Cargando…
p53 Mediates Failure of Human Definitive Hematopoiesis in Dyskeratosis Congenita
Dyskeratosis congenita (DC) is a bone marrow failure syndrome associated with telomere dysfunction. The progression and molecular determinants of hematopoietic failure in DC remain poorly understood. Here, we use the directed differentiation of human embryonic stem cells harboring clinically relevan...
Autores principales: | Fok, Wilson Chun, Niero, Evandro Luis de Oliveira, Dege, Carissa, Brenner, Kirsten Ann, Sturgeon, Christopher Michael, Batista, Luis Francisco Zirnberger |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5550027/ https://www.ncbi.nlm.nih.gov/pubmed/28757166 http://dx.doi.org/10.1016/j.stemcr.2017.06.015 |
Ejemplares similares
-
Telomere Dysfunction Activates p53 and Represses HNF4α Expression Leading to Impaired Human Hepatocyte Development and Function
por: Munroe, Michael, et al.
Publicado: (2020) -
Dyskeratosis congenita
por: Gitto, Lorenzo, et al.
Publicado: (2020) -
Differential impact of a dyskeratosis congenita mutation in TPP1 on mouse hematopoiesis and germline
por: Graniel, Jacqueline V, et al.
Publicado: (2021) -
Dyskeratosis congenita presenting with dysphagia
por: Gupta, Kalpana, et al.
Publicado: (2016) -
Dyskeratosis congenita, stem cells and telomeres
por: Kirwan, Michael, et al.
Publicado: (2009)