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GP1BA wt Allele

Known as: Platelet Glycoprotein Ib, Alpha Polypeptide Gene, BSS, CD42B 
Human GP1BA wild-type allele is located in the vicinity of 17p13.2 and is approximately 3 kb in length. This allele, which encodes platelet… 
National Institutes of Health

Papers overview

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Highly Cited
2010
Highly Cited
2010
Background— Although many genetic epidemiology and biomarker studies have been conducted to examine associations of genetic… 
Highly Cited
2008
Highly Cited
2008
Beside their main physiological function in hemostasis, platelets are also highly involved in pathological processes, such as… 
Highly Cited
2007
Highly Cited
2007
Summary.  Background: The major antigen implicated in the antiphospholipid syndrome is beta2‐glycoprotein I (β2GPI). Dimerized… 
Review
2006
Review
2006
Bernard-Soulier syndrome (BSS), also known as Hemorrhagiparous thrombocytic dystrophy, is a hereditary bleeding disorder… 
Highly Cited
2005
Highly Cited
2005
BACKGROUND: Several strategies are being developed to reduce the risk of pathogen transmission associated with platelet (PLT… 
Highly Cited
2003
Highly Cited
2003
ABSTRACT Friend leukemia integration 1 (Fli-1) is a member of the Ets family of transcriptional activators that has been shown to… 
Highly Cited
2000
Highly Cited
2000
The pathogenic effects of antiplatelet antibodies were investigated in mice. Monoclonal antibodies (mAbs) of different… 
Highly Cited
1998
Highly Cited
1998
Although it has been reported that activated platelets can adhere to intact endothelium, the receptors involved have not been… 
Highly Cited
1998
Highly Cited
1998
The platelet GPIb-V-IX complex is the receptor for the initial binding of von Willebrand factor (vWF) mediating platelet adhesion… 
Highly Cited
1996
Highly Cited
1996
Bernard-Soulier Syndrome (BSS) is a rare congenital bleeding disorder due to absent or decreased expression of the glycoprotein…