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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
1996-7-30
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pubmed:databankReference |
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pubmed:abstractText |
The polymorphic Bcl I site in the human ucp gene associated to percentage fat gain over time in the Québec Family Study cohort (Oppert et al. Int J Obesity 1994; 18: 526-531) has been positioned to the 5'-flanking region. This polymorphism results from a unique A/G mutation. Oligonucleotides used to amplify the polymorphic region, and allowing future studies of any cohort of patients, are described.
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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 |
Mar
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pubmed:issn |
0307-0565
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
20
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
278-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:8653151-Base Sequence,
pubmed-meshheading:8653151-Carrier Proteins,
pubmed-meshheading:8653151-DNA,
pubmed-meshheading:8653151-Deoxyribonucleases, Type II Site-Specific,
pubmed-meshheading:8653151-Humans,
pubmed-meshheading:8653151-Ion Channels,
pubmed-meshheading:8653151-Membrane Proteins,
pubmed-meshheading:8653151-Mitochondrial Proteins,
pubmed-meshheading:8653151-Molecular Sequence Data,
pubmed-meshheading:8653151-Obesity,
pubmed-meshheading:8653151-Point Mutation,
pubmed-meshheading:8653151-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:8653151-Restriction Mapping
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pubmed:year |
1996
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pubmed:articleTitle |
The Bcl I polymorphism of the human uncoupling protein (ucp) gene is due to a point mutation in the 5'-flanking region.
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pubmed:affiliation |
Centre de Recherche sur l'Endocrinologie Moléculaire et le Développement, Centre National de la Recherche Scientifique, Meudon, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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