Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.
about
Differentiation of the lateral compartment of the cochlea requires a temporally restricted FGF20 signalChimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyDistinct populations within Isl1 lineages contribute to appendicular and facial skeletogenesis through the β-catenin pathwayTbx1 controls the morphogenesis of pharyngeal pouch epithelia through mesodermal Wnt11r and Fgf8a.Elevated levels of Wnt signaling disrupt thymus morphogenesis and function.Endothelial neuropilin disruption in mice causes DiGeorge syndrome-like malformations via mechanisms distinct to those caused by loss of Tbx1A novel role for the T-box transcription factor Tbx1 as a negative regulator of tumor cell growth in mice.WNT signaling suppression in the senescent human thymus.Differentially regulated splice variants and systems biology analysis of Kaposi's sarcoma-associated herpesvirus-infected lymphatic endothelial cells.Histone deacetylase 3 regulates smooth muscle differentiation in neural crest cells and development of the cardiac outflow tractGenome-wide occupancy links Hoxa2 to Wnt-β-catenin signaling in mouse embryonic development.Partitioning the heart: mechanisms of cardiac septation and valve developmentSuperoxide Dismutase 1 In Vivo Ameliorates Maternal Diabetes Mellitus-Induced Apoptosis and Heart Defects Through Restoration of Impaired Wnt Signaling.Reduced dosage of β-catenin provides significant rescue of cardiac outflow tract anomalies in a Tbx1 conditional null mouse model of 22q11.2 deletion syndrome.Novel insights into the development and maintenance of the blood-brain barrier.Mouth development.Mesenchymal fibroblast growth factor receptor signaling regulates palatal shelf elevation during secondary palate formation.Expression, function, and regulation of the embryonic transcription factor TBX1 in parathyroid tumors.Pax2 may play a role in kidney development by regulating the expression of TBX1.Cranial neural crest cells on the move: their roles in craniofacial development.
P2860
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P2860
Beta-catenin deficiency causes DiGeorge syndrome-like phenotypes through regulation of Tbx1.
description
2010 nî lūn-bûn
@nan
2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年学术文章
@wuu
2010年学术文章
@zh-cn
2010年学术文章
@zh-hans
2010年学术文章
@zh-my
2010年学术文章
@zh-sg
2010年學術文章
@yue
name
Beta-catenin deficiency causes ...... es through regulation of Tbx1.
@ast
Beta-catenin deficiency causes ...... es through regulation of Tbx1.
@en
type
label
Beta-catenin deficiency causes ...... es through regulation of Tbx1.
@ast
Beta-catenin deficiency causes ...... es through regulation of Tbx1.
@en
prefLabel
Beta-catenin deficiency causes ...... es through regulation of Tbx1.
@ast
Beta-catenin deficiency causes ...... es through regulation of Tbx1.
@en
P2860
P356
P1433
P1476
Beta-catenin deficiency causes ...... pes through regulation of Tbx1
@en
P2093
Sung-Ho Huh
P2860
P304
P356
10.1242/DEV.045534
P407
P577
2010-04-01T00:00:00Z