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Yasuko Miyake

Osaka University

42

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internalization-defective familial hypercholesterolemia Histochemical characterization of low density lipoprotein receptors in

2010
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Update of Japanese common LDLR gene mutations and their phenotypes: Mild type mutation L547V might predominate in the Japanese population

2009 Atherosclerosis
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Genetic variants in PCSK9 in the Japanese population: Rare genetic variants in PCSK9 might collectively contribute to plasma LDL cholesterol levels in the general population

2008 Atherosclerosis
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CD36 Expression in Human Monocytic Leukemia Cell Lines: THP-1 and THP-1 Subtype, Show Different Expressions of Type I and Type II Scavenger Receptors

2000
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Low density lipoprotein (LDL) binding affinity for the LDL receptor in hyperlipoproteinemia

1999 Atherosclerosis
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LDLR Database (second edition): New additions to the database and the software, and results of the first molecular analysis

1998 Nucleic Acids Research
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A novel point mutation in a splice acceptor site of intron 1 of the human low density lipoprotein receptor gene which causes severe hypercholesterolemia: An unexpected absence of exon skipping

1998 Human Mutation
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4.P.399 Implication of apolipoprotein E2 in plasma lipoprotein metabolism - lipoprotein composition and the risk of atherosclerosis -

1997 Atherosclerosis
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A compound heterozygote for familial hypercholesterolaemia with a homozygous mother

1996 Journal of Internal Medicine
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Common Mutations in the Low-Density-Lipoprotein–Receptor Gene Causing Familial Hypercholesterolemia in the Japanese Population

1995 Arteriosclerosis, Thrombosis, and Vascular Biology
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Citations (39)