小松 代表的な論文業績

  • Ding J, Komatsu H, Iida S, Yano H, Kusumoto S, Inagaki A, Mori F, Ri M, Ito A, Wakita A, Ishida T, Nitta M, Ueda R. The Asn505 mutation of the c-MPL gene, which causes familial essential thrombocythemia, induces autonomous homodimerization of the c-Mpl protein due to strong amino acid polarity. Blood. 2009 Oct 8;114(15):3325-8.
  • Ding J, Komatsu H, Wakita A, Kato-Uranishi M, Ito M, Satoh A, Tsuboi K, Nitta M, Miyazaki H, Iida S, Ueda R. Familial essential thrombocythemia associated with a dominant-positive activating mutation of the c-MPL gene, which encodes for the receptor for thrombopoietin. Blood. 103(11):4198-200, 2004.
  • Hayami Y, Komatsu H, Iida S, Utsunomiya A, Hanada S, Hua XJ, Huiping N, Harada S, Tsuboi K, Banno S, Wakita A, Kato T, Ueda R. Microsatellite instability as a potential marker for poor prognosis in adult T cell leukemia/lymphoma. Leuk Lymphoma. 32(3-4):345-9, 1999.
  • Harada S, Komatsu H, Seto M, Ni H, Xu JH, Hayami Y, Tsuboi K, Wakita A, Nitta M, Kato T, Ueda R. Microsatellite instability is rare in the clinical course of myelodysplastic syndrome studied with DNA from fresh and paraffin-embedded tissues. J Cancer Res Clin Oncol. 124(5):231-5, 1998.
  • Ni H, Nitta M, Komatsu H, Kojima S, Suzuki S, Harada S, Tsuboi K, Banno S, Wakita A, Yazaki M, Ren L, Kato T, Ueda R. Detection of bcr/abl fusion transcripts by semiquantitative multiplex RT-PCR combined with a colormetric assay in Ph positive leukemia. Cancer Lett. 124(2):173-80, 1998.
  • Komatsu H, Iida S, Yamamoto K, Mikuni C, Nitta M, Takahashi T, Ueda R, Seto M. A variant chromosome translocation at 11q13 identifying PRAD1/cyclin D1 as the BCL-1 gene. Blood. 84(4):1226-31, 1994.
  • Komatsu H, Yoshida K, Seto M, Iida S, Aikawa T, Ueda R, Mikuni C. Overexpression of PRAD1 in a mantle zone lymphoma patient with a t(11;22)(q13;q11) translocation. Br J Haematol. 85(2):427-9, 1993.