Fibroblast activation and abnormal extracellular matrix remodelling as common hallmarks in three cancer‐prone genodermatoses

BACKGROUND: Recessive dystrophic epidermolysis bullosa (RDEB), Kindler syndrome (KS) and xeroderma pigmentosum complementation group C (XPC) are three cancer‐prone genodermatoses whose causal genetic mutations cannot fully explain, on their own, the array of associated phenotypic manifestations. Rec...

Descripción completa

Detalles Bibliográficos
Autores principales: Chacón‐Solano, E., León, C., Díaz, F., García‐García, F., García, M., Escámez, M.J., Guerrero‐Aspizua, S., Conti, C.J., Mencía, Á., Martínez‐Santamaría, L., Llames, S., Pévida, M., Carbonell‐Caballero, J., Puig‐Butillé, J.A., Maseda, R., Puig, S., de Lucas, R., Baselga, E., Larcher, F., Dopazo, J., del Río, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850467/
https://www.ncbi.nlm.nih.gov/pubmed/30693469
http://dx.doi.org/10.1111/bjd.17698

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6850467/
https://www.ncbi.nlm.nih.gov/pubmed/30693469
http://dx.doi.org/10.1111/bjd.17698

Ejemplares similares