| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-121 |
Sentence |
denotes |
Sialyl cholesterol is translocated into cell nuclei and it promotes neurite outgrowth in a mouse neuroblastoma cell line. |
| T1 |
0-121 |
Sentence |
denotes |
Sialyl cholesterol is translocated into cell nuclei and it promotes neurite outgrowth in a mouse neuroblastoma cell line. |
| T1 |
0-121 |
Sentence |
denotes |
Sialyl cholesterol is translocated into cell nuclei and it promotes neurite outgrowth in a mouse neuroblastoma cell line. |
| TextSentencer_T2 |
122-347 |
Sentence |
denotes |
To determine the mechanisms of the neuritogenesis induced by synthetic sialyl cholesterol (SC) in a mouse neuroblastoma cell line, Neuro2a, the biochemical fate of SC and ganglioside GM1 (IV3NeuAc-GgOse4Cer) was investigated. |
| T2 |
122-347 |
Sentence |
denotes |
To determine the mechanisms of the neuritogenesis induced by synthetic sialyl cholesterol (SC) in a mouse neuroblastoma cell line, Neuro2a, the biochemical fate of SC and ganglioside GM1 (IV3NeuAc-GgOse4Cer) was investigated. |
| T2 |
122-347 |
Sentence |
denotes |
To determine the mechanisms of the neuritogenesis induced by synthetic sialyl cholesterol (SC) in a mouse neuroblastoma cell line, Neuro2a, the biochemical fate of SC and ganglioside GM1 (IV3NeuAc-GgOse4Cer) was investigated. |
| TextSentencer_T3 |
348-438 |
Sentence |
denotes |
The kinetics of incorporation of SC and GM1 into cells for the two compounds were similar. |
| T3 |
348-438 |
Sentence |
denotes |
The kinetics of incorporation of SC and GM1 into cells for the two compounds were similar. |
| T3 |
348-438 |
Sentence |
denotes |
The kinetics of incorporation of SC and GM1 into cells for the two compounds were similar. |
| TextSentencer_T4 |
439-612 |
Sentence |
denotes |
SC was not degraded nor modified for at least 24 h after the incorporation, indicating that SC itself and not its metabolites were responsible for the neuritogenic activity. |
| T4 |
439-612 |
Sentence |
denotes |
SC was not degraded nor modified for at least 24 h after the incorporation, indicating that SC itself and not its metabolites were responsible for the neuritogenic activity. |
| T4 |
439-612 |
Sentence |
denotes |
SC was not degraded nor modified for at least 24 h after the incorporation, indicating that SC itself and not its metabolites were responsible for the neuritogenic activity. |
| TextSentencer_T5 |
613-800 |
Sentence |
denotes |
Cell fractionation experiments showed that approximately 40% of the incorporated SC was localized in the nucleus, 25% in the plasma membrane fractions, and 11-14% in the granule fraction. |
| T5 |
613-800 |
Sentence |
denotes |
Cell fractionation experiments showed that approximately 40% of the incorporated SC was localized in the nucleus, 25% in the plasma membrane fractions, and 11-14% in the granule fraction. |
| T5 |
613-800 |
Sentence |
denotes |
Cell fractionation experiments showed that approximately 40% of the incorporated SC was localized in the nucleus, 25% in the plasma membrane fractions, and 11-14% in the granule fraction. |
| TextSentencer_T6 |
801-850 |
Sentence |
denotes |
This distribution was different from that of GM1. |
| T6 |
801-850 |
Sentence |
denotes |
This distribution was different from that of GM1. |
| T6 |
801-850 |
Sentence |
denotes |
This distribution was different from that of GM1. |
| TextSentencer_T7 |
851-988 |
Sentence |
denotes |
The nuclear SC was found to affect de novo RNA synthesis, indicating its biological effect may be mediated at the level of transcription. |
| T7 |
851-988 |
Sentence |
denotes |
The nuclear SC was found to affect de novo RNA synthesis, indicating its biological effect may be mediated at the level of transcription. |
| T7 |
851-988 |
Sentence |
denotes |
The nuclear SC was found to affect de novo RNA synthesis, indicating its biological effect may be mediated at the level of transcription. |
| TextSentencer_T8 |
989-1115 |
Sentence |
denotes |
SC also increased the rates of both Ca2+ influx and efflux, although the intracellular level of total Ca2+ remained unchanged. |
| T8 |
989-1115 |
Sentence |
denotes |
SC also increased the rates of both Ca2+ influx and efflux, although the intracellular level of total Ca2+ remained unchanged. |
| T8 |
989-1115 |
Sentence |
denotes |
SC also increased the rates of both Ca2+ influx and efflux, although the intracellular level of total Ca2+ remained unchanged. |
| TextSentencer_T9 |
1116-1299 |
Sentence |
denotes |
Levels of inositol 1,4,5-triphosphate (IP3) also remained unchanged and the SC dependent neuritogenesis was not inhibited by an excess amount of W-7, an inhibitor of Ca2+/CaM kinases. |
| T9 |
1116-1299 |
Sentence |
denotes |
Levels of inositol 1,4,5-triphosphate (IP3) also remained unchanged and the SC dependent neuritogenesis was not inhibited by an excess amount of W-7, an inhibitor of Ca2+/CaM kinases. |
| T9 |
1116-1299 |
Sentence |
denotes |
Levels of inositol 1,4,5-triphosphate (IP3) also remained unchanged and the SC dependent neuritogenesis was not inhibited by an excess amount of W-7, an inhibitor of Ca2+/CaM kinases. |
| TextSentencer_T10 |
1300-1441 |
Sentence |
denotes |
These results again accord with the suggestion that SC and GM1 do not utilize Ca2+, IP3 or Ca2+/CaM as a second messenger for neuritogenesis. |
| T10 |
1300-1441 |
Sentence |
denotes |
These results again accord with the suggestion that SC and GM1 do not utilize Ca2+, IP3 or Ca2+/CaM as a second messenger for neuritogenesis. |
| T10 |
1300-1441 |
Sentence |
denotes |
These results again accord with the suggestion that SC and GM1 do not utilize Ca2+, IP3 or Ca2+/CaM as a second messenger for neuritogenesis. |
| TextSentencer_T11 |
1442-1540 |
Sentence |
denotes |
Rather it appears very likely that the nuclear localized SC may play a key role in neuritogenesis. |
| T11 |
1442-1540 |
Sentence |
denotes |
Rather it appears very likely that the nuclear localized SC may play a key role in neuritogenesis. |
| T11 |
1442-1540 |
Sentence |
denotes |
Rather it appears very likely that the nuclear localized SC may play a key role in neuritogenesis. |