Evaluation of NLRP1 Gene Polymorphisms in Vogt-Koyanagi-Harada Disease
スポンサーリンク
概要
- 論文の詳細を見る
- Springerの論文
- 2011-01-01
著者
-
Morisaki Takayuki
国立循環器病センター 心臓血管内科
-
Morisaki T
Department Of Bioscience National Cardiovascular Center Research Institute
-
Saito Wataru
Department Of Ophthalmology And Visual Sciences Hokkaido University Graduate School Of Medicine
-
Ishida Susumu
Department Of Anesthesia And Intensive Care Nagoya Daini Red Cross Hospital
-
Ohno Shigeaki
Department Of Ocular Inflammation And Immunology Hokkaido University Graduate School Of Medicine
-
Ohno Shigeaki
Department Of Ophthalmology And Visual Sciences Hokkaido University Graduate School Of Medicine
-
Kitaichi Nobuyoshi
Department Of Ophthalmology And Visual Science Hokkaido University Graduate School Of Medicine
-
Saito Wataru
Department Of Ophthalmology Hokkaido University Graduate School Of Medicine
-
Ohno S
Department Of Ocular Inflammation And Immunology Hokkaido University Graduate School Of Medicine
-
Saito Wataru
Department Of Electrical And Electronic Engineering Tokyo Institute Of Technology
-
Miura Toshie
Department Of Craniofacial Growth And Development Dentistry Kanagawa Dental College
-
HORIE Yukihiro
Department of Ophthalmology, Hokkaido University Graduate School of Medicine
-
Kitaichi Nobuyoshi
Department Of Ophthalmology Health Sciences University Of Hokkaido
-
Horie Yukihiro
Department Of Ophthalmology Hokkaido University Graduate School Of Medicine
-
Kaibara Nobuaki
Department Of Ophthalmology Hokkaido University Graduate School Of Medicine
-
Miura Toshie
Department Of Ophthalmology Hokkaido University Graduate School Of Medicine
-
OHNO Shigeaki
Department of Ocular Inflammation and Immunology
関連論文
- Prevention of experimental autoimmune uveoretinitis by blockade of osteopontin with small interfering RNA
- 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
- PE-441 Essential Role of p300 in Post-natal Cardiac Mitochondrial Gene Expression and Maintenance of Normal Cardiac Function(Heart failure, basic-5, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- 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
- Involvement of IL-32 in activation-induced cell death in T cells
- 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 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
- 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
- Treatment of Vogt-Koyanagi-Harada's Disease During Pregnancy
- Identification of a novel insertion mutation in GATA3 with HDR syndrome
- Remote Reperfusion Lung Injury is Associated With AMP Deaminase 3 Activation and Attenuated by Inosine Monophosphate
- 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
- SEROTYPING OF CHLAMYDIA TRACHOMATIS FROM INCLUSION CONJUNCTIVITIS BY POLYMERASE CHAIN REACTION AND RESTRICTION FRAGMENT LENGTH POLYMORPHISM ANALYSIS
- Increase in macrophage migration inhibitory factor levels in lacrimal fluid of patients with severe atopic dermatitis
- Ciclosporin Microemulsion Preconcentrate Treatment of Patients With Behcet's Disease
- Episcleritis Associated with Pigmentary Retinal Degeneration in an HTLV-I Carrier
- 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
- Retinal Blood Flow in the Macular Area Before and After Scleral Buckling Procedures for Rhegmatogenous Retinal Detachment Without Macular Involvement
- Posterior Synechia of the Iris After Combined Pars Plana Vitrectomy, Phacoemulsification, and Intraocular Lens Implantation
- A New Method for Quantification of Metamorphopsia in Patients with Epiretinal Membrane
- Evaluation of FcεRI-binding serum IgE in patients with ocular allergic diseases
- Surgical correction of spinal deformity in patients with congenital muscular dystrophy
- Borrelia burgdorferi Sensu Lato in an Endemic Environment: Wild Sika Deer (Cervus nippon yesoensis) with Infected Ticks and Antibodies
- Role of matrix metalloproteinase-7 in angiogenesis associated with age-related macular degeneration
- 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
- 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
- High-risk for Bradyarrhythmic Complications in Patients with Brugada Syndrome Caused by SCN5A Gene Mutations(Arrhythmia, Basic (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 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
