Cargando…
Single-Molecule Analysis of the Human Telomerase RNA·Dyskerin Interaction and the Effect of Dyskeratosis Congenita Mutations
[Image: see text] It has been proposed that human telomerase RNA (hTR) interacts with dyskerin, prior to assembly of the telomerase holoenzyme. The direct interaction of dyskerin and hTR has not been demonstrated and is an experimentally challenging research problem because of difficulties in expres...
Autores principales: | Ashbridge, Beth, Orte, Angel, Yeoman, Justin A., Kirwan, Michael, Vulliamy, Tom, Dokal, Inderjeet, Klenerman, David, Balasubramanian, Shankar |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2009
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778356/ https://www.ncbi.nlm.nih.gov/pubmed/19835419 http://dx.doi.org/10.1021/bi901373e |
Ejemplares similares
-
Dyskeratosis congenita and the DNA damage response
por: Kirwan, Michael, et al.
Publicado: (2011) -
Dyskeratosis congenita, stem cells and telomeres
por: Kirwan, Michael, et al.
Publicado: (2009) -
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)