[一组患有家族性全骨髓病（范可尼型）的亲属血细胞中的己糖激酶缺乏症] - Suppr

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超能文献

[Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)].

作者信息

Löhr G W, Waller H D, Anschütz F, Knopp A

出版信息

Klin Wochenschr. 1965 Aug 15;43(16):870-5. doi: 10.1007/BF01711251.

DOI:10.1007/BF01711251

PMID:5862690

Abstract

摘要

相似文献

[Hexokinase deficiency in blood cells in a group of kin with familial panmyelopathy (Fanconi type)].[一组患有家族性全骨髓病（范可尼型）的亲属血细胞中的己糖激酶缺乏症]

Klin Wochenschr. 1965 Aug 15;43(16):870-5. doi: 10.1007/BF01711251.

Regulation of glycolysis in human red cells.人类红细胞中糖酵解的调节

Folia Haematol Int Mag Klin Morphol Blutforsch. 1968;89(4):357-75.

[Biochemical defects in the blood cells in familial panmyelopathy (Fanconi type)].[家族性全骨髓病（范科尼型）血细胞中的生化缺陷]

Humangenetik. 1965;1(4):383-7. doi: 10.1007/BF00273980.

[Cytogenetic finding and etiology of Fanconi's anemia. A case of Fanconi's anemia without hexokinase deficiency].[范科尼贫血的细胞遗传学发现及病因。一例无己糖激酶缺乏的范科尼贫血病例]

Humangenetik. 1966;3(1):76-81. doi: 10.1007/BF00273021.

[Cytogenic and biochemical studies of 8 cases of Fanconi's anemia].

Ann Genet. 1972 Mar;15(1):29-40.

[Behavior of the hexokinase activity in rickets in man].[人类佝偻病中己糖激酶活性的表现]

Folia Haematol Int Mag Klin Morphol Blutforsch. 1965;83(3):340-6.

Behaviour of enzyme systems in cercopithecus and rhesus kidney cells in consequence of SV40 virus action.猿猴和恒河猴肾细胞中酶系统在SV40病毒作用下的行为。

Prog Immunobiol Stand. 1967;3:136-8.

Carbohydrate metabolism in rat uterus during the oestrous cycle.大鼠发情周期中子宫的碳水化合物代谢

Steroids Lipids Res. 1973;4(5):341-50.

[Attempt at a mathematical description of the effect of ATP and F6P on the HK-PFK system in erythrocytes at pH 8.4].[对pH 8.4时ATP和F6P对红细胞中HK-PFK系统影响的数学描述尝试]

Acta Biol Med Ger. 1970;24(3):253-62.

[Chromosome abnormalities in constitutional cytopenia].[体质性血细胞减少中的染色体异常]

Nouv Rev Fr Hematol. 1970 Jan-Feb;10(1):107-17.

引用本文的文献

Proliferative kinetics and mitomycin C-induced chromosome damage in Fanconi's anemia lymphocytes.范科尼贫血淋巴细胞的增殖动力学及丝裂霉素C诱导的染色体损伤

Hum Genet. 1983;63(1):19-23. doi: 10.1007/BF00285391.

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[Cytogenetic and cytologic findings in enzymopenic panmyelopathies and pancytopenias. Familial myelopathy of Fanconi, glutathione-reductase deficiency anemia and megaloblastic B12 deficiency anemia].

Humangenetik. 1966;2(3):287-316. doi: 10.1007/BF00395947.

Bloom's syndrome. I. Genetical and clinical observations in the first twenty-seven patients.布卢姆综合征。一、首批27例患者的遗传学和临床观察。

Am J Hum Genet. 1969 Mar;21(2):196-227.

[Glutathione reduction in erythrocytes of healthy persons and enzyme defect carriers. Use of the azoester test by Kosower et al. in glucose-6-P-dehydrogenase and glutathione reductase deficiency].[健康人和酶缺陷携带者红细胞中的谷胱甘肽还原。科索尔等人的偶氮酯试验在葡萄糖-6-磷酸脱氢酶和谷胱甘肽还原酶缺乏症中的应用]

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[Hexokinase isoenzymes in normal erythrocytes of adults and newborns and in various hyperregenerative anemias].[成人及新生儿正常红细胞和各种增生性贫血中的己糖激酶同工酶]

Klin Wochenschr. 1969 Jul 15;47(14):772-8. doi: 10.1007/BF01880123.

Chromosomal peculiarities and "in vitro" examinations in Fanconi's anaemia.范科尼贫血的染色体特性及“体外”检查

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[Contribution to the pathogenesis of the Fanconi anemia].[对范可尼贫血发病机制的贡献]

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Diagnosis of red blood cell enzymopathies in infants, children and adolescents.婴幼儿、儿童及青少年红细胞酶病的诊断

Indian J Pediatr. 1987 May-Jun;54(3):355-67. doi: 10.1007/BF02748920.

Clinical and cytogenetic observations during a six-year period in an adult with Fanconi's anaemia.

Blut. 1977 Feb;34(2):119-32. doi: 10.1007/BF00999858.

本文引用的文献

Spectrophotometric measurement of hexokinase and phosphohexokinase activity.分光光度法测定己糖激酶和磷酸己糖激酶活性。

J Biol Chem. 1947 Mar;167(3):843-54.

[Sensitive photometric method for the determination of hemoglobin and hemoglobin].用于测定血红蛋白和血红蛋白的灵敏光度法。

Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1947;204(1-3):190-202.

Biosynthesis of tricarboxylic acids by carbon dioxide fixation; enzymatic mechanisms.通过二氧化碳固定进行三羧酸的生物合成；酶促机制。

J Biol Chem. 1948 May;174(1):133-57.

Chronic pancytopenia with multiple congenital abnormalities (Fanconi's anaemia).

Acta Paediatr (Stockh). 1960 Jul;49:518-29. doi: 10.1111/j.1651-2227.1960.tb07767.x.

[FAMILIAL PANMYELOPATHY].[家族性全骨髓病]

Schweiz Med Wochenschr. 1964 Sep 19;94:1309-18.

[STUDIES ON HEMOLYSIS IN FANCONI'S ANEMIA. INCREASE OF ATP-ASE AS A POSSIBLE CAUSE FOR DECEASED ATP VALUES].[范科尼贫血中的溶血研究。ATP酶增加作为ATP值降低的可能原因]

Dtsch Med Wochenschr. 1965 Feb 12;90:290-6. doi: 10.1055/s-0028-1111334.

[HYPOTHESIS OF CHROMOSOMAL TRANSLOCATION AS A GENETIC INTERPRETATION OF FANCONI'S FAMILIAL CONSTITUTIONAL PANMYELOPATHY].[染色体易位假说作为范可尼家族性体质性全骨髓病的遗传学解释]

Helv Paediatr Acta. 1964 Jun;19:29-33.

ADENOSINE-TRIPHOSPHATASE DEFICIENCY IN PATIENTS WITH NON-SPHEROCYTIC HAEMOLYTIC ANAEMIA.非球形红细胞溶血性贫血患者的三磷酸腺苷酶缺乏症

Lancet. 1964 Jul 4;2(7349):18-9. doi: 10.1016/s0140-6736(64)90009-1.

PURIFICATION AND PROPERTIES OF GLUTATHIONE REDUCTASE OF HUMAN ERYTHROCYTES.人红细胞谷胱甘肽还原酶的纯化及性质

J Biol Chem. 1963 Dec;238:3928-33.

[Panmyelopathies in childhood. Study of Fanconi's anemia].

Helv Paediatr Acta. 1961 Dec;16:752-94.

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