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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | Nevertheless, some trends can be mentioned. | [
"16",
"11"
] | 43 | 42,419 | 0 | false | Nevertheless, some trends can be mentioned. | [] | Nevertheless, some trends can be mentioned. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | Positions located on the 5′ side of a G in the third strand were more likely to accommodate an adenine than those located on the 3′ side. | [
"16",
"11"
] | 137 | 42,420 | 0 | false | Positions located on the 5′ side of a G in the third strand were more likely to accommodate an adenine than those located on the 3′ side. | [] | Positions located on the 5′ side of a G in the third strand were more likely to accommodate an adenine than those located on the 3′ side. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | AT base pairs that were surrounded by only AT base pairs were more likely to be recognized by thymines. | [
"16",
"11"
] | 103 | 42,421 | 0 | false | AT base pairs that were surrounded by only AT base pairs were more likely to be recognized by thymines. | [] | AT base pairs that were surrounded by only AT base pairs were more likely to be recognized by thymines. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | Only one AT base pair (position 15) seemed to prefer an adenine (85%). | [
"16",
"11"
] | 70 | 42,422 | 0 | false | Only one AT base pair (position 15) seemed to prefer an adenine (85%). | [] | Only one AT base pair seemed to prefer an adenine (85%). | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 11 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | Preference for A or T may be related to the existence of distortions in the third strand at TpG and GpT steps within antiparallel triple helices with GT third strands (11), and/or to preferential binding sites for intercalation of BIQ. | [
"16",
"11"
] | 235 | 42,423 | 1 | false | Preference for A or T may be related to the existence of distortions in the third strand at TpG and GpT steps within antiparallel triple helices with GT third strands, and/or to preferential binding sites for intercalation of BIQ. | [
"11"
] | Preference for A or T may be related to the existence of distortions in the third strand at TpG and GpT steps within antiparallel triple helices with GT third strands, and/or to preferential binding sites for intercalation of BIQ. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | It is also possible that the selection process favours sequences that do not fold into competing structures. | [
"16",
"11"
] | 108 | 42,424 | 0 | false | It is also possible that the selection process favours sequences that do not fold into competing structures. | [] | It is also possible that the selection process favours sequences that do not fold into competing structures. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | We were not able to explain the presence of adenine at specific positions by such a mechanism. | [
"16",
"11"
] | 94 | 42,425 | 0 | false | We were not able to explain the presence of adenine at specific positions by such a mechanism. | [] | We were not able to explain the presence of adenine at specific positions by such a mechanism. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | We measured the dissociation constant for clone 20, which corresponded to the consensus sequence involving G, T and a single A in the triplex forming region. | [
"16",
"11"
] | 157 | 42,426 | 0 | false | We measured the dissociation constant for clone 20, which corresponded to the consensus sequence involving G, T and a single A in the triplex forming region. | [] | We measured the dissociation constant for clone 20, which corresponded to the consensus sequence involving G, T and a single A in the triplex forming region. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | The affinity of this sequence for the target was slightly higher than that of clone 19, which has the highest number of adenines. | [
"16",
"11"
] | 129 | 42,427 | 0 | false | The affinity of this sequence for the target was slightly higher than that of clone 19, which has the highest number of adenines. | [] | The affinity of this sequence for the target was slightly higher than that of clone 19, which has the highest number of adenines. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | This difference is probably not very significant, and may be explained by the effects of adjacent sequences. | [
"16",
"11"
] | 108 | 42,428 | 0 | false | This difference is probably not very significant, and may be explained by the effects of adjacent sequences. | [] | This difference is probably not very significant, and may be explained by the effects of adjacent sequences. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | Experiments performed with 20-mer oligonucleotides did not show significant differences between the binding affinities of the various selected sequences. | [
"16",
"11"
] | 153 | 42,429 | 0 | false | Experiments performed with 20-mer oligonucleotides did not show significant differences between the binding affinities of the various selected sequences. | [] | Experiments performed with 20-mer oligonucleotides did not show significant differences between the binding affinities of the various selected sequences. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | Although two pyrimidine rich oligonucleotides were present among the selected sequences, binding of these oligonucleotides could not be detected. | [
"16",
"11"
] | 145 | 42,430 | 0 | false | Although two pyrimidine rich oligonucleotides were present among the selected sequences, binding of these oligonucleotides could not be detected. | [] | Although two pyrimidine rich oligonucleotides were present among the selected sequences, binding of these oligonucleotides could not be detected. | true | true | true | true | true | 7,353 |
1 | DISCUSSION | 1 | 16 | [
"B16",
"B11"
] | 20,007,154 | pmid-7596824|pmid-7819208|pmid-9862797|NA|pmid-18954091|NA|NA | The binding scheme and the reason for the presence of these sequences remains to be investigated. | [
"16",
"11"
] | 97 | 42,431 | 0 | false | The binding scheme and the reason for the presence of these sequences remains to be investigated. | [] | The binding scheme and the reason for the presence of these sequences remains to be investigated. | true | true | true | true | true | 7,353 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | Interesting questions are raised by the issue of our selections. | [
"38",
"39"
] | 64 | 42,432 | 0 | false | Interesting questions are raised by the issue of our selections. | [] | Interesting questions are raised by the issue of our selections. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | One may wonder why only TFOs were selected. | [
"38",
"39"
] | 43 | 42,433 | 0 | false | One may wonder why only TFOs were selected. | [] | One may wonder why only TFOs were selected. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | Given the tremendous variety of structures that are adopted by aptamers for the recognition of small molecules [see ref. | [
"38",
"39"
] | 120 | 42,434 | 0 | false | Given the tremendous variety of structures that are adopted by aptamers for the recognition of small molecules [see ref. | [] | Given the tremendous variety of structures that are adopted by aptamers for the recognition of small molecules [see ref. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | (38) for review], one may expect the possibility for recognition of a DNA–intercalator complex by a selected oligonucleotide within a new structural framework. | [
"38",
"39"
] | 159 | 42,435 | 1 | false | for review], one may expect the possibility for recognition of a DNA–intercalator complex by a selected oligonucleotide within a new structural framework. | [
"38"
