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ITGB3 wt Allele

Known as: GPIIIa, Platelet Fibrinogen Receptor, Beta Subunit Gene, Integrin, Beta-3 Gene 
Human ITGB3 wild-type allele is located in the vicinity of 17q21.32 and is approximately 59 kb in length. This allele, which encodes integrin beta-3… 
National Institutes of Health

Papers overview

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2014
2014
Introduction: Bernard–Soulier syndrome is a rare autosomal recessive disease that causes a deficiency of glycoprotein Ib, the… 
2010
2010
The authors analyse effect of GPIIIA gene (PI a allele) polymorphism on the frequency of complicated coronary heart disease in… 
2010
2010
Background Disturbances in affective state are known to cause platelet activation, which may relate to evidence linking major… 
2010
2010
The authors analyse effect of GPIIIA gene (PI a allele) polymorphism on the frequency of complicated coronary heart disease in… 
2004
2004
Sedimentation equilibrium and low-angle laser-light scattering were used to determine the molar mass of the glycoprotein moieties… 
1999
1999
AIM: To investigate gene PIA1/A2 polymorphism and some parameters of plasma hemostasis in postmyocardial infarction (PMI… 
1999
1999
AIM To investigate gene PIA1/A2 polymorphism and some parameters of plasma hemostasis in postmyocardial infarction (PMI) patients… 
1995
1995
The ultrastructure of the leukemic cells in transient leukemia (six cases), myelodysplasia (five cases) and acute… 
Highly Cited
1992
Highly Cited
1992
The genetic basis for Glanzmann's thrombasthenia (GT) was elucidated on a compound heterozygote with glycoprotein (GP)IIb gene…