Role of osteoclasts and interleukin-17 in the pathogenesis of rheumatoid arthritis : crucial 'human osteoclastology'
スポンサーリンク
概要
- 論文の詳細を見る
- 2012-03-30
著者
-
Kawamoto Manabu
Institute Of Rheumatology Tokyo Women's Medical University
-
Nanke Yuki
Institute Of Rheumatology Tokyo Women's Medical University
-
Kotake Shigeru
Institute Of Rheumatology Tokyo Women's Medical University
-
Yago Toru
Institute Of Rheumatology Aoyama Hospital Tokyo Women's Medical University
-
Yago Toru
Institute of Rheumatology, Tokyo Women's Medical University
関連論文
- A Case of Mikuliczs Disease, IgG4-related Plasmacytic Syndrome, Successfully Treated by Corticosteroid and Mizoribine, Followed by Mizoribine Alone
- Genetic Variations and Haplotypes of ABCC2 Encoding MRP2 in a Japanese Population
- Genetic variations and haplotype structures of the DPYD gene encoding dihydropyrimidine dehydrogenase in Japanese and their ethnic differences
- Genetic Variations of the ABC Transporter Gene ABCB11 Encoding the Human Bile Salt Export Pump (BSEP) in a Japanese Population
- Familial Mediterranean fever in three Japanese patients, and a comparison of the frequency of MEFV gene mutations in Japanese and Mediterranean populations
- 日本人におけるGSTT1及びGSTM1の遺伝子多型の同定及びハプロタイプ構造の解析
- Twenty Novel Genetic Variations and Haplotype Structures of the DCK Gene Encoding Human Deoxycytidine Kinase (dCK)
- Genetic Variations of VDR/NR1I1 Encoding Vitamin D Receptor in a Japanese Population
- Genetic Variations and Frequencies of Major Haplotypes in SLCO1B1 Encoding the Transporter OATP1B1 in Japanese Subjects : SLCO1B1^*17 is More Prevalent Than ^*15
- Genetic Variations and Haplotype Structures of the ABC Transporter Gene ABCC1 in a Japanese Population
- 日本人における Denaturing HPLC を用いた Thiopurine S-Methyltransferase 遺伝子の新規SNPスクリーニング
- 日本人におけるヒトSLC29A1の新規遺伝子多型の同定
- Genetic Variation and Haplotype Structure of the ABC Transporter Gene ABCG2 in a Japanese Population
- Genetic Variations and Haplotypes of UGT1A4 in a Japanese Population
- Genetic Polymorphisms of UGT1A6 in a Japanese Population
- Genetic Variations of the AHR Gene Encoding Aryl Hydrocarbon Receptor in a Japanese Population
- A case of Chlamydia-associated arthritis
- Combining effects of polymorphism of tumor necrosis factor α5'-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis
- Decreased percentages of regulatory T cells in peripheral blood of patients with Behcet's disease before ocular attack : a possible predictive marker of ocular attack
- The effect of geranylgeranylacetone on human osteoclastogenesis and synovitis in patients with rheumatoid arthritis
- Roles of osteoblasts, osteoclasts, T cells and cytokines in glucocorticoid-induced osteoporosis
- Raised plasma adrenomedullin level in Behcet's disease patients
- A new syndrome : multiple dislocations of distal interphalangeal joints associated with interstitial pneumonia, Sjogren's syndrome, and positive autoantibodies
- The study of bone mineral density and bone turnover markers in postmenopausal women with active rheumatoid arthritis
- Usefulness of three-dimensional echocardiography in assessing right ventricular function in patients with primary pulmonary hypertension
- Inhibition of Cardiac Remodeling by Pravastatin Is Associated with Amelioration of Endoplasmic Reticulum Stress
- Plasma Adiponectin Is Associated with Plasma Brain Natriuretic Peptide and Cardiac Function in Healthy Subjects
- Sequence-based Analysis of the CYP2D6^*36-CYP2D6^*10 Tandem-type Arrangement, a Major CYP2D6^*10 Haplotype in the Japanese Population
- Stereoselective Effect of Amiodarone on the Pharmacokinetics of Racemic Carvedilol
- Novel Nonsynonymous Single Nucleotide Polymorphisms in the CYP2D6 Gene
- Seven Novel Single Nucleotide Polymorphisms in the Human SLC22A1 Gene Encoding Organic Cation Transporter 1 (OCT1)
- Fourteen Novel Single Nucleotide Polymorphisms in the SLC22A2 Gene Encoding Human Organic Cation Transporter (OCT2)
- Atorvastatin Slows the Progression of Cardiac Remodeling in Mice with Pressure Overload and Inhibits Epidermal Growth Factor Receptor Activation
- Impact of Adenosine Receptor Signaling and Metabolism on Pathophysiology in Patients with Chronic Heart Failure
- INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
- Variations in the FTO gene are associated with severe obesity in the Japanese
- Abnormal Glucose Tolerance Contributes to the Progression of Chronic Heart Failure in Patients with Dilated Cardiomyopathy
- Genetic Variations of CYP2C9 in 724 Japanese Individuals and Their Impact on the Antihypertensive Effects of Losartan
- PE-166 Superoxide-Dependent Activation of Cathepsin System is Associated with Hypertensive Myocardial Remodeling and Represents a Target for AT1R Blocker Therapy(Cardiovascular pharmacology, basic/clinical(03)(H),Poster Session(English),The 72nd Annual Sc
