遗传性球形红细胞增多症中红细胞膜特定蛋白质的异常。 - Suppr

Suppr

超能文献

Abnormality in a specific protein of the erythrocyte membrane in hereditary spherocytosis.

作者信息

Hayashi S, Koomoto R, Yano A, Ishigami S, Tsujino G

出版信息

Biochem Biophys Res Commun. 1974 Apr 23;57(4):1038-44. doi: 10.1016/0006-291x(74)90801-8.

DOI:10.1016/0006-291x(74)90801-8

PMID:4830746

Abstract

摘要

相似文献

Abnormality in a specific protein of the erythrocyte membrane in hereditary spherocytosis.遗传性球形红细胞增多症中红细胞膜特定蛋白质的异常。

Biochem Biophys Res Commun. 1974 Apr 23;57(4):1038-44. doi: 10.1016/0006-291x(74)90801-8.

A red cell membrane protein abnormality in hereditary spherocytosis.遗传性球形红细胞增多症中的红细胞膜蛋白异常。

Br J Haematol. 1972 Sep;23(3):363-70. doi: 10.1111/j.1365-2141.1972.tb08883.x.

Hereditary spherocytosis with normal osmotic fragility after incubation. Is the autohemolysis test really obsolete?孵育后渗透脆性正常的遗传性球形红细胞增多症。自体溶血试验真的过时了吗？

JAMA. 1979 Jul 6;242(1):63-4.

Modified osmotic fragility test for the laboratory diagnosis of hereditary spherocytosis.

Am J Hematol. 1989 Jun;31(2):136-7. doi: 10.1002/ajh.2830310214.

Erythrocyte membrane vacuole formation in hereditary spherocytosis.遗传性球形红细胞增多症中的红细胞膜空泡形成

Br J Haematol. 1974 Jan;26(1):59-69. doi: 10.1111/j.1365-2141.1974.tb00449.x.

[Flow-assisted differential diagnosis of hemolytic anemia with spherocytosis: a case report].[流式细胞术辅助诊断球形红细胞增多症所致溶血性贫血：一例报告]

Korean J Lab Med. 2010 Aug;30(4):339-44. doi: 10.3343/kjlm.2010.30.4.339.

Extramedullary haematopoiesis in hereditary spherocytosis simulating mediastinal tumour.遗传性球形红细胞增多症中模拟纵隔肿瘤的髓外造血

Eur J Haematol. 1997 Feb;58(2):124-6. doi: 10.1111/j.1600-0609.1997.tb00936.x.

Hemolytic anemia with abnormal membrane protein.伴有异常膜蛋白的溶血性贫血

Clin Chim Acta. 1973 Aug 30;47(2):319-21. doi: 10.1016/0009-8981(73)90331-8.

[Anemia (with splenomegaly since childhood): congenital spherocytosis (with special reference to abnormalities of erythrocyte membrane proteins].[贫血（自幼伴有脾肿大）：先天性球形红细胞增多症（特别提及红细胞膜蛋白异常）]

Nihon Rinsho. 1975 Apr 10;Spec No:986-7, 1518-21.

Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis.遗传性球形红细胞增多症中红细胞水通道蛋白-1的表达降低。

Ann Hematol. 2016 Oct;95(10):1595-601. doi: 10.1007/s00277-016-2757-0. Epub 2016 Jul 28.

引用本文的文献

Deficiency of protein 4.2 in erythrocytes from a patient with a Coombs negative hemolytic anemia. Evidence for a role of protein 4.2 in stabilizing ankyrin on the membrane.一位库姆斯试验阴性溶血性贫血患者红细胞中蛋白质4.2的缺乏。蛋白质4.2在稳定膜上锚蛋白中的作用证据。

J Clin Invest. 1988 Mar;81(3):893-901. doi: 10.1172/JCI113400.

Complete amino acid sequence and homologies of human erythrocyte membrane protein band 4.2.人红细胞膜蛋白4.2的完整氨基酸序列及其同源性

Proc Natl Acad Sci U S A. 1990 Jan;87(2):613-7. doi: 10.1073/pnas.87.2.613.

Gel electrophoresis of the human erythrocyte membrane proteins: aberrant patterns in hematological and non-hematological diseases.人红细胞膜蛋白的凝胶电泳：血液学和非血液学疾病中的异常模式

Blut. 1978 Mar 15;36(3):135-44. doi: 10.1007/BF00996652.

Hemolytic disorders associated with a primary red cell membrane defect.与原发性红细胞膜缺陷相关的溶血性疾病。

Experientia. 1976 May 15;32(5):537-42. doi: 10.1007/BF01990150.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验