Makita Naomasa | Department Of Gastroenterology National Hospital Organization Kyushu Medical Center

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著作論文

Analysis of HLA-DRB1 polymorphisms in Japanese patients with primary biliary cirrhosis (PBC) : The HLA-DRB1 polymorphism determines the relative risk of antinuclear antibodies for disease progression in PBC
State-Dependent Blocking Actions of Azimilide Dihydrochloride (NE-10064) on Human Cardiac Na^+ Channels
L-Cysteine Prevents Oxidation-Induced Block of the Cardiac Na^+ Channel Via Interaction With Heart-Specific Cysteinyl Residues in the P-Loop Region
Absence of a Trafficking Defect in R1232W/T1620M, a Double SCN5A Mutant Responsible for Brugada Syndrome
Liver X receptor in cooperation with SREBP-1c is a major lipid synthesis regulator in nonalcoholic fatty liver disease
Partial splenic embolization facilitates completion of interferon therapy in patients with chronic HCV infection and hypersplenism
Long-term fibrate treatment for PBC
Lemierre's Syndrome : Porphyromonas asaccharolytica as a Putative Pathogen
Body surface area is an independent factor contributing to the effects of lamivudine treatment
Primary hepatic lymphoma in a patient with Sjogren's syndrome
ANTI-MONOCYTE CHEMOATTRACTANT PROTEIN-1 GENE THERAPY PREVENTS DIMETHYLNITROSAMINE-INDUCED HEPATIC FIBROSIS IN RATS
PREVENTION OF HEPATIC FIBROSIS BY MODULATING RHO-ROCK SIGNALING PATHWAY
Serum levels of HCV RNA and core protein before and after incubation at 37℃ for 24h
1 Molecular Basis for Low Penetrance in the Long QT Syndrome(Meet the Expert 7 (ME7) (A) : Issues on Sudden Cardiac Death)(Special Program)
OE-133 Novel intrinsic mechanism of the enhanced rate-dependant QT Shortening in R1623Q mutant of the LQT3 syndrome(Arrhythmia, Basic 4 (A) : OE16)(Oral Presentation (English))
OJ-009 A Common KCNE1 Polymorphism, D85N, is a Genetic Modifier of Long QT Syndrome(Arrhythmia, diagnosis/ Pathophysiology/ EPS(03)(A),Oral Presentation(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
A single mutation of cardiac sodium channel gene confers phenotypes of both Brugada and long QT syndromes
Ion channel mutations and polymorphisms in Japanese patients with acquired long QT syndrome
Genetic analysis of expression profile involved in retinoid metabolism in non-alcoholic fatty liver disease
FRS-119 Familial Isolated Cardiac Conduction Defect Associated with a Mutation in the Connexin40 Gene GJA5(FRS24,Novel Mechanisms of Ventricular Arrhythmia (A),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulat
Human intrahepatic biliary epithelial cell as possible modulator of hepatic regeneration : Potential role of biliary epithelial cell for hepatic remodeling in vivo
An SCN5A Mutation Associated With Idiopathic Ventricular Fibrillation Alters The Na^+ Channel Pore Structure And Responses To Antiarrhythmic Drugs
Predictive role of anti-gp210 and anticentromere antibodies in long-term outcome of primary biliary cirrhosis
Expression profile of lipid metabolism-associated genes in hepatitis C virus-infected human liver
Dermatomyositis Associated with Invasive Thymoma
Establishment and structural analysis of human mAb to E2 component of the 2-oxoglutarate dehydrogenase complex generated from a patient with primary biliary cirrhosis
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)
5 Overlap Between LQT3 and Brugada Syndrome : Clinical Features in a Common Mutation and Underlying Biophysical Mechanisms(Plenary Session 4 (PL-4) (A) New Scientific Approaches to QT Prolongation,Special Program,The 72nd Annual Scientific Meeting of the
2-1). Antigen Peptide Analog : Induction of T cell Anergy in Primary Biliary Cirrhosis
NORADRENALINE-INDUCED ALTERATIONS IN ADENYLATE CYCLASE SYSTEM OF RAT HEART MEMBRANES : Cardiovascular Drugs : 53 Annual Scientific Meeting, Japanese Circulation Society
Genetic Polymorphisms and Arrhythmia Susceptibility(Genetics of Arrhythmias)
Molecular Basis for the Phenotypic Variability of Cardiac Sodium Channelopathies(Ion Channels and Cardiac Arrhythmias : Current Understanding and Future, The 69th Annual Scientific Meeting of the Japanese Circulation Society)
Association analysis of cytotoxic T-lymphocyte antigen 4 gene polymorphisms with primary biliary cirrhosis in Japanese patients
PE-307 Left Ventricular Noncompaction Associated With Mutations in Cardiac Na Channel Gene SCN5A(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OE-085 Genetic Factors Conferring Congenital Sick Sinus Syndrome in SCN5A Mutation Carriers(Arrhythmia, basic-1, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
ALTERATIONS OF PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE C AND PROTEIN KINASE C ACTIVITIES IN THE MYOCARDIUM OF SPONTANEOUSLY HYPERTENSIVE RATS (SHR) : Cardiomyopathy, Myocarditis : 53 Annual Scientific Meeting, Japanese Circulation Society
-P163- PARTIAL PURIFICATION AND CHARACTERIZATION OF PHOSPHATIDYLINOSITOL-SPECIFIC PHOSPHOLIPASE C IN RAT MYOCARDIUM
1 Genotype-Phenotypes Relations of SCN5A-Positive Brugada Syndrome(Brugada Syndrome:From Cell to Bedside,Plenary Session 2 (PL2) (A),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
Aborted Sudden Cardiac Death Associated with Short QT Syndrome
Enhanced sodium channel intermediate inactivation in Brugada syndrome
Molecular and Biophysical Bases of Brugada Syndrome
-0532-ALTERATIONS OF MEMBRANE PHOSPHOINOSITIDE METABOLISM IN THE HEART OF CARDIOMYOPATHIC SYRIAN HAMSTER BIO 14.6 (BIO)
Iron state in association with retinoid metabolism in non-alcoholic fatty liver disease
A polymorphism in the integrin αV subunit gene affects the progression of primary biliary cirrhosis in Japanese patients
Evaluation of risk factors for the development of cirrhosis in autoimmune hepatitis : Japanese NHO-AIH prospective study
Alpha-fetoprotein above normal levels as a risk factor for the development of hepatocellular carcinoma in patients infected with hepatitis C virus
Genetic polymorphisms in CTLA4 and SLC4A2 are differentially associated with the pathogenesis of primary biliary cirrhosis in Japanese patients

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