- PE-343 A Elastolytic Cathepsin Induction/Activation System Exists in the Rat and Human Myocardium and is Upregulated in Hypertensive Heart Failure(Heart failure, clinical-09, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-677 Comparison of Bypass Surgery with Drug-Eluting Stents for Diabetic Patients with Left Main Coronary Artery (LMCA) Stenosis(PJ114,Coronary Revascularization, PCI (DES) 4 (IHD),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japan
- PJ-179 Mechanisms Underlying the Impairment of Ischemia-induced Neovascularization in Aging Mice : the Pivotal Role for Matirx-Metalloproteinase-2(Regeneration(angiogenesis/myocardial regeneration)(04)(M),Poster Session(Japanese),The 72nd Annual Scientifi
- PJ-039 Treatment of ApoE-Deficient Mice with Statin Inhibits the Oxidative Stress-dependent Lysosomal Protease Cathepsin Activation System : Implication for Plaque Stability(Atherosclerosis, basic(05)(IHD),Poster Session(Japanese),The 72nd Annual Scientif
- 2 Mechanisms underlying the impairment of ischemia-induced neovascularization in MMP-2-deficient mice(The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- 2 Current Status of the Prevalence and Trend of Risk Factors for Cardiovascular Diseases in Nishiarita-Cho Cohort Study(Long-Term Prediction and Prevention of Cardiac Diseases and the Risk Factors,Symposium 10 (SY10) (H),The 70th Anniversary Annual Scient
- Dynamic Change in ST-Segment and Spontaneous Occurrence of Ventricular Fibrillation in Brugada Syndrome With a Novel Nonsense Mutation in the SCN5A Gene During Long-Term Follow-up
- Gene Expression Property of High-Density Three-Dimensional Tissue of HepG2 Cells Formed in Radial-Flow Bioreactor(BIOINFORMATICS)
- Three-Dimensional High-Density Culture of HepG2 Cells in a 5-ml Radial-Flow Bioreactor for Construction of Artificial Liver(Biochemical Engineering)
- OE-234 Plasma level of BMP but not systolic BP becomes a predictive marker of left ventricular hypertrophy in community screening(Preventive Medicine/Epidemiology/Education 2 (H) : OE29)(Oral Presentation (English))
- 日本人で新たに見いだされた低活性型CYP2D6ハプロタイプ
- Angiotensin II Type 1 Receptor Blocker Prevents Atrial Structural Remodeling in Rats with Hypertension Induced by Chronic Nitric Oxide Inhibition
- 日本人におけるABCC3遺伝子の多型解析
- The role of a common TNNT2 polymorphism in cardiac hypertrophy
- A Japanese case of Behcet's disease complicated by recurrent optic neuropathy involving both eyes : a third case in the English literature
- Geranglgeranylacetone, a non-toxic inducer of heat shock protein, induces cell death in fibroblast-like synoviocytes from patients with rheumatoid arthritis
- Bone erosion of the sternocostal joint in a patient with Behcet's disease
- Risk factors associated with incident fractures in Japanese men with rheumatoid arthritis : a prospective observational cohort study
- A huge congenital arachnoid cyst in a rheumatoid arthritis patient
- Practical Approach for Detecting Cardiac Sarcoidosis in Patients with AV Block(Arrhythmia, Diagnosis/Pathophysiology/EPS 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Electrophysiological Study as Prognostic Factor for Recurrence after Catheter Ablation for Post-operative Right Atrial Flutter(Arrhythmia, Diagnosis/Pathophysiology/EPS 4 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Long-Term Follow-up of Electrocardiographic Features in Patients with Brugada Syndrome : Comparison between SCN5A Mutation Carriers and Non-Mutation carriers(ECG/Body Surface Potential Mapping/Holter 2 (A), The 69th Annual Scientific Meeting of the Japane
- Clinical Significance of Body Surface Area of ST-segment Elevation in Patients with Brugada Syndrome(ECG/Body Surface Potential Mapping/Holter 2 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- A1330V polymorphism of low-density lipoprotein receptor-related protein 5 gene and self-reported incident fractures in Japanese female patients with rheumatoid arthritis
- Therapeutic efficacy of intravenous cyclophosphamide concomitant with moderate- to high-dose prednisolone in two patients with fasciitis panniculitis syndrome
- PJ-706 MMP-2 Deficiency Attenuates Ischemia-induced Angiogenesis and Vasculogenesis in MMP-2-Deficient Mice(Regeneration (angionenesis/myocardial regeneration)-7 (M) PJ119,Poster Session (Japanese),The 70th Anniversary Annual Scientific Meeting of the Jap
- 6 Current Status of the Prevalence of Smoking in Nishiarita-Cho Cohort Study and Its Conjunction with Cardiovascular and Cerebrovascular Diseases(Tobacco Free Symposium: The Present Condition of Tobacco Control in Japan, the Risk of Smoking to Cardio-and
