EFFECT OF 5-AZACYTIDINE TREATMENT ON MOUSE EMBRYONAL CARCINOMA-CELLS

被引：14
作者：
CREMISI, C
机构：
来源：
JOURNAL OF CELLULAR PHYSIOLOGY | 1983年 / 116卷 / 02期
关键词：
D O I：
10.1002/jcp.1041160209
中图分类号：
Q2 [细胞生物学];
学科分类号：
071009 ; 090102 ;
摘要：
引用
收藏
页码：181 / 190
页数：10
相关论文
共 50 条
[41]   THE CHARACTERISTICS OF EMBRYONAL CARCINOMA-CELLS IN TERATOCARCINOMAS [J].
BRAWN, PN .
CANCER, 1987, 59 (12) :2042-2046
[42]   INTERFERON ENHANCES 2-5A SYNTHETASE IN EMBRYONAL CARCINOMA-CELLS [J].
WOOD, JN ;
HOVANESSIAN, AG .
NATURE, 1979, 282 (5734) :74-76
[43]   PYCNOTIC DEGENERATION OF CENTRICULAR CELLS OF EMBRYONIC MOUSE BRAIN CAUSED BY 5-AZACYTIDINE [J].
SEIFERTO.M .
STUDIA BIOPHYSICA, 1972, 31 :375-382
[44]   ONCOGENE EXPRESSION IN DIFFERENTIATING F9 MOUSE EMBRYONAL CARCINOMA-CELLS [J].
LOCKETT, TJ ;
SLEIGH, MJ .
EXPERIMENTAL CELL RESEARCH, 1987, 173 (02) :370-378
[45]   CYTO-TOXICITY OF PLANT-LECTINS FOR MOUSE EMBRYONAL CARCINOMA-CELLS [J].
DRABER, P ;
STANLEY, P .
SOMATIC CELL AND MOLECULAR GENETICS, 1984, 10 (05) :435-443
[46]   INDUCTION OF MOUSE 8-CELL BLASTOMERE POLARIZATION BY EMBRYONAL CARCINOMA-CELLS [J].
ADLER, RR ;
ZIOMEK, CA .
JOURNAL OF CELL BIOLOGY, 1986, 103 (05) :A88-A88
[47]   JUNCTIONAL MODULATION IN MOUSE EMBRYONAL CARCINOMA-CELLS BY FAB FRAGMENTS OF RABBIT ANTI-EMBRYONAL CARCINOMA CELL SERUM [J].
DUNIA, I ;
NICOLAS, JF ;
JAKOB, H ;
BENEDETTI, EL ;
JACOB, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (07) :3387-3391
[48]   COMPARATIVE-ANALYSIS OF RETROVIRAL VECTOR EXPRESSION IN MOUSE EMBRYONAL CARCINOMA-CELLS [J].
HAWLEY, TS ;
SABOURIN, LA ;
HAWLEY, RG .
PLASMID, 1989, 22 (02) :120-131
[49]   INCREASED SIALYLATION OF COMPLEX GLYCOPEPTIDES DURING DIFFERENTIATION OF MOUSE EMBRYONAL CARCINOMA-CELLS [J].
COSSU, G ;
CORTESI, E ;
WARREN, L .
DIFFERENTIATION, 1985, 29 (01) :63-67
[50]   Effects of 5-azacytidine on the development of parthenogenetic mouse embryos [J].
Penkov, LI ;
Platonov, ES ;
Mironova, OV ;
Konyukhov, BV .
DEVELOPMENT GROWTH & DIFFERENTIATION, 1996, 38 (03) :263-270
12345