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Biochemical Characterization of Warsaw Breakage Syndrome Helicase
Mutations in the human ChlR1 gene are associated with a unique genetic disorder known as Warsaw breakage syndrome characterized by cellular defects in sister chromatid cohesion and hypersensitivity to agents that induce replication stress. A role of ChlR1 helicase in sister chromatid cohesion was fi...
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| Hoofdauteurs: | , , , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society for Biochemistry and Molecular Biology
2012
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3256869/ https://ncbi.nlm.nih.gov/pubmed/22102414 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.276022 |
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