] | for review], one may expect the possibility for recognition of a DNA–intercalator complex by a selected oligonucleotide within a new structural framework. | false | true | true | true | false | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | Aptamers may indeed potentially establish stacking interactions with planar aliphatic rings as well as electrostatic interactions with the side chains. | [
"38",
"39"
] | 151 | 42,436 | 0 | false | Aptamers may indeed potentially establish stacking interactions with planar aliphatic rings as well as electrostatic interactions with the side chains. | [] | Aptamers may indeed potentially establish stacking interactions with planar aliphatic rings as well as electrostatic interactions with the side chains. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 39 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | It should be noted that aptamer can recognize chemical moieties as small as ethanolamine (39), which resembles the side chain of our triplex stabilizing agent. | [
"38",
"39"
] | 159 | 42,437 | 1 | false | It should be noted that aptamer can recognize chemical moieties as small as ethanolamine, which resembles the side chain of our triplex stabilizing agent. | [
"39"
] | It should be noted that aptamer can recognize chemical moieties as small as ethanolamine, which resembles the side chain of our triplex stabilizing agent. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | Despite the presence of this large intercalating compound in our selection scheme, no DNA binding solutions that differed from triple-helix formation were discovered. | [
"38",
"39"
] | 166 | 42,438 | 0 | false | Despite the presence of this large intercalating compound in our selection scheme, no DNA binding solutions that differed from triple-helix formation were discovered. | [] | Despite the presence of this large intercalating compound in our selection scheme, no DNA binding solutions that differed from triple-helix formation were discovered. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | Several factors may have biased selection toward recovery of sequences that bound via triple-helix formation: the chosen DNA contained an oligopurine–oligopyrimidine stretch and therefore was typically suited to form conventional triple helices with an appropriate DNA, and conventional triple helix formation may afford... | [
"38",
"39"
] | 361 | 42,439 | 0 | false | Several factors may have biased selection toward recovery of sequences that bound via triple-helix formation: the chosen DNA contained an oligopurine–oligopyrimidine stretch and therefore was typically suited to form conventional triple helices with an appropriate DNA, and conventional triple helix formation may afford... | [] | Several factors may have biased selection toward recovery of sequences that bound via triple-helix formation: the chosen DNA contained an oligopurine–oligopyrimidine stretch and therefore was typically suited to form conventional triple helices with an appropriate DNA, and conventional triple helix formation may afford... | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | The size of the pool that we used (250 pmol, i.e. | [
"38",
"39"
] | 49 | 42,440 | 0 | false | The size of the pool that we used (250 pmol, i.e. | [] | The size of the pool that we used (250 pmol, i.e. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | ∼1.5 × 1014 molecules) is sufficient to screen all possible sequences with a length of 22 nt (each sequence is present on average 10 times). | [
"38",
"39"
] | 140 | 42,441 | 0 | false | ∼1.5 × 1014 molecules) is sufficient to screen all possible sequences with a length of 22 nt (each sequence is present on average 10 times). | [] | ∼1.5 × 1014 molecules) is sufficient to screen all possible sequences with a length of 22 nt (each sequence is present on average 10 times). | false | false | true | true | false | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | All the selected sequences seemed to provide maximal recognition with the same length of 20 nucleotides, as there appears to be little nucleotide sequence conservation outside of the canonical recognition sequence. | [
"38",
"39"
] | 214 | 42,442 | 0 | false | All the selected sequences seemed to provide maximal recognition with the same length of 20 nucleotides, as there appears to be little nucleotide sequence conservation outside of the canonical recognition sequence. | [] | All the selected sequences seemed to provide maximal recognition with the same length of 20 nucleotides, as there appears to be little nucleotide sequence conservation outside of the canonical recognition sequence. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | This suggests that additional interactions involving two additional nucleotides did not improve binding sufficiently to make a difference. | [
"38",
"39"
] | 138 | 42,443 | 0 | false | This suggests that additional interactions involving two additional nucleotides did not improve binding sufficiently to make a difference. | [] | This suggests that additional interactions involving two additional nucleotides did not improve binding sufficiently to make a difference. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | This does not exclude that better solutions involving more than 23 nucleotides may exist and have been missed in our screening. | [
"38",
"39"
] | 127 | 42,444 | 0 | false | This does not exclude that better solutions involving more than 23 nucleotides may exist and have been missed in our screening. | [] | This does not exclude that better solutions involving more than 23 nucleotides may exist and have been missed in our screening. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | One may also not exclude that some binding solutions other than the representatives of the triple helix may have been present in the oligonucleotide pool solution but were eliminated due to a lower affinity. | [
"38",
"39"
] | 207 | 42,445 | 0 | false | One may also not exclude that some binding solutions other than the representatives of the triple helix may have been present in the oligonucleotide pool solution but were eliminated due to a lower affinity. | [] | One may also not exclude that some binding solutions other than the representatives of the triple helix may have been present in the oligonucleotide pool solution but were eliminated due to a lower affinity. | true | true | true | true | true | 7,354 |
2 | DISCUSSION | 1 | 38 | [
"B38",
"B39"
] | 20,007,154 | pmid-10637355|pmid-1609278|NA|pmid-9520410|NA|pmid-8639533|pmid-8604349|pmid-9547278|pmid-10657289|pmid-16289104 | Such other solutions would be recovered by using a target with a much shorter or no oligopurine–oligopyrimidine stretch at all. | [
"38",
"39"
] | 127 | 42,446 | 0 | false | Such other solutions would be recovered by using a target with a much shorter or no oligopurine–oligopyrimidine stretch at all. | [] | Such other solutions would be recovered by using a target with a much shorter or no oligopurine–oligopyrimidine stretch at all. | true | true | true | true | true | 7,354 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | One may also wonder why we did recover only TFOs within the antiparallel motif, contrary to previous studies. | [
"40",
"41"
] | 109 | 42,447 | 0 | false | One may also wonder why we did recover only TFOs within the antiparallel motif, contrary to previous studies. | [] | One may also wonder why we did recover only TFOs within the antiparallel motif, contrary to previous studies. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | Our target sequence does not contain long stretches of GC base pairs, and the proportion of GC base pairs (35%), should in principle be favourable for the binding of pyrimidine rich TFOs. | [
"40",
"41"
