Early postnatal ataxia and abnormal cerebellar development in mice lacking Xeroderma pigmentosum Group A and Cockayne Syndrome Group B DNA repair genes

Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are rare autosomal recessive disorders associated with a defect in the nucleotide excision repair (NER) pathway required for the removal of DNA damage induced by UV light and distorting chemical adducts. Although progressive neurological dysfunct...

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Dettagli Bibliografici
Autori principali: Murai, Machiko, Enokido, Yasushi, Inamura, Naoko, Yoshino, Masafumi, Nakatsu, Yoshimichi, van der Horst, Gijsbertus T. J., Hoeijmakers, Jan H. J., Tanaka, Kiyoji, Hatanaka, Hiroshi
Natura: Artigo
Lingua:Inglês
Pubblicazione: The National Academy of Sciences 2001
Soggetti:
Biological Sciences
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC60879/
https://ncbi.nlm.nih.gov/pubmed/11687625
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.231329598
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