OJ-029 Suppression of Anastomotic Intimal Hyperplasia in Rabbit Hypercholesterolemic Model using Chimeric Decoy Oligodeoxynucleotides against NF κ B and E2F(Restenosis, basic/clinical-1 (IHD) OJ5,Oral Presentation (Japanese),The 70th Anniversary Annual Sc
スポンサーリンク
概要
- 論文の詳細を見る
- 社団法人日本循環器学会の論文
- 2006-03-01
著者
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Miyata Toshiyuki
Research Institute National Cardiovascular Center
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Aoki Motokuni
Department Of Clinical Gene Therapy Osaka University Graduate School Of Medicine
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Aoki Motokuni
大阪大学 臨床遺伝子治療学
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Aoki Motokuni
Department Of Geriatric Medicine
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Aoki Motokuni
Department Of Geriatric Medicine Osaka University Medical School
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Morishita Ryuichi
Division Of Gene Therapy Science Osaka University Graduate School Of Medicine
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Morisaki Takayuki
国立循環器病センター 心臓血管内科
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Miyata Toshiyuki
Department Of Clinical Gene Therapy Osaka University Graduate School Of Medicine
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Miyake Takashi
Division of Gene Therapy Science, Osaka University Graduate School of Medicine
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Takano Makoto
Division Of Molecular Physiology And Biophysics Department Of Physiology Jichi Medical University
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Takano M
Division Of Biophysics Department Of Physiology Jichii Medical School
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Mannami Toshifumi
Department Of Preventive Cardiology National Cardiovascular Center
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Morishita Ryuichi
Division Of Clinical Gene Therapy
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Miyata Toshiyuki
Department Of Preventive Cardiology National Cardiovascular Center:hygiene And Public Health Social
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Miyake Takashi
Division Of Clinical Gene Therapy Osaka University Graduate School Of Medicine
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Morishita Ryuichi
Department Cf Clinical Gene Therapy Graduate School Of Medicine Osaka University
関連論文
- Identification of Genetic Markers Associated With High-Density Lipoprotein-Cholesterol by Genome-Wide Screening in a Japanese Population : The Suita Study
- FRS-007 Functional inhibition of p300 in the post-natal heart leads to mitochondrial dysfunction and cell death in mice(Novel Pathophysiological Mechanisms of Heart Failure(M),Featured Research Session,The 72nd Annual Scientific Meeting of the Japanese Ci
- OE-362 Genome-wide Search for Polymorphic Markers Associated with Lipid and Blood Pressure Levels in Japanese(OE61,Lipid Disorders (H),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- PJ-104 Delayed Onset of Beating and Decreased Expression of T-type Ca^ Channel in Mouse ES Cell-Derived Cardiocytes Carrying Human Chromosome 21(Excitation-contraction coupling/Ion channel, The 71st Annual Scientific Meeting of the Japanese Circulatio
- FRS-091 Impairment of Ubiquitin-Proteasome System Caused by a Missense MYBPC3 Mutation and Associated with Cardiac Dysfunction in Hypertrophic Cardiomyopathy(FRS19,Genetic Abnormalities in Cardiac Hypertrophy and Cardiomyopathy (M),Featured Research Sessi
- Association of Genetic Polymorphisms of Endothelin-Converting Enzyme-1 Gene with Hypertension in a Japanese Population and Rare Missense Mutation in Preproendothelin-1 in Japanese Hypertensives
- Association of Genetic Polymorphisms of Sodium-Calcium Exchanger 1 Gene, NCX1, with Hypertension in a Japanese General Population
- Identification of 108 SNPs in TSC, WNK1, and WNK4 and their association with hypertension in a Japanese general population