] | 187 | 42,448 | 0 | false | Our target sequence does not contain long stretches of GC base pairs, and the proportion of GC base pairs (35%), should in principle be favourable for the binding of pyrimidine rich TFOs. | [] | Our target sequence does not contain long stretches of GC base pairs, and the proportion of GC base pairs (35%), should in principle be favourable for the binding of pyrimidine rich TFOs. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | The issue of our selection may result from a much better stability of antiparallel TFOs in the presence of BIQ. | [
"40",
"41"
] | 111 | 42,449 | 0 | false | The issue of our selection may result from a much better stability of antiparallel TFOs in the presence of BIQ. | [] | The issue of our selection may result from a much better stability of antiparallel TFOs in the presence of BIQ. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | It may also be due to the presence of magnesium, which favours the antiparallel motif. | [
"40",
"41"
] | 86 | 42,450 | 0 | false | It may also be due to the presence of magnesium, which favours the antiparallel motif. | [] | It may also be due to the presence of magnesium, which favours the antiparallel motif. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | Other parameters, such as binding kinetics, may also be important in such experiments. | [
"40",
"41"
] | 86 | 42,451 | 0 | false | Other parameters, such as binding kinetics, may also be important in such experiments. | [] | Other parameters, such as binding kinetics, may also be important in such experiments. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | The formation of pyrimidine motif triple helices is a slow process, which may have been disfavoured by our fast binding step. | [
"40",
"41"
] | 125 | 42,452 | 0 | false | The formation of pyrimidine motif triple helices is a slow process, which may have been disfavoured by our fast binding step. | [] | The formation of pyrimidine motif triple helices is a slow process, which may have been disfavoured by our fast binding step. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | Further work will be necessary to evaluate how modifications of the selection protocol will affect the repertory of selected sequences. | [
"40",
"41"
] | 135 | 42,453 | 0 | false | Further work will be necessary to evaluate how modifications of the selection protocol will affect the repertory of selected sequences. | [] | Further work will be necessary to evaluate how modifications of the selection protocol will affect the repertory of selected sequences. | true | true | true | true | true | 7,355 |
3 | DISCUSSION | 1 | 40 | [
"B40",
"B41"
] | 20,007,154 | pmid-2200121|pmid-1697402|pmid-10995196|pmid-10960261|pmid-17634987|pmid-17627883|pmid-8855239|pmid-10449422|pmid-12867086|pmid-15681618|pmid-7506827|pmid-7529405 | One should also keep in mind that, in addition to slightly acidic conditions, previous studies were aimed at selecting RNA oligonucleotides, which are known to be poorly compatible with the formation of antiparallel triple-helices (40,41). | [
"40",
"41"
] | 239 | 42,454 | 0 | false | One should also keep in mind that, in addition to slightly acidic conditions, previous studies were aimed at selecting RNA oligonucleotides, which are known to be poorly compatible with the formation of antiparallel triple-helices. | [
"40,41"
] | One should also keep in mind that, in addition to slightly acidic conditions, previous studies were aimed at selecting RNA oligonucleotides, which are known to be poorly compatible with the formation of antiparallel triple-helices. | true | true | true | true | true | 7,355 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | Our SELEX process was performed in the presence of a low molecular weight compound expected to enhance interactions between the target and the oligonucleotide pool. | [
"42"
] | 164 | 42,455 | 0 | false | Our SELEX process was performed in the presence of a low molecular weight compound expected to enhance interactions between the target and the oligonucleotide pool. | [] | Our SELEX process was performed in the presence of a low molecular weight compound expected to enhance interactions between the target and the oligonucleotide pool. | true | true | true | true | true | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | This is an original strategy which to our knowledge has never been used before. | [
"42"
] | 79 | 42,456 | 0 | false | This is an original strategy which to our knowledge has never been used before. | [] | This is an original strategy which to our knowledge has never been used before. | true | true | true | true | true | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | The presence of the ligand resulted in selection of oligonucleotides that bound to the target only in the presence of the small molecule, although no counterselection was introduced to remove sequences that would bind in the absence of the compound. | [
"42"
] | 249 | 42,457 | 0 | false | The presence of the ligand resulted in selection of oligonucleotides that bound to the target only in the presence of the small molecule, although no counterselection was introduced to remove sequences that would bind in the absence of the compound. | [] | The presence of the ligand resulted in selection of oligonucleotides that bound to the target only in the presence of the small molecule, although no counterselection was introduced to remove sequences that would bind in the absence of the compound. | true | true | true | true | true | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | This is likely due to the very high stability of the complexes formed by the target, the ligand and the selected oligonucleotide. | [
"42"
] | 129 | 42,458 | 0 | false | This is likely due to the very high stability of the complexes formed by the target, the ligand and the selected oligonucleotide. | [] | This is likely due to the very high stability of the complexes formed by the target, the ligand and the selected oligonucleotide. | true | true | true | true | true | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | A great effort has been devoted to the expansion of the catalytic repertoire of nucleic acids by addition of protein like functionalities to the nucleic acids to be selected | [
"42"
] | 173 | 42,459 | 0 | false | A great effort has been devoted to the expansion of the catalytic repertoire of nucleic acids by addition of protein like functionalities to the nucleic acids to be selected | [] | A great effort has been devoted to the expansion of the catalytic repertoire of nucleic acids by addition of protein like functionalities to the nucleic acids to be selected | true | true | false | true | false | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | and references therein]. | [
"42"
] | 24 | 42,460 | 0 | false | and references therein]. | [] | and references therein]. | false | true | true | true | false | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | The number of modifications that can be incorporated into aptamers is still limited. | [
"42"
] | 84 | 42,461 | 0 | false | The number of modifications that can be incorporated into aptamers is still limited. | [] | The number of modifications that can be incorporated into aptamers is still limited. | true | true | true | true | true | 7,356 |
4 | DISCUSSION | 1 | 42 | [
"B42"
] | 20,007,154 | pmid-1716784|pmid-8656424|pmid-19153138 | The use of another functional group, in this case an intercalator, in order to provide these additional functionalities represents an interesting solution to this problem. | [
"42"
