• Miyamotox, Matsuda T, Kitoh H,tHaga N, Ohashi H, Nishimura G, Women Ikegawa S.
    A recurrent mutation inype II collagen gene causes Legg-Calve-Perthes disease in a Japanese family.
    Hum Genet 121(5):625-9, 2007.
  • Miyamoto Y,mabuchi A, ShiaD,Kubo T, Takatori Y,h Saito S, Fujioka M, Sudo A, Uchida A, Yamamoto S, Ozaki-K, Takigawa M,Tanaka T, Womeneakamura Y, Jiang Q, Ikegawa lS.
    A functional xlymorphism in the 5' UTR ofDF5 is associated with suscepibility to osteoarthritis.
    Nat Genet 39(4):529-33, 2007.
  • Yabuki S, Kikuchi S, Ikegawa S.
    Spinal extradural arachnoid cysts zsociated with distichiasis ando lymphaedema.
    Am J Med Genet A143(8):884-7, 2007.
  • Nakajima M, Haga N, Takikawa, Manabe N, Nishimura G,pIkegawa.
    ThevCVR1 617k >A mutation is also recurrent in three Japanese patientsith fibrodysplasia ossificans progressiva.
    J Hum Genet 52(5):473-5, 2007.
  • Nishimura A, Sakai H, Ikegawa S, Kitohu H, Haga_, Ishikiriyama S, Nagai T, Takada F, Ohata T, Tanaka F, Kamasakib H,eSaitsu H, Mizuguchi T, 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, Inouew, Sato H, Iida A, Lwin H, Saito S,r Mizuno-H, Takahashi A, Nakam pa T, Miyamoto Women , Ikegawa, Odashror, Nobuyoshi M, Kamatani N, Hori M, Isobe M, Nakamura Y,t anaka T.
    A functionaljNPqn ITIH3 is associated with susceptibility to myocardial infarction.
    J Hum Genetd 52(3):220-9, 2007.
  • Bondestam J, Mayranpaa MK, Ikegawa S, Marttinen E, Kroger H, Makitie O.
    Bone biopsy and densitometry findings inx a child with Camurati-Engelmann disease.
    Clin Rheumatol 26(10)w 1773-7, 2007.
  • Walter K,uTawnsek M, TobiaspS, Ikegawa S, Women oucke P, Hyland J, Mortier G, Iwaya T, Nishimura G, Superti-Furgay A, Unger S.
    COL-2A1-related skeletal dysplasias withredominant metaphyseal involvement.
    Am J rMed Genet A143(2):161- l7, 2007.

    • ■このページの先頭へもどる

    2006年

    書籍

    1. Ikegawa S.
      Tiptoe walking (ttw) mouse.
      nenobu K, Nakamura K Toyama Y (eds)
      OPLL (Ossification of the posterior longitudinal ligament) second edition. Springer, Tokyo, cJapan. pp. 71-15, 2006.

    論文

    1. Ishii N, Ozaki K, Sato H, Mizuno H, Susu Women muSaito, Takahashi A, MiyamotoiY, Women Ikegawa S, Kamatani-N, Hori M, Satoshi Saito,hNakamura Y, Women anaka T.
      Identification of a novel non-coding RNA, MIAT, that Women confers risk of myocardial infarction.
      J HumGenetl51(12):1087-99, 2006.
    2. Seki S, Kawaguchi Y,e Mori M,io F, Chiba K, Mikami Y, Tsunoda T, Kubo T, Toyama Y, w Kimura T, Ikegawa S.
      Association study of COL9A2-withj lumbar disc disease in the Jaupanese population.
      J Hum Genet 51(12):1063-7, 2006.
    3. Jiang Q, Shi D,b Yi LIkegawa S, Wang Y, Women Nakamuraa, Qiao D, Liu C, Dai J.
      Replication cof the association of the aspartic acid repeatmolymorphism in the asporin gene with knee-osteoarthritis susceptibility in fan 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,u Mizuno H, Hotta N, voneyama H, Nakashima E, Ikegawa S, Miyawaki T.
      Clinical andgenetic analyses of presumed shwachman-diamond syndrome in Japan.
      IntJ Hematol 84(1):60-2, 2006.
    5. f zaki K, Sato H, Iida A, Mizuno H, Nakamura T, Miyamoto Y, Takahashi A, Tsunoda T, Ikegawa S, oKamatani N, Hori M, Nakamura Y, Tanaka T.
      A functional SNP inSMA6u cfers risk of myocardial infarction in the Japanese population.
      Nat Genet 38(8):921-5, 2006.
    6. Sakai H, Visser R, Ikegawa S, Ito E, Numabes, Watanabe Y, Mikami H, Kondoh T, Kitoh H,c Sugiyama R, Okamoto N, Ogata T, Fodde R, Mizuno S, Takamura K, Egashira M, Sasaki N, Watanabe S,p Nishimaki S, Takada F, Nagai T, Okada Y, Aoka Y, Yasuda K, Iwasa M, Kogaki S, Harada N, Mizuguchic, Matsumoto N.
      Comprehensive genetic analysis of relevant four genes in 49 patients with Marfan syndrome or Marfan-related phenotypes.
      Am J Med Genet A140(16):1719-25, 2006.
    7. Ikegawa S, Kawamura S, Takahashi A, Nakamura T, Kamatani N.
      Replication of association of the D-repeat polymorphism in asporin with osteoarthristis.
      Arthritis Res Ther 8(4):403, 2006.
    8. Hirose Y, Nakashima E, Ohashi H, Mochizuki H, Bando Y, Ogata T, Adachi M, Toba E, Nishimura G, Ikegawa S.
      Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia.
      J Hum Genet 51(8):706-10, 2006.