Art
J-GLOBAL ID：200902135592804055
Reference number：01A0209275
Glanzmann Thrombasthenia: Integrin αIIbβ3 Deficiency.
Glanzmann血小板無力症 インテグリンαIIbβ3欠損症
Author (1)：
Material：
Volume：
72
Issue：
4
Page：
448-454
Publication year：
Dec. 2000
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
文献レビュー
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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Semi thesaurus term：
Thesaurus term/Semi thesaurus term
Keywords indexed to the article.
All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
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JST classification (3)：
JST classification
Category name(code) classified by JST.
Congenital diseases,deformities in general.
, Hematologic diseases
, Molecular genetics in general
Reference (73)：
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HYNES, R. O. Integrins: versatility, modulation, and signaling in cell adhesion. Cell. 1992, 69, 11-25
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RUOSLAHTI, E. Integrins. J Clin Invest. 1991, 87, 1-5
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GEORGE, J. N. Glanzmann's thrombasthenia: the spectrum of clinical disease. Blood. 1990, 75, 1383-1395
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ETZIONI, A. Of man and mouse: leukocyte and endothelial adhesion molecule deficiencies. Blood. 1999, 94, 3281-3288
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BRAY, P. F. Inherited diseases of platelet glycoproteins: consideration for rapid molecular characterization. Thromb Haemost. 1994, 72, 492-502
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Terms in the title (3)：
Terms in the title
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