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Intersection of mechanisms of type 2A VWD through defects in VWF multimerization, secretion, ADAMTS-13 susceptibility, and regulated storage

Type 2A VWD is characterized by the absence of large VWF multimers and decreased platelet-binding function. Historically, type 2A variants are subdivided into group 1, which have impaired assembly and secretion of VWF multimers, or group 2, which have normal secretion of VWF multimers and increased...

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Detaylı Bibliyografya
Asıl Yazarlar: Jacobi, Paula M., Gill, Joan Cox, Flood, Veronica H., Jakab, David A., Friedman, Kenneth D., Haberichter, Sandra L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Hematology 2012
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3362367/
https://ncbi.nlm.nih.gov/pubmed/22431572
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2011-06-360875
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