Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells.

Janel, N; Leroy, C; Laude, I; Toti, F; Fressinaud, E; Meyer, D; Freyssinet, J M; Kerbiriou-Nabias, D

Janel, N; Leroy, C; Laude, I; Toti, F; Fressinaud, E; Meyer, D; Freyssinet, J M; Kerbiriou-Nabias, D.

Thromb Haemost ; 81(2): 322-3, 1999 Feb.

Article in En | MEDLINE | ID: mdl-10064019

Subject(s)

Amino Acid Substitution; Blood Coagulation Disorders/enzymology; Carrier Proteins/genetics; Membrane Proteins/genetics; Mutation, Missense; Phospholipid Transfer Proteins; Point Mutation; Adult; Biological Transport; Blood Coagulation Disorders/genetics; Carrier Proteins/biosynthesis; Cell Membrane/metabolism; DNA Mutational Analysis; DNA, Complementary/genetics; Female; Gene Expression; Gene Frequency; Genes, Recessive; Genotype; Humans; Male; Membrane Lipids/physiology; Membrane Proteins/biosynthesis; Phosphatidylserines/physiology; Polymerase Chain Reaction; RNA, Messenger/genetics; Syndrome

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Collection: 01-internacional Database: MEDLINE Main subject: Blood Coagulation Disorders / Carrier Proteins / Point Mutation / Amino Acid Substitution / Mutation, Missense / Phospholipid Transfer Proteins / Membrane Proteins Limits: Adult / Female / Humans / Male Language: En Journal: Thromb Haemost Year: 1999 Document type: Article Country of publication: Germany

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