rs104893891
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
|
8896568 |
1996 |
rs104893891
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
|
8968758 |
1996 |
rs104893891
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
|
8896569 |
1996 |
rs104893891
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
Pathogenesis of Hirschsprung's disease.
|
10917288 |
2000 |
rs121918536
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
|
8896569 |
1996 |
rs121918536
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
|
8896568 |
1996 |
rs121918536
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
Pathogenesis of Hirschsprung's disease.
|
10917288 |
2000 |
rs121918536
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.800 |
GeneticVariation |
UNIPROT |
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
|
8968758 |
1996 |
rs36119840
|
GDNF;GDNF-AS1
|
Pheochromocytoma
|
|
0.710 |
GeneticVariation |
BEFREE |
No GDNF mutations were identified in patients with familial phaeochromocytoma disease, but a c277C-->T (R93W) sequence variant was identified in one of 28 sporadic tumours.
|
9215674 |
1997 |
rs36119840
|
GDNF;GDNF-AS1
|
Pheochromocytoma
|
|
0.710 |
GeneticVariation |
UNIPROT |
No GDNF mutations were identified in patients with familial phaeochromocytoma disease, but a c277C-->T (R93W) sequence variant was identified in one of 28 sporadic tumours.
|
9215674 |
1997 |
rs36119840
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
|
8896569 |
1996 |
rs36119840
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
|
8968758 |
1996 |
rs36119840
|
GDNF;GDNF-AS1
|
Congenital central hypoventilation
|
|
0.700 |
GeneticVariation |
UNIPROT |
An official ATS clinical policy statement: Congenital central hypoventilation syndrome: genetic basis, diagnosis, and management.
|
20208042 |
2010 |
rs36119840
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
|
8896568 |
1996 |
rs36119840
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
Pathogenesis of Hirschsprung's disease.
|
10917288 |
2000 |
rs36119840
|
GDNF;GDNF-AS1
|
Congenital central hypoventilation
|
|
0.700 |
GeneticVariation |
UNIPROT |
Mutations of the RET-GDNF signaling pathway in Ondine's curse.
|
9497256 |
1998 |
rs4574573
|
GDNF-AS1;LINC02117
|
Serum total cholesterol measurement
|
|
0.700 |
GeneticVariation |
GWASCAT |
Very low-depth whole-genome sequencing in complex trait association studies.
|
30576415 |
2019 |
rs777451569
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
De novo mutation of GDNF, ligand for the RET/GDNFR-alpha receptor complex, in Hirschsprung disease.
|
8968758 |
1996 |
rs777451569
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
Pathogenesis of Hirschsprung's disease.
|
10917288 |
2000 |
rs777451569
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
|
8896568 |
1996 |
rs777451569
|
GDNF;GDNF-AS1
|
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 3
|
|
0.700 |
GeneticVariation |
UNIPROT |
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.
|
8896569 |
1996 |
rs760097344
|
GDNF;GDNF-AS1
|
Amyotrophic Lateral Sclerosis
|
|
0.030 |
GeneticVariation |
BEFREE |
To evaluate the therapeutic potential of human neural progenitor cells (hNPs) in amyotrophic lateral sclerosis (ALS), we transplanted hNPs or growth factor (GF)-expressing hNPs into the central nervous system (CNS) of mutant Cu/Zn superoxide dismutase (SOD1(G93A)) transgenic mice.
|
19322031 |
2009 |
rs760097344
|
GDNF;GDNF-AS1
|
Amyotrophic Lateral Sclerosis
|
|
0.030 |
GeneticVariation |
BEFREE |
Because adeno-associated virus (AAV) has been developed as an attractive gene delivery system with proven safety, we explored the therapeutic efficacy of intramuscular delivery of the GDNF gene mediated by an AAV vector (AAV-GDNF) in the G93A mouse model of ALS.
|
12177190 |
2002 |
rs760097344
|
GDNF;GDNF-AS1
|
Amyotrophic Lateral Sclerosis
|
|
0.030 |
GeneticVariation |
BEFREE |
Intraspinal administration of human spinal cord-derived neural progenitor cells in the G93A-SOD1 mouse model of ALS delays symptom progression, prolongs survival and increases expression of endogenous neurotrophic factors.
|
25641599 |
2017 |
rs1110149
|
GDNF;GDNF-AS1
|
Tinnitus
|
|
0.010 |
GeneticVariation |
BEFREE |
Heterozygosity was significantly lower for GDNF rs1110149 polymorphism in tinnitus subjects compared to the controls (p < 0.05).
|
27180191 |
2016 |