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 | 19,654,939 | null | Furthermore, we could not exclude the effect of current medication or atherosclerotic risk factors, such as diabetes, smoking, or hypercholesterolemia. | null | 151 | 41,719 | 0 | false | null | null | Furthermore, we could not exclude the effect of current medication or atherosclerotic risk factors, such as diabetes, smoking, or hypercholesterolemia. | true | true | true | true | true | 7,196 |
8 | DISCUSSION | 0 | null | null | 19,654,939 | null | However, the study population included subjects who suffered non-cardiac deaths, such as motor vehicle injury, stab wound injury, and fall injury. | null | 146 | 41,720 | 0 | false | null | null | However, the study population included subjects who suffered non-cardiac deaths, such as motor vehicle injury, stab wound injury, and fall injury. | true | true | true | true | true | 7,196 |
8 | DISCUSSION | 0 | null | null | 19,654,939 | null | Hence, the study population appeared to represent the general population, and we believe our data accurately indicated the natural course of atherosclerosis and its relation to Nogo-B. | null | 184 | 41,721 | 0 | false | null | null | Hence, the study population appeared to represent the general population, and we believe our data accurately indicated the natural course of atherosclerosis and its relation to Nogo-B. | true | true | true | true | true | 7,196 |
9 | DISCUSSION | 0 | null | null | 19,654,939 | null | In conclusion, the present study shows that Nogo-B expression is down-regulated and inversely correlated with FA progression. | null | 125 | 41,722 | 0 | false | null | null | In conclusion, the present study shows that Nogo-B expression is down-regulated and inversely correlated with FA progression. | true | true | true | true | true | 7,197 |
9 | DISCUSSION | 0 | null | null | 19,654,939 | null | This is specifically represented by the increasing size of the necrotic core. | null | 77 | 41,723 | 0 | false | null | null | This is specifically represented by the increasing size of the necrotic core. | true | true | true | true | true | 7,197 |
9 | DISCUSSION | 0 | null | null | 19,654,939 | null | Our findings support the hypothesis that local Nogo-B reduction may contribute to plaque formation and/or vulnerability. | null | 120 | 41,724 | 0 | false | null | null | Our findings support the hypothesis that local Nogo-B reduction may contribute to plaque formation and/or vulnerability. | true | true | true | true | true | 7,197 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6"
] | 18,653,524 | pmid-15289578|pmid-11606270|NA|pmid-17493823|NA|pmid-16891171 | DNA is often viewed as a relatively rigid biological macromolecule (1–3), with RNA and proteins thought of as exhibiting broader ranges of both intrinsic three-dimensional structural variability as well as dynamical flexibility. | [
"1–3",
"4",
"5",
"6"
] | 228 | 41,725 | 1 | false | DNA is often viewed as a relatively rigid biological macromolecule, with RNA and proteins thought of as exhibiting broader ranges of both intrinsic three-dimensional structural variability as well as dynamical flexibility. | [
"1–3"
] | DNA is often viewed as a relatively rigid biological macromolecule, with RNA and proteins thought of as exhibiting broader ranges of both intrinsic three-dimensional structural variability as well as dynamical flexibility. | true | true | true | true | true | 7,198 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6"
] | 18,653,524 | pmid-15289578|pmid-11606270|NA|pmid-17493823|NA|pmid-16891171 | This perspective of a locally rigid, globally flexible biopolymer is consistent with the rather passive biological role of DNA as the repository of genetic information—the genome is read-out by the process of transcription. | [
"1–3",
"4",
"5",
"6"
] | 223 | 41,726 | 0 | false | This perspective of a locally rigid, globally flexible biopolymer is consistent with the rather passive biological role of DNA as the repository of genetic information—the genome is read-out by the process of transcription. | [] | This perspective of a locally rigid, globally flexible biopolymer is consistent with the rather passive biological role of DNA as the repository of genetic information—the genome is read-out by the process of transcription. | true | true | true | true | true | 7,198 |
0 | INTRODUCTION | 1 | 4 | [
"B1 B2 B3",
"B4",
"B5",
"B6"
] | 18,653,524 | pmid-15289578|pmid-11606270|NA|pmid-17493823|NA|pmid-16891171 | Links between structure and potential biological functions (both normal and aberrant) have been explored for conformations that deviate from the standard B-form double helix—including such varieties as multi-stranded triplexes, quadruplex structures found in telomeric G-rich tracts, cruciforms adopted by inverted repea... | [
"1–3",
"4",
"5",
"6"
] | 370 | 41,727 | 1 | false | Links between structure and potential biological functions (both normal and aberrant) have been explored for conformations that deviate from the standard B-form double helix—including such varieties as multi-stranded triplexes, quadruplex structures found in telomeric G-rich tracts, cruciforms adopted by inverted repea... | [
"4"
] | Links between structure and potential biological functions (both normal and aberrant) have been explored for conformations that deviate from the standard B-form double helix—including such varieties as multi-stranded triplexes, quadruplex structures found in telomeric G-rich tracts, cruciforms adopted by inverted repea... | true | true | true | true | true | 7,198 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6"
] | 18,653,524 | pmid-15289578|pmid-11606270|NA|pmid-17493823|NA|pmid-16891171 | However, beyond these alternative secondary structures, it is also becoming increasingly apparent that the structure and dynamics of the canonical Watson–Crick DNA double helix on a very local (base pair) level play pivotal roles in specific biological functions, such as the site-specific binding of transcription facto... | [
"1–3",
"4",
"5",
"6"
] | 346 | 41,728 | 0 | false | However, beyond these alternative secondary structures, it is also becoming increasingly apparent that the structure and dynamics of the canonical Watson–Crick DNA double helix on a very local (base pair) level play pivotal roles in specific biological functions, such as the site-specific binding of transcription facto... | [] | However, beyond these alternative secondary structures, it is also becoming increasingly apparent that the structure and dynamics of the canonical Watson–Crick DNA double helix on a very local (base pair) level play pivotal roles in specific biological functions, such as the site-specific binding of transcription facto... | true | true | true | true | true | 7,198 |
0 | INTRODUCTION | 1 | 1–3 | [
"B1 B2 B3",
"B4",
"B5",
"B6"
] | 18,653,524 | pmid-15289578|pmid-11606270|NA|pmid-17493823|NA|pmid-16891171 | This idea of a functional role for sequence-specific DNA fine structure and dynamics is embodied in the concept of ‘indirect readout’ (5,6), wherein features of protein···DNA recognition are dictated by subtle conformational and dynamical properties of DNA beyond the stereochemical code provided by the specific linear ... | [
"1–3",
"4",
"5",
"6"
] | 424 | 41,729 | 0 | false | This idea of a functional role for sequence-specific DNA fine structure and dynamics is embodied in the concept of ‘indirect readout’, wherein features of protein···DNA recognition are dictated by subtle conformational and dynamical properties of DNA beyond the stereochemical code provided by the specific linear array ... | [
"5,6"
] | This idea of a functional role for sequence-specific DNA fine structure and dynamics is embodied in the concept of ‘indirect readout’, wherein features of protein···DNA recognition are dictated by subtle conformational and dynamical properties of DNA beyond the stereochemical code provided by the specific linear array ... | true | true | true | true | true | 7,198 |
1 | INTRODUCTION | 1 | 7 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | Despite the vast literature dedicated to DNA structural biology since the first atomic-resolution crystal structures of both left- (7) and right-handed (8) double helices, many aspects of DNA structure and dynamics remain unclear—including the intrinsic coupling between structure and conformational dynamics that is the... | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 347 | 41,730 | 1 | false | Despite the vast literature dedicated to DNA structural biology since the first atomic-resolution crystal structures of both left- and right-handed double helices, many aspects of DNA structure and dynamics remain unclear—including the intrinsic coupling between structure and conformational dynamics that is the basis o... | [
