Código QR (código de barras bidimensional)

Skeletal muscle cell protein dysregulation highlights the pathogenesis mechanism of myopathy-associated p97/VCP R155H mutations

p97/VCP, a hexametric member of the AAA-ATPase superfamily, has been associated with a wide range of cellular protein pathways, such as proteasomal degradation, the unfolding of polyubiquitinated proteins, and autophagosome maturation. Autosomal dominant p97/VCP mutations cause a rare hereditary mul...

תיאור מלא

שמור ב:
Principais autores: Anna Luzzi, Feng Wang, Shan Li, Michelina Iacovino, Tsui-Fen Chou
פורמט: Artigo
שפה:Inglês
יצא לאור: Frontiers Media S.A. 2023-08-01
סדרה:Frontiers in Neurology
נושאים:
VCP/p97
IBMPFD/ALS
iPSCs
skeletal muscle
myopathy
R155H mutation
גישה מקוונת:https://www.frontiersin.org/articles/10.3389/fneur.2023.1211635/full
תגים: הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!

פריטים דומים