スポンサーリンク
Second Department of Internal Medicine Nagoya University School of Medicine | 論文
- Cloning and sequencing of a novel human gene that encodes a putative target protein of Nesh-SH3
- Molecular cloning of a novel human gene (SIRP-B2) which encodes a new member of the SIRP/SHPS-1 protein family
- Sustained High Levels of Circulatory Interleukin-8 are Associated with a Poor Outcome in Patients with Adult Respiratory Distress Syndrome
- A Rapidly Progressive Case of Interstitial Pneumonia
- Mutation at codon 130 in hepatitis B virus (HBV) core region increases markedly during acute exacerbation of hepatitis in chronic HBV carriers
- Randomized controlled trial of twice-a-day administration of natural interferon β for chronic hepatitis C
- Interleukin 2 and γ/δ T-cell receptors in peripheral blood of patients with chronic hepatitis C virus infection
- Identification of a Phosphatase-Sensitive Epitope of Rabies Virus Nucleoprotein Which ls Recognized by a Monoclonal Antibody 5-2-26
- Monoclonal Antibody #5-2-26 Recognizes the Phosphatase-Sensitive Epitope of Rabies Virus Nucleoprotein
- Clinical and Immunohistochemical Evaluation of Acute Imterstitial pneumonia, Bronchiolitis Obliterans Organizing Pneumonia, and acute Exacerbation of Idiopathic Pulmonary Fibrosis
- DECREASED RESPONSE OF LYMPHOCYTES TO β-ADRENERGIC STIMULATION IN HEART FAILURE : Arrhythmia I, Immunity & Heredity, Contractile Protein : IVth Auditorium : Proceedings of the 43rd Annual Meeting of the Japanese Circulation Society, Tokyo, 1979
- Activation of Trypsinogen in Experimental Models of Acute Pancreatitis in Rats
- A Patient with Chronic Hepatitis C Who Obtained Sustained Response by Retreatment of Interferon after Decrease of Viral Load and Mutation in Interferon Sensitivity Determining Region
- Are Autoantibodies against Lewis Antigens Involved in the Pathogenesis of Helicobacter pylori-Induced Peptic Ulcers?
- RobA-Induced Multiple Antibiotic Resistance Largely Depends on the Activation of the AcrAB Efflux
- Special stain and X-ray probe microanalysis of livers with Wilson disease
- Mutational analysis of the MRP2 gene and long-term follow-up of Dubin-Johnson syndrome in Japan
- Identification of a novel 2026G→C mutation of the MRP2 gene in a Japanese patient with Dubin-Johnson syndrome
- AVAQ 594-597 deletion of the TfR2 gene in a Japanese family with hemochromatosis
- C282Y and H63D Mutations in the HFE Gene Have No Effect on Iron Overload Disorders in Japan