"7",
"8"
] | Despite the vast literature dedicated to DNA structural biology since the first atomic-resolution crystal structures of both left- and right-handed double helices, many aspects of DNA structure and dynamics remain unclear—including the intrinsic coupling between structure and conformational dynamics that is the basis o... | true | true | true | true | true | 7,199 |
1 | INTRODUCTION | 1 | 9–12 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | For instance, controversy surrounds the relative significance of extrinsic/environmental factors (such as hydration and counterion-binding) versus intrinsic factorsm (such as local base pair interactions) in mediating sequence-specific DNA fine structure, as gauged by helical axis bending, groove widths and related pro... | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 335 | 41,731 | 1 | false | For instance, controversy surrounds the relative significance of extrinsic/environmental factors (such as hydration and counterion-binding) versus intrinsic factorsm (such as local base pair interactions) in mediating sequence-specific DNA fine structure, as gauged by helical axis bending, groove widths and related pro... | [
"9–12"
] | For instance, controversy surrounds the relative significance of extrinsic/environmental factors (such as hydration and counterion-binding) versus intrinsic factorsm (such as local base pair interactions) in mediating sequence-specific DNA fine structure, as gauged by helical axis bending, groove widths and related pro... | true | true | true | true | true | 7,199 |
1 | INTRODUCTION | 1 | 7 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | Quantitative frameworks have been developed for the description of DNA structure in terms of the local geometry of bases, base pairs (bp), bp steps and higher-order structural units [e.g. | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 187 | 41,732 | 0 | false | Quantitative frameworks have been developed for the description of DNA structure in terms of the local geometry of bases, base pairs (bp), bp steps and higher-order structural units [e.g. | [] | Quantitative frameworks have been developed for the description of DNA structure in terms of the local geometry of bases, base pairs (bp), bp steps and higher-order structural units [e.g. | true | true | true | true | true | 7,199 |
1 | INTRODUCTION | 1 | 13 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | (13)], but progress in elucidating those structural and dynamical phenomena thought to occur via transient, short-lived intermediates [such as occurs in base flipping (14,15)] remains hindered by the difficulty of using existing experimental methods to extract dynamical information at both atomic resolution and over th... | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 362 | 41,733 | 1 | false | ], but progress in elucidating those structural and dynamical phenomena thought to occur via transient, short-lived intermediates remains hindered by the difficulty of using existing experimental methods to extract dynamical information at both atomic resolution and over the potentially relevant timescales (ns→ms). | [
"13",
"such as occurs in base flipping (14,15)"
] | ], but progress in elucidating those structural and dynamical phenomena thought to occur via transient, short-lived intermediates remains hindered by the difficulty of using existing experimental methods to extract dynamical information at both atomic resolution and over the potentially relevant timescales (ns→ms). | false | false | true | true | false | 7,199 |
1 | INTRODUCTION | 1 | 7 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | Emblematic of this difficulty, crystallographic models generally represent spatially and temporally averaged structures of individual molecules, the averages being taken over more than 1012 unit cells (a conservative estimate, for micrometer-sized crystals of typical cell dimensions) and time periods greater than hundr... | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 420 | 41,734 | 0 | false | Emblematic of this difficulty, crystallographic models generally represent spatially and temporally averaged structures of individual molecules, the averages being taken over more than 1012 unit cells (a conservative estimate, for micrometer-sized crystals of typical cell dimensions) and time periods greater than hundr... | [] | Emblematic of this difficulty, crystallographic models generally represent spatially and temporally averaged structures of individual molecules, the averages being taken over more than 1012 unit cells (a conservative estimate, for micrometer-sized crystals of typical cell dimensions) and time periods greater than hundr... | true | true | true | true | true | 7,199 |
1 | INTRODUCTION | 1 | 7 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | Thus, detailed knowledge remains somewhat obscure of the factors modulating the mean structural and conformational properties of DNA, the dynamical processes mediating inter-conversions between these average conformational states, and the interactions of these (sub-)states with transcription factors, histone proteins, ... | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 383 | 41,735 | 0 | false | Thus, detailed knowledge remains somewhat obscure of the factors modulating the mean structural and conformational properties of DNA, the dynamical processes mediating inter-conversions between these average conformational states, and the interactions of these (sub-)states with transcription factors, histone proteins, ... | [] | Thus, detailed knowledge remains somewhat obscure of the factors modulating the mean structural and conformational properties of DNA, the dynamical processes mediating inter-conversions between these average conformational states, and the interactions of these (sub-)states with transcription factors, histone proteins, ... | true | true | true | true | true | 7,199 |
1 | INTRODUCTION | 1 | 16 | [
"B7",
"B8",
"B9 B10 B11 B12",
"B13",
"B14",
"B15",
"B16",
"B17"
] | 18,653,524 | pmid-514347|pmid-7432492|pmid-9622486|pmid-10497024|pmid-11493048|pmid-15465909|pmid-11601858|pmid-7606789|pmid-9759487|pmid-16683746|NA | Computational approaches such as molecular dynamics (MD) simulation (16) provide an alternative route towards exploring biomolecular structure and dynamics in fully atomic detail, and have yielded a wealth of nucleic acid simulations over the past dozen years [reviewed in (17)]. | [
"7",
"8",
"9–12",
"13",
"14",
"15",
"16",
"17"
] | 279 | 41,736 | 1 | false | Computational approaches such as molecular dynamics (MD) simulation provide an alternative route towards exploring biomolecular structure and dynamics in fully atomic detail, and have yielded a wealth of nucleic acid simulations over the past dozen years. | [
"16",
"reviewed in (17)"
] | Computational approaches such as molecular dynamics (MD) simulation provide an alternative route towards exploring biomolecular structure and dynamics in fully atomic detail, and have yielded a wealth of nucleic acid simulations over the past dozen years. | true | true | true | true | true | 7,199 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | The NF-κB transcription factor family illustrates the many potential complexities of protein···DNA recognition. | [
"18",
"18",
"19",
"20"
] | 111 | 41,737 | 0 | false | The NF-κB transcription factor family illustrates the many potential complexities of protein···DNA recognition. | [] | The NF-κB transcription factor family illustrates the many potential complexities of protein···DNA recognition. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | This family occurs in a wide variety of eukaryotes and regulates a similarly broad array of cellular pathways, ranging from morphogenesis in insects to adaptive immunity in humans (18). | [
"18",
"18",
"19",
"20"
] | 185 | 41,738 | 1 | false | This family occurs in a wide variety of eukaryotes and regulates a similarly broad array of cellular pathways, ranging from morphogenesis in insects to adaptive immunity in humans. | [
"18"
