Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
about
Cloning and characterisation of the Sry-related transcription factor gene Sox8.Domains of Brn-2 that mediate homodimerization and interaction with general and melanocytic transcription factorsThe MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patientsBrachyury-related transcription factor Tbx2 and repression of the melanocyte-specific TRP-1 promoter.A new long form of Sox5 (L-Sox5), Sox6 and Sox9 are coexpressed in chondrogenesis and cooperatively activate the type II collagen geneSox10 is an active nucleocytoplasmic shuttle protein, and shuttling is crucial for Sox10-mediated transactivationGpnmb is a melanoblast-expressed, MITF-dependent geneThe armadillo repeat-containing protein, ARMCX3, physically and functionally interacts with the developmental regulatory factor Sox10Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factorsTransplanting the enteric nervous system: a step closer to treatment for aganglionosisSox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal deathInduction of the neural crest state: control of stem cell attributes by gene regulatory, post-transcriptional and epigenetic interactionsA dual role for SOX10 in the maintenance of the postnatal melanocyte lineage and the differentiation of melanocyte stem cell progenitorsDevelopment of the zebrafish enteric nervous system.The Effect of Microbiota and the Immune System on the Development and Organization of the Enteric Nervous SystemGenerating human intestinal tissues from pluripotent stem cells to study development and diseaseMolecular control of the neural crest and peripheral nervous system developmentFurther complexity of the human SOX gene family revealed by the combined use of highly degenerate primers and nested PCRA molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathiesMyelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutationMelanocyte-specific expression of dopachrome tautomerase is dependent on synergistic gene activation by the Sox10 and Mitf transcription factorsMolecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutationsRegulatory mechanisms for neural crest formationSOX10 mutations in patients with Waardenburg-Hirschsprung diseaseA Sox10 expression screen identifies an amino acid essential for Erbb3 function.Neuropilin 1 signaling guides neural crest cells to coordinate pathway choice with cell specificationAdult-onset degeneration of adipose tissue in mice deficient for the Sox8 transcription factorThe homeobox gene Phox2b is essential for the development of autonomic neural crest derivativesSOX7 and SOX17 regulate the parietal endoderm-specific enhancer activity of mouse laminin alpha1 geneMice null for sox18 are viable and display a mild coat defectTerminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8The Sox9 transcription factor determines glial fate choice in the developing spinal cordThe novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear.Sox8 is a critical regulator of adult Sertoli cell function and male fertilityThe high mobility group transcription factor Sox8 is a negative regulator of osteoblast differentiationSox8 is a specific marker for muscle satellite cells and inhibits myogenesisA sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathyCharacterization of Solt, a novel SoxLZ/Sox6 binding protein expressed in adult mouse testis
P2860
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P2860
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
description
1998 nî lūn-bûn
@nan
1998 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
name
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@ast
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en-gb
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@nl
type
label
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@ast
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en-gb
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@nl
prefLabel
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@ast
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en-gb
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@nl
P3181
P356
P1433
P1476
Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model
@en
P2093
P2888
P3181
P356
10.1038/NG0198-60
P407
P577
1998-01-01T00:00:00Z
P6179
1012646897