FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Masayuki Hakoda

Research Profile

Chemicals & Drugs

Geographic Areas

Japan

Genes & Molecular Sequences

Alleles

Procedures

Physiology

Disorders

Rheumatoid Arthritis

Anatomy

Living Beings

Homozygote

Concepts & Ideas

Molecular Sequence Data

Phenomena

Co-author Network

Publications

TOP 3
Atsuo Taniguchi; Y Yamada; Masayuki Hakoda; H Kaneko; M Kawamoto; C Sekita; Hisashi Yamanaka
Molecular characterization of a deletion in the HPRT1 gene in a patient with Lesch-Nyhan syndrome.
Naomi Ichikawa; Shigeru Kotake; Masayuki Hakoda; Kenshi Higami; Aya Kawasaki; Takefumi Furuya; Yuki Nanke; Naoyuki Tsuchiya; Katsushi Tokunaga; Naoyuki Kamatani
Combining effects of polymorphism of tumor necrosis factor alpha 5'-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis.
Takefumi Furuya; I Matsumoto; Naoyuki Tsuchiya; Masayuki Hakoda; Naomi Ichikawa; Toru Yago; Kenshi Higami; Yuki Nanke; T Sumida; Naoyuki Kamatani; Shigeru Kotake
Anti-glucose-6-phosphate isomerase, anti-cyclic citrullinated peptide antibodies and HLA-DRB1 genotypes in Japanese patients with early rheumatoid arthritis.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Masayuki Hakoda (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2011: Atsuo Taniguchi; Y Yamada; Masayuki Hakoda; H Kaneko; M Kawamoto; C Sekita; Hisashi Yamanaka
Molecular characterization of a deletion in the HPRT1 gene in a patient with Lesch-Nyhan syndrome.
Nucleosides, nucleotides & nucleic acids 2011;30(12):1266-71.
2009: Naomi Ichikawa; Shigeru Kotake; Masayuki Hakoda; Kenshi Higami; Aya Kawasaki; Takefumi Furuya; Yuki Nanke; Naoyuki Tsuchiya; Katsushi Tokunaga; Naoyuki Kamatani
Combining effects of polymorphism of tumor necrosis factor alpha 5'-flanking region and HLA-DRB1 on radiological progression in patients with rheumatoid arthritis.
Modern rheumatology / the Japan Rheumatism Association 2009;19(2):134-9.
2008: Takefumi Furuya; I Matsumoto; Naoyuki Tsuchiya; Masayuki Hakoda; Naomi Ichikawa; Toru Yago; Kenshi Higami; Yuki Nanke; T Sumida; Naoyuki Kamatani; Shigeru Kotake
Anti-glucose-6-phosphate isomerase, anti-cyclic citrullinated peptide antibodies and HLA-DRB1 genotypes in Japanese patients with early rheumatoid arthritis.
Clinical and experimental rheumatology 2008;26(5):918-21.
2008: Masayuki Hakoda
[Epidemiology of hyperuricemia and gout in Japan].
Nihon rinsho. Japanese journal of clinical medicine 2008;66(4):647-52.
2007: Takefumi Furuya; Masayuki Hakoda; Naomi Ichikawa; Kenshi Higami; Yuki Nanke; Toru Yago; Naoyuki Kamatani; Shigeru Kotake
Associations between HLA-DRB1, RANK, RANKL, OPG, and IL-17 genotypes and disease severity phenotypes in Japanese patients with early rheumatoid arthritis.
Clinical rheumatology 2007;26(12):2137-41.
2007: Takefumi Furuya; Masayuki Hakoda; Naomi Ichikawa; Kenshi Higami; Yuki Nanke; Toru Yago; Tsuyoshi Kobashigawa; Katsushi Tokunaga; Naoyuki Tsuchiya; Naoyuki Kamatani; Shigeru Kotake
Differential association of HLA-DRB1 alleles in Japanese patients with early rheumatoid arthritis in relationship to autoantibodies to cyclic citrullinated peptide.
Clinical and experimental rheumatology 2007;25(2):219-24.
2004: Takefumi Furuya; Masayuki Hakoda; Naoyuki Tsuchiya; Shigeru Kotake; Naomi Ichikawa; Yuki Nanke; Ayako Nakajima; Megumi Takeuchi; Makoto Nishinarita; Hirobumi Kondo; Aya Kawasaki; Shio Kobayashi; Tsuneyo Mimori; Katsushi Tokunaga; Naoyuki Kamatani
Immunogenetic features in 120 Japanese patients with idiopathic inflammatory myopathy.
The Journal of rheumatology 2004;31(9):1768-74.
2001: Naomi Ichikawa; Shigeru Kotake; Masayuki Hakoda; Naoyuki Kamatani
Microchimerism in Japanese patients with systemic sclerosis.
Arthritis and rheumatism 2001;44(5):1226-8.
2001: Shigeru Kotake; N Udagawa; Masayuki Hakoda; M Mogi; K Yano; E Tsuda; K Takahashi; Takefumi Furuya; S Ishiyama; K J Kim; Seiji Saito; T Nishikawa; N Takahashi; A Togari; Taisuke Tomatsu; T Suda; Naoyuki Kamatani
