Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development
about
A zebrafish screen for craniofacial mutants identifies wdr68 as a highly conserved gene required for endothelin-1 expressionTbx1 regulates population, proliferation and cell fate determination of otic epithelial cellsIn vivo genetic ablation of the periotic mesoderm affects cell proliferation survival and differentiation in the cochlea.Tissue-specific roles of Tbx1 in the development of the outer, middle and inner ear, defective in 22q11DS patients.T-Box transcription factor Tbx20 regulates a genetic program for cranial motor neuron cell body migrationMesodermal Tbx1 is required for patterning the proximal mandible in miceConnecting the ear to the brain: Molecular mechanisms of auditory circuit assembly.Developmental expression patterns of Tbx1, Tbx2, Tbx5, and Tbx20 in Xenopus tropicalisMature middle and inner ears express Chd7 and exhibit distinctive pathologies in a mouse model of CHARGE syndrome.Can you hear me now? Understanding vertebrate middle ear development.A 200-kb region of human chromosome 22q11.2 confers antipsychotic-responsive behavioral abnormalities in mice.Common molecular etiologies are rare in nonsyndromic Tibetan Chinese patients with hearing impairment.Inactivation of Bmp4 from the Tbx1 expression domain causes abnormal pharyngeal arch artery and cardiac outflow tract remodeling.A defect in early myogenesis causes Otitis media in two mouse models of 22q11.2 Deletion Syndrome.Hard to swallow: Developmental biological insights into pediatric dysphagia.A molecular and genetic outline of cardiac morphogenesis.What have we learned from murine models of otitis media?Identification of downstream genetic pathways of Tbx1 in the second heart field.Canonical Wnt signaling modulates Tbx1, Eya1, and Six1 expression, restricting neurogenesis in the otic vesicle.Loss of Tbx1 induces bone phenotypes similar to cleidocranial dysplasia.Pax2 may play a role in kidney development by regulating the expression of TBX1.Altered Tbx1 gene expression is associated with abnormal oesophageal development in the adriamycin mouse model of oesophageal atresia/tracheo-oesophageal fistula.The 22q11 deletion: DiGeorge and velocardiofacial syndromes and the role of TBX1.Dual role for neural crest cells during outflow tract septation in the neural crest-deficient mutant Splotch(2H).
P2860
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P2860
Tbx1 is required for proper neural crest migration and to stabilize spatial patterns during middle and inner ear development
description
2005 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2005
@ast
im Februar 2005 veröffentlichter wissenschaftlicher Artikel
@de
scientific journal article
@en
vedecký článok (publikovaný 2005/02/01)
@sk
vědecký článek publikovaný v roce 2005
@cs
wetenschappelijk artikel (gepubliceerd op 2005/02/01)
@nl
наукова стаття, опублікована в лютому 2005
@uk
مقالة علمية (نشرت في فبراير 2005)
@ar
name
Tbx1 is required for proper ne ...... ddle and inner ear development
@ast
Tbx1 is required for proper ne ...... ddle and inner ear development
@en
Tbx1 is required for proper ne ...... ddle and inner ear development
@nl
type
label
Tbx1 is required for proper ne ...... ddle and inner ear development
@ast
Tbx1 is required for proper ne ...... ddle and inner ear development
@en
Tbx1 is required for proper ne ...... ddle and inner ear development
@nl
prefLabel
Tbx1 is required for proper ne ...... ddle and inner ear development
@ast
Tbx1 is required for proper ne ...... ddle and inner ear development
@en
Tbx1 is required for proper ne ...... ddle and inner ear development
@nl
P50
P1476
Tbx1 is required for proper ne ...... ddle and inner ear development
@en
P2093
Filipa Moraes
Loydie A Jerome-Majewska
P304
P356
10.1016/J.MOD.2004.10.004
P577
2005-02-01T00:00:00Z