] | This family occurs in a wide variety of eukaryotes and regulates a similarly broad array of cellular pathways, ranging from morphogenesis in insects to adaptive immunity in humans. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | The five mammalian NF-κBs [p50, p52, p65 (RelA), c-Rel and RelB] contain an ≈300-residue Rel Homology Region (RHR), consisting of two immunoglobulin-like folds joined by a flexible linker. | [
"18",
"18",
"19",
"20"
] | 188 | 41,739 | 0 | false | The five mammalian NF-κBs [p50, p52, p65 (RelA), c-Rel and RelB] contain an ≈300-residue Rel Homology Region (RHR), consisting of two immunoglobulin-like folds joined by a flexible linker. | [] | The five mammalian NF-κBs [p50, p52, p65 (RelA), c-Rel and RelB] contain an ≈300-residue Rel Homology Region (RHR), consisting of two immunoglobulin-like folds joined by a flexible linker. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | NF-κBs associate into homo- and hetero-dimers that modulate gene expression by binding to target κB DNA-enhancer sites. | [
"18",
"18",
"19",
"20"
] | 119 | 41,740 | 0 | false | NF-κBs associate into homo- and hetero-dimers that modulate gene expression by binding to target κB DNA-enhancer sites. | [] | NF-κBs associate into homo- and hetero-dimers that modulate gene expression by binding to target κB DNA-enhancer sites. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | The remarkably loose κB consensus sequence 5′GGGRNWYYCC3′ [N = any nucleotide, R = purine, Y = pyrimidine (often Thy) and W = Ade or Thy] consists of two ‘half sites’ (underlined). | [
"18",
"18",
"19",
"20"
] | 180 | 41,741 | 0 | false | The remarkably loose κB consensus sequence 5′GGGRNWYYCC3′ [N = any nucleotide, R = purine, Y = pyrimidine (often Thy) and W = Ade or Thy] consists of two ‘half sites’ (underlined). | [] | The remarkably loose κB consensus sequence 5′GGGRNWYYCC3′ [N = any nucleotide, R = purine, Y = pyrimidine (often Thy) and W = Ade or Thy] consists of two ‘half sites’ (underlined). | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | The 5-bp GGGRN half sites are preferentially bound by p50 and p52 subunits, while RelA, RelB and c-Rel prefer the 4-bp YYCC half sites. | [
"18",
"18",
"19",
"20"
] | 135 | 41,742 | 0 | false | The 5-bp GGGRN half sites are preferentially bound by p50 and p52 subunits, while RelA, RelB and c-Rel prefer the 4-bp YYCC half sites. | [] | The 5-bp GGGRN half sites are preferentially bound by p50 and p52 subunits, while RelA, RelB and c-Rel prefer the 4-bp YYCC half sites. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | Thus, in addition to immense sequence variability and intrinsically different NF-κB-binding preferences for different half sites, κB elements also vary in length. | [
"18",
"18",
"19",
"20"
] | 162 | 41,743 | 0 | false | Thus, in addition to immense sequence variability and intrinsically different NF-κB-binding preferences for different half sites, κB elements also vary in length. | [] | Thus, in addition to immense sequence variability and intrinsically different NF-κB-binding preferences for different half sites, κB elements also vary in length. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | Known κB sites can be grouped into 9-bp ‘class I’ sites (4 + 1 + 4 arrangement, for c-Rel and RelA homodimers) and 10- or 11-bp ‘class II’ sites (5 + 1 + 5, for p50 and p52 homodimers). | [
"18",
"18",
"19",
"20"
] | 185 | 41,744 | 0 | false | Known κB sites can be grouped into 9-bp ‘class I’ sites (4 + 1 + 4 arrangement, for c-Rel and RelA homodimers) and 10- or 11-bp ‘class II’ sites (5 + 1 + 5, for p50 and p52 homodimers). | [] | Known κB sites can be grouped into 9-bp ‘class I’ sites and 10- or 11-bp ‘class II’ sites. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | However, even the above rules and consensus sequences are likely to be too restrictive: Some sequence-specific trends are known, but there is great degeneracy in terms of both (i) optimal DNA sequences for a given NF-κB dimer and (ii) the relative affinities of different NF-κB dimers for a given κB DNA sequence (18). | [
"18",
"18",
"19",
"20"
] | 318 | 41,745 | 1 | false | However, even the above rules and consensus sequences are likely to be too restrictive: Some sequence-specific trends are known, but there is great degeneracy in terms of both (i) optimal DNA sequences for a given NF-κB dimer and (ii) the relative affinities of different NF-κB dimers for a given κB DNA sequence. | [
"18"
] | However, even the above rules and consensus sequences are likely to be too restrictive: Some sequence-specific trends are known, but there is great degeneracy in terms of both (i) optimal DNA sequences for a given NF-κB dimer and (ii) the relative affinities of different NF-κB dimers for a given κB DNA sequence. | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 18 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | Thus, an outstanding question in the NF-κB field is the detailed mechanism of indirect readout—What are the determinants of sequence-specific binding of NF-κB to target κB sites? | [
"18",
"18",
"19",
"20"
] | 178 | 41,746 | 0 | false | Thus, an outstanding question in the NF-κB field is the detailed mechanism of indirect readout—What are the determinants of sequence-specific binding of NF-κB to target κB sites? | [] | Thus, an outstanding question in the NF-κB field is the detailed mechanism of indirect readout—What are the determinants of sequence-specific binding of NF-κB to target κB sites? | true | true | true | true | true | 7,200 |
2 | INTRODUCTION | 1 | 19 | [
"B18",
"B18",
"B19",
"B20"
] | 18,653,524 | pmid-17072323|pmid-17072323|pmid-10825175|pmid-15663934 | Biophysical studies have demonstrated that NF-κB···DNA-binding affinity is largely entropically driven (19), but the issue of site specificity remains far murkier, with it now thought that ‘the conformation and flexibility of κB DNA sequences play a critical role in the recognition of NF-κB dimers’ (20). | [
"18",
"18",
"19",
"20"
] | 305 | 41,747 | 1 | false | Biophysical studies have demonstrated that NF-κB···DNA-binding affinity is largely entropically driven, but the issue of site specificity remains far murkier, with it now thought that ‘the conformation and flexibility of κB DNA sequences play a critical role in the recognition of NF-κB dimers’. | [
"19",
"20"
] | Biophysical studies have demonstrated that NF-κB···DNA-binding affinity is largely entropically driven, but the issue of site specificity remains far murkier, with it now thought that ‘the conformation and flexibility of κB DNA sequences play a critical role in the recognition of NF-κB dimers’. | true | true | true | true | true | 7,200 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | Therefore, as an initial step in elucidating protein···DNA recognition and the mechanism of indirect readout in the context of differential binding of NF-κB transcription factors to κB DNA elements, we performed MD simulations of a 20-bp κB DNA of known structure (Figure 1, S1). | [
"21"
] | 279 | 41,748 | 0 | false | Therefore, as an initial step in elucidating protein···DNA recognition and the mechanism of indirect readout in the context of differential binding of NF-κB transcription factors to κB DNA elements, we performed MD simulations of a 20-bp κB DNA of known structure (Figure 1, S1). | [] | Therefore, as an initial step in elucidating protein···DNA recognition and the mechanism of indirect readout in the context of differential binding of NF-κB transcription factors to κB DNA elements, we performed MD simulations of a 20-bp κB DNA of known structure. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | This DNA duplex consists of the sequence d(GGGTTTAAAGAAATTCCAGA), and encompasses a κB element (underlined) recognized by the c-Rel NF-κB homodimer and its oncogenic variant ‘v-Rel’ (21). | [
"21"
] | 187 | 41,749 | 1 | false | This DNA duplex consists of the sequence d(GGGTTTAAAGAAATTCCAGA), and encompasses a κB element (underlined) recognized by the c-Rel NF-κB homodimer and its oncogenic variant ‘v-Rel’. | [
"21"
] | This DNA duplex consists of the sequence d(GGGTTTAAAGAAATTCCAGA), and encompasses a κB element (underlined) recognized by the c-Rel NF-κB homodimer and its oncogenic variant ‘v-Rel’. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | Simulations of the DNA were extended to the microsecond timescale, affording insights that would have remained undiscovered in a shorter simulation. | [
"21"
