BCM Department of Medicine
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Thrombosis Research Section Faculty

 

Full-Time Faculty (Primary Appointment)

VAHID AFSHAR-KHARGHAN, M.D.

 

 

 

 

 

 

Research Interest:

One of my research interests is to identify new functional polymorphisms in the platelet and neutrophil receptors. My goal is to translate the knowledge obtained by basic research in this field to the information applicable in prevention and treatment of thrombotic disease. I am also interested in studying the molecular basis and physiologic consequences of interaction between platelets and complement system. Research in this field is important in better understanding of the connection between thrombosis and inflammation.

Recent Publications:

1. Afshar-Kharghan V, Matijevic-Aleksic N, Ahn C, Boerwinkle E, Wu KK, and López JA: The Variable Number of Tandem Repeat Polymorphism of Platelet Glycoprotein Iba and Risk of Coronary Heart Disease (submitted).

2. Afshar-Kharghan V, Diz-Küçükkaya R, Ludwig EH, Marian AJ, and López JA: Human polymorphism of P-selectin glycoprotein ligand 1 attributable to variable numbers of tandem decameric repeats in the mucinlike region, Blood, 15 May 2001, 97(10): 3306-3307

3. Baker RI, Eikelboom J, Lofthouse E, Staples N, Afshar-Kharghan V, Lopez JA, Shen Y, Berndt MC, and Hankey G: Platelet glycoprotein Iba Kozak polymorphism is associated with an increased risk of ischemic stroke, Blood, 1 July 2001, 98(1): 36-40.

4. Afshar-Kharghan V, Sae-Tung G, Li CQ, Sun L, Dong JF, López JA: Necessity of conserved residues in the leucine-rich repeats of glycoprotein Iba for proper conformation and stability of the ligand-binding region. Biochemistry, March 28, 2000, 39(12): 3384-91.

5. Afshar-Kharghan V, López JA: Bernard-Soulier syndrome in a patient doubly heterozygous for two frame shift mutations in the Glycoprotein Iba gene. British Journal of Haematology, 2000, 110: 919-924.

6. Afshar-Kharghan V, Khoshnevis-Asl M, López JA: Kozak sequence polymorphism is a major determinant of the surface levels of a platelet adhesion receptor. Blood, July 1, 1999, 94(1): 186-191.

7. Afshar-Kharghan V, López JA: Bernard-Soulier syndrome caused by a dinucleotide deletion and reading frame shift in the region encoding the glycoprotein Iba transmembrane domain. Blood, October 1, 1997, 90(7): 2634-2643.

8. Sachs UJH, Kiefel V, Böhringer M, Afshar-Kharghan V, Kroll H, and Santoso S: Single amino acid substitution in human platelet Glycoprotein Ibb is responsible for the formation of the platelet-specific alloantigen Iya. Blood, March 1, 2000, 95(5): 1849-55.

9. López JA, Andrews RK, Afshar-Kharghan V, Berndt MC: Review: Bernard-Soulier Syndrome. Blood, June 15, 1998, 91(12): 4397-4418.

10. Dong JF, Li CQ, Sae-Tung G, Hyun W, Afshar-Kharghan V, López J A: The cytoplasmic domain of glycoprotein(GP) Iba constrains the lateral diffusion of the GP Ib-IX complex and modulates von Willebrand Factor binding. Biochemistry, October 14, 1997, 36(41): 12421-12427.

 



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