- Association of PLA2G7 polymorphisms with carotid atherosclerosis in hypertensive Japanese
- Genetic Variations of CYP2C9 in 724 Japanese Individuals and Their Impact on the Antihypertensive Effects of Losartan
- Leptin Gene and Leptin Receptor Gene Polymorphisms Are Associated with Sweet Preference and Obesity
- Associations of Hypertension and Its Complications with Variations in the Xanthine Dehydrogenase Gene
- Single Nucleotide Polymorphisms in the Interleukin-6 Gene Associated with Blood Pressure and Atherosclerosis in a Japanese General Population
- An association analysis between ApoA1 polymorphisms and the high-density lipoprotein (HDL) cholesterol level and myocardial infarction (MI) in Japanese
- 1 Role of the Ubiquitin Proteasome System in the Development of Heart Failure in Hypertrophic Cardiomyopathy(Young Investigator's Award for International Students Finalists Lecture (YIA International),Special Program,The 72nd Annual Scientific Meeting of
- PJ-180 Subtype Swithing of T-type Ca^ Channels from Cav3.2 to Cav3.1 during Differentiation of Embryonic Stem Cells to Cardiac Cell Lineage(Excitation-contraction coupling/Ion channel-2 (A) PJ30,Poster Session (Japanese),The 70th Anniversary Annual Sc
- Subtype Switching of T-Type Ca^ Channels From Cav3.2 to Cav3.1 During Differentiation of Embryonic Stem Cells to Cardiac Cell Lineage
- Identification of a novel insertion mutation in GATA3 with HDR syndrome
- Recovery of Learning and Memory by Gene Therapy Using Hepatocyte Growth Factor Gene After Focal Cerebral Ishcemia in Rats(Gene Therapy/Genetic Engineering (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Inhibitory Effect of Chimera Decoy Oligodeoxynucleotides (ODN) against Ets and NFκ B on the Progression of Rabbit Experimental Aortic Aneurysms (AAA)
- Gene Therapy for Abdominal Aortic Aneurysm (AAA) using Decoy Strategy against ets binding site
- Effect of E2F decoy on inhibitation of neointima formation in pig coronary arteries after balloon injury and stent implantation
- Transcription factor, ets-1, is a novel angiogenic molecule : Implication to ciene therapy to treat peripheral arterial disease
- Novel molecular intervention to treat abdominal aortic aneurysms (AAA) using chimera decoy oligodeoxynucleotides (ODN) against ets and NFkB binding sites
- Remote Reperfusion Lung Injury is Associated With AMP Deaminase 3 Activation and Attenuated by Inosine Monophosphate
- Increase in DNA Synthesis of Cardiac Myocytes by Transfection ofP53 and Rb Antisense : Possibility of Cardiac Myocytes Regeneration
- OE-193 Exaggeration of Remote Reperfusion Pulmonary Injury in AMP Deaminase 3 Knockout Mice(Metabolism/Biochemistry/Energetics-1 (H) OE33,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Genetic Polymorphisms of L-Type Calcium Channel α1c and α1D Subunit Genes are Associated With Sensitivity to the Antihypertensive Effects of L-Type Dihydropyridine Calcium-Channel Blockers
- PE-298 Feasibility of Undifferentiated ES Cell Engraftment to Diseased Hearts is Limited by Tumorigenesis and Apoptosis through Leukemia Inhibitory Factor (LIF)(Regeneration (angionenesis/myocardial regeneration)-5 (M) PE50,Poster Session (English),The 70
- PJ-086 Regression of Experimental Rabbit Aortic Aneurysm by The Treatment with Chimera Decoy Oligodeoxynucleotides (ODN) against ets and NFkB(Gene Therapy 1 (IHD) : PJ15)(Poster Session (Japanese))
- Characterization of Subclinical Thyroid Dysfunction From Cardiovascular and Metabolic Viewpoints : The Suita Study
- Association of Sixty-One Non-Synonymous Polymorphisms in Forty-One Hypertension Candidate Genes with Blood Pressure Variation and Hypertension
- IS033 UP-REGULATION OF KEY TRANSCRIPTIONAL FACTOR FOR ANGIOGENESIS, ETS, AND INDUCTION OF ANGIOGENESIS BY IN VIVO GENE TRANSFER OF HUMAN HEPATOCYTE GROWTH FACTOR (HGF) INTO MYOCARDIUM
- Contribution of a Vascular Modulator, Hepatocyte Growth factor (HGF), to the Pathogenesis of Cardiovascular Disease
