| scholarly article | Q13442814 |
| P50 | author | E. Michelle Southard-Smith | Q63436814 |
| P2093 | author name string | Hernan Correa | |
| Melissa A Musser | |||
| P2860 | cites work | Temporal control of neural crest lineage generation by Wnt/β-catenin signaling. | Q51785160 |
| Cell-intrinsic differences between stem cells from different regions of the peripheral nervous system regulate the generation of neural diversity. | Q52115703 | ||
| The Sox10(Dom) mouse: modeling the genetic variation of Waardenburg-Shah (WS4) syndrome | Q57281748 | ||
| Development and degeneration of dorsal root ganglia in the absence of the HMG-domain transcription factor Sox10 | Q57911328 | ||
| Survival and glial fate acquisition of neural crest cells are regulated by an interplay between the transcription factor Sox10 and extrinsic combinatorial signaling | Q57911330 | ||
| Accurate measurement of intestinal transit in the rat | Q71069600 | ||
| Early death of neural crest cells is responsible for total enteric aganglionosis in Sox10(Dom)/Sox10(Dom) mouse embryos | Q73047295 | ||
| Widespread changes in neurotransmitter expression and number of enteric neurons and interstitial cells of Cajal in lethal spotted mice: an explanation for persisting dysmotility after operation for Hirschsprung's disease? | Q74129610 | ||
| Sox10 haploinsufficiency affects maintenance of progenitor cells in a mouse model of Hirschsprung disease | Q78477481 | ||
| Interactions between Sox10 and EdnrB modulate penetrance and severity of aganglionosis in the Sox10Dom mouse model of Hirschsprung disease | Q80418548 | ||
| Anatomic modifications in the enteric nervous system of piebald mice and physiological consequences to colonic motor activity | Q81597920 | ||
| Sox10 mutation disrupts neural crest development in Dom Hirschsprung mouse model | Q24319465 | ||
| Neural crest stem cells persist in the adult gut but undergo changes in self-renewal, neuronal subtype potential, and factor responsiveness | Q24650279 | ||
| Role of enteric neurotransmission in host defense and protection of the gastrointestinal tract | Q26827692 | ||
| Contribution of rare and common variants determine complex diseases-Hirschsprung disease as a model | Q26866340 | ||
| The role of SOX10 during enteric nervous system development | Q28290131 | ||
| Dual roles for glucokinase in glucose homeostasis as determined by liver and pancreatic beta cell-specific gene knock-outs using Cre recombinase | Q28508079 | ||
| SOX10 Maintains Multipotency and Inhibits Neuronal Differentiation of Neural Crest Stem Cells | Q28579735 | ||
| Genome-wide linkage identifies novel modifier loci of aganglionosis in the Sox10Dom model of Hirschsprung disease | Q28589643 | ||
| Estrogen actions in the brain and the basis for differential action in men and women: a case for sex-specific medicines | Q30478476 | ||
| 5-HT4 receptor-mediated neuroprotection and neurogenesis in the enteric nervous system of adult mice | Q30490465 | ||
| Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease | Q31021758 | ||
| Genetic background impacts developmental potential of enteric neural crest-derived progenitors in the Sox10Dom model of Hirschsprung disease. | Q34211976 | ||
| Hirschsprung disease, associated syndromes and genetics: a review | Q34584242 | ||
| Murine model of Hirschsprung-associated enterocolitis. I: phenotypic characterization with development of a histopathologic grading system | Q34617639 | ||
| Prenatal intestinal obstruction affects the myenteric plexus and causes functional bowel impairment in fetal rat experimental model of intestinal atresia | Q34717098 | ||
| Expression level of Hand2 affects specification of enteric neurons and gastrointestinal function in mice | Q35154143 | ||
| Glial cells in the mouse enteric nervous system can undergo neurogenesis in response to injury. | Q35187149 | ||
| Isolation and live imaging of enteric progenitors based on Sox10-Histone2BVenus transgene expression | Q35540338 | ||
| Of mice and MEN1: Insulinomas in a conditional mouse knockout | Q35660901 | ||
| Enteric nervous system specific deletion of Foxd3 disrupts glial cell differentiation and activates compensatory enteric progenitors | Q35782972 | ||
| Altered neuronal density and neurotransmitter expression in the ganglionated region of Ednrb null mice: implications for Hirschsprung's disease | Q36625882 | ||
| Fate mapping using Cited1-CreERT2 mice demonstrates that the cap mesenchyme contains self-renewing progenitor cells and gives rise exclusively to nephronic epithelia. | Q37235452 | ||
| Long-term outcomes of Hirschsprung's disease. | Q38044132 | ||
| Balancing on the crest - Evidence for disruption of the enteric ganglia via inappropriate lineage segregation and consequences for gastrointestinal function | Q38078731 | ||
| Hirschsprung-associated enterocolitis: pathogenesis, treatment and prevention | Q38126434 | ||
| Toll-like receptor 2 regulates intestinal inflammation by controlling integrity of the enteric nervous system | Q39102142 | ||
| Disturbances of colonic motility in mouse models of Hirschsprung's disease. | Q40012892 | ||
| Conditional ablation of GFRalpha1 in postmigratory enteric neurons triggers unconventional neuronal death in the colon and causes a Hirschsprung's disease phenotype. | Q40132055 | ||
| 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. | Q40296066 | ||
| GDNF availability determines enteric neuron number by controlling precursor proliferation. | Q40659699 | ||
| Murine model of Hirschsprung-associated enterocolitis II: Surgical correction of aganglionosis does not eliminate enterocolitis | Q41818786 | ||
| Oscillatory control of factors determining multipotency and fate in mouse neural progenitors | Q42258504 | ||
| Environmental factors unveil dormant developmental capacities in multipotent progenitors of the trunk neural crest | Q42446040 | ||
| Requirement for Foxd3 in the maintenance of neural crest progenitors | Q43139378 | ||
| Immunohistochemical analysis of neuron types in the mouse small intestine | Q46316774 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 87-101 | |
| P577 | publication date | 2015-01-01 | |
| P1433 | published in | Cellular and molecular gastroenterology and hepatology | Q27726289 |
| P1476 | title | Enteric neuron imbalance and proximal dysmotility in ganglionated intestine of the Sox10Dom/+ Hirschsprung mouse model | |
| P478 | volume | 1 |
| Q42322599 | All Is Not Normal in "Normoganglionic" Bowel Regions of Hirschsprung Disease Model Mice |
| Q38915958 | Arundic Acid Prevents Developmental Upregulation of S100B Expression and Inhibits Enteric Glial Development. |
| Q42703839 | Bowel dysfunction following pullthrough surgery is associated with an overabundance of nitrergic neurons in Hirschsprung disease |
| Q33747014 | Colitis promotes neuronal differentiation of Sox2+ and PLP1+ enteric cells |
| Q89526910 | Dlx1/2 mice have abnormal enteric nervous system function |
| Q93176238 | Down syndrome mouse models have an abnormal enteric nervous system |
| Q64883765 | Enteric nervous system development: what could possibly go wrong? |
| Q61444384 | Gut microbiota-mediated Gene-Environment interaction in the TashT mouse model of Hirschsprung disease |
| Q50196075 | Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes |
| Q47833563 | Medial preoptic circuit induces hunting-like actions to target objects and prey. |
| Q38883845 | Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players |
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