] | 148 | 41,750 | 0 | false | Simulations of the DNA were extended to the microsecond timescale, affording insights that would have remained undiscovered in a shorter simulation. | [] | Simulations of the DNA were extended to the microsecond timescale, affording insights that would have remained undiscovered in a shorter simulation. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | Unanticipated κB DNA structural transitions discovered at the long times sampled in this trajectory include cross-strand intercalative stacking (‘XSIS’) of nucleotides followed by spontaneous base flipping at a neighboring nucleotide, as well as a peculiar minor groove-bound ‘barbed’ terminus. | [
"21"
] | 294 | 41,751 | 0 | false | Unanticipated κB DNA structural transitions discovered at the long times sampled in this trajectory include cross-strand intercalative stacking (‘XSIS’) of nucleotides followed by spontaneous base flipping at a neighboring nucleotide, as well as a peculiar minor groove-bound ‘barbed’ terminus. | [] | Unanticipated κB DNA structural transitions discovered at the long times sampled in this trajectory include cross-strand intercalative stacking (‘XSIS’) of nucleotides followed by spontaneous base flipping at a neighboring nucleotide, as well as a peculiar minor groove-bound ‘barbed’ terminus. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | In addition to illuminating the microsecond-scale structural and dynamical behavior of this particular κB sequence, the simulation provides a broad, atomic-resolution glimpse into the dynamical properties of two turns of double helical DNA over a wide range of timescales (nine orders of magnitude). | [
"21"
] | 299 | 41,752 | 0 | false | In addition to illuminating the microsecond-scale structural and dynamical behavior of this particular κB sequence, the simulation provides a broad, atomic-resolution glimpse into the dynamical properties of two turns of double helical DNA over a wide range of timescales (nine orders of magnitude). | [] | In addition to illuminating the microsecond-scale structural and dynamical behavior of this particular κB sequence, the simulation provides a broad, atomic-resolution glimpse into the dynamical properties of two turns of double helical DNA over a wide range of timescales (nine orders of magnitude). | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | The terascale body of data presents opportunities for detailed analyses of methodological issues (such as the approximations inherent in the empirical force fields used in MD), but the present report focuses instead upon the intriguing XSIS, flipping and barbing transitions, as well as suggesting specific experimental ... | [
"21"
] | 407 | 41,753 | 0 | false | The terascale body of data presents opportunities for detailed analyses of methodological issues (such as the approximations inherent in the empirical force fields used in MD), but the present report focuses instead upon the intriguing XSIS, flipping and barbing transitions, as well as suggesting specific experimental ... | [] | The terascale body of data presents opportunities for detailed analyses of methodological issues (such as the approximations inherent in the empirical force fields used in MD), but the present report focuses instead upon the intriguing XSIS, flipping and barbing transitions, as well as suggesting specific experimental ... | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | While technical issues pertaining to force field parameterization lie beyond the scope of the present work, an initial assessment of the quality of this extended trajectory was made by considering microsecond-scale DNA backbone dynamics in terms of potential BI/BII and α/γ backbone substate sampling problems. | [
"21"
] | 310 | 41,754 | 0 | false | While technical issues pertaining to force field parameterization lie beyond the scope of the present work, an initial assessment of the quality of this extended trajectory was made by considering microsecond-scale DNA backbone dynamics in terms of potential BI/BII and α/γ backbone substate sampling problems. | [] | While technical issues pertaining to force field parameterization lie beyond the scope of the present work, an initial assessment of the quality of this extended trajectory was made by considering microsecond-scale DNA backbone dynamics in terms of potential BI/BII and α/γ backbone substate sampling problems. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | Figure 1.Overview of the κB DNA element and simulation system. | [
"21"
] | 62 | 41,755 | 0 | false | Figure 1.Overview of the κB DNA element and simulation system. | [] | Figure 1.Overview of the κB DNA element and simulation system. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | The microsecond-scale dynamics of the κB DNA element shown in this sequence schematic (a) were explored, the MD simulation system consisting of the 20-bp duplex immersed in a bath of explicit water and 50 mM NaCl (b; dark blue line indicates perimeter of cut-away frontal slice). | [
"21"
] | 279 | 41,756 | 0 | false | The microsecond-scale dynamics of the κB DNA element shown in this sequence schematic (a) were explored, the MD simulation system consisting of the 20-bp duplex immersed in a bath of explicit water and 50 mM NaCl (b; dark blue line indicates perimeter of cut-away frontal slice). | [] | The microsecond-scale dynamics of the κB DNA element shown in this sequence schematic (a) were explored, the MD simulation system consisting of the 20-bp duplex immersed in a bath of explicit water and 50 mM NaCl (b; dark blue line indicates perimeter of cut-away frontal slice). | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | This particular κB DNA sequence is bound by the (c-Rel)2 NF-κB homodimer, and is essentially a composite recognition element consisting of AGAA and TTCC κB ‘half sites’. | [
"21"
] | 169 | 41,757 | 0 | false | This particular κB DNA sequence is bound by the (c-Rel)2 NF-κB homodimer, and is essentially a composite recognition element consisting of AGAA and TTCC κB ‘half sites’. | [] | This particular κB DNA sequence is bound by the (c-Rel)2 NF-κB homodimer, and is essentially a composite recognition element consisting of AGAA and TTCC κB ‘half sites’. | true | true | true | true | true | 7,201 |
3 | INTRODUCTION | 1 | 21 | [
"B21"
] | 18,653,524 | pmid-11587641 | Much of the interesting structural and dynamical behavior of this A/T-rich duplex (A-rich regions are accentuated in red) arose within the nonameric κB element (grey background in a, CPK spheres in b), including the cross-strand intercalative stacking (XSIS) and base flipping events. | [
"21"
] | 284 | 41,758 | 0 | false | Much of the interesting structural and dynamical behavior of this A/T-rich duplex (A-rich regions are accentuated in red) arose within the nonameric κB element (grey background in a, CPK spheres in b), including the cross-strand intercalative stacking (XSIS) and base flipping events. | [] | Much of the interesting structural and dynamical behavior of this A/T-rich duplex (A-rich regions are accentuated in red) arose within the nonameric κB element (grey background in a, CPK spheres in b), including the cross-strand intercalative stacking (XSIS) and base flipping events. | true | true | true | true | true | 7,201 |
4 | INTRODUCTION | 0 | null | null | 18,653,524 | null | Overview of the κB DNA element and simulation system. | null | 53 | 41,759 | 0 | false | null | null | Overview of the κB DNA element and simulation system. | true | true | true | true | true | 7,202 |
4 | INTRODUCTION | 0 | null | null | 18,653,524 | null | The microsecond-scale dynamics of the κB DNA element shown in this sequence schematic (a) were explored, the MD simulation system consisting of the 20-bp duplex immersed in a bath of explicit water and 50 mM NaCl (b; dark blue line indicates perimeter of cut-away frontal slice). | null | 279 | 41,760 | 0 | false | null | null | The microsecond-scale dynamics of the κB DNA element shown in this sequence schematic (a) were explored, the MD simulation system consisting of the 20-bp duplex immersed in a bath of explicit water and 50 mM NaCl (b; dark blue line indicates perimeter of cut-away frontal slice). | true | true | true | true | true | 7,202 |
4 | INTRODUCTION | 0 | null | null | 18,653,524 | null | This particular κB DNA sequence is bound by the (c-Rel)2 NF-κB homodimer, and is essentially a composite recognition element consisting of AGAA and TTCC κB ‘half sites’. | null | 169 | 41,761 | 0 | false | null | null | This particular κB DNA sequence is bound by the (c-Rel)2 NF-κB homodimer, and is essentially a composite recognition element consisting of AGAA and TTCC κB ‘half sites’. | true | true | true | true | true | 7,202 |