- IS053 ANTI-APOPTOTIC ACTION OF HEPATOCYTE GROWTH FACTOR ON HUMAN AORTIC ENDOTHELIAL CELLS
- Potential Role of a Novel Vascular Modulator, Hepatocyte Growth Factor (HGF), in Cardiovascular Disease: Characterization and Regulation of Local HGF System
- Polymorphisms in Vitamin K-Dependent γ-Carboxylation-Related Genes Influence Interindividual Variability in Plasma Protein C and Protein S Activities in the General Population
- Genetic Variations of HSD11B2 in Hypertensive Patients and in the General Population, Six Rare Missense/Frameshift Mutations
- OJ-041 A Common Genetic Variation in the ABCA1 Gene is Associated with Left Ventricular Diastolic Dysfunction in Men with Essential Hypertension(Atherosclerosis, clinical-3 (H) OJ7,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meetin
- OE-045 Gene Polymorphisms of Circadian Rhythm Related Genes may be Contributed to Insulin Resistance in Patients with Hypertension(Hypertension, clinical-1 (H) OE8,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese
- OE-044 Polymorphisms of the Genes in Angiotensin II Signal Transduction May Influence the Antihypertensive Effect of Angiotensin II Receptor Blockers(Hypertension, clinical-1 (H) OE8,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeti
- A Novel Missense Mutation, F826Y, in the Mineralocorticoid Receptor Gene in Japanese Hypertensives : Its Implications for Clinical Phenotypes
- Contribution of Single Nucleotide Polymorphisms in Protein-Tyrosin Kinase 2 to the Progression of Atherosclerosis in Patients with Essential Hypertension(Hypertension, Clinical 5 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Association of Plasma Platelet Activating Factor-acetylhydrolase (PAF-AH) Gene Polymorphism with Carotid Atherosclerosis in Essential Hypertension(The Frontier of Atherosclerosis Research (IHD), The 69th Annual Scientific Meeting of the Japanese Circulati
- The Thiazide-Sensitive Na^+-Cl^- Cotransporter Gene, C1784T, and Adrenergic Receptor-β3 Gene, T727C, May Be Gene Polymorphisms Susceptible to the Antihypertensive Effect of Thiazide Diuretics
- Six Missense Mutations of the Epithelial Sodium Channel β and γ Subunits in Japanese Hypertensives
- PE-452 Catalogue of Matrix Metalloproteinase Gene Polymorphisms and Susceptibility to Cardiovascular Hypertrophy in Japanese Hypertensive Patients(Hypertension, Clinical 6 (H) : PE77)(Poster Session (English))
- PE-293 Single polymorphism of Lipocalin-type prostaglandin D synthase gene is associated with HDL-cholesterol levels and carotid plaques in hypertensive patients(Heart Failure, Clinical 11 (M) : PE50)(Poster Session (English))
- PE-204 Single Nucleotide Polymorphisms for Determining the Renal Blood Flow in the Patients with Essential Hypertension(Kidney/Renal Circulation 1 (H) : PE35)(Poster Session (English))
- PJ-477 A Therapeutic Strategy to Treat Brain Ischemia : Over-expression of Hepatocyte Growth Factor Gene Reduced Ischemic Injury in Rat Model(Cerebrovascular Circulation/Stroke 1 (H) : PJ80)(Poster Session (Japanese))
- OE-217 Genetic Variation of Thrombomodulin Gene in Japanese Deep Vein Thrombosis Patients and in the General Population(Thromboembolism/Antithrombotic therapy/Thrombolysis-1 (H) OE37,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeti
- PE-114 Angiotensin II Blocker, Valsartan, Supresses the Development of Experimental Abdominal Aortic Aneurysm in Rats(Peripheral circulation/Vascular disease(03)(H),Poster Session(English),The 72nd Annual Scientific Meeting of the Japanese Circulation Soc
- PJ-691 Inhibition of Development of Experimental Aortic Abdominal Aneurysm in Rat Model by Atorvastatin through Inhibition of Macrophage Migration(Peripheral circulation/Vascular disease-6, The 71st Annual Scientific Meeting of the Japanese Circulation So
