| scholarly article | Q13442814 |
| P819 | ADS bibcode | 1998PNAS...95.5161H |
| P356 | DOI | 10.1073/PNAS.95.9.5161 |
| P932 | PMC publication ID | 20231 |
| P698 | PubMed publication ID | 9560246 |
| P5875 | ResearchGate publication ID | 13720681 |
| P2093 | author name string | Goossens M | |
| Pingault V | |||
| Hermans-Borgmeyer I | |||
| Bondurand N | |||
| Wegner M | |||
| Kuhlbrodt K | |||
| Puliti A | |||
| Herbarth B | |||
| Lemort N | |||
| P2860 | cites work | Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model | Q24319465 |
| Waardenburg syndrome | Q24517935 | ||
| Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene | Q28242642 | ||
| Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene SOX9 | Q28243215 | ||
| Interaction of endothelin-3 with endothelin-B receptor is essential for development of epidermal melanocytes and enteric neurons | Q28243225 | ||
| Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype | Q28253613 | ||
| Defects in cardiac outflow tract formation and pro-B-lymphocyte expansion in mice lacking Sox-4 | Q28505545 | ||
| Sox10, a novel transcriptional modulator in glial cells | Q28582624 | ||
| Association of megacolon with a new dominant spotting gene (Dom) in the mouse | Q28586637 | ||
| Multiple essential functions of neuregulin in development | Q28587914 | ||
| A gene mapping to the sex-determining region of the mouse Y chromosome is a member of a novel family of embryonically expressed genes | Q29618455 | ||
| Construction of a mouse yeast artificial chromosome library in a recombination-deficient strain of yeast | Q31157900 | ||
| Genomic analysis using a yeast artificial chromosome library with mouse DNA inserts | Q31162138 | ||
| Yeast artificial chromosome libraries containing large inserts from mouse and human DNA | Q33546790 | ||
| Targeted and natural (piebald-lethal) mutations of endothelin-B receptor gene produce megacolon associated with spotted coat color in mice | Q34328245 | ||
| A genetic study of Hirschsprung disease | Q34644543 | ||
| SOX genes: architects of development. | Q36437950 | ||
| Expression of a candidate sex-determining gene during mouse testis differentiation. | Q38338182 | ||
| Development of the peripheral nervous system from the neural crest | Q39544468 | ||
| Genes and lineages in the formation of the enteric nervous system | Q41130786 | ||
| Requirement for neuregulin receptor erbB2 in neural and cardiac development | Q41269625 | ||
| Sox genes find their feet | Q41536268 | ||
| Cellular and molecular biology of neural crest cell lineage determination | Q41549759 | ||
| Human homology and candidate genes for the Dominant megacolon locus, a mouse model of Hirschsprung disease | Q48056092 | ||
| A high-resolution genetic map of mouse chromosome 15 encompassing the Dominant megacolon (Dom) locus | Q70992246 | ||
| Contributions of placodal and neural crest cells to avian cranial peripheral ganglia | Q71755691 | ||
| A somatic cell hybrid panel for mouse gene mapping characterized by PCR and FISH | Q71989849 | ||
| Two rhombomeres are altered in Hoxa-1 mutant mice | Q72723151 | ||
| Association of Megacolon with Two Recessive Spotting Genes in the Mouse | Q72795387 | ||
| P433 | issue | 9 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | megacolon | Q1754226 |
| P304 | page(s) | 5161-5165 | |
| P577 | publication date | 1998-04-01 | |
| P1433 | published in | Proceedings of the National Academy of Sciences of the United States of America | Q1146531 |
| P1476 | title | Mutation of the Sry-related Sox10 gene in Dominant megacolon, a mouse model for human Hirschsprung disease | |
| P478 | volume | 95 |
| Q30490465 | 5-HT4 receptor-mediated neuroprotection and neurogenesis in the enteric nervous system of adult mice |
| Q34286431 | A curated online resource for SOX10 and pigment cell molecular genetic pathways |
| Q27321082 | A dual role for SOX10 in the maintenance of the postnatal melanocyte lineage and the differentiation of melanocyte stem cell progenitors |
| Q28141732 | A molecular analysis of the yemenite deaf-blind hypopigmentation syndrome: SOX10 dysfunction causes different neurocristopathies |
| Q41556263 | A reporter mouse model for in vivo tracing and in vitro molecular studies of melanocytic lineage cells and their diseases. |
| Q58782380 | Ablation of Ezh2 in neural crest cells leads to aberrant enteric nervous system development in mice |
