Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
about
Muscle differentiation is antagonized by SOX15, a new member of the SOX protein familyNeurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain.A 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 mutationsThe VCAM-1 gene that encodes the vascular cell adhesion molecule is a target of the Sry-related high mobility group box gene, Sox18Sox8 is a critical regulator of adult Sertoli cell function and male fertilityNeuropathy-Associated Egr2 Mutants Disrupt Cooperative Activation of Myelin Protein Zero by Egr2 and Sox10Sox10-Venus mice: a new tool for real-time labeling of neural crest lineage cells and oligodendrocytes.Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis.The Dual-specificity phosphatase Dusp15 is regulated by Sox10 and Myrf in Myelinating Oligodendrocytes.Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish.An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10.Developmental biology of the enteric nervous system: pathogenesis of Hirschsprung's disease and other congenital dysmotilities.Protein stability and domain topology determine the transcriptional activity of the mammalian glial cells missing homolog, GCMb.Transcriptional regulation by activation and repression elements located at the 5'-noncoding region of the human alpha9 nicotinic receptor subunit gene.Intestinal motility disorders and development of the enteric nervous system.1998 ASHG presidential address. Making genomic medicine a realityGnRH, anosmia and hypogonadotropic hypogonadism--where are we?Mouse models for four types of Waardenburg syndrome.Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cellsSOX10, a novel HMG-box-containing tumor suppressor, inhibits growth and metastasis of digestive cancers by suppressing the Wnt/β-catenin pathway.Antagonistic cross-regulation between Sox9 and Sox10 controls an anti-tumorigenic program in melanoma.The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia.SOXE transcription factors form selective dimers on non-compact DNA motifs through multifaceted interactions between dimerization and high-mobility group domainsThe chemokine SDF-1/CXCL12 regulates the migration of melanocyte progenitors in mouse hair follicles.Elevated Levels of SOX10 in Serum from Vitiligo and Melanoma Patients, Analyzed by Proximity Ligation Assay.Cellular and ultrastructural characterization of the grey-morph phenotype in southern right whales (Eubalaena australis).Cooperative binding of Sox10 to DNA: requirements and consequencesKnockout mouse models of Hirschsprung's disease.Microphthalmia-associated transcription factor is expressed in projection neurons of the mouse olfactory bulb.Sox10 promotes the formation and maintenance of giant congenital naevi and melanoma.Protein zero gene expression is regulated by the glial transcription factor Sox10The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences.Loss of tumorigenic potential upon transdifferentiation from keratinocytic into melanocytic lineage.The transcription factor Sox5 modulates Sox10 function during melanocyte development.The transcription factor Sox10 is a key regulator of peripheral glial development.Identification and functional analysis of SOX10 phosphorylation sites in melanoma.Transcription factor Sox10 regulates oligodendroglial Sox9 levels via microRNAs.
P2860
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P2860
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
description
1998 nî lūn-bûn
@nan
1998 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
1998 թվականի սեպտեմբերին 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
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@ast
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en-gb
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@nl
type
label
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@ast
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en-gb
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@nl
prefLabel
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@ast
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en-gb
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@nl
P2093
P2860
P921
P3181
P356
P1476
Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients
@en
P2093
P2860
P304
P3181
P356
10.1074/JBC.273.36.23033
P407
P577
1998-09-04T00:00:00Z