Cell migration is impaired in XPA‐deficient cells

Xeroderma pigmentosum (XP) is a hereditary disorder characterized by photosensitivity, predisposition to skin cancers, and neurological abnormalities including microcephaly and progressive neurodegeneration. A lack of nucleotide excision repair (NER) in patients with XP can cause hypersensitivity to...

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Detalles Bibliográficos
Autores principales: Takeuchi, Seiji, Fukumoto, Takeshi, Takemori, Chihiro, Saito, Naoaki, Nishigori, Chikako, Sato, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927838/
https://www.ncbi.nlm.nih.gov/pubmed/36816512
http://dx.doi.org/10.1096/fba.2022-00084

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927838/
https://www.ncbi.nlm.nih.gov/pubmed/36816512
http://dx.doi.org/10.1096/fba.2022-00084

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