| Q28504812 | Adult-onset degeneration of adipose tissue in mice deficient for the Sox8 transcription factor |
| Q33379291 | An evolutionarily conserved intronic region controls the spatiotemporal expression of the transcription factor Sox10. |
| Q37714233 | An ongoing role for Wnt signaling in differentiating melanocytes in vivo |
| Q36332520 | Animal models in pediatric surgery |
| Q35023613 | Antagonistic cross-regulation between Sox9 and Sox10 controls an anti-tumorigenic program in melanoma. |
| Q35251314 | Anterior Hox genes interact with components of the neural crest specification network to induce neural crest fates |
| Q39397994 | Beyond MITF: Multiple transcription factors directly regulate the cellular phenotype in melanocytes and melanoma. |
| Q38061180 | Building a brain in the gut: development of the enteric nervous system |
| Q30273715 | Cell type-specific activation of neuronal nicotinic acetylcholine receptor subunit genes by Sox10. |
| Q44233362 | Characterization of cultured multipotent zebrafish neural crest cells |
| Q42629090 | Chick sox10, a transcription factor expressed in both early neural crest cells and central nervous system |
| Q34720641 | Chromosome 21 scan in Down syndrome reveals DSCAM as a predisposing locus in Hirschsprung disease |
| Q58379822 | Colonic Epithelial Expression of ErbB2 Is Required for Postnatal Maintenance of the Enteric Nervous System |
| Q34428830 | Comparison of melanoblast expression patterns identifies distinct classes of genes |
| Q52095660 | Complementation of melanocyte development in SOX10 mutant neural crest using lineage-directed gene transfer. |
| Q24676478 | Control of cell fate and differentiation by Sry-related high-mobility-group box (Sox) transcription factors |
| Q38359542 | Cooperative binding of Sox10 to DNA: requirements and consequences |
| Q33556276 | Defining the transcriptomic landscape of the developing enteric nervous system and its cellular environment |
| Q57911328 | Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10 |
| Q34580794 | Development of the zebrafish inner ear. |
| Q35009580 | Disrupted SOX10 function causes spongiform neurodegeneration in gray tremor mice |
| Q40296066 | Distant regulatory elements in a Sox10-beta GEO BAC transgene are required for expression of Sox10 in the enteric nervous system and other neural crest-derived tissues. |
| Q52431322 | Distinct interactions of Sox5 and Sox10 in fate specification of pigment cells in medaka and zebrafish. |
| Q24290395 | Domains of Brn-2 that mediate homodimerization and interaction with general and melanocytic transcription factors |
| Q93344047 | Dual embryonic origin of the mammalian enteric nervous system |
| Q91600448 | Efficacy of Sox10 Promoter Methylation in the Diagnosis of Intestinal Neuronal Dysplasia From the Peripheral Blood |
| Q35998016 | Elevated Levels of SOX10 in Serum from Vitiligo and Melanoma Patients, Analyzed by Proximity Ligation Assay |
| Q35561135 | Elevated in vivo levels of a single transcription factor directly convert satellite glia into oligodendrocyte-like cells |
| Q34081737 | Embryology and development of the enteric nervous system |
| Q39413846 | Endoderm-derived Sonic hedgehog and mesoderm Hand2 expression are required for enteric nervous system development in zebrafish. |
| Q34352040 | Endogenous retrovirus insertion in the KIT oncogene determines white and white spotting in domestic cats |
| Q36827186 | Enteric nervous system development and Hirschsprung's disease: advances in genetic and stem cell studies |
| Q26745493 | Enteric nervous system development in avian and zebrafish models |
| Q64883765 | Enteric nervous system development: what could possibly go wrong? |
| Q48659025 | Establishment of myelinating Schwann cells and barrier integrity between central and peripheral nervous systems depend on Sox10. |
| Q38288184 | Expression and characterization of Xenopus laevis SRY-related cDNAs, xSox17alpha1, xSox17alpha2, xSox18alpha and xSox18beta |
| Q52003127 | Expression of Hand2 is sufficient for neurogenesis and cell type-specific gene expression in the enteric nervous system. |
| Q28591270 | Expression of Ret-, p75(NTR)-, Phox2a-, Phox2b-, and tyrosine hydroxylase-immunoreactivity by undifferentiated neural crest-derived cells and different classes of enteric neurons in the embryonic mouse gut |
