15579037

Source:http://linkedlifedata.com/resource/pubmed/id/15579037

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0022665, umls-concept:C1704981
pubmed:issue	8
pubmed:dateCreated	2004-12-6
pubmed:abstractText	Hyperparathyroidism-jaw tumor (HPT-JT) syndrome is a familial multi-tumor syndrome resulting from mutations in the HRPT2 tumor suppressor gene, which encodes a protein product named parafibromin. We review current knowledge of the renal manifestations of the HPT-JT syndrome, and examine recent advances in understanding the biological function of parafibromin.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101093076
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Dec
pubmed:issn	1566-5240
pubmed:author	pubmed-author:KakV KVK, pubmed-author:TehB TBT
pubmed:issnType	Print
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	895-7
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:15579037-Bone Neoplasms, pubmed-meshheading:15579037-Genes, Tumor Suppressor, pubmed-meshheading:15579037-Humans, pubmed-meshheading:15579037-Hyperparathyroidism, pubmed-meshheading:15579037-Kidney Neoplasms, pubmed-meshheading:15579037-Syndrome
pubmed:year	2004
pubmed:articleTitle	Renal neoplasia in the hyperparathyroidism-jaw tumor syndrome.
pubmed:affiliation	Laboratory of Cancer Genetics, Van Andel Research Institute, Grand Rapids, MI 49503, USA.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't