Výsledky vyhledávání - "D K, Sanghera"

The p22 phox polymorphism C242T is not associated with CHD risk in Asian Indians and Chinese

Autor: N, Saha, D K, Sanghera, M I, Kamboh

Publikováno v: European journal of clinical investigation. 29(12)

Oxygen free radicals such as superoxide anion have been implicated in the pathogenesis of atherosclerosis and coronary heart disease (CHD). The nonglycosylated 22 kDa alpha-subunit of the NADH/NADPH oxidase (p22 phox) of the vasculature acts as the f

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0aac5df4fa0a577518fed6a221599641
https://pubmed.ncbi.nlm.nih.gov/10583446

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Apolipoprotein J polymorphisms and serum HDL cholesterol levels in African blacks

Autor: C S, Nestlerode, C H, Bunker, D K, Sanghera, C E, Aston, F A, Ukoli, M I, Kamboh

Publikováno v: Human biology. 71(2)

Apolipoprotein J (apoJ, protein; APOJ, gene) is found in serum associated with high-density lipoprotein (HDL) subfractions, which also contain apolipoprotein A-I (apoA1) and cholesteryl ester transfer protein. ApoJ has been shown to be involved in a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1151ba454ed694bd5f742ab232b75738
https://pubmed.ncbi.nlm.nih.gov/10222643

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Identification of structural mutations in the fifth domain of apolipoprotein H (beta 2-glycoprotein I) which affect phospholipid binding

Autor: D R Wagenknecht, M I Kamboh, J A McIntyre, D K Sanghera

Publikováno v: Human molecular genetics. 6(2)

Apolipoprotein H (apoH), also known as beta 2-glycoprotein-I, is considered to be a cofactor for the binding of certain antiphospholipid autoantibodies to negatively charged phospholipids. Genetically determined structural abnormalities in the lipid

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0eddcde4ff6fa7da4124d7f150ac02d6
https://pubmed.ncbi.nlm.nih.gov/9063752

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Gender-specific nonrandom association between the alpha 1-antichymotrypsin and apolipoprotein E polymorphisms in the general population and its implication for the risk of Alzheimer's disease

Autor: M I, Kamboh, D K, Sanghera, C E, Aston, C H, Bunker, R F, Hamman, R E, Ferrell, S T, DeKosky

Publikováno v: Genetic epidemiology. 14(2)

A common polymorphism in the alpha 1-antichymotrypsin (ACT) gene has been found co modify the APOE*4-associated risk of Alzheimer's disease due to an apparent interaction between the two loci. This study was undertaken to determine the gender- and ag

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d752b5305cac9f77d55fa63ed29bcdc9
https://pubmed.ncbi.nlm.nih.gov/9129962

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Short report on DNA marker at candidate locus. Two new alleles in the tetranucleotide repeat polymorphism in the LDL-receptor-related protein (LRP) gene

Autor: M, Harris, D K, Sanghera, M I, Kamboh

Publikováno v: Clinical genetics. 50(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::94694ea6c60ab872e737069321402e7b
https://pubmed.ncbi.nlm.nih.gov/8891388

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