| Q57829890 | Expression of the SOX10 gene during human development |
| Q49159530 | Expression of the Sox10 gene during mouse inner ear development |
| Q34199653 | Expression of transcription factors during oligodendroglial development |
| Q36788451 | Feeder-free Derivation of Melanocytes from Human Pluripotent Stem Cells |
| Q30447868 | Feline deafness |
| Q50026122 | First Report of Prenatal Ascertainment of a Fetus With Homozygous Loss of the SOX10 Gene and Phenotypic Correlation by Autopsy Examination |
| Q36645563 | Function of Armcx3 and Armc10/SVH Genes in the Regulation of Progenitor Proliferation and Neural Differentiation in the Chicken Spinal Cord. |
| Q24309053 | Functional analysis of Sox10 mutations found in human Waardenburg-Hirschsprung patients |
| Q50432807 | Functional analysis of Waardenburg syndrome-associated PAX3 and SOX10 mutations: report of a dominant-negative SOX10 mutation in Waardenburg syndrome type II. |
| Q43123316 | Genetic ablation of neural crest cell diversification |
| Q34986444 | Genetic basis of Hirschsprung's disease. |
| Q51854582 | Genetic interaction between Sox10 and Zfhx1b during enteric nervous system development. |
| Q33699347 | Genetic model system studies of the development of the enteric nervous system, gut motility and Hirschsprung's disease |
| Q28589643 | Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease |
| Q37027769 | Glial cells: old cells with new twists |
| Q34443063 | GnRH, anosmia and hypogonadotropic hypogonadism--where are we? |
| Q90405710 | Gonadotropin-releasing hormone neuron development in vertebrates |
| Q38534660 | Hearing loss in Waardenburg syndrome: a systematic review |
| Q60418230 | Heterogeneity and phenotypic plasticity of glial cells in the mammalian enteric nervous system |
| Q33688226 | Hirschsprung disease and other enteric dysganglionoses |
| Q34428513 | Hirschsprung disease, associated syndromes, and genetics: a review |
| Q38316691 | Homologue of Sox10 in Misgurnus anguillicaudatus: sequence, expression pattern during early embryogenesis |
| Q52055087 | Hoxb3 vagal neural crest-specific enhancer element for controlling enteric nervous system development. |
| Q33346003 | Human hereditary hearing impairment: mouse models can help to solve the puzzle |
| Q28506101 | Identification of Sox8 as a modifier gene in a mouse model of Hirschsprung disease reveals underlying molecular defect |
| Q52119538 | Identification of a distal enhancer for the melanocyte-specific promoter of the MITF gene. |
| Q43185873 | Identification of a novel nonsense mutation on the Pax3 gene in ENU-derived white belly spotting mice and its genetic interaction with c-Kit |
| Q33367100 | Identification of neural crest and glial enhancers at the mouse Sox10 locus through transgenesis in zebrafish |
| Q28512330 | Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8 |
| Q34482177 | Influence and timing of arrival of murine neural crest on pancreatic beta cell development and maturation |
| Q98781870 | Insights into olfactory ensheathing cell development from a laser-microdissection and transcriptome-profiling approach |
| Q50465179 | Interactions between Sox10, Edn3 and Ednrb during enteric nervous system and melanocyte development. |
| Q34694810 | Interspecies difference in the regulation of melanocyte development by SOX10 and MITF. |
| Q34236122 | Intestinal motility disorders and development of the enteric nervous system |
| Q28188758 | Is there a role for the IHH gene in Hirschsprung's disease? |
| Q28505432 | Isolation and characterization of a mouse SRY-related cDNA, mSox7 |
| Q35540338 | Isolation and live imaging of enteric progenitors based on Sox10-Histone2BVenus transgene expression |
| Q38542132 | Knockout mouse models of Hirschsprung's disease |
| Q39661589 | Master regulator for chondrogenesis, Sox9, regulates transcriptional activation of the endoplasmic reticulum stress transducer BBF2H7/CREB3L2 in chondrocytes |
| Q37303304 | Mechanisms for reaching the differentiated state: Insights from neural crest-derived melanocytes |
| Q28237203 | Melanocyte-specific expression of dopachrome tautomerase is dependent on synergistic gene activation by the Sox10 and Mitf transcription factors |
| Q52118710 | Migration and function of a glial subtype in the vertebrate peripheral nervous system. |
