FAMILY STUDIES ON GLUTATHIONE REDUCTASE FROM RED BLOOD CELLS

被引：21

作者：

BLUME, KG

GOTTWIK, M

LOHR, GW

RUDIGER, HW

机构：

[1] Medizinische Poliklinik der Universität Marburg a. d. Lahn, Marburg a. d. Lahn

来源：

HUMANGENETIK | 1968年 / 6卷 / 02期

关键词：

D O I：

10.1007/BF00297725

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

We report on formal genetical studies of glutathione reductase from human red blood cells. Heterozygotes can he distinguished from normals by determination of glutathione reductase activity, electrophoresis of this enzyme, and Heinz-body-test. Probably the enzyme protein are qualitatively and quantitatively different (biochemical data and electrophoretic behaviour). The mode of inheritance of glutathione reductase deficiency is autosomally dominant. © 1968 Springer-Verlag.

引用

页码：163 / +

页数：1

共 39 条

[1] BERGMEYER HU, METHODEN ENZYMATI ED, P758
[2] A SERIES OF NEW SCREENING PROCEDURES FOR PYRUVATE KINASE DEFICIENCY GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND GLUTATHIONE REDUCTASE DEFICIENCY
BEUTLER, E
[J]. BLOOD-THE JOURNAL OF HEMATOLOGY, 1966, 28 (04): : 553 - &
[3] BEUTLER E, 1954, J LAB CLIN MED, V44, P177
[4] ERYTHROCYTE GLUTATHIONE REDUCTASE
BEUTLER, E
YEH, MKY
[J]. BLOOD, 1963, 21 (05) : 573 - &
[5] BEUTLER E, 1956, J CLIN INVEST, V35, P690
[6] ELECTROPHORESIS OF GLUTATHIONE REDUCTASE FROM HUMAN RES BLOOD CELLS
BLUME, KG
RUDIGER, HW
LOHR, GW
[J]. BIOCHIMICA ET BIOPHYSICA ACTA, 1968, 151 (03) : 686 - &
[7] BLUME KG, IN PRESS
[8] ANGEBORENE NICHTSPHAROCYTARE HAMOLYTISCHE ANAMIE BEI FAMILIAREM MANGEL AN DPNH- UND TPNH-ABHANGIGER GLUTATHIONREDUKTASE DER ERYTHROCYTEN
BRITTING.G
LOFFLER, G
KONIG, E
[J]. KLINISCHE WOCHENSCHRIFT, 1965, 43 (08): : 427 - &
[9] BUZARD JA, 1963, J BIOL CHEM, V238, P464
[10] GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND RELATED DISORDERS OF PENTOSE PHOSPHATE PATHWAY
CARSON, PE
FRISCHER, H
[J]. AMERICAN JOURNAL OF MEDICINE, 1966, 41 (05) : 744 - +

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