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Fujio Takeuchi

Research Profile

Geographic Areas

Japan

Disorders

Genes & Molecular Sequences

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Chemicals & Drugs

Physiology

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Polymerase Chain Reaction

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Polymorphism, Single-Stranded Conformational

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Publications

TOP 3
Shinji Harihara; Kennichi Nakamura; Kaiyo Takubo; Fujio Takeuchi
Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twins.
Hee Jung Ryu; Fujio Takeuchi; Shoji Kuwata; Yoon Jun Kim; Eun Young Lee; Eun Bong Lee; Yeong Wook Song
The diagnostic utilities of anti-agalactosyl IgG antibodies, anti-cyclic citrullinated peptide antibodies, and rheumatoid factors in rheumatoid arthritis.
Toshikatsu Kaburaki; Mitsuko Takamoto; Jiro Numaga; Hidetoshi Kawashima; Makoto Araie; Yuka Ohnogi; Shinji Harihara; S Kuwata; Fujio Takeuchi
Genetic association of HLA-A*2601 with ocular Behçet's disease in Japanese patients.

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All Publications

2013: Shinji Harihara; Kennichi Nakamura; Kaiyo Takubo; Fujio Takeuchi
Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twins.
Mitochondrial DNA 2013;24(2):158-62.
2011: Hee Jung Ryu; Fujio Takeuchi; Shoji Kuwata; Yoon Jun Kim; Eun Young Lee; Eun Bong Lee; Yeong Wook Song
The diagnostic utilities of anti-agalactosyl IgG antibodies, anti-cyclic citrullinated peptide antibodies, and rheumatoid factors in rheumatoid arthritis.
Rheumatology international 2011;31(3):315-9.
2010: Toshikatsu Kaburaki; Mitsuko Takamoto; Jiro Numaga; Hidetoshi Kawashima; Makoto Araie; Yuka Ohnogi; Shinji Harihara; S Kuwata; Fujio Takeuchi
Genetic association of HLA-A*2601 with ocular Behçet's disease in Japanese patients.
Clinical and experimental rheumatology 2010;28(4 Suppl 60):S39-44.
2009: Daisuke Son; Hiroko Kanda; Akihiro Yamaguchi; Kimito Kawabata; Takahisa Kawakami; Kanae Kubo; Masaaki Higashihara; Jun Shimizu; Hiroshi Uozaki; Shigeru Kuramochi; Yoshikata Misaki; Fujio Takeuchi; Kazuhiko Yamamoto
Myeloperoxidase antineutrophil cytoplasmic antibody-associated vasculitis with diffuse tubulointerstitial nephritis.
Journal of nephrology 2009;22(3):417-20.
2008: Fujio Takeuchi; N Nakaue; N Kobayashi; S Kuwata; T Murayama; Kaname Kawasugi; Masatomo Mori; Kunio Matsuta
Genetic contribution of the CD14 -159C/T dimorphism in the promoter region in Japanese RA.
Clinical and experimental rheumatology 2008;26(2):337-9.
2008: Shinji Harihara; Kenichi Nakamura; Mutsunori Fujiwara; Tomio Arai; Motoji Sawabe; Fujio Takeuchi; Kaiyo Takubo
Markedly different clinical features in 2 diabetes mellitus patients with extremely high tissue levels of the mitochondrial DNA A3243G mutation.
Gerontology 2008;54(3):168-72.
2007: Fujio Takeuchi; Naoko Nakaue; Kaname Kawasugi; Masaki Mori; Shoji Kuwata; Kiyoaki Tanimoto
The CTLA-4 -1661A/G and -1772T/C dimorphisms in Japanese patients with systemic sclerosis.
Rheumatology international 2007;27(8):785-7.
2006: Fujio Takeuchi; Kaname Kawasugi; M Mori; N Nakaue; N Kobayashi; S Kuwata; T Murayama; Kunio Matsuta
