| scholarly article | Q13442814 |
| P50 | author | William J Pavan | Q55426393 |
| E. Michelle Southard-Smith | Q63436814 | ||
| P2093 | author name string | Chakravarti A | |
| Agarwala R | |||
| Baxevanis AD | |||
| Angrist M | |||
| Ellison JS | |||
| P433 | issue | 3 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetic variation | Q349856 |
| P304 | page(s) | 215-225 | |
| P577 | publication date | 1999-03-01 | |
| P1433 | published in | Genome Research | Q5533485 |
| P1476 | title | The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome | |
| P478 | volume | 9 |
| Q28657851 | 2013 William Allan Award: My multifactorial journey |
| Q35561874 | A Sox10(rtTA/+) Mouse Line Allows for Inducible Gene Expression in the Auditory and Balance Organs of the Inner Ear. |
| Q37149716 | A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus. |
| Q90158813 | A novel frameshift mutation in SOX10 causes Waardenburg syndrome with peripheral demyelinating neuropathy, visual impairment and the absence of Hirschsprung disease |
| Q28590547 | A sensitized mutagenesis screen identifies Gli3 as a modifier of Sox10 neurocristopathy |
| Q64041991 | Case of Waardenburg Shah syndrome in a family with review of literature |
| Q34428830 | Comparison of melanoblast expression patterns identifies distinct classes of genes |
| Q35061675 | Cranial neural crest cell contribution to craniofacial formation, pathology, and future directions in tissue engineering |
| Q36512067 | Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4 |
| Q33717205 | Developmental biology of the enteric nervous system: pathogenesis of Hirschsprung's disease and other congenital dysmotilities |
| Q35950365 | Differential gene expression and functional analysis implicate novel mechanisms in enteric nervous system precursor migration and neuritogenesis. |
| Q42366787 | Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease |
| Q35234669 | Enteric neuron imbalance and proximal dysmotility in ganglionated intestine of the Sox10Dom/+ Hirschsprung mouse model. |
| Q34211976 | Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease. |
| Q30474153 | Genetic background strongly modifies the severity of symptoms of Hirschsprung disease, but not hearing loss in rats carrying Ednrb(sl) mutations |
| Q34986444 | Genetic basis of Hirschsprung's disease. |
| Q34374616 | Genetic evidence does not support direct regulation of EDNRB by SOX10 in migratory neural crest and the melanocyte lineage |
| Q43010652 | Genetic interactions and modifier genes in Hirschsprung's disease |
| Q34428513 | Hirschsprung disease, associated syndromes, and genetics: a review |
| Q28512330 | Idiopathic weight reduction in mice deficient in the high-mobility-group transcription factor Sox8 |
| Q55407497 | Key Genes and Pathways Associated With Inner Ear Malformation in SOX10 p.R109W Mutation Pigs. |
| Q28508181 | Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome |
| Q24540201 | Neurological phenotype in Waardenburg syndrome type 4 correlates with novel SOX10 truncating mutations and expression in developing brain |
| Q33714632 | Oligodendroglial and pan-neural crest expression of Cre recombinase directed by Sox10 enhancer |
| Q34762174 | Phenotype variation in two-locus mouse models of Hirschsprung disease: tissue-specific interaction between Ret and Ednrb |
| Q39452670 | Protein zero gene expression is regulated by the glial transcription factor Sox10 |
| Q34087982 | QTL analysis identifies a modifier locus of aganglionosis in the rat model of Hirschsprung disease carrying Ednrb(sl) mutations |
| Q35364550 | SOX10 is abnormally expressed in aganglionic bowel of Hirschsprung's disease infants |
| Q39318116 | Sox10 promotes the formation and maintenance of giant congenital naevi and melanoma |
| Q28511593 | Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10 |
| Q24304297 | The MADS box transcription factor MEF2C regulates melanocyte development and is a direct transcriptional target and partner of SOX10 |
| Q36951687 | The developmental etiology and pathogenesis of Hirschsprung disease. |
| Q34360888 | The genetic inheritance of the blue-eyed white phenotype in alpacas (Vicugna pacos). |
| Q39572483 | The glial transcription factor Sox10 binds to DNA both as monomer and dimer with different functional consequences |
| Q40423560 | The transcription factor Sox10 is a key regulator of peripheral glial development. |
| Q39990892 | Transcription factor Sox10 orchestrates activity of a neural crest-specific enhancer in the vicinity of its gene |
| Q92258462 | Waardenburg Syndrome Expression and Penetrance |
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