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Gray platelet syndrome. Demonstration of alpha granule membranes that can fuse with the cell surface.

Platelets from patients with the gray platelet syndrome have decreased recognizable alpha granules and are markedly deficient in some alpha-granule secretory proteins. Using immunocytochemical techniques with antibodies to an alpha-granule membrane protein, GMP-140, we identified the membranes of in...

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Detalhes bibliográficos
Main Authors: Rosa, J P, George, J N, Bainton, D F, Nurden, A T, Caen, J P, McEver, R P
Formato: Artigo
Idioma:Inglês
Publicado em: 1987
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC442357/
https://ncbi.nlm.nih.gov/pubmed/2443536
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