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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3 | INTRODUCTION | 1 | 22 | [
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | Adenine quartets (22), uracil quartets (23) and bulges may also be accommodated in RNA quadruplexes (24), expanding the structural repertoire of quadruplexes. | [
"18",
"19",
"20",
"21",
"22",
"23",
"24"
] | 158 | 4,600 | 1 | false | Adenine quartets, uracil quartets and bulges may also be accommodated in RNA quadruplexes, expanding the structural repertoire of quadruplexes. | [
"22",
"23",
"24"
] | Adenine quartets, uracil quartets and bulges may also be accommodated in RNA quadruplexes, expanding the structural repertoire of quadruplexes. | true | true | true | true | true | 777 |
3 | INTRODUCTION | 1 | 18 | [
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | However, the contributions of these non-G quartets to the kinetics and energetics of the quadruplex are poorly understood, and structural methods provide only clues to the effects of these modifications. | [
"18",
"19",
"20",
"21",
"22",
"23",
"24"
] | 203 | 4,601 | 0 | false | However, the contributions of these non-G quartets to the kinetics and energetics of the quadruplex are poorly understood, and structural methods provide only clues to the effects of these modifications. | [] | However, the contributions of these non-G quartets to the kinetics and energetics of the quadruplex are poorly understood, and structural methods provide only clues to the effects of these modifications. | true | true | true | true | true | 777 |
3 | INTRODUCTION | 1 | 18 | [
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | Little data is available for sequences in which the G-tract is interrupted by a ‘mismatch,’ i.e. | [
"18",
"19",
"20",
"21",
"22",
"23",
"24"
] | 96 | 4,602 | 0 | false | Little data is available for sequences in which the G-tract is interrupted by a ‘mismatch,’ i.e. | [] | Little data is available for sequences in which the G-tract is interrupted by a ‘mismatch,’ i.e. | true | true | true | true | true | 777 |
3 | INTRODUCTION | 1 | 18 | [
"B18",
"B19",
"B20",
"B21",
"B22",
"B23",
"B24"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | any base (natural or synthetic) different from a guanine. | [
"18",
"19",
"20",
"21",
"22",
"23",
"24"
] | 57 | 4,603 | 0 | false | any base (natural or synthetic) different from a guanine. | [] | any base (natural or synthetic) different from a guanine. | false | true | true | true | false | 777 |
4 | INTRODUCTION | 0 | null | null | 17,452,368 | pmid-11159416 | Using the canonical tetramolecular quadruplexes formed by TG4T and TG5T, we substituted each of the four or five guanines, respectively, with a variety of bases (the natural bases A, T, C and U, and the non-natural bases represented in Figure 1) and analyzed the impacts of these modifications on the kinetics of formati... | null | 364 | 4,604 | 0 | false | null | null | Using the canonical tetramolecular quadruplexes formed by TG4T and TG5T, we substituted each of the four or five guanines, respectively, with a variety of bases (the natural bases A, T, C and U, and the non-natural bases represented in Figure 1) and analyzed the impacts of these modifications on the kinetics of formati... | true | true | true | true | true | 778 |
4 | INTRODUCTION | 0 | null | null | 17,452,368 | pmid-11159416 | We demonstrate that, in most cases, the incorporation of a single modified quartet not only leads to decreased melting temperature but also to a decreased association rate. | null | 172 | 4,605 | 0 | false | null | null | We demonstrate that, in most cases, the incorporation of a single modified quartet not only leads to decreased melting temperature but also to a decreased association rate. | true | true | true | true | true | 778 |
4 | INTRODUCTION | 0 | null | null | 17,452,368 | pmid-11159416 | Non-guanine base quartets are, at best, tolerated in a parallel quadruplex and generally do not contribute to the stability of the structure, two exceptions being the 8-bromo-guanine (X) and 6-methyl-isoxanthopterin (P) substitutions. | null | 234 | 4,606 | 0 | false | null | null | Non-guanine base quartets are, at best, tolerated in a parallel quadruplex and generally do not contribute to the stability of the structure, two exceptions being the 8-bromo-guanine (X) and 6-methyl-isoxanthopterin (P) substitutions. | true | true | true | true | true | 778 |
0 | DISCUSSION | 1 | 17 | [
"B17"
] | 17,452,368 | pmid-12831878|pmid-17012276|pmid-13947099|pmid-15079086|pmid-11438689|pmid-15231739|pmid-16142245|NA|pmid-17036128|pmid-17146462|pmid-17226803|pmid-16287312 | In the present study, we analyzed the effects of 12 different base substitutions on the kinetics and thermodynamics of parallel tetramolecular quadruplexes. | [
"17"
] | 156 | 4,607 | 0 | false | In the present study, we analyzed the effects of 12 different base substitutions on the kinetics and thermodynamics of parallel tetramolecular quadruplexes. | [] | In the present study, we analyzed the effects of 12 different base substitutions on the kinetics and thermodynamics of parallel tetramolecular quadruplexes. | true | true | true | true | true | 779 |
0 | DISCUSSION | 1 | 17 | [
"B17"
] | 17,452,368 | pmid-12831878|pmid-17012276|pmid-13947099|pmid-15079086|pmid-11438689|pmid-15231739|pmid-16142245|NA|pmid-17036128|pmid-17146462|pmid-17226803|pmid-16287312 | The data were compared with the parallel-stranded tetramolecular quadruplexes formed by TG4T and TG5T. | [
"17"
] | 102 | 4,608 | 0 | false | The data were compared with the parallel-stranded tetramolecular quadruplexes formed by TG4T and TG5T. | [] | The data were compared with the parallel-stranded tetramolecular quadruplexes formed by TG4T and TG5T. | true | true | true | true | true | 779 |
0 | DISCUSSION | 1 | 17 | [
"B17"
] | 17,452,368 | pmid-12831878|pmid-17012276|pmid-13947099|pmid-15079086|pmid-11438689|pmid-15231739|pmid-16142245|NA|pmid-17036128|pmid-17146462|pmid-17226803|pmid-16287312 | Most isothermal and melting experiments could be analyzed in the framework of an all-or-none process, in agreement with Petraccone et al., who demonstrated that the quadruplex-to-single strand transition of TG4T involved only two significant spectral species, suggesting a simple dissociation pathway (17). | [
"17"
] | 306 | 4,609 | 1 | false | Most isothermal and melting experiments could be analyzed in the framework of an all-or-none process, in agreement with Petraccone et al., who demonstrated that the quadruplex-to-single strand transition of TG4T involved only two significant spectral species, suggesting a simple dissociation pathway. | [
"17"
] | Most isothermal and melting experiments could be analyzed in the framework of an all-or-none process, in agreement with Petraccone et al., who demonstrated that the quadruplex-to-single strand transition of TG4T involved only two significant spectral species, suggesting a simple dissociation pathway. | true | true | true | true | true | 779 |
0 | DISCUSSION | 1 | 17 | [
"B17"
] | 17,452,368 | pmid-12831878|pmid-17012276|pmid-13947099|pmid-15079086|pmid-11438689|pmid-15231739|pmid-16142245|NA|pmid-17036128|pmid-17146462|pmid-17226803|pmid-16287312 | To our knowledge, the present work is the first experimental attempt to quantify and compare a variety of modified quadruplex sequences. | [
"17"
] | 136 | 4,610 | 0 | false | To our knowledge, the present work is the first experimental attempt to quantify and compare a variety of modified quadruplex sequences. | [] | To our knowledge, the present work is the first experimental attempt to quantify and compare a variety of modified quadruplex sequences. | true | true | true | true | true | 779 |
1 | DISCUSSION | 1 | 37 | [
"B37",
"B38"
] | 17,452,368 | pmid-5138337|pmid-1390713 | Although many oligomers adopt relatively similar conformations, the kinetics of these complexes may vary greatly. | [
"37",
"38"
