Akihiro Inazu

Ontology type: schema:Person     

Person Info





Publications in SciGraph latest 50 shown

  • 2016-04-02 Changes in lipoprotein lipase and endothelial lipase mass in familial hypercholesterolemia during three-drug lipid-lowering combination therapy in LIPIDS IN HEALTH AND DISEASE
  • 2015-03-13 Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia in JIMD REPORTS, VOLUME 22
  • 2015-02-10 Infantile Cases of Sitosterolaemia with Novel Mutations in the ABCG5 Gene: Extreme Hypercholesterolaemia is Exacerbated by Breastfeeding in JIMD REPORTS, VOLUME 21
  • 2010-02-03 Human Cholesteryl Ester Transfer Protein in Human HDL Metabolism in HIGH DENSITY LIPOPROTEINS, DYSLIPIDEMIA, AND CORONARY HEART DISEASE
  • 2007-10-24 Comparison of Effects of Pitavastatin and Atorvastatin on Plasma Coenzyme Q10 in Heterozygous Familial Hypercholesterolemia: Results From a Crossover Study in CLINICAL PHARMACOLOGY & THERAPEUTICS
  • 2003-03-26 Haplotype analyses of cholesteryl ester transfer protein gene promoter: a clue to an unsolved mystery of TaqIB polymorphism in JOURNAL OF MOLECULAR MEDICINE
  • 2002-06 Double deletions and missense mutations in the first nucleotide-binding fold of the ATP-binding cassette transporter A1 (ABCA1) gene in Japanese patients with Tangier disease in JOURNAL OF HUMAN GENETICS
  • 2001-04 Effects of hepatic lipase gene promoter nucleotide variations on serum HDL cholesterol concentration in the general Japanese population in JOURNAL OF HUMAN GENETICS
  • 2000 Common Mutation of 5, 10-Methylenetetrahydrofolate Reductase Accelerates Coronary Artery Disease in Familial Hypercholesterolemia in LIPOPROTEIN METABOLISM AND ATHEROGENESIS
  • 1996 Molecular Genetics of Cholesterol Transport and Cholesterol Reverse Transport Disorders, and Coronary Heart Disease in DRUGS AFFECTING LIPID METABOLISM
  • 1993-03 Rapid detection and prevalence of cholesteryl ester transfer protein deficiency caused by an intron 14 splicing defect in hyperalphalipoproteinemia in HUMAN GENETICS
  • 1989-11-01 Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins in NATURE
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