AAAAAA

   
Results: 1-22 |
Results: 22
A LOW-PREVALENCE OF CORONARY HEART-DISEASE AMONG SUBJECTS WITH INCREASED HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL LEVELS, INCLUDING THOSE WITH PLASMA CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY
Authors: MORIYAMA Y OKAMURA T INAZU A DOI M ISO H MOURI Y ISHIKAWA Y SUZUKI H IIDA M KOIZUMI J MABUCHI H KOMACHI Y
Citation: Y. Moriyama et al., A LOW-PREVALENCE OF CORONARY HEART-DISEASE AMONG SUBJECTS WITH INCREASED HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL LEVELS, INCLUDING THOSE WITH PLASMA CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY, Preventive medicine, 27(5), 1998, pp. 659-667
FDG UPTAKE IN GLUCOSE-UTILIZING ORGANS OF MODY PATIENTS WITH HNF-1 ALPHA-GENE MUTATION
Authors: YAGI K SEKI H KITATANI M YONEDA T NOHARA A INAZU A HIFUMI S KOIZUMI J TAKEKOSHI N MABUCHI H
Citation: K. Yagi et al., FDG UPTAKE IN GLUCOSE-UTILIZING ORGANS OF MODY PATIENTS WITH HNF-1 ALPHA-GENE MUTATION, Diabetes, 47, 1998, pp. 682-682
ENZYME-IMMUNOASSAY FOR CHOLESTERYL ESTER TRANSFER PROTEIN IN HUMAN SERUM
Authors: KIYOHARA T KIRIYAMA R ZAMMA S INAZU A KOIZUMI J MABUCHI H CHICHIBU K
Citation: T. Kiyohara et al., ENZYME-IMMUNOASSAY FOR CHOLESTERYL ESTER TRANSFER PROTEIN IN HUMAN SERUM, Clinica chimica acta, 271(2), 1998, pp. 109-118
A CASE OF ABETALIPOPROTEINEMIA CAUSED BY MATERNAL ISODISOMY OF CHROMOSOME 4Q CONTAINING AN INTRON-9 SPLICE ACCEPTOR MUTATION IN THE MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN GENE
Authors: YANG XP INAZU A YAGI K KAJINAMI K KOIZUMI J MABUCHI H
Citation: Xp. Yang et al., A CASE OF ABETALIPOPROTEINEMIA CAUSED BY MATERNAL ISODISOMY OF CHROMOSOME 4Q CONTAINING AN INTRON-9 SPLICE ACCEPTOR MUTATION IN THE MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN GENE, Circulation, 98(17), 1998, pp. 172-172
COMMON MUTATION OF 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE ACCERALATES CORONARY-ARTERY DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA
Authors: KAWASHIRI M KAJINAMI K INAZU A KOIZUMI J MASBUCHI H
Citation: M. Kawashiri et al., COMMON MUTATION OF 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE ACCERALATES CORONARY-ARTERY DISEASE IN FAMILIAL HYPERCHOLESTEROLEMIA, Circulation, 98(17), 1998, pp. 210-210
LOW-DENSITY-LIPOPROTEIN RECEPTOR GENOTYPE-DEPENDENT RESPONSE TO CHOLESTEROL-LOWERING BY COMBINED PRAVASTATIN AND CHOLESTYRAMINE IN FAMILIALHYPERCHOLESTEROLEMIA
Authors: KAJINAMI K YAGI K HIGASHIKATA T INAZU A KOIZUMI J MABUCHI H
Citation: K. Kajinami et al., LOW-DENSITY-LIPOPROTEIN RECEPTOR GENOTYPE-DEPENDENT RESPONSE TO CHOLESTEROL-LOWERING BY COMBINED PRAVASTATIN AND CHOLESTYRAMINE IN FAMILIALHYPERCHOLESTEROLEMIA, The American journal of cardiology, 82(1), 1998, pp. 113-117
CHOLESTERYL ESTER TRANSFER PROTEIN-ACTIVITY ENHANCES PLASMA CHOLESTERYL ESTER FORMATION - STUDIES IN CETP TRANSGENIC MICE AND HUMAN GENETICCETP DEFICIENCY
Authors: OLIVEIRA HCF MA LM MILNE R MARCOVINA SM INAZU A MABUCHI H TALL AR
Citation: Hcf. Oliveira et al., CHOLESTERYL ESTER TRANSFER PROTEIN-ACTIVITY ENHANCES PLASMA CHOLESTERYL ESTER FORMATION - STUDIES IN CETP TRANSGENIC MICE AND HUMAN GENETICCETP DEFICIENCY, Arteriosclerosis, thrombosis, and vascular biology, 17(6), 1997, pp. 1045-1052
