Art
J-GLOBAL ID：200902109840324803
Reference number：01A0633539
GenomeからPostgenomeの時代へ 赤血球膜異常症の研究から
Author (1)：
Material：
Volume：
42
Issue：
5
Page：
343-351
Publication year：
May. 30, 2001
JST Material Number：
Z0688A
ISSN：
0485-1439
Document type：
Article
Country of issue：
Japan (JPN)
Language：
JAPANESE (JA)
Reference (31)：
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1) Gallagher PG, Jarolim P: Red cell membrane disorders. Hoffman R et al. (ed), Hematology: Basic Principles and Practice, pp576∼610, Livingston, New York, 2000
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2) Yawata A, et al.: A surface replica method: A useful tool for studies of the cytoskeletal network in red cell membranes of normal subjects and patients with a β-spectrin mutant (spectrin Le Puy: β220/214). Virchows Arch [B] 425: 297∼304, 1994
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3) Yawata A, et al.: A markedly disrupted skeletal network with abnormally distributed intramembrane particles in complete protein 4.1-deficient red blood cells (allele Madrid): Implications regarding a critical role of protein 4.1 in maintenance of the integrity of the blood cell membrane. Blood 90: 2471∼2481, 1997
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4) Yawata Y, et al.: Characteristic features of genotype and phenotype of hereditary spherocytosis in the Japanese population. Int J Hematol 71: 118∼135, 2000
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5) Kanzaki A, et al.: A deletional frameshift mutation of the β-spectrin gene associated with elliptocytosis in spectrin Tokyo (β220/216). Blood 80: 2115∼2127, 1992
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