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The role of gelsolin domain 3 in familial amyloidosis (Finnish type)

In the disease familial amyloidosis, Finnish type (FAF), also known as AGel amyloidosis (AGel), the mechanism by which point mutations in the calcium-regulated actin-severing protein gelsolin lead to furin cleavage is not understood in the intact protein. Here, we provide a structural and biochemica...

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Detalhes bibliográficos
Publicado no:Proc Natl Acad Sci U S A
Main Authors: Zorgati, Habiba, Larsson, Mårten, Ren, Weitong, Sim, Adelene Y. L., Gettemans, Jan, Grimes, Jonathan M., Li, Wenfei, Robinson, Robert C.
Formato: Artigo
Idioma:Inglês
Publicado em: National Academy of Sciences 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6628662/
https://ncbi.nlm.nih.gov/pubmed/31243148
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1902189116
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