Cargando…
A Mutation in the Srrm4 Gene Causes Alternative Splicing Defects and Deafness in the Bronx Waltzer Mouse
Sensory hair cells are essential for hearing and balance. Their development from epithelial precursors has been extensively characterized with respect to transcriptional regulation, but not in terms of posttranscriptional influences. Here we report on the identification and functional characterizati...
Autores principales: | Nakano, Yoko, Jahan, Israt, Bonde, Gregory, Sun, Xingshen, Hildebrand, Michael S., Engelhardt, John F., Smith, Richard J. H., Cornell, Robert A., Fritzsch, Bernd, Bánfi, Botond |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3464207/ https://www.ncbi.nlm.nih.gov/pubmed/23055939 http://dx.doi.org/10.1371/journal.pgen.1002966 |
Ejemplares similares
-
Inhibition of a transcriptional repressor rescues hearing in a splicing factor–deficient mouse
por: Nakano, Yoko, et al.
Publicado: (2020) -
Double homozygous waltzer and Ames waltzer mice provide no evidence of retinal degeneration
por: Ahmed, Zubair M., et al.
Publicado: (2008) -
SRRM2 organizes splicing condensates to regulate alternative splicing
por: Xu, Shaohai, et al.
Publicado: (2022) -
Auditory Neural Activity in Congenitally Deaf Mice Induced by Infrared Neural Stimulation
por: Tan, Xiaodong, et al.
Publicado: (2018) -
Presence of interstereocilial links in waltzer mutants suggests Cdh23 is not essential for tip Link formation
por: Rzadzinska, A.K., et al.
Publicado: (2009)