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- Two different PABPN1 expanded alleles in a Mexican population with...
Two different PABPN1 expanded alleles in a Mexican population with oculopharyngeal muscular dystrophy arising from independent founder effects. - Living with oculopharyngeal muscular dystrophy: a phenomenological
Related Articles Living with oculopharyngeal muscular dystrophy: a phenomenological study. Can J Neurosci Nurs. 2008;30(1):35-9... - [The clinical-genealogic and molecular-genetic characteristics of...
[The clinical-genealogic and molecular-genetic characteristics of oculopharyngeal muscular dystrophy in the Republic of Sakha (Yakutia).] - [Original articles - Laboratory science] Two different PABPN1
- Lentiviral-based gene therapy for oculopharyngeal muscular dystrophy
Lentiviral-based gene therapy for oculopharyngeal muscular dystrophy. Bales, O; Yanez, R; Talbot, G; et al. HUMAN GENE THERAPY 19 (4): 415-415... - Expression and siRNA targeting of PABPN1 as a model for...
Expression and siRNA targeting of PABPN1 as a model for oculopharyngeal muscular dystrophy (OPMd) Trollet, C; Benstead, J; Graham, I; et al. - Short GCG expansions in the PAB II gene for oculopharyngeal muscular
...in nucleus, such as polyalanine accumulation, a disease related with swallowing difficulties, such as oculopharyngeal muscular dystrophy. - Wild-type PABPN1 is anti-apoptotic and reduces toxicity of the...
Related Articles Wild-type PABPN1 is anti-apoptotic and reduces toxicity of the oculopharyngeal muscular dystrophy mutation. Hum Mol Genet. - A case of rare recessive oculopharyngeal muscular dystrophy (OPMD)...
Oculopharyngeal muscular dystrophy (OPMD) is typically inherited in an autosomal dominant fashion and is characterized by late onset proximal muscle