Hematopoiesis and the defect in paroxysmal nocturnal hemoglobinuria.
作者信息
Rosse W F
出版信息
J Clin Invest. 1997 Sep 1;100(5):953-4. doi: 10.1172/JCI119645.
Abstract
摘要
相似文献
1
Hematopoiesis and the defect in paroxysmal nocturnal hemoglobinuria.造血作用与阵发性夜间血红蛋白尿症中的缺陷。
J Clin Invest. 1997 Sep 1;100(5):953-4. doi: 10.1172/JCI119645.
2
[Molecular abnormality of paroxysmal nocturnal hemoglobinuria].阵发性睡眠性血红蛋白尿的分子异常
Nihon Naika Gakkai Zasshi. 1994 May 10;83(5):840-5.
3
[Paroxysmal nocturnal hemoglobinuria].[阵发性夜间血红蛋白尿]
Nihon Rinsho. 1991 Mar;49(3):667-71.
4
[Paroxysmal nocturnal hemoglobinuria--pathophysiological implication of altered glycosylation].[阵发性夜间血红蛋白尿——糖基化改变的病理生理意义]
Seikagaku. 1994 Feb;66(2):137-49.
5
[Paroxysmal nocturnal hemoglobinuria--an acquired genetic defect of the hematopoietic stem cells].阵发性夜间血红蛋白尿——造血干细胞的一种获得性遗传缺陷
Dtsch Med Wochenschr. 1995 Jan 5;120(1-2):31-4. doi: 10.1055/s-2008-1043195.
6
[GPI-anchored proteins and paroxysmal nocturnal hemoglobinuria].[糖基磷脂酰肌醇锚定蛋白与阵发性睡眠性血红蛋白尿症]
Nihon Saikingaku Zasshi. 1993 May;48(3):533-9. doi: 10.3412/jsb.48.533.
7
PIG-A--the target gene in paroxysmal nocturnal hemoglobinuria.
N Engl J Med. 1994 Jan 27;330(4):283-4. doi: 10.1056/NEJM199401273300410.
8
[Paroxysmal nocturnal hemoglobinuria--molecular mechanism of abnormal hemolysis].阵发性夜间血红蛋白尿——异常溶血的分子机制
Tanpakushitsu Kakusan Koso. 1993 Nov;38(14):2333-46.
9
On the origin of multiple mutant clones in paroxysmal nocturnal hemoglobinuria.阵发性夜间血红蛋白尿中多个突变克隆的起源
Stem Cells. 2007 Dec;25(12):3081-4. doi: 10.1634/stemcells.2007-0427. Epub 2007 Sep 6.
10
[Paroxysmal nocturnal hemoglobinuria].[阵发性夜间血红蛋白尿]
Duodecim. 1998;114(24):2561-8.
引用本文的文献
1
Clinical paroxysmal nocturnal hemoglobinuria is the result of expansion of glycosyl-phosphatidyl-inositol-anchored protein-deficient clone in the condition of deficient hematopoiesis.临床阵发性夜间血红蛋白尿是造血功能不足情况下糖基磷脂酰肌醇锚定蛋白缺陷克隆扩增的结果。
Int J Hematol. 2001 Jan;73(1):64-70. doi: 10.1007/BF02981904.
Zotero 插件