The genetic contribution of CTLA-4 dimorphisms in promoter and exon 1 regions in Japanese patients with rheumatoid arthritis.
Scandinavian journal of rheumatology 2006;35(2):154-5.
2005: Fujio Takeuchi; H Nabeta; GH Hong; Kaname Kawasugi; M Mori; Kunio Matsuta; S Kuwata; T Murayama; K Nakano
The genetic contribution of the TNFa11 microsatellite allele and the TNFb + 252*2 allele in Japanese RA.
Clinical and experimental rheumatology 2005;23(4):494-8.
2005: Fujio Takeuchi; K Nakano; H Nabeta; GH Hong; Kaname Kawasugi; M Mori; H Okudaira; S Kuwata; K Tanimoto
Genetic contribution of the tumour necrosis factor (TNF) B + 252*2/2 genotype, but not the TNFa,b microsatellite alleles, to systemic lupus erythematosus in Japanese patients.
International journal of immunogenetics 2005;32(3):173-8.
2003: Fujio Takeuchi; Kaname Kawasugi; H Nabeta; M Mori; K Tanimoto
CTLA-4 dimorphisms in Japanese patients with systemic lupus erythematosus.
Clinical and experimental rheumatology 2003;21(4):527-8.
2003: Fujio Takeuchi; Shinji Harihara; Kenichi Nakamura; Kaiyo Takubo; Masao Kanamori; Makoto Goto
The mitochondrial DNA A3243G mutation in Werner's syndrome.
Experimental gerontology 2003;38(3):339-42.
2003: Kaname Kawasugi; Fujio Takeuchi
[PRPP synthetase deficiency].
Nihon rinsho. Japanese journal of clinical medicine 2003;61 Suppl 1():383-5.
2003: Kaname Kawasugi; Fujio Takeuchi
[PRPP synthetase superactivity].
Nihon rinsho. Japanese journal of clinical medicine 2003;61 Suppl 1():284-7.
2003: Kaname Kawasugi; Fujio Takeuchi
[Phosphoribosylpyrophosphate(PRPP) synthetase].
Nihon rinsho. Japanese journal of clinical medicine 2003;61 Suppl 1():20-3.
2002: Fujio Takeuchi; Kaname Kawasugi; H Nabeta; M Mori; K Tanimoto
Association of CTLA-4 with systemic sclerosis in Japanese patients.
Clinical and experimental rheumatology 2002;20(6):823-8.
2002: Shinji Harihara; Kenichi Nakamura; Kaiyo Takubo; Fujio Takeuchi
Comparison of the level of mitochondrial DNA A3243G mutation in esophageal epithelium and myocardium from individuals of very advanced age.
Experimental gerontology 2002;37(7):917-23.
2002: Fujio Takeuchi; M Mori; M Goto; Kunio Matsuta; A Yamada; Teiji Chihara; T Hanyu; T Murayama; S Yamamoto; Naoko Takubo; N Murata; T Matsubara; M Itakura; H Sakuta
Mode of inheritance of HLA-DRB1 shared epitope in Japanese familial rheumatoid arthritis.
Clinical and experimental rheumatology 2002;20(3):395-8.
2000: Fujio Takeuchi; Kaname Kawasugi; H Nabeta; M Mori; M Moritani; M Goto; Kunio Matsuta; A Yamada; Teiji Chihara; T Hanyu; T Murayama; S Yamamoto; N Murata; T Matsubara; M Itakura
HLA-DR shared epitope in familial cases of Japanese rheumatoid arthritis.
Clinical and experimental rheumatology 2000;18(3):423-4.
2000: Fujio Takeuchi; H Nabeta; Monika Füssel; Karsten Conrad; KH Frank
Association of the TNFa13 microsatellite with systemic sclerosis in Japanese patients.
Annals of the rheumatic diseases 2000;59(4):293-6.
1998: Fujio Takeuchi; H Nabeta; GH Hong; Kunio Matsuta; Katsushi Tokunaga; K Tanimoto; K Nakano
C4A and C4B null alleles are genetic markers of different types of systemic sclerosis in Japanese patients.
