异常红细胞丙酮酸激酶的一些特性。 - Suppr

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超能文献

Some properties of abnormal red blood cell pyruvate kinase.

作者信息

Staal G E, Koster J F, van Milligen-Boersma L

出版信息

Biochim Biophys Acta. 1970 Dec 16;220(3):613-6. doi: 10.1016/0005-2744(70)90293-7.

DOI:10.1016/0005-2744(70)90293-7

PMID:5499640

Abstract

摘要

相似文献

Some properties of abnormal red blood cell pyruvate kinase.异常红细胞丙酮酸激酶的一些特性。

Biochim Biophys Acta. 1970 Dec 16;220(3):613-6. doi: 10.1016/0005-2744(70)90293-7.

Screening of hereditary spherocytosis and pyruvate kinase deficiency by automated blood count using erythrocytic and reticulocytic parameters.应用红细胞和网织红细胞参数的自动化血细胞计数筛选遗传性球形红细胞增多症和丙酮酸激酶缺乏症。

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Intracellular free magnesium and phosphorylated metabolites in hexokinase- and pyruvate kinase-deficient red cells measured using 31P-NMR spectroscopy.使用31P核磁共振波谱法测量己糖激酶和丙酮酸激酶缺陷红细胞中的细胞内游离镁和磷酸化代谢物。

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Red blood cell age, pyruvate kinase activity, and insulin receptors. Evidence that monocytes and RBCs may behave differently.

Diabetes. 1983 Nov;32(11):1017-22. doi: 10.2337/diab.32.11.1017.

Familial hemolytic anemia resulting from an abnormal red blood cell pyruvate kinase.由异常红细胞丙酮酸激酶引起的家族性溶血性贫血。

J Lab Clin Med. 1968 Sep;72(3):359-62.

Free and bound pyruvate kinase from fish brain: properties and redistribution after hypoxia.鱼脑游离和结合丙酮酸激酶：缺氧后的性质与重新分布

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[Effect of methylguanidine and guanidinosuccinic acid on pyruvate kinase activity in human red cells].

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Purification and properties of pyruvate kinase in normal and in pyruvate kinase deficient human red blood cells.正常及丙酮酸激酶缺乏的人红细胞中丙酮酸激酶的纯化及性质

Biochim Biophys Acta. 1971 Feb 10;227(2):364-72. doi: 10.1016/0005-2744(71)90068-4.

A modified screening procedure to detect pyruvate kinase deficiency.一种用于检测丙酮酸激酶缺乏症的改良筛查程序。

Am J Clin Pathol. 1993 Feb;99(2):128-31. doi: 10.1093/ajcp/99.2.128.

Cord blood transplantation in a young child with pyruvate kinase deficiency.丙酮酸激酶缺乏症幼儿的脐血移植

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引用本文的文献

Hereditary erythrocyte pyruvate-kinase (PK) deficiency and chronic hemolytic anemia: clinical, genetic and molecular studies in six new Spanish patients.遗传性红细胞丙酮酸激酶（PK）缺乏症与慢性溶血性贫血：对6名西班牙新患者的临床、遗传及分子研究

Hum Genet. 1980;53(3):401-8. doi: 10.1007/BF00287063.

A new pyruvate kinase variant (PK Osaka) demonstrated by partial purification and condensation.通过部分纯化和浓缩鉴定出一种新的丙酮酸激酶变体（大阪丙酮酸激酶）。

Am J Hum Genet. 1976 Sep;28(5):474-81.

[Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].非球形红细胞性溶血性贫血中红细胞糖酵解及核苷酸代谢的酶缺乏（作者译）

Klin Wochenschr. 1976 Sep 1;54(17):803-21. doi: 10.1007/BF01469302.

A monomeric form of pyruvate kinase in human pyruvate kinase deficiency.人类丙酮酸激酶缺乏症中的丙酮酸激酶单体形式。

Proc Natl Acad Sci U S A. 1977 Feb;74(2):501-4. doi: 10.1073/pnas.74.2.501.

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