Search Results - "Saha, Nilmani"
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Mitochondrial DNA analysis reveals diverse histories of tribal populations from India
Published in European journal of human genetics : EJHG (01-03-2003)“…We analyzed 370 bp of the first hypervariable region of the mitochondrial DNA (mtDNA) control region in 752 individuals from 17 tribal and four nontribal…”
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Polynesian Origins: Insights from the Y Chromosome
Published in Proceedings of the National Academy of Sciences - PNAS (18-07-2000)“…The question surrounding the colonization of Polynesia has remained controversial. Two hypotheses, one postulating Taiwan as the putative homeland and the…”
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Genetic Polymorphism of Paraoxonase and the Risk of Coronary Heart Disease
Published in Arteriosclerosis, thrombosis, and vascular biology (01-06-1997)“…Recent studies have implicated paraoxonase, an HDL-associated enzyme, in providing protection against LDL oxidation, thus affecting the risk of coronary heart…”
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ABCA1 gene polymorphisms and their associations with coronary artery disease and plasma lipids in males from three ethnic populations in Singapore
Published in Human genetics (01-07-2003)“…Mutations in the ATP-binding cassette transporter ABCA1 underlie Tangier disease and familial hypoalphaliproteinemia (FHA), disorders that are characterised by…”
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Racial and genetic determinants of plasma factor XIII activity
Published in Genetic epidemiology (01-12-2000)“…Factor XIII (F XIII), a plasma transglutaminase, is essential for normal hemostasis and fibrinolysis. Plasma F XIII consists of two catalytic A (F XIIIA) and…”
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Association of CETP Taq1B and -629C > A polymorphisms with coronary artery disease and lipid levels in the multi-ethnic Singaporean population
Published in Lipids in health and disease (08-06-2013)“…Hyperlipidaemia is a major risk factor for coronary artery disease (CAD) and cholesteryl ester transfer protein (CETP) gene polymorphisms are known to be…”
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The northeast Indian passageway: a barrier or corridor for human migrations?
Published in Molecular biology and evolution (01-08-2004)“…The northeast Indian passageway connecting the Indian subcontinent to East/Southeast Asia is thought to have been a major corridor for human migrations…”
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Lactase Haplotype Diversity in the Old World
Published in American journal of human genetics (01-01-2001)“…Lactase persistence, the genetic trait in which intestinal lactase activity persists at childhood levels into adulthood, varies in frequency in different human…”
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Alu insertion polymorphisms and human evolution: evidence for a larger population size in Africa
Published in Genome research (01-11-1997)“…Alu insertion polymorphisms (polymorphisms consisting of the presence/absence of an Alu element at a particular chromosomal location) offer several advantages…”
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DNA Polymorphisms in Two Paraoxonase Genes (PON1 and PON2) Are Associated with the Risk of Coronary Heart Disease
Published in American journal of human genetics (01-01-1998)“…A common polymorphism at codon 192 in the human paraoxonase (PON) 1 gene has been shown to be associated with increased risk for coronary heart disease (CHD)…”
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Association of Three Lipoprotein Lipase Polymorphisms with Coronary Artery Disease in Chinese and Asian Indians
Published in International journal of cardiology (24-09-2010)“…Abstract We evaluated the impact of three polymorphisms in the lipoprotein lipase gene (LPL) on coronary artery disease (CAD) susceptibility in Chinese and…”
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The apolipoprotein E polymorphism : a comparison of allele frequencies and effects in nine populations
Published in American journal of human genetics (01-08-1991)“…Application of uniform methods for measuring the apolipoprotein (apo) E polymorphism and plasma cholesterol levels in nine populations (Tyrolean, Sudanese,…”
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Apo(a) isoforms predict risk for coronary heart disease : a study in six populations
Published in Arteriosclerosis and thrombosis (01-10-1992)“…Elevated concentrations of lipoprotein(a) (Lp[a]) in plasma are associated with premature coronary heart disease (CHD). Lp(a) levels are largely determined by…”
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The codon 55 polymorphism in the paraoxonase 1 gene is not associated with the risk of coronary heart disease in Asian Indians and Chinese
Published in Atherosclerosis (01-02-1998)“…Recently several but not all studies have implicated the codon 192 polymorphism in the paraoxonase 1 ( PON1) gene with the risk of coronary heart disease…”
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Acyl-CoA : cholesterol acyltransferase-2 gene polymorphisms and their association with plasma lipids and coronary artery disease risks
Published in Human genetics (01-12-2005)“…Acyl-CoA: cholesterol acyltransferase-2 (ACAT2), an intracellular cholesterol esterification enzyme found only in the intestine and liver, has been…”
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Variation of the platelet glycoprotein IIIa PI(A1/A2) allele frequencies in the three ethnic groups of Singapore
Published in International journal of cardiology (01-08-2003)“…Polymorphisms of the glycoprotein IIIa receptor have been shown to be associated with differences in platelet aggregability. The PI(A2) variant of the…”
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Variation of the platelet glycoprotein IIIa PIA1/A2 allele frequencies in the three ethnic groups of Singapore
Published in International journal of cardiology (01-08-2003)Get full text
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Variation of the platelet glycoprotein IIIa PI A1/A2 allele frequencies in the three ethnic groups of Singapore
Published in International journal of cardiology (2003)“…Background: Polymorphisms of the glycoprotein IIIa receptor have been shown to be associated with differences in platelet aggregability. The PI A2 variant of…”
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Acute phase proteins in male Chinese schizophrenic patients in Singapore
Published in Schizophrenia research (15-11-1996)“…Changes in the concentration of some serum acute phase proteins ( α 1-antitrypsin, α 2-macroglobulin, complement C 3, haptoglobin, ceruloplasmin, transferrin,…”
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The impact of factor XIIIa V34L polymorphism on plasma factor XIII activity in the Chinese and Asian Indians from Singapore
Published in Human genetics (2004)“…Factor XIII (FXIII) is a plasma transglutaminase that is essential for normal haemostasis and fibrinolysis. A few polymorphic sites have been identified in the…”
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