CONTROLLER-GENE DISEASES - OPERON MODEL AS APPLIED TO BETA-THALASSEMIA FAMILIAL FETAL HEMOGLOBINEMIA + NORMAL SWITCH FROM PRODUCTION OF FETAL HEMOGLOBIN TO THAT OF ADULT HEMOGLOBIN

被引:80
作者
ZUCKERKANDL, E
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D O I
10.1016/S0022-2836(64)80154-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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页码:128 / &
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共 44 条
[1]  
BAGLIONI C, 1963, MOLECULAR GENETICS 1, P405
[2]  
BRADLEY TB, 1960, T ASSOC AM PHYSICIAN, V73, P72
[3]  
CEPPELLINI R, 1959, BIOCHEMISTRY HUMAN G, P133
[4]  
CRICK F H, 1958, Symp Soc Exp Biol, V12, P138
[6]   GENETIC CODE - EMERGENCE OF A SYMMETRICAL PATTERN [J].
ECK, RV .
SCIENCE, 1963, 140 (356) :477-&
[7]   HEMOGLOBIN METABOLISM IN THALASSEMIA - INVIVO STUDIES [J].
GRINSTEIN, M ;
BANNERMAN, RM ;
VAVRA, JD ;
MOORE, CV .
AMERICAN JOURNAL OF MEDICINE, 1960, 29 (01) :18-32
[8]  
GUIDOTTI G, 1962, SCIENCE, V138, P996
[9]   HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN - A FAMILY STUDY [J].
HERMAN, EC ;
CONLEY, CL .
AMERICAN JOURNAL OF MEDICINE, 1960, 29 (01) :9-17
[10]   REACTION OF HAEMOGLOBIN ALPHAA WITH HAEMOGLOBIN H [J].
HUEHNS, ER ;
SHOOTER, EM .
NATURE, 1962, 193 (4820) :1083-&