Source:http://linkedlifedata.com/resource/pubmed/id/18249304
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2008-2-5
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pubmed:abstractText |
The co-occurrence of parathyroid hyperplasia with pancreatic endocrine tumours and/or pituitary adenoma is classified as Multiple Endocrine Neoplasia type 1 (MEN-1) and is caused by a germ-line mutation in MEN-1 gene encoding a tumour suppressor protein, menin. This review presents clinical expressions, diagnosis and management of the MEN-1 syndrome. Properties and mechanisms of menin functions are also reviewed.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1879-0828
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
99-103
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pubmed:dateRevised |
2009-5-20
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pubmed:meshHeading |
pubmed-meshheading:18249304-Gastrinoma,
pubmed-meshheading:18249304-Gene Expression,
pubmed-meshheading:18249304-Humans,
pubmed-meshheading:18249304-Hyperparathyroidism,
pubmed-meshheading:18249304-Insulinoma,
pubmed-meshheading:18249304-Multiple Endocrine Neoplasia Type 1,
pubmed-meshheading:18249304-Mutation,
pubmed-meshheading:18249304-Prolactinoma,
pubmed-meshheading:18249304-Proto-Oncogene Proteins
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pubmed:year |
2008
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pubmed:articleTitle |
Multiple Endocrine Neoplasia type 1.
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pubmed:affiliation |
Department of Nephrology, Endocrinology and Metabolic Diseases, Medical University of Silesia, Katowice, ul. Francuska 20/24, 40-027 Katowice, Poland.
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pubmed:publicationType |
Journal Article,
Review
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