4 | INTRODUCTION | 0 | null | null | 18,653,524 | null | Much of the interesting structural and dynamical behavior of this A/T-rich duplex (A-rich regions are accentuated in red) arose within the nonameric κB element (grey background in a, CPK spheres in b), including the cross-strand intercalative stacking (XSIS) and base flipping events. | null | 284 | 41,762 | 0 | false | null | null | Much of the interesting structural and dynamical behavior of this A/T-rich duplex (A-rich regions are accentuated in red) arose within the nonameric κB element (grey background in a, CPK spheres in b), including the cross-strand intercalative stacking (XSIS) and base flipping events. | true | true | true | true | true | 7,202 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B3",
"B4",
"B9",
"B10"
] | 18,607,120 | pmid-9279630|pmid-3821363|pmid-9366704|NA|pmid-528821 | A narrow IAC is a rare congenital malformation of the temporal bone and it usually exists along with several other abnormalities of the temporal bone and various systemic developmental anomalies, including cardiac, renal, skeletal, and intestinal malformations (1). | [
"1",
"3",
"4",
"9",
"10"
] | 265 | 41,763 | 1 | false | A narrow IAC is a rare congenital malformation of the temporal bone and it usually exists along with several other abnormalities of the temporal bone and various systemic developmental anomalies, including cardiac, renal, skeletal, and intestinal malformations. | [
"1"
] | A narrow IAC is a rare congenital malformation of the temporal bone and it usually exists along with several other abnormalities of the temporal bone and various systemic developmental anomalies, including cardiac, renal, skeletal, and intestinal malformations. | true | true | true | true | true | 7,203 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B3",
"B4",
"B9",
"B10"
] | 18,607,120 | pmid-9279630|pmid-3821363|pmid-9366704|NA|pmid-528821 | This malformation comprises only 12% of congenital temporal bone anomalies, and it is usually unilateral (3, 4, 9). | [
"1",
"3",
"4",
"9",
"10"
] | 115 | 41,764 | 0 | false | This malformation comprises only 12% of congenital temporal bone anomalies, and it is usually unilateral. | [
"3, 4, 9"
] | This malformation comprises only 12% of congenital temporal bone anomalies, and it is usually unilateral. | true | true | true | true | true | 7,203 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B3",
"B4",
"B9",
"B10"
] | 18,607,120 | pmid-9279630|pmid-3821363|pmid-9366704|NA|pmid-528821 | Rarely, this malformation may exist in isolation. | [
"1",
"3",
"4",
"9",
"10"
] | 49 | 41,765 | 0 | false | Rarely, this malformation may exist in isolation. | [] | Rarely, this malformation may exist in isolation. | true | true | true | true | true | 7,203 |
0 | DISCUSSION | 1 | 10 | [
"B1",
"B3",
"B4",
"B9",
"B10"
] | 18,607,120 | pmid-9279630|pmid-3821363|pmid-9366704|NA|pmid-528821 | Congenital isolated narrowing of the IAC implies that there are no associated abnormalities in the inner ear, middle or external ear structures, and the absence of any acquired osseous condition predisposing to stenosis of the IAC (10). | [
"1",
"3",
"4",
"9",
"10"
] | 236 | 41,766 | 1 | false | Congenital isolated narrowing of the IAC implies that there are no associated abnormalities in the inner ear, middle or external ear structures, and the absence of any acquired osseous condition predisposing to stenosis of the IAC. | [
"10"
] | Congenital isolated narrowing of the IAC implies that there are no associated abnormalities in the inner ear, middle or external ear structures, and the absence of any acquired osseous condition predisposing to stenosis of the IAC. | true | true | true | true | true | 7,203 |
0 | DISCUSSION | 1 | 1 | [
"B1",
"B3",
"B4",
"B9",
"B10"
] | 18,607,120 | pmid-9279630|pmid-3821363|pmid-9366704|NA|pmid-528821 | In this case, the IAC was unilateral and there was no evidence of other temporal bone or systemic developmental anomalies. | [
"1",
"3",
"4",
"9",
"10"
] | 122 | 41,767 | 0 | false | In this case, the IAC was unilateral and there was no evidence of other temporal bone or systemic developmental anomalies. | [] | In this case, the IAC was unilateral and there was no evidence of other temporal bone or systemic developmental anomalies. | true | true | true | true | true | 7,203 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | There are two widely accepted hypotheses that explain the association of a narrow IAC with sensorineural hearing loss. | [
"1",
"4",
"1"
] | 118 | 41,768 | 0 | false | There are two widely accepted hypotheses that explain the association of a narrow IAC with sensorineural hearing loss. | [] | There are two widely accepted hypotheses that explain the association of a narrow IAC with sensorineural hearing loss. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | One hypothesis is that the embryonic cochlear and vestibule induce the growth of the vestibulocochlear nerve and the bony canal develops around the nerve together with the facial nerve by chondrification and ossification of the mesoderm in the eighth week of gestation. | [
"1",
"4",
"1"
] | 269 | 41,769 | 0 | false | One hypothesis is that the embryonic cochlear and vestibule induce the growth of the vestibulocochlear nerve and the bony canal develops around the nerve together with the facial nerve by chondrification and ossification of the mesoderm in the eighth week of gestation. | [] | One hypothesis is that the embryonic cochlear and vestibule induce the growth of the vestibulocochlear nerve and the bony canal develops around the nerve together with the facial nerve by chondrification and ossification of the mesoderm in the eighth week of gestation. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | When the vestibulocochlear nerve is aplastic or hypoplastic, the IAC fails to develop and becomes stenotic (1, 4). | [
"1",
"4",
"1"
] | 114 | 41,770 | 0 | false | When the vestibulocochlear nerve is aplastic or hypoplastic, the IAC fails to develop and becomes stenotic. | [
"1, 4"
] | When the vestibulocochlear nerve is aplastic or hypoplastic, the IAC fails to develop and becomes stenotic. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | The other hypothesis is that the primary defect is bony stenosis that inhibits the growth of the vestibulocochlear nerve and causes impaired transmission of an induction signal from the intact cochlea and vestibule. | [
"1",
"4",
"1"
] | 215 | 41,771 | 0 | false | The other hypothesis is that the primary defect is bony stenosis that inhibits the growth of the vestibulocochlear nerve and causes impaired transmission of an induction signal from the intact cochlea and vestibule. | [] | The other hypothesis is that the primary defect is bony stenosis that inhibits the growth of the vestibulocochlear nerve and causes impaired transmission of an induction signal from the intact cochlea and vestibule. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | However, given the fact that the facial nerve function is usually preserved and it has a normal gross morphology in most cases of narrow IAC, this hypothesis is less likely (1). | [
"1",
"4",
"1"
] | 177 | 41,772 | 1 | false | However, given the fact that the facial nerve function is usually preserved and it has a normal gross morphology in most cases of narrow IAC, this hypothesis is less likely. | [
"1"
] | However, given the fact that the facial nerve function is usually preserved and it has a normal gross morphology in most cases of narrow IAC, this hypothesis is less likely. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | The facial nerve develops separately and it is later surrounded as the canal forms around the vestibulocochlear nerve. | [
"1",
"4",
"1"
] | 118 | 41,773 | 0 | false | The facial nerve develops separately and it is later surrounded as the canal forms around the vestibulocochlear nerve. | [] | The facial nerve develops separately and it is later surrounded as the canal forms around the vestibulocochlear nerve. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | This may cause the duplication of the IAC in some cases of a narrow IAC with the aplastic or hypoplastic vestibulocochlear nerve. | [
"1",
"4",
"1"
