially problematic, because the shRNA will target the viral RNA genome during vector production, thus reducing the titer. | [] | For instance, the incorporation of shRNA cassettes in a lentiviral vector is potentially problematic, because the shRNA will target the viral RNA genome during vector production, thus reducing the titer. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Such self-targeting has not been reported (52,53), we think because the target is not accessible as part of the perfectly base-paired shRNA hairpin. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 148 | 9,378 | 0 | false | Such self-targeting has not been reported, we think because the target is not accessible as part of the perfectly base-paired shRNA hairpin. | [
"52,53"
] | Such self-targeting has not been reported, we think because the target is not accessible as part of the perfectly base-paired shRNA hairpin. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | The apparent absence of such self-targeting is particularly important for the development of multi-shRNA lentiviral vectors without titer reduction. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 148 | 9,379 | 0 | false | The apparent absence of such self-targeting is particularly important for the development of multi-shRNA lentiviral vectors without titer reduction. | [] | The apparent absence of such self-targeting is particularly important for the development of multi-shRNA lentiviral vectors without titer reduction. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | However, placing many tight RNA structures in the vector genome may negatively influence the titer by other means. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 114 | 9,380 | 0 | false | However, placing many tight RNA structures in the vector genome may negatively influence the titer by other means. | [] | However, placing many tight RNA structures in the vector genome may negatively influence the titer by other means. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 54 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | For instance, reverse transcription is very sensitive to excessively stable RNA structure (54) and RNA polymerase II transcription may pause at sites where the RNA products folds stable hairpin structures (55). | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 210 | 9,381 | 1 | false | For instance, reverse transcription is very sensitive to excessively stable RNA structure and RNA polymerase II transcription may pause at sites where the RNA products folds stable hairpin structures. | [
"54",
"55"
] | For instance, reverse transcription is very sensitive to excessively stable RNA structure and RNA polymerase II transcription may pause at sites where the RNA products folds stable hairpin structures. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | We did indeed observe that four shRNA cassettes reduce the lentiviral vector titer (ter Brake, unpublished data). | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 113 | 9,382 | 0 | false | We did indeed observe that four shRNA cassettes reduce the lentiviral vector titer (ter Brake, unpublished data). | [] | We did indeed observe that four shRNA cassettes reduce the lentiviral vector titer (ter Brake, unpublished data). | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 56 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Destabilizing the introduced shRNAs may avoid such vector problems, and provide additional benefits for cloning and sequencing of inverted repeat sequences (56). | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 161 | 9,383 | 1 | false | Destabilizing the introduced shRNAs may avoid such vector problems, and provide additional benefits for cloning and sequencing of inverted repeat sequences. | [
"56"
