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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
2010-10-26
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pubmed:abstractText |
Melanocortin-4 receptor (MC4R) deficiency is the most common cause of monogenic obesity. In the present study, we screened the MC4R gene for mutations in a population of overweight and obese children and adolescents.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1662-4025
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pubmed:author |
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pubmed:copyrightInfo |
Copyright © 2010 S. Karger AG, Basel.
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pubmed:issnType |
Print
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pubmed:volume |
3
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
304-11
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pubmed:meshHeading |
pubmed-meshheading:20975296-Adolescent,
pubmed-meshheading:20975296-Adult,
pubmed-meshheading:20975296-Animals,
pubmed-meshheading:20975296-Belgium,
pubmed-meshheading:20975296-Body Mass Index,
pubmed-meshheading:20975296-Body Weight,
pubmed-meshheading:20975296-COS Cells,
pubmed-meshheading:20975296-Case-Control Studies,
pubmed-meshheading:20975296-Cercopithecus aethiops,
pubmed-meshheading:20975296-Child,
pubmed-meshheading:20975296-Cross-Sectional Studies,
pubmed-meshheading:20975296-DNA Mutational Analysis,
pubmed-meshheading:20975296-Female,
pubmed-meshheading:20975296-Genetic Predisposition to Disease,
pubmed-meshheading:20975296-Humans,
pubmed-meshheading:20975296-Male,
pubmed-meshheading:20975296-Microscopy, Confocal,
pubmed-meshheading:20975296-Mutation,
pubmed-meshheading:20975296-Obesity,
pubmed-meshheading:20975296-Overweight,
pubmed-meshheading:20975296-Pedigree,
pubmed-meshheading:20975296-Phenotype,
pubmed-meshheading:20975296-Protein Transport,
pubmed-meshheading:20975296-Receptor, Melanocortin, Type 4,
pubmed-meshheading:20975296-Risk Assessment,
pubmed-meshheading:20975296-Risk Factors,
pubmed-meshheading:20975296-Signal Transduction,
pubmed-meshheading:20975296-Transfection
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pubmed:year |
2010
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pubmed:articleTitle |
Identification and functional characterization of novel mutations in the melanocortin-4 receptor.
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pubmed:affiliation |
Department of Medical Genetics, University of Antwerp and Antwerp University Hospital, Antwerp, Belgium.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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