PROTEIN TYROSINE KINASES, PROTEIN SERINE KINASES, AND THE MECHANISM OF ACTION OF INSULIN

被引：0
作者：
ROSEN, OM
机构：
来源：
HARVEY LECTURES | 1988年 / 82卷
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中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
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页码：105 / 122
页数：18
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共 49 条
[1]   TRANSFORMATION OF RAT FIBROBLASTS BY FSV RAPIDLY INCREASES GLUCOSE TRANSPORTER GENE-TRANSCRIPTION [J].
BIRNBAUM, MJ ;
HASPEL, HC ;
ROSEN, OM .
SCIENCE, 1987, 235 (4795) :1495-1498
[2]   CLONING AND CHARACTERIZATION OF A CDNA-ENCODING THE RAT-BRAIN GLUCOSE-TRANSPORTER PROTEIN [J].
BIRNBAUM, MJ ;
HASPEL, HC ;
ROSEN, OM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :5784-5788
[3]  
BRIDGES MA, 1987, CELL BIOCH C S, V11, P64
[4]   CELL-TRANSFORMATION BY PP60C-SRC MUTATED IN THE CARBOXY-TERMINAL REGULATORY DOMAIN [J].
CARTWRIGHT, CA ;
ECKHART, W ;
SIMON, S ;
KAPLAN, PL .
CELL, 1987, 49 (01) :83-91
[5]  
CHOU CK, 1987, J BIOL CHEM, V262, P1842
[6]  
COHEN P, 1985, MOL BASIS INSULIN AC, P213
[7]   THE NATURE AND REGULATION OF THE INSULIN-RECEPTOR - STRUCTURE AND FUNCTION [J].
CZECH, MP .
ANNUAL REVIEW OF PHYSIOLOGY, 1985, 47 :357-381
[8]   LATENT INSULIN-RECEPTORS AND POSSIBLE RECEPTOR PRECURSORS IN 3T3-L1 ADIPOCYTES [J].
DEUTSCH, PJ ;
WAN, CF ;
ROSEN, OM ;
RUBIN, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (01) :133-136
[9]   REPLACEMENT OF LYSINE RESIDUE 1030 IN THE PUTATIVE ATP-BINDING REGION OF THE INSULIN-RECEPTOR ABOLISHES INSULIN-STIMULATED AND ANTIBODY-STIMULATED GLUCOSE-UPTAKE AND RECEPTOR KINASE-ACTIVITY [J].
EBINA, Y ;
ARAKI, E ;
TAIRA, M ;
SHIMADA, F ;
MORI, M ;
CRAIK, CS ;
SIDDLE, K ;
PIERCE, SB ;
ROTH, RA ;
RUTTER, WJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (03) :704-708
[10]   REPLACEMENT OF INSULIN-RECEPTOR TYROSINE RESIDUES 1162 AND 1163 COMPROMISES INSULIN-STIMULATED KINASE-ACTIVITY AND UPTAKE OF 2-DEOXYGLUCOSE [J].
ELLIS, L ;
CLAUSER, E ;
MORGAN, DO ;
EDERY, M ;
ROTH, RA ;
RUTTER, WJ .
CELL, 1986, 45 (05) :721-732
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