About: A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma

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About: A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma Goto Sponge NotDistinct Permalink

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scientific article published in Nature

Attributes	Values
rdf:type	Item
description	artículu científicu (ast) wetenschappelijk artikel (nl) article publié dans la revue scientifique Nature (fr) im Januar 1994 veröffentlichter wissenschaftlicher Artikel (de) নেচারে প্রকাশিত বৈজ্ঞানিক প্রবন্ধ (bn) scientific article published in Nature (en) наукова стаття, опублікована в Nature в січні 1994 (uk)
publication date	wds:Q55670928-2FA28C2E-9FAC-482A-A2F0-0050705B62C0
publication date	1994-01-27 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q55670928-F8D25598-4878-4521-8C04-53318CFBC838
language of work or name	English
exact match	wds:Q55670928-B982578C-2791-4B81-B231-FCFF9D5C96B2
exact match	https://scigraph.springernature.com/pub.10.1038/367375a0
cites work	wds:Q55670928-1E8F14D3-043B-46E6-99FB-63CA5892CA2D wds:Q55670928-39377BC4-9863-4B4F-B51B-E4581D8CD855 wds:Q55670928-57D5086E-F272-4B6D-9353-19F07E0023A9 wds:Q55670928-779CBE28-6D80-4305-A6EE-DBB394D377F6 wds:Q55670928-7A1C895F-DDFB-414C-95CD-E50512DFAC08 wds:Q55670928-8B9333D4-79E4-4AB2-B818-5C2AFC87A404 wds:Q55670928-95FECAE1-0AED-4062-8EEB-507334F9491D wds:Q55670928-A7929C44-5EFE-4495-8E7C-2B86B13074C3 wds:Q55670928-BC81D0B8-2D9C-4A50-86F1-80DAD7C7A49C wds:Q55670928-D682181E-AAF2-4E49-90BA-F6014F7581BA
cites work	A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10 The human protooncogene ret: a communicative cadherin? Mutations in the RET proto-oncogene are associated with MEN 2A and FMTC. The protein kinase family: conserved features and deduced phylogeny of the catalytic domains Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction Germ-line mutations of the RET proto-oncogene in multiple endocrine neoplasia type 2A. Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage Linkage of the multiple endocrine neoplasia type 2B gene (MEN2B) to chromosome 10 markers linked to MEN2A. Exon structure and flanking intronic sequences of the human RET proto-oncogene Development of multiple endocrine neoplasia type 2A does not involve substantial deletions of chromosome 10
author name string	wds:Q55670928-28778511-9652-49C5-B0FC-49A6035358C7 wds:Q55670928-76124B3A-B8F9-4FBA-941B-5AB731709813 wds:Q55670928-B467DD8B-A4B2-44FE-8A79-0CBA911FEB17 wds:Q55670928-B86622F9-24F1-4BC3-8E87-D2D1C9208F7E wds:Q55670928-C06A2039-1CEC-447E-BDFC-4B646D6E7B7E wds:Q55670928-E0AF3821-CCA4-4C4A-9374-87A7F06437D7 wds:Q55670928-E3E786F7-B088-412D-A318-CF4492132828 wds:Q55670928-F4F7A615-E776-4642-80E6-E7A5A5447C32 wds:Q55670928-FDD70AA1-12F3-42B3-B008-8E1A08A69FDB
author name string	Y Luo J W Höppener G Romeo R M Hofstra R P Stulp B Pasini R M Landsvater H K van Amstel T Stelwagen
rdfs:label	A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (en) A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (nl)
skos:prefLabel	A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (en) A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (nl)
name	A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (en) A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (nl)
author	wds:Q55670928-2AF57123-B03A-4F5A-889A-7A4914BFAF2B
author	Isabella Ceccherini
title	wds:Q55670928-71914EEC-62DA-4FF5-B006-402F0750AFE9
title	A mutation in the RET proto-oncogene associated with multiple endocrine neoplasia type 2B and sporadic medullary thyroid carcinoma (en)
page(s)	wds:Q55670928-838A3C91-E6C5-47FD-B911-BAADCA0FF1A5
page(s)	375-6
instance of	wds:Q55670928-9189B9FF-EA34-4843-8D28-B322F426713A
instance of	scholarly article
main subject	wds:Q55670928-ACC61BA1-4560-4B60-BC03-54686804BBD4 wds:Q55670928-CD9A200A-C3B8-4862-9581-9A9F36806EB1
main subject	multiple endocrine neoplasia type 2B thyroid carcinoma
PubMed ID	wds:Q55670928-ECD1FABB-1861-400B-984C-0C852B35925E
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7906866
PubMed ID	7906866
published in	wds:Q55670928-507874F5-5B49-4854-BC11-3042C69F5394
published in	Nature
issue	wds:Q55670928-C5A8DCCC-6BDC-4AD1-B206-5FD92F9E6FDE
volume	wds:Q55670928-CED6EDF4-C7BD-40B3-B470-2F8C6A93FB24
issue	6461
volume	367
DOI	wds:Q55670928-42FFCA34-99D2-41DB-97FE-00698551A787
DOI	http://dx.doi.org/10.1038/367375A0
DOI	10.1038/367375A0
Dimensions Publication ID	wds:Q55670928-697FB925-85E9-4C96-80F6-4624F79CDA82
Dimensions Publication ID	1004801930
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q55670928
is cites work of	Molecular genetic diagnosis of von Hippel-Lindau disease in familial phaeochromocytoma Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome GDNF-induced activation of the ret protein tyrosine kinase is mediated by GDNFR-alpha, a novel receptor for GDNF UMD (Universal mutation database): a generic software to build and analyze locus-specific databases Phenotypic diversity, allelic series and modifier genes Analysis of Somatic Mutations in Cancer: Molecular Mechanisms of Activation in the ErbB Family of Receptor Tyrosine Kinases Intestinal motility during ontogeny and intestinal pseudo-obstruction in children Neurocristopathy: its growth and development in 20 years Association of RET protooncogene codon 45 polymorphism with Hirschsprung disease A homozygous missense mutation in the tyrosine E kinase domain of the RET proto-oncogene in an infant with total intestinal aganglionosis Point mutations and overexpression of Ron induce transformation, tumor formation, and metastasis Flying under the radar: the new wave of BCR-ABL inhibitors Nuclear orphan receptor Nurr1 directly transactivates the osteocalcin gene in osteoblasts Biological and biochemical properties of Ret with kinase domain mutations identified in multiple endocrine neoplasia type 2B and familial medullary thyroid carcinoma

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