Masafumi Matsuo

Overview

Best Publications

• Effect of the mutation (C3435T) at exon 26 of the MDR1 gene on expression level of MDR1 messenger ribonucleic acid in duodenal enterocytes of healthy Japanese subjects

  Tsutomu Nakamura;Toshiyuki Sakaeda;Masanori Horinouchi;Takao Tamura

  385
  Citations

• Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.

  Yasuhiro Takeshima;Mariko Yagi;Yo Okizuka;Hiroyuki Awano

  287
  Citations

• Insertion of a 5' truncated L1 element into the 3' end of exon 44 of the dystrophin gene resulted in skipping of the exon during splicing in a case of Duchenne muscular dystrophy.

  N Narita;H Nishio;Y Kitoh;Y Ishikawa

  274
  Citations

• Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.

  M Matsuo;T Masumura;H Nishio;T Nakajima

  253
  Citations

• Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy.

  Christophe Béroud;Sylvie Tuffery-Giraud;Masafumi Matsuo;Dalil Hamroun

  241
  Citations

• Autonomous regulation of osteosarcoma cell invasiveness by Wnt5a/Ror2 signaling

  M Enomoto;S Hayakawa;S Itsukushima;D Y Ren

  219
  Citations

• Auditory nerve and brainstem responses in newborn infants with hyperbilirubinemia.

  Hajime Nakamura;Satoshi Takada;Roberto Shimabuku;Masafumi Matsuo

  190
  Citations

• Rituximab treatment for posttransplant lymphoproliferative disorder (PTLD) induces complete remission of recurrent nephrotic syndrome.

  Kandai Nozu;Kazumoto Iijima;Masato Fujisawa;Atsuko Nakagawa

  188
  Citations

• Real-Time Quantitative Polymerase Chain Reaction for MDR1, MRP1, MRP2, and CYP3A-mRNA Levels in Caco-2 Cell Lines, Human Duodenal Enterocytes, Normal Colorectal Tissues, and Colorectal Adenocarcinomas

  Tsutomu Nakamura;Toshiyuki Sakaeda;Nobuko Ohmoto;Takao Tamura

  187
  Citations

• Genetic origins of the Ainu inferred from combined DNA analyses of maternal and paternal lineages

  Atsushi Tajima;Masanori Hayami;Katsushi Tokunaga;Takeo Juji

  170
  Citations

• Effects of polymorphisms of MDR1, MRP1, and MRP2 genes on their mRNA expression levels in duodenal enterocytes of healthy Japanese subjects.

  Yuka Moriya;Yuka Moriya;Tsutomu Nakamura;Masanori Horinouchi;Toshiyuki Sakaeda

  166
  Citations

• