paragraph_index int64 | sec string | p_has_citation int64 | cites string | citeids list | pmid int64 | cited_id string | sentences string | all_sent_cites list | sent_len int64 | sentence_batch_index int64 | sent_has_citation float64 | qc_fail bool | cited_sentence string | cites_in_sentence list | cln_sentence string | is_cap bool | is_alpha bool | ends_wp bool | cit_qc bool | lgtm bool | __index_level_0__ int64 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
2 | INTRODUCTION | 1 | 11 | [
"B11",
"B12 B13 B14"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | It is shown that repeated or periodic variations in β sequence give rise to different types of helical and looped conformations and that helical conformations are able to associate pairwise as a zip, to form double helices, intercalate and contract to a high density. | [
"11",
"12–14"
] | 267 | 37,916 | 0 | false | It is shown that repeated or periodic variations in β sequence give rise to different types of helical and looped conformations and that helical conformations are able to associate pairwise as a zip, to form double helices, intercalate and contract to a high density. | [] | It is shown that repeated or periodic variations in β sequence give rise to different types of helical and looped conformations and that helical conformations are able to associate pairwise as a zip, to form double helices, intercalate and contract to a high density. | true | true | true | true | true | 6,500 |
2 | INTRODUCTION | 1 | 11 | [
"B11",
"B12 B13 B14"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | Finally, the irregular conformation of a filament with a random β sequence is described as well as how it can be converted into a regular helix by chromatin remodeling and limited twisting of the linkers. | [
"11",
"12–14"
] | 204 | 37,917 | 0 | false | Finally, the irregular conformation of a filament with a random β sequence is described as well as how it can be converted into a regular helix by chromatin remodeling and limited twisting of the linkers. | [] | Finally, the irregular conformation of a filament with a random β sequence is described as well as how it can be converted into a regular helix by chromatin remodeling and limited twisting of the linkers. | true | true | true | true | true | 6,500 |
2 | INTRODUCTION | 1 | 11 | [
"B11",
"B12 B13 B14"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | Although physical models are static and do not account for the linker flexibility, they might be useful in studies of chromatin ultrastructure and serve as reference models for the analysis of transmission electron microscopic images. | [
"11",
"12–14"
] | 234 | 37,918 | 0 | false | Although physical models are static and do not account for the linker flexibility, they might be useful in studies of chromatin ultrastructure and serve as reference models for the analysis of transmission electron microscopic images. | [] | Although physical models are static and do not account for the linker flexibility, they might be useful in studies of chromatin ultrastructure and serve as reference models for the analysis of transmission electron microscopic images. | true | true | true | true | true | 6,500 |
0 | DISCUSSION | 1 | 24 | [
"B24",
"B29",
"B15",
"B16"
] | 17,704,136 | pmid-9305837|pmid-2660830|NA|pmid-8138564|pmid-1757505|pmid-3955173|pmid-9826673|pmid-8522597|pmid-9635737|pmid-14645090 | A major result of the present study is the demonstration of the significance of α for the conformational freedom of the nucleosomal filament. | [
"24",
"29",
"15",
"16"
] | 141 | 37,919 | 0 | false | A major result of the present study is the demonstration of the significance of α for the conformational freedom of the nucleosomal filament. | [] | A major result of the present study is the demonstration of the significance of α for the conformational freedom of the nucleosomal filament. | true | true | true | true | true | 6,501 |
0 | DISCUSSION | 1 | 24 | [
"B24",
"B29",
"B15",
"B16"
] | 17,704,136 | pmid-9305837|pmid-2660830|NA|pmid-8138564|pmid-1757505|pmid-3955173|pmid-9826673|pmid-8522597|pmid-9635737|pmid-14645090 | When α is smaller than 60° the filament thus remains a helix with little space for variations in the β sequence, while larger values of α provide it with a freedom to attain conformations, which are not dependent on a helical symmetry, by allowing for an increased variation in β sequence. | [
"24",
"29",
"15",
"16"
] | 289 | 37,920 | 0 | false | When α is smaller than 60° the filament thus remains a helix with little space for variations in the β sequence, while larger values of α provide it with a freedom to attain conformations, which are not dependent on a helical symmetry, by allowing for an increased variation in β sequence. | [] | When α is smaller than 60° the filament thus remains a helix with little space for variations in the β sequence, while larger values of α provide it with a freedom to attain conformations, which are not dependent on a helical symmetry, by allowing for an increased variation in β sequence. | true | true | true | true | true | 6,501 |
0 | DISCUSSION | 1 | 24 | [
"B24",
"B29",
"B15",
"B16"
] | 17,704,136 | pmid-9305837|pmid-2660830|NA|pmid-8138564|pmid-1757505|pmid-3955173|pmid-9826673|pmid-8522597|pmid-9635737|pmid-14645090 | The size of α in chromatin is not known with certainty, but α has been shown by cryo-EM imaging of native chromatin fibers (24,29) to decrease from 85 to 35° when the salt concentration is increased. | [
"24",
"29",
"15",
"16"
] | 199 | 37,921 | 0 | false | The size of α in chromatin is not known with certainty, but α has been shown by cryo-EM imaging of native chromatin fibers to decrease from 85 to 35° when the salt concentration is increased. | [
"24,29"
] | The size of α in chromatin is not known with certainty, but α has been shown by cryo-EM imaging of native chromatin fibers to decrease from 85 to 35° when the salt concentration is increased. | true | true | true | true | true | 6,501 |
0 | DISCUSSION | 1 | 24 | [
"B24",
"B29",
"B15",
"B16"
] | 17,704,136 | pmid-9305837|pmid-2660830|NA|pmid-8138564|pmid-1757505|pmid-3955173|pmid-9826673|pmid-8522597|pmid-9635737|pmid-14645090 | These relatively small DNA entry–exit angles have been suggested to be caused by the stem motive, which has not been observed by scanning force microscopy (SFM). | [
"24",
"29",
"15",
"16"
] | 161 | 37,922 | 0 | false | These relatively small DNA entry–exit angles have been suggested to be caused by the stem motive, which has not been observed by scanning force microscopy (SFM). | [] | These relatively small DNA entry–exit angles have been suggested to be caused by the stem motive, which has not been observed by scanning force microscopy (SFM). | true | true | true | true | true | 6,501 |
0 | DISCUSSION | 1 | 15 | [
"B24",
"B29",
"B15",
"B16"
] | 17,704,136 | pmid-9305837|pmid-2660830|NA|pmid-8138564|pmid-1757505|pmid-3955173|pmid-9826673|pmid-8522597|pmid-9635737|pmid-14645090 | Studies by SFM of chromatin fibers fixed at low ionic strength have yielded average values of α of 100 ± 40° in the presence and 130 ± 40° in the absence of linker histones (15), and unfixed mononucleosomes at 10 mM MgCl2 showed two maxima of α at around 80 and 136° in the absence of H1 and one maximum at 85–88° in the... | [
"24",
"29",
"15",
"16"
] | 411 | 37,923 | 1 | false | Studies by SFM of chromatin fibers fixed at low ionic strength have yielded average values of α of 100 ± 40° in the presence and 130 ± 40° in the absence of linker histones, and unfixed mononucleosomes at 10 mM MgCl2 showed two maxima of α at around 80 and 136° in the absence of H1 and one maximum at 85–88° in the pres... | [
"15",
"16"
] | Studies by SFM of chromatin fibers fixed at low ionic strength have yielded average values of α of 100 ± 40° in the presence and 130 ± 40° in the absence of linker histones, and unfixed mononucleosomes at 10 mM MgCl2 showed two maxima of α at around 80 and 136° in the absence of H1 and one maximum at 85–88° in the pres... | true | true | true | true | true | 6,501 |
0 | DISCUSSION | 1 | 24 | [
"B24",
"B29",
"B15",
"B16"
] | 17,704,136 | pmid-9305837|pmid-2660830|NA|pmid-8138564|pmid-1757505|pmid-3955173|pmid-9826673|pmid-8522597|pmid-9635737|pmid-14645090 | These large values of α thus correspond to a polygon fiber geometry. | [
"24",
"29",
"15",
"16"
] | 68 | 37,924 | 0 | false | These large values of α thus correspond to a polygon fiber geometry. | [] | These large values of α thus correspond to a polygon fiber geometry. | true | true | true | true | true | 6,501 |
1 | DISCUSSION | 0 | null | null | 17,704,136 | pmid-15377519|pmid-16622406|pmid-9514762|pmid-11171316 | An important property of the polygon fiber is the length expansion at 0° < | null | 74 | 37,925 | 0 | false | null | null | An important property of the polygon fiber is the length expansion at 0° < | true | true | false | true | false | 6,502 |
1 | DISCUSSION | 0 | null | null | 17,704,136 | pmid-15377519|pmid-16622406|pmid-9514762|pmid-11171316 | β < 180° (in contrast to the star fiber, which contracts) and the more than 90° change in direction at β > 180°. | null | 112 | 37,926 | 0 | false | null | null | β < 180° (in contrast to the star fiber, which contracts) and the more than 90° change in direction at β > 180°. | false | true | true | true | false | 6,502 |
