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Antithrombotic effects of losartan in patients with hypertension complicated by atrial fibrillation: 4A (Angiotensin II Antagonist of platelet Aggregation in patients with Atrial fibrillation), a pilot study

Hypertension research, 2014-06, Vol.37 (6), p.513-518

2014

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Tailored Adjunctive Cilostazol Therapy Based on CYP2C19 Genotyping in Patients With Acute Myocardial Infarction　― The CALDERA-GENE Study

Circulation Journal, 2018/05/25, Vol.82(6), pp.1517-1525

2018

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Selective neuronal damage and chronic hemodynamic cerebral ischemia

Annals of neurology, 2007-05, Vol.61 (5), p.454-465

2007

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Design and Synthesis of Cyclic ADP-4-Thioribose as a Stable Equivalent of Cyclic ADP-Ribose, a Calcium Ion-Mobilizing Second Messenger

Angewandte Chemie (International ed.), 2013-06, Vol.52 (26), p.6633-6637

International ed. in English, 2013

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Substitution at the 8-position of 3-deoxy-cyclic ADP-carbocyclic-ribose, a highly potent Ca2+-mobilizing agent, provides partial agonists

Bioorganic & medicinal chemistry, 2007-04, Vol.15 (8), p.3032-3040

2007

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Reproducibility of Semi-quantitative Parameters in FDG-PET Using Two Different PET Scanners: Influence of Attenuation Correction Method and Examination Interval

Molecular imaging and biology, 2008-05, Vol.10 (3), p.162-166

2008

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Epidermal nevus syndrome associated with anterior scleral staphyloma and ectopic bone and cartilaginous intraocular tissue

Japanese journal of ophthalmology, 2010-01, Vol.54 (1), p.15-18

2010

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The Role of Tc-99m-HSA-D scintigraphy in the diagnosis of protein-losing enteropathy: A Comprehensive Review of recent 10 years experience

The Journal of nuclear medicine (1978), 2017-05, Vol.58, p.942

2017

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A Multicenter, Phase 2, Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Dose-Finding Trial of the Oral Factor XIa Inhibitor Asundexian to Prevent Adverse Cardiovascular Outcomes After Acute Myocardial Infarction

Circulation (New York, N.Y.), 2022-10, Vol.146 (16), p.1196-1206

2022

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Shape of Silkworm cocoon changes with size in some races

Journal of Insect Biotechnology and Sericology, 2013, Vol.82(3), pp.3_055-3_059

2013

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Synthesis of 5-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent : The first antagonists modified at the N1-ribose moiety

Bioorganic & medicinal chemistry letters, 2008-07, Vol.18 (13), p.3814-3818

2008

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Increased Plasma Levels of Thioredoxin in Patients with Glucose Intolerance

Internal Medicine, 2005, Vol.44(11), pp.1127-1132

2005

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Usefulness of Preprocedural Platelet Aggregation to Predict Restenosis After Percutaneous Coronary Intervention

The American journal of cardiology, 2005-07, Vol.96 (1), p.71-73

2005

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Angiotensin II Receptor Blocker-based Therapy in Japanese Elderly, High-risk, Hypertensive Patients

The American journal of medicine, 2012-10, Vol.125 (10), p.981-990

2012

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Myocardial ischemia in Kawasaki disease: Evaluation with dipyridamole stress technetium 99m tetrofosmin scintigraphy

Journal of nuclear cardiology, 2002-11, Vol.9 (6), p.632-637

2002

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Class A macrophage scavenger receptor gene expression levels in peripheral blood mononuclear cells specifically increase in patients with acute coronary syndrome

Atherosclerosis, 2008-06, Vol.198 (2), p.426-433

2008

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Differential effectiveness of ARB plus CCB therapy and high-dose ARB therapy in high-risk elderly hypertensive patients: subanalysis of the OSCAR study

Hypertension research, 2015-03, Vol.38 (3), p.199-207

2015

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Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca(2+)-mobilizing second messenger. Structure--activity relationship of the N1-ribose moiety

Journal of the American Chemical Society, 2005-06, Vol.127 (24), p.8846-8855

2005

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Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca2+-mobilizing second messenger. structure-activity relationship of the N1-ribose moiety

Journal of the American Chemical Society, 2005-06, Vol.127 (24), p.8846-8855

2005

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Mevalonate analogues as substrates of enzymes in the isoprenoid biosynthetic pathway of Streptococcus pneumoniae

Bioorganic & medicinal chemistry, 2010-02, Vol.18 (3), p.1124-1134

2010

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Recent advances in nuclear cardiology in the study of coronary artery disease

