Cargando…
Genetic Background of Prop1(df) Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment
Hypothyroidism is a cause of genetic and environmentally induced deafness. The sensitivity of cochlear development and function to thyroid hormone (TH) mandates understanding TH action in this sensory organ. Prop1 (df) and Pou1f1 (dw) mutant mice carry mutations in different pituitary transcription...
Autores principales: | Fang, Qing, Giordimaina, Alicia M., Dolan, David F., Camper, Sally A., Mustapha, Mirna |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3298611/ https://www.ncbi.nlm.nih.gov/pubmed/22143287 http://dx.doi.org/10.1007/s10162-011-0302-3 |
Ejemplares similares
-
Hearing Impairment in Congenitally Hypothyroid Patients
por: Hashemipour, Mahin, et al.
Publicado: (2012) -
The 133-kDa N-terminal domain enables myosin 15 to maintain mechanotransducing stereocilia and is essential for hearing
por: Fang, Qing, et al.
Publicado: (2015) -
PROP1 triggers epithelial-mesenchymal transition-like process in pituitary stem cells
por: Pérez Millán, María Inés, et al.
Publicado: (2016) -
Tequila, DF /
por: Mejía Madrid, Fabrizio, 1967-
Publicado: (2008) -
Effect of new polyherbal formulations DF1911, DF2112 and DF2813 on CFA induced inflammation in rat model
por: Nagarkar, Bhagyashri, et al.
Publicado: (2017)