About: First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene

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About: First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene Goto Sponge NotDistinct Permalink

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scientific article published on 16 September 2013

Attributes	Values
rdf:type	Item
description	videnskabelig artikel (da) article científic (ca) articolo scientifico (it) artigo científico (pt) bilimsel makale (tr) vedecký článok (sk) vetenskaplig artikel (sv) vědecký článek (cs) wetenschappelijk artikel (nl) wissenschaftlicher Artikel (de) научни чланак (sr) article scientifique (fr) artículu científicu espublizáu en 2013 (ast) наукова стаття, опублікована у вересні 2013 (uk) مقالة علمية نشرت في 16 سبتمبر 2013 (ar) scientific article published on 16 September 2013 (en)
publication date	wds:Q37579771-F4376F62-CFB1-4E3A-83EE-4AC0BBE13212
publication date	2013-09-16 00:00:00Z (xsd:dateTime)
cites work	wds:Q37579771-40DE8E9B-BE24-4AF1-91DB-D91FBAB30C4F wds:Q37579771-9E3892F6-1BF8-4CAE-B5E1-661E7E56CA00 wds:Q37579771-C5920E1F-9C7C-47B5-8BE9-50E7CEDE3E72 wds:Q37579771-CC43A0B9-CFC7-47AF-AED3-8FA8A29DCEF3 wds:Q37579771-CCC280AB-4C08-464B-990E-B465712EA2C3
cites work	Multiple endocrine neoplasia type 2A in two families with the familial medullary thyroid carcinoma associated G533C mutation of the RET proto-oncogene The RET p.G533C mutation confers predisposition to multiple endocrine neoplasia type 2A in a Brazilian kindred and is able to induce a malignant phenotype in vitro and in vivo A newly detected mutation of the RET protooncogene in exon 8 as a cause of multiple endocrine neoplasia type 2A. Multiple endocrine neoplasia type 2A due to an exon 8 (G533C) mutation in a large North American kindred A novel 9-base pair duplication in RET exon 8 in familial medullary thyroid carcinoma
author name string	wds:Q37579771-4D86F949-635C-422E-945B-74896600AF17 wds:Q37579771-7C1C8EE4-A907-45A3-92A4-5F20FE0B000C wds:Q37579771-AAABA4CB-D9CB-4721-8580-8B348FF8E818
author name string	D O'Halloran R Casey S Prendeville
rdfs:label	First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (en) First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (nl) First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (ast)
skos:prefLabel	First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (en) First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (nl) First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (ast)
name	First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (en) First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (nl) First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (ast)
author	wds:Q37579771-63A8C5A9-CB77-4E1F-9DAD-4C3E212F82A3
author	Caroline Joyce
title	wds:Q37579771-BFE1EB67-0E2E-48C1-B982-BF474D42627A
title	First reported case in Ireland of MEN2A due to a rare mutation in exon 8 of the RET oncogene (en)
page(s)	wds:Q37579771-C0D7A995-C719-4245-9296-BDC87493E56F
page(s)	130044
instance of	wds:Q37579771-11b50dd0-0b37-4cc1-a364-93305962d41c wds:Q37579771-4F5C80A5-43F6-46B3-A926-585B10802165
instance of	scholarly article case report
PubMed ID	wds:Q37579771-2A6E6933-B45A-4E25-831B-0F6AD2FFA00B
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/24616773
PubMed ID	24616773
published in	wds:Q37579771-6359F348-D45C-45A1-A4A8-B6928B2F6F3B
published in	Endocrinology, diabetes & metabolism case reports
volume	wds:Q37579771-B49FA7B9-CAB9-4F9B-B231-1AE46F8ACCCA
volume	2013
DOI	wds:Q37579771-1BCFE9CC-A410-4F5D-8F64-F76644AEBF2C
DOI	http://dx.doi.org/10.1530/EDM-13-0044
DOI	10.1530/EDM-13-0044
ResearchGate publication ID	wds:Q37579771-3908BBBA-96DB-4CEC-B083-3A4D515EE87A
ResearchGate publication ID	260684936
PMCID	wds:Q37579771-E68F389C-9DCF-4E0A-970F-47AEA1FFF824
PMCID	3922143
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37579771
is cites work of	Familial MTC with RET exon 8 Gly533Cys mutation: origin and prevalence of second malignancy Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
is cites work of	wds:Q42635292-D723993C-1FA1-492B-83A1-C20E50794B4C wds:Q64253642-DBB3DD8D-5A6C-4F5C-84A6-9E40BC6924B0

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