Pages that link to "Q30373367"
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The following pages link to Functional loss of semaphorin 3C and/or semaphorin 3D and their epistatic interaction with ret are critical to Hirschsprung disease liability (Q30373367):
Displaying 40 items.
- Enteric nervous system development in avian and zebrafish models (Q26745493) (← links)
- White paper on guidelines concerning enteric nervous system stem cell therapy for enteric neuropathies (Q26750556) (← links)
- A collagen VI-dependent pathogenic mechanism for Hirschsprung's disease (Q27330447) (← links)
- Defining the transcriptomic landscape of the developing enteric nervous system and its cellular environment (Q33556276) (← links)
- Next-generation-based targeted sequencing as an efficient tool for the study of the genetic background in Hirschsprung patients (Q35799615) (← links)
- Effects of SEMA3 polymorphisms in Hirschsprung disease patients. (Q36089076) (← links)
- A Novel Zebrafish ret Heterozygous Model of Hirschsprung Disease Identifies a Functional Role for mapk10 as a Modifier of Enteric Nervous System Phenotype Severity (Q36207993) (← links)
- Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease (Q36272727) (← links)
- Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes (Q36301311) (← links)
- Intestinal Neuronal Dysplasia-Like Submucosal Ganglion Cell Hyperplasia at the Proximal Margins of Hirschsprung Disease Resections (Q36734014) (← links)
- Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patients (Q37295706) (← links)
- Effects of RET, NRG1 and NRG3 Polymorphisms in a Chinese Population with Hirschsprung Disease (Q37679036) (← links)
- Decreased expression of semaphorin 3D is associated with genesis and development in colorectal cancer (Q37713342) (← links)
- Potential association between ITPKC genetic variations and Hirschsprung disease (Q38701047) (← links)
- Hirschsprung's disease: clinical dysmorphology, genes, micro-RNAs, and future perspectives (Q38800868) (← links)
- Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. (Q38814873) (← links)
- Mouse models of Hirschsprung disease and other developmental disorders of the enteric nervous system: Old and new players (Q38883845) (← links)
- Genetics of enteric neuropathies. (Q38899834) (← links)
- Advances in understanding functional variations in the Hirschsprung disease spectrum (variant Hirschsprung disease). (Q39042354) (← links)
- Enhancer Variants Synergistically Drive Dysfunction of a Gene Regulatory Network In Hirschsprung Disease (Q42366787) (← links)
- Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus (Q48146651) (← links)
- Gut feelings: Studying enteric nervous system development, function, and disease in the zebrafish model system (Q48248078) (← links)
- Hirschsprung disease - integrating basic science and clinical medicine to improve outcomes (Q50196075) (← links)
- RET somatic mutations are underrecognized in Hirschsprung disease (Q50424264) (← links)
- Testing the Ret and Sema3d genetic interaction in mouse enteric nervous system development. (Q51089610) (← links)
- Deregulation of the planar cell polarity genes CELSR3 and FZD3 in Hirschsprung disease. (Q51516980) (← links)
- Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing. (Q52372462) (← links)
- Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. (Q52588852) (← links)
- Semaphorin 3C and Its Receptors in Cancer and Cancer Stem-Like Cells. (Q55457324) (← links)
- Human Semaphorin 3 Variants Link Melanocortin Circuit Development and Energy Balance (Q61797817) (← links)
- Intestinal dysmotility in a zebrafish () mutant model of autism (Q61805365) (← links)
- AKT signaling displays multifaceted functions in neural crest development (Q88959381) (← links)
- MicroRNA-4516-mediated regulation of MAPK10 relies on 3' UTR cis-acting variants and contributes to the altered risk of Hirschsprung disease (Q89747179) (← links)
- Long non-coding RNA FAL1 functions as a ceRNA to antagonize the effect of miR-637 on the down-regulation of AKT1 in Hirschsprung's disease (Q90657655) (← links)
- Aberrant Expressions and Variant Screening of SEMA3D in Indonesian Hirschsprung Patients (Q90699620) (← links)
- Increased miR-214 expression suppresses cell migration and proliferation in Hirschsprung disease by interacting with PLAGL2 (Q92046663) (← links)
- Molecular Genetic Anatomy and Risk Profile of Hirschsprung's Disease (Q93002902) (← links)
- Common variation of the NSD1 gene is associated with susceptibility to Hirschsprung's disease in Chinese Han population (Q94541178) (← links)
- The advances of genetics research on Hirschsprung's disease (Q98772360) (← links)
- Semaphorin 3A controls enteric neuron connectivity and is inversely associated with synapsin 1 expression in Hirschsprung disease (Q99551247) (← links)