] | 113 | 4,611 | 0 | false | Although many oligomers adopt relatively similar conformations, the kinetics of these complexes may vary greatly. | [] | Although many oligomers adopt relatively similar conformations, the kinetics of these complexes may vary greatly. | true | true | true | true | true | 780 |
1 | DISCUSSION | 1 | 37 | [
"B37",
"B38"
] | 17,452,368 | pmid-5138337|pmid-1390713 | We showed that the consideration of Tm (or T1/2) as the sole indicator of quadruplex thermodynamics may lead to a profound underestimation of the energetic penalty imposed by a single guanine replacement. | [
"37",
"38"
] | 204 | 4,612 | 0 | false | We showed that the consideration of Tm (or T1/2) as the sole indicator of quadruplex thermodynamics may lead to a profound underestimation of the energetic penalty imposed by a single guanine replacement. | [] | We showed that the consideration of Tm (or T1/2) as the sole indicator of quadruplex thermodynamics may lead to a profound underestimation of the energetic penalty imposed by a single guanine replacement. | true | true | true | true | true | 780 |
1 | DISCUSSION | 1 | 37 | [
"B37",
"B38"
] | 17,452,368 | pmid-5138337|pmid-1390713 | It is essential to evaluate the kinetics of both dissociation and association to obtain a reliable estimate of the thermodynamic penalty imposed by the sequence modification. | [
"37",
"38"
] | 174 | 4,613 | 0 | false | It is essential to evaluate the kinetics of both dissociation and association to obtain a reliable estimate of the thermodynamic penalty imposed by the sequence modification. | [] | It is essential to evaluate the kinetics of both dissociation and association to obtain a reliable estimate of the thermodynamic penalty imposed by the sequence modification. | true | true | true | true | true | 780 |
1 | DISCUSSION | 1 | 37 | [
"B37",
"B38"
] | 17,452,368 | pmid-5138337|pmid-1390713 | It is striking that for quadruplexes, a ‘mismatch’ has a deleterious impact on both the association and dissociation processes, whereas for duplexes and triplexes, a mismatched base-pair or base-triplet affects the dissociation process (37,38). | [
"37",
"38"
] | 244 | 4,614 | 0 | false | It is striking that for quadruplexes, a ‘mismatch’ has a deleterious impact on both the association and dissociation processes, whereas for duplexes and triplexes, a mismatched base-pair or base-triplet affects the dissociation process. | [
"37,38"
] | It is striking that for quadruplexes, a ‘mismatch’ has a deleterious impact on both the association and dissociation processes, whereas for duplexes and triplexes, a mismatched base-pair or base-triplet affects the dissociation process. | true | true | true | true | true | 780 |
1 | DISCUSSION | 1 | 37 | [
"B37",
"B38"
] | 17,452,368 | pmid-5138337|pmid-1390713 | A possible explanation for this behavior comes from the differences in length among these motifs. | [
"37",
"38"
] | 97 | 4,615 | 0 | false | A possible explanation for this behavior comes from the differences in length among these motifs. | [] | A possible explanation for this behavior comes from the differences in length among these motifs. | true | true | true | true | true | 780 |
1 | DISCUSSION | 1 | 37 | [
"B37",
"B38"
] | 17,452,368 | pmid-5138337|pmid-1390713 | Only four to five base quartets are formed in quadruplexes, and a mismatch is more likely to affect the nucleation event for initial quadruplex association. | [
"37",
"38"
] | 156 | 4,616 | 0 | false | Only four to five base quartets are formed in quadruplexes, and a mismatch is more likely to affect the nucleation event for initial quadruplex association. | [] | Only four to five base quartets are formed in quadruplexes, and a mismatch is more likely to affect the nucleation event for initial quadruplex association. | true | true | true | true | true | 780 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | The 5′/3′ asymmetry observed in the influence of stabilizing modifications also gives interesting insights into the nucleation process. | [
"39",
"40",
"41–46"
] | 135 | 4,617 | 0 | false | The 5′/3′ asymmetry observed in the influence of stabilizing modifications also gives interesting insights into the nucleation process. | [] | The 5′/3′ asymmetry observed in the influence of stabilizing modifications also gives interesting insights into the nucleation process. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | One may therefore be tempted to propose that the rate-limiting step involves the 5′ side of the strands. | [
"39",
"40",
"41–46"
] | 104 | 4,618 | 0 | false | One may therefore be tempted to propose that the rate-limiting step involves the 5′ side of the strands. | [] | One may therefore be tempted to propose that the rate-limiting step involves the 5′ side of the strands. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | All three favorable modifications (8, X and P) accelerated formation or decelerated dissociation of quadruplexes only when located on the 5′ side. | [
"39",
"40",
"41–46"
] | 146 | 4,619 | 0 | false | All three favorable modifications (8, X and P) accelerated formation or decelerated dissociation of quadruplexes only when located on the 5′ side. | [] | All three favorable modifications (8, X and P) accelerated formation or decelerated dissociation of quadruplexes only when located on the 5′ side. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | In X and P modifications, the respective bromo- and methyl substituents may favor the initial hydrophobic collapse that brings strands together. | [
"39",
"40",
"41–46"
] | 144 | 4,620 | 0 | false | In X and P modifications, the respective bromo- and methyl substituents may favor the initial hydrophobic collapse that brings strands together. | [] | In X and P modifications, the respective bromo- and methyl substituents may favor the initial hydrophobic collapse that brings strands together. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | However, as this asymmetry is not observed for all substitutions, this putative directional nucleation-zipping mechanism for quadruplex formation is probably less pronounced than for triplexes (39). | [
"39",
"40",
"41–46"
] | 198 | 4,621 | 1 | false | However, as this asymmetry is not observed for all substitutions, this putative directional nucleation-zipping mechanism for quadruplex formation is probably less pronounced than for triplexes. | [
"39"
] | However, as this asymmetry is not observed for all substitutions, this putative directional nucleation-zipping mechanism for quadruplex formation is probably less pronounced than for triplexes. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | The extremely deleterious impact of a central guanine substitution on association also indicates that the central guanines participate in the rate-limiting step. | [
"39",
"40",
"41–46"
] | 161 | 4,622 | 0 | false | The extremely deleterious impact of a central guanine substitution on association also indicates that the central guanines participate in the rate-limiting step. | [] | The extremely deleterious impact of a central guanine substitution on association also indicates that the central guanines participate in the rate-limiting step. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 40 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | It is also worth noticing that with these three modifications (P, X and 8), the syn conformation is (or is likely to be) favored as compared to a regular guanine (40) suggesting the implication of the syn G at the 5′ end in the nucleation process. | [
"39",
"40",
"41–46"
] | 247 | 4,623 | 1 | false | It is also worth noticing that with these three modifications (P, X and 8), the syn conformation is (or is likely to be) favored as compared to a regular guanine suggesting the implication of the syn G at the 5′ end in the nucleation process. | [
"40"
