Cargando…
Dyskeratosis congenita, stem cells and telomeres
Dyskeratosis congenita (DC) is a multi-system disorder which in its classical form is characterised by abnormalities of the skin, nails and mucous membranes. In approximately 80% of cases, it is associated with bone marrow dysfunction. A variety of other abnormalities (including bone, brain, cancer,...
Autores principales: | Kirwan, Michael, Dokal, Inderjeet |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Elsevier Pub. Co
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686081/ https://www.ncbi.nlm.nih.gov/pubmed/19419704 http://dx.doi.org/10.1016/j.bbadis.2009.01.010 |
Ejemplares similares
-
Dyskeratosis congenita and the DNA damage response
por: Kirwan, Michael, et al.
Publicado: (2011) -
Constitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
por: Walne, Amanda J., et al.
Publicado: (2013) -
TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes
por: Walne, Amanda J., et al.
Publicado: (2008) -
Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund–Thomson syndrome
por: Walne, Amanda J., et al.
Publicado: (2010) -
Dyskeratosis Congenita Links Telomere Attrition to
Age-Related Systemic Energetics
por: James, Emma Naomi, et al.
Publicado: (2023)