CATALYTICALLY INACTIVE LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) CAUSED BY A GLY-30 TO SER MUTATION IN A FAMILY WITH LCAT DEFICIENCY
Authors: YANG XP INAZU A HONJO A KOIZUMI I KAJINAMI K KOIZUMI J MARCOVINA SM ALBERS JJ MABUCHI H
Citation: Xp. Yang et al., CATALYTICALLY INACTIVE LECITHIN - CHOLESTEROL ACYLTRANSFERASE (LCAT) CAUSED BY A GLY-30 TO SER MUTATION IN A FAMILY WITH LCAT DEFICIENCY, Journal of lipid research, 38(3), 1997, pp. 585-591
LDL-RECEPTOR GENOTYPE-DEPENDENT RESPONSE TO CHOLESTEROL-LOWERING THERAPY IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Authors: KAJINAMI K YAGI K HIGASHIKATA T INAZU A KOIZUMI J MABUCHI H
Citation: K. Kajinami et al., LDL-RECEPTOR GENOTYPE-DEPENDENT RESPONSE TO CHOLESTEROL-LOWERING THERAPY IN PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, Atherosclerosis, 134(1-2), 1997, pp. 56-56
VARIETY OF LOW-DENSITY-LIPOPROTEIN-RECEPTOR GENE-MUTATIONS AND EXPRESSION OF CORONARY-ARTERY DISEASE IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Authors: HIGASHIKATA T KAJINAMI K YAGI K INAZU A MATSUSHITA H NOHARA A KOIZUMI J MABUCHI H
Citation: T. Higashikata et al., VARIETY OF LOW-DENSITY-LIPOPROTEIN-RECEPTOR GENE-MUTATIONS AND EXPRESSION OF CORONARY-ARTERY DISEASE IN HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, Atherosclerosis, 134(1-2), 1997, pp. 69-69
PLASMA HOMOCYSTEINE LEVELS AND PREMATURE CORONARY-ARTERY DISEASE IN MALE-PATIENTS
Authors: KAWASHIRI M KAJINAMI K NOHARA A INAZU A KOIZUMI J MABUCHI H
Citation: M. Kawashiri et al., PLASMA HOMOCYSTEINE LEVELS AND PREMATURE CORONARY-ARTERY DISEASE IN MALE-PATIENTS, Atherosclerosis, 134(1-2), 1997, pp. 160-160
CLINICAL CHARACTERISTICS OF DOUBLE HETEROZYGOTES WITH FAMILIAL HYPERCHOLESTEROLEMIA AND CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY
Authors: HARAKI T INAZU A YAGI K KAJINAMI K KOIZUMI J MABUCHI H
Citation: T. Haraki et al., CLINICAL CHARACTERISTICS OF DOUBLE HETEROZYGOTES WITH FAMILIAL HYPERCHOLESTEROLEMIA AND CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY, Atherosclerosis, 132(2), 1997, pp. 229-236
DIABETIC-PATIENTS ASSOCIATED WITH POSITIVE GAD-ANTIBODIES AND MITOCHONDRIAL-DNA ABNORMALITY IN JAPAN
Authors: KITATANI M YAGI K INAZU A NAKAGAWA A KAJINAMI K KOIZUMI J MABUCHI H
Citation: M. Kitatani et al., DIABETIC-PATIENTS ASSOCIATED WITH POSITIVE GAD-ANTIBODIES AND MITOCHONDRIAL-DNA ABNORMALITY IN JAPAN, Diabetologia, 40, 1997, pp. 797-797
FAMILIAL COMBINED HYPERLIPIDEMIA IN DIABETIC-PATIENTS
Authors: KOIZUMI J NOHARA A KITATANI M HIGASHIKATA T HARAKI T YAGI K INAZU A KAJINAMI K MABUCHI H
Citation: J. Koizumi et al., FAMILIAL COMBINED HYPERLIPIDEMIA IN DIABETIC-PATIENTS, Diabetes, 45, 1996, pp. 137-137
A 4-YEAR TRIAL OF SIMVASTATIN IN THE TREATMENT OF PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA
Authors: KITATANI M KOIZUMI J INAZU A KAJINAMI K MABUCHI H
Citation: M. Kitatani et al., A 4-YEAR TRIAL OF SIMVASTATIN IN THE TREATMENT OF PATIENTS WITH HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA, Current therapeutic research, 57(1), 1996, pp. 62-71
