A genetic analysis of integrin function: Glanzmann thrombasthenia in vitro

Glanzmann thrombasthenia, an inherited bleeding disorder, can be caused by a defect or deficiency in platelet integrin α(IIb)β(3) (GPIIb-IIIa). Studies of thrombasthenia variants have facilitated identification of sites involved in the functions of α(IIb)β(3) and other integrins. Such sites include...

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izdano v:	Proc Natl Acad Sci U S A
Principais autores:	Baker, Elizabeth K., Tozer, Eileen Collins, Pfaff, Martin, Shattil, Sanford J., Loftus, Joseph C., Ginsberg, Mark H.
Format:	Artigo
Jezik:	Inglês
Izdano:	National Academy of Sciences 1997
Teme:	Biological Sciences
Online dostop:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC20027/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9050889/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.94.5.1973
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