DETECTION OF PHOSPHOHEXOSE ISOMERASE DEFICIENCY IN HUMAN FIBROBLAST CULTURES

被引：13

作者：

KRONE, W

SCHNEIDE.G

SCHULZ, D

ARNOLD, H

BLUME, KG

机构：

来源：

HUMANGENETIK | 1970年 / 10卷 / 03期

关键词：

D O I：

10.1007/BF00295784

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：224 / &

共 11 条

[1]

ARNOLD H, IN PRESS

[2] HEREDITARY HEMOLYTIC ANEMIA ASSOCIATED WITH GLUCOSEPHOSPHATE ISOMERASE (GPI) DEFICIENCY - A NEW ENZYME DEFECT OF HUMAN ERYTHROCYTES [J].

BAUGHAN, MA ;

VALENTINE, WN ;

PAGLIA, DE ;

WAYS, PO ;

SIMONS, ER ;

DEMARSH, QB .

BLOOD, 1968, 32 (02) :236-+

[3]

DAVIDSON RG, 1970, MODERN TRENDS HUMAN, V1, P143

[4]

DEMARS R, 1964, 13 NAT CANC I MON, P181

[5] INHERITED VARIATIONS IN HUMAN PHOSPHOHEXOSE ISOMERASE [J].

DETTER, JC ;

WAYS, PO ;

GIBLETT, ER ;

BAUGHAN, MA ;

HOPKINSO.DA ;

POVEY, S ;

HARRIS, H .

ANNALS OF HUMAN GENETICS, 1968, 31 :329-&

[6]

EVANS VJ, 1947, J NATL CANCER I, V8, P103

[7]

LOWRY OH, 1951, J BIOL CHEM, V193, P265

[8] OCCURRENCE OF DEFECTIVE HEXOSEPHOSPHATE ISOMERIZATION IN HUMAN ERYTHROCYTES AND LEUKOCYTES [J].

PAGLIA, DE ;

HOLLAND, P ;

BAUGHAN, MA ;

VALENTINE, WN .

NEW ENGLAND JOURNAL OF MEDICINE, 1969, 280 (02) :66-+

[9]

SCHIMKE RT, 1969, CURRENT TOPICS CELLU, V1, P77

[10]

SELVYN JG, 1954, BLOOD, V9, P414

← 1 2 →