] | It is also worth noticing that with these three modifications (P, X and 8), the syn conformation is (or is likely to be) favored as compared to a regular guanine suggesting the implication of the syn G at the 5′ end in the nucleation process. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 41–46 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | In the publications reporting quadruplex structures based on the (3 + 1) or mixed parallel–antiparallel scaffold (41–46) the Gs on the 5′ part of the quadruplex are mostly syn. | [
"39",
"40",
"41–46"
] | 176 | 4,624 | 1 | false | In the publications reporting quadruplex structures based on the (3 + 1) or mixed parallel–antiparallel scaffold the Gs on the 5′ part of the quadruplex are mostly syn. | [
"41–46"
] | In the publications reporting quadruplex structures based on the or mixed parallel–antiparallel scaffold the Gs on the 5′ part of the quadruplex are mostly syn. | true | true | true | true | true | 781 |
2 | DISCUSSION | 1 | 39 | [
"B39",
"B40",
"B41 B42 B43 B44 B45 B46"
] | 17,452,368 | NA|pmid-12944293|pmid-8672504|pmid-15642696|pmid-16682446|pmid-8672504|pmid-15642696|pmid-16287312|pmid-12490709|NA|pmid-7704525|pmid-16332077|pmid-16433524|pmid-16714449|pmid-16866556|pmid-17040899 | These 5′ syn bases might also participate in the stability of the quadruplex (for X and 8). | [
"39",
"40",
"41–46"
] | 91 | 4,625 | 0 | false | These 5′ syn bases might also participate in the stability of the quadruplex (for X and 8). | [] | These 5′ syn bases might also participate in the stability of the quadruplex (for X and 8). | true | true | true | true | true | 781 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | The structure of this kinetic intermediate remains elusive but some observations help to eliminate some possibilities: (i) a Hoogsteen duplex or triplex is an extremely unstable, and therefore unlikely, intermediate (13), (ii) transient strand dimers and trimers have been evidenced by mass spectrometry (47), (iii) mono... | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 575 | 4,626 | 1 | false | The structure of this kinetic intermediate remains elusive but some observations help to eliminate some possibilities: (i) a Hoogsteen duplex or triplex is an extremely unstable, and therefore unlikely, intermediate, (ii) transient strand dimers and trimers have been evidenced by mass spectrometry, (iii) monocations pa... | [
"13",
"47",
"15,16",
"15",
"14–17"
] | The structure of this kinetic intermediate remains elusive but some observations help to eliminate some possibilities: (i) a Hoogsteen duplex or triplex is an extremely unstable, and therefore unlikely, intermediate, (ii) transient strand dimers and trimers have been evidenced by mass spectrometry, (iii) monocations pa... | true | true | true | true | true | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | Starting from the double-dimer to tetramer pathway proposed by Wyatt et al. | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 75 | 4,627 | 0 | false | Starting from the double-dimer to tetramer pathway proposed by Wyatt et al. | [] | Starting from the double-dimer to tetramer pathway proposed by Wyatt et al. | true | true | true | true | true | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | and the ‘cross-like’ two-stranded assemblies proposed by Stefl et al. | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 69 | 4,628 | 0 | false | and the ‘cross-like’ two-stranded assemblies proposed by Stefl et al. | [] | and the ‘cross-like’ two-stranded assemblies proposed by Stefl et al. | false | true | true | true | false | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | (13), one may envision that the rate-limiting step is the formation of ‘nucleation’ quartets, with four guanines unlikely to originate from four different strands. | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 163 | 4,629 | 1 | false | , one may envision that the rate-limiting step is the formation of ‘nucleation’ quartets, with four guanines unlikely to originate from four different strands. | [
"13"
] | , one may envision that the rate-limiting step is the formation of ‘nucleation’ quartets, with four guanines unlikely to originate from four different strands. | false | false | true | true | false | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | Two of these guanines must then originate from the same strand (for example, one ‘central’ and the other towards the 5′ end, thereby explaining a certain asymmetry) and some of these bases transiently adopt a syn conformation. | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 226 | 4,630 | 0 | false | Two of these guanines must then originate from the same strand (for example, one ‘central’ and the other towards the 5′ end, thereby explaining a certain asymmetry) and some of these bases transiently adopt a syn conformation. | [] | Two of these guanines must then originate from the same strand (for example, one ‘central’ and the other towards the 5′ end, thereby explaining a certain asymmetry) and some of these bases transiently adopt a syn conformation. | true | true | true | true | true | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | This transient geometry could be facilitated by the presence of some modifications, (X or P for example), for which the syn conformation is preferred. | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 150 | 4,631 | 0 | false | This transient geometry could be facilitated by the presence of some modifications, (X or P for example), for which the syn conformation is preferred. | [] | This transient geometry could be facilitated by the presence of some modifications, (X or P for example), for which the syn conformation is preferred. | true | true | true | true | true | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | A long guanine tract facilitates the formation of two (and perhaps three) stacked quartet, which captures one to two monocations and defines the nucleation event. | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 162 | 4,632 | 0 | false | A long guanine tract facilitates the formation of two (and perhaps three) stacked quartet, which captures one to two monocations and defines the nucleation event. | [] | A long guanine tract facilitates the formation of two (and perhaps three) stacked quartet, which captures one to two monocations and defines the nucleation event. | true | true | true | true | true | 782 |
3 | DISCUSSION | 1 | 15 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | This could explain the puzzling observation that the longer the guanine tract, the faster the association and this is in agreement with the negative activation energy of association (Eon = −29 kcal/mol for TG4T) found for tetramolecular quadruplexes (15). | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 255 | 4,633 | 1 | false | This could explain the puzzling observation that the longer the guanine tract, the faster the association and this is in agreement with the negative activation energy of association (Eon = −29 kcal/mol for TG4T) found for tetramolecular quadruplexes. | [
"15"
] | This could explain the puzzling observation that the longer the guanine tract, the faster the association and this is in agreement with the negative activation energy of association (Eon = −29 kcal/mol for TG4T) found for tetramolecular quadruplexes. | true | true | true | true | true | 782 |
3 | DISCUSSION | 1 | 13 | [
"B13",
"B47",
"B15",
"B16",
"B15",
"B14 B15 B16 B17",
"B14",
"B13",
"B15"
] | 17,452,368 | pmid-14747859|pmid-15614794|pmid-10352174|pmid-10772934|pmid-12842044|pmid-1382577|pmid-14604532|pmid-12944293|NA|pmid-15642696|pmid-16682446|pmid-15642696|pmid-8672504|pmid-15642696|pmid-16682446|pmid-16287312|pmid-8672504|pmid-12944293|pmid-15642696 | These initial quartet(s) are embedded in a two-stranded dimer, rather than a Hoogsteen duplex, and will then undergo a series of rearrangements involving the association of additional strands, possible formation of a trimer, syn to anti conversion (again, the presence of syn bases in the final structure may be proposed... | [
