Pages that link to "Q34428513"
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The following pages link to Hirschsprung disease, associated syndromes, and genetics: a review (Q34428513):
Displaying 50 items.
- Mowat-Wilson syndrome (Q21202963) (← links)
- Apolipoprotein B is a new target of the GDNF/RET and ET-3/EDNRB signalling pathways (Q24296634) (← links)
- Mowat-Wilson syndrome (Q24677663) (← links)
- Transplanting the enteric nervous system: a step closer to treatment for aganglionosis (Q24679657) (← links)
- Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome) (Q24682812) (← links)
- The bowel and beyond: the enteric nervous system in neurological disorders (Q28069344) (← links)
- Is there a role for the IHH gene in Hirschsprung's disease? (Q28188758) (← links)
- Pediatric disorders with autonomic dysfunction: what role for PHOX2B? (Q28251570) (← links)
- Fluorescence Visualization of the Enteric Nervous Network in a Chemically Induced Aganglionosis Model (Q28550569) (← links)
- Deficiency in endothelin receptor B reduces proliferation of neuronal progenitors and increases apoptosis in postnatal rat cerebellum (Q28580802) (← links)
- Inhibition of neural crest migration underlies craniofacial dysmorphology and Hirschsprung's disease in Bardet-Biedl syndrome (Q28585667) (← links)
- Diminished Ret expression compromises neuronal survival in the colon and causes intestinal aganglionosis in mice. (Q30481679) (← links)
- Novel mechanisms of early upper and lower urinary tract patterning regulated by RetY1015 docking tyrosine in mice (Q30514572) (← links)
- In vivo transplantation of neurosphere-like bodies derived from the human postnatal and adult enteric nervous system: a pilot study (Q31157437) (← links)
- Organotypic specificity of key RET adaptor-docking sites in the pathogenesis of neurocristopathies and renal malformations in mice (Q33685678) (← links)
- Developmental biology of the enteric nervous system: pathogenesis of Hirschsprung's disease and other congenital dysmotilities (Q33717205) (← links)
- Hirschsprung's disease in children: a five year experience at a university teaching hospital in northwestern Tanzania (Q33850725) (← links)
- Fine mapping of the 9q31 Hirschsprung's disease locus. (Q33853719) (← links)
- Expression of the SMADIP1 gene during early human development (Q34144195) (← links)
- Mutational analysis of the RNX gene in congenital central hypoventilation syndrome (Q34156952) (← links)
- Hirschsprung's Disease and Associated Congenital Heart Defects: A Prospective Observational Study from a Single Institution. (Q34198135) (← links)
- Complex pathogenesis of Hirschsprung's disease in a patient with hydrocephalus, vesico-ureteral reflux and a balanced translocation t(3;17)(p12;q11). (Q34326028) (← links)
- Polymerase chain reaction-single strand conformational polymorphism analysis of rearranged during transfection proto-oncogene in Chinese familial Hirschsprung's disease (Q34382706) (← links)
- Identifying candidate Hirschsprung disease-associated RET variants (Q34401758) (← links)
- Trisomy 7 mosaicism, maternal uniparental heterodisomy 7 and Hirschsprung's disease in a child with Silver-Russell syndrome (Q34421272) (← links)
- A prospective observational study of associated anomalies in Hirschsprung's disease (Q34461709) (← links)
- Diagnosis of Hirschsprung's disease with particular emphasis on histopathology. A systematic review of current literature (Q34466628) (← links)
- Functional outcome after Swenson's operation for Hirshsprung's disease. (Q34501312) (← links)
- Advances in ontogeny of the enteric nervous system (Q34564719) (← links)
- The contribution of associated congenital anomalies in understanding Hirschsprung's disease (Q34565449) (← links)
- Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease (Q34614037) (← links)
- Pigment pattern formation in zebrafish: a model for developmental genetics and the evolution of form (Q34872754) (← links)
- Beyond Mendel: an evolving view of human genetic disease transmission (Q34932051) (← links)
- Genetic basis of Hirschsprung's disease. (Q34986444) (← links)
- RET and PHOX2B genetic polymorphisms and Hirschsprung's disease susceptibility: a meta-analysis (Q35126633) (← links)
- Comparative study of Hsp27, GSK3β, Wnt1 and PRDX3 in Hirschsprung's disease (Q35158630) (← links)
- Genes modulating chemical breathing control: lessons from mutant animals (Q35174345) (← links)
- Diagnosis and treatment of chronic gastroparesis and chronic intestinal pseudo-obstruction. (Q35176981) (← links)
- Down-regulation of miR-206 is associated with Hirschsprung disease and suppresses cell migration and proliferation in cell models (Q35198095) (← links)
- The genetics of Hirschsprung disease (Q35561249) (← links)
- Multiple endocrine neoplasias type 2B and RET proto-oncogene. (Q36012582) (← links)
- Multiple endocrine neoplasia type 2B and Hirschsprung's disease (Q36119799) (← links)
- Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report. (Q36125601) (← links)
- Alternative splicing results in RET isoforms with distinct trafficking properties. (Q36284502) (← links)
- Epithelial-mesenchymal transition in development and cancer: role of phosphatidylinositol 3' kinase/AKT pathways (Q36313178) (← links)
- Animal models in pediatric surgery (Q36332520) (← links)
- Detection and preliminary screening of the human gene expression profile for Hirschsprung's disease (Q36390408) (← links)
- Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4 (Q36512067) (← links)
- Enteric nervous system and developmental abnormalities in childhood (Q36603964) (← links)
- Symptomatology, pathophysiology, diagnostic work-up, and treatment of Hirschsprung disease in infancy and childhood (Q36826195) (← links)