] | Destabilizing the introduced shRNAs may avoid such vector problems, and provide additional benefits for cloning and sequencing of inverted repeat sequences. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | In our target model system, we mutated the antisense strand of the shRNA hairpin, leaving the sense target sequence intact. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 123 | 9,384 | 0 | false | In our target model system, we mutated the antisense strand of the shRNA hairpin, leaving the sense target sequence intact. | [] | In our target model system, we mutated the antisense strand of the shRNA hairpin, leaving the sense target sequence intact. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | In the case of a true shRNA expression cassette, modifications will be made in the sense (target) strand to leave the guide/antisense siRNA strand unaltered. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 157 | 9,385 | 0 | false | In the case of a true shRNA expression cassette, modifications will be made in the sense (target) strand to leave the guide/antisense siRNA strand unaltered. | [] | In the case of a true shRNA expression cassette, modifications will be made in the sense (target) strand to leave the guide/antisense siRNA strand unaltered. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | The obvious advantage will be reduced complementarity between the target and the siRNA inhibitor. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 97 | 9,386 | 0 | false | The obvious advantage will be reduced complementarity between the target and the siRNA inhibitor. | [] | The obvious advantage will be reduced complementarity between the target and the siRNA inhibitor. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | The impact of such mutations on self-targeting is likely to depend on the position and type of mismatches that are introduced (57,58). | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 134 | 9,387 | 0 | false | The impact of such mutations on self-targeting is likely to depend on the position and type of mismatches that are introduced. | [
"57,58"
] | The impact of such mutations on self-targeting is likely to depend on the position and type of mismatches that are introduced. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | It is therefore impossible to make general rules for shRNA design and destabilization as each hairpin RNA structure will have its unique characteristics as target and effector in the RNAi mechanism. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 198 | 9,388 | 0 | false | It is therefore impossible to make general rules for shRNA design and destabilization as each hairpin RNA structure will have its unique characteristics as target and effector in the RNAi mechanism. | [] | It is therefore impossible to make general rules for shRNA design and destabilization as each hairpin RNA structure will have its unique characteristics as target and effector in the RNAi mechanism. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Here we demonstrate a ΞG window for shRNA-Pol destabilization without activating RNAi self-targeting, which may provide a guideline for other shRNAs. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 149 | 9,389 | 0 | false | Here we demonstrate a ΞG window for shRNA-Pol destabilization without activating RNAi self-targeting, which may provide a guideline for other shRNAs. | [] | Here we demonstrate a ΞG window for shRNA-Pol destabilization without activating RNAi self-targeting, which may provide a guideline for other shRNAs. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | Positional effects should be considered, and hairpins may be destabilized to ΞG = β25βkcal/mol as long as the target 3β² end remains base-paired. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 144 | 9,390 | 0 | false | Positional effects should be considered, and hairpins may be destabilized to ΞG = β25 kcal/mol as long as the target 3β² end remains base-paired. | [] | Positional effects should be considered, and hairpins may be destabilized to ΞG = β25 kcal/mol as long as the target 3β² end remains base-paired. | true | true | true | true | true | 1,492 |
4 | DISCUSSION | 1 | 52 | [
"B52",
"B53",
"B54",
"B55",
"B56",
"B57",
"B58"
] | 17,576,691 | pmid-12888501|pmid-15110788|pmid-14762201|pmid-15843020|pmid-15014042|pmid-15170178|pmid-14738896|pmid-14670130|pmid-11058109|pmid-6322106|pmid-15241778|pmid-15781493|pmid-16113241 | It is too early to define more general guidelines for structured RNA motifs other than the man-made, perfectly base-paired shRNA hairpins, as natural RNA structures differ significantly in their topology and architecture. | [
"52",
"53",
"54",
"55",
"56",
"57",
"58"