] | 171 | 42,462 | 0 | false | The use of another functional group, in this case an intercalator, in order to provide these additional functionalities represents an interesting solution to this problem. | [] | The use of another functional group, in this case an intercalator, in order to provide these additional functionalities represents an interesting solution to this problem. | true | true | true | true | true | 7,356 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | Although great progress have been made toward the design of new chemically modified oligonucleotides that permit recognition of a wider variety of sequences by TFOs (43,44), there is still no general solution that is easy to apply to any sequence of interest. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 259 | 42,463 | 0 | false | Although great progress have been made toward the design of new chemically modified oligonucleotides that permit recognition of a wider variety of sequences by TFOs, there is still no general solution that is easy to apply to any sequence of interest. | [
"43,44"
] | Although great progress have been made toward the design of new chemically modified oligonucleotides that permit recognition of a wider variety of sequences by TFOs, there is still no general solution that is easy to apply to any sequence of interest. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | Our SELEX approach provides an interesting solution for the design of TFOs for applications that can accommodate the presence of an intercalator. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 145 | 42,464 | 0 | false | Our SELEX approach provides an interesting solution for the design of TFOs for applications that can accommodate the presence of an intercalator. | [] | Our SELEX approach provides an interesting solution for the design of TFOs for applications that can accommodate the presence of an intercalator. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | The same selection scheme could by applied to other target DNA sequences, with interesting potential applications. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 114 | 42,465 | 0 | false | The same selection scheme could by applied to other target DNA sequences, with interesting potential applications. | [] | The same selection scheme could by applied to other target DNA sequences, with interesting potential applications. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | First, the repertoire of target sequences for triple-helix formation may be extended in the presence of DNA binding agents. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 123 | 42,466 | 0 | false | First, the repertoire of target sequences for triple-helix formation may be extended in the presence of DNA binding agents. | [] | First, the repertoire of target sequences for triple-helix formation may be extended in the presence of DNA binding agents. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 46 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | It has already been demonstrated that addition of a triplex-stabilizing agent could enhance the formation of triple helices at sites containing inversions within the oligopurine–oligopyrimidine sequence (19,45) or at (GT)n tracts (46). | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 235 | 42,467 | 1 | false | It has already been demonstrated that addition of a triplex-stabilizing agent could enhance the formation of triple helices at sites containing inversions within the oligopurine–oligopyrimidine sequence or at (GT)n tracts. | [
"19,45",
"46"
] | It has already been demonstrated that addition of a triplex-stabilizing agent could enhance the formation of triple helices at sites containing inversions within the oligopurine–oligopyrimidine sequence or at (GT)n tracts. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 10 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | Triplex-specific intercalators have also been shown to promote the formation of triple helices which switch from one strand to the other strand of DNA (10). | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 156 | 42,468 | 1 | false | Triplex-specific intercalators have also been shown to promote the formation of triple helices which switch from one strand to the other strand of DNA. | [
"10"
] | Triplex-specific intercalators have also been shown to promote the formation of triple helices which switch from one strand to the other strand of DNA. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 47 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | In such cases, molecular modelling has suggested a code for designing the best switch oligonucleotide (47). | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 107 | 42,469 | 1 | false | In such cases, molecular modelling has suggested a code for designing the best switch oligonucleotide. | [
"47"
] | In such cases, molecular modelling has suggested a code for designing the best switch oligonucleotide. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | Although this code has received some experimental validation (10,48), our strategy would provide the best oligonucleotide solution for this switch problem. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 155 | 42,470 | 0 | false | Although this code has received some experimental validation, our strategy would provide the best oligonucleotide solution for this switch problem. | [
"10,48"
] | Although this code has received some experimental validation, our strategy would provide the best oligonucleotide solution for this switch problem. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | It would also be interesting to perform selections with other DNA binding agents. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 81 | 42,471 | 0 | false | It would also be interesting to perform selections with other DNA binding agents. | [] | It would also be interesting to perform selections with other DNA binding agents. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | Large molecules, such as echinomycin, may be more likely to be recognized by folded oligonucleotides. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 101 | 42,472 | 0 | false | Large molecules, such as echinomycin, may be more likely to be recognized by folded oligonucleotides. | [] | Large molecules, such as echinomycin, may be more likely to be recognized by folded oligonucleotides. | true | true | true | true | true | 7,357 |
5 | DISCUSSION | 1 | 43 | [
"B43",
"B44",
"B19",
"B45",
"B46",
"B10",
"B47",
"B10",
"B48"
] | 20,007,154 | pmid-15274215|pmid-15911633|pmid-9547278|pmid-9380499|pmid-9685475|pmid-9862797|NA|pmid-9862797|pmid-10454596 | Work is in progress in order to explore all those possibilities. | [
"43",
"44",
"19",
"45",
"46",
"10",
"47",
"10",
"48"
] | 64 | 42,473 | 0 | false | Work is in progress in order to explore all those possibilities. | [] | Work is in progress in order to explore all those possibilities. | true | true | true | true | true | 7,357 |
0 | INTRODUCTION | 1 | 1 | [
"B1"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | Pain following spinal cord injury (SCI) is a major challenge for patients coping with the physical and life-threatening consequences of SCI [1]. | [
"1"
] | 144 | 42,474 | 1 | false | Pain following spinal cord injury (SCI) is a major challenge for patients coping with the physical and life-threatening consequences of SCI. | [
"1"
] | Pain following spinal cord injury (SCI) is a major challenge for patients coping with the physical and life-threatening consequences of SCI. | true | true | true | true | true | 7,358 |
0 | INTRODUCTION | 1 | 1 | [
"B1"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | For the development of more effective treatments for pain of spinal origin, the pathophysiological and neurochemical changes following spinal injury should be clearly illustrated. | [
"1"
] | 179 | 42,475 | 0 | false | For the development of more effective treatments for pain of spinal origin, the pathophysiological and neurochemical changes following spinal injury should be clearly illustrated. | [] | For the development of more effective treatments for pain of spinal origin, the pathophysiological and neurochemical changes following spinal injury should be clearly illustrated. | true | true | true | true | true | 7,358 |
