Human intrahepatic biliary epithelial cell as possible modulator of hepatic regeneration : Potential role of biliary epithelial cell for hepatic remodeling in vivo

スポンサーリンク

概要

• 論文の詳細を見る
• 2007-10-01

著者

• Yatsuhashi Hiroshi

  Clinical Research Center, National Nagasaki Medical Center

• Yatsuhashi Hiroshi

  長崎大学 医歯薬学総合研究科内科学第一

• Yatsuhashi Hiroshi

  国立病院機構長崎医療センター 呼吸器科

• Yatsuhashi Hiroshi

  Clinical Research Center National Nagasaki Medical Center

• Yatsuhashi Hiroshi

  National Hospital Organization (nho) Nagasaki Medical Center

• Ida H

  First Department Of Internal Medicine Nagasaki University Hospital Of Medicine And Dentistry Graduat

• Ida Hiroaki

  The First Department Of Internal Medicine Nagasaki University School Of Medicine

• NAKAMURA Minoru

  Clinical Research Center, National Hospital Organization (NHO) Nagasaki Medical Center

• KOMORI Atsumasa

  Clinical Research Center, National Hospital Organization (NHO) Nagasaki Medical Center

• MIGITA Kiyoshi

  Clinical Research Center, National Hospital Organization (NHO) Nagasaki Medical Center

• ISHIBASHI Hiromi

  Clinical Research Center, National Hospital Organization (NHO) Nagasaki Medical Center

• Nakamuta Makoto

  九州大学 医学系学府病態制御内科学

• Nakamuta M

  The Department Of Medicine And Bioregulatory Science Graduate School Of Medical Sciences Kyushu Univ

• Nakamuta Makoto

  九州大学 医学研究院病態制御内科学分野

• Makita Naomasa

  Department Of Gastroenterology National Hospital Organization Kyushu Medical Center

• Migita Kiyoshi

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

• Migita Kiyoshi

  国立病院機構長崎医療センター

• Nakashima M

  鳥取大学 医学系研究科遺伝子医療学

• Fujioka Hikaru

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

• Fujiwara Shinsuke

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

• YANO Koji

  Clinical Research Center, National Hospital Organization (NHO) Nagasaki Medical Center

• YANO Koji

  National Hospital Organization (NHO) Nagasaki Medical Center

• ISHIBASHI Hiromi

  National Hospital Organization (NHO) Nagasaki Medical Center

• Ishibashi Hiromi

  Clinical Research Center And Department Of General Internal Medicine Nho Nagasaki Medical Center

• Ishibashi Hiromi

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

• Nakamuta Makoto

  Department Of Gastroenterology National Hospital Organization Kyushu Medical Center

• Komori Atsumasa

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

• Yatsuhashi Hiroshi

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

• Yano Koji

  Clinical Research Center National Nagasaki Medical Center

• Nakamura Minoru

  Clinical Research Center National Hospital Organization (nho) Nagasaki Medical Center