] | 221 | 9,391 | 0 | false | It is too early to define more general guidelines for structured RNA motifs other than the man-made, perfectly base-paired shRNA hairpins, as natural RNA structures differ significantly in their topology and architecture. | [] | It is too early to define more general guidelines for structured RNA motifs other than the man-made, perfectly base-paired shRNA hairpins, as natural RNA structures differ significantly in their topology and architecture. | true | true | true | true | true | 1,492 |
0 | INTRODUCTION | 1 | 1β4 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8",
"B9",
"B3",
"B4"
] | 17,311,812 | pmid-2124274|pmid-1645868|pmid-15152202|pmid-16064056|pmid-9217051|pmid-7947755|pmid-8197162|pmid-8768071|pmid-10688366|pmid-15152202|pmid-16064056 | Like most retroviruses, the human immunodeficiency virus type I (HIV-1) selectively packages two copies of its RNA genome (1β4). | [
"1β4",
"5β7",
"8",
"9",
"3",
"4"
] | 128 | 9,392 | 1 | false | Like most retroviruses, the human immunodeficiency virus type I (HIV-1) selectively packages two copies of its RNA genome. | [
"1β4"
] | Like most retroviruses, the human immunodeficiency virus type I selectively packages two copies of its RNA genome. | true | true | true | true | true | 1,493 |
0 | INTRODUCTION | 1 | 5β7 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8",
"B9",
"B3",
"B4"
] | 17,311,812 | pmid-2124274|pmid-1645868|pmid-15152202|pmid-16064056|pmid-9217051|pmid-7947755|pmid-8197162|pmid-8768071|pmid-10688366|pmid-15152202|pmid-16064056 | The two copies are held together as a non-covalent dimer at the dimer linkage structure (DLS) (5β7) in the 5β²-leader RNA (8,9). | [
"1β4",
"5β7",
"8",
"9",
"3",
"4"
] | 127 | 9,393 | 1 | false | The two copies are held together as a non-covalent dimer at the dimer linkage structure (DLS) in the 5β²-leader RNA. | [
"5β7",
"8,9"
] | The two copies are held together as a non-covalent dimer at the dimer linkage structure (DLS) in the 5β²-leader RNA. | true | true | true | true | true | 1,493 |
0 | INTRODUCTION | 1 | 1β4 | [
"B1 B2 B3 B4",
"B5 B6 B7",
"B8",
"B9",
"B3",
"B4"
] | 17,311,812 | pmid-2124274|pmid-1645868|pmid-15152202|pmid-16064056|pmid-9217051|pmid-7947755|pmid-8197162|pmid-8768071|pmid-10688366|pmid-15152202|pmid-16064056 | The RNA dimer has been shown to exert advantageous roles in reverse transcription, including in promoting recombination and generation of drug-resistant strains and its formation has been linked to packaging of the genomic RNA and viral maturation (3,4). | [
"1β4",
"5β7",
"8",
"9",
"3",
"4"
] | 254 | 9,394 | 0 | false | The RNA dimer has been shown to exert advantageous roles in reverse transcription, including in promoting recombination and generation of drug-resistant strains and its formation has been linked to packaging of the genomic RNA and viral maturation. | [
"3,4"
] | The RNA dimer has been shown to exert advantageous roles in reverse transcription, including in promoting recombination and generation of drug-resistant strains and its formation has been linked to packaging of the genomic RNA and viral maturation. | true | true | true | true | true | 1,493 |
1 | INTRODUCTION | 1 | 6 | [
"B6",
"B7",
"B10",
"B1",
"B2",
"B6",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B41"
] | 17,311,812 | pmid-7947755|pmid-8197162|pmid-8955907|pmid-2124274|pmid-1645868|pmid-7947755|pmid-8197162|pmid-8350405|pmid-8035501|pmid-11533179|pmid-10400801|pmid-8083960|pmid-9223458|pmid-16603544|pmid-12225748|pmid-12225748|pmid-8709210 | Stem loop1 (SL1) is a highly conserved 35-nt hairpin in the HIV-1 5β²-leader RNA (Figure 1A) and a key component of the DLS structure (6,7,10). | [
"6",
"7",
"10",
"1",
"2",
"6",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"41"
] | 142 | 9,395 | 0 | false | Stem loop1 is a highly conserved 35-nt hairpin in the HIV-1 5β²-leader RNA and a key component of the DLS structure. | [
"SL1",
"Figure 1A",
"6,7,10"
] | Stem loop1 is a highly conserved 35-nt hairpin in the HIV-1 5β²-leader RNA and a key component of the DLS structure. | true | true | true | true | true | 1,494 |
1 | INTRODUCTION | 1 | 6 | [
"B6",
"B7",
"B10",
"B1",
"B2",
"B6",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B41"