"13",
"47",
"15",
"16",
"15",
"14–17",
"14",
"13",
"15"
] | 572 | 4,634 | 0 | false | These initial quartet(s) are embedded in a two-stranded dimer, rather than a Hoogsteen duplex, and will then undergo a series of rearrangements involving the association of additional strands, possible formation of a trimer, syn to anti conversion (again, the presence of syn bases in the final structure may be proposed... | [] | These initial quartet(s) are embedded in a two-stranded dimer, rather than a Hoogsteen duplex, and will then undergo a series of rearrangements involving the association of additional strands, possible formation of a trimer, syn to anti conversion (again, the presence of syn bases in the final structure may be proposed... | true | true | true | true | true | 782 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | The wealth of data compiled here can serve as a basis for future structural interpretation. | [
"48"
] | 91 | 4,635 | 0 | false | The wealth of data compiled here can serve as a basis for future structural interpretation. | [] | The wealth of data compiled here can serve as a basis for future structural interpretation. | true | true | true | true | true | 783 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | Interestingly, Stefl et al. | [
"48"
] | 27 | 4,636 | 0 | false | Interestingly, Stefl et al. | [] | Interestingly, Stefl et al. | true | true | true | true | true | 783 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | already performed molecular dynamics simulations of DNA quadruplex molecules containing modified bases (48). | [
"48"
] | 108 | 4,637 | 1 | false | already performed molecular dynamics simulations of DNA quadruplex molecules containing modified bases. | [
"48"
] | already performed molecular dynamics simulations of DNA quadruplex molecules containing modified bases. | false | true | true | true | false | 783 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | The incorporation of 6-thioguanine (6) or 6-methylguanine (M) sharply destabilized four-stranded G-DNA structures, whereas inosine (I) had a limited effect. | [
"48"
] | 156 | 4,638 | 0 | false | The incorporation of 6-thioguanine (6) or 6-methylguanine (M) sharply destabilized four-stranded G-DNA structures, whereas inosine (I) had a limited effect. | [] | The incorporation of 6-thioguanine (6) or 6-methylguanine (M) sharply destabilized four-stranded G-DNA structures, whereas inosine (I) had a limited effect. | true | true | true | true | true | 783 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | The first two modifications prevented proper cation coordination and created a steric clash in the central part of the quartet, whereas inosine could still form a quartet, even though the external ring of H-bonds is lost. | [
"48"
] | 221 | 4,639 | 0 | false | The first two modifications prevented proper cation coordination and created a steric clash in the central part of the quartet, whereas inosine could still form a quartet, even though the external ring of H-bonds is lost. | [] | The first two modifications prevented proper cation coordination and created a steric clash in the central part of the quartet, whereas inosine could still form a quartet, even though the external ring of H-bonds is lost. | true | true | true | true | true | 783 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | All these predictions are verified in our experiments. | [
"48"
] | 54 | 4,640 | 0 | false | All these predictions are verified in our experiments. | [] | All these predictions are verified in our experiments. | true | true | true | true | true | 783 |
4 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,452,368 | pmid-11159416 | Also, the higher destabilization observed with central modifications, together with the mass spectrometry measurements of the number of coordinated cations, suggest that the stability should be interpreted in terms of nearest neighbors (two neighboring quartets and the associated cations) instead of quartets only. | [
"48"
] | 315 | 4,641 | 0 | false | Also, the higher destabilization observed with central modifications, together with the mass spectrometry measurements of the number of coordinated cations, suggest that the stability should be interpreted in terms of nearest neighbors (two neighboring quartets and the associated cations) instead of quartets only. | [] | Also, the higher destabilization observed with central modifications, together with the mass spectrometry measurements of the number of coordinated cations, suggest that the stability should be interpreted in terms of nearest neighbors (two neighboring quartets and the associated cations) instead of quartets only. | true | true | true | true | true | 783 |
5 | DISCUSSION | 0 | null | null | 17,452,368 | null | One of the major findings of our study is that most substitutions are extremely detrimental to quadruplex stability, as shown by substantial decreases in both the association rate and the thermal stability of the complex. | null | 221 | 4,642 | 0 | false | null | null | One of the major findings of our study is that most substitutions are extremely detrimental to quadruplex stability, as shown by substantial decreases in both the association rate and the thermal stability of the complex. | true | true | true | true | true | 784 |
5 | DISCUSSION | 0 | null | null | 17,452,368 | null | In particular, all natural bases (A, C, T and U) fall in this category. | null | 71 | 4,643 | 0 | false | null | null | In particular, all natural bases (A, C, T and U) fall in this category. | true | true | true | true | true | 784 |
5 | DISCUSSION | 0 | null | null | 17,452,368 | null | Non-G quartets in genomic DNA are therefore clearly not favorable to the energetics of the quadruplexes: they are tolerated at best. | null | 132 | 4,644 | 0 | false | null | null | Non-G quartets in genomic DNA are therefore clearly not favorable to the energetics of the quadruplexes: they are tolerated at best. | true | true | true | true | true | 784 |
5 | DISCUSSION | 0 | null | null | 17,452,368 | null | This is independent of the nature of the monocation: with a few exceptions, an unfavorable substitution in K+ remains unfavorable in Na+ and . | null | 142 | 4,645 | 0 | false | null | null | This is independent of the nature of the monocation: with a few exceptions, an unfavorable substitution in K+ remains unfavorable in Na+ and . | true | true | true | true | true | 784 |
5 | DISCUSSION | 0 | null | null | 17,452,368 | null | Despite the presence of well-defined non-guanine base quartets in a number of NMR and X-ray structures, our data suggest that these quartets do not participate favorably in structural stability and are formed only by virtue of the docking platform provided by neighboring G-quartets. | null | 283 | 4,646 | 0 | false | null | null | Despite the presence of well-defined non-guanine base quartets in a number of NMR and X-ray structures, our data suggest that these quartets do not participate favorably in structural stability and are formed only by virtue of the docking platform provided by neighboring G-quartets. | true | true | true | true | true | 784 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | Our study also provides useful guidelines for the future conception of synthetic DNA assemblies based on quadruplex formation. | [
"49"
] | 126 | 4,647 | 0 | false | Our study also provides useful guidelines for the future conception of synthetic DNA assemblies based on quadruplex formation. | [] | Our study also provides useful guidelines for the future conception of synthetic DNA assemblies based on quadruplex formation. | true | true | true | true | true | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | Comparing the association constants found for a variety of substitutions led us to propose the following conclusions: (i) the central part of the quartet (the central ring of H-bonds and O6 carbonyl groups) is vital to its stability: altering this part not only leads to the loss of one H-bond, but may also hamper coord... | [