1 | INTRODUCTION | 1 | 2 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | An important consideration in the study of injury-induced spinal pain using an animal model is the pathological and/or behavioral responses associated with human SCI. | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 166 | 42,476 | 0 | false | An important consideration in the study of injury-induced spinal pain using an animal model is the pathological and/or behavioral responses associated with human SCI. | [] | An important consideration in the study of injury-induced spinal pain using an animal model is the pathological and/or behavioral responses associated with human SCI. | true | true | true | true | true | 7,359 |
1 | INTRODUCTION | 1 | 2 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Numerous experimental models, including photochemical [2], hemisection [3], contusion [4] and clip compression [5] models, have been developed to explicate the complex pathophysiological mechanisms of spinal cord injury. | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 220 | 42,477 | 1 | false | Numerous experimental models, including photochemical, hemisection, contusion and clip compression models, have been developed to explicate the complex pathophysiological mechanisms of spinal cord injury. | [
"2",
"3",
"4",
"5"
] | Numerous experimental models, including photochemical, hemisection, contusion and clip compression models, have been developed to explicate the complex pathophysiological mechanisms of spinal cord injury. | true | true | true | true | true | 7,359 |
1 | INTRODUCTION | 1 | 2 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Although these models share many pathological characteristics with the human condition, the specific neural substrates responsible for the injury-induced abnormal sensations are not yet elucidated. | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 197 | 42,478 | 0 | false | Although these models share many pathological characteristics with the human condition, the specific neural substrates responsible for the injury-induced abnormal sensations are not yet elucidated. | [] | Although these models share many pathological characteristics with the human condition, the specific neural substrates responsible for the injury-induced abnormal sensations are not yet elucidated. | true | true | true | true | true | 7,359 |
1 | INTRODUCTION | 1 | 2 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Based on previous studies documenting the elevated excitatory amino acid levels commonly associated with spinal injury [6,7], Yezierski et al. | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 142 | 42,479 | 0 | false | Based on previous studies documenting the elevated excitatory amino acid levels commonly associated with spinal injury, Yezierski et al. | [
"6,7"
] | Based on previous studies documenting the elevated excitatory amino acid levels commonly associated with spinal injury, Yezierski et al. | true | true | true | true | true | 7,359 |
1 | INTRODUCTION | 1 | 8 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | [8] injected the AMPA-metabotropic receptor agonist quisqualic acid into the grey matter of the spinal cord in an effort to simulate injury-induced elevations of excitatory amino acids. | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 185 | 42,480 | 1 | false | injected the AMPA-metabotropic receptor agonist quisqualic acid into the grey matter of the spinal cord in an effort to simulate injury-induced elevations of excitatory amino acids. | [
"8"
] | injected the AMPA-metabotropic receptor agonist quisqualic acid into the grey matter of the spinal cord in an effort to simulate injury-induced elevations of excitatory amino acids. | false | true | true | true | false | 7,359 |
1 | INTRODUCTION | 1 | 2 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | They reported that intraspinal injections of the AMPA-metabotropic receptor agonist quisqualic acid induce the progressive pathological sequela resembling the cascade of events described following ischemic and traumatic SCI, and that the morphological changes of the spinal cord following intraspinal injection correlate... | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 414 | 42,481 | 0 | false | They reported that intraspinal injections of the AMPA-metabotropic receptor agonist quisqualic acid induce the progressive pathological sequela resembling the cascade of events described following ischemic and traumatic SCI, and that the morphological changes of the spinal cord following intraspinal injection correlate... | [] | They reported that intraspinal injections of the AMPA-metabotropic receptor agonist quisqualic acid induce the progressive pathological sequela resembling the cascade of events described following ischemic and traumatic SCI, and that the morphological changes of the spinal cord following intraspinal injection correlate... | true | true | true | true | true | 7,359 |
1 | INTRODUCTION | 1 | 9 | [
"B2",
"B3",
"B4",
"B5",
"B6",
"B7",
"B8",
"B9"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Moreover, it has also been demonstrated that the injection of N-methyl-D-aspartate (NMDA) into the ventral horn of the spinal cord induces intense neuronal degeneration and acute inflammation in both the grey and white matter [9]. | [
"2",
"3",
"4",
"5",
"6",
"7",
"8",
"9"
] | 230 | 42,482 | 1 | false | Moreover, it has also been demonstrated that the injection of N-methyl-D-aspartate (NMDA) into the ventral horn of the spinal cord induces intense neuronal degeneration and acute inflammation in both the grey and white matter. | [
"9"
] | Moreover, it has also been demonstrated that the injection of N-methyl-D-aspartate (NMDA) into the ventral horn of the spinal cord induces intense neuronal degeneration and acute inflammation in both the grey and white matter. | true | true | true | true | true | 7,359 |
2 | INTRODUCTION | 0 | null | null | 20,556,212 | pmid-11844532|pmid-15530884|pmid-12125741 | The present study was designed to evaluate the morphological changes of the dorsal horn of the spinal cord and profiles of pain behaviors following intraspinal injection of NMDA in rats. | null | 186 | 42,483 | 0 | false | null | null | The present study was designed to evaluate the morphological changes of the dorsal horn of the spinal cord and profiles of pain behaviors following intraspinal injection of NMDA in rats. | true | true | true | true | true | 7,360 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | The purpose of this study was to evaluate the morphological changes of the dorsal horn of the spinal cord and profiles of pain behaviors following intraspinal injection of NMDA in rats. | [
"2",
"11"
] | 185 | 42,484 | 0 | false | The purpose of this study was to evaluate the morphological changes of the dorsal horn of the spinal cord and profiles of pain behaviors following intraspinal injection of NMDA in rats. | [] | The purpose of this study was to evaluate the morphological changes of the dorsal horn of the spinal cord and profiles of pain behaviors following intraspinal injection of NMDA in rats. | true | true | true | true | true | 7,361 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | A major finding of the present study is that intrarspinal injection of NMDA induced excessive grooming behaviors and intense neuronal degeneration in the ipsilateral dorsal horn of the spinal cord. | [
"2",
"11"
] | 197 | 42,485 | 0 | false | A major finding of the present study is that intrarspinal injection of NMDA induced excessive grooming behaviors and intense neuronal degeneration in the ipsilateral dorsal horn of the spinal cord. | [] | A major finding of the present study is that intrarspinal injection of NMDA induced excessive grooming behaviors and intense neuronal degeneration in the ipsilateral dorsal horn of the spinal cord. | true | true | true | true | true | 7,361 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | The histopathological findings were similar to those previously reported quisqualic acid-induced excitotoxic damage to the spinal cord [2,11]. | [