Annals of nuclear medicine, 1997-06, Vol.11 (2), p.55-66

1997

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Synthesis of 5"-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca super(2+)-mobilizing agent: The first antagonists modified at the N1- ribose moiety

Bioorganic & medicinal chemistry, 2008-07, Vol.18 (13), p.3814-3818

2008

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Substitution at the 8-position of 3″-deoxy-cyclic ADP-carbocyclic-ribose, a highly potent Ca 2+-mobilizing agent, provides partial agonists 1

Bioorganic & medicinal chemistry, 2007, Vol.15 (8), p.3032-3040

2007

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Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca 2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (13), p.3814-3818

2008

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Assessment of regional and global left ventricular function by reinjection Tl-201 and rest Tc-99m sestamibi ECG-gated SPECT : Comparison with three-dimensional magnetic resonance imaging

Journal of the American College of Cardiology, 1999-03, Vol.33 (4), p.991-997

1999

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Antithrombotic effects of losartan in patients with hypertension complicated by atrial fibrillation: 4A (Angiotensin II Antagonist of platelet Aggregation in patients with Atrial fibrillation), a pilot study

Tailored Adjunctive Cilostazol Therapy Based on CYP2C19 Genotyping in Patients With Acute Myocardial Infarction　― The CALDERA-GENE Study

Selective neuronal damage and chronic hemodynamic cerebral ischemia

Design and Synthesis of Cyclic ADP-4-Thioribose as a Stable Equivalent of Cyclic ADP-Ribose, a Calcium Ion-Mobilizing Second Messenger

Substitution at the 8-position of 3-deoxy-cyclic ADP-carbocyclic-ribose, a highly potent Ca2+-mobilizing agent, provides partial agonists

Reproducibility of Semi-quantitative Parameters in FDG-PET Using Two Different PET Scanners: Influence of Attenuation Correction Method and Examination Interval

Epidermal nevus syndrome associated with anterior scleral staphyloma and ectopic bone and cartilaginous intraocular tissue

The Role of Tc-99m-HSA-D scintigraphy in the diagnosis of protein-losing enteropathy: A Comprehensive Review of recent 10 years experience

A Multicenter, Phase 2, Randomized, Placebo-Controlled, Double-Blind, Parallel-Group, Dose-Finding Trial of the Oral Factor XIa Inhibitor Asundexian to Prevent Adverse Cardiovascular Outcomes After Acute Myocardial Infarction

Shape of Silkworm cocoon changes with size in some races

Synthesis of 5-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca2+-mobilizing agent : The first antagonists modified at the N1-ribose moiety

Increased Plasma Levels of Thioredoxin in Patients with Glucose Intolerance

Usefulness of Preprocedural Platelet Aggregation to Predict Restenosis After Percutaneous Coronary Intervention

Angiotensin II Receptor Blocker-based Therapy in Japanese Elderly, High-risk, Hypertensive Patients

Myocardial ischemia in Kawasaki disease: Evaluation with dipyridamole stress technetium 99m tetrofosmin scintigraphy

Class A macrophage scavenger receptor gene expression levels in peripheral blood mononuclear cells specifically increase in patients with acute coronary syndrome

Differential effectiveness of ARB plus CCB therapy and high-dose ARB therapy in high-risk elderly hypertensive patients: subanalysis of the OSCAR study

Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca(2+)-mobilizing second messenger. Structure--activity relationship of the N1-ribose moiety

Synthesis of stable and cell-type selective analogues of cyclic ADP-ribose, a Ca2+-mobilizing second messenger. structure-activity relationship of the N1-ribose moiety

Mevalonate analogues as substrates of enzymes in the isoprenoid biosynthetic pathway of Streptococcus pneumoniae

Recent advances in nuclear cardiology in the study of coronary artery disease

Synthesis of 5"-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca super(2+)-mobilizing agent: The first antagonists modified at the N1- ribose moiety

Substitution at the 8-position of 3″-deoxy-cyclic ADP-carbocyclic-ribose, a highly potent Ca 2+-mobilizing agent, provides partial agonists 1

Synthesis of 5″-branched derivatives of cyclic ADP-carbocyclic-ribose, a potent Ca 2+-mobilizing agent: The first antagonists modified at the N1-ribose moiety

Assessment of regional and global left ventricular function by reinjection Tl-201 and rest Tc-99m sestamibi ECG-gated SPECT : Comparison with three-dimensional magnetic resonance imaging

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