Cargando…
Vitamin C alters the amount of specific endoplasmic reticulum associated proteins involved in lipid metabolism in the liver of mice synthesizing a nonfunctional Werner syndrome (Wrn) mutant protein
Werner syndrome (WS) is a premature aging disorder caused by mutations in a protein containing both a DNA exonuclease and DNA helicase domain. Mice lacking the helicase domain of the Wrn protein orthologue exhibit transcriptomic and metabolic alterations, some of which are reversed by vitamin C. Rec...
Autores principales: | Aumailley, Lucie, Roux-Dalvai, Florence, Kelly, Isabelle, Droit, Arnaud, Lebel, Michel |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5832228/ https://www.ncbi.nlm.nih.gov/pubmed/29494634 http://dx.doi.org/10.1371/journal.pone.0193170 |
Ejemplares similares
-
Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice
por: Aumailley, Lucie, et al.
Publicado: (2015) -
Vitamin C modulates the levels of several proteins of the mitochondrial complex III and its activity in the mouse liver
por: Aumailley, Lucie, et al.
Publicado: (2022) -
CDK2 phosphorylation of Werner protein (WRN) contributes to WRN’s DNA double‐strand break repair pathway choice
por: Lee, Jong‐Hyuk, et al.
Publicado: (2021) -
Werner syndrome with refractory cystoid macular edema and immunohistochemical analysis of WRN proteins in human retinas
por: Oshitari, Toshiyuki, et al.
Publicado: (2014) -
Strand exchange of telomeric DNA catalyzed by the Werner syndrome protein (WRN) is specifically stimulated by TRF2
por: Edwards, Deanna N., et al.
Publicado: (2014)