D J Galton


Ontology type: schema:Person     


Person Info

NAME

D J

SURNAME

Galton

Publications in SciGraph latest 50 shown

  • 2003-12 Genetic study of common variants at the Apo E, Apo AI, Apo CIII, Apo B, lipoprotein lipase (LPL) and hepatic lipase (LIPC) genes and coronary artery disease (CAD): variation in LIPC gene associates with clinical outcomes in patients with established CAD in BMC MEDICAL GENETICS
  • 1999-09 Genetic markers to predict polygenic disease in CURRENT ATHEROSCLEROSIS REPORTS
  • 1998-06 Human cloning: Safety is the issue in NATURE MEDICINE
  • 1996-09 Genetic contribution of polymorphism of the GLUT1 and GLUT4 genes to the susceptibility to type 2 (non-insulin-dependent) diabetes mellitus in different populations in ACTA DIABETOLOGICA
  • 1996 Environment-by-Gene Interactions: Polymorphisms at the Lipoprotein Lipase (Lpl) Locus in DRUGS AFFECTING LIPID METABOLISM
  • 1994-06 Affected sib-pair analysis of the GLUT1 glucose transporter gene locus in non-insulin-dependent diabetes mellitus (NIDDM): evidence for no linkage in HUMAN GENETICS
  • 1994 Plasma Triglyceride Transport in GENETIC FACTORS IN CORONARY HEART DISEASE
  • 1993 Lipoprotein lipase: Gene variants and coronary atherosclerosis in HUMAN APOLIPOPROTEIN MUTANTS III
  • 1993 Common Mutations Underlying the Hypertriglyceridaemia/Low HDL Syndrome in CELLULAR METABOLISM OF THE ARTERIAL WALL AND CENTRAL NERVOUS SYSTEM
  • 1992-03 Polymorphisms at the GLUT1 (HepG2) and GLUT4 (muscle/adipocyte) glucose transporter genes and non-insulin-dependent diabetes mellitus (NIDDM) in HUMAN GENETICS
  • 1992-01 Common genetic variants relating to familial hypertriglyceridaemia in JOURNAL OF ANALYTICAL CHEMISTRY
  • 1991-04 Insulin receptor gene polymorphisms in Type 2 (non-insulin-dependent) diabetes mellitus in DIABETOLOGIA
  • 1991 DNA Polymorphisms as Disease Markers in DNA POLYMORPHISMS AS DISEASE MARKERS
  • 1991 Atherosclerosis: The Genetic Analysis of a Multi-Factorial Disease in DNA POLYMORPHISMS AS DISEASE MARKERS
  • 1991 Lipoprotein Lipase Gene Variants in Subjects with Hypertriglyceridaemia and Coronary Atherosclerosis in DNA POLYMORPHISMS AS DISEASE MARKERS
  • 1990 Genetic Variation at the Lipoprotein Lipase Gene Associates with Coronary Arteriosclerosis in HYPERCHOLESTEROLEMIA, HYPOCHOLESTEROLEMIA, HYPERTRIGLYCERIDEMIA, IN VIVO KINETICS
  • 1989 DNA Polymorphisms of the Glucose Transporter Gene in Non-Insulin Dependent Diabetes Mellitus (NIDDM) in HUMAN APOLIPOPROTEIN MUTANTS 2
  • 1988-12 DNA haplotypes of the human apoprotein B gene in coronary atherosclerosis in HUMAN GENETICS
  • 1988-11 Linkage analysis of the human insulin receptor gene in Type 2 (non-insulin-dependent) diabetic families and a family with maturity onset diabetes of the young in DIABETOLOGIA
  • 1988 Molecular Genetics of Coronary Heart Disease in EICOSANOIDS, APOLIPOPROTEINS, LIPOPROTEIN PARTICLES, AND ATHEROSCLEROSIS
  • 1988-01 A DNA polymorphism of an apoprotein gene associates with the hypertriglyceridaemia of primary gout in HUMAN GENETICS
  • 1987-03 DNA polymorphic patterns and haplotype arrangements of the apo A-1, apo C-III, apo A-IV gene cluster in different ethnic groups in HUMAN GENETICS
  • 1987 The management of the hyperlipidaemias in DRUGS FOR HEART DISEASE
  • 1987 DNA Polymorphisms of the Insulin Receptor Gene and Non-Insulin-Dependent Diabetes Mellitus in KONGREß
  • 1986-11 A DNA polymorphism of the apoprotein AII gene in hypertriglyceridaemia in HUMAN GENETICS
  • 1986-07 Haplotypes of the human apoprotein AI-CIII-AIV gene cluster in coronary atherosclerosis in HUMAN GENETICS
  • 1986-03 Acipimox in the treatment of patients with hyperlipidaemia: A double blind trial in EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
  • 1986-02 haplotypes identified by DNA polymorphisms at the apolipoprotein A-1 and C-III loci and hypertriglyceridaemia in HUMAN GENETICS
  • 1986 An Apoprotein AII Gene Polymorphism and Hyperlipidaemia in HUMAN APOLIPOPROTEIN MUTANTS
  • 1985-11 Allelic variation adjacent to the human insulin and apolipoprotein C-II genes in different ethnic groups in HUMAN GENETICS
  • 1985-04 849 THE INSULIN GENE POLYMORPHISM IN TYPE I DIABETES (IDDM) FAMILIES in PEDIATRIC RESEARCH
  • 1985-04 Type 1 (insulin-dependent) diabetes and a highly variable locus close to the insulin gene on chromosome 11 in DIABETOLOGIA
  • 1985-03 DNA polymorphisms flanking the apo A-1 and insulin genes and type III hyperlipidaemia in HUMAN GENETICS
  • 1984-08 Insulin and apolipoprotein A-1/C-III gene polymorphisms relating to hypertriglyceridaemia and diabetes mellitus in DIABETOLOGIA
  • 1984-07 Familial apolipoprotein CII deficiency: A preliminary analysis of the gene defect in two independent families in HUMAN GENETICS
  • 1981 Symposium: Substratumsatz menschlicher Gewebe bei normalem und gestörtem Stoffwechsel in VERHANDLUNGEN DER DEUTSCHEN GESELLSCHAFT FÜR INNERE MEDIZIN
  • 1980-03 Activation of the phospholipase A1 activity of lipoprotein lipase by apoprotein C-II in LIPIDS
  • 1980 Regulation der Sterin-Synthese in menschlichen Leukozyten in VERHANDLUNGEN DER DEUTSCHEN GESELLSCHAFT FÜR INNERE MEDIZIN
  • 1979-05 Insulin-independent diabetes: A defect in the activity of lipoprotein lipase in adipose tissue in DIABETOLOGIA
  • 1979-03 A new simple assay for total blood lipids by refractometry in CELLULAR AND MOLECULAR LIFE SCIENCES
  • 1976-08 Catecholamine receptor sensitivity and the regulation of lipolysis in adult diabetes in DIABETOLOGIA
  • 1975 Adipose Tissue Metabolism in OBESITY: ITS PATHOGENESIS AND MANAGEMENT
  • 1974-04 The effect of a glucose load on plasma fatty acids and lipolysis in adipose tissue of obese diabetic and non-diabetic patients in DIABETOLOGIA
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