A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse
about
Beyond generalized hair cells: molecular cues for hair cell typesMice with conditional deletion of Cx26 exhibit no vestibular phenotype despite secondary loss of Cx30 in the vestibular end organsThe candidate splicing factor Sfswap regulates growth and patterning of inner ear sensory organsThe neurogenetics of alternative splicingN-acetyl-cysteine prevents age-related hearing loss and the progressive loss of inner hair cells in γ-glutamyl transferase 1 deficient mice.A mutation in the mouse ttc26 gene leads to impaired hedgehog signalingInner ear development: building a spiral ganglion and an organ of Corti out of unspecified ectodermCharacterization of the transcriptome of nascent hair cells and identification of direct targets of the Atoh1 transcription factorPax2-Islet1 Transgenic Mice Are Hyperactive and Have Altered Cerebellar Foliation.Characterization of Lgr5+ progenitor cell transcriptomes in the apical and basal turns of the mouse cochlea.NOVA2-mediated RNA regulation is required for axonal pathfinding during developmentEvolving gene regulatory networks into cellular networks guiding adaptive behavior: an outline how single cells could have evolved into a centralized neurosensory system.Sensational placodes: neurogenesis in the otic and olfactory systems.Essential roles for the splicing regulator nSR100/SRRM4 during nervous system development.Alternative splicing of inner-ear-expressed genes.A global regulatory mechanism for activating an exon network required for neurogenesisLSD1 Neurospecific Alternative Splicing Controls Neuronal Excitability in Mouse Models of Epilepsy.Rest represses maturation within migrating facial branchiomotor neurons.Angulin proteins ILDR1 and ILDR2 regulate alternative pre-mRNA splicing through binding to splicing factors TRA2A, TRA2B, or SRSF1SRRM4-dependent neuron-specific alternative splicing of protrudin transcripts regulates neurite outgrowth.CDC14A Phosphatase is Essential for Hearing and Male Fertility in Mouse and Human.ESRP1 Mutations Cause Hearing Loss due to Defects in Alternative Splicing that Disrupt Cochlear Development.Intracellular Regulome Variability Along the Organ of Corti: Evidence, Approaches, Challenges, and Perspective.Development of Neuroendocrine Prostate Cancers by the Ser/Arg Repetitive Matrix 4-Mediated RNA Splicing Network.
P2860
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P2860
A mutation in the Srrm4 gene causes alternative splicing defects and deafness in the Bronx waltzer mouse
description
2012 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հունվարին հրատարակված գիտական հոդված
@hy
artikull shkencor
@sq
artículu científicu espublizáu en 2012
@ast
im Januar 2012 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
wetenschappelijk artikel
@nl
наукова стаття, опублікована в січні 2012
@uk
مقالة علمية (نشرت عام 2012)
@ar
name
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@ast
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@en
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@nl
type
label
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@ast
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@en
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@nl
prefLabel
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@ast
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@en
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@nl
P2093
P2860
P3181
P1433
P1476
A mutation in the Srrm4 gene c ...... ess in the Bronx waltzer mouse
@en
P2093
Bernd Fritzsch
Botond Bánfi
Gregory Bonde
Israt Jahan
John F. Engelhardt
Michael S. Hildebrand
Richard J. H. Smith
Robert A. Cornell
Xingshen Sun
Yoko Nakano
P2860
P304
P3181
P356
10.1371/JOURNAL.PGEN.1002966
P577
2012-01-01T00:00:00Z