Another link between phospholipid transmembrane migration and ABC transporter gene family, inferred from a rare inherited disorder of phosphatidylserine externalization

Biochemical and Biophysical Research Communications

Volumn 241, Issue 2, 1997, Pages 548-552

  Toti, Florence ^a,b   Schindler, Véronique ^a,c   Riou, Jean François ^c   Lombard Platet, Gaël ^c,d   Fressinaud, Edith ^b,e   Meyer, Dominique ^b   Uzan, André ^c   Le Pecq, Jean Bernard ^c   Mandel, Jean Louis ^d   Freyssinet, Jean Marie ^a,b  

^a UNIVERSITÉ DE STRASBOURG   (France)

^b BICÊTRE HOSPITAL   (France)

^c SANOFI   (France)

^d INSTITUT DE GÉNÉTIQUE ET DE BIOLOGIE MOLÉCULAIRE ET CELLULAIRE   (France)

^e HÔTEL DIEU   (France)

Author keywords

Apoptosis; Lipid translocases; Microsatellite analysis; Multidrug transport; Procoagulant phospholipids; Scott syndrome

Indexed keywords

ABC TRANSPORTER; GLYCOPROTEIN P; MEMBRANE PHOSPHOLIPID; MICROSATELLITE DNA; PHOSPHATIDYLSERINE; PROCOAGULANT;

AGED; ARTICLE; B LYMPHOBLAST; BLEEDING; CASE REPORT; CHROMOSOME 7Q; CONTROLLED STUDY; GENE EXPRESSION; GENETIC DISORDER; HUMAN; HUMAN CELL; LIPID TRANSPORT; MEMBRANE TRANSPORT; MULTIDRUG RESISTANCE; MULTIGENE FAMILY; PRIORITY JOURNAL;

MAMMALIA; SACCHAROMYCES CEREVISIAE;

EID: 0031577724     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1997.7836     Document Type: Article

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