関連論文

• Semi-quantitative discrimination of HBV mutants using allele-specific oligonucleotide hybridization with Handy Bio-Strand(METHODS)
• Semi-quantitative discrimination of HBV mutants using allele-specific oligonucleotide hybridization with Handy Bio-Strand
• 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
• Hepatitis B Related Polyarteritis Nodosa Presenting Necrotizing Vasculitis in the Hepatobiliary System Successfully Treated with Lamivudine, Plasmapheresis and Glucocorticoid
• Case-control study for the identification of virological factors associated with fulminant hepatitis B
• Spatial and chronological differences in hepatitis B virus genotypes from patients with acute hepatitis B in Japan
• 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
• The efficacy of ursodeoxycholic acid and bezafibrate combination therapy for primary biliary cirrhosis : A prospective, multicenter study
• 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
• Reversibility of Serum NH_3 Level in a Case of Sudden Onset and Rapidly Progressive Case of Type 2 Citrullinemia
• Transforming Growth Factor-α Induces the Differentiation of Sarcomatoid Cholangiocarcinoma Cells
• The Significance of Enzyme Immunoassay for the Assessment of Hepatitis B Virus Core-Related Antigen following Liver Transplantation
• A Case of Granulocyte-Colony Stimulating Factor-Producing Hepatocellular Carcinoma Confirmed by Immunohistochemistry
• 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
• Risk Factors and Prediction of Long-term Outcome in Primary Biliary Cirrhosis
• Prediction of DAS28-ESR remission at 6 months by baseline variables in patients with rheumatoid arthritis treated with etanercept in Japanese population
• 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
• Autoimmune hepatitis in a patient with systemic lupus erythematosus : a case report
• Catastrophic transverse myelitis in a patient with systemic lupus erythematosus
• A significantly impaired natural killer cell activity due to a low activity on a per-cell basis in rheumatoid arthritis
• Twenty-four-week follow-up examination of a leukocytapheresis therapy in rheumatoid arthritis
• Characterization of anticytoplasmic antibodies in patients with systemic autoimmune diseases
• A case of amyloidosis secondary to rheumatoid arthritis complicated with Graves' ophthalmopathy
• Atypical mycobacteriosis in two patients with rheumatoid arthritis
• Human intrahepatic biliary epithelial cell as possible modulator of hepatic regeneration : Potential role of biliary epithelial cell for hepatic remodeling in vivo
• Increasing hepatitis C virus-associated hepatocellular carcinoma mortality and aging : Long term trends in Japan
• Nonalcoholic Steatohepatitis with Improved Hepatic Fibrosis after Weight Reduction
• Amyloid a Protein Amyloidosis in a Patient with Plasma Cell Dyscrasia
• Geranylgeraniol, an Intermediate Product in Mevalonate Pathway, Induces Apoptotic Cell Death in Human Hepatoma Cells : Death Receptor-independent Activation of Caspase-8 with Down-regulation of Bcl-xL Expression
• Attenuation of Responsiveness to Interferon-α Treatment by Preceded Overactivation of Interferon-mediated Pathway in Patients Chronically Infected by Hepatitis C Virus
• Two cases of hepatopulmonary syndrome with improved liver function following long-term oxygen therapy
• An SCN5A Mutation Associated With Idiopathic Ventricular Fibrillation Alters The Na^+ Channel Pore Structure And Responses To Antiarrhythmic Drugs
• A case of cold agglutinin disease in the course of treatment for polymyalgia rheumatica
• Predictive role of anti-gp210 and anticentromere antibodies in long-term outcome of primary biliary cirrhosis
• Reactive Arthritis which Occurred One Year After Acute Chlamydial Urethritis
• Successful plasmapheresis in alveolar hemorrhage associated with systemic lupus erythematosus
• Expression profile of lipid metabolism-associated genes in hepatitis C virus-infected human liver
• Elevated serum soluble CD8 level in autoimmune hepatitis and the effect of corticosteroid therapy
• Dermatomyositis Associated with Invasive Thymoma
• Propylthiouracil-Induced severe hepatitis: A case report and review of the literature
• Establishment and structural analysis of human mAb to E2 component of the 2-oxoglutarate dehydrogenase complex generated from a patient with primary biliary cirrhosis
• Tyrphostin AG 1478 Accelerates Hydrogen Peroxide-Induced Apoptosis in A431 Cells
• 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
• A case of periodic-fever-syndrome-like disorder with lipodystrophy, myositis, and autoimmune abnormalities
• 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)
• Effective prediction of outcome of combination therapy with pegylated interferon alpha 2b plus ribavirin in Japanese patients with genotype-1 chronic hepatitis C using early viral kinetics and new indices
• Efficacy of early retreatment with interferon β for relapse in patients with genotype Ib chronic hepatitis C
• Pilot study of prolonged interferon-α retreatment in chronic hepatitis C patients with genotype 1b
• Aneurysmal Intraheptic Portosystemic Venous Shunt Associated with Idiopathic Portal Hypertension : A Lesion Evaluated by a 3 D Image Reconstructed from Power Doppler Flow Imaging
• Multicentric reticulohistiocytosis associated with ovarian cancer
• Aborted Sudden Cardiac Death Associated with Short QT Syndrome
• Enhanced sodium channel intermediate inactivation in Brugada syndrome
• Molecular and Biophysical Bases of Brugada Syndrome
• Cutaneous vasculitis induced by TNF inhibitors : a report of three cases
• Switching to the anti-interleukin-6 receptor antibody tocilizumab in rheumatoid arthritis patients refractory to antitumor necrosis factor biologics
• Prediction of DAS28-CRP remission in patients with rheumatoid arthritis treated with tacrolimus at 6 months by baseline variables
• Autoreactive T-cell responses in primary biliary cirrhosis are proinflammatory whereas those of controls are regulatory
• -0532-ALTERATIONS OF MEMBRANE PHOSPHOINOSITIDE METABOLISM IN THE HEART OF CARDIOMYOPATHIC SYRIAN HAMSTER BIO 14.6 (BIO)
• Hen and egg, you mitochondria! PBC revisits mitochondria again
• Interobserver variation in assessing small bile duct lesions in PBC, CVH, and AIH
• Successful treatment of chronic lupus myocarditis with prednisolone and mizoribine
• Long-term efficacy of intravenously administered immunoglobulin in a case of polymyositis with limited application of steroid therapy.
• ITPA gene variant protects against anemia induced by pegylated interferon-α and ribavirin therapy for Japanese patients with chronic hepatitis C
• 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
• Integrated fibrosis scoring by ultrasonography predicts the occurrence of hepatocellular carcinoma in patients with chronic hepatitis C virus infection
• Contribution of an adenine to guanine single nucleotide polymorphism of the matrix metalloproteinase-13 (MMP-13) -77 promoter region to the production of anticyclic citrullinated peptide antibodies in patients with HLA-DRB1^*shared epitope-negative rheuma
• Reduction in serum levels of substance P in patients with rheumatoid arthritis by etanercept, a tumor necrosis factor inhibitor
• A case of lupus-associated pancreatitis with ruptured pseudoaneurysms
• Genetic polymorphisms in CTLA4 and SLC4A2 are differentially associated with the pathogenesis of primary biliary cirrhosis in Japanese patients
• Delayed treatment with tumor necrosis factor inhibitors in incomplete responders to synthetic disease-modifying anti-rheumatic drugs shows and excellent effect in patients with very early rheumatoid arthritis with poor prognosis factors
• Treatment discontinuation in patients with very early rheumatoid arthritis in sustained simplified disease activity index remission after synthetic disease-modifying anti-rheumatic drug administration
• Anti-hypoalbuminemic effect of branched-chain amino acid granules in patients with liver cirrhosis is independent of dietary energy and protein intake

もっと見る 閉じる

スポンサーリンク