| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-128 |
Sentence |
denotes |
DNA-sequence rearrangement required for the adaptation of JC polyomavirus to growth in a human neuroblastoma cell line (IMR-32). |
| T1 |
0-128 |
Sentence |
denotes |
DNA-sequence rearrangement required for the adaptation of JC polyomavirus to growth in a human neuroblastoma cell line (IMR-32). |
| TextSentencer_T2 |
129-326 |
Sentence |
denotes |
Infection of a human neuroblastoma cell line (IMR-32) with the JC polyomavirus (JCV) strain Mad-1 with subsequent serial passage results in the generation of a virus adapted to growth in IMR-32 (K. |
| T2 |
129-326 |
Sentence |
denotes |
Infection of a human neuroblastoma cell line (IMR-32) with the JC polyomavirus (JCV) strain Mad-1 with subsequent serial passage results in the generation of a virus adapted to growth in IMR-32 (K. |
| TextSentencer_T3 |
327-338 |
Sentence |
denotes |
Akatani, M. |
| T3 |
327-338 |
Sentence |
denotes |
Akatani, M. |
| TextSentencer_T4 |
339-347 |
Sentence |
denotes |
Imai, M. |
| T4 |
339-347 |
Sentence |
denotes |
Imai, M. |
| TextSentencer_T5 |
348-358 |
Sentence |
denotes |
Kimura, K. |
| T5 |
348-358 |
Sentence |
denotes |
Kimura, K. |
| TextSentencer_T6 |
359-376 |
Sentence |
denotes |
Nagashima, and N. |
| T6 |
359-376 |
Sentence |
denotes |
Nagashima, and N. |
| TextSentencer_T7 |
377-388 |
Sentence |
denotes |
Ikegami, J. |
| T7 |
377-388 |
Sentence |
denotes |
Ikegami, J. |
| TextSentencer_T8 |
389-393 |
Sentence |
denotes |
Med. |
| T8 |
389-393 |
Sentence |
denotes |
Med. |
| TextSentencer_T9 |
394-412 |
Sentence |
denotes |
Virol., in press). |
| T9 |
394-412 |
Sentence |
denotes |
Virol., in press). |
| TextSentencer_T10 |
413-511 |
Sentence |
denotes |
To understand the basis of this adaptation, we molecularly cloned JCV DNAs from the adapted virus. |
| T10 |
413-511 |
Sentence |
denotes |
To understand the basis of this adaptation, we molecularly cloned JCV DNAs from the adapted virus. |
| TextSentencer_T11 |
512-634 |
Sentence |
denotes |
The cloned JCV DNAs consisted of essentially three species (M1-IMRa, -IMRb, and -IMRc) with rearranged regulatory regions. |
| T11 |
512-634 |
Sentence |
denotes |
The cloned JCV DNAs consisted of essentially three species (M1-IMRa, -IMRb, and -IMRc) with rearranged regulatory regions. |
| TextSentencer_T12 |
635-816 |
Sentence |
denotes |
Two TATA sequences are present in the regulatory region of the parental virus Mad-1, but one distal from the origin of replication was commonly deleted in M1-IMRa, -IMRb, and -IMRc. |
| T12 |
635-816 |
Sentence |
denotes |
Two TATA sequences are present in the regulatory region of the parental virus Mad-1, but one distal from the origin of replication was commonly deleted in M1-IMRa, -IMRb, and -IMRc. |
| TextSentencer_T13 |
817-913 |
Sentence |
denotes |
We showed that these regulatory regions were required for the efficient growth of JCV in IMR-32. |
| T13 |
817-913 |
Sentence |
denotes |
We showed that these regulatory regions were required for the efficient growth of JCV in IMR-32. |
| TextSentencer_T14 |
914-1040 |
Sentence |
denotes |
Various JCV strains should be propagated in IMR-32, if their regulatory regions are replaced with those defined in this study. |
| T14 |
914-1040 |
Sentence |
denotes |
Various JCV strains should be propagated in IMR-32, if their regulatory regions are replaced with those defined in this study. |
| TextSentencer_T15 |
1041-1207 |
Sentence |
denotes |
Since it is difficult to propagate JCV in cells other than primary human fetal glial cells, this system may be useful for structural and immunological studies of JCV. |
| T15 |
1041-1207 |
Sentence |
denotes |
Since it is difficult to propagate JCV in cells other than primary human fetal glial cells, this system may be useful for structural and immunological studies of JCV. |