×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Protecting thyroid cancer patients from untoward effects of radioactive iodine treatment.
19731974 2009
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
The inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN 2) is caused by mutations of the RET receptor tyrosine kinase and is characterized by medullary thyroid carcinoma.
19226610 2009
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Head and neck paragangliomas in von Hippel-Lindau disease and multiple endocrine neoplasia type 2.
19336503 2009
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Medullary thyroid cancer: management guidelines of the American Thyroid Association.
19469690 2009
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Multiple endocrine neoplasia type 2 RET protooncogene database: repository of MEN2-associated RET sequence variation and reference for genotype/phenotype correlations.
19177457 2009
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Familial prevalence and age of RET germline mutations: implications for screening.
18062802 2008
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
RET proto-oncogene testing in infants presenting with Hirschsprung disease identifies 2 new multiple endocrine neoplasia 2A kindreds.
18206480 2008
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
The occurrence and the type of germline mutations in the RET gene in patients with medullary thyroid carcinoma and their unaffected kindred's from Central Poland.
18058472 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
RET genetic screening in patients with medullary thyroid cancer and their relatives: experience with 807 individuals at one center.
17895320 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
In humans, activating RET mutations are found in the inherited cancer syndrome multiple endocrine neoplasia 2 and in sporadic medullary and papillary thyroid carcinomas.
17916994 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Pheochromocytoma penetrance varies by RET mutation in MEN 2A.
18063059 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
Mutations of the RET proto-oncogene cause the inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN 2).
17213820 2007
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Impact of RET proto-oncogene analysis on the clinical management of multiple endocrine neoplasia type 2.
16532227 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Hereditary medullary thyroid cancer in Slovenia--genotype-phenotype correlations.
16865646 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
A rare extracellular D631Y germline mutation of the RET proto-oncogene in two Korean families with multiple endocrine neoplasia 2A.
16839264 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
Germline mutations in RET are responsible for multiple endocrine neoplasia type 2 (MEN2), an autosomal dominantly inherited cancer syndrome that is characterized by medullary thyroid carcinoma (MTC), pheochromocytoma, and parathyroid hyperplasia/adenoma.
16707008 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
Germ line missense mutations in the RET proto-oncogene are responsible for the inherited cancer syndrome multiple endocrine neoplasia type 2A (MEN2A).
16424056 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Occurrence of the Cys611Tyr mutation and a novel Arg886Trp substitution in the RET proto-oncogene in multiple endocrine neoplasia type 2 families and sporadic medullary thyroid carcinoma cases originating from the central region of Portugal.
16712668 2006
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease.
15744028 2005
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Nine novel germline gene variants in the RET proto-oncogene identified in twelve unrelated cases.
15858153 2005
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
GeneticVariation
group
BEFREE
Mutations of the RET proto-oncogene are found in the majority of patients with the inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN 2).
15592530 2005
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Multiple endocrine neoplasia type 2: evaluation of the genotype-phenotype relationship.
12686527 2003
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations.
12409662 2002
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Papillary thyroid carcinoma in patients with RET proto-oncogene germline mutation.
12193298 2002
×
Entrez Id: 5979
Gene Symbol: RET
RET
0.200
CausalMutation
group
CLINVAR
Germ-line mutations in nonsyndromic pheochromocytoma.
12000816 2002