PARTIAL BLOCK TO TRANSCRIPTION OF HUMAN ADENOVIRUS TYPE-2 LATE GENES IN ABORTIVELY INFECTED MONKEY CELLS

被引：35

作者：

JOHNSTON, JM

ANDERSON, KP

KLESSIG, DF

机构：

[1] UNIV UTAH,SCH MED,DEPT CELLULAR VIRAL & MOLEC BIOL,SALT LAKE CITY,UT 84132

[2] UNIV UTAH,SCH MED,CTR INFECT DIS DIAGNOST MICROBIOL & IMMUNOL,SALT LAKE CITY,UT 84132

来源：

JOURNAL OF VIROLOGY | 1985年 / 56卷 / 02期

关键词：

D O I：

10.1128/JVI.56.2.378-385.1985

中图分类号：

Q93 [微生物学];

学科分类号：

071005 ; 100705 ;

摘要：

引用

页码：378 / 385

页数：8

共 45 条

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[2] INDEPENDENT, SPONTANEOUS MUTANTS OF ADENOVIRUS TYPE 2-SIMIAN VIRUS-40 HYBRID AD2+ND3 THAT GROW EFFICIENTLY IN MONKEY CELLS POSSESS INDENTICAL MUTATIONS IN THE ADENOVIRUS TYPE-2 DNA-BINDING PROTEIN GENE [J].

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[3]

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[4] SYNTHESIS OF HUMAN ADENOVIRUS EARLY RNA SPECIES IS SIMILAR IN PRODUCTIVE AND ABORTIVE INFECTIONS OF MONKEY AND HUMAN-CELLS [J].

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[5] ALTERED MESSENGER-RNA SPLICING IN MONKEY CELLS ABORTIVELY INFECTED WITH HUMAN ADENOVIRUS MAY BE RESPONSIBLE FOR INEFFICIENT SYNTHESIS OF THE VIRION FIBER POLYPEPTIDE [J].

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[6] THE STABILITY OF EARLY ADENOVIRUS MESSENGER-RNA IS CONTROLLED BY THE VIRAL 72KD DNA-BINDING PROTEIN [J].

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[7] EFFECT OF ADENOVIRUS ON METABOLISM OF SPECIFIC HOST MESSENGER-RNAS - TRANSPORT CONTROL AND SPECIFIC TRANSLATIONAL DISCRIMINATION [J].

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[8] INHIBITION OF HELA-CELL PROTEIN-SYNTHESIS DURING ADENOVIRUS INFECTION - RESTRICTION OF CELLULAR MESSENGER-RNA SEQUENCES TO THE NUCLEUS [J].

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[9] RESTRICTED CHANGES IN THE ADENOVIRUS DNA-BINDING PROTEIN THAT LEAD TO EXTENDED HOST RANGE OR TEMPERATURE-SENSITIVE PHENOTYPES [J].

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[10] COMPLEX SPLICING PATTERNS OF RNAS FROM THE EARLY REGIONS OF ADENOVIRUS-2 [J].

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