| Q38356293 | Molecular cloning and expression of Sox17 in gonads during sex reversal in the rice field eel, a teleost fish with a characteristic of natural sex transformation. |
| Q48232579 | Molecular cloning and mRNA expression pattern of Sox10 in Paramisgurnus dabryanus |
| Q34793348 | Molecular dissection of craniofacial development using zebrafish |
| Q39449898 | Molecular fingerprinting delineates progenitor populations in the developing zebrafish enteric nervous system |
| Q28248837 | Molecular mechanism for distinct neurological phenotypes conveyed by allelic truncating mutations |
| Q52062410 | Morphogenesis of the jaw: development beyond the embryo. |
| Q34536726 | Mouse models for four types of Waardenburg syndrome |
| Q38883845 | Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players |
| Q30499506 | Multiple conserved regulatory elements with overlapping functions determine Sox10 expression in mouse embryogenesis |
| Q28144228 | Myelin deficiencies in both the central and the peripheral nervous systems associated with a SOX10 mutation |
| Q39539932 | Neural crest cells retain their capability for multipotential differentiation even after lineage-restricted stages. |
| Q26775970 | Neural crest: The fourth germ layer |
| Q34299988 | Neuropathology of paediatric chronic intestinal pseudo-obstruction and related animal models |
| Q41768904 | Olfactory ensheathing glia are required for embryonic olfactory axon targeting and the migration of gonadotropin-releasing hormone neurons |
| Q48743716 | Oligodendroglial-specific transcriptional factor SOX10 is ubiquitously expressed in human gliomas |
| Q33939049 | Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disorders. |
| Q44474587 | Pathogenesis of axonal dystrophy and demyelination in alphaA-crystallin-expressing transgenic mice |
| Q38292266 | Pax3 down-regulation and shut-off of melanogenesis in melanoma B16/F10.9 by interleukin-6 receptor signaling |
| Q40432015 | Pax3 is required for enteric ganglia formation and functions with Sox10 to modulate expression of c-ret |
| Q34687551 | Prospective identification and isolation of enteric nervous system progenitors using Sox2. |
| Q39452670 | Protein zero gene expression is regulated by the glial transcription factor Sox10 |
| Q48608385 | Radial glia phagocytose axonal debris from degenerating overextending axons in the developing olfactory bulb |
| Q38262962 | Regulation of SOX10 stability via ubiquitination-mediated degradation by Fbxw7α modulates melanoma cell migration |
| Q36041868 | Regulators of gene expression in Enteric Neural Crest Cells are putative Hirschsprung disease genes. |
| Q51915545 | Replacement of mouse Sox10 by the Drosophila ortholog Sox100B provides evidence for co-option of SoxE proteins into vertebrate-specific gene-regulatory networks through altered expression. |
| Q37686450 | Review and update of mutations causing Waardenburg syndrome. |
| Q37086064 | Riding the crest of the wave: parallels between the neural crest and cancer in epithelial-to-mesenchymal transition and migration |
| Q28579735 | SOX10 Maintains Multipotency and Inhibits Neuronal Differentiation of Neural Crest Stem Cells |
| Q33932242 | SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer |
| Q35364550 | SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants |
| Q39017271 | SOX10 promotes melanoma cell invasion by regulating melanoma inhibitory activity. |
| Q38314140 | SOX10, in combination with Sp1, regulates the endothelin receptor type B gene in human melanocyte lineage cells |
| Q34005547 | Sox proteins in melanocyte development and melanoma |
| Q39162325 | Sox10 and Itgb1 interaction in enteric neural crest cell migration. |
| Q36295516 | Sox10 contributes to the balance of fate choice in dorsal root ganglion progenitors |
| Q30437030 | Sox10 expressing cells in the lateral wall of the aged mouse and human cochlea |
| Q24537637 | Sox10 is an active nucleocytoplasmic shuttle protein, and shuttling is crucial for Sox10-mediated transactivation |
| Q41775433 | Sox10 is required for Schwann cell identity and progression beyond the immature Schwann cell stage |
| Q57911290 | Sox10 is required for Schwann-cell homeostasis and myelin maintenance in the adult peripheral nerve |
| Q38352189 | Sox10 is required for the early development of the prospective neural crest in Xenopus embryos. |