Clinical and experimental rheumatology 1998;16(1):55-60.
1998: Fujio Takeuchi; H Nabeta; GH Hong; S Kuwata; K Tanimoto; Kyoko Ito
Polymorphisms of DMA and DMB genes in Japanese systemic lupus erythematosus.
British journal of rheumatology 1998;37(1):95-7.
1997: Fujio Takeuchi; H Nabeta; S Kuwata; K Tanimoto; Kyoko Ito
Association of DMA and DMB with RA in Japanese.
Clinical and experimental rheumatology 1997;15(2):189-92.
1997: Fujio Takeuchi; K Nakano; Kunio Matsuta; K Takizawa; H Nabeta; S Kuwata; Kyoko Ito
Polymorphism of TAP1 and TAP2 in Japanese patients with rheumatoid arthritis.
Tissue antigens 1997;49(3 Pt 1):280-2.
1997: Fujio Takeuchi; K Takizawa; H Nabeta; S Kuwata; Kyoko Ito
Association of DM genes in systemic sclerosis is secondary to the association with HLA genes.
Scandinavian journal of rheumatology 1997;26(3):174-9.
1996: Fujio Takeuchi; K Nakano; H Nabeta; GH Hong; S Kuwata; K Ito
Polymorphisms of the TAP1 and TAP2 transporter genes in Japanese SLE.
Annals of the rheumatic diseases 1996;55(12):924-6.
1996: M H Park; M D Oh; Y W Song; H J Pai; Fujio Takeuchi; Katsushi Tokunaga; GH Hong; K S Park
Association of complement alleles C4AQ0 and C4B5 with rheumatoid arthritis in Koreans.
Annals of the rheumatic diseases 1996;55(10):776-8.
1996: GH Hong; M H Park; Fujio Takeuchi; M D Oh; Y W Song; H Nabeta; K Nakano; K Ito; K S Park
Association of specific amino acid sequence of HLA-DR with rheumatoid arthritis in Koreans and its diagnostic value.
The Journal of rheumatology 1996;23(10):1699-703.
1996: Fujio Takeuchi; S Kuwata; K Nakano; H Nabeta; GH Hong; Y Shibata; K Tanimoto; K Ito
Association of TAP1 and TAP2 with systemic sclerosis in Japanese.
Clinical and experimental rheumatology 1996;14(5):513-21.
1996: S Pattanakitsakul; Fujio Takeuchi; H Nabeta; K Nakano; S Kuwata; M Yanagisawa; Y Shibata; K Ito
A novel TAP 2 gene RFLP observed in a Japanese.
Tissue antigens 1996;47(4):353-5.
1996: Fujio Takeuchi; K Nakano; Kunio Matsuta; H Nabeta; Makoto Bannai; K Tanimoto; K Ito
Positive and negative association of HLA-DR genotypes with Japanese rheumatoid arthritis.
Clinical and experimental rheumatology 1996;14(1):17-22.
1994: Fujio Takeuchi; K Nakano; H Yamada; GH Hong; H Nabeta; A Yoshida; Kunio Matsuta; Makoto Bannai; Katsushi Tokunaga; K Ito
Association of HLA-DR with progressive systemic sclerosis in Japanese.
The Journal of rheumatology 1994;21(5):857-63.
1994: GH Hong; H Y Kim; Fujio Takeuchi; K Nakano; H Yamada; Kunio Matsuta; H Han; Katsushi Tokunaga; K Ito; K S Park
Association of complement C4 and HLA-DR alleles with systemic lupus erythematosus in Koreans.
The Journal of rheumatology 1994;21(3):442-7.
1993: Naoyuki Tsuchiya; T Endo; Kunio Matsuta; S Yoshinoya; Fujio Takeuchi; Y Nagano; M Shiota; K Furukawa; N Kochibe; K Ito
Detection of glycosylation abnormality in rheumatoid IgG using N-acetylglucosamine-specific Psathyrella velutina lectin.
Journal of immunology (Baltimore, Md. : 1950) 1993;151(2):1137-46.
1993: Fujio Takeuchi; K Nakano; H Yamada; E Kosuge; M Hirai; H Maeda; Y Moroi
Chromosome abnormalities in peripheral lymphocytes from patients with progressive systemic sclerosis.
Rheumatology international 1993;12(6):243-6.