ABSENCE OF FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 IN JAPANESE PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA
Authors: NOHARA A YAGI K INAZU A KAJINAMI K KOIZUMI J MABUCHI H
Citation: A. Nohara et al., ABSENCE OF FAMILIAL DEFECTIVE APOLIPOPROTEIN B-100 IN JAPANESE PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA, Lancet, 345(8962), 1995, pp. 1438-1438
CLINICAL EFFICACY OF FLUVASTATIN IN THE LONG-TERM TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA
Authors: KOIZUMI J HARAKI T YAGI K INAZU A KAJINAMI K MIYAMOTO S UEDA K OHTA M TAKEGOSHI T TAKEDA M UNO Y MABUCHI H TAKEDA R
Citation: J. Koizumi et al., CLINICAL EFFICACY OF FLUVASTATIN IN THE LONG-TERM TREATMENT OF FAMILIAL HYPERCHOLESTEROLEMIA, The American journal of cardiology, 76(2), 1995, pp. 47-50
PURIFICATION AND CHARACTERIZATION OF A NOVEL DIMERIC 20-ALPHA-HYDROXYSTEROID DEHYDROGENASE FROM TETRAHYMENA-PYRIFORMIS
Authors: INAZU A SATO K NAKAYAMA T DEYASHIKI Y HARA A NOZAWA Y
Citation: A. Inazu et al., PURIFICATION AND CHARACTERIZATION OF A NOVEL DIMERIC 20-ALPHA-HYDROXYSTEROID DEHYDROGENASE FROM TETRAHYMENA-PYRIFORMIS, Biochemical journal, 297, 1994, pp. 195-200
GENETIC CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY CAUSED BY 2 PREVALENT MUTATIONS AS A MAJOR DETERMINANT OF INCREASED LEVELS OF HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL
Authors: INAZU A JIANG XC HARAKI T YAGI K KAMON N KOIZUMI J MABUCHI H TAKEDA R TAKATA K MORIYAMA Y DOI M TALL A
Citation: A. Inazu et al., GENETIC CHOLESTERYL ESTER TRANSFER PROTEIN-DEFICIENCY CAUSED BY 2 PREVALENT MUTATIONS AS A MAJOR DETERMINANT OF INCREASED LEVELS OF HIGH-DENSITY-LIPOPROTEIN CHOLESTEROL, The Journal of clinical investigation, 94(5), 1994, pp. 1872-1882
STEREOSPECIFICITY OF TRANS-DIHYDRODIOL OXIDATION BY DIMERIC AND MONOMERIC DIHYDRODIOL DEHYDROGENASES FROM MAMMALIAN-TISSUES
Authors: YAMAGUCHI S INAZU A DEYASHIKI Y NAKAYAMA T SATO K MIYABE Y HARA A
Citation: S. Yamaguchi et al., STEREOSPECIFICITY OF TRANS-DIHYDRODIOL OXIDATION BY DIMERIC AND MONOMERIC DIHYDRODIOL DEHYDROGENASES FROM MAMMALIAN-TISSUES, Journal of Biochemistry, 115(3), 1994, pp. 493-496
REDUCTION OF LIPOPROTEIN(A) BY LDL-APHERESIS USING A DEXTRAN SULFATE CELLULOSE COLUMN IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA
Authors: KOIZUMI J KOIZUMI I UNO Y INAZU A KAJINAMI K HARAKI T YAGI K KAMON N MIYAMOTO S TAKEGOSHI T MABUCHI H TAKEDA R TANI N TAKADA S
Citation: J. Koizumi et al., REDUCTION OF LIPOPROTEIN(A) BY LDL-APHERESIS USING A DEXTRAN SULFATE CELLULOSE COLUMN IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA, Atherosclerosis, 100(1), 1993, pp. 65-74
MONKEY 3-DEOXYGLUCOSONE REDUCTASE - TISSUE DISTRIBUTION AND PURIFICATION OF 3 MULTIPLE FORMS OF THE KIDNEY ENZYME THAT ARE IDENTICAL WITH DIHYDRODIOL DEHYDROGENASE, ALDEHYDE REDUCTASE, AND ALDOSE REDUCTASE
Authors: SATO K INAZU A YAMAGUCHI S NAKAYAMA T DEYASHIKI Y SAWADA H HARA A
Citation: K. Sato et al., MONKEY 3-DEOXYGLUCOSONE REDUCTASE - TISSUE DISTRIBUTION AND PURIFICATION OF 3 MULTIPLE FORMS OF THE KIDNEY ENZYME THAT ARE IDENTICAL WITH DIHYDRODIOL DEHYDROGENASE, ALDEHYDE REDUCTASE, AND ALDOSE REDUCTASE, Archives of biochemistry and biophysics, 307(2), 1993, pp. 286-294
Risultati: 1-22 |