遗传性球形红细胞增多症中99钼与红细胞膜蛋白的结合无变化。
Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis.
作者信息
Marík T, Kselíková M, Bíbr B, Brabec V, Lener J
出版信息
Folia Haematol Int Mag Klin Morphol Blutforsch. 1983;110(1):81-5.
PMID:6192057
Abstract
The interaction of 99Mo with red cell membrane proteins was found specific for spectrin both in normal red cells and those of hereditary spherocytosis. In addition, no significant quantitative differences were observed in labeling patterns between these two types of red cells, thus indicating no major alterations in the spectrin molecules of hereditary spherocytosis.
摘要
在正常红细胞和遗传性球形红细胞增多症患者的红细胞中均发现，99Mo与红细胞膜蛋白的相互作用对血影蛋白具有特异性。此外，这两种类型的红细胞在标记模式上未观察到显著的定量差异，因此表明遗传性球形红细胞增多症患者血影蛋白分子无重大改变。
相似文献
1
Unchanged binding of 99molybdenum to red cell membrane proteins in hereditary spherocytosis.遗传性球形红细胞增多症中99钼与红细胞膜蛋白的结合无变化。
Folia Haematol Int Mag Klin Morphol Blutforsch. 1983;110(1):81-5.
2
A genetic defect in the binding of protein 4.1 to spectrin in a kindred with hereditary spherocytosis.在一个患有遗传性球形红细胞增多症的家族中，蛋白质4.1与血影蛋白结合存在基因缺陷。
N Engl J Med. 1982 Nov 25;307(22):1367-74. doi: 10.1056/NEJM198211253072203.
3
Spectrin oligomers of the red cell membrane extracts in hereditary spherocytosis.遗传性球形红细胞增多症中红细胞膜提取物的血影蛋白寡聚体。
Biomed Biochim Acta. 1983;42(11-12):S32-7.
4
Role of the interaction between Lu/BCAM and the spectrin-based membrane skeleton in the increased adhesion of hereditary spherocytosis red cells to laminin.Lu/BCAM 与基于血影蛋白的膜骨架之间的相互作用在遗传性球形红细胞增多症红细胞与层粘连蛋白黏附增加中的作用。
Br J Haematol. 2010 Feb;148(3):456-65. doi: 10.1111/j.1365-2141.2009.07973.x.
5
[Cytoskeleton anomalies in disorders of red cell membrane proteins].[红细胞膜蛋白疾病中的细胞骨架异常]
Rinsho Ketsueki. 1991 Jun;32(6):573-9.
6
Erythrocyte membrane phosphorylation in hereditary spherocytosis.遗传性球形红细胞增多症中的红细胞膜磷酸化作用
Biomedicine. 1977 Jan 31;27(1):34-6.
7
Study of spectrin phosphorylation and polymerization in normal and spherocytic red blood-cells [proceedings].
Arch Int Physiol Biochim. 1979 Oct;87(4):805-7.
8
Red cell membrane protein phosphorylation in hemolytic anemias and muscular dystrophies.溶血性贫血和肌肉萎缩症中的红细胞膜蛋白磷酸化
Muscle Nerve. 1980 Jan-Feb;3(1):55-69. doi: 10.1002/mus.880030107.
9
Oxidative erythrocyte membrane damage in hereditary spherocytosis.
Biochem Int. 1992 Feb;26(2):265-74.
10
The abnormal phosphorylation of spectrin in human hereditary spherocytosis.人遗传性球形红细胞增多症中血影蛋白的异常磷酸化
Biochim Biophys Acta. 1981 Nov 20;649(1):31-7. doi: 10.1016/0005-2736(81)90005-5.
Zotero 插件