NOVEL 2',5'-OLIGOADENYLATES SYNTHESIZED IN INTERFERON-TREATED, VACCINA VIRUS-INFECTED CELLS

被引：28

作者：

RICE, AP ^{[1
]}

KERR, SM ^{[1
]}

ROBERTS, WK ^{[1
]}

BROWN, RE ^{[1
]}

KERR, IM ^{[1
]}

机构：

[1] IMPERIAL CANC RES FUND,LONDON WC2A 3PX,ENGLAND

来源：

JOURNAL OF VIROLOGY | 1985年 / 56卷 / 03期

关键词：

D O I：

10.1128/JVI.56.3.1041-1044.1985

中图分类号：

Q93 [微生物学];

学科分类号：

071005 ; 100705 ;

摘要：

引用

页码：1041 / 1044

页数：4

共 17 条

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[3]

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[4]

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[5] ACTIVATION OF THE PPP(A2'P)NA SYSTEM IN INTERFERON-TREATED, HERPES-SIMPLEX VIRUS-INFECTED CELLS AND EVIDENCE FOR NOVEL INHIBITORS OF THE PPP(A2'P)NA-DEPENDENT RNASE [J].

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[7] THE 2'5' OLIGOADENYLATE SYNTHETASE HAS A MULTIFUNCTIONAL 2'5' NUCLEOTIDYL-TRANSFERASE ACTIVITY [J].

FERBUS, D ;

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[8]

GOSWAMI BB, 1984, J BIOL CHEM, V259, P1371

[9] ANALOGS AND ANALOG INHIBITORS OF PPP(A2'P)NA - THEIR STABILITY AND BIOLOGICAL-ACTIVITY [J].

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[10]

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