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Alexander disease causing mutations in the C-terminal domain of GFAP are deleterious both to assembly and network formation with the potential to both activate caspase 3 and decrease cell viability

Alexander disease is a primary genetic disorder of astrocyte caused by dominant mutations in the astrocyte-specific intermediate filament glial fibrillary acidic protein (GFAP). While most of the disease-causing mutations described to date have been found in the conserved α-helical rod domain, some...

תיאור מלא

שמור ב:
מידע ביבליוגרפי
הוצא לאור ב:Exp Cell Res
Main Authors: Chen, Yi-Song, Lim, Suh-Ciuan, Chen, Mei-Hsuan, Quinlan, Roy A., Perng, Ming-Der
פורמט: Artigo
שפה:Inglês
יצא לאור: 2011
נושאים:
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC4308095/
https://ncbi.nlm.nih.gov/pubmed/21756903
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yexcr.2011.06.017
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