UPTAKE OF [6,7-H-3]OESTRADIOL-17BETA BY NORMAL AND ABNORMAL HUMAN ENDOMETRIUM

被引:48
作者
CROCKER, SG
MILTON, PJD
KING, RJB
机构
[1] IMPERIAL CANC RES FUND,HORMONE BIOCHEM DEPT,LONDON WC2A 3PX,ENGLAND
[2] ST THOMASS HOSP,GYNAECOL DEPT,LONDON SE1 7EH,ENGLAND
关键词
D O I
10.1677/joe.0.0620145
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:145 / 152
页数:8
相关论文
共 24 条
[1]   ESTROGEN AND NUCLEAR BINDING-SITES - DETERMINATION OF SPECIFIC SITES BY [H-3]OESTRADIOL EXCHANGE [J].
ANDERSON, J ;
PECK, EJ ;
CLARK, JH .
BIOCHEMICAL JOURNAL, 1972, 126 (03) :561-&
[3]   UPTAKE OF [6,7-3H]OESTRADIOL BY NORMAL HUMAN FEMALE REPRODUCTIVE TRACT [J].
BRUSH, MG ;
TAYLOR, RW ;
KING, RJB .
JOURNAL OF ENDOCRINOLOGY, 1967, 39 (04) :599-&
[5]   OESTROGEN RECEPTORS IN HUMAN UTERINE TISSUE [J].
EVANS, LH ;
HAHNEL, R .
JOURNAL OF ENDOCRINOLOGY, 1971, 50 (02) :209-&
[6]   SULFONYL FLUORIDES AS INHIBITORS OF ESTERASES .1. RATES OF REACTION WITH ACETYLCHOLINESTERASE, ALPHA-CHYMOTRYPSIN, AND TRYPSIN [J].
FAHRNEY, DE ;
GOLD, AM .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1963, 85 (07) :997-&
[7]  
GUSBERG SB, 1973, ENDOMETRIAL CANCER
[8]  
King R.J.B., 1974, STEROID CELL INTERAC
[9]  
KING RJB, 1973, ENDOMETRIAL CANCER