10876191

Source:http://linkedlifedata.com/resource/pubmed/id/10876191

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0003442, umls-concept:C0026882, umls-concept:C0543431, umls-concept:C0678226, umls-concept:C0694890, umls-concept:C1833921, umls-concept:C1861403
pubmed:issue	1
pubmed:dateCreated	2000-8-1
pubmed:abstractText	Multiple endocrine neoplasia type 2 (MEN 2) and familial medullary thyroid carcinoma (FMTC) are autosomal dominantly inherited cancer syndromes that predispose to C-cell hyperplasia and MTC. MEN 2A and FMTC are caused by mutations in the RET proto-oncogene.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/0417347
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-ret, http://linkedlifedata.com/resource/pubmed/chemical/Receptor Protein-Tyrosine Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Ret oncogene protein, Drosophila
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	0039-6060
pubmed:author	pubmed-author:AinsworthP JPJ, pubmed-author:EdmondsM WMW, pubmed-author:FeldmanG LGL, pubmed-author:JacksonC ECE, pubmed-author:LenoirG MGM, pubmed-author:PetrucelliNN, pubmed-author:RobersonJJ, pubmed-author:SaxeA WAW, pubmed-author:SchuffeneckerII, pubmed-author:TalposG BGB
pubmed:issnType	Print
pubmed:volume	128
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	93-8
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:10876191-Adult, pubmed-meshheading:10876191-Age of Onset, pubmed-meshheading:10876191-Aged, pubmed-meshheading:10876191-Aged, 80 and over, pubmed-meshheading:10876191-Carcinoma, Medullary, pubmed-meshheading:10876191-Drosophila Proteins, pubmed-meshheading:10876191-Exons, pubmed-meshheading:10876191-Family Health, pubmed-meshheading:10876191-Female, pubmed-meshheading:10876191-Humans, pubmed-meshheading:10876191-Male, pubmed-meshheading:10876191-Middle Aged, pubmed-meshheading:10876191-Pedigree, pubmed-meshheading:10876191-Phenotype, pubmed-meshheading:10876191-Point Mutation, pubmed-meshheading:10876191-Proto-Oncogene Proteins, pubmed-meshheading:10876191-Proto-Oncogene Proteins c-ret, pubmed-meshheading:10876191-Receptor Protein-Tyrosine Kinases, pubmed-meshheading:10876191-Thyroid Neoplasms, pubmed-meshheading:10876191-Thyroidectomy
pubmed:year	2000
pubmed:articleTitle	Variable expressivity of familial medullary thyroid carcinoma (FMTC) due to a RET V804M (GTG-->ATG) mutation.
pubmed:affiliation	Department of Medical Genetics, Henry Ford Hospital, the Center for Molecular Medicine and Genetics, Detroit, MI 48201, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't