terai chihiro

FacultyComprehensiveMedicine1
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Profile

Research Keywords

    Rheumatology, Clinical Immunology

Research Areas

  • Basic medicine / Immunology
  • Clinical internal medicine / General internal medicine (including psychosomatic medicine)
  • Clinical internal medicine / Kidney internal medicine

Research Activities

Papers(other)

  • Pyrimidine nucleotide and nucleic acid synthesis in human monocytes and macrophages.
    Exp. Cell Res. 193 1991
  • Apoptosis as a mechanism of cell death in cultured T lymphoblasts acutely infected with HIV-l.
    J. Clin. Invest. 87 1991
  • Dependence of cell survival on DNA repair in human mononuclear phagocytes
    J. Immunol 147(12) 1991
  • Potent toxicity of 2-chlorodeoxyadenosine toward human monocytes in vitro and in vivo. (共著)
    J. Clin. Invest 86 1990
  • Induction of programmed cell death in lymphocytes but not monocytes by inoizing radiation
    FASEB J. 1990
  • Determination of urinary albumin excretion by radioimmunoassay in patients with subclinical lupus nephritis
    Clin. Nephrol 27(2) 1987
  • Low C3b receptor reactivity on erythrocytes from patients with systemic lupus erythematosus detected by immune adherence hemagglutination and radioimmuno(共著)
    Arth. Rheum. 27(12) 1984
  • Selection of human cells having two different types of mutations in individual cells(genetic/artificial mutants). (共著)
    Hum. Genet. 76 1987
  • Genetic and clinical studies on 19 families with adenine phosphoribosyltransferase deficiencies(共著)
    Hum. Genet. 75 1987
  • Low capacity of erythrocytes to bind with immune complexes via C3b receptor in patients with systemic lupus erythematosus : correlation with pathological(共著)
    Clin. Immunol. Immunopathol 34 1985
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Papers(other)close
  • Pyrimidine nucleotide and nucleic acid synthesis in human monocytes and macrophages.
    Exp. Cell Res. 193 1991
  • Apoptosis as a mechanism of cell death in cultured T lymphoblasts acutely infected with HIV-l.
    J. Clin. Invest. 87 1991
  • Dependence of cell survival on DNA repair in human mononuclear phagocytes
    J. Immunol 147(12) 1991
  • Potent toxicity of 2-chlorodeoxyadenosine toward human monocytes in vitro and in vivo. (共著)
    J. Clin. Invest 86 1990
  • Induction of programmed cell death in lymphocytes but not monocytes by inoizing radiation
    FASEB J. 1990
  • Determination of urinary albumin excretion by radioimmunoassay in patients with subclinical lupus nephritis
    Clin. Nephrol 27(2) 1987
  • Low C3b receptor reactivity on erythrocytes from patients with systemic lupus erythematosus detected by immune adherence hemagglutination and radioimmuno(共著)
    Arth. Rheum. 27(12) 1984
  • Selection of human cells having two different types of mutations in individual cells(genetic/artificial mutants). (共著)
    Hum. Genet. 76 1987
  • Genetic and clinical studies on 19 families with adenine phosphoribosyltransferase deficiencies(共著)
    Hum. Genet. 75 1987
  • Low capacity of erythrocytes to bind with immune complexes via C3b receptor in patients with systemic lupus erythematosus : correlation with pathological(共著)
    Clin. Immunol. Immunopathol 34 1985
  • Adenine phosphorybosyltransferase deficiency identified by urinary sediment analysis : cellular and molecular confirmation
    Clinical Genetics 48 246-250 1995
  • Differential cytotoxic effects of mizoribine and its aglycone on human and murine cells and on normal and enzyme deficient human cells
    Biochemical Pharmacology 50(7) 1099-1102 1995
  • Molecular basis for the interaction between human IgM and staphylococcal protain A(共著)
    Clinical Immunological Immunopathology 72 394 1994
  • 2-Chlorodeoxyadenosine chemotherapy triggers programmed cell death in normal and malignant lymphocytes(共著)
    Advances in Experimental Medcine and Biology 309A 15 1991
  • Diagnosis of genotypes for adenine phosphoribosyltransferase (APRT) deficiency(共著)
    Advances in Experimental Medicine and Biology 253A 51 1989
  • Defection of an amino acid substitution in the mutant enzyme for a special type of adenine phosphoribosyltransferase (APRT) deficiency by sequence specific protein cleavage(共著)
