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[Studies on the activity of galactokinase in the blood of normal persons and of patients with GDo trisomy].

作者信息

Krone W, Wolf U, Goedde H W, Baitsch H

出版信息

Humangenetik. 1965;1(3):279-88. doi: 10.1007/BF00395658.

DOI:10.1007/BF00395658
PMID:4223835
Abstract
摘要

相似文献

1
[Studies on the activity of galactokinase in the blood of normal persons and of patients with GDo trisomy].[关于正常人及21-三体综合征患者血液中半乳糖激酶活性的研究]
Humangenetik. 1965;1(3):279-88. doi: 10.1007/BF00395658.
2
Blood cell galactose-1-phosphate uridyl transferase activity in dysplastic patients, with and without chromosomal aberrations.发育异常患者（有和没有染色体畸变）的血细胞半乳糖-1-磷酸尿苷酰转移酶活性
Hum Hered. 1969;19(6):628-40. doi: 10.1159/000152277.
3
Galactose-1-phosphate-uridyl-transferase activity in blood in translocation Down's syndrome.易位型唐氏综合征患者血液中的半乳糖-1-磷酸尿苷转移酶活性
Lancet. 1969 Oct 25;2(7626):907-8. doi: 10.1016/s0140-6736(69)92367-8.
4
Maternal enzymes of galactose metabolism and the "inexplicable" infantile cataract.
Lancet. 1974 Aug 3;2(7875):259-61. doi: 10.1016/s0140-6736(74)91417-2.
5
A patient with hereditary galactokinase deficiency.一名患有遗传性半乳糖激酶缺乏症的患者。
Acta Paediatr Scand. 1970 Nov;59(6):669-75. doi: 10.1111/j.1651-2227.1970.tb17703.x.
6
Enzymes in cultivated human fibroblasts derived from patients with autosomal trisomy syndromes.源自常染色体三体综合征患者的培养人成纤维细胞中的酶。
Am J Hum Genet. 1967 Mar;19(2):94-9.
7
ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY.
Lancet. 1964 Sep 12;2(7359):590. doi: 10.1016/s0140-6736(64)90660-9.
8
Galactokinase deficiency as a cause of cataracts.半乳糖激酶缺乏症作为白内障的一个病因
N Engl J Med. 1973 Jun 7;288(23):1203-6. doi: 10.1056/NEJM197306072882303.
9
Galactokinase: evidence for a new racial polymorphism.半乳糖激酶：一种新的种族多态性的证据。
Science. 1972 Oct 13;178(4057):176-8. doi: 10.1126/science.178.4057.176.
10
ENHANCEMENT OF ERYTHROCYTE-GALACTOKINASE ACTIVITY IN LANGDON-DOWN TRISOMY.
Lancet. 1965 Mar 6;1(7384):553. doi: 10.1016/s0140-6736(65)92057-x.

引用本文的文献

1
Elevated galactokinase activity in blood cells of patients with G-trisomy: a belated correction.G三体综合征患者血细胞中半乳糖激酶活性升高：迟来的纠正。
Humangenetik. 1970;11(1):81-2. doi: 10.1007/BF00296310.
2
[On the problem of assigning genes to definite human autosomes with the aid of chromosome aberrations].[关于借助染色体畸变将基因定位到特定人类常染色体的问题]
Humangenetik. 1967;4(2):85-103. doi: 10.1007/BF00291253.
3
[Comparative enzyme studies in blood, erythrocytes and leukocytes of mentally retarded hospitalized patients].

本文引用的文献

1
The enzymatic transformation of uridine diphosphate glucose into a galactose derivative.尿苷二磷酸葡萄糖向半乳糖衍生物的酶促转化。
Arch Biochem Biophys. 1951 Sep;33(2):186-90. doi: 10.1016/0003-9861(51)90096-3.
2
The abnormality of tryptophane metabolism in children with mongolism.蒙古症儿童色氨酸代谢异常。
Arch Dis Child. 1962 Feb;37(191):17-20. doi: 10.1136/adc.37.191.17.
3
URINARY EXCRETION OF BETA-AMINO-ISOBUTYRIC ACID AND TAURINE MONGOLISM.
Nature. 1964 Nov 14;204:650-2. doi: 10.1038/204650a0.
[住院智障患者血液、红细胞和白细胞中的酶比较研究]
Humangenetik. 1969;7(3):203-17. doi: 10.1007/BF00273169.
4
[Enzyme determination of erythrocytes of children with Down syndrome].[唐氏综合征患儿红细胞的酶测定]
Humangenetik. 1968;5(4):305-9. doi: 10.1007/BF00291638.
4
HAPTOGLOBINS AND TRANSFERRINS IN PATIENTS WITH DOWN'S SYNDROME.唐氏综合征患者体内的触珠蛋白和转铁蛋白
Ann Hum Genet. 1964 Jun;27:413-5. doi: 10.1111/j.1469-1809.1963.tb01538.x.
5
STUDIES ON GALACTOSE OXIDATION IN DOWN'S SYNDROME.
N Engl J Med. 1964 May 21;270:1085-8. doi: 10.1056/NEJM196405212702103.
6
THE ASSAY OF GALACTOKINASE AND GALACTOSE-1-PHOSPHATE URIDYL TRANSFERASE ACTIVITY IN HUMAN ERYTHROCYTES. A PRESUMED TEST FOR HETEROZYGOUS CARRIERS OF THE GALACTOSEMIC DEFECT.人红细胞中半乳糖激酶和1-磷酸半乳糖尿苷酰转移酶活性的测定。一种针对半乳糖血症缺陷杂合子携带者的推测性检测。
J Exp Med. 1963 Sep 1;118(3):359-70. doi: 10.1084/jem.118.3.359.
7
[REGULATORY MECHANISMS IN THE BIOSYNTHESIS OF THE ENZYMES OF GALACTOSE METABOLISM IN ESCHERICHIA COLI K 12. I. THE INDUCED BIOSYNTHESIS OF GALACTOKINASE AND THE SIMULTANEOUS INDUCTION OF THE ENZYMATIC SEQUENCE].[大肠杆菌K12中半乳糖代谢酶生物合成的调控机制。I. 半乳糖激酶的诱导生物合成及酶序列的同步诱导]
J Mol Biol. 1963 Aug;7:164-82. doi: 10.1016/s0022-2836(63)80044-3.
8
GALACTOSAEMIA LOCUS AND THE DOWN'S SYNDROME CHROMOSOME.半乳糖血症基因座与唐氏综合征染色体
Lancet. 1963 Oct 5;2(7310):700-3. doi: 10.1016/s0140-6736(63)90345-3.
9
STUDIES OF LEUKOCYTE ALKALINE PHOSPHATASE IN MONGOLISM: A POSSIBLE CHROMOSOME MARKER.
Blood. 1963 Aug;22:165-77.
10
Alkaline-phosphatase activity of polymorphs in mongolism.
Lancet. 1962 Dec 22;2(7269):1302-5. doi: 10.1016/s0140-6736(62)90851-6.