] | 129 | 41,774 | 0 | false | This may cause the duplication of the IAC in some cases of a narrow IAC with the aplastic or hypoplastic vestibulocochlear nerve. | [] | This may cause the duplication of the IAC in some cases of a narrow IAC with the aplastic or hypoplastic vestibulocochlear nerve. | true | true | true | true | true | 7,204 |
1 | DISCUSSION | 1 | 1 | [
"B1",
"B4",
"B1"
] | 18,607,120 | pmid-9279630|pmid-9366704|pmid-9279630 | In this case, the right IAC was duplicated with a bony septum that separated the canal into a relatively large anterosuperior portion containing an intact facial nerve and empty stenotic inferoposterior portion. | [
"1",
"4",
"1"
] | 211 | 41,775 | 0 | false | In this case, the right IAC was duplicated with a bony septum that separated the canal into a relatively large anterosuperior portion containing an intact facial nerve and empty stenotic inferoposterior portion. | [] | In this case, the right IAC was duplicated with a bony septum that separated the canal into a relatively large anterosuperior portion containing an intact facial nerve and empty stenotic inferoposterior portion. | true | true | true | true | true | 7,204 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | To date, only five cases of a narrow IAC with duplication have been reported. | [
"6",
"8",
"5",
"2",
"7"
] | 77 | 41,776 | 0 | false | To date, only five cases of a narrow IAC with duplication have been reported. | [] | To date, only five cases of a narrow IAC with duplication have been reported. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | The first case was reported by Casselman et al. | [
"6",
"8",
"5",
"2",
"7"
] | 47 | 41,777 | 0 | false | The first case was reported by Casselman et al. | [] | The first case was reported by Casselman et al. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | (6) in 1997. | [
"6",
"8",
"5",
"2",
"7"
] | 12 | 41,778 | 1 | false | in 1997. | [
"6"
] | in 1997. | false | true | true | true | false | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | These investigators described a case of unilateral narrow IAC with duplication. | [
"6",
"8",
"5",
"2",
"7"
] | 79 | 41,779 | 0 | false | These investigators described a case of unilateral narrow IAC with duplication. | [] | These investigators described a case of unilateral narrow IAC with duplication. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | However, there were no imaging findings of this case in the report. | [
"6",
"8",
"5",
"2",
"7"
] | 67 | 41,780 | 0 | false | However, there were no imaging findings of this case in the report. | [] | However, there were no imaging findings of this case in the report. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | Vilain et al. | [
"6",
"8",
"5",
"2",
"7"
] | 13 | 41,781 | 0 | false | Vilain et al. | [] | Vilain et al. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 8 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | (8) reported a second case in 1999. | [
"6",
"8",
"5",
"2",
"7"
] | 35 | 41,782 | 1 | false | reported a second case in 1999. | [
"8"
] | reported a second case in 1999. | false | true | true | true | false | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | These investigators described a case of narrow IAC with duplicated canals that joined at the fundus of the IAC. | [
"6",
"8",
"5",
"2",
"7"
] | 111 | 41,783 | 0 | false | These investigators described a case of narrow IAC with duplicated canals that joined at the fundus of the IAC. | [] | These investigators described a case of narrow IAC with duplicated canals that joined at the fundus of the IAC. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 5 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | (5) reported a third case in 2000 and it was a case of narrow IAC with duplication. | [
"6",
"8",
"5",
"2",
"7"
] | 83 | 41,784 | 1 | false | reported a third case in 2000 and it was a case of narrow IAC with duplication. | [
"5"
] | reported a third case in 2000 and it was a case of narrow IAC with duplication. | false | true | true | true | false | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | However, two separate canaliculi of the IAC showed similar diameters and did not join at the fundus of IAC. | [
"6",
"8",
"5",
"2",
"7"
] | 107 | 41,785 | 0 | false | However, two separate canaliculi of the IAC showed similar diameters and did not join at the fundus of IAC. | [] | However, two separate canaliculi of the IAC showed similar diameters and did not join at the fundus of IAC. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | A fourth case was reported by Ferreira et al. | [
"6",
"8",
"5",
"2",
"7"
] | 45 | 41,786 | 0 | false | A fourth case was reported by Ferreira et al. | [] | A fourth case was reported by Ferreira et al. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 2 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | (2) in 2003. | [
"6",
"8",
"5",
"2",
"7"
] | 12 | 41,787 | 1 | false | in 2003. | [
"2"
] | in 2003. | false | true | true | true | false | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | These investigators described a similar case of narrow IAC which was associated with bilateral enlargement of the vestibule and the lateral semicircular canal and bilateral dysplastic cochleae. | [
"6",
"8",
"5",
"2",
"7"
] | 193 | 41,788 | 0 | false | These investigators described a similar case of narrow IAC which was associated with bilateral enlargement of the vestibule and the lateral semicircular canal and bilateral dysplastic cochleae. | [] | These investigators described a similar case of narrow IAC which was associated with bilateral enlargement of the vestibule and the lateral semicircular canal and bilateral dysplastic cochleae. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | A fifth case was reported by Demir et al. | [
"6",
"8",
"5",
"2",
"7"
] | 41 | 41,789 | 0 | false | A fifth case was reported by Demir et al. | [] | A fifth case was reported by Demir et al. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 7 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | (7) in 2005. | [
"6",
"8",
"5",
"2",
"7"
] | 12 | 41,790 | 1 | false | in 2005. | [
"7"
] | in 2005. | false | true | true | true | false | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | This was a case of a narrow IAC that was separated into two narrow bony canals. | [
"6",
"8",
"5",
"2",
"7"
] | 79 | 41,791 | 0 | false | This was a case of a narrow IAC that was separated into two narrow bony canals. | [] | This was a case of a narrow IAC that was separated into two narrow bony canals. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | The contralateral external auditory canal was stenotic and the ossicles were dysplastic. | [
"6",
"8",
"5",
"2",
"7"
] | 88 | 41,792 | 0 | false | The contralateral external auditory canal was stenotic and the ossicles were dysplastic. | [] | The contralateral external auditory canal was stenotic and the ossicles were dysplastic. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | Our case was an isolated unilateral narrow IAC that was not associated with any other labyrinthine abnormality. | [
"6",
"8",
"5",
"2",
"7"
] | 111 | 41,793 | 0 | false | Our case was an isolated unilateral narrow IAC that was not associated with any other labyrinthine abnormality. | [] | Our case was an isolated unilateral narrow IAC that was not associated with any other labyrinthine abnormality. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | In this case, the IAC was divided by a bony septum into two bony canals that were joined at the fundus of IAC. | [
"6",
"8",
"5",
"2",
"7"
] | 110 | 41,794 | 0 | false | In this case, the IAC was divided by a bony septum into two bony canals that were joined at the fundus of IAC. | [] | In this case, the IAC was divided by a bony septum into two bony canals that were joined at the fundus of IAC. | true | true | true | true | true | 7,205 |
2 | DISCUSSION | 1 | 6 | [
"B6",
"B8",
"B5",
"B2",
"B7"
] | 18,607,120 | pmid-9051033|pmid-10102042|pmid-10912275|pmid-12743665|pmid-16079980 | These cases are summarized in Table 1. | [
"6",
"8",
"5",
"2",
"7"
] | 38 | 41,795 | 0 | false | These cases are summarized in Table 1. | [] | These cases are summarized in Table 1. | true | true | true | true | true | 7,205 |
3 | DISCUSSION | 1 | 9 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | The normal range of the IAC is 2-8 mm, with an average of 4 mm, and a narrow IAC is defined when a canal is smaller than 2 mm in vertical diameter as seen on HRCT (9). | [
"9",
"1",
"6",
