ISOLATION AND CHARACTERIZATION OF VARIANT CDNAS ENCODING MOUSE TYROSINASE

被引：29

作者：

TERAO, M ^{[1
]}

TABE, L ^{[1
]}

GARATTINI, E ^{[1
]}

SARTORI, D ^{[1
]}

STUDER, M ^{[1
]}

MINTZ, B ^{[1
]}

机构：

[1] FOX CHASE CANC CTR,INST CANC RES,PHILADELPHIA,PA 19111

来源：

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | 1989年 / 159卷 / 02期

关键词：

D O I：

10.1016/0006-291X(89)90072-7

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：848 / 853

页数：6

共 21 条

[1] ALTERNATIVE SPLICING - A UBIQUITOUS MECHANISM FOR THE GENERATION OF MULTIPLE PROTEIN ISOFORMS FROM SINGLE GENES [J].

BREITBART, RE ;

ANDREADIS, A ;

NADALGINARD, B .

ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :467-495

[2]

BURNETT JB, 1967, CANCER RES, V27, P880

[3]

FREIBERG AP, 1984, ANAL BIOCHEM, V137, P266

[4] MAMMALIAN TYROSINASE - STRUCTURAL AND FUNCTIONAL INTERRELATIONSHIP OF ISOZYMES [J].

HEARING, VJ ;

NICHOLSON, JM ;

MONTAGUE, PM ;

EKEL, TM ;

TOMECKI, KJ .

BIOCHIMICA ET BIOPHYSICA ACTA, 1978, 522 (02) :327-339

[5] UNIDIRECTIONAL DIGESTION WITH EXONUCLEASE-III CREATES TARGETED BREAKPOINTS FOR DNA SEQUENCING [J].

HENIKOFF, S .

GENE, 1984, 28 (03) :351-359

[6]

Huynh TV, 1985, DNA CLONING TECHNIQU, V1, P49

[7] MAMMALIAN TYROSINASE CATALYZES 3 REACTIONS IN THE BIOSYNTHESIS OF MELANIN [J].

KORNER, A ;

PAWELEK, J .

SCIENCE, 1982, 217 (4565) :1163-1165

[8] FUNCTIONAL MESSENGER-RNAS ARE PRODUCED BY SP6 INVITRO TRANSCRIPTION OF CLONED CDNAS [J].

KRIEG, PA ;

MELTON, DA .

NUCLEIC ACIDS RESEARCH, 1984, 12 (18) :7057-7070

[9] SEQUENCE-ANALYSIS OF MOUSE TYROSINASE CDNA AND THE EFFECT OF MELANOTROPIN ON ITS GENE-EXPRESSION [J].

KWON, BS ;

WAKULCHIK, M ;

HAQ, AK ;

HALABAN, R ;

KESTLER, D .

BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (03) :1301-1309

[10] ISOLATION AND SEQUENCE OF A CDNA CLONE FOR HUMAN TYROSINASE THAT MAPS AT THE MOUSE C-ALBINO LOCUS [J].

KWON, BS ;

HAQ, AK ;

POMERANTZ, SH ;

HALABAN, R .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7473-7477

← 1 2 3 →