"49"
] | 350 | 4,648 | 0 | false | Comparing the association constants found for a variety of substitutions led us to propose the following conclusions: (i) the central part of the quartet (the central ring of H-bonds and O6 carbonyl groups) is vital to its stability: altering this part not only leads to the loss of one H-bond, but may also hamper coord... | [] | Comparing the association constants found for a variety of substitutions led us to propose the following conclusions: (i) the central part of the quartet (the central ring of H-bonds and O6 carbonyl groups) is vital to its stability: altering this part not only leads to the loss of one H-bond, but may also hamper coord... | true | true | true | true | true | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | (ii) Removal of the external ring of H-bonds leads to a moderate decrease in the association rate (ex: inosine). | [
"49"
] | 112 | 4,649 | 0 | false | (ii) Removal of the external ring of H-bonds leads to a moderate decrease in the association rate (ex: inosine). | [] | (ii) Removal of the external ring of H-bonds leads to a moderate decrease in the association rate (ex: inosine). | false | false | true | true | false | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | However, if one not only remove these H-bonds but perturbs the geometry/planarity of the quartet as a result of a steric clash, as for 7-deazaguanine, the penalty is more severe. | [
"49"
] | 178 | 4,650 | 0 | false | However, if one not only remove these H-bonds but perturbs the geometry/planarity of the quartet as a result of a steric clash, as for 7-deazaguanine, the penalty is more severe. | [] | However, if one not only remove these H-bonds but perturbs the geometry/planarity of the quartet as a result of a steric clash, as for 7-deazaguanine, the penalty is more severe. | true | true | true | true | true | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | (iii) One is left with a limited freedom to play with the 8-position and, in a few cases (8-bromo-guanine), substitutions may even become favorable. | [
"49"
] | 148 | 4,651 | 0 | false | (iii) One is left with a limited freedom to play with the 8-position and, in a few cases (8-bromo-guanine), substitutions may even become favorable. | [] | (iii) One is left with a limited freedom to play with the 8-position and, in a few cases (8-bromo-guanine), substitutions may even become favorable. | false | false | true | true | false | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | Modifications that do not affect the cyclic hydrogen bond pattern nor the central carbonyl groups are well tolerated and may effectively replace guanines, although syn/anti sugar configuration preferences play a role. | [
"49"
] | 217 | 4,652 | 0 | false | Modifications that do not affect the cyclic hydrogen bond pattern nor the central carbonyl groups are well tolerated and may effectively replace guanines, although syn/anti sugar configuration preferences play a role. | [] | Modifications that do not affect the cyclic hydrogen bond pattern nor the central carbonyl groups are well tolerated and may effectively replace guanines, although syn/anti sugar configuration preferences play a role. | true | true | true | true | true | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | (iv) Finally, the purine geometry is not an absolute requirement to form a stable quartet: isoxanthopterine is fully compatible with quadruplex formation, and other planar bicyclic groups may also form a quartet. | [
"49"
] | 212 | 4,653 | 0 | false | (iv) Finally, the purine geometry is not an absolute requirement to form a stable quartet: isoxanthopterine is fully compatible with quadruplex formation, and other planar bicyclic groups may also form a quartet. | [] | (iv) Finally, the purine geometry is not an absolute requirement to form a stable quartet: isoxanthopterine is fully compatible with quadruplex formation, and other planar bicyclic groups may also form a quartet. | false | false | true | true | false | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | In that case, we believe that the presence of a central carbonyl group is required (i.e. | [
"49"
] | 88 | 4,654 | 0 | false | In that case, we believe that the presence of a central carbonyl group is required (i.e. | [] | In that case, we believe that the presence of a central carbonyl group is required (i.e. | true | true | true | true | true | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | at a position equivalent to the O6 group of guanine) and should be H-bonded to a H-bond donor group (likely an amino group) from another base. | [
"49"
] | 142 | 4,655 | 0 | false | at a position equivalent to the O6 group of guanine) and should be H-bonded to a H-bond donor group (likely an amino group) from another base. | [] | at a position equivalent to the O6 group of guanine) and should be H-bonded to a H-bond donor group (likely an amino group) from another base. | false | true | true | true | false | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | (v) The conclusions reached here apply to base quartets in which, by virtue of the tetramolecular system, all four bases are substituted. | [
"49"
] | 137 | 4,656 | 0 | false | (v) The conclusions reached here apply to base quartets in which, by virtue of the tetramolecular system, all four bases are substituted. | [] | (v) The conclusions reached here apply to base quartets in which, by virtue of the tetramolecular system, all four bases are substituted. | false | false | true | true | false | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | It should be interesting to compare this system with intramolecular quadruplexes, in which a single base may be replaced in each quartet | [
"49"
] | 136 | 4,657 | 0 | false | It should be interesting to compare this system with intramolecular quadruplexes, in which a single base may be replaced in each quartet | [] | It should be interesting to compare this system with intramolecular quadruplexes, in which a single base may be replaced in each quartet | true | true | false | true | false | 785 |
6 | DISCUSSION | 1 | 49 | [
"B49"
] | 17,452,368 | pmid-16292787 | [for example: (49)]. | [
"49"
] | 20 | 4,658 | 0 | false | . | [
"for example: (49)"
] | . | false | false | true | true | false | 785 |
7 | DISCUSSION | 0 | null | null | 17,452,368 | null | The two ‘non-canonical’ modifications X and P even lead to faster quadruplex formations than the all-guanine reference sequences. | null | 129 | 4,659 | 0 | false | null | null | The two ‘non-canonical’ modifications X and P even lead to faster quadruplex formations than the all-guanine reference sequences. | true | true | true | true | true | 786 |
7 | DISCUSSION | 0 | null | null | 17,452,368 | null | The only substitution that leads to a stability improvement in both association and dissociation parameters (as compared to guanine) is 8-bromo-guanine (X), when inserted at the 5′ end (position 1). | null | 198 | 4,660 | 0 | false | null | null | The only substitution that leads to a stability improvement in both association and dissociation parameters (as compared to guanine) is 8-bromo-guanine (X), when inserted at the 5′ end (position 1). | true | true | true | true | true | 786 |
7 | DISCUSSION | 0 | null | null | 17,452,368 | null | However, the case of P substitution is also highly interesting on the application point of view, because this modification in the 5′ side leads to an increase of both the association and dissociation rates. | null | 206 | 4,661 | 0 | false | null | null | However, the case of P substitution is also highly interesting on the application point of view, because this modification in the 5′ side leads to an increase of both the association and dissociation rates. | true | true | true | true | true | 786 |
