Search Results - "Sakamaki, Tateo"

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  1. 1

    HLA-DRB1 14 and DQB1 05 are associated with Japanese anti-MuSK antibody-positive myasthenia gravis patients by Kanai, Tetsuya, Uzawa, Akiyuki, Kawaguchi, Naoki, Sakamaki, Tateo, Yoshiyama, Yasumasa, Himuro, Keiichi, Oda, Fumiko, Kuwabara, Satoshi

    Published in Journal of the neurological sciences (15-04-2016)
    “…Abstract Background Myasthenia gravis (MG) is an autoimmune disorder presumed to be associated with genetic susceptibility. This study aims to determine…”
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  2. 2

    HLA-DRB114 and DQB105 are associated with Japanese anti-MuSK antibody-positive myasthenia gravis patients by Kanai, Tetsuya, Uzawa, Akiyuki, Kawaguchi, Naoki, Sakamaki, Tateo, Yoshiyama, Yasumasa, Himuro, Keiichi, Oda, Fumiko, Kuwabara, Satoshi

    Published in Journal of the neurological sciences (15-04-2016)
    “…Myasthenia gravis (MG) is an autoimmune disorder presumed to be associated with genetic susceptibility. This study aims to determine whether HLA is associated…”
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    Journal Article
  3. 3

    T cell epitopes of type II collagen in HLA-DRB10101 or DRB10405-positive Japanese patients with rheumatoid arthritis by Ohnishi, Yasuyuki, Tsutsumi, Akito, Sakamaki, Tateo, Sumida, Takayuki

    “…Rheumatoid arthritis (RA) is a T cell-mediated autoimmune disease, but target antigens (autoantigens) responsible for T cell activation remain unclear. Type II…”
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  4. 4

    DNA typing of HLA class II genes; DRB10803 increases the susceptibility of Japanese to primary biliary cirrhosis by Onishi, S, Sakamaki, T, Maeda, T, Iwamura, S, Tomita, A, Saibara, T, Yamamoto, Y

    Published in Journal of hepatology (1994)
    “…The association between human leukocyte antigens and primary biliary cirrhosis is controversial, but major histocompatibility complex class II antigen DR8 was…”
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  5. 5

    Association of HLA-DR, -DQ genotype and CTLA-4 gene polymorphism with Graves' disease in Japanese children by Iwama, Saika, Ikezaki, Ayako, Kikuoka, Noriko, Kim, Hye-Sook, Matsuoka, Hisafumi, Yanagawa, Tatsuo, Sato, Hirokazu, Hoshi, Mari, Sakamaki, Tateo, Sugihara, Shigetaka

    Published in Hormone research (01-01-2005)
    “…Childhood onset Graves' disease (GD) has been documented to be clinically distinct from adult onset GD, and an association with the genes encoding HLA and…”
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  6. 6
  7. 7

    Association of HLA-DR, DQ genotype with different β-cell functions at IDDM diagnosis in Japanese children by SUGIHARA, S, SAKAMAKI, T, KONDA, S, MURATA, A, WATAKI, K, KOBAYASHI, Y, MINAMITANI, K, MIYAMOTO, S, SASAKI, N, NIIMI, H

    Published in Diabetes (New York, N.Y.) (01-11-1997)
    “…Japanese IDDM patients have been demonstrated to have unique and different HLA associations from white patients. To elucidate the effect of HLA-associated…”
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  8. 8
  9. 9

    Involvement of platelet-derived growth factor and histocompatibility of DRB 1 in chronic renal allograft nephropathy by YAMADA, Kenichi, HATAKEYAMA, Emiko, SAKAMAKI, Tateo, NISHIMURA, Motonobu, ARITA, Seiji, SAKAMOTO, Kaoru, HAMAGUCHI, Kinichi, NAKAJIMA, Kazuaki, OTSUKA, Masaaki, TANABE, Kazunari

    Published in Transplantation (15-04-2001)
    “…The role of activated T cells in graft arteriosclerosis, which is observed in chronic renal allograft nephropathy, and the involvement of major…”
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  10. 10

    Retrovirus Produced by a Lymphoid Cell Line from an Infant with Acute Lymphoblastic Leukemia by MIKI, Takashi, SATO, Takeyuki, NAKAJIMA, Hironori, KOYAMA, Shigeko, TOYAMA, Yoshiro, FUSE, Akira, SUZUKI, Nobuo, KANNO, Harushige, SAKAMAKI, Tateo, KATO, Iwao

    “…A lymphoid cell line CK-a was established from peripheral blood of an infant with acute lymphoblastic leukemia of non-T, non-B cell type with mediastinal…”
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  11. 11

    Identification of the disease-related T cell epitope of ovalbumin and epitope-targeted T cell inactivation in egg allergy by Shimojo, N, Katsuki, T, Coligan, J E, Nishimura, Y, Sasazuki, T, Tsunoo, H, Sakamaki, T, Kohno, Y, Niimi, H

    “…An ovalbumin (OVA)-specific T cell line (TCL) was established from a patient with hen egg allergy. The TCL was CD4+, expressed alpha beta T cell receptor, and…”
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  12. 12

    A de novo deletion in the C1 inhibitor gene in a case of sporadic hereditary angioneurotic edema by Ariga, T, Hoshioka, A, Kohno, Y, Sakamaki, T, Matsumoto, S

    Published in Clinical immunology and immunopathology (01-10-1993)
    “…A sporadic case of hereditary angioneurotic edema (HANE) is reported here. The patient was a 15-year-old girl who for 4 years had suffered recurrent episodes…”
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