] | 17,311,812 | pmid-7947755|pmid-8197162|pmid-8955907|pmid-2124274|pmid-1645868|pmid-7947755|pmid-8197162|pmid-8350405|pmid-8035501|pmid-11533179|pmid-10400801|pmid-8083960|pmid-9223458|pmid-16603544|pmid-12225748|pmid-12225748|pmid-8709210 | SL1 contains a self-complementary GC-rich apical loop that promotes dimerization of the HIV-1 genome by forming metastable kissing dimers that are held together by intermolecular base-pairing (Figure 1B) (1,2,6,7). | [
"6",
"7",
"10",
"1",
"2",
"6",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"41"
] | 214 | 9,396 | 0 | false | SL1 contains a self-complementary GC-rich apical loop that promotes dimerization of the HIV-1 genome by forming metastable kissing dimers that are held together by intermolecular base-pairing. | [
"Figure 1B",
"1,2,6,7"
] | SL1 contains a self-complementary GC-rich apical loop that promotes dimerization of the HIV-1 genome by forming metastable kissing dimers that are held together by intermolecular base-pairing. | true | true | true | true | true | 1,494 |
1 | INTRODUCTION | 1 | 6 | [
"B6",
"B7",
"B10",
"B1",
"B2",
"B6",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B41"
] | 17,311,812 | pmid-7947755|pmid-8197162|pmid-8955907|pmid-2124274|pmid-1645868|pmid-7947755|pmid-8197162|pmid-8350405|pmid-8035501|pmid-11533179|pmid-10400801|pmid-8083960|pmid-9223458|pmid-16603544|pmid-12225748|pmid-12225748|pmid-8709210 | During viral maturation, the metastable kissing dimer undergoes a transition into a more stable dimer in which the two genome copies are more strongly associated (11,12). | [
"6",
"7",
"10",
"1",
"2",
"6",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"41"
] | 170 | 9,397 | 0 | false | During viral maturation, the metastable kissing dimer undergoes a transition into a more stable dimer in which the two genome copies are more strongly associated. | [
"11,12"
] | During viral maturation, the metastable kissing dimer undergoes a transition into a more stable dimer in which the two genome copies are more strongly associated. | true | true | true | true | true | 1,494 |
1 | INTRODUCTION | 1 | 13 | [
"B6",
"B7",
"B10",
"B1",
"B2",
"B6",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B41"
] | 17,311,812 | pmid-7947755|pmid-8197162|pmid-8955907|pmid-2124274|pmid-1645868|pmid-7947755|pmid-8197162|pmid-8350405|pmid-8035501|pmid-11533179|pmid-10400801|pmid-8083960|pmid-9223458|pmid-16603544|pmid-12225748|pmid-12225748|pmid-8709210 | This transition occurs following the proteolytic release of the N-terminus domain of nucleocapsid (NC) protein from the Gag precursor (13). | [
"6",
"7",
"10",
"1",
"2",
"6",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"41"
] | 139 | 9,398 | 1 | false | This transition occurs following the proteolytic release of the N-terminus domain of nucleocapsid (NC) protein from the Gag precursor. | [
"13"
] | This transition occurs following the proteolytic release of the N-terminus domain of nucleocapsid (NC) protein from the Gag precursor. | true | true | true | true | true | 1,494 |
1 | INTRODUCTION | 1 | 14 | [
"B6",
"B7",
"B10",
"B1",
"B2",
"B6",
"B7",
"B11",
"B12",
"B13",
"B14",
"B15",
"B16",
"B41"
] | 17,311,812 | pmid-7947755|pmid-8197162|pmid-8955907|pmid-2124274|pmid-1645868|pmid-7947755|pmid-8197162|pmid-8350405|pmid-8035501|pmid-11533179|pmid-10400801|pmid-8083960|pmid-9223458|pmid-16603544|pmid-12225748|pmid-12225748|pmid-8709210 | The processing of Gag has also been shown to be dependent on formation of the RNA dimer (14) and on interactions with the HIV-1 RNA genome (15,16), indicating that maturation of viral proteins and RNA are tightly coupled events. | [
"6",
"7",
"10",
"1",
"2",
"6",
"7",
"11",
"12",
"13",
"14",
"15",
"16",
"41"
] | 228 | 9,399 | 1 | false | The processing of Gag has also been shown to be dependent on formation of the RNA dimer and on interactions with the HIV-1 RNA genome, indicating that maturation of viral proteins and RNA are tightly coupled events. | [
"14",
"15,16"
] | The processing of Gag has also been shown to be dependent on formation of the RNA dimer and on interactions with the HIV-1 RNA genome, indicating that maturation of viral proteins and RNA are tightly coupled events. | true | true | true | true | true | 1,494 |
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