"2",
"11"
] | 142 | 42,486 | 0 | false | The histopathological findings were similar to those previously reported quisqualic acid-induced excitotoxic damage to the spinal cord. | [
"2,11"
] | The histopathological findings were similar to those previously reported quisqualic acid-induced excitotoxic damage to the spinal cord. | true | true | true | true | true | 7,361 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | Although the incidence of mechanical and cold allodynia following intraspinal injection was low, excessive grooming behavior commonly seen in animals suffering from experimental central neuropathic pain was evident, especially in the 100 mM NMDA group. | [
"2",
"11"
] | 252 | 42,487 | 0 | false | Although the incidence of mechanical and cold allodynia following intraspinal injection was low, excessive grooming behavior commonly seen in animals suffering from experimental central neuropathic pain was evident, especially in the 100 mM NMDA group. | [] | Although the incidence of mechanical and cold allodynia following intraspinal injection was low, excessive grooming behavior commonly seen in animals suffering from experimental central neuropathic pain was evident, especially in the 100 mM NMDA group. | true | true | true | true | true | 7,361 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | On the spinal cord sections of the 100 mM NMDA group prepared after four-week survival periods, dilation of the central canal and formation of intraspinal cavities were observed. | [
"2",
"11"
] | 178 | 42,488 | 0 | false | On the spinal cord sections of the 100 mM NMDA group prepared after four-week survival periods, dilation of the central canal and formation of intraspinal cavities were observed. | [] | On the spinal cord sections of the 100 mM NMDA group prepared after four-week survival periods, dilation of the central canal and formation of intraspinal cavities were observed. | true | true | true | true | true | 7,361 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | Intraspinal NMDA-induced neuronal loss occurred mainly at the lamina III-V. | [
"2",
"11"
] | 75 | 42,489 | 0 | false | Intraspinal NMDA-induced neuronal loss occurred mainly at the lamina III-V. | [] | Intraspinal NMDA-induced neuronal loss occurred mainly at the lamina III-V. | true | true | true | true | true | 7,361 |
0 | DISCUSSION | 1 | 2 | [
"B2",
"B11"
] | 20,556,212 | pmid-19154757|pmid-1589248|pmid-9187327 | The present data suggest the existence of a causal relationship between the neuronal loss of the dorsal horn and the evoked/spontaneous pain-like behavior. | [
"2",
"11"
] | 155 | 42,490 | 0 | false | The present data suggest the existence of a causal relationship between the neuronal loss of the dorsal horn and the evoked/spontaneous pain-like behavior. | [] | The present data suggest the existence of a causal relationship between the neuronal loss of the dorsal horn and the evoked/spontaneous pain-like behavior. | true | true | true | true | true | 7,361 |
1 | DISCUSSION | 1 | 12 | [
"B12",
"B13",
"B14",
"B8"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Concentrated excitatory amino acids following trauma or ischemia can lead to a prolonged period of depolarization and the initiation of a cellular cascade that ultimately results in neuronal death. | [
"12",
"13",
"14",
"8"
] | 197 | 42,491 | 0 | false | Concentrated excitatory amino acids following trauma or ischemia can lead to a prolonged period of depolarization and the initiation of a cellular cascade that ultimately results in neuronal death. | [] | Concentrated excitatory amino acids following trauma or ischemia can lead to a prolonged period of depolarization and the initiation of a cellular cascade that ultimately results in neuronal death. | true | true | true | true | true | 7,362 |
1 | DISCUSSION | 1 | 12 | [
"B12",
"B13",
"B14",
"B8"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Both NMDA and non-NMDA receptors contribute to the excitotoxic effects of elevated glutamate levels in the spinal cord [12]. | [
"12",
"13",
"14",
"8"
] | 124 | 42,492 | 1 | false | Both NMDA and non-NMDA receptors contribute to the excitotoxic effects of elevated glutamate levels in the spinal cord. | [
"12"
] | Both NMDA and non-NMDA receptors contribute to the excitotoxic effects of elevated glutamate levels in the spinal cord. | true | true | true | true | true | 7,362 |
1 | DISCUSSION | 1 | 13 | [
"B12",
"B13",
"B14",
"B8"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Several classes of excitatory amino acid receptors are thought to be involved in glutamate excitotoxicity, including NMDA, AMPA, kainate and metabotropic receptors [13]. | [
"12",
"13",
"14",
"8"
] | 169 | 42,493 | 1 | false | Several classes of excitatory amino acid receptors are thought to be involved in glutamate excitotoxicity, including NMDA, AMPA, kainate and metabotropic receptors. | [
"13"
] | Several classes of excitatory amino acid receptors are thought to be involved in glutamate excitotoxicity, including NMDA, AMPA, kainate and metabotropic receptors. | true | true | true | true | true | 7,362 |
1 | DISCUSSION | 1 | 14 | [
"B12",
"B13",
"B14",
"B8"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | Ionotropic receptors regulate the opening of voltage-gated ion channels, and metabotropic receptors are linked via G-proteins to phospholipase C. Glutamate-induced cell death that results from NMDA ionotropic receptor activation is well documented as largely due to the excessive influx of sodium and calcium ions [14]. | [
"12",
"13",
"14",
"8"
] | 319 | 42,494 | 1 | false | Ionotropic receptors regulate the opening of voltage-gated ion channels, and metabotropic receptors are linked via G-proteins to phospholipase C. Glutamate-induced cell death that results from NMDA ionotropic receptor activation is well documented as largely due to the excessive influx of sodium and calcium ions. | [
"14"
] | Ionotropic receptors regulate the opening of voltage-gated ion channels, and metabotropic receptors are linked via G-proteins to phospholipase C. Glutamate-induced cell death that results from NMDA ionotropic receptor activation is well documented as largely due to the excessive influx of sodium and calcium ions. | true | true | true | true | true | 7,362 |
1 | DISCUSSION | 1 | 12 | [
"B12",
"B13",
"B14",
"B8"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | The role of non-NMDA receptors in the injury of spinal neurons has been studied with a simulated excitotoxic spinal cord injury model using intraspinal quisqualic acid injection. | [
"12",
"13",
"14",
"8"
] | 178 | 42,495 | 0 | false | The role of non-NMDA receptors in the injury of spinal neurons has been studied with a simulated excitotoxic spinal cord injury model using intraspinal quisqualic acid injection. | [] | The role of non-NMDA receptors in the injury of spinal neurons has been studied with a simulated excitotoxic spinal cord injury model using intraspinal quisqualic acid injection. | true | true | true | true | true | 7,362 |
1 | DISCUSSION | 1 | 8 | [
"B12",
"B13",
"B14",
"B8"
] | 20,556,212 | pmid-1589248|pmid-18353556|pmid-11186233|pmid-12460606|pmid-1977091|pmid-1884213|pmid-9539683|pmid-15530884|pmid-19154757|pmid-1361523|pmid-1697342|pmid-9539683 | The results suggest that the specific non-NMDA receptor agonist AMPA produces histological changes similar to those observed following quisqualic acid injections [8]. | [
"12",
"13",
"14",
"8"
] | 166 | 42,496 | 1 | false | The results suggest that the specific non-NMDA receptor agonist AMPA produces histological changes similar to those observed following quisqualic acid injections. | [