    American Journal of Human Genetics 45 325 1989
  • Correlative expression of C3b receptors in the glomerulus and on erythrocytes(共著)
    Clin. Immunol. Immunopathol. 38 85 1986
  • Tubulointerstitial immune complex nephritis in a patient with cutaneous vasculitis(共著)
    Clinical Nephrology 25 48 1986
  • Search for the mechanisms of high incidence of APRT deficiency among Japanese.
    Adv. Exp. Med. Biol 370 327-330 1995
  • Analysis of the genotypes for aldehyde dehydrogenase 2in Japanese patients with primary gout.
    Adv. Exp. Med. Biol. 370 53-56 1995
  • Selection against blood cells dficient in hypoxanthine phosphoribosyltransferase(HPRT)in Lesch-Nyhan heterozygoes occurs at the level of multipotent stem cells.
    Hum. Genet. 96(6) 674-680 1995
  • Origin of the most common mutation of adenine phosphoribosyltransferase among Japanese goes back to prehistoric era.
    Hum. Genet. 98(5) 596-600 1996
  • Differential binding avidities of human IgM for staphylococcal protein A derive from specific germ-line VH3 gene usage.
    J. Immunol. 157 2976-2981 1996
  • Generation and molecular characterisation of monoclonal IgG4 rheumatoid factor from a patient with rheumatoid arthritis.
    Ann. Rheum. Dis. 56 74-77 1997
  • Intervention of somatic mutational events in vivo by a germline defect at the adenine phosphoribosyltransferase locus.
    Hum. Genet. 99(2) 164-170 1997
  • Sclerosing cholangitis associated with hypereosinophilic syndrome
    Naomi ICHIKAWA, Atsuo TANIGUCHI, Hideto AKAMA, Hisataka ISHIGURO, Takeshi KURIHARA, Chihiro TERAI, Masako KARA, Sadao KASHIWAZAKI
    Internal Medicine 36(8) 561-564 1997
  • A case of eosinophilic fasciitis complicated with peripheral neuropathy
    Masato MORIGUCHI, Chihiro TERAI, Soemu KUROKI, Eiichi TANAKA, Noriyuki SOMEYA, Yoshiho TSUNODA, Sadao KASHIWAZAKI
    Internal Medicine 37(4) 417-420 1998
  • A germline mutation abolishing the original stop codon of the human adenine phosphoribosyltransferase(APRT)gene leads to complete loss of the enzyme protein
    Human Genetics 102(2) 197-202 1998
  • Optimal range of serum urate concentrations to minimize risk of gouty attacks during antihyperuricemic treatment
    Adv. Exp. Med. Biol. 13 1998
  • The origin of APRT*J : The most common disease-related mutation of APRT gene among Japanese goes back to a prehistoric era
    Adv. Exp. Med. Biol. 135 1998
  • Acute sympathetic hyperfunction in overlapping syndromes of systemic lupus erythematosus and polymyostis
    J. Rheumatol. 25 1638 1998
  • Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis
    Human Genetics 105 360 1999
  • Influence of genotypes at SAA1 and SAA2 loci on the development and the length of latent period of secondary AA-amyloidosis in patients with rheumatoid arthritis
    Human Genetics 105 360-366 1999
  • Renal function estimated from serum creatinine is overestimated in patients with rheumatoid arthritis because of their muscle atrophy
    Modern Rheumatology 10 230-234 2000
  • Rapidly progressive glomerulonephritis with D-penicillamine
    Am J Med Sci 320 398-402 2000
  • A prospective study on renal involvement in patients with early rheumatoid arthritis.
    Ann Rheum Dis 82 327-331 2001
  • Identification of a single nucleotide polymorphism in the 5' flanking region of SAA1 primarily associated with the risk of AA-amyloidosis in rheumatoid arthiritis patients.
    Arth Rheum 44 1266-2272 2001
  • Genotypes at ┣DBSAA1(/)-┫DB locus correlate with the clinical severity of AA-amyloidosis.
    Amyloid 8 115-120 2001
  • Antiphospholipid syndrome with complete abdominal aorta occlusion and chondritis.
    Mod Rheumatol 11 159-161 2001

Outside Fund Adoption

  • Secondary Amyloidosis AA-amyloidosis
  • Renal involvement in collagen diseases
  • Molecular diagnosis of APRT deficiency
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Outside Fund Adoptionclose
  • Secondary Amyloidosis AA-amyloidosis
  • Renal involvement in collagen diseases
  • Molecular diagnosis of APRT deficiency


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