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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

Atherosclerosis, 2008-01, Vol.196 (1), p.29-36

2008

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Atrial electrical abnormality in patients with Brugada syndrome assessed by signal-averaged electrocardiography

Indian heart journal, 2017-11, Vol.69 (6), p.714-719

2017

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Effects of number of flowers per raceme and number of racemes per plant on bumblebee visits and female reproductive success in Salvia nipponica (Labiatae)

Ecological research, 2005-07, Vol.20 (4), p.395-403

2005

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Ventricular fibrillation followed by the augmentation of Brugada-like electrocardiographic changes caused by ischemia of the conus branch in a patient with coronary artery disease

IHJ cardiovascular case reports, 2018-01, Vol.2 (1), p.58-60

2018

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

Atherosclerosis, 2009-03, Vol.203 (1), p.153-160

2009

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Common mutations in the low-density-lipoprotein-receptor gene causing familial hypercholesterolemia in the Japanese population

Arteriosclerosis, thrombosis, and vascular biology, 1995-10, Vol.15 (10), p.1713

1995

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Partial left superior pulmonary vein potential elimination by an inferior ganglionated plexus ablation

Clinical case reports, 2017-11, Vol.5 (11), p.1826-1829

2017

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Maintenance-Type DNA Methyltransferase Is Highly Expressed in Post-Mitotic Neurons and Localized in the Cytoplasmic Compartment

Journal of biochemistry (Tokyo), 2000-08, Vol.128 (2), p.315-321

2000

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

Atherosclerosis, 1999-11, Vol.147 (1), p.77-86

1999

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Rate of Cholesteryl Ester Transfer between High and Low Density Lipoproteins in Human Serum and a Case with Decreased Transfer Rate in Association with Hyperalphalipoproteinemia

Journal of biochemistry (Tokyo), 1985-12, Vol.98 (6), p.1499-1508

1985

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Cells of a human monocytic leukemia cell line (THP-1) synthesize and secrete apolipoprotein E and lipoprotein lipase

Biochemical and biophysical research communications, 1985-01, Vol.126 (1), p.526-531

1985

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

Nucleic acids research, 1998-01, Vol.26 (1), p.248

1998

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Uptake of oxidized low-density lipoprotein in a THP-1 cell line lacking scavenger receptor A

Atherosclerosis, 2001-10, Vol.158 (2), p.351-357

2001

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Low-Density Lipoprotein Receptor Mutation That Deletes Exons 2 and 3 by Alu-Alu Recombination

Journal of biochemistry (Tokyo), 1993-03, Vol.113 (3), p.372-376

1993

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Cells of an Internalization-Defective Familial Hypercholesterolemia Mutant Secrete Low Density Lipoprotein Receptors

Journal of biochemistry (Tokyo), 1987, Vol.101 (6), p.1355-1360

1987

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A point mutation of low‐density‐lipoprotein receptor causing rapid degradation of the receptor

European journal of biochemistry, 1992-11, Vol.210 (1), p.1-7

1992

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Transformation of intramembrane particles of HVJ (Sendai virus) envelopes from an invisible to visible form on aging of virions

Virology (New York, N.Y.), 1979-06, Vol.95 (2), p.523-535

1979

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Parasexual Hybridization in Cellular Slime Molds.II. The Appearance and Characterization of Interspecific Hybrids between Dictyostelium discoideum and D. mucoroides

Cell Structure and Function, 1976, Vol.1(2), pp.147-154

1976

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Parasexual Hybridization in Cellular Slime Molds

Cell structure and function, 1975-01, Vol.1 (1), p.23

1975

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Parasexual Hybridization in Cellular Slime Molds: I. Appearance of Hybrid Clones at High Frequency in a Short Period and Its Relation to Cell Fusion in Dictyostelium discoideum

Cell Structure and Function, 1975, Vol.1(1), pp.23-31

1975

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Genomic organization of the mouse AZ1 gene that encodes the protein localized to preacrosomes of spermatids

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.138-141

1997

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Genomic Organization of the MouseAZ1Gene That Encodes the Protein Localized to Preacrosomes of Spermatids

Genomics (San Diego, Calif.), 1997-02, Vol.40 (1), p.138-141

1997

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Three mutations including two deletions of the low density lipoprotein receptor gene in Japanese patients with homozygous familial hypercholesterolemia

Japanese journal of medicine, 1989, Vol.28 (5), p.661-662

1989

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1-Methoxycarbonylindolizine-3,5-dicarbaldehyde as a derivatization reagent for amino compounds in high-performance capillary electrophoresis

Analyst (London), 1995, Vol.120 (1), p.63-68

1995

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Siblings with normal LDL receptor activity and severe hypercholesterolemia

Arteriosclerosis and thrombosis, 1992-09, Vol.12 (9), p.1071

1992

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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

Atrial electrical abnormality in patients with Brugada syndrome assessed by signal-averaged electrocardiography

Effects of number of flowers per raceme and number of racemes per plant on bumblebee visits and female reproductive success in Salvia nipponica (Labiatae)

Ventricular fibrillation followed by the augmentation of Brugada-like electrocardiographic changes caused by ischemia of the conus branch in a patient with coronary artery disease

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

Common mutations in the low-density-lipoprotein-receptor gene causing familial hypercholesterolemia in the Japanese population

Partial left superior pulmonary vein potential elimination by an inferior ganglionated plexus ablation

Maintenance-Type DNA Methyltransferase Is Highly Expressed in Post-Mitotic Neurons and Localized in the Cytoplasmic Compartment

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

Rate of Cholesteryl Ester Transfer between High and Low Density Lipoproteins in Human Serum and a Case with Decreased Transfer Rate in Association with Hyperalphalipoproteinemia

Cells of a human monocytic leukemia cell line (THP-1) synthesize and secrete apolipoprotein E and lipoprotein lipase

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

Uptake of oxidized low-density lipoprotein in a THP-1 cell line lacking scavenger receptor A

Low-Density Lipoprotein Receptor Mutation That Deletes Exons 2 and 3 by Alu-Alu Recombination

Cells of an Internalization-Defective Familial Hypercholesterolemia Mutant Secrete Low Density Lipoprotein Receptors

A point mutation of low‐density‐lipoprotein receptor causing rapid degradation of the receptor

Transformation of intramembrane particles of HVJ (Sendai virus) envelopes from an invisible to visible form on aging of virions

Parasexual Hybridization in Cellular Slime Molds.II. The Appearance and Characterization of Interspecific Hybrids between Dictyostelium discoideum and D. mucoroides

Parasexual Hybridization in Cellular Slime Molds

Parasexual Hybridization in Cellular Slime Molds: I. Appearance of Hybrid Clones at High Frequency in a Short Period and Its Relation to Cell Fusion in Dictyostelium discoideum

Genomic organization of the mouse AZ1 gene that encodes the protein localized to preacrosomes of spermatids

Genomic Organization of the MouseAZ1Gene That Encodes the Protein Localized to Preacrosomes of Spermatids

Three mutations including two deletions of the low density lipoprotein receptor gene in Japanese patients with homozygous familial hypercholesterolemia

1-Methoxycarbonylindolizine-3,5-dicarbaldehyde as a derivatization reagent for amino compounds in high-performance capillary electrophoresis

Siblings with normal LDL receptor activity and severe hypercholesterolemia

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