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Volumn 6, Issue 6, 1997, Pages 869-876

Leptin receptor gene variation and obesity: Lack of association in a white British male population

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; HORMONE RECEPTOR; LEPTIN; MESSENGER RNA;

EID: 0030927064     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/6.6.869     Document Type: Article
Times cited : (172)

References (26)
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    • Recombinant mouse OB protein: Evidence for a peripheral signal linking adiposity and central neural networks
    • Campfield, L.A., Smith, F.J., Guisez, Y., Devos, R. and Burn P. (1995) Recombinant mouse OB protein: evidence for a peripheral signal linking adiposity and central neural networks. Science, 269, 546-549.
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    • Campfield, L.A.1    Smith, F.J.2    Guisez, Y.3    Devos, R.4    Burn, P.5
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    • 0030006511 scopus 로고    scopus 로고
    • Mapping of the OB receptor to 1p in a region of nonconserved gene order from mouse and rat to human
    • Chung, W.K., Power-Kehoe, L., Chua, M. and Leibel, R.L. (1996) Mapping of the OB receptor to 1p in a region of nonconserved gene order from mouse and rat to human. Genome Res., 6, 431-438.
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    • The hypothalamic leptin receptor in humans: Identification of incidental sequence polymorphisms and absence of the db/db mouse and fa/fa rat mutations
    • Considine, R.V., Considine, E.L., Williams, C.J., Hyde, T.M. and Caro, J.F. (1996) The hypothalamic leptin receptor in humans: identification of incidental sequence polymorphisms and absence of the db/db mouse and fa/fa rat mutations. Diabetes, 45, 992-994.
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    • Considine, R.V.1    Considine, E.L.2    Williams, C.J.3    Hyde, T.M.4    Caro, J.F.5
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    • Relation of central obesity and insulin resistance with high diabetes prevalence and cardiovascular risk in South Asians
    • McKeigue, P.M., Shah, B. and Marmot, M.G. (1991) Relation of central obesity and insulin resistance with high diabetes prevalence and cardiovascular risk in South Asians. Lancet, 337, 382-386.
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    • Occurrence of multiple aberrantly spliced mRNAs upon a donor splice site mutation that causes familial lipoprotein lipase deficiency
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.