1 | DISCUSSION | 0 | null | null | 17,704,136 | pmid-15377519|pmid-16622406|pmid-9514762|pmid-11171316 | These properties are essential for creation of swivel-linkers and for transformation of helical coils into loops by reversing the pitch of the filament. | null | 152 | 37,927 | 0 | false | null | null | These properties are essential for creation of swivel-linkers and for transformation of helical coils into loops by reversing the pitch of the filament. | true | true | true | true | true | 6,502 |
1 | DISCUSSION | 0 | null | null | 17,704,136 | pmid-15377519|pmid-16622406|pmid-9514762|pmid-11171316 | Swivel-linkers can make space for close contacts between two fibers by separating two coils in a filament, thereby forming a pocket of 5–6 nucleosomes in which a nucleosome from another filament can bind. | null | 204 | 37,928 | 0 | false | null | null | Swivel-linkers can make space for close contacts between two fibers by separating two coils in a filament, thereby forming a pocket of 5–6 nucleosomes in which a nucleosome from another filament can bind. | true | true | true | true | true | 6,502 |
1 | DISCUSSION | 0 | null | null | 17,704,136 | pmid-15377519|pmid-16622406|pmid-9514762|pmid-11171316 | Tandem repeats of the β sequences of such pockets allow for the side-by-side association of two fibers like a zip, and the separation of helical coils by swivel-linkers can also provide space for the formation of double helices. | null | 228 | 37,929 | 0 | false | null | null | Tandem repeats of the β sequences of such pockets allow for the side-by-side association of two fibers like a zip, and the separation of helical coils by swivel-linkers can also provide space for the formation of double helices. | true | true | true | true | true | 6,502 |
1 | DISCUSSION | 0 | null | null | 17,704,136 | pmid-15377519|pmid-16622406|pmid-9514762|pmid-11171316 | It is tempting to speculate that tandem repeated DNA sequences, which often contain regularly positioned nucleosomes, might be stabilized and compacted by such types of fiber interactions. | null | 188 | 37,930 | 0 | false | null | null | It is tempting to speculate that tandem repeated DNA sequences, which often contain regularly positioned nucleosomes, might be stabilized and compacted by such types of fiber interactions. | true | true | true | true | true | 6,502 |
2 | DISCUSSION | 1 | 30 | [
"B30",
"B31 B32 B33 B34",
"B35"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | Another type of double fiber, which does not involve regularly spaced nucleosomes, is represented by the left-handed coiling of two polygon fibers around each other by intercalation of every second nucleosome (Figure 5C). | [
"30",
"31–34",
"35"
] | 221 | 37,931 | 0 | false | Another type of double fiber, which does not involve regularly spaced nucleosomes, is represented by the left-handed coiling of two polygon fibers around each other by intercalation of every second nucleosome (Figure 5C). | [] | Another type of double fiber, which does not involve regularly spaced nucleosomes, is represented by the left-handed coiling of two polygon fibers around each other by intercalation of every second nucleosome (Figure 5C). | true | true | true | true | true | 6,503 |
2 | DISCUSSION | 1 | 30 | [
"B30",
"B31 B32 B33 B34",
"B35"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | The positions of close contacts between the intercalated nucleosomes in this type of fiber appear to fit well with the positions of alternating asymmetric protection of nucleosomes in isolated nuclei against digestion by DNase I (30), which were shown to give rise to a dinucleosomal DNA repeat pattern (31–34). | [
"30",
"31–34",
"35"
] | 311 | 37,932 | 1 | false | The positions of close contacts between the intercalated nucleosomes in this type of fiber appear to fit well with the positions of alternating asymmetric protection of nucleosomes in isolated nuclei against digestion by DNase I, which were shown to give rise to a dinucleosomal DNA repeat pattern. | [
"30",
"31–34"
] | The positions of close contacts between the intercalated nucleosomes in this type of fiber appear to fit well with the positions of alternating asymmetric protection of nucleosomes in isolated nuclei against digestion by DNase I, which were shown to give rise to a dinucleosomal DNA repeat pattern. | true | true | true | true | true | 6,503 |
2 | DISCUSSION | 1 | 35 | [
"B30",
"B31 B32 B33 B34",
"B35"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | However, this type of double fiber may not provide the high degree of protection of the linkers, as inferred from analysis of the cleavage pattern, which was explained as a result of intercalation of nucleosomes in helical crosslinker model with linkers being buried in the interior of the fiber (35). | [
"30",
"31–34",
"35"
] | 301 | 37,933 | 1 | false | However, this type of double fiber may not provide the high degree of protection of the linkers, as inferred from analysis of the cleavage pattern, which was explained as a result of intercalation of nucleosomes in helical crosslinker model with linkers being buried in the interior of the fiber. | [
"35"
] | However, this type of double fiber may not provide the high degree of protection of the linkers, as inferred from analysis of the cleavage pattern, which was explained as a result of intercalation of nucleosomes in helical crosslinker model with linkers being buried in the interior of the fiber. | true | true | true | true | true | 6,503 |
2 | DISCUSSION | 1 | 30 | [
"B30",
"B31 B32 B33 B34",
"B35"
] | 17,704,136 | pmid-7673231|pmid-8415647|NA|pmid-11259307|pmid-10931924|pmid-7439531|pmid-6268454|pmid-6278427|pmid-6216116|NA | Although the interdigitated model may not be able to fully explain these observations, the polygon fiber geometry has the potential to provide the chromatin with architectural properties by facilitating the formation of double fibers, thus enabling the filaments to form 3D networks. | [
"30",
"31–34",
"35"
] | 283 | 37,934 | 0 | false | Although the interdigitated model may not be able to fully explain these observations, the polygon fiber geometry has the potential to provide the chromatin with architectural properties by facilitating the formation of double fibers, thus enabling the filaments to form 3D networks. | [] | Although the interdigitated model may not be able to fully explain these observations, the polygon fiber geometry has the potential to provide the chromatin with architectural properties by facilitating the formation of double fibers, thus enabling the filaments to form 3D networks. | true | true | true | true | true | 6,503 |
3 | DISCUSSION | 1 | 36 | [
"B36",
"B18",
"B17",
"B37"
] | 17,704,136 | pmid-3479765|NA|pmid-12892727|pmid-16387302 | A special property of the helical conformation formed by β sequence (333)n is the ability to compact to a high density by a decrease in α, followed by interdigitation. | [
"36",
"18",
"17",
"37"
] | 167 | 37,935 | 0 | false | A special property of the helical conformation formed by β sequence (333)n is the ability to compact to a high density by a decrease in α, followed by interdigitation. | [] | A special property of the helical conformation formed by β sequence n is the ability to compact to a high density by a decrease in α, followed by interdigitation. | true | true | true | true | true | 6,504 |
3 | DISCUSSION | 1 | 36 | [
"B36",
"B18",
"B17",
"B37"
] | 17,704,136 | pmid-3479765|NA|pmid-12892727|pmid-16387302 | The extent of compaction (∼6 nucleosomes/11 nm), as well as the radius of gyration (32 nm), agrees with results of neutron scattering and scanning electron microscopy of isolated chromatin at elevated ionic strength (36), but the volume of the fiber is smaller because the cross-section area is smaller, and the shape of... | [
"36",
"18",
"17",
"37"
] | 443 | 37,936 | 1 | false | The extent of compaction (∼6 nucleosomes/11 nm), as well as the radius of gyration (32 nm), agrees with results of neutron scattering and scanning electron microscopy of isolated chromatin at elevated ionic strength, but the volume of the fiber is smaller because the cross-section area is smaller, and the shape of the ... | [
"36"
] | The extent of compaction, as well as the radius of gyration, agrees with results of neutron scattering and scanning electron microscopy of isolated chromatin at elevated ionic strength, but the volume of the fiber is smaller because the cross-section area is smaller, and the shape of the fiber allows for interdigitatio... | true | true | true | true | true | 6,504 |
3 | DISCUSSION | 1 | 18 | [
"B36",
"B18",
"B17",
"B37"
] | 17,704,136 | pmid-3479765|NA|pmid-12892727|pmid-16387302 | This high density is so far only exceeded by two other models in which the compaction was caused by bending of the linkers (18) and by nucleosome gaping (17,37). | [
"36",
"18",
"17",
"37"
] | 161 | 37,937 | 1 | false | This high density is so far only exceeded by two other models in which the compaction was caused by bending of the linkers and by nucleosome gaping. | [
"18",
"17,37"
] | This high density is so far only exceeded by two other models in which the compaction was caused by bending of the linkers and by nucleosome gaping. | true | true | true | true | true | 6,504 |
4 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 17,704,136 | pmid-15919827|pmid-17060627 | Energy analyses have indicated that the balance between repulsion among linker DNA and internucleosome interactions determines the salt-dependent condensation of the nucleosomal filament (38), and positively charged core histone N-terminal tails are important in this process by mediating favorable internucleosomal inte... | [
"38",
"39"
] | 362 | 37,938 | 1 | false | Energy analyses have indicated that the balance between repulsion among linker DNA and internucleosome interactions determines the salt-dependent condensation of the nucleosomal filament, and positively charged core histone N-terminal tails are important in this process by mediating favorable internucleosomal interacti... | [
"38",
"39"
] | Energy analyses have indicated that the balance between repulsion among linker DNA and internucleosome interactions determines the salt-dependent condensation of the nucleosomal filament, and positively charged core histone N-terminal tails are important in this process by mediating favorable internucleosomal interacti... | true | true | true | true | true | 6,505 |
4 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 17,704,136 | pmid-15919827|pmid-17060627 | Compaction of the fiber would seem to require a high degree of charge neutralization, as linker DNA and nucleosomal DNA are brought very close to each other, while face-to-face internucleosomal interactions are only involved in interdigitation of the fibers and in apposition of layers of interdigitated fibers. | [
"38",
"39"
] | 311 | 37,939 | 0 | false | Compaction of the fiber would seem to require a high degree of charge neutralization, as linker DNA and nucleosomal DNA are brought very close to each other, while face-to-face internucleosomal interactions are only involved in interdigitation of the fibers and in apposition of layers of interdigitated fibers. | [] | Compaction of the fiber would seem to require a high degree of charge neutralization, as linker DNA and nucleosomal DNA are brought very close to each other, while face-to-face internucleosomal interactions are only involved in interdigitation of the fibers and in apposition of layers of interdigitated fibers. | true | true | true | true | true | 6,505 |
5 | DISCUSSION | 1 | 40 | [
"B40"
] | 17,704,136 | NA | Since a regular spacing of nucleosomes is rare, it is noteworthy that repeated β sequences required for double fiber formation and compaction can also be formed by fibers with a random distribution of β values after displacement of nucleosomes and limited twisting of the linkers. | [
"40"
] | 280 | 37,940 | 0 | false | Since a regular spacing of nucleosomes is rare, it is noteworthy that repeated β sequences required for double fiber formation and compaction can also be formed by fibers with a random distribution of β values after displacement of nucleosomes and limited twisting of the linkers. | [] | Since a regular spacing of nucleosomes is rare, it is noteworthy that repeated β sequences required for double fiber formation and compaction can also be formed by fibers with a random distribution of β values after displacement of nucleosomes and limited twisting of the linkers. | true | true | true | true | true | 6,506 |
5 | DISCUSSION | 1 | 40 | [
"B40"
] | 17,704,136 | NA | This supports speculations that the nucleosome repositioning activity of chromatin remodeling factors may provide the chromatin fiber with dynamic properties at the supra-nucleosomal level (40). | [
"40"
] | 194 | 37,941 | 1 | false | This supports speculations that the nucleosome repositioning activity of chromatin remodeling factors may provide the chromatin fiber with dynamic properties at the supra-nucleosomal level. | [
"40"
] | This supports speculations that the nucleosome repositioning activity of chromatin remodeling factors may provide the chromatin fiber with dynamic properties at the supra-nucleosomal level. | true | true | true | true | true | 6,506 |
5 | DISCUSSION | 1 | 40 | [
"B40"
] | 17,704,136 | NA | It furthermore shows that variations in β may not only be caused by differences in linker length but also by twisting of the linker. | [
"40"
] | 132 | 37,942 | 0 | false | It furthermore shows that variations in β may not only be caused by differences in linker length but also by twisting of the linker. | [] | It furthermore shows that variations in β may not only be caused by differences in linker length but also by twisting of the linker. | true | true | true | true | true | 6,506 |
5 | DISCUSSION | 1 | 40 | [
"B40"
] | 17,704,136 | NA | There is therefore no unambiguous correlation between β and linker length. | [
"40"
] | 74 | 37,943 | 0 | false | There is therefore no unambiguous correlation between β and linker length. | [] | There is therefore no unambiguous correlation between β and linker length. | true | true | true | true | true | 6,506 |
5 | DISCUSSION | 1 | 40 | [
"B40"
] | 17,704,136 | NA | In addition, linkers of the same length can differ slightly in their β values owing to sequence-dependent variations in the helical twist angle of base pairs in the linker DNA. | [
"40"
] | 176 | 37,944 | 0 | false | In addition, linkers of the same length can differ slightly in their β values owing to sequence-dependent variations in the helical twist angle of base pairs in the linker DNA. | [] | In addition, linkers of the same length can differ slightly in their β values owing to sequence-dependent variations in the helical twist angle of base pairs in the linker DNA. | true | true | true | true | true | 6,506 |
6 | DISCUSSION | 1 | 3 | [
"B3"
] | 17,704,136 | NA | An important consequence of the polygon fiber geometry is the ability of the filament to form loops in response to variations in β. | [
"3"
] | 131 | 37,945 | 0 | false | An important consequence of the polygon fiber geometry is the ability of the filament to form loops in response to variations in β. | [] | An important consequence of the polygon fiber geometry is the ability of the filament to form loops in response to variations in β. | true | true | true | true | true | 6,507 |
6 | DISCUSSION | 1 | 3 | [
"B3"
] | 17,704,136 | NA | Closed and locked loops formed by periodic variations in β(0), β(+), β(5) and β(−) remained compact at many different combinations of β values, and the flexibility of the filament was caused only by the interconnecting linkers. | [
"3"
] | 227 | 37,946 | 0 | false | Closed and locked loops formed by periodic variations in β(0), β(+), β(5) and β(−) remained compact at many different combinations of β values, and the flexibility of the filament was caused only by the interconnecting linkers. | [] | Closed and locked loops formed by periodic variations in β(0), β(+), β(5) and β(−) remained compact at many different combinations of β values, and the flexibility of the filament was caused only by the interconnecting linkers. | true | true | true | true | true | 6,507 |
6 | DISCUSSION | 1 | 3 | [
"B3"
] | 17,704,136 | NA | The fact that some of these types of loops required the addition of one nucleosome at each terminal linker to provide space for being serially connected is reminiscent of the supranucleosomal organization of the chromatin. | [
"3"
] | 222 | 37,947 | 0 | false | The fact that some of these types of loops required the addition of one nucleosome at each terminal linker to provide space for being serially connected is reminiscent of the supranucleosomal organization of the chromatin. | [] | The fact that some of these types of loops required the addition of one nucleosome at each terminal linker to provide space for being serially connected is reminiscent of the supranucleosomal organization of the chromatin. | true | true | true | true | true | 6,507 |
6 | DISCUSSION | 1 | 3 | [
"B3"
] | 17,704,136 | NA | The size of supranucleosomes isolated by nuclease digestion thus varies from a minimum of 6 or 8 nucleosomes up to 40 nucleosomes (3). | [
"3"
] | 134 | 37,948 | 1 | false | The size of supranucleosomes isolated by nuclease digestion thus varies from a minimum of 6 or 8 nucleosomes up to 40 nucleosomes. | [
"3"
] | The size of supranucleosomes isolated by nuclease digestion thus varies from a minimum of 6 or 8 nucleosomes up to 40 nucleosomes. | true | true | true | true | true | 6,507 |
6 | DISCUSSION | 1 | 3 | [
"B3"
] | 17,704,136 | NA | Filaments with random variations in β sequence also seem to be able to attain a supranucleosomal organization by the formation of relatively stable loop clusters separated by more flexible segments. | [
"3"
] | 198 | 37,949 | 0 | false | Filaments with random variations in β sequence also seem to be able to attain a supranucleosomal organization by the formation of relatively stable loop clusters separated by more flexible segments. | [] | Filaments with random variations in β sequence also seem to be able to attain a supranucleosomal organization by the formation of relatively stable loop clusters separated by more flexible segments. | true | true | true | true | true | 6,507 |
7 | DISCUSSION | 1 | 41 | [
"B41",
"B42"
] | 17,704,136 | pmid-11130729|pmid-11467737 | It is generally recognized that the nucleosome filament is highly dynamic owing to limited twisting of the linkers within the twist constraints and a rapid exchange between free and bound histone H1 (41). | [
"41",
"42"
] | 204 | 37,950 | 1 | false | It is generally recognized that the nucleosome filament is highly dynamic owing to limited twisting of the linkers within the twist constraints and a rapid exchange between free and bound histone H1. | [
"41"
] | It is generally recognized that the nucleosome filament is highly dynamic owing to limited twisting of the linkers within the twist constraints and a rapid exchange between free and bound histone H1. | true | true | true | true | true | 6,508 |
7 | DISCUSSION | 1 | 42 | [
"B41",
"B42"
] | 17,704,136 | pmid-11130729|pmid-11467737 | The major significance of static models may well be to show conformations that have the potential to be stabilized, either by double fiber formation, by the presence of closed and locked loops, or by cross linking of nucleosomes by nuclear proteins (42). | [
"41",
"42"
] | 254 | 37,951 | 1 | false | The major significance of static models may well be to show conformations that have the potential to be stabilized, either by double fiber formation, by the presence of closed and locked loops, or by cross linking of nucleosomes by nuclear proteins. | [
"42"
] | The major significance of static models may well be to show conformations that have the potential to be stabilized, either by double fiber formation, by the presence of closed and locked loops, or by cross linking of nucleosomes by nuclear proteins. | true | true | true | true | true | 6,508 |
7 | DISCUSSION | 1 | 41 | [
"B41",
"B42"
] | 17,704,136 | pmid-11130729|pmid-11467737 | The stability of loop clusters in filaments with a random distribution of β may thus be increased by cross-linking of nearby nucleosomes. | [
"41",
"42"
] | 137 | 37,952 | 0 | false | The stability of loop clusters in filaments with a random distribution of β may thus be increased by cross-linking of nearby nucleosomes. | [] | The stability of loop clusters in filaments with a random distribution of β may thus be increased by cross-linking of nearby nucleosomes. | true | true | true | true | true | 6,508 |
8 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B45",
"B39"
] | 17,704,136 | NA|pmid-11381129|pmid-16167325|pmid-17060627 | In light of the importance of α, β and the linker length for the conformation of the nucleosomal filament, what is then the role of these parameters for the organization of chromatin in the nucleus? | [
"43",
"44",
"45",
"39"
] | 198 | 37,953 | 0 | false | In light of the importance of α, β and the linker length for the conformation of the nucleosomal filament, what is then the role of these parameters for the organization of chromatin in the nucleus? | [] | In light of the importance of α, β and the linker length for the conformation of the nucleosomal filament, what is then the role of these parameters for the organization of chromatin in the nucleus? | true | true | true | true | true | 6,509 |
8 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B45",
"B39"
] | 17,704,136 | NA|pmid-11381129|pmid-16167325|pmid-17060627 | A discussion of this question has to take into account that the geometry of the linker can be affected by bending. | [
"43",
"44",
"45",
"39"
] | 114 | 37,954 | 0 | false | A discussion of this question has to take into account that the geometry of the linker can be affected by bending. | [] | A discussion of this question has to take into account that the geometry of the linker can be affected by bending. | true | true | true | true | true | 6,509 |
8 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B45",
"B39"
] | 17,704,136 | NA|pmid-11381129|pmid-16167325|pmid-17060627 | Stretches of poly(dAdT) are often bent and have an increased likelihood of being present in linkers (43) and linkers may also bend as a result of binding of H1. | [
"43",
"44",
"45",
"39"
] | 160 | 37,955 | 1 | false | Stretches of poly(dAdT) are often bent and have an increased likelihood of being present in linkers and linkers may also bend as a result of binding of H1. | [
"43"
] | Stretches of poly(dAdT) are often bent and have an increased likelihood of being present in linkers and linkers may also bend as a result of binding of H1. | true | true | true | true | true | 6,509 |
8 | DISCUSSION | 1 | 44 | [
"B43",
"B44",
"B45",
"B39"
] | 17,704,136 | NA|pmid-11381129|pmid-16167325|pmid-17060627 | Moreover, theoretical calculations do not exclude that electrostatic interactions with core histone tail domains (44) can bend the linker DNA, despite the known large persistence length of the DNA (45). | [
"43",
"44",
"45",
"39"
] | 202 | 37,956 | 1 | false | Moreover, theoretical calculations do not exclude that electrostatic interactions with core histone tail domains can bend the linker DNA, despite the known large persistence length of the DNA. | [
"44",
"45"
] | Moreover, theoretical calculations do not exclude that electrostatic interactions with core histone tail domains can bend the linker DNA, despite the known large persistence length of the DNA. | true | true | true | true | true | 6,509 |
8 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B45",
"B39"
] | 17,704,136 | NA|pmid-11381129|pmid-16167325|pmid-17060627 | Mesoscopic computer models have indeed shown that when chromatin fiber models include real DNA flexibility and charge, then the internucleosome interactions overcome the pre-designed linker DNA geometry and result in establishing new nucleosome chain configurations. | [
"43",
"44",
"45",
"39"
] | 266 | 37,957 | 0 | false | Mesoscopic computer models have indeed shown that when chromatin fiber models include real DNA flexibility and charge, then the internucleosome interactions overcome the pre-designed linker DNA geometry and result in establishing new nucleosome chain configurations. | [] | Mesoscopic computer models have indeed shown that when chromatin fiber models include real DNA flexibility and charge, then the internucleosome interactions overcome the pre-designed linker DNA geometry and result in establishing new nucleosome chain configurations. | true | true | true | true | true | 6,509 |
8 | DISCUSSION | 1 | 39 | [
"B43",
"B44",
"B45",
"B39"
] | 17,704,136 | NA|pmid-11381129|pmid-16167325|pmid-17060627 | However, the internucleosomal interactions appeared to be relatively weak and probably insufficient to maintain highly bent linker DNA (39). | [
"43",
"44",
"45",
"39"
] | 140 | 37,958 | 1 | false | However, the internucleosomal interactions appeared to be relatively weak and probably insufficient to maintain highly bent linker DNA. | [
"39"
] | However, the internucleosomal interactions appeared to be relatively weak and probably insufficient to maintain highly bent linker DNA. | true | true | true | true | true | 6,509 |
9 | DISCUSSION | 1 | 28 | [
"B28"
] | 17,704,136 | pmid-8415708 | Bending and twisting of linker DNA may be the result of aggregation of nucleosomes (28), which have a propensity to aggregate at high concentration and in high salt, and the sequence of aggregation of newly synthesized nucleosomes to their nearest neighbors, might in fact function as a folding path for nucleosomal fila... | [
"28"
] | 341 | 37,959 | 1 | false | Bending and twisting of linker DNA may be the result of aggregation of nucleosomes, which have a propensity to aggregate at high concentration and in high salt, and the sequence of aggregation of newly synthesized nucleosomes to their nearest neighbors, might in fact function as a folding path for nucleosomal filaments... | [
"28"
] | Bending and twisting of linker DNA may be the result of aggregation of nucleosomes, which have a propensity to aggregate at high concentration and in high salt, and the sequence of aggregation of newly synthesized nucleosomes to their nearest neighbors, might in fact function as a folding path for nucleosomal filaments... | true | true | true | true | true | 6,510 |
9 | DISCUSSION | 1 | 28 | [
"B28"
] | 17,704,136 | pmid-8415708 | The potential importance of a folding path is seen from models of fibers consisting of hexanucleosomal loops, some of which needed an extra nucleosome at the terminals to give space for being serially connected. | [
"28"
] | 211 | 37,960 | 0 | false | The potential importance of a folding path is seen from models of fibers consisting of hexanucleosomal loops, some of which needed an extra nucleosome at the terminals to give space for being serially connected. | [] | The potential importance of a folding path is seen from models of fibers consisting of hexanucleosomal loops, some of which needed an extra nucleosome at the terminals to give space for being serially connected. | true | true | true | true | true | 6,510 |
9 | DISCUSSION | 1 | 28 | [
"B28"
] | 17,704,136 | pmid-8415708 | Such sequences of eight nucleosomes could not be folded from preformed filaments and are therefore unlikely to be generated from pre-existing filaments as a result of a thermodynamic equilibrium. | [
"28"
] | 195 | 37,961 | 0 | false | Such sequences of eight nucleosomes could not be folded from preformed filaments and are therefore unlikely to be generated from pre-existing filaments as a result of a thermodynamic equilibrium. | [] | Such sequences of eight nucleosomes could not be folded from preformed filaments and are therefore unlikely to be generated from pre-existing filaments as a result of a thermodynamic equilibrium. | true | true | true | true | true | 6,510 |
10 | DISCUSSION | 1 | 27 | [
"B27",
"B46",
"B47"
] | 17,704,136 | pmid-1736292|pmid-16506093|NA | The narrow distribution of NRLs in every cell type and organism around a single mean value suggests that there is a range of preferred β values in the chromatin. | [
"27",
"46",
"47"
] | 161 | 37,962 | 0 | false | The narrow distribution of NRLs in every cell type and organism around a single mean value suggests that there is a range of preferred β values in the chromatin. | [] | The narrow distribution of NRLs in every cell type and organism around a single mean value suggests that there is a range of preferred β values in the chromatin. | true | true | true | true | true | 6,511 |
10 | DISCUSSION | 1 | 27 | [
"B27",
"B46",
"B47"
] | 17,704,136 | pmid-1736292|pmid-16506093|NA | NRLs for a large number of different organisms and cell types have been shown to be quantized by integral multiples of ∼10 bp, corresponding to integral multiples of helical turns of linker DNA (27), suggesting that preferred β values might be the same for these organisms. | [
"27",
"46",
"47"
] | 273 | 37,963 | 1 | false | NRLs for a large number of different organisms and cell types have been shown to be quantized by integral multiples of ∼10 bp, corresponding to integral multiples of helical turns of linker DNA, suggesting that preferred β values might be the same for these organisms. | [
"27"
] | NRLs for a large number of different organisms and cell types have been shown to be quantized by integral multiples of ∼10 bp, corresponding to integral multiples of helical turns of linker DNA, suggesting that preferred β values might be the same for these organisms. | true | true | true | true | true | 6,511 |
10 | DISCUSSION | 1 | 27 | [
"B27",
"B46",
"B47"
] | 17,704,136 | pmid-1736292|pmid-16506093|NA | However, as the NRL can be changed experimentally by up to 15 bp without fatal effects (46,47), it seems that chromatin higher order structure can accommodate to a wide range of β values. | [
"27",
"46",
"47"
] | 187 | 37,964 | 0 | false | However, as the NRL can be changed experimentally by up to 15 bp without fatal effects, it seems that chromatin higher order structure can accommodate to a wide range of β values. | [
"46,47"
] | However, as the NRL can be changed experimentally by up to 15 bp without fatal effects, it seems that chromatin higher order structure can accommodate to a wide range of β values. | true | true | true | true | true | 6,511 |
10 | DISCUSSION | 1 | 27 | [
"B27",
"B46",
"B47"
] | 17,704,136 | pmid-1736292|pmid-16506093|NA | This is in fact the case for the closed and locked hexanucleosomal looping of the filament, which depends more on the distribution of (+)- and (−)-linkers than on the actual values of β(+) and β(−). | [
"27",
"46",
"47"
] | 198 | 37,965 | 0 | false | This is in fact the case for the closed and locked hexanucleosomal looping of the filament, which depends more on the distribution of (+)- and (−)-linkers than on the actual values of β(+) and β(−). | [] | This is in fact the case for the closed and locked hexanucleosomal looping of the filament, which depends more on the distribution of (+)- and (−)-linkers than on the actual values of β(+) and β(−). | true | true | true | true | true | 6,511 |
10 | DISCUSSION | 1 | 27 | [
"B27",
"B46",
"B47"
] | 17,704,136 | pmid-1736292|pmid-16506093|NA | While looping appears to be an inherent property of the filament, occurring even as a result of a stochastic distribution of linker lengths, the location, conformation and length of the loops depend on the actual β sequence. | [
"27",
"46",
"47"
] | 224 | 37,966 | 0 | false | While looping appears to be an inherent property of the filament, occurring even as a result of a stochastic distribution of linker lengths, the location, conformation and length of the loops depend on the actual β sequence. | [] | While looping appears to be an inherent property of the filament, occurring even as a result of a stochastic distribution of linker lengths, the location, conformation and length of the loops depend on the actual β sequence. | true | true | true | true | true | 6,511 |
10 | DISCUSSION | 1 | 27 | [
"B27",
"B46",
"B47"
] | 17,704,136 | pmid-1736292|pmid-16506093|NA | This suggests that for a supranucleosomal organization of the chromatin, changes in linker lengths have a modulating effect on the conformation of the filament, leaving some loops unaltered, changing the conformation of others, destroying some loops and creating new ones, thus leaving the principal structure of the fib... | [
"27",
"46",
"47"
] | 380 | 37,967 | 0 | false | This suggests that for a supranucleosomal organization of the chromatin, changes in linker lengths have a modulating effect on the conformation of the filament, leaving some loops unaltered, changing the conformation of others, destroying some loops and creating new ones, thus leaving the principal structure of the fib... | [] | This suggests that for a supranucleosomal organization of the chromatin, changes in linker lengths have a modulating effect on the conformation of the filament, leaving some loops unaltered, changing the conformation of others, destroying some loops and creating new ones, thus leaving the principal structure of the fib... | true | true | true | true | true | 6,511 |
11 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,704,136 | pmid-16862119 | The models predict that this will be different for conformations, which are more dependent on a specific β sequence, as expected for regular fibers and for some types of double fibers with repeated β sequences. | [
"48"
] | 210 | 37,968 | 0 | false | The models predict that this will be different for conformations, which are more dependent on a specific β sequence, as expected for regular fibers and for some types of double fibers with repeated β sequences. | [] | The models predict that this will be different for conformations, which are more dependent on a specific β sequence, as expected for regular fibers and for some types of double fibers with repeated β sequences. | true | true | true | true | true | 6,512 |
11 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,704,136 | pmid-16862119 | Since these types of fibers have a potential architectural role in the large-scale organization of the chromatin, changes in β within these segments of the filaments might have fatal effects. | [
"48"
] | 191 | 37,969 | 0 | false | Since these types of fibers have a potential architectural role in the large-scale organization of the chromatin, changes in β within these segments of the filaments might have fatal effects. | [] | Since these types of fibers have a potential architectural role in the large-scale organization of the chromatin, changes in β within these segments of the filaments might have fatal effects. | true | true | true | true | true | 6,512 |
11 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,704,136 | pmid-16862119 | An invariable placement of nucleosomes in these regions may therefore be more important than in others. | [
"48"
] | 103 | 37,970 | 0 | false | An invariable placement of nucleosomes in these regions may therefore be more important than in others. | [] | An invariable placement of nucleosomes in these regions may therefore be more important than in others. | true | true | true | true | true | 6,512 |
11 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,704,136 | pmid-16862119 | Maintenance of the higher order organization of the genome might thus depend on the existence of series of ‘architectural’ nucleosomes located in invariable positions. | [
"48"
] | 167 | 37,971 | 0 | false | Maintenance of the higher order organization of the genome might thus depend on the existence of series of ‘architectural’ nucleosomes located in invariable positions. | [] | Maintenance of the higher order organization of the genome might thus depend on the existence of series of ‘architectural’ nucleosomes located in invariable positions. | true | true | true | true | true | 6,512 |
11 | DISCUSSION | 1 | 48 | [
"B48"
] | 17,704,136 | pmid-16862119 | Such nucleosomes might possibly belong to the most firmly bound nucleosomes whose positions are encoded by the DNA (48). | [
"48"
] | 120 | 37,972 | 1 | false | Such nucleosomes might possibly belong to the most firmly bound nucleosomes whose positions are encoded by the DNA. | [
"48"
] | Such nucleosomes might possibly belong to the most firmly bound nucleosomes whose positions are encoded by the DNA. | true | true | true | true | true | 6,512 |
0 | DISCUSSION | 1 | 1 | [
"bib1",
"bib8",
"bib2"
] | 16,567,385 | pmid-11861612|pmid-8600537|pmid-15102369 | Acute infections have the potential to generate high levels of protective CD8 T cell memory that can persist for the life of the organism (1, 8). | [
"1",
"8",
"2"
] | 145 | 37,973 | 0 | false | Acute infections have the potential to generate high levels of protective CD8 T cell memory that can persist for the life of the organism. | [
"1, 8"
] | Acute infections have the potential to generate high levels of protective CD8 T cell memory that can persist for the life of the organism. | true | true | true | true | true | 6,513 |
0 | DISCUSSION | 1 | 1 | [
"bib1",
"bib8",
"bib2"
] | 16,567,385 | pmid-11861612|pmid-8600537|pmid-15102369 | Although an extensive body of literature describing CD8 T cell memory has been amassed, the vast majority of these studies have focused on primary memory cells that arise after a single infection or vaccination. | [
"1",
"8",
"2"
] | 211 | 37,974 | 0 | false | Although an extensive body of literature describing CD8 T cell memory has been amassed, the vast majority of these studies have focused on primary memory cells that arise after a single infection or vaccination. | [] | Although an extensive body of literature describing CD8 T cell memory has been amassed, the vast majority of these studies have focused on primary memory cells that arise after a single infection or vaccination. | true | true | true | true | true | 6,513 |
0 | DISCUSSION | 1 | 2 | [
"bib1",
"bib8",
"bib2"
] | 16,567,385 | pmid-11861612|pmid-8600537|pmid-15102369 | Importantly, in the case of vaccination, a single immunization may not be sufficient to generate an adequate level of immunity for protection from infection, and a temporally separated booster immunization may be required (2). | [
"1",
"8",
"2"
] | 226 | 37,975 | 1 | false | Importantly, in the case of vaccination, a single immunization may not be sufficient to generate an adequate level of immunity for protection from infection, and a temporally separated booster immunization may be required. | [
"2"
] | Importantly, in the case of vaccination, a single immunization may not be sufficient to generate an adequate level of immunity for protection from infection, and a temporally separated booster immunization may be required. | true | true | true | true | true | 6,513 |
0 | DISCUSSION | 1 | 1 | [
"bib1",
"bib8",
"bib2"
] | 16,567,385 | pmid-11861612|pmid-8600537|pmid-15102369 | The characteristics of secondary responses, specifically the extent to which secondary CD8 T memory differs from primary CD8 T memory is, therefore, critical for the optimization of vaccination protocols. | [
"1",
"8",
"2"
] | 204 | 37,976 | 0 | false | The characteristics of secondary responses, specifically the extent to which secondary CD8 T memory differs from primary CD8 T memory is, therefore, critical for the optimization of vaccination protocols. | [] | The characteristics of secondary responses, specifically the extent to which secondary CD8 T memory differs from primary CD8 T memory is, therefore, critical for the optimization of vaccination protocols. | true | true | true | true | true | 6,513 |
1 | DISCUSSION | 0 | null | null | 16,567,385 | null | Here we have shown, in infection models that differ with respect to mouse strain, pathogen, antigen, and host environment, that secondary CD8 T cell responses result in memory populations that have unique qualities that distinguish them from primary memory CD8 T cell populations. | null | 280 | 37,977 | 0 | false | null | null | Here we have shown, in infection models that differ with respect to mouse strain, pathogen, antigen, and host environment, that secondary CD8 T cell responses result in memory populations that have unique qualities that distinguish them from primary memory CD8 T cell populations. | true | true | true | true | true | 6,514 |
1 | DISCUSSION | 0 | null | null | 16,567,385 | null | As defined by CD62L expression and IL-2 production, primary CD8 T cell responses after acute infection pass relatively rapidly through an effector–memory phase and stabilize as a predominantly TCM population. | null | 208 | 37,978 | 0 | false | null | null | As defined by CD62L expression and IL-2 production, primary CD8 T cell responses after acute infection pass relatively rapidly through an effector–memory phase and stabilize as a predominantly TCM population. | true | true | true | true | true | 6,514 |
1 | DISCUSSION | 0 | null | null | 16,567,385 | null | In contrast, secondary memory CD8 T cells appear to be severely delayed in this progression. | null | 92 | 37,979 | 0 | false | null | null | In contrast, secondary memory CD8 T cells appear to be severely delayed in this progression. | true | true | true | true | true | 6,514 |
1 | DISCUSSION | 0 | null | null | 16,567,385 | null | Furthermore, secondary memory CD8 T cells, besides sharing a similarly low CD62L expression level, are clearly not the same as primary TEM; secondary memory CD8 T cells display reduced basal proliferation, a higher level of expression of cytolytic molecules, exhibit more potent cytolytic capabilities, and are more prot... | null | 344 | 37,980 | 0 | false | null | null | Furthermore, secondary memory CD8 T cells, besides sharing a similarly low CD62L expression level, are clearly not the same as primary TEM; secondary memory CD8 T cells display reduced basal proliferation, a higher level of expression of cytolytic molecules, exhibit more potent cytolytic capabilities, and are more prot... | true | true | true | true | true | 6,514 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | The IL-15–driven basal proliferation important for the long-term maintenance of primary memory CD8 T cells is substantially reduced in secondary memory CD8 T cells, which may account for the delayed acquisition of TCM characteristics. | [
"14",
"14"
] | 234 | 37,981 | 0 | false | The IL-15–driven basal proliferation important for the long-term maintenance of primary memory CD8 T cells is substantially reduced in secondary memory CD8 T cells, which may account for the delayed acquisition of TCM characteristics. | [] | The IL-15–driven basal proliferation important for the long-term maintenance of primary memory CD8 T cells is substantially reduced in secondary memory CD8 T cells, which may account for the delayed acquisition of TCM characteristics. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | This correlation between the rate of cell division and the acquisition of a central–memory phenotype for memory CD8 T cells may be explained by several possibilities. | [
"14",
"14"
] | 166 | 37,982 | 0 | false | This correlation between the rate of cell division and the acquisition of a central–memory phenotype for memory CD8 T cells may be explained by several possibilities. | [] | This correlation between the rate of cell division and the acquisition of a central–memory phenotype for memory CD8 T cells may be explained by several possibilities. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | One possibility is that cell division is a necessary step before memory cells can reexpress CD62L. | [
"14",
"14"
] | 98 | 37,983 | 0 | false | One possibility is that cell division is a necessary step before memory cells can reexpress CD62L. | [] | One possibility is that cell division is a necessary step before memory cells can reexpress CD62L. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | However, studies by others (14) do not support this hypothesis. | [
"14",
"14"
] | 63 | 37,984 | 1 | false | However, studies by others do not support this hypothesis. | [
"14"
] | However, studies by others do not support this hypothesis. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | Another possibility that may explain the correlation between cell division and CD62L acquisition is that TCM may accumulate faster than TEM, resulting in an increase in the representation of TEM over time. | [
"14",
"14"
] | 205 | 37,985 | 0 | false | Another possibility that may explain the correlation between cell division and CD62L acquisition is that TCM may accumulate faster than TEM, resulting in an increase in the representation of TEM over time. | [] | Another possibility that may explain the correlation between cell division and CD62L acquisition is that TCM may accumulate faster than TEM, resulting in an increase in the representation of TEM over time. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | Proponents of this hypothesis often cite data that indicate that TCM undergo a faster rate of basal proliferation than TEM (14). | [
"14",
"14"
] | 128 | 37,986 | 1 | false | Proponents of this hypothesis often cite data that indicate that TCM undergo a faster rate of basal proliferation than TEM. | [
"14"
] | Proponents of this hypothesis often cite data that indicate that TCM undergo a faster rate of basal proliferation than TEM. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | However, it is necessary that the death rate of this population is also known to invoke preferential accumulation; it is possible for a dividing population to decrease in total numbers if its death rate is greater than that which can be replenished by cell division. | [
"14",
"14"
] | 266 | 37,987 | 0 | false | However, it is necessary that the death rate of this population is also known to invoke preferential accumulation; it is possible for a dividing population to decrease in total numbers if its death rate is greater than that which can be replenished by cell division. | [] | However, it is necessary that the death rate of this population is also known to invoke preferential accumulation; it is possible for a dividing population to decrease in total numbers if its death rate is greater than that which can be replenished by cell division. | true | true | true | true | true | 6,515 |
2 | DISCUSSION | 1 | 14 | [
"bib14",
"bib14"
] | 16,567,385 | pmid-12563257|pmid-12563257 | Resolution of this issue will likely require progress in understanding the death rate of memory T cell populations. | [
"14",
"14"
] | 115 | 37,988 | 0 | false | Resolution of this issue will likely require progress in understanding the death rate of memory T cell populations. | [] | Resolution of this issue will likely require progress in understanding the death rate of memory T cell populations. | true | true | true | true | true | 6,515 |
3 | DISCUSSION | 0 | null | null | 16,567,385 | null | We found that secondary memory CD8 T cells are not only equally able to undergo expansion in response to antigen, but are better at immediate cytolysis and protecting hosts against challenge by a virulent pathogen compared with primary memory CD8 T cells of the same specificity. | null | 279 | 37,989 | 0 | false | null | null | We found that secondary memory CD8 T cells are not only equally able to undergo expansion in response to antigen, but are better at immediate cytolysis and protecting hosts against challenge by a virulent pathogen compared with primary memory CD8 T cells of the same specificity. | true | true | true | true | true | 6,516 |
3 | DISCUSSION | 0 | null | null | 16,567,385 | null | Additionally, their decreased representation in the lymph nodes and therefore increased representation in the peripheral organs may be a mechanism to maintain highly lytic memory CD8 T cells for longer periods at potential sites of pathogen entry. | null | 247 | 37,990 | 0 | false | null | null | Additionally, their decreased representation in the lymph nodes and therefore increased representation in the peripheral organs may be a mechanism to maintain highly lytic memory CD8 T cells for longer periods at potential sites of pathogen entry. | true | true | true | true | true | 6,516 |
3 | DISCUSSION | 0 | null | null | 16,567,385 | null | In this way, the host may tailor memory CD8 T cell migration to circumstances in which infection with the same pathogens are a recurring event. | null | 143 | 37,991 | 0 | false | null | null | In this way, the host may tailor memory CD8 T cell migration to circumstances in which infection with the same pathogens are a recurring event. | true | true | true | true | true | 6,516 |
4 | DISCUSSION | 1 | 43 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Immediately after an infection, the preexisting naive CD8 T cell population becomes activated by receiving antigenic and costimulatory signals in the secondary lymphoid organs and will eventually differentiate into a memory CD8 T cell population (43, 44). | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 255 | 37,992 | 0 | false | Immediately after an infection, the preexisting naive CD8 T cell population becomes activated by receiving antigenic and costimulatory signals in the secondary lymphoid organs and will eventually differentiate into a memory CD8 T cell population. | [
"43, 44"
] | Immediately after an infection, the preexisting naive CD8 T cell population becomes activated by receiving antigenic and costimulatory signals in the secondary lymphoid organs and will eventually differentiate into a memory CD8 T cell population. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 45 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Throughout these responses, new naive CD8 T cells of the same specificity will be populating the periphery, either through thymic or extrathymic development (45). | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 162 | 37,993 | 1 | false | Throughout these responses, new naive CD8 T cells of the same specificity will be populating the periphery, either through thymic or extrathymic development. | [
"45"
] | Throughout these responses, new naive CD8 T cells of the same specificity will be populating the periphery, either through thymic or extrathymic development. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 46 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Also, it may be possible that, during an initial infection, not all of the preexisting naive CD8 T cells will have been recruited to respond (46). | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 146 | 37,994 | 1 | false | Also, it may be possible that, during an initial infection, not all of the preexisting naive CD8 T cells will have been recruited to respond. | [
"46"
] | Also, it may be possible that, during an initial infection, not all of the preexisting naive CD8 T cells will have been recruited to respond. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 20 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Therefore, it is likely that most anamnestic CD8 T cell responses include both primary and secondary responses (20). | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 116 | 37,995 | 1 | false | Therefore, it is likely that most anamnestic CD8 T cell responses include both primary and secondary responses. | [
"20"
] | Therefore, it is likely that most anamnestic CD8 T cell responses include both primary and secondary responses. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 43 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Here, we show that trafficking into lymph nodes by secondary memory CD8 T cells is severely decreased compared with primary memory CD8 T cells, which more rapidly adopt a CD62Lhi central–memory phenotype. | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 204 | 37,996 | 0 | false | Here, we show that trafficking into lymph nodes by secondary memory CD8 T cells is severely decreased compared with primary memory CD8 T cells, which more rapidly adopt a CD62Lhi central–memory phenotype. | [] | Here, we show that trafficking into lymph nodes by secondary memory CD8 T cells is severely decreased compared with primary memory CD8 T cells, which more rapidly adopt a CD62Lhi central–memory phenotype. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 42 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Because primary memory CD8 T cells are present in lymph nodes, they are able to suppress a new naive CD8 T cell response from occurring by, most simply, competing for presented antigen on dendritic cells (42). | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 209 | 37,997 | 1 | false | Because primary memory CD8 T cells are present in lymph nodes, they are able to suppress a new naive CD8 T cell response from occurring by, most simply, competing for presented antigen on dendritic cells. | [
"42"
] | Because primary memory CD8 T cells are present in lymph nodes, they are able to suppress a new naive CD8 T cell response from occurring by, most simply, competing for presented antigen on dendritic cells. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 43 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Because secondary memory CD8 T cells, on the other hand, are excluded from entering the lymph nodes until very late time points after infection, they are more permissive for the initiation of a new naive CD8 T cell response. | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 224 | 37,998 | 0 | false | Because secondary memory CD8 T cells, on the other hand, are excluded from entering the lymph nodes until very late time points after infection, they are more permissive for the initiation of a new naive CD8 T cell response. | [] | Because secondary memory CD8 T cells, on the other hand, are excluded from entering the lymph nodes until very late time points after infection, they are more permissive for the initiation of a new naive CD8 T cell response. | true | true | true | true | true | 6,517 |
4 | DISCUSSION | 1 | 43 | [
"bib43",
"bib44",
"bib45",
"bib46",
"bib20",
"bib42"
] | 16,567,385 | pmid-10376601|pmid-10073942|pmid-8946921|pmid-11323695|pmid-12734336|pmid-11034600 | Their exclusion from the lymph nodes, therefore, increases the potential for the generation of a higher number of replacement memory cells in future exposures to the same pathogen. | [
"43",
"44",
"45",
"46",
"20",
"42"
] | 180 | 37,999 | 0 | false | Their exclusion from the lymph nodes, therefore, increases the potential for the generation of a higher number of replacement memory cells in future exposures to the same pathogen. | [] | Their exclusion from the lymph nodes, therefore, increases the potential for the generation of a higher number of replacement memory cells in future exposures to the same pathogen. | true | true | true | true | true | 6,517 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | In terms of immune function, is there a compelling reason to keep secondary memory CD8 T cells out of lymph nodes for extended periods? | [
"47",
"48"
] | 135 | 38,000 | 0 | false | In terms of immune function, is there a compelling reason to keep secondary memory CD8 T cells out of lymph nodes for extended periods? | [] | In terms of immune function, is there a compelling reason to keep secondary memory CD8 T cells out of lymph nodes for extended periods? | true | true | true | true | true | 6,518 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | Secondary memory CD8 T cells are, by definition, the progeny of many rounds of division caused by the expansion phase of their initial response, their maintenance by basal proliferation as primary memory CD8 T cells, and the expansion phase of their secondary response. | [
"47",
"48"
] | 269 | 38,001 | 0 | false | Secondary memory CD8 T cells are, by definition, the progeny of many rounds of division caused by the expansion phase of their initial response, their maintenance by basal proliferation as primary memory CD8 T cells, and the expansion phase of their secondary response. | [] | Secondary memory CD8 T cells are, by definition, the progeny of many rounds of division caused by the expansion phase of their initial response, their maintenance by basal proliferation as primary memory CD8 T cells, and the expansion phase of their secondary response. | true | true | true | true | true | 6,518 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | Although telomerase is thought to be activated in responding CD8 T cells (47, 48), potentially permitting many more divisions before senescence compared with other cells, even memory T cells will likely reach a limit of division. | [
"47",
"48"
] | 229 | 38,002 | 0 | false | Although telomerase is thought to be activated in responding CD8 T cells, potentially permitting many more divisions before senescence compared with other cells, even memory T cells will likely reach a limit of division. | [
"47, 48"
] | Although telomerase is thought to be activated in responding CD8 T cells, potentially permitting many more divisions before senescence compared with other cells, even memory T cells will likely reach a limit of division. | true | true | true | true | true | 6,518 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | Thus, delayed acquisition of CD62L by secondary memory CD8 T cells may be a mechanism to allow for a new population of CD8 T cell memory to be generated from naive precursors while maintaining adequate or even enhanced protection from infection. | [
"47",
"48"
] | 245 | 38,003 | 0 | false | Thus, delayed acquisition of CD62L by secondary memory CD8 T cells may be a mechanism to allow for a new population of CD8 T cell memory to be generated from naive precursors while maintaining adequate or even enhanced protection from infection. | [] | Thus, delayed acquisition of CD62L by secondary memory CD8 T cells may be a mechanism to allow for a new population of CD8 T cell memory to be generated from naive precursors while maintaining adequate or even enhanced protection from infection. | true | true | true | true | true | 6,518 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | These results have practical implications for vaccines that rely on multiple immunizations by defining an optimal window for the third boost, before the reacquisition of CD62L. | [
"47",
"48"
] | 176 | 38,004 | 0 | false | These results have practical implications for vaccines that rely on multiple immunizations by defining an optimal window for the third boost, before the reacquisition of CD62L. | [] | These results have practical implications for vaccines that rely on multiple immunizations by defining an optimal window for the third boost, before the reacquisition of CD62L. | true | true | true | true | true | 6,518 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | This may result in both efficient boosting of secondary memory CD8 T cells as well as the most effective generation of new primary CD8 T cell responses. | [
"47",
"48"
] | 152 | 38,005 | 0 | false | This may result in both efficient boosting of secondary memory CD8 T cells as well as the most effective generation of new primary CD8 T cell responses. | [] | This may result in both efficient boosting of secondary memory CD8 T cells as well as the most effective generation of new primary CD8 T cell responses. | true | true | true | true | true | 6,518 |
5 | DISCUSSION | 1 | 47 | [
"bib47",
"bib48"
] | 16,567,385 | pmid-8992976|pmid-9729035 | This approach to timing may ensure that the induced memory is long lasting and able to respond to multiple encounters with the specific pathogen. | [
"47",
"48"
] | 145 | 38,006 | 0 | false | This approach to timing may ensure that the induced memory is long lasting and able to respond to multiple encounters with the specific pathogen. | [] | This approach to timing may ensure that the induced memory is long lasting and able to respond to multiple encounters with the specific pathogen. | true | true | true | true | true | 6,518 |
6 | DISCUSSION | 1 | 49 | [
"bib49"
] | 16,567,385 | pmid-12001996 | In cases where the induction of humoral responses by vaccination is not sufficient to protect against pathogenic infection, the generation of CD8 T cell memory has substantial potential in the rational design of vaccines (49). | [
"49"
] | 226 | 38,007 | 1 | false | In cases where the induction of humoral responses by vaccination is not sufficient to protect against pathogenic infection, the generation of CD8 T cell memory has substantial potential in the rational design of vaccines. | [
"49"
] | In cases where the induction of humoral responses by vaccination is not sufficient to protect against pathogenic infection, the generation of CD8 T cell memory has substantial potential in the rational design of vaccines. | true | true | true | true | true | 6,519 |
6 | DISCUSSION | 1 | 49 | [
"bib49"
] | 16,567,385 | pmid-12001996 | Insufficient primary memory CD8 T cell responses may be boosted by secondary immunizations, which quantitatively enhance memory cell numbers and alter certain qualitative aspects of memory. | [
"49"
] | 189 | 38,008 | 0 | false | Insufficient primary memory CD8 T cell responses may be boosted by secondary immunizations, which quantitatively enhance memory cell numbers and alter certain qualitative aspects of memory. | [] | Insufficient primary memory CD8 T cell responses may be boosted by secondary immunizations, which quantitatively enhance memory cell numbers and alter certain qualitative aspects of memory. | true | true | true | true | true | 6,519 |
6 | DISCUSSION | 1 | 49 | [
"bib49"
] | 16,567,385 | pmid-12001996 | Whether secondary memory CD8 T cells will be more protective, as shown in our studies with L. monocytogenes against all, or only a subset, of pathogens, is a critical issue for the design of the most potent vaccines. | [
"49"
] | 216 | 38,009 | 0 | false | Whether secondary memory CD8 T cells will be more protective, as shown in our studies with L. monocytogenes against all, or only a subset, of pathogens, is a critical issue for the design of the most potent vaccines. | [] | Whether secondary memory CD8 T cells will be more protective, as shown in our studies with L. monocytogenes against all, or only a subset, of pathogens, is a critical issue for the design of the most potent vaccines. | true | true | true | true | true | 6,519 |
6 | DISCUSSION | 1 | 49 | [
"bib49"
] | 16,567,385 | pmid-12001996 | For example, a potent CD8 T cell response to a single immunization may be most effective against one subset of pathogens, whereas a low priming vaccination and robust booster immunization to generate secondary CD8 T cell memory may be more effective against another subset of pathogens. | [
"49"
] | 286 | 38,010 | 0 | false | For example, a potent CD8 T cell response to a single immunization may be most effective against one subset of pathogens, whereas a low priming vaccination and robust booster immunization to generate secondary CD8 T cell memory may be more effective against another subset of pathogens. | [] | For example, a potent CD8 T cell response to a single immunization may be most effective against one subset of pathogens, whereas a low priming vaccination and robust booster immunization to generate secondary CD8 T cell memory may be more effective against another subset of pathogens. | true | true | true | true | true | 6,519 |
6 | DISCUSSION | 1 | 49 | [
"bib49"
] | 16,567,385 | pmid-12001996 | Comparison of primary and secondary memory CD8 T cells for protection against a variety of pathogens will be required to resolve this issue. | [
"49"
] | 140 | 38,011 | 0 | false | Comparison of primary and secondary memory CD8 T cells for protection against a variety of pathogens will be required to resolve this issue. | [] | Comparison of primary and secondary memory CD8 T cells for protection against a variety of pathogens will be required to resolve this issue. | true | true | true | true | true | 6,519 |
0 | INTRODUCTION | 0 | null | null | 19,503,677 | null | Disability evaluation typically requires an assessment of the activities of daily life (ADL) and instrumental ADL (I-ADL). | null | 122 | 38,012 | 0 | false | null | null | Disability evaluation typically requires an assessment of the activities of daily life (ADL) and instrumental ADL (I-ADL). | true | true | true | true | true | 6,520 |
0 | INTRODUCTION | 0 | null | null | 19,503,677 | null | In Japan, a physical disability certificate is based on the patient's ADL and I-ADL grades. | null | 91 | 38,013 | 0 | false | null | null | In Japan, a physical disability certificate is based on the patient's ADL and I-ADL grades. | true | true | true | true | true | 6,520 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | The independent ADL scale, which is widely considered within the field of rehabilitation medicine to be a particularly important component in the evaluation (1, 2), considers both individual and universal factors (Fig. | [
"1",
"2"
] | 218 | 38,014 | 0 | false | The independent ADL scale, which is widely considered within the field of rehabilitation medicine to be a particularly important component in the evaluation, considers both individual and universal factors (Fig. | [
"1, 2"
] | The independent ADL scale, which is widely considered within the field of rehabilitation medicine to be a particularly important component in the evaluation, considers both individual and universal factors (Fig. | true | true | true | true | true | 6,521 |
1 | INTRODUCTION | 1 | 1 | [
"B1",
"B2"
] | 19,503,677 | NA|NA | Assessment is performed by analyzing the results of test activities relating the patient's personal life. | [
"1",
"2"
] | 105 | 38,015 | 0 | false | Assessment is performed by analyzing the results of test activities relating the patient's personal life. | [] | Assessment is performed by analyzing the results of test activities relating the patient's personal life. | true | true | true | true | true | 6,521 |
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