Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice

Werner syndrome (WS) is a premature aging disorder caused by mutations in a RecQ-family DNA helicase, WRN. Mice lacking part of the helicase domain of the WRN orthologue exhibit many phenotypic features of WS, including metabolic abnormalities and a shorter mean life span. In contrast, mice lacking...

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Detalles Bibliográficos
Autores principales: Aumailley, Lucie, Garand, Chantal, Dubois, Marie Julie, Johnson, F. Brad, Marette, André, Lebel, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598085/
https://www.ncbi.nlm.nih.gov/pubmed/26447695
http://dx.doi.org/10.1371/journal.pone.0140292

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4598085/
https://www.ncbi.nlm.nih.gov/pubmed/26447695
http://dx.doi.org/10.1371/journal.pone.0140292

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