- Secondary Macular Hole Associated with Central Retinal Vein Occlusion Treated with Corticosteroid Injection
- OJ-021 Blockade of T-type Calcium Channel Reduced the Arrythmogenicity in the Dominant Negative NRSF Transgenic Mice(Heart failure, basic-2 (M) OJ4,Oral Presentation (Japanese),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Soc
- Pathophysiological Significance of T-type Ca^ Channels : Transcriptional Regulation of T-type Ca^ Channel : Regulation of CACNA1H by Neuron-Restrictive Silencer Factor
- Resistin Gene Polymorphism Positively Associated with the Metabolic Syndrome in Japanese Men(Gene Therapy/Genetic Engineering (IHD), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 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)
- 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)
- 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-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
- 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)
- Low prevalence of juvenile-onset Behçet's disease with uveitis in East/South Asian people
- Association of Major Histocompatibility Complex Class I Chain-Related Gene A and HLA-B Alleles with Behcet's Disease in Turkey
- A Novel Approach to Treat Complete Atrio-ventricular (AV) Block by Transplantation of Embryonic Stem Cell-derived cardiac cells(Arrhythmia, Basic (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Genetic Risk Factors for Deep Vein Thrombosis among Japanese : Importance of Protein S K196E Mutation
- Current concept of the pathogenesis of age-related macular degeneration : the role of oxidative stress and inflammation
- Evaluation of PTPN22 polymorphisms and Vogt-Koyanagi-Harada disease in Japanese patients
- Intravitreal anti-vascular endothelial growth factor therapy with bevacizumab for tuberous sclerosis with macular oedema
- Inhibition of nuclear factor-kappa B activation attenuates hydrogen peroxide-induced cytotoxicity in human lens epithelial cells
- Interleukin-6 (IL-6) in patients with Behcet's disease
- Seroepidemiological Studies on Silk Road Ethnic Groups
- Ultrasonic Study of the High Temperature Phase of Fe_3O_4
- Epidemiological Survey of Intraocular Inflammation in Japan
- Nano-Sized Carbon Black Exposure Exacerbates Atherosclerosis in LDL-Receptor Knockout Mice
- Transcriptional Regulation of the Pacemaker Channel HCN4 (Excitation-contraction Coupling/Ion Channel 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Expression of erythropoietin receptor in human Merkel cell carcinoma of the eyelid
- Expression of thymidine phosphorylase in choroidal malignant melanoma associated with neovascular glaucoma.
- Is It Possible to Detect the Presence of Adenovirus Antigen in Conjunctiva Before the Onset of Conjunctivitis?
- Pseudomonas Scleral Abscess Following Pars Plana Vitrectomy
- Secondary Macular Hole Formation with Presumed Evulsion of Foveal Hard Exudates in a Patient with Diabetic Retinopathy
- Elevation of Surfactant Protein D, a Pulmonary Disease Biomarker, in the Sera of Uveitis Patients with Sarcoidosis
- Cardiac output increases the rate of carbon monoxide elimination in hyperpneic but not normally ventilated dogs
- 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)
- Uveal Effusion Syndrome Caused by Choroidal Invasion of Malignant Lymphoma
- Indocyanine Green Angiography in a Case of Punctate Inner Choroidopathy Associated with Acute Zonal Occult Outer Retinopathy
- Chronic panuveitis and scleritis in a patient with cryptogenic organizing pneumonia.
- Two-year results for scoliosis secondary to Duchenne muscular dystrophy fused to lumbar 5 with segmental pedicle screw instrumentation
- Shortening of Detection Time for Observation of Hot Electron Spatial Distribution by Scanning Hot Electron Microscopy
- 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
- Calcium Channel Blocker Nilvadipine, but Not Diltiazem, Inhibits Ocular Inflammation in Endotoxin-Induced Uveitis
- Evaluation of NLRP1 Gene Polymorphisms in Vogt-Koyanagi-Harada Disease
- The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts
- Hunting for genes for hypertension : the Millennium Genome Project for Hypertension
- Trabecular meshwork depigmentation in Vogt-Koyanagi-Harada disease