Cargando…
Xeroderma Pigmentosum C: A Valuable Tool to Decipher the Signaling Pathways in Skin Cancers
Xeroderma pigmentosum (XP) is a rare autosomal genodermatosis that manifests clinically with pronounced sensitivity to ultraviolet (UV) radiation and the high probability of the occurrence of different skin cancer types in XP patients. XP is mainly caused by mutations in XP-genes that are involved i...
Autores principales: | Nasrallah, A., Fayyad, N., Kobaisi, F., Badran, B., Fayyad-Kazan, H., Fayyad-Kazan, M., Sève, M., Rachidi, W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495593/ https://www.ncbi.nlm.nih.gov/pubmed/34630850 http://dx.doi.org/10.1155/2021/6689403 |
Ejemplares similares
-
Isoconazole and Clemizole Hydrochloride Partially Reverse the Xeroderma Pigmentosum C Phenotype
por: Kobaisi, Farah, et al.
Publicado: (2021) -
Xeroderma Pigmentosum C (XPC) Mutations in Primary Fibroblasts Impair Base Excision Repair Pathway and Increase Oxidative DNA Damage
por: Fayyad, Nour, et al.
Publicado: (2020) -
Signaling Pathways, Chemical and Biological Modulators of Nucleotide Excision Repair: The Faithful Shield against UV Genotoxicity
por: Kobaisi, F., et al.
Publicado: (2019) -
High-throughput synthetic rescue for exhaustive characterization of suppressor mutations in human genes
por: Kobaisi, Farah, et al.
Publicado: (2020) -
Effect of Ultraviolet Radiation and Benzo[a]pyrene Co-Exposure on Skin Biology: Autophagy as a Potential Target
por: Fayyad-Kazan, Mohammad, et al.
Publicado: (2023)