- PE-543 Inhibiton of Experimental Aortic Abdominal Aneurysm by Angiotensin Receptor Blocker, Valsartan(Peripheral circulation/Vascular disease-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- Two Years Follow-up of Clinical Trial of Human Gene Therapy for Peripheral Arterial Disease Using Hepatocyte Growth Factor Gene Transfer(Peripheral Circulation/Vascular Disease (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Clinical Trial of Human Gene Therapy Using Hepatocyte Growth Factor Gene Transfer(Translational Research in Cardiovascular Disease, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- FRS-013 Long Term Evaluation of Clinical Trial of Human Gene Therapy for Peripheral Arterial Disease Using Hepatocyte Growth Factor Gene Transfer(Angiogenesis and Regeneration Medicine in Cardiovascular Medicine (M) : FRS3)(Featured Research Session (Engl
- Increase in Peripheral Blood Flow by Intravenous Administration of Prostaglandin E1 in Patients with Peripheral Arterial Disease, Accompanied by Up-Regulation of Hepatocyte Growth Factor
- Inhibition of Restenosis by Beraprost Sodium (a Prostaglandin 12 Analogue) in the Porcine Coronary Artery after Angioplasty
- Results of Safety from Human Clinical Gene Therapy Using HGF (TREAT-HGF)
- Long Term Evaluation of Results from the First Stage in the Clinical Trial of Gene Therapy for Peripheral Arterial Disease
- Clinical Results of TREAT-HGF (Japan Trial to Treat Peripheral Arterial Disease by Therapeutic Angiogenesis Using Hepatocyte Growth Factor Gene Transfer)
- Evaluation of utility of prostagrandin E1 in the patients with ASO : Protective effect on endothelial function through up-regulation of HGF
- No increase in human HGF concentration in the patients transfected with human HGF plasmid : preliminary clinical results from TREAT-HGF
- Preliminary clinical results from TREAT-HGF (Japan Trial to Treat Peripheral Arterial Disease by Therapeutic Angiogenesis Using HGF Gene Transfer)
- Preliminary clinical results from TREAT-HGF : Gene therapy for PAD
- 4 Pharmacogenomic Approaches Targeted on the Tailor-made Medicine for Hypertension(Plenary Session 7 (PL-7) (M) Genomic Approaches to Cardiovascular Diseases : Present and Future,Special Program,The 72nd Annual Scientific Meeting of the Japanese Circulati
- Hypertension Susceptibility Genes on Chromosome 2p24-p25 in a General Japanese Population(Hypertension, Clinical 6 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-213 Prevention of Abdominal Aortic Aneurysm using Ribbon-type Chimeric Decoy Oligodeoxynucleotides against NF κ B and Ets in a Rat Model(Genetics/Genetically engineered models/Gene therapy-2(H/M), The 71st Annual Scientific Meeting of the Japanese Circ
- OJ-028 Role of NF κ B and Ets in Development of Abdominal Aortic Aneurysm in Human(Peripheral circulation/Vascular disease-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- 5 Clinical Trial of Human Gene Therapy for Peripheral Arterial Disease Using Hepatocyte Growth Factor Gene Transfer(Clinical Trials of Regeneration Therapy in Japan, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-391 Hypertension Accelerated Experimental Abdominal Aortic Aneurysm through Up-regulation of Transcription Factors, NFkB and Ets(Peripheral circulation-2 (H) OJ66,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japane
- OJ-338 Long Term Results and Sub-analysis from Clinical Trial of Human Gene Therapy for Peripheral Arterial Disease (PAD)(Genetics/Genetically engineered models/Gene therapy-1 (M) OJ57,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Me
- OJ-337 Regression of Abdominal Aortic Aneurysms by Chimeric Decoy Oligonucleotides against NF κ B and Ets Binding Sites in Rabbit Model(Genetics/Genetically engineered models/Gene therapy-1 (M) OJ57,Oral Presentation (Japanese),The 70th Anniversary Annual
- OJ-029 Suppression of Anastomotic Intimal Hyperplasia in Rabbit Hypercholesterolemic Model using Chimeric Decoy Oligodeoxynucleotides against NF κ B and E2F(Restenosis, basic/clinical-1 (IHD) OJ5,Oral Presentation (Japanese),The 70th Anniversary Annual Sc
