Cargando…
MOZ Regulates the Tbx1 Locus, and Moz Mutation Partially Phenocopies DiGeorge Syndrome
DiGeorge syndrome, caused by a 22q11 microdeletion or mutation of the TBX1 gene, varies in severity greatly, even among monozygotic twins. Epigenetic phenomena have been invoked to explain phenotypic differences in individuals of identical genetic composition, although specific chromatin modificatio...
Autores principales: | Voss, Anne K., Vanyai, Hannah K., Collin, Caitlin, Dixon, Mathew P., McLennan, Tamara J., Sheikh, Bilal N., Scambler, Peter, Thomas, Tim |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3442180/ https://www.ncbi.nlm.nih.gov/pubmed/22921202 http://dx.doi.org/10.1016/j.devcel.2012.07.010 |
Ejemplares similares
-
MOZ is critical for the development of MOZ/MLL fusion–induced leukemia through regulation of Hoxa9/Meis1 expression
por: Katsumoto, Takuo, et al.
Publicado: (2022) -
MOZ-TIF2 repression of nuclear receptor-mediated transcription requires multiple domains in MOZ and in the CID domain of TIF2
por: Yin, Hong, et al.
Publicado: (2007) -
Inbound marketing and SEO: insights from the Moz Blog
por: Fishkin, Rand, et al.
Publicado: (2013) -
Expression of the MOZ-TIF2 oncoprotein in mice represses senescence
por: Largeot, Anne, et al.
Publicado: (2016) -
DiGeorge’s syndrome presenting as hypocalcemia in an adult
por: Aljabri, K.S., et al.
Publicado: (2005)