About: A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A

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About: A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A Goto Sponge NotDistinct Permalink

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scientific article published on 01 March 1998

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1998 (uk) article scientifique publié en 1998 (fr) im März 1998 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu en marzu de 1998 (ast) scientific article published on 01 March 1998 (en)
publication date	wds:Q74324586-291F1D16-3AF7-45CC-8459-55D48965A159
publication date	1998-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q74324586-1111EB00-226F-468C-A4B3-E30F7DCAF66F
language of work or name	English
author name string	wds:Q74324586-0276FAE2-660D-4CB3-BCF8-F4A9A59BD207 wds:Q74324586-04206AD5-E7EA-4B7D-BF1E-3703CF899DBA wds:Q74324586-09D3ED1F-FAD9-468F-A4E8-2F35E79592DB wds:Q74324586-1DC684FB-4BE1-4F11-88F1-B9D67F2557E2 wds:Q74324586-41774EBB-0C96-4922-BDD7-702BBD71BD63 wds:Q74324586-6D400256-17BA-4031-9A2B-9561C482C1D7 wds:Q74324586-843B2BD0-8C03-4E44-B8E9-304AC97B0E4C wds:Q74324586-C78F2CF6-366C-46D3-A111-F11D041B7214 wds:Q74324586-E82F64FF-6933-4B34-9CC2-B17E2DF8876E
author name string	M Reuter P Groth F Raue K Frank-Raue M M Ritter M Grussendorf W Höppner B Saller I Berndt
rdfs:label	A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (en) A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (nl)
skos:prefLabel	A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (en) A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (nl)
name	A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (en) A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (nl)
title	wds:Q74324586-8133FD10-0963-4A48-9F13-F8064F0DE323
title	A new hot spot for mutations in the ret protooncogene causing familial medullary thyroid carcinoma and multiple endocrine neoplasia type 2A (en)
page(s)	wds:Q74324586-749047DB-0F62-4DB3-A302-012B20D608EF
page(s)	770-774
instance of	wds:Q74324586-27D6FBAD-E4BE-42B1-B127-F84C2ACD7307
instance of	scholarly article
main subject	wds:Q74324586-2A78D10A-2330-446B-AE1E-79676DC7D102 wds:Q74324586-7A9C702D-D276-41E0-8D22-FE270DFE3C0B wds:Q74324586-B342EF42-E4AC-4270-B2E7-18F7F6699E18
main subject	multiple endocrine neoplasia type 2A thyroid carcinoma familial medullary thyroid carcinoma
PubMed ID	wds:Q74324586-2AF37361-41F5-4669-B6BD-52C8A07C5203
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9506724
PubMed ID	9506724
published in	wds:Q74324586-8E488FA7-3AE6-403C-A3BD-D582071E6413
published in	The Journal of Clinical Endocrinology and Metabolism
issue	wds:Q74324586-9718E169-B135-4618-ACA3-A4730F6440C8
volume	wds:Q74324586-0C133EF8-3E21-4ABF-B392-94F8C8A2149E
issue	3
volume	83
DOI	wds:Q74324586-0D10FB01-6025-44AC-AE2D-C7F8275700B4
DOI	http://dx.doi.org/10.1210/JCEM.83.3.4619
DOI	10.1210/JCEM.83.3.4619
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q74324586
is cites work of	Codon Y791F mutations in a large kindred: is prophylactic thyroidectomy always indicated? A RET Mutation with Decreased Penetrance in the Family of a Patient with a Multiple endocrine neoplasia type 2 and RET: from neoplasia to neurogenesis RET and neuroendocrine tumors Multiple endocrine neoplasia type 2: achievements and current challenges Multiple endocrine neoplasia type 2 and familial medullary thyroid carcinoma: an update RET revisited: expanding the oncogenic portfolio Multiple endocrine neoplasia type 2. Novel mutations of the MET proto-oncogene in papillary renal carcinomas. Prophylactic thyroidectomy in multiple endocrine neoplasia: the impact of molecular mechanisms of RET proto-oncogene. Genotype-phenotype correlation in multiple endocrine neoplasia type 2 Genotype-phenotype based surgical concept of hereditary medullary thyroid carcinoma Comprehensive analysis of RET gene should be performed in patients with multiple endocrine neoplasia type 2 (MEN 2) syndrome and no apparent genotype-phenotype correlation: an appraisal of p.Y791F and p.C634Y RET mutations in five unrelated Brazilia Various penetrance of familial medullary thyroid carcinoma in patients with RET protooncogene codon 790/791 germline mutations Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models Disease variants in genomes of 44 centenarians. Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility The finding of a somaticdeletion in RET exon 15 clarified the sporadic nature of amedullary thyroid carcinoma suspected to be familial Molecular mechanisms of RET activation in human neoplasia RET proto-oncogene mutations in thyroid carcinomas: clinical relevance Timing and extent of surgery in patients with familial medullary thyroid carcinoma/multiple endocrine neoplasia 2A-related RET mutations not affecting codon 634. Hereditary medullary thyroid cancer in Slovenia--genotype-phenotype correlations. Update multiple endocrine neoplasia type 2. RET mutation Tyr791Phe: the genetic cause of different diseases derived from neural crest. Outcomes of Children and Adolescents with Advanced Hereditary Medullary Thyroid Carcinoma Treated with Vandetanib. A differential diagnosis of inherited endocrine tumors and their tumor counterparts Medullary thyroid cancer: RET testing of an archival material Incidence and prevalence of sporadic and hereditary MTC in Denmark 1960-2014: a nationwide study. Somatic mutations in RET exons 12 and 15 in sporadic medullary thyroid carcinomas: different spectrum of mutations in sporadic type from hereditary type. Molecular mechanisms of RET receptor-mediated oncogenesis in multiple endocrine neoplasia 2. Genotype-Phenotype Correlation in Indian Patients with MEN2-Associated Pheochromocytoma and Comparison of Clinico-Pathological Attributes with Apparently Sporadic Adrenal Pheochromocytoma. RET proto-oncogene genotyping using unlabeled probes, the masking technique, and amplicon high-resolution melting analysis Incidentally found medullary thyroid cancer: treatment rationale for small tumors Multiple endocrine neoplasia type 2 and the practice of molecular medicine Exon 5 of the RET proto-oncogene: a newly detected risk exon for familial medullary thyroid carcinoma, a novel germ-line mutation Gly321Arg. Screening of RET gene mutations in Chinese patients with medullary thyroid carcinoma and their relatives. RET proto-oncogene mutations are restricted to codon 618 in Cypriot families with multiple endocrine neoplasia 2 Genotype-phenotype correlations in Hungarian patients with hereditary medullary thyroid cancer. Penetrance of inherited medullary thyroid carcinoma and genotype-phenotype correlation in a large multiple endocrine neoplasia type 2A family with C634Y RET mutation. State-of-the-Art Strategies for Targeting RET-Dependent Cancers

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