- Improvement of Myocardial Dysfunction by Therapeutic Angiogenesis Induced by Transfection of HGF Gene in Porcine Chronic Myocardial Ischemia Model(Gene Therapy 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Regression of Experimental Rabbit Aortic Aneurysm by the Treatment with Chimeric Decoy Oligodeoxynucleotides (ODN) against Ets and NFkB(Gene Therapy 1 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Inhibitory Effect of NFκB Decoy Oligodeoxynucleotides (ODN) on the Neointimal Hyperplasia in Rabbit Vein Graft Model(Cardiovascular Surgery/CABG 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Hereditary Protein S Deficiency With a History of Recurrent Myocardial Infarction : A Case Report
- Kynureninase Is a Novel Candidate Gene for Hypertension in Spontaneously Hypertensive Rats
- Genetic Risk Factors for Deep Vein Thrombosis among Japanese : Importance of Protein S K196E Mutation
- Nano-Sized Carbon Black Exposure Exacerbates Atherosclerosis in LDL-Receptor Knockout Mice
- PE-129 Exposure to Nano-Sized Carbon Black Accelerates Atherosclerosis in a Low Density Lipoprotein Receptor Knockout Mouse(Atherosclerosis, basic-7, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-224 Genetic Contribution to Left Ventricular Diastolic Dysfunction in Essential Hypertension : Combined Effects of AT1, ETA, and MT1-MMP Gene Polymorphisms(Hypertension, clinical-9 (H) PJ38,Poster Session (Japanese),The 70th Anniversary Annual Scientif
- 5 Susceptible single nucleotide polymorphisms to the hypertensive complications and effectiveness of antihypertensive drugs(Perspectives of Genome-wide Study to Identify Genes Underlying Cardiovascular Diseases,Roundtable Discussion 10 (RT10) (M),The 70th
- Novel Genetic Polymorphisms of Orphan G-protein-coupled Receptors GPR91 and GPR99 Associated with Anti-atherosclerosis(Preventive Medicine/Epidemiology/Education/Health Policy 1 (H), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Evaluation of the Lys198Asn and - 134delA Genetic Polymorphisms of the Endothelin-1 Gene
- FRS-160 Single Nucleotide Polymorphisms Relating to Low-Renin Essential Hypertension(Hypertension (H) : FRS19)(Featured Research Session (English))
- Polymorphism of Na+/Ca2+ Exchanger Gene and AntihypertensiveResponse to Calcium Channel Blockers in Patients with Essential Hypertension
- Susceptible Gene Polymorphisms to the Antihypertensive Effect of Angiotensin Converting Enzyme Inhibitors
- Association between Polymorphisms of Kallikrein Gene and Resistant to Anti-Hypertensive Therapy
- Susceptible Gene Polymorphisms to the Antihypertensive Effect of Thiazide Diuretics
- Pathophysiological Remodeling of Mouse Cardiac Myocytes Expressing Dominant Negative Mutant of Neuron Restrictive Silencing Factor
- Association of carotid atherosclerosis with genetic polymorphisms of the klotho gene in patients with hypertension
- Impact of RGS2 deficiency on the therapeutic effect of telmisartan in angiotensin II-induced aortic aneurysm
- Usefulness of antithrombin deficiency phenotypes for risk assessment of venous thromboembolism : type I deficiency as a strong risk factor for venous thromboembolism
- FRS-090 Association of Apolipoprotein A5 Genetic Polymorphism with Serum Triglyceride Levels in a Japanese General Population : The Suita Study(Preventive Medicine in Cardiovascular Disease (H) : FRS11)(Featured Research Session (English))
- 3 Susceptible single nucleotide polymorphisms to the hypertensive complications : Possible application to the tailor-made medicine for hypertension(Symposium 2 (SY2) (H) : Hypertension : From Molecular Mechanisms to Tailored Therapy)(Special Program)
- Hunting for genes for hypertension : the Millennium Genome Project for Hypertension
- Association of intima-media thickening of carotid artery with genetic polymorphisms of the regulator of G-protein signaling 2 gene in patients with hypertension and in the general population