The Werner Syndrome Protein Is Involved in RNA Polymerase II Transcription

Werner syndrome (WS) is a human progeroid syndrome characterized by the early onset of a large number of clinical features associated with the normal aging process. The complex molecular and cellular phenotypes of WS involve characteristic features of genomic instability and accelerated replicative...

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Pubblicato in:	Mol Biol Cell
Autori principali:	Balajee, Adayabalam S., Machwe, Amrita, May, Alfred, Gray, Matthew D., Oshima, Junko, Martin, George M., Nehlin, Jan O., Brosh, Robert, Orren, David K., Bohr, Vilhelm A.
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	American Society for Cell Biology 1999
Soggetti:	Article
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC25497/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10436020/ https://ncbi.nlm.nih.govhttps://doi.org/10.1091/mbc.10.8.2655
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