Werner Syndrome Protein and DNA Replication

Werner Syndrome (WS) is an autosomal recessive disorder characterized by the premature development of aging features. Individuals with WS also have a greater predisposition to rare cancers that are mesenchymal in origin. Werner Syndrome Protein (WRN), the protein mutated in WS, is unique among RecQ...

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Vydáno v:Int J Mol Sci
Hlavní autoři: Mukherjee, Shibani, Sinha, Debapriya, Bhattacharya, Souparno, Srinivasan, Kalayarasan, Abdisalaam, Salim, Asaithamby, Aroumougame
Médium: Artigo
Jazyk:Inglês
Vydáno: MDPI 2018
Témata:
Review
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6274846/
https://ncbi.nlm.nih.gov/pubmed/30400178
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms19113442
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