7 | DISCUSSION | 0 | null | null | 17,452,368 | null | Reversible devices based on P-modified quadruplexes could therefore have a higher turnover than the classical G-quadruplexes. | null | 125 | 4,662 | 0 | false | null | null | Reversible devices based on P-modified quadruplexes could therefore have a higher turnover than the classical G-quadruplexes. | true | true | true | true | true | 786 |
7 | DISCUSSION | 0 | null | null | 17,452,368 | null | The thermodynamic and kinetic data compiled here is highly valuable for the design of DNA quadruplex assemblies with tunable association/dissociation properties. | null | 161 | 4,663 | 0 | false | null | null | The thermodynamic and kinetic data compiled here is highly valuable for the design of DNA quadruplex assemblies with tunable association/dissociation properties. | true | true | true | true | true | 786 |
7 | DISCUSSION | 0 | null | null | 17,452,368 | null | So far, guanines are still a quartet′s best friends! | null | 52 | 4,664 | 0 | false | null | null | So far, guanines are still a quartet′s best friends! | true | true | true | true | true | 786 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Small regulatory RNAs (sRNAs) are expressed in both prokaryotes and eukaryotes, primarily as posttranscriptional regulators. | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 124 | 4,665 | 0 | false | Small regulatory RNAs (sRNAs) are expressed in both prokaryotes and eukaryotes, primarily as posttranscriptional regulators. | [] | Small regulatory RNAs (sRNAs) are expressed in both prokaryotes and eukaryotes, primarily as posttranscriptional regulators. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Over the past six years, about 70 sRNAs have been discovered in E. coli, and about 20 of them have been assigned a function. | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 124 | 4,666 | 0 | false | Over the past six years, about 70 sRNAs have been discovered in E. coli, and about 20 of them have been assigned a function. | [] | Over the past six years, about 70 sRNAs have been discovered in E. coli, and about 20 of them have been assigned a function. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Many of these trans-encoded RNAs are involved in metabolic processes [e.g. | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 74 | 4,667 | 0 | false | Many of these trans-encoded RNAs are involved in metabolic processes [e.g. | [] | Many of these trans-encoded RNAs are involved in metabolic processes [e.g. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Spot42, DsrA, RprA, RyhB, SgrS, GadY, reviewed in (1)] and at least eight sRNAs regulate the expression of membrane proteins [reviewed in (2)]. | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 143 | 4,668 | 1 | false | Spot42, DsrA, RprA, RyhB, SgrS, GadY, reviewed in ] and at least eight sRNAs regulate the expression of membrane proteins. | [
"1",
"reviewed in (2)"
] | Spot42, DsrA, RprA, RyhB, SgrS, GadY, reviewed in ] and at least eight sRNAs regulate the expression of membrane proteins. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | To date, relatively few systematic searches have been performed in Gram-positive bacteria. | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 90 | 4,669 | 0 | false | To date, relatively few systematic searches have been performed in Gram-positive bacteria. | [] | To date, relatively few systematic searches have been performed in Gram-positive bacteria. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 3 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Among the recently discovered sRNAs in Gram-positive hosts are RatA from the Bacillus subtilis chromosome (3), which came up in a systematic search (4) together with 12 other sRNAs that proved to be sporulation-controlled, but still await the identification of their targets (5). | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 279 | 4,670 | 1 | false | Among the recently discovered sRNAs in Gram-positive hosts are RatA from the Bacillus subtilis chromosome, which came up in a systematic search together with 12 other sRNAs that proved to be sporulation-controlled, but still await the identification of their targets. | [
"3",
"4",
"5"
] | Among the recently discovered sRNAs in Gram-positive hosts are RatA from the Bacillus subtilis chromosome, which came up in a systematic search together with 12 other sRNAs that proved to be sporulation-controlled, but still await the identification of their targets. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 6 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Furthermore, in addition to the well-studied RNAIII from Staphylococcus aureus (6), 12 novel sRNAs from Staphylococcus aureus pathogenicity islands have been detected (7) as well as three Hfq-binding sRNAs of Listeria monocytogenes with still unknown function (8), and nine novel sRNAs from Listeria monocytogenes within... | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 380 | 4,671 | 1 | false | Furthermore, in addition to the well-studied RNAIII from Staphylococcus aureus, 12 novel sRNAs from Staphylococcus aureus pathogenicity islands have been detected as well as three Hfq-binding sRNAs of Listeria monocytogenes with still unknown function, and nine novel sRNAs from Listeria monocytogenes within intergenic ... | [
"6",
"7",
"8",
"9"
] | Furthermore, in addition to the well-studied RNAIII from Staphylococcus aureus, 12 novel sRNAs from Staphylococcus aureus pathogenicity islands have been detected as well as three Hfq-binding sRNAs of Listeria monocytogenes with still unknown function, and nine novel sRNAs from Listeria monocytogenes within intergenic ... | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Additionally, more than 100 potential 6S RNA species have been identified by bioinformatics approaches, and many of them were verified experimentally, among them two 6S RNA species in B. subtilis (10,11). | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 204 | 4,672 | 0 | false | Additionally, more than 100 potential 6S RNA species have been identified by bioinformatics approaches, and many of them were verified experimentally, among them two 6S RNA species in B. subtilis. | [
"10,11"
] | Additionally, more than 100 potential 6S RNA species have been identified by bioinformatics approaches, and many of them were verified experimentally, among them two 6S RNA species in B. subtilis. | true | true | true | true | true | 787 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9",
"B10",
"B11"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Still, the identification of mRNA targets of the recently discovered sRNAs is a challenging issue, and has been successful only in less than one-third of all cases. | [
"1",
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9",
"10",
"11"
] | 164 | 4,673 | 0 | false | Still, the identification of mRNA targets of the recently discovered sRNAs is a challenging issue, and has been successful only in less than one-third of all cases. | [] | Still, the identification of mRNA targets of the recently discovered sRNAs is a challenging issue, and has been successful only in less than one-third of all cases. | true | true | true | true | true | 787 |
1 | INTRODUCTION | 1 | 12 | [
"B12",
"B13",
"B14",
"B15",
"B16"
] | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | One important hallmark of many trans-encoded regulatory RNAs from E. coli is their ability to bind the Sm-like abundant RNA chaperone Hfq (12). | [
"12",
"13",
"14",
"15",
"16"
] | 143 | 4,674 | 1 | false | One important hallmark of many trans-encoded regulatory RNAs from E. coli is their ability to bind the Sm-like abundant RNA chaperone Hfq. | [
"12"
] | One important hallmark of many trans-encoded regulatory RNAs from E. coli is their ability to bind the Sm-like abundant RNA chaperone Hfq. | true | true | true | true | true | 788 |
1 | INTRODUCTION | 1 | 12 | [
"B12",
"B13",
"B14",
"B15",
"B16"
] | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | While several sRNAs have been found to require Hfq for their stability, some were shown to need Hfq for efficient complex formation with their target RNA (13,14). | [
"12",
"13",
"14",
"15",
"16"
] | 162 | 4,675 | 0 | false | While several sRNAs have been found to require Hfq for their stability, some were shown to need Hfq for efficient complex formation with their target RNA. | [
"13,14"
] | While several sRNAs have been found to require Hfq for their stability, some were shown to need Hfq for efficient complex formation with their target RNA. | true | true | true | true | true | 788 |
1 | INTRODUCTION | 1 | 15 | [
"B12",
"B13",
"B14",
"B15",
"B16"
] | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | For DsrA/rpoS/Hfq, the pathway of complex formation has been investigated by biophysical techniques (15). | [
"12",
"13",
"14",
"15",
"16"
] | 105 | 4,676 | 1 | false | For DsrA/rpoS/Hfq, the pathway of complex formation has been investigated by biophysical techniques. | [
"15"
] | For DsrA/rpoS/Hfq, the pathway of complex formation has been investigated by biophysical techniques. | true | true | true | true | true | 788 |
1 | INTRODUCTION | 1 | 12 | [
"B12",
"B13",
"B14",
"B15",
"B16"
] | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | However, for sRNAs from Gram-positive bacteria, the putative function of Hfq is still elusive. | [
"12",
"13",
"14",
"15",
"16"
] | 94 | 4,677 | 0 | false | However, for sRNAs from Gram-positive bacteria, the putative function of Hfq is still elusive. | [] | However, for sRNAs from Gram-positive bacteria, the putative function of Hfq is still elusive. | true | true | true | true | true | 788 |
1 | INTRODUCTION | 1 | 16 | [
"B12",
"B13",
"B14",
"B15",
"B16"
] | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | At least in one case, staphylococcal RNAIII/spa interaction, no influence of Hfq has been found (16). | [
"12",
"13",
"14",
"15",
"16"
] | 101 | 4,678 | 1 | false | At least in one case, staphylococcal RNAIII/spa interaction, no influence of Hfq has been found. | [
"16"
] | At least in one case, staphylococcal RNAIII/spa interaction, no influence of Hfq has been found. | true | true | true | true | true | 788 |
2 | INTRODUCTION | 1 | 17 | [
"B17",
"B18",
"B19",
"B20",
"B14",
"B21",
"B22"
] | 17,576,690 | NA|pmid-7534474|pmid-12101127|pmid-14739933|pmid-16313626|pmid-16204185|pmid-15678100|NA | In contrast to the cis-encoded sRNAs from accessory genetic elements like plasmids, phages, transposons that have been studied in detail over the past 25 years [reviewed in (17)], relatively little is known about structural requirements, binding kinetics and mechanisms or degradation pathways of these new trans-encoded... | [
"17",
"18",
"19",
"20",
"14",
"21",
"22"
] | 338 | 4,679 | 0 | false | In contrast to the cis-encoded sRNAs from accessory genetic elements like plasmids, phages, transposons that have been studied in detail over the past 25 years, relatively little is known about structural requirements, binding kinetics and mechanisms or degradation pathways of these new trans-encoded regulatory sRNAs. | [
"reviewed in (17)"
] | In contrast to the cis-encoded sRNAs from accessory genetic elements like plasmids, phages, transposons that have been studied in detail over the past 25 years, relatively little is known about structural requirements, binding kinetics and mechanisms or degradation pathways of these new trans-encoded regulatory sRNAs. | true | true | true | true | true | 789 |
2 | INTRODUCTION | 1 | 17 | [
"B17",
"B18",
"B19",
"B20",
"B14",
"B21",
"B22"
] | 17,576,690 | NA|pmid-7534474|pmid-12101127|pmid-14739933|pmid-16313626|pmid-16204185|pmid-15678100|NA | Although complexes between sRNA and mRNA have been detected in vitro in some instances, only in five cases secondary structures of such complexes predicted by Mfold have been confirmed by experimental secondary structure probing. | [
"17",
"18",
"19",
"20",
"14",
"21",
"22"
] | 229 | 4,680 | 0 | false | Although complexes between sRNA and mRNA have been detected in vitro in some instances, only in five cases secondary structures of such complexes predicted by Mfold have been confirmed by experimental secondary structure probing. | [] | Although complexes between sRNA and mRNA have been detected in vitro in some instances, only in five cases secondary structures of such complexes predicted by Mfold have been confirmed by experimental secondary structure probing. | true | true | true | true | true | 789 |
2 | INTRODUCTION | 1 | 18 | [
"B17",
"B18",
"B19",
"B20",
"B14",
"B21",
"B22"
] | 17,576,690 | NA|pmid-7534474|pmid-12101127|pmid-14739933|pmid-16313626|pmid-16204185|pmid-15678100|NA | These include MicF/ompF (18), Spot42/galK (19), RyhB/sodB (20), MicA/ompA (14,21) from E. coli and RNAIII/spa from Staphylococcus aureus (22). | [
"17",
"18",
"19",
"20",
"14",
"21",
"22"
] | 142 | 4,681 | 1 | false | These include MicF/ompF, Spot42/galK, RyhB/sodB, MicA/ompA from E. coli and RNAIII/spa from Staphylococcus aureus. | [
"18",
"19",
"20",
"14,21",
"22"
] | These include MicF/ompF, Spot42/galK, RyhB/sodB, MicA/ompA from E. coli and RNAIII/spa from Staphylococcus aureus. | true | true | true | true | true | 789 |
2 | INTRODUCTION | 1 | 17 | [
"B17",
"B18",
"B19",
"B20",
"B14",
"B21",
"B22"
] | 17,576,690 | NA|pmid-7534474|pmid-12101127|pmid-14739933|pmid-16313626|pmid-16204185|pmid-15678100|NA | So far, the region of initial contact between a trans-encoded sRNA and a target RNA sharing more than one complementary region has not been narrowed down. | [
"17",
"18",
"19",
"20",
"14",
"21",
"22"
] | 154 | 4,682 | 0 | false | So far, the region of initial contact between a trans-encoded sRNA and a target RNA sharing more than one complementary region has not been narrowed down. | [] | So far, the region of initial contact between a trans-encoded sRNA and a target RNA sharing more than one complementary region has not been narrowed down. | true | true | true | true | true | 789 |
2 | INTRODUCTION | 1 | 17 | [
"B17",
"B18",
"B19",
"B20",
"B14",
"B21",
"B22"
] | 17,576,690 | NA|pmid-7534474|pmid-12101127|pmid-14739933|pmid-16313626|pmid-16204185|pmid-15678100|NA | The mechanism of action has been proposed in some cases, but not always corroborated by a combination of in vivo and in vitro experiments. | [
"17",
"18",
"19",
"20",
"14",
"21",
"22"
] | 138 | 4,683 | 0 | false | The mechanism of action has been proposed in some cases, but not always corroborated by a combination of in vivo and in vitro experiments. | [] | The mechanism of action has been proposed in some cases, but not always corroborated by a combination of in vivo and in vitro experiments. | true | true | true | true | true | 789 |
3 | INTRODUCTION | 1 | 23 | [
"B23",
"B24"
] | 17,576,690 | pmid-16164558|pmid-17020585 | The 205-nt untranslated RNA SR1 from the B. subtilis genome was found in our group by a combination of computer predictions and northern blotting (23). | [
"23",
"24"
] | 151 | 4,684 | 1 | false | The 205-nt untranslated RNA SR1 from the B. subtilis genome was found in our group by a combination of computer predictions and northern blotting. | [
"23"
] | The 205-nt untranslated RNA SR1 from the B. subtilis genome was found in our group by a combination of computer predictions and northern blotting. | true | true | true | true | true | 790 |
3 | INTRODUCTION | 1 | 24 | [
"B23",
"B24"
] | 17,576,690 | pmid-16164558|pmid-17020585 | Recently, we have shown that SR1 is a bona fide antisense RNA that acts by basepairing with its primary target, ahrC mRNA, the transcriptional activator of the rocABC and rocDEF arginine catabolic operons (24). | [
"23",
"24"
] | 210 | 4,685 | 1 | false | Recently, we have shown that SR1 is a bona fide antisense RNA that acts by basepairing with its primary target, ahrC mRNA, the transcriptional activator of the rocABC and rocDEF arginine catabolic operons. | [
"24"