| Q39318116 | Sox10 promotes the formation and maintenance of giant congenital naevi and melanoma |
| Q44826007 | Sox10 promotes the survival of cochlear progenitors during the establishment of the organ of Corti |
| Q34651020 | Sox10 regulates ciliary neurotrophic factor gene expression in Schwann cells |
| Q52103988 | Sox10 regulates the development of neural crest-derived melanocytes in Xenopus. |
| Q35569050 | Sox10--a marker for not only schwannian and melanocytic neoplasms but also myoepithelial cell tumors of soft tissue: a systematic analysis of 5134 tumors |
| Q40502328 | Sox10-rtTA mouse line for tetracycline-inducible expression of transgenes in neural crest cells and oligodendrocytes |
| Q28587628 | Sox8 is a specific marker for muscle satellite cells and inhibits myogenesis |
| Q36536675 | SoxE proteins are differentially required in mouse adrenal gland development |
| Q47413249 | Spatiotemporal regulation of endothelin receptor-B by SOX10 in neural crest-derived enteric neuron precursors. |
| Q35771686 | Spotlight on spotted mice: a review of white spotting mouse mutants and associated human pigmentation disorders |
| Q35787988 | Sympathoadrenal hyperplasia causes renal malformations in Ret(MEN2B)-transgenic mice |
| Q40846928 | Synergistic transcriptional activation by Sox10 and Sp1 family members |
| Q28511593 | Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10 |
| Q28594564 | The Hlx homeobox transcription factor is required early in enteric nervous system development |
| Q24304297 | The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10 |
| Q22011211 | The SOX8 gene is located within 700 kb of the tip of chromosome 16p and is deleted in a patient with ATR-16 syndrome |
| Q28512816 | The Sox9 transcription factor determines glial fate choice in the developing spinal cord |
| Q24647979 | The armadillo repeat-containing protein, ARMCX3, physically and functionally interacts with the developmental regulatory factor Sox10 |
| Q34250716 | The enteric nervous system |
| Q92751197 | The gene regulatory basis of genetic compensation during neural crest induction |
| Q39572483 | The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences |
| Q28586194 | The high mobility group transcription factor Sox8 is a negative regulator of osteoblast differentiation |
| Q24337898 | The high-mobility group transcription factor Sox10 interacts with the N-myc-interacting protein Nmi |
| Q28505510 | The homeobox gene Phox2b is essential for the development of autonomic neural crest derivatives |
| Q35146531 | The importance of having your SOX on: role of SOX10 in the development of neural crest-derived melanocytes and glia |
| Q44067013 | The projections of early enteric neurons are influenced by the direction of neural crest cell migration. |
| Q38296070 | The receptor tyrosine kinase RET regulates hindgut colonization by sacral neural crest cells |
| Q28290131 | The role of SOX10 during enteric nervous system development |
| Q40423560 | The transcription factor Sox10 is a key regulator of peripheral glial development. |
| Q100750439 | The transcription factor Sox10 is an essential determinant of branching morphogenesis and involution in the mouse mammary gland |
| Q39950581 | The transcription factor Sox5 modulates Sox10 function during melanocyte development |
| Q36202037 | The transcription factors Ets1 and Sox10 interact during murine melanocyte development |
| Q34374352 | The ubiquitin ligase Nedd4 regulates craniofacial development by promoting cranial neural crest cell survival and stem-cell like properties |
| Q40651259 | Tissue culture methods to study neurological disorders: establishment of immortalized Schwann cells from murine disease models |
| Q39990892 | Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene |
| Q38370706 | Transcriptional control of neural crest specification into peripheral glia |
| Q34968711 | Zebrafish as a model for hearing and deafness. |
| Q33355991 | Zebrafish endzone regulates neural crest-derived chromatophore differentiation and morphology |
| Q37118111 | lessen encodes a zebrafish trap100 required for enteric nervous system development |
| Q41827449 | prdm1a Regulates sox10 and islet1 in the development of neural crest and Rohon‐Beard sensory neurons |
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