INHIBITION OF RIBONUCLEASES BY RIBONUCLEOTIDES AND TRANSITION-STATE ANALOGS IN CELL-FREE-EXTRACTS FROM EHRLICH ASCITES TUMOR-CELLS

被引：12

作者：

EGBERTS, E ^{[1
]}

HACKETT, PB ^{[1
]}

TRAUB, P ^{[1
]}

机构：

[1] MAX PLANCK INST ZELLBIOL,D-2940 WILHELMSHAVEN,FED REP GER

来源：

HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE | 1977年 / 358卷 / 04期

关键词：

D O I：

10.1515/bchm2.1977.358.1.475

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

引用

页码：475 / 490

页数：16

共 24 条

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[12] PURIFICATION AND PROPERTIES OF A NUCLEAR EXORIONUCLEASE FROM EHRLICH ASCITES TUMOR CELLS
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 57 (05) : 1386 - &
[13] STUDIES ON ALLOSTERIC PROPERTIES OF NUCLEAR EXORIBONUCLEASE FROM EHRLICH ASCITES TUMOR
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SPORN, MB
[J]. BIOCHEMISTRY, 1971, 10 (03) : 505 - &
[14] A NEW KINETIC MODEL FOR POLYNUCLEOTIDE METABOLISM
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[J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1968, 60 (04) : 1503 - &
[15] ENZYMATIC CATALYSIS AND TRANSITION-STATE THEORY OF REACTION-RATES - TRANSITION-STATE ANALOGS
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LINDQUIS.RN
SECEMSKI, II
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[J]. COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY, 1971, 36 : 45 - +
[16] ISOLATION OF MESSENGER-RNA FROM KB-CELLS BY AFFINITY CHROMATOGRAPHY ON POLYURIDYLIC ACID COVALENTLY LINKED TO SEPHAROSE
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PERSSON, T
[J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1972, 31 (02): : 246 - &
[17] CHARACTERIZATION OF A HIGHLY EFFICIENT PROTEIN SYNTHESIZING SYSTEM DERIVED FROM COMMERCIAL WHEAT-GERM
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[J]. NUCLEIC ACIDS RESEARCH, 1974, 1 (11) : 1385 - 1397
[18] MAMMALIAN CELL-FREE PROTEIN SYNTHESIS DIRECTED BY VIRAL RIBONUCLEIC ACID
MATHEWS, MB
KORNER, A
[J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1970, 17 (02): : 328 - &
[19] ION-EXCHANGE THIN-LAYER CHROMATOGRAPHY .14. SEPARATION OF NUCLEOTIDE SUGARS AND NUCLEOSIDE MONOPHOSPHATES ON PEI-CELLULOSE
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RANDERATH, E
[J]. ANALYTICAL BIOCHEMISTRY, 1965, 13 (03) : 575 - +
[20] RIBONUCLEASE .2. ACTIVATORS AND INHIBITORS FOR RIBONUCLEASE
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[J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1953, 44 (02) : 265 - 270

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