- Lesson from the Constitution of Infrastructure of a Large-scale Clinical Trail and a Epidemiological Cohort Study(How to Make Japanese Original Evidence in Cardiology, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- Stromal cell activity in bone marrow from the tibia and iliac crest of patients with rheumatoid arthritis
- Cilostazol Reduces Target Lesion Revascularization After Percutaneous Transluminal Angioplasty in the Femoropopliteal Artery
- Cilostazol Reduces Target Lesion Revascularization (TLR) after Percutaneous Transluminal Angioplasty (PTA) in the Iliac and Femoro-Popliteal Region(Restenosis after Angioplasty, Basic/Clinical 2 (IHD), The 69th Annual Scientific Meeting of the Japanese Ci
- 2 Future Challenge in Brugada syndrome : Gender and Ethnic Differences(Brugada Syndrome:From Cell to Bedside,Plenary Session 2 (PL2) (A),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
- Testosterone Associated with Low Body Mass Index Contribute to Male Predominance in Brugada Syndrome(Arrhythmia, Diagnosis/Pathophysiology/EPS 9 (A), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
- 2 Systematic Linkage between the Genomic and Clinical Database of Cardiovascular Disease to Find New Pathophysiology or Effective Treatment(Symposium 5 (SY5) (IHD) : Genome Informatics of Cardiovascular System)(Special Program)
- 5 A new strategy for fishing individual risk factors of life-style related disease in lifestyle, biochemical data and genomics in Nishiarita(Plenary Session 7 (PL7) (H) : Health Promotion Act and Cardiovascular Disease Prevention)(Special Program)
- Genetic Polymorphisms of Copper- and Platinum Drug-efflux Transporters ATP7A and ATP7B in Japanese Cancer Patients
- Ethnic Differences of two Non-synonymous Single Nucleotide Polymorphisms in CDA Gene
- OJ-298 MEKK1 is Required in Vascular Remodeling after Injury in Carotid Ligation Model(Restenosis after Angioplasty, Basic/Clinical 2 (IHD) : OJ36)(Oral Presentation (Japanese))
- Radiographic repair in three Japanese patients with rheumatoid arthritis treated with bucillamine
- Associations between methotrexate treatment and methylenetetrahydrofolate reductase gene polymorphisms with incident fractures in Japanese female rheumatoid arthritis patients
- Atrioventricular Block-Induced Torsades de Pointes With Clinical and Molecular Backgrounds Similar to Congenital Long QT Syndrome
- Genetic Polymorphisms of FCGRT Encoding FcRn in a Japanese Population and Their Functional Analysis
- Efficacy of methotrexate in the treatment of a HLA-B27-positive Japanease patient with reactive arthritis
- Interferon-induced helicase (IFIH1) polymorphism with systemic lupus erythematosus and dermatomyositis/polymyositis
- Single nucleotide polymorphisms of CD244 gene predispose to renal and neuropsychiatric manifestations with systemic lupus erythematosus
- Impact of reduced left atrial functions on diagnosis of paroxysmal atrial fibrillation : Results from analysis of time-left atrial volume curve determined by two-dimensional speckle tracking
- Different Characteristics of Peripartum Cardiomyopathy Between Patients Complicated With and Without Hypertensive Disorders : Results From the Japanese Nationwide Survey of Peripartum Cardiomyopathy
- Interleukin-18 promoter polymorphisms in Japanese patients with rheumatoid arthritis : protective effect of the T allele and T/T genotype at rs360722
- A case of Weber-Christian disease with later development of rheumatoid arthritis
- The effects of disease modifying anti-rheumatic drugs on osteoclastogenesis and bone destruction in rheumatoid arthritis
- Is there evidence in support of the use of intra-articular hyaluronate in treating rheumatoid arthritis of the knee? A meta-analysis of the published literature
- Seasonal and Circadian Distributions of Cardiac Events in Genotyped Patients With Congenital Long QT Syndrome
- Carvedilol, a Non-Selective β-with α_1-Blocker is Effective in Long QT Syndrome Type 2
- Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population
- Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population
- "Possible Primary Antiphospholipid Syndrome" with Concurrent Diffuse Alveolar Hemorrhaging and Libman-Sacks Endocarditis Mimicking Catastrophic Antiphospholipid Syndrome
- Serum Blood Urea Nitrogen and Plasma Brain Natriuretic Peptide and Low Diastolic Blood Pressure Predict Cardiovascular Morbidity and Mortality Following Discharge in Acute Decompensated Heart Failure Patients
- Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility in Japanese rheumatoid arthritis patients
- Role of osteoclasts and interleukin-17 in the pathogenesis of rheumatoid arthritis : crucial 'human osteoclastology'