1992: Fujio Takeuchi; E Kosuge; Y Hashimoto; Kunio Matsuta; F Hanaoka; K Tanimoto; K Ito
Lobenzarit disodium (CCA) inhibits the proliferation of human endothelial cells and the activity of DNA polymerase alpha.
Agents and actions 1992;36(3-4):312-6.
1992: U Shu; Fujio Takeuchi; K Tanimoto; Y Moroi; K Uchida; K Ito
Transient myopia with severe chemosis associated with exacerbation of disease activity in systemic lupus erythematosus.
The Journal of rheumatology 1992;19(2):297-301.
1991: Fujio Takeuchi; A Takeuchi
Chromosome aberration in lymphocytes from Behçet's disease.
The Journal of rheumatology 1991;18(8):1207-10.
1990: Fujio Takeuchi; E Kosuge; Kunio Matsuta; K Nakano; Katsushi Tokunaga; T Juji; T Miyamoto
Antibody to a specific HLA-DR beta 1 sequence in Japanese patients with rheumatoid arthritis.
Arthritis and rheumatism 1990;33(12):1867-8.
1990: H Yamada; A Watanabe; A Mimori; K Nakano; Fujio Takeuchi; Kunio Matsuta; K Tanimoto; T Miyamoto; Y Yukiyama; Katsushi Tokunaga
Lack of gene deletion for complement C4A deficiency in Japanese patients with systemic lupus erythematosus.
The Journal of rheumatology 1990;17(8):1054-7.
1990: A Mimori; Fujio Takeuchi; Katsushi Tokunaga; H Maeda; K Matsuki; Kunio Matsuta; K Nakano; E Kosuge; Y Yukiyama; K Omoto
Restriction fragment length polymorphism of complement C4 in Japanese patients with rheumatoid arthritis and normal Japanese.
Tissue antigens 1990;35(5):197-202.
1990: K Furukawa; Kunio Matsuta; Fujio Takeuchi; E Kosuge; T Miyamoto; Akira Kobata
Kinetic study of a galactosyltransferase in the B cells of patients with rheumatoid arthritis.
International immunology 1990;2(1):105-12.
1989: Fujio Takeuchi; Kunio Matsuta; Y Watanabe; K Tokunaga; T Juji; T Miyamoto
Susceptibility epitope on HLA-DR beta chain for rheumatoid arthritis and the effect of the positivity on the clinical features.
Journal of immunogenetics 1989;16(6):475-83.
1989: Fujio Takeuchi; F Hanaoka; Kunio Matsuta; T Miyamoto
Inhibitory effects of gold sodium thiomalate on DNA polymerase alpha.
Clinical and experimental rheumatology 1989;7(6):595-601.
1989: Y Watanabe; K Tokunaga; K Matsuki; Fujio Takeuchi; Kunio Matsuta; H Maeda; K Omoto; T Juji
Putative amino acid sequence of HLA-DRB chain contributing to rheumatoid arthritis susceptibility.
The Journal of experimental medicine 1989;169(6):2263-8.
1989: Fujio Takeuchi; A Mimori; Kunio Matsuta; K Nakano; T Miyamoto; K Matsuki; Takeo Juji; H Maeda; K Omoto; Katsushi Tokunaga
Association of complement alleles C4AQ0 and C4B5 with rheumatoid arthritis in Japanese patients.
Arthritis and rheumatism 1989;32(6):691-8.
1989: Naoyuki Tsuchiya; T Endo; Kunio Matsuta; S Yoshinoya; T Aikawa; E Kosuge; Fujio Takeuchi; T Miyamoto; Akira Kobata
Effects of galactose depletion from oligosaccharide chains on immunological activities of human IgG.
The Journal of rheumatology 1989;16(3):285-90.
1987: I Komuro; H Kato; T Nakagawa; K Takahashi; A Mimori; Fujio Takeuchi; Y Nishida; T Miyamoto
The longest-lived patient with homozygous familial hypercholesterolemia secondary to a defect in internalization of the LDL receptor.
The American journal of the medical sciences 1987;294(5):341-5.