Activated human T cells directly induce osteoclastogenesis from human monocytes: possible role of T cells in bone destruction in rheumatoid arthritis patients.
Arthritis and rheumatism 2001;44(5):1003-12.
2000: Hiroshi Nakajima; Masayoshi Harigai; Masako Hara; Masayuki Hakoda; H Tokuda; F Sakai; Naoyuki Kamatani; S Kashiwazaki
KL-6 as a novel serum marker for interstitial pneumonia associated with collagen diseases.
The Journal of rheumatology 2000;27(5):1164-70.
1998: Takefumi Furuya; Masayuki Hakoda; Kenshi Higami; H Ueda; Naoyuki Tsuchiya; Katsushi Tokunaga; Naoyuki Kamatani; S Kashiwazaki
Association of HLA class I and class II alleles with myositis in Japanese patients.
The Journal of rheumatology 1998;25(6):1109-14.
1998: Atsuo Taniguchi; Masayuki Hakoda; Hisashi Yamanaka; Chihiro Terai; K Hikiji; R Kawaguchi; N Konishi; S Kashiwazaki; Naoyuki Kamatani
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 1998;102(2):197-202.
1998: Naoyuki Kamatani; Chihiro Terai; S Y Kim; C L Chen; Hisashi Yamanaka; Masayuki Hakoda; S Totokawa; S Kashiwazaki
The origin of APRT*J. The most common disease-related mutation of APRT gene among Japanese goes back to a prehistoric era.
Advances in experimental medicine and biology 1998;431():135-9.
1998: Hisashi Yamanaka; R Togashi; Masayuki Hakoda; Chihiro Terai; S Kashiwazaki; T Dan; Naoyuki Kamatani
Optimal range of serum urate concentrations to minimize risk of gouty attacks during anti-hyperuricemic treatment.
Advances in experimental medicine and biology 1998;431():13-8.
1997: Kenshi Higami; Masayuki Hakoda; Yuko Matsuda; H Ueda; S Kashiwazaki
Lack of association of HLA-DRB1 genotype with radiologic progression in Japanese patients with early rheumatoid arthritis.
Arthritis and rheumatism 1997;40(12):2241-7.
1997: Masayuki Hakoda; Naoyuki Kamatani; S Kurumada; Y Hirai; K Sakamoto; Hisashi Yamanaka; Chihiro Terai; S Kashiwazaki
Intervention of somatic mutational events in vivo by a germline defect at the adenine phosphoribosyltransferase locus.
Human genetics 1997;99(2):164-70.
1997: Masayuki Hakoda
[APRT deficiency].
Ryōikibetsu shōkōgun shirīzu 1997;(17 Pt 2):235-8.
1997: Masayuki Hakoda; Naoyuki Kamatani; Atsuo Taniguchi; H Ueda; Hisashi Yamanaka; Chihiro Terai; S Kashiwazaki
Generation and molecular characterisation of monoclonal IgG4 rheumatoid factor from a patient with rheumatoid arthritis.
Annals of the rheumatic diseases 1997;56(1):74-7.
1996: Naoyuki Kamatani; Chihiro Terai; S Y Kim; C L Chen; Hisashi Yamanaka; Masayuki Hakoda; S Totokawa; S Kashiwazaki
The origin of the most common mutation of adenine phosphoribosyltransferase among Japanese goes back to a prehistoric era.
Human genetics 1996;98(5):596-600.
1996: Masayuki Hakoda; Naoyuki Kamatani; Chihiro Terai; Hisashi Yamanaka; Atsuo Taniguchi; H Ueda; S Kashiwazaki
Similarity of in vivo somatic mutations at an autosomal adenine phosphoribosyltransferase locus between T- and B-cells in human peripheral blood.
Mutation research 1996;357(1-2):107-13.
1996: Masayuki Hakoda; Naoyuki Kamatani; S Hayashimoto-Kurumada; G J Silverman; H Yamanaka; Chihiro Terai; S Kashiwazaki
Differential binding avidities of human IgM for staphylococcal protein A derive from specific germ-line VH3 gene usage.
Journal of immunology (Baltimore, Md. : 1950) 1996;157(7):2976-81.
1996: A Nakajima; Masayuki Hakoda; H Yamanaka; Naoyuki Kamatani; S Kashiwazaki
Divergent effects of methotrexate on the clonal growth of T and B lymphocytes and synovial adherent cells from patients with rheumatoid arthritis.
Annals of the rheumatic diseases 1996;55(4):237-42.
1995: Masayuki Hakoda; Y Hirai; M Akiyama; Hisashi Yamanaka; Chihiro Terai; Naoyuki Kamatani; S Kashiwazaki
Selection against blood cells deficient in hypoxanthine phosphoribosyltransferase (HPRT) in Lesch-Nyhan heterozygotes occurs at the level of multipotent stem cells.
Human genetics 1995;96(6):674-80.
1995: Chihiro Terai; Masayuki Hakoda; Hisashi Yamanaka; Naoyuki Kamatani; M Okai; F Takahashi; S Kashiwazaki