"8"
] | The results suggest that the specific non-NMDA receptor agonist AMPA produces histological changes similar to those observed following quisqualic acid injections. | true | true | true | true | true | 7,362 |
2 | DISCUSSION | 1 | 15 | [
"B15",
"B9",
"B16"
] | 20,556,212 | pmid-11844532|pmid-15530884|pmid-12125741 | NMDA receptors are present on the endothelial cells of grey matter vasculature and damage to blood vessels in the grey matter can induce damage to the adjacent white matter [15]. | [
"15",
"9",
"16"
] | 178 | 42,497 | 1 | false | NMDA receptors are present on the endothelial cells of grey matter vasculature and damage to blood vessels in the grey matter can induce damage to the adjacent white matter. | [
"15"
] | NMDA receptors are present on the endothelial cells of grey matter vasculature and damage to blood vessels in the grey matter can induce damage to the adjacent white matter. | true | true | true | true | true | 7,363 |
2 | DISCUSSION | 1 | 15 | [
"B15",
"B9",
"B16"
] | 20,556,212 | pmid-11844532|pmid-15530884|pmid-12125741 | NMDA molecules can bind to receptors in the endothelial cells, inducing blood-brain barrier breakdown, acute inflammation and tissue damage. | [
"15",
"9",
"16"
] | 140 | 42,498 | 0 | false | NMDA molecules can bind to receptors in the endothelial cells, inducing blood-brain barrier breakdown, acute inflammation and tissue damage. | [] | NMDA molecules can bind to receptors in the endothelial cells, inducing blood-brain barrier breakdown, acute inflammation and tissue damage. | true | true | true | true | true | 7,363 |
2 | DISCUSSION | 1 | 9 | [
"B15",
"B9",
"B16"
] | 20,556,212 | pmid-11844532|pmid-15530884|pmid-12125741 | The expansion of the primary necrotic area is a secondary pathological phenomenon involving a multitude of mechanisms, including pathological release of excitatory amino acids, free radical formation, nitric oxide synthesis, and inflammation [9]. | [
"15",
"9",
"16"
] | 246 | 42,499 | 1 | false | The expansion of the primary necrotic area is a secondary pathological phenomenon involving a multitude of mechanisms, including pathological release of excitatory amino acids, free radical formation, nitric oxide synthesis, and inflammation. | [
"9"
] | The expansion of the primary necrotic area is a secondary pathological phenomenon involving a multitude of mechanisms, including pathological release of excitatory amino acids, free radical formation, nitric oxide synthesis, and inflammation. | true | true | true | true | true | 7,363 |
2 | DISCUSSION | 1 | 16 | [
"B15",
"B9",
"B16"
] | 20,556,212 | pmid-11844532|pmid-15530884|pmid-12125741 | Neuronal degeneration and activated macrophages/microglia in the grey matter could also release cytokines and other diffusible factors, such as nitric oxide, which can induce damage to white matter or potentiate deleterious tissue damage by pathological activation of non-NMDA receptors [16]. | [
"15",
"9",
"16"
] | 292 | 42,500 | 1 | false | Neuronal degeneration and activated macrophages/microglia in the grey matter could also release cytokines and other diffusible factors, such as nitric oxide, which can induce damage to white matter or potentiate deleterious tissue damage by pathological activation of non-NMDA receptors. | [
"16"
] | Neuronal degeneration and activated macrophages/microglia in the grey matter could also release cytokines and other diffusible factors, such as nitric oxide, which can induce damage to white matter or potentiate deleterious tissue damage by pathological activation of non-NMDA receptors. | true | true | true | true | true | 7,363 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | In the present study, excessive grooming behavior correlated with a lesion sparing the superficial laminae (lamina I-II, superficial in Fig. | [
"17",
"1",
"17",
"18"
] | 140 | 42,501 | 0 | false | In the present study, excessive grooming behavior correlated with a lesion sparing the superficial laminae (lamina I-II, superficial in Fig. | [] | In the present study, excessive grooming behavior correlated with a lesion sparing the superficial laminae (lamina I-II, superficial in Fig. | true | true | true | true | true | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | 3) and neuronal damage in the neck of the dorsal horn (lamina III-IV, neck in Fig. | [
"17",
"1",
"17",
"18"
] | 82 | 42,502 | 0 | false | 3) and neuronal damage in the neck of the dorsal horn (lamina III-IV, neck in Fig. | [] | 3) and neuronal damage in the neck of the dorsal horn (lamina III-IV, neck in Fig. | false | false | true | true | false | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | These results are consistent with those of the previous study, documenting that destruction of lamina I cells can prevent or eliminate excessive grooming behavior | [
"17",
"1",
"17",
"18"
] | 162 | 42,503 | 0 | false | These results are consistent with those of the previous study, documenting that destruction of lamina I cells can prevent or eliminate excessive grooming behavior | [] | These results are consistent with those of the previous study, documenting that destruction of lamina I cells can prevent or eliminate excessive grooming behavior | true | true | false | true | false | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | Pain associated with spinal cord injury can be divided into nociceptive (including musculoskeletal and visceral) and neuropathic (including above-, at- and below-level) | [
"17",
"1",
"17",
"18"
] | 168 | 42,504 | 0 | false | Pain associated with spinal cord injury can be divided into nociceptive (including musculoskeletal and visceral) and neuropathic (including above-, at- and below-level) | [] | Pain associated with spinal cord injury can be divided into nociceptive (including musculoskeletal and visceral) and neuropathic (including above-, at- and below-level) | true | true | false | true | false | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | The primary characteristic of at-level pain is a hypersensitive band of skin in dermatomes associated with spinal segments adjacent to the site of injury. | [
"17",
"1",
"17",
"18"
] | 154 | 42,505 | 0 | false | The primary characteristic of at-level pain is a hypersensitive band of skin in dermatomes associated with spinal segments adjacent to the site of injury. | [] | The primary characteristic of at-level pain is a hypersensitive band of skin in dermatomes associated with spinal segments adjacent to the site of injury. | true | true | true | true | true | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | Injury-induced loss of intrinsic inhibitory control and changes in the functional state of neurons adjacent to the site of injury represent the current view of a mechanism responsible for this condition [17]. | [
"17",
"1",
"17",
"18"
] | 208 | 42,506 | 1 | false | Injury-induced loss of intrinsic inhibitory control and changes in the functional state of neurons adjacent to the site of injury represent the current view of a mechanism responsible for this condition. | [
"17"
] | Injury-induced loss of intrinsic inhibitory control and changes in the functional state of neurons adjacent to the site of injury represent the current view of a mechanism responsible for this condition. | true | true | true | true | true | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | Consistent with the clinical profile of at-level pain, hypersensitivity to thermal and mechanical stimuli are characteristics of the area targeted for excessive grooming behavior. | [
"17",
"1",
"17",
"18"