] | Recently, we have shown that SR1 is a bona fide antisense RNA that acts by basepairing with its primary target, ahrC mRNA, the transcriptional activator of the rocABC and rocDEF arginine catabolic operons. | true | true | true | true | true | 790 |
3 | INTRODUCTION | 1 | 23 | [
"B23",
"B24"
] | 17,576,690 | pmid-16164558|pmid-17020585 | In vitro translation data and translational reporter gene fusions suggested that SR1 might inhibit ahrC translation at a post-initiation stage. | [
"23",
"24"
] | 143 | 4,686 | 0 | false | In vitro translation data and translational reporter gene fusions suggested that SR1 might inhibit ahrC translation at a post-initiation stage. | [] | In vitro translation data and translational reporter gene fusions suggested that SR1 might inhibit ahrC translation at a post-initiation stage. | true | true | true | true | true | 790 |
3 | INTRODUCTION | 1 | 23 | [
"B23",
"B24"
] | 17,576,690 | pmid-16164558|pmid-17020585 | Hfq was shown to be dispensable for the stability of SR1. | [
"23",
"24"
] | 57 | 4,687 | 0 | false | Hfq was shown to be dispensable for the stability of SR1. | [] | Hfq was shown to be dispensable for the stability of SR1. | true | true | true | true | true | 790 |
4 | INTRODUCTION | 0 | null | null | 17,576,690 | pmid-11931231|pmid-17259613|NA | Here, we provide a detailed in vitro characterization of SR1 and the SR1/ahrC complex with and without Hfq. | null | 107 | 4,688 | 0 | false | null | null | Here, we provide a detailed in vitro characterization of SR1 and the SR1/ahrC complex with and without Hfq. | true | true | true | true | true | 791 |
4 | INTRODUCTION | 0 | null | null | 17,576,690 | pmid-11931231|pmid-17259613|NA | We determined the region of initial contact between SR1 and ahrC. | null | 65 | 4,689 | 0 | false | null | null | We determined the region of initial contact between SR1 and ahrC. | true | true | true | true | true | 791 |
4 | INTRODUCTION | 0 | null | null | 17,576,690 | pmid-11931231|pmid-17259613|NA | Furthermore, a combination of toeprinting and SR1/ahrC complex probing studies demonstrated that SR1 inhibits translation initiation of ahrC mRNA by inducing structural changes between the ahrC SD sequence and the first complementary region G. | null | 243 | 4,690 | 0 | false | null | null | Furthermore, a combination of toeprinting and SR1/ahrC complex probing studies demonstrated that SR1 inhibits translation initiation of ahrC mRNA by inducing structural changes between the ahrC SD sequence and the first complementary region G. | true | true | true | true | true | 791 |
4 | INTRODUCTION | 0 | null | null | 17,576,690 | pmid-11931231|pmid-17259613|NA | In contrast to many E. coli sense/antisense systems, Hfq was shown to be exclusively required for translation of ahrC RNA, but not for promoting the SR1/ahrC interaction. | null | 170 | 4,691 | 0 | false | null | null | In contrast to many E. coli sense/antisense systems, Hfq was shown to be exclusively required for translation of ahrC RNA, but not for promoting the SR1/ahrC interaction. | true | true | true | true | true | 791 |
4 | INTRODUCTION | 0 | null | null | 17,576,690 | pmid-11931231|pmid-17259613|NA | The intracellular concentration of SR1 in B. subtilis was calculated to be 30 nM in log phase and 315 nM in stationary phase in complex TY medium. | null | 146 | 4,692 | 0 | false | null | null | The intracellular concentration of SR1 in B. subtilis was calculated to be 30 nM in log phase and 315 nM in stationary phase in complex TY medium. | true | true | true | true | true | 791 |
0 | DISCUSSION | 1 | 24 | [
"B24"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | For all recently discovered trans-encoded sRNAs the targets of which have been identified, only one or two complementary regions were found. | [
"24"
] | 140 | 4,693 | 0 | false | For all recently discovered trans-encoded sRNAs the targets of which have been identified, only one or two complementary regions were found. | [] | For all recently discovered trans-encoded sRNAs the targets of which have been identified, only one or two complementary regions were found. | true | true | true | true | true | 792 |
0 | DISCUSSION | 1 | 24 | [
"B24"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | In the majority of cases, these regions covered the 5′ part of the target RNA, mostly including the SD sequence, and the mechanism of action was found to be inhibition or activation of translation initiation. | [
"24"
] | 208 | 4,694 | 0 | false | In the majority of cases, these regions covered the 5′ part of the target RNA, mostly including the SD sequence, and the mechanism of action was found to be inhibition or activation of translation initiation. | [] | In the majority of cases, these regions covered the 5′ part of the target RNA, mostly including the SD sequence, and the mechanism of action was found to be inhibition or activation of translation initiation. | true | true | true | true | true | 792 |
0 | DISCUSSION | 1 | 24 | [
"B24"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | Rather unusually, SR1 and ahrC mRNA contain seven regions of complementarity that comprise the 3′ half of SR1 and the central and 3′ portion of ahrC mRNA (24). | [
"24"
] | 159 | 4,695 | 1 | false | Rather unusually, SR1 and ahrC mRNA contain seven regions of complementarity that comprise the 3′ half of SR1 and the central and 3′ portion of ahrC mRNA. | [
"24"
] | Rather unusually, SR1 and ahrC mRNA contain seven regions of complementarity that comprise the 3′ half of SR1 and the central and 3′ portion of ahrC mRNA. | true | true | true | true | true | 792 |
0 | DISCUSSION | 1 | 24 | [
"B24"
] | 17,576,690 | pmid-15952886|pmid-17055775|pmid-16166525|pmid-11717296|pmid-16385044|pmid-7556100|pmid-16183745|pmid-16373489|pmid-17259222|pmid-15811922|pmid-15793584|pmid-17020585 | This prompted us to determine the secondary structures of SR1 and the ahrC/SR1 complex and to investigate the structural requirements for efficient ahrC/SR1 pairing. | [
"24"
] | 165 | 4,696 | 0 | false | This prompted us to determine the secondary structures of SR1 and the ahrC/SR1 complex and to investigate the structural requirements for efficient ahrC/SR1 pairing. | [] | This prompted us to determine the secondary structures of SR1 and the ahrC/SR1 complex and to investigate the structural requirements for efficient ahrC/SR1 pairing. | true | true | true | true | true | 792 |
1 | DISCUSSION | 0 | null | null | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | Figure 1B shows that SR1 is composed of one large 5′ stem-loop (SL1) structure with a prominent bulge, a central small stem-loop SL2 and the terminator stem-loop SL3 separated by two single-stranded regions. | null | 207 | 4,697 | 0 | false | null | null | Figure 1B shows that SR1 is composed of one large 5′ stem-loop (SL1) structure with a prominent bulge, a central small stem-loop SL2 and the terminator stem-loop SL3 separated by two single-stranded regions. | true | true | true | true | true | 793 |
1 | DISCUSSION | 0 | null | null | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | Six out of seven regions of complementarity to ahrC RNA (B to G) are located in the 3′ 100 nt of SR1. | null | 101 | 4,698 | 0 | false | null | null | Six out of seven regions of complementarity to ahrC RNA (B to G) are located in the 3′ 100 nt of SR1. | true | true | true | true | true | 793 |
1 | DISCUSSION | 0 | null | null | 17,576,690 | pmid-15009882|pmid-11804582|pmid-16313626|pmid-17259214|pmid-17291347 | Secondary structure probing of labelled SR1 in complex with increasing concentrations of unlabelled ahrC and vice versa (Figure 3A and B) revealed structural alterations in six of the seven complementary regions. | null | 212 | 4,699 | 0 | false | null | null | Secondary structure probing of labelled SR1 in complex with increasing concentrations of unlabelled ahrC and vice versa (Figure 3A and B) revealed structural alterations in six of the seven complementary regions. | true | true | true | true | true | 793 |
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