"4"
] | 167 | 41,796 | 1 | false | The normal range of the IAC is 2-8 mm, with an average of 4 mm, and a narrow IAC is defined when a canal is smaller than 2 mm in vertical diameter as seen on HRCT. | [
"9"
] | The normal range of the IAC is 2-8 mm, with an average of 4 mm, and a narrow IAC is defined when a canal is smaller than 2 mm in vertical diameter as seen on HRCT. | true | true | true | true | true | 7,206 |
3 | DISCUSSION | 1 | 1 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | The HRCT scan is the diagnostic modality of choice as it provides excellent bony detail and high sensitivity and specificity in demonstrating the congenital inner ear and temporal bone abnormalities (1). | [
"9",
"1",
"6",
"4"
] | 203 | 41,797 | 1 | false | The HRCT scan is the diagnostic modality of choice as it provides excellent bony detail and high sensitivity and specificity in demonstrating the congenital inner ear and temporal bone abnormalities. | [
"1"
] | The HRCT scan is the diagnostic modality of choice as it provides excellent bony detail and high sensitivity and specificity in demonstrating the congenital inner ear and temporal bone abnormalities. | true | true | true | true | true | 7,206 |
3 | DISCUSSION | 1 | 9 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | However, a CT scan has a limited role in assessing the neural components of the IAC. | [
"9",
"1",
"6",
"4"
] | 84 | 41,798 | 0 | false | However, a CT scan has a limited role in assessing the neural components of the IAC. | [] | However, a CT scan has a limited role in assessing the neural components of the IAC. | true | true | true | true | true | 7,206 |
3 | DISCUSSION | 1 | 9 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | Casselman et al. | [
"9",
"1",
"6",
"4"
] | 16 | 41,799 | 0 | false | Casselman et al. | [] | Casselman et al. | true | true | true | true | true | 7,206 |
3 | DISCUSSION | 1 | 6 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | (6) described seven cases with congenital or unexplained sensorineural hearing loss and five of those cases with a normal IAC showed aplasia or hypoplasia of the vestibulocochlear nerve or of only the cochlear branch on MR imaging. | [
"9",
"1",
"6",
"4"
] | 231 | 41,800 | 1 | false | described seven cases with congenital or unexplained sensorineural hearing loss and five of those cases with a normal IAC showed aplasia or hypoplasia of the vestibulocochlear nerve or of only the cochlear branch on MR imaging. | [
"6"
] | described seven cases with congenital or unexplained sensorineural hearing loss and five of those cases with a normal IAC showed aplasia or hypoplasia of the vestibulocochlear nerve or of only the cochlear branch on MR imaging. | false | true | true | true | false | 7,206 |
3 | DISCUSSION | 1 | 4 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | In patients with a narrow IAC, assessment of the cochlear nerve is crucial for selecting patients for cochlear implantation (4). | [
"9",
"1",
"6",
"4"
] | 128 | 41,801 | 1 | false | In patients with a narrow IAC, assessment of the cochlear nerve is crucial for selecting patients for cochlear implantation. | [
"4"
] | In patients with a narrow IAC, assessment of the cochlear nerve is crucial for selecting patients for cochlear implantation. | true | true | true | true | true | 7,206 |
3 | DISCUSSION | 1 | 9 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | Patients with aplastic cochlear nerves may not respond to the electric stimulation of the cochlear implantation. | [
"9",
"1",
"6",
"4"
] | 112 | 41,802 | 0 | false | Patients with aplastic cochlear nerves may not respond to the electric stimulation of the cochlear implantation. | [] | Patients with aplastic cochlear nerves may not respond to the electric stimulation of the cochlear implantation. | true | true | true | true | true | 7,206 |
3 | DISCUSSION | 1 | 9 | [
"B9",
"B1",
"B6",
"B4"
] | 18,607,120 | NA|pmid-9279630|pmid-9051033|pmid-9366704 | These reports emphasized that an HRCT scan alone is not sufficient to rule out the risk of aplasia or hypoplasia of the vestibulocochlear nerve and that MR imaging should be performed to look for the defect of neural structures in the IAC of patients with sensorineural hearing loss. | [
"9",
"1",
"6",
"4"
] | 283 | 41,803 | 0 | false | These reports emphasized that an HRCT scan alone is not sufficient to rule out the risk of aplasia or hypoplasia of the vestibulocochlear nerve and that MR imaging should be performed to look for the defect of neural structures in the IAC of patients with sensorineural hearing loss. | [] | These reports emphasized that an HRCT scan alone is not sufficient to rule out the risk of aplasia or hypoplasia of the vestibulocochlear nerve and that MR imaging should be performed to look for the defect of neural structures in the IAC of patients with sensorineural hearing loss. | true | true | true | true | true | 7,206 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | MR imaging has become the modality of choice along with HRCT for the assessment of abnormalities in patients with sensorineural hearing loss. | [
"6",
"5",
"7",
"5"
] | 141 | 41,804 | 0 | false | MR imaging has become the modality of choice along with HRCT for the assessment of abnormalities in patients with sensorineural hearing loss. | [] | MR imaging has become the modality of choice along with HRCT for the assessment of abnormalities in patients with sensorineural hearing loss. | true | true | true | true | true | 7,207 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | Especially, the use of high-resolution gradient-echo imaging provides detailed anatomical images of the vestibulocochlear and facial nerves of an IAC and is essential for cochlear implant candidates (6). | [
"6",
"5",
"7",
"5"
] | 203 | 41,805 | 1 | false | Especially, the use of high-resolution gradient-echo imaging provides detailed anatomical images of the vestibulocochlear and facial nerves of an IAC and is essential for cochlear implant candidates. | [
"6"
] | Especially, the use of high-resolution gradient-echo imaging provides detailed anatomical images of the vestibulocochlear and facial nerves of an IAC and is essential for cochlear implant candidates. | true | true | true | true | true | 7,207 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | There are several newly developed high-resolution gradient-echo MR imaging sequences which include 3D magnetization prepared rapid gradient echo (MP-RAGE), 3D balanced fast field echo (B-FFE), 3D Fourier transformation-constructive interference in the steady state (3D FT-CISS), and 3D DRIVE sequences (5, 7). | [
"6",
"5",
"7",
"5"
] | 309 | 41,806 | 0 | false | There are several newly developed high-resolution gradient-echo MR imaging sequences which include 3D magnetization prepared rapid gradient echo (MP-RAGE), 3D balanced fast field echo (B-FFE), 3D Fourier transformation-constructive interference in the steady state (3D FT-CISS), and 3D DRIVE sequences. | [
"5, 7"
] | There are several newly developed high-resolution gradient-echo MR imaging sequences which include 3D magnetization prepared rapid gradient echo (MP-RAGE), 3D balanced fast field echo (B-FFE), 3D Fourier transformation-constructive interference in the steady state (3D FT-CISS), and 3D DRIVE sequences. | true | true | true | true | true | 7,207 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | These sequences are all three-dimensional for data acquisition and submillimetric in spatial resolution, which are optimal to evaluate the neural structures less than 1 mm in diameter, such as the auditory and facial nerves. | [
"6",
"5",
"7",
"5"
] | 224 | 41,807 | 0 | false | These sequences are all three-dimensional for data acquisition and submillimetric in spatial resolution, which are optimal to evaluate the neural structures less than 1 mm in diameter, such as the auditory and facial nerves. | [] | These sequences are all three-dimensional for data acquisition and submillimetric in spatial resolution, which are optimal to evaluate the neural structures less than 1 mm in diameter, such as the auditory and facial nerves. | true | true | true | true | true | 7,207 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | In this case, we used a 3D DRIVE sequence with a high field 3-Tesla MRI scanner to obtain detailed images for the neural structures of the IAC. | [
"6",
"5",
"7",
"5"
