| Id |
Subject |
Object |
Predicate |
Lexical cue |
| TextSentencer_T1 |
0-48 |
Sentence |
denotes |
Influenza virus infection of desialylated cells. |
| T1 |
0-48 |
Sentence |
denotes |
Influenza virus infection of desialylated cells. |
| T1 |
0-48 |
Sentence |
denotes |
Influenza virus infection of desialylated cells. |
| TextSentencer_T2 |
49-130 |
Sentence |
denotes |
Sialic acid has long been considered to be the sole receptor for influenza virus. |
| T2 |
49-130 |
Sentence |
denotes |
Sialic acid has long been considered to be the sole receptor for influenza virus. |
| T2 |
49-130 |
Sentence |
denotes |
Sialic acid has long been considered to be the sole receptor for influenza virus. |
| TextSentencer_T3 |
131-344 |
Sentence |
denotes |
The viral hemagglutinin (HA) is known to bind cell surface sialic acid, and sialic acids on viral glyco-proteins are cleaved by the viral neuraminidase (NA) to promote efficient release of progeny virus particles. |
| T3 |
131-344 |
Sentence |
denotes |
The viral hemagglutinin (HA) is known to bind cell surface sialic acid, and sialic acids on viral glyco-proteins are cleaved by the viral neuraminidase (NA) to promote efficient release of progeny virus particles. |
| T3 |
131-344 |
Sentence |
denotes |
The viral hemagglutinin (HA) is known to bind cell surface sialic acid, and sialic acids on viral glyco-proteins are cleaved by the viral neuraminidase (NA) to promote efficient release of progeny virus particles. |
| TextSentencer_T4 |
345-488 |
Sentence |
denotes |
However, NWS-Mvi, a mutant virus completely lacking NA, grows well in MDCK cells continuously treated with exogenous neuraminidase (sialidase). |
| T4 |
345-488 |
Sentence |
denotes |
However, NWS-Mvi, a mutant virus completely lacking NA, grows well in MDCK cells continuously treated with exogenous neuraminidase (sialidase). |
| T4 |
345-488 |
Sentence |
denotes |
However, NWS-Mvi, a mutant virus completely lacking NA, grows well in MDCK cells continuously treated with exogenous neuraminidase (sialidase). |
| TextSentencer_T5 |
489-670 |
Sentence |
denotes |
Exogenous sialidase quantitatively releases all sialic acids from purified glycoproteins and glycolipids of MDCK cells and efficiently removes surface sialic acid from intact cells. |
| T5 |
489-670 |
Sentence |
denotes |
Exogenous sialidase quantitatively releases all sialic acids from purified glycoproteins and glycolipids of MDCK cells and efficiently removes surface sialic acid from intact cells. |
| T5 |
489-670 |
Sentence |
denotes |
Exogenous sialidase quantitatively releases all sialic acids from purified glycoproteins and glycolipids of MDCK cells and efficiently removes surface sialic acid from intact cells. |
| TextSentencer_T6 |
671-821 |
Sentence |
denotes |
Binding of NWS-Mvi and parent influenza viruses to MDCK cells is indistinguishable, and is only partially reduced by sialidase treatment of the cells. |
| T6 |
671-821 |
Sentence |
denotes |
Binding of NWS-Mvi and parent influenza viruses to MDCK cells is indistinguishable, and is only partially reduced by sialidase treatment of the cells. |
| T6 |
671-821 |
Sentence |
denotes |
Binding of NWS-Mvi and parent influenza viruses to MDCK cells is indistinguishable, and is only partially reduced by sialidase treatment of the cells. |
| TextSentencer_T7 |
822-922 |
Sentence |
denotes |
Both mutant and wild-type viruses enter enzymatically desialylated cells and initiate transcription. |
| T7 |
822-922 |
Sentence |
denotes |
Both mutant and wild-type viruses enter enzymatically desialylated cells and initiate transcription. |
| T7 |
822-922 |
Sentence |
denotes |
Both mutant and wild-type viruses enter enzymatically desialylated cells and initiate transcription. |
| TextSentencer_T8 |
923-1113 |
Sentence |
denotes |
The ability of influenza A reassortant viruses to infect desialylated cells is shared by recent H3N2 clinical isolates, suggesting that this may be a general property of influenza A viruses. |
| T8 |
923-1113 |
Sentence |
denotes |
The ability of influenza A reassortant viruses to infect desialylated cells is shared by recent H3N2 clinical isolates, suggesting that this may be a general property of influenza A viruses. |
| T8 |
923-1113 |
Sentence |
denotes |
The ability of influenza A reassortant viruses to infect desialylated cells is shared by recent H3N2 clinical isolates, suggesting that this may be a general property of influenza A viruses. |
| TextSentencer_T9 |
1114-1250 |
Sentence |
denotes |
We propose that influenza virus infection can result from sialic acid-independent receptors, either directly or in a multistage process. |
| T9 |
1114-1250 |
Sentence |
denotes |
We propose that influenza virus infection can result from sialic acid-independent receptors, either directly or in a multistage process. |
| T9 |
1114-1250 |
Sentence |
denotes |
We propose that influenza virus infection can result from sialic acid-independent receptors, either directly or in a multistage process. |
| TextSentencer_T10 |
1251-1402 |
Sentence |
denotes |
When sialic acid is present, it may act to enhance virus binding to the cell surface to increase interaction with secondary receptors to mediate entry. |
| T10 |
1251-1402 |
Sentence |
denotes |
When sialic acid is present, it may act to enhance virus binding to the cell surface to increase interaction with secondary receptors to mediate entry. |
| T10 |
1251-1402 |
Sentence |
denotes |
When sialic acid is present, it may act to enhance virus binding to the cell surface to increase interaction with secondary receptors to mediate entry. |
| TextSentencer_T11 |
1403-1501 |
Sentence |
denotes |
Understanding virus entry will be critical to further efforts in infection control and prevention. |
| T11 |
1403-1501 |
Sentence |
denotes |
Understanding virus entry will be critical to further efforts in infection control and prevention. |
| T11 |
1403-1501 |
Sentence |
denotes |
Understanding virus entry will be critical to further efforts in infection control and prevention. |