Yasuhide Hayashi

Overview

Best Publications

• Oncogenic mutations of ALK kinase in neuroblastoma.

  Yuyan Chen;Junko Takita;Young Lim Choi;Motohiro Kato

  1058
  Citations

• Charcot-Marie-Tooth Disease Type 2A Caused by Mutation in a Microtubule Motor KIF1Bβ

  Chunjie Zhao;Junko Takita;Yosuke Tanaka;Mitsutoshi Setou

  927
  Citations

• Frequent inactivation of A20 in B-cell lymphomas

  Motohiro Kato;Masashi Sanada;Itaru Kato;Yasuharu Sato

  672
  Citations

• Gain-of-function of mutated C-CBL tumour suppressor in myeloid neoplasms.

  Masashi Sanada;Takahiro Suzuki;Lee-Yung Shih;Makoto Otsu

  476
  Citations

• The landscape of somatic mutations in Down syndrome-related myeloid disorders

  Kenichi Yoshida;Tsutomu Toki;Yusuke Okuno;Rika Kanezaki

  441
  Citations

• LCX, Leukemia-associated Protein with a CXXC Domain, Is Fused to MLL in Acute Myeloid Leukemia with Trilineage Dysplasia Having t(10;11)(q22;q23)

  Ryoichi Ono;Tomohiko Taki;Takeshi Taketani;Masafumi Taniwaki

  397
  Citations

• An RNA-binding Protein Gene, TLS/FUS , Is Fused to ERG in Human Myeloid Leukemia with t(16;21) Chromosomal Translocation

  Hitoshi Ichikawa;Kimiko Shimizu;Yasuhide Hayashi;Misao Ohki

  355
  Citations

• Adenoviral E1A-associated protein p300 is involved in acute myeloid leukemia with t(11;22)(q23;q13).

  Kohmei Ida;Issay Kitabayashi;Tomohiko Taki;Masafumi Taniwaki

  352
  Citations

• The t(11;16)(q23;p13) translocation in myelodysplastic syndrome fuses the MLL gene to the CBP gene.

  Tomohiko Taki;Masahiro Sako;Masahiro Tsuchida;Yasuhide Hayashi

  346
  Citations

• FLT3 mutations in the activation loop of tyrosine kinase domain are frequently found in infant ALL with MLL rearrangements and pediatric ALL with hyperdiploidy

  Takeshi Taketani;Tomohiko Taki;Kanji Sugita;Yoshiyuki Furuichi

  302
  Citations

• An Inv(16)(p13.3q24.3)-encoded CBFA2T3-GLIS2 fusion protein defines an aggressive subtype of pediatric acute megakaryoblastic leukemia.

  Tanja A. Gruber;Amanda Larson Gedman;Jinghui Zhang;Cary S. Koss

  283
  Citations

• The Partner Gene of AML1 in t(16;21) Myeloid Malignancies Is a Novel Member of the MTG8(ETO) Family

  Toshie Gamou;Eiko Kitamura;Fumie Hosoda;Kimiko Shimizu

  282
  Citations

• Tandem duplication of the FLT3 gene is found in acute lymphoblastic leukaemia as well as acute myeloid leukaemia but not in myelodysplastic syndrome or juvenile chronic myelogenous leukaemia in children.

  F. Xu;T. Taki;H. W. Yang;R. Hanada

  267
  Citations

• Spontaneous regression of localized neuroblastoma detected by mass screening.

  Keiko Yamamoto;Ryoji Hanada;Akira Kikuchi;Masataka Ichikawa

  264
  Citations

• KIT mutations, and not FLT3 internal tandem duplication, are strongly associated with a poor prognosis in pediatric acute myeloid leukemia with t(8;21): a study of the Japanese Childhood AML Cooperative Study Group

  Akira Shimada;Tomohiko Taki;Ken Tabuchi;Akio Tawa

  257
  Citations

• Establishment of a human leukaemic cell line (CMK) with megakaryocytic characteristics from a Down's syndrome patient with acute megakaryoblastic leukaemia

  Takeyuki Sato;Akira Fuse;Mitsuoki Eguchi;Yasuhide Hayashi

  249
  Citations

• The inv(11)(p15q22) Chromosome Translocation of De Novo and Therapy-Related Myeloid Malignancies Results in Fusion of the Nucleoporin Gene, NUP98, With the Putative RNA Helicase Gene, DDX10

  Yasuhito Arai;Fumie Hosoda;Hirofumi Kobayashi;Kyoko Arai

  240
  Citations

• Frequent mutations in the GATA-1 gene in the transient myeloproliferative disorder of Down syndrome.

  Gang Xu;Masumi Nagano;Rika Kanezaki;Tsutomu Toki

  231
  Citations

• Defect of histone acetyltransferase activity of the nuclear transcriptional coactivator CBP in Rubinstein–Taybi syndrome

  Takashi Murata;Riki Kurokawa;Anna Krones;Ken Tatsumi

  227
  Citations

• Fbxw7 acts as a critical fail-safe against premature loss of hematopoietic stem cells and development of T-ALL

  Sahoko Matsuoka;Yuichi Oike;Yuichi Oike;Ichiro Onoyama;Atsushi Iwama

  211
  Citations