] | 143 | 41,808 | 0 | false | In this case, we used a 3D DRIVE sequence with a high field 3-Tesla MRI scanner to obtain detailed images for the neural structures of the IAC. | [] | In this case, we used a 3D DRIVE sequence with a high field 3-Tesla MRI scanner to obtain detailed images for the neural structures of the IAC. | true | true | true | true | true | 7,207 |
4 | DISCUSSION | 1 | 5 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | (5) reported a case of narrow IAC syndrome with aplasia of the vestibulocochlear nerve and intact facial nerve that were successfully demonstrated by using parasagittal reconstruction MR imaging. | [
"6",
"5",
"7",
"5"
] | 195 | 41,809 | 1 | false | reported a case of narrow IAC syndrome with aplasia of the vestibulocochlear nerve and intact facial nerve that were successfully demonstrated by using parasagittal reconstruction MR imaging. | [
"5"
] | reported a case of narrow IAC syndrome with aplasia of the vestibulocochlear nerve and intact facial nerve that were successfully demonstrated by using parasagittal reconstruction MR imaging. | false | true | true | true | false | 7,207 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | In this case, the IAC was narrow and was composed of two separate canaliculi as seen on HRCT. | [
"6",
"5",
"7",
"5"
] | 93 | 41,810 | 0 | false | In this case, the IAC was narrow and was composed of two separate canaliculi as seen on HRCT. | [] | In this case, the IAC was narrow and was composed of two separate canaliculi as seen on HRCT. | true | true | true | true | true | 7,207 |
4 | DISCUSSION | 1 | 6 | [
"B6",
"B5",
"B7",
"B5"
] | 18,607,120 | pmid-9051033|pmid-10912275|pmid-16079980|pmid-10912275 | On 3-T MR images using 3D DRIVE and a T2-weighted FSE sequence with axial and parasagittal planes perpendicular to the course of the IAC, there were a relatively larger anterosuperior portion containing the intact facial nerve and a stenotic inferoposterior portion without any neural contents. | [
"6",
"5",
"7",
"5"
] | 294 | 41,811 | 0 | false | On 3-T MR images using 3D DRIVE and a T2-weighted FSE sequence with axial and parasagittal planes perpendicular to the course of the IAC, there were a relatively larger anterosuperior portion containing the intact facial nerve and a stenotic inferoposterior portion without any neural contents. | [] | On 3-T MR images using 3D DRIVE and a T2-weighted FSE sequence with axial and parasagittal planes perpendicular to the course of the IAC, there were a relatively larger anterosuperior portion containing the intact facial nerve and a stenotic inferoposterior portion without any neural contents. | true | true | true | true | true | 7,207 |
5 | DISCUSSION | 0 | null | null | 18,607,120 | null | In conclusion, an isolated narrow IAC with duplication associated with congenital sensorineural hearing loss and normal facial nerve function is extremely rare, and to the best of our knowledge, this is the sixth case reported for this malformation. | null | 249 | 41,812 | 0 | false | null | null | In conclusion, an isolated narrow IAC with duplication associated with congenital sensorineural hearing loss and normal facial nerve function is extremely rare, and to the best of our knowledge, this is the sixth case reported for this malformation. | true | true | true | true | true | 7,208 |
5 | DISCUSSION | 0 | null | null | 18,607,120 | null | An examination of this anomaly should include a past medical history and physical examination, auditometry including auditory brainstem response, a high-resolution CT scan, and high-resolution MR imaging. | null | 204 | 41,813 | 0 | false | null | null | An examination of this anomaly should include a past medical history and physical examination, auditometry including auditory brainstem response, a high-resolution CT scan, and high-resolution MR imaging. | true | true | true | true | true | 7,208 |
5 | DISCUSSION | 0 | null | null | 18,607,120 | null | It is of great importance to make a diagnosis of aplasia or hypoplasia of the vestibulocochlear nerve in the IAC for cochlear implant candidates. | null | 145 | 41,814 | 0 | false | null | null | It is of great importance to make a diagnosis of aplasia or hypoplasia of the vestibulocochlear nerve in the IAC for cochlear implant candidates. | true | true | true | true | true | 7,208 |
5 | DISCUSSION | 0 | null | null | 18,607,120 | null | For this purpose, high-resolution submillimetric gradient-echo MR images, such as 3D-CISS and 3D DRIVE, or T2-weighted FSE sequences should be obtained in the parasagittal plane perpendicular to the course of the vestibulocochlear and facial nerves. | null | 249 | 41,815 | 0 | false | null | null | For this purpose, high-resolution submillimetric gradient-echo MR images, such as 3D-CISS and 3D DRIVE, or T2-weighted FSE sequences should be obtained in the parasagittal plane perpendicular to the course of the vestibulocochlear and facial nerves. | true | true | true | true | true | 7,208 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B3"
] | 16,941,739 | pmid-11918468|NA|pmid-2502382|pmid-11918468 | Infantile spasm is a catastrophic childhood epilepsy syndrome1 that was first described by West in 1841.2 The combination of infantile spasm, a characteristic electroencephalographic pattern and psychomotor retardation in the majority of patients is known as West Syndrome.3 | [
"1",
"2",
"3"
] | 274 | 41,816 | 0 | false | Infantile spasm is a catastrophic childhood epilepsy syndrome1 that was first described by West in 1841.2 The combination of infantile spasm, a characteristic electroencephalographic pattern and psychomotor retardation in the majority of patients is known as West Syndrome.3 | [] | Infantile spasm is a catastrophic childhood epilepsy syndrome1 that was first described by West in 1841.2 The combination of infantile spasm, a characteristic electroencephalographic pattern and psychomotor retardation in the majority of patients is known as West Syndrome.3 | true | true | false | true | false | 7,209 |
1 | INTRODUCTION | 1 | 4 | [
"B4",
"B5",
"B6",
"B12"
] | 16,941,739 | pmid-11701267|pmid-10757471|pmid-2821097|pmid-11999624|NA|pmid-11701267|pmid-11781414|pmid-6312008|pmid-2821097|pmid-3017235|pmid-6244378 | For the management of infantile spasm, ACTH/steroid or vigabatrin (VGB) are widely and frequently as the first-line of treatment.4,5 Because the usefulness of these drugs is limited by the occurrence of side effects, scientists are searching for new antiepileptic drugs to treat infantile spasm.6-12 | [
"4",
"5",
"6",
"12"
] | 299 | 41,817 | 0 | false | For the management of infantile spasm, ACTH/steroid or vigabatrin (VGB) are widely and frequently as the first-line of treatment.4,5 Because the usefulness of these drugs is limited by the occurrence of side effects, scientists are searching for new antiepileptic drugs to treat infantile spasm.6-12 | [] | For the management of infantile spasm, ACTH/steroid or vigabatrin (VGB) are widely and frequently as the first-line of treatment.4,5 Because the usefulness of these drugs is limited by the occurrence of side effects, scientists are searching for new antiepileptic drugs to treat infantile spasm.6-12 | true | true | false | true | false | 7,210 |
2 | INTRODUCTION | 1 | 13 | [
"B13",
"B14",
"B15",
"B16",
"B17"
] | 16,941,739 | pmid-2217531|pmid-8641230|pmid-10227614|pmid-10227615|pmid-10768308|pmid-6275826|pmid-7919570|pmid-3102998|pmid-11981230 | Topiramate (TPM) is a drug with multiple mechanisms of action, including the state-dependent inhibition of sodium channels, the potentiation of γ-aminobutyric acid (GABA)-induced chloride influx, the blockade of glutamate related excitatory neurotransmission, and the inhibition of carbonic anhydrase.13 TMP has been use... | [
"13",
"14",
"15",
"16",
"17"
] | 585 | 41,818 | 0 | false | Topiramate (TPM) is a drug with multiple mechanisms of action, including the state-dependent inhibition of sodium channels, the potentiation of γ-aminobutyric acid (GABA)-induced chloride influx, the blockade of glutamate related excitatory neurotransmission, and the inhibition of carbonic anhydrase.13 TMP has been use... | [] | Topiramate (TPM) is a drug with multiple mechanisms of action, including the state-dependent inhibition of sodium channels, the potentiation of γ-aminobutyric acid (GABA)-induced chloride influx, the blockade of glutamate related excitatory neurotransmission, and the inhibition of carbonic anhydrase.13 TMP has been use... | true | true | false | true | false | 7,211 |
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