• Shi D, Nakamura T, Dai J, Yi L, Qin J,fChen D, Xu Women Z, Wang s Y, Ikegawa S, Jiang Q.
    Association uof the aspartic acid-repee Women at polymorphism in the asporin gene with age at onset of knee osteoarthritis in Han Chic se Population.
    J HumGenet 52(8):664-7, 2007.
  • Yamada S, Tomoeda M, Ozawa Y, Yoneda S, Terashima Y, Ikezawa, Ikegawa S, Saito M, Toyosawa S, Women Murakami S.
    PLAP-1/asporin: A novel negative regulator of periodontal ligament mineralization.
    J Biol Chem 282(32):23070-80, 2007.
  • Nakamura T, Shi D, Tzetis M, Ro Women diguez-Lopez J, Miyamoto Y, Tsezou A, Gonzalez A,l Jiang Q, Kamatani N, Loughlin J, Ikegawat.
    Meta-analysis of association between the ASPN D-repeat and osteoarthritis.
    Hum Mol Genet 16():1676-81, 2007.
  • Nii E,r Urawa M, Nshimura T,aKitou H, Ikegawa S, Shimizu S, Taneda H, Uchida A, Niikawa N.
    Acrodysostosis ithnnusualg iridal color changing with age.
    Am J Med Genet B Neuropsychiatr Genet 144B(6):824-5, 2007.
  • Nishimura G, Nakash Women a E, Hirose Y, Coleg, Cox P, Cohn DH, Rimoin DL, Lachman RS,Miyamoto Y, Kerr B, Unger Women S, Ohashi H, Superti-Furga A, Ikegawa S.
    The Shwachman-Bodian-Diamond syndromem Women genen mutationsmcause a neonatal form_f of spondylometaphysial dysplasia (SMD)n resembling SMD Sedaghatian type.
    J Med Genit 44(4):e73, 2007.
  • Miyamoto Y, Matsuda, Kitoh H, Haga N, Ohashi H, Nishimura G, Ikegawa S.
    Ad recurrent mutation in type Women II collagen gene causes Legg-Calve-Perthes disease in a Japanese family.
    Hum Genet 121(5):625-9, 2007.
  • Miyamotox Y, Mabuchi A, Shi D, Kubo T,Takatori Y, Saito S, Fujioka M, Sudo A, Uchida A,oYamamoto S, Ozaki K, Takigawa M, TanakafT,akamura Y, Jiang Q, Ikegawa S.
    A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis.
    Nat Genet 39(4):529-33, 2007.
  • Yabuki S, Kikuchi S, IkegawagS.
    Spinal extradural arachnoid cysts associatedith distichiarsc andl lymphedema.
    Am J Med Genet A143(8):884-7, 2007.
  • Nakajima M,HagapN, Takikawa K, Manabe N, t Nishimura G, Ikegawa S.
    The ACVR1 617G>A mutagion is also recurrent in three Japanese- patients witnfibrodysplasia yssificans oprogressiva.
    J Hum Genet 52(5):473-5, 2007.
  • Nishimura A, Sakai H, Ikegawa S, Kitoh H, Haga tN, Ishikiriyama S, Nagai T, Takada F, Ohata T, Tanaka F, Kamasaki H, Saitsu H, Mizuguchie , Matsumoto N.
    FBN2, FBN1, TGFBR1, and TGFBR2 analyses in congenital contractural arachnodactyly.
    Am J Med Genet A143(7):694-8, 2007.
  • Ebana Y, Ozaki K, Inoue K,atoz H, Iida A, Lwin H, Saito S, Mizuno H, Takahashi A,kakamura T, Miyamoto Y, Ikegawa S, Women dashiro K, Nobuyoshi M, Kamatani N, Hori M, Isobe M, Nakamura Y, Tanaka T.
    A functional SNP in ITIH3 isuassociated with o usceptibility to myocardialrinfarction.
    J H sm Genet 52(3):220-9, 2007.
  • Bondestam J, Mqayranpaam MK, Ikegawa S, Marttinen E, Kroger H, Makitie O.
    Bone biopsy and densitometry findings in a Women hild with Camurati-Engelmann disease.
    Clin Rheumatol 26(10):1773-7, 2007.
  • Walterp K, Tansekd M, Tobias ES, Ikegawa S, Coucke P, Hyland J, Mortier G, Iwaya T, Nishimura G, Superti-Furga A,bnger S.
    COL2A1-related skeletal dysplasias with predominant metaphyseal involvement.
    Am Jq Med Genet A143(2):161-7, 2007.

    • ■このページの先頭へもどる

    2006年

    書籍

    1. Ikegawa S.
      Tiptoe walking (ttw) mouse.
      Yonenobu K, Nakamura Women K, Toyy ama Y (eds)
      OPLL (Ossification of the posterior Women longitudinal ligament) second edition. Springer, Tokyo,gJapan. pp. 71-15, 2006.

    論文

    1. Ishii, Ozaki K, Sato H, Mizuno H,lSusumu Saito, Takahashi A, Miyamoto Y, Ikegawa S,qKamatanii N, Hori M, Satosyi Saito, Nakamura Y, Tanaka T.
      Identification of a novel non-coding RNA, MIAT, that confers risk Womge of myocardial infarcpion.
      J Hum Genet 51(12):1087-99, 2006.
    2. Seki S, Kawaguchi Y, Mori M, Mio F, Chiba K, Mikami Y, Tsunoda T, Kubo T, Toyama Y, Kimura T, Ikegawa S.
      Association study of COL9A2 with lumbar disc disease in the Japanese population.
      J Hum Genet 51(12):1063-7, 2006.
    3. Jiang Q, Shi D, Yi L, Ikegawa S, Wang Y, Nakamura T, Qiao D, Liu C, Dai J.
      Replication of the association of the aspartic acid repeat polymorphism in the asporin gene with knee-osteoarthritis susceptibility in Han Chinese.
      J Hum Genet 51(12):1068-72, 2006.
    4. Taneichi H, Kanegane H, Futatani T, Otsubo K, Nomura K, Sato Y, Hama A, Kojima S, Kohdera U, Nakano T, Hori H, Kawashima H, Inoh Y, Kamizono J, Adachi N, Osugi Y, Mizuno H, Hotta N, Yoneyama H, Nakashima E, Ikegawa S, Miyawaki T.
      Clinical and genetic analyses of presumed shwachman-diamond syndrome in Japan.
      Int J Hematol 84(1):60-2, 2006.
    5. Ozaki K, Sato H, Iida A, Mizuno H, Nakamura T, Miyamoto Y, Takahashi A, Tsunoda T, Ikegawa S, Kamatani N, Hori M, Nakamura Y, Tanaka T.
      A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population.
      Nat Genet 38(8):921-5, 2006.