] | 179 | 42,507 | 0 | false | Consistent with the clinical profile of at-level pain, hypersensitivity to thermal and mechanical stimuli are characteristics of the area targeted for excessive grooming behavior. | [] | Consistent with the clinical profile of at-level pain, hypersensitivity to thermal and mechanical stimuli are characteristics of the area targeted for excessive grooming behavior. | true | true | true | true | true | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | Pain can be present in NMDA-injected animals without excessive grooming behavior, as evidenced by the finding that a few of the injected animals developed cold and mechanical allodynia below the level of injury without any signs of excessive grooming. | [
"17",
"1",
"17",
"18"
] | 251 | 42,508 | 0 | false | Pain can be present in NMDA-injected animals without excessive grooming behavior, as evidenced by the finding that a few of the injected animals developed cold and mechanical allodynia below the level of injury without any signs of excessive grooming. | [] | Pain can be present in NMDA-injected animals without excessive grooming behavior, as evidenced by the finding that a few of the injected animals developed cold and mechanical allodynia below the level of injury without any signs of excessive grooming. | true | true | true | true | true | 7,364 |
3 | DISCUSSION | 1 | 17 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | In this study, efforts to correlate the pattern of neuronal loss with the development of hypersensitivity to cold and mechanical stimuli proved unsuccessful. | [
"17",
"1",
"17",
"18"
] | 157 | 42,509 | 0 | false | In this study, efforts to correlate the pattern of neuronal loss with the development of hypersensitivity to cold and mechanical stimuli proved unsuccessful. | [] | In this study, efforts to correlate the pattern of neuronal loss with the development of hypersensitivity to cold and mechanical stimuli proved unsuccessful. | true | true | true | true | true | 7,364 |
3 | DISCUSSION | 1 | 18 | [
"B17",
"B1",
"B17",
"B18"
] | 20,556,212 | pmid-15135936|pmid-19154757|pmid-15135936|pmid-18619906 | It can be postulated that cold and mechanical allodynia were not developed due to somatosensory dysfunction associated with NMDA-induced injury to the white matter and death of the entire primary afferent neuron as a consequence of the central nervous system lesion [18]. | [
"17",
"1",
"17",
"18"
] | 271 | 42,510 | 1 | false | It can be postulated that cold and mechanical allodynia were not developed due to somatosensory dysfunction associated with NMDA-induced injury to the white matter and death of the entire primary afferent neuron as a consequence of the central nervous system lesion. | [
"18"
] | It can be postulated that cold and mechanical allodynia were not developed due to somatosensory dysfunction associated with NMDA-induced injury to the white matter and death of the entire primary afferent neuron as a consequence of the central nervous system lesion. | true | true | true | true | true | 7,364 |
4 | DISCUSSION | 0 | null | null | 20,556,212 | null | In conclusion, intraspinal injection of NMDA leads to the pathological sequela in the spinal cord and to excessive grooming behavior. | null | 133 | 42,511 | 0 | false | null | null | In conclusion, intraspinal injection of NMDA leads to the pathological sequela in the spinal cord and to excessive grooming behavior. | true | true | true | true | true | 7,365 |
4 | DISCUSSION | 0 | null | null | 20,556,212 | null | The morphological changes of the spinal cord resemble the cascade of events described following ischemic and traumatic SCI. | null | 123 | 42,512 | 0 | false | null | null | The morphological changes of the spinal cord resemble the cascade of events described following ischemic and traumatic SCI. | true | true | true | true | true | 7,365 |
4 | DISCUSSION | 0 | null | null | 20,556,212 | null | Excessive grooming behavior was associated with neuronal damage in the neck of the spinal dorsal horn and with sparing the superficial laminae. | null | 143 | 42,513 | 0 | false | null | null | Excessive grooming behavior was associated with neuronal damage in the neck of the spinal dorsal horn and with sparing the superficial laminae. | true | true | true | true | true | 7,365 |
4 | DISCUSSION | 0 | null | null | 20,556,212 | null | These results support the use of NMDA and excessive grooming behavior to study central neuropathic pain following SCI. | null | 118 | 42,514 | 0 | false | null | null | These results support the use of NMDA and excessive grooming behavior to study central neuropathic pain following SCI. | true | true | true | true | true | 7,365 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B1",
"B3",
"B4",
"B5",
"B6",
"B6",
"B7"
] | 20,664,777 | pmid-16514137|NA|pmid-16514137|pmid-15069304|pmid-16492908|pmid-8903474|pmid-11833360|pmid-11833360|pmid-11390274|pmid-8701470|pmid-8701470|pmid-4953930 | Prostate cancer (CaP) has the highest incidence among cancers in the US and is the second leading cause of cancer-associated death in men [1]. | [
"1",
"2",
"1",
"3",
"4",
"5",
"6",
"6",
"7"
] | 142 | 42,515 | 1 | false | Prostate cancer (CaP) has the highest incidence among cancers in the US and is the second leading cause of cancer-associated death in men. | [
"1"
] | Prostate cancer (CaP) has the highest incidence among cancers in the US and is the second leading cause of cancer-associated death in men. | true | true | true | true | true | 7,366 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B1",
"B3",
"B4",
"B5",
"B6",
"B6",
"B7"
] | 20,664,777 | pmid-16514137|NA|pmid-16514137|pmid-15069304|pmid-16492908|pmid-8903474|pmid-11833360|pmid-11833360|pmid-11390274|pmid-8701470|pmid-8701470|pmid-4953930 | In Korea, its incidence is still increasing, compared to that of other cancers and it ranked fifth in incidence in 2005 | [
"1",
"2",
"1",
"3",
"4",
"5",
"6",
"6",
"7"
] | 119 | 42,516 | 0 | false | In Korea, its incidence is still increasing, compared to that of other cancers and it ranked fifth in incidence in 2005 | [] | In Korea, its incidence is still increasing, compared to that of other cancers and it ranked fifth in incidence in 2005 | true | true | false | true | false | 7,366 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B1",
"B3",
"B4",
"B5",
"B6",
"B6",
"B7"
] | 20,664,777 | pmid-16514137|NA|pmid-16514137|pmid-15069304|pmid-16492908|pmid-8903474|pmid-11833360|pmid-11833360|pmid-11390274|pmid-8701470|pmid-8701470|pmid-4953930 | Despite recent improvements in diagnosis and therapeutic techniques, the survival rate of CaP patients is poor because of the recurrence of the disease [1,3]. | [
"1",
"2",
"1",
"3",
"4",
"5",
"6",
"6",
"7"
] | 158 | 42,517 | 0 | false | Despite recent improvements in diagnosis and therapeutic techniques, the survival rate of CaP patients is poor because of the recurrence of the disease. | [
"1,3"
] | Despite recent improvements in diagnosis and therapeutic techniques, the survival rate of CaP patients is poor because of the recurrence of the disease. | true | true | true | true | true | 7,366 |
0 | INTRODUCTION | 1 | 1 | [
"B1",
"B2",
"B1",
"B3",
"B4",
"B5",
"B6",
"B6",
"B7"
] | 20,664,777 | pmid-16514137|NA|pmid-16514137|pmid-15069304|pmid-16492908|pmid-8903474|pmid-11833360|pmid-11833360|pmid-11390274|pmid-8701470|pmid-8701470|pmid-4953930 | The lack of effective therapies for advanced CaP is related to a large extent to poor understanding of the molecular mechanisms underlying the progression of this disease (invasion and metastasis) | [
"1",
"2",
"1",
"3",
"4",
"5",
"6",
"6",
"7"
] | 196 | 42,518 | 0 | false | The lack of effective therapies for advanced CaP is related to a large extent to poor understanding of the molecular mechanisms underlying the progression of this disease (invasion and metastasis) | [] | The lack of effective therapies for advanced CaP is related to a large extent to poor understanding of the molecular mechanisms underlying the progression of this disease (invasion and metastasis) | true | true | false | true | false | 7,366 |
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