Adenine phosphoribosyltransferase deficiency identified by urinary sediment analysis: cellular and molecular confirmation.
Clinical genetics 1995;48(5):246-50.
1995: Chihiro Terai; Masayuki Hakoda; Hisashi Yamanaka; Naoyuki Kamatani; S Kashiwazaki
Differential cytotoxic effects of mizoribine and its aglycone on human and murine cells and on normal and enzyme-deficient human cells.
Biochemical pharmacology 1995;50(7):1099-102.
1994: Masayuki Hakoda; S Hayashimoto; H Yamanaka; Chihiro Terai; Naoyuki Kamatani; S Kashiwazaki
Molecular basis for the interaction between human IgM and staphylococcal protein A.
Clinical immunology and immunopathology 1994;72(3):394-401.
1994: Hisashi Yamanaka; Naoyuki Kamatani; Masayuki Hakoda; Chihiro Terai; R Kawaguchi; S Kashiwazaki
Analysis of the genotypes for aldehyde dehydrogenase 2 in Japanese patients with primary gout.
Advances in experimental medicine and biology 1994;370():53-6.
1994: Naoyuki Kamatani; Hisashi Yamanaka; Masayuki Hakoda; Chihiro Terai; S Kashiwazaki
Search for the mechanisms of high incidence of APRT deficiency among Japanese.
Advances in experimental medicine and biology 1994;370():327-30.
1993: Masayuki Hakoda; T Ishimoto; S Hayashimoto; K Inoue; Atsuo Taniguchi; Naoyuki Kamatani; S Kashiwazaki
Selective infiltration of B cells committed to the production of monoreactive rheumatoid factor in synovial tissue of patients with rheumatoid arthritis.
Clinical immunology and immunopathology 1993;69(1):16-22.
1992: Masayuki Hakoda; Naoyuki Kamatani
[Genotype and genetic diagnosis of APRT deficiency].
Nihon rinsho. Japanese journal of clinical medicine 1992;50(12):3110-5.
1992: Naoyuki Kamatani; Masayuki Hakoda; S Otsuka; H Yoshikawa; S Kashiwazaki
Only three mutations account for almost all defective alleles causing adenine phosphoribosyltransferase deficiency in Japanese patients.
The Journal of clinical investigation 1992;90(1):130-5.
1991: R Kawaguchi; H Higashimoto; Kazumasa Hikiji; Masayuki Hakoda; Naoyuki Kamatani
Detection of the most common mutation of adenine phosphoribosyltransferase deficiency among Japanese by a non-radioactive method.
Clinica chimica acta; international journal of clinical chemistry 1991;203(2-3):183-90.
1991: Masayuki Hakoda; Hisashi Yamanaka; Naoyuki Kamatani; N Kamatani
Diagnosis of heterozygous states for adenine phosphoribosyltransferase deficiency based on detection of in vivo somatic mutants in blood T cells: application to screening of heterozygotes.
American journal of human genetics 1991;48(3):552-62.
1991: Masayuki Hakoda; Naoyuki Kamatani; S Ohtsuka; S Kashiwazaki
Germline and somatic mutations leading to adenine phosphoribosyltransferase (APRT) deficiency.
Advances in experimental medicine and biology 1991;309B():87-90.
1990: Masayuki Hakoda; T Ishimoto; K Yamamoto; K Inoue; Naoyuki Kamatani; N Miyasaka; K Nishioka
Clonal analysis of T cell infiltrates in synovial tissue of patients with rheumatoid arthritis.
Clinical immunology and immunopathology 1990;57(3):387-98.
1990: Naoyuki Kamatani; S Kuroshima; Masayuki Hakoda; T D Palella; Y Hidaka
Crossovers within a short DNA sequence indicate a long evolutionary history of the APRT*J mutation.
Human genetics 1990;85(6):600-4.
1990: Naoyuki Kamatani; S Kuroshima; Hisashi Yamanaka; S Nakashe; H Take; Masayuki Hakoda
Identification of a compound heterozygote for adenine phosphoribosyltransferase deficiency (APRT*J/APART*Q0) leading to 2,8-dihydroxyadenine urolithiasis.
Human genetics 1990;85(5):500-4.
1990: Masayuki Hakoda; K Nishioka; Naoyuki Kamatani
Homozygous deficiency at autosomal locus aprt in human somatic cells in vivo induced by two different mechanisms.
Cancer research 1990;50(6):1738-41.
1989: Naoyuki Kamatani; S Kuroshima; Chihiro Terai; Masayuki Hakoda; K Nishioka; K Mikanagi
Diagnosis of genotypes for adenine phosphoribosyltransferase (APRT) deficiency.
Advances in experimental medicine and biology 1989;253A():51-8.