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Plastin 3 in X-Linked Osteoporosis: Imbalance of Ca(2+)-Dependent Regulation Is Equivalent to Protein Loss

Osteogenesis imperfecta is a genetic disorder disrupting bone development and remodeling. The primary causes of osteogenesis imperfecta are pathogenic variants of collagen and collagen processing genes. However, recently variants of the actin bundling protein plastin 3 have been identified as anothe...

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Detalhes bibliográficos
Publicado no:Front Cell Dev Biol
Main Authors: Schwebach, Christopher L., Kudryashova, Elena, Kudryashov, Dmitri S.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7859272/
https://ncbi.nlm.nih.gov/pubmed/33553175
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fcell.2020.635783
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