Search Results - "Dammerman, M."
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Common genetic variation in the promoter of the human apo CIII gene abolishes regulation by insulin and may contribute to hypertriglyceridemia
Published in The Journal of clinical investigation (01-12-1995)“…Overexpression of plasma apolipoprotein CIII (apo CIII) causes hypertriglyceridemia in transgenic mice. A genetically variant form of the human apo CIII…”
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2
Absence of mutations in the human OB gene in obese/diabetic subjects
Published in Diabetes (New York, N.Y.) (01-05-1996)“…Absence of mutations in the human OB gene in obese/diabetic subjects. M Maffei , M Stoffel , M Barone , B Moon , M Dammerman , E Ravussin , C Bogardus , D S…”
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3
An Apolipoprotein CIII Haplotype Protective Against Hypertriglyceridemia is Specified by Promoter and 3' Untranslated Region Polymorphisms
Published in Proceedings of the National Academy of Sciences - PNAS (15-05-1993)“…Five DNA polymorphisms were detected in the promoter of the apolipoprotein CIII gene of a type III hyperlipidemic subject with severe hypertriglyceridemia…”
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4
Genetic determinants of myocardial infarction
Published in Advances in experimental medicine and biology (1995)“…There is a strong familial and genetic nature of CAD and predisposing metabolic disorders. This should encourage health care workers to focus additional…”
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5
A monoclonal antibody equivalent to anti-rat neural antigen-1 as a marker for Schwann cells
Published in Neuroscience (01-07-1985)“…The monoclonal antibody 217c, raised by Peng et al. [(1982) Science, Wash. 215, 1102-1104] in mice against the rat glioma cell line C6, can be used as a marker…”
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6
Sequence of a human MAP-2 region sharing epitopes with Alzheimer neurofibrillary tangles
Published in Journal of neuroscience research (01-12-1989)“…Microtubule-associated protein 2 (MAP-2), an abundant neuronal protein, consists of a short microtubule-binding domain and a long projection arm. MAP-2 shares…”
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Isolation and characterization of cDNA clones encoding epitopes shared with Alzheimer neurofibrillary tangles
Published in Journal of neuroscience research (1988)“…A pool of ten monoclonal antibodies to SDS-insoluble epitopes of Alzheimer neurofibrillary tangles (NFT) was used to screen an adult human brain cDNA…”
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8
Absence of mutations in the human OB gene in obese/diabetic subjects
Published in Diabetes (New York, N.Y.) (01-05-1996)“…The product of the obese (ob) gene, leptin, is a secreted protein that is important in the regulation of body weight. Mice with mutations in the ob gene are…”
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Genetic basis of lipoprotein disorders
Published in Circulation (New York, N.Y.) (15-01-1995)Get full text
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An apolipoprotein CIII marker associated with hypertriglyceridemia in Caucasians also confers increased risk in a west Japanese population
Published in Human genetics (01-04-1995)“…Polymorphisms and haplotypes at the adjacent apolipoprotein (apo) AI and CIII gene loci were investigated in 61 Japanese patients with triglycerides greater…”
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11
Localization and characterization of the binding site for the regulatory subunit of type II cAMP-dependent protein kinase on MAP2
Published in Neuron (Cambridge, Mass.) (01-11-1989)“…Microtubule-associated protein 2 (MAP2) binds, and is a substrate for, type II cAMP-dependent protein kinase. The structural domain in MAP2 that binds the…”
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