Phenotypic consequence of the gene abnormality in the platelet glycoprotein IX gene observed in a patient with Bernard-Soulier syndrome through mammalian cell expression system

Thrombosis Research

Volumn 95, Issue 6, 1999, Pages 295-302

  Suzuki, Keijiroh ^a   Hayashi, Tomohiro ^a   Akiba, Jiroh ^a   Satoh, Shinji ^a   Kato, Takeo ^a  

^a YAMAGATA UNIVERSITY   (Japan)

Author keywords

Bernard Soulier syndrome; Gene expression; Leucine rich motif; Platelet glycoprotein IX

Indexed keywords

GLYCOPROTEIN; LEUCINE; PLATELET GLYCOPROTEIN 9; UNCLASSIFIED DRUG;

ARTICLE; BERNARD SOULIER DISEASE; CHO CELL; CONTROLLED STUDY; GENE EXPRESSION REGULATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MISSENSE MUTATION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN DEFECT; PROTEIN EXPRESSION; SITE DIRECTED MUTAGENESIS;

ANIMALS; BERNARD-SOULIER SYNDROME; CHO CELLS; CRICETINAE; FLOW CYTOMETRY; GENE EXPRESSION REGULATION; HUMANS; MUTATION, MISSENSE; PLATELET GLYCOPROTEIN GPIB-IX COMPLEX; TRANSFECTION;

EID: 0032828403     PISSN: 00493848     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0049-3848(99)00047-X     Document Type: Article

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