The involvement of human RECQL4 in DNA double strand break repair

Rothmund-Thomson syndrome (RTS) is an autosomal recessive hereditary disorder associated with mutation in RECQL4 gene, a member of the human RecQ helicases. The disease is characterized by genomic instability, skeletal abnormalities and predisposition to malignant tumors, especially osteosarcomas. T...

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Xehetasun bibliografikoak
Argitaratua izan da:Aging Cell
Egile Nagusiak: Singh, Dharmendra Kumar, Karmakar, Parimal, Aamann, Maria, Schurman, Shepherd H., May, Alfred, Croteau, Deborah L., Burks, Lynnette, Plon, Sharon E., Bohr, Vilhelm A.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2010
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC4624395/
https://ncbi.nlm.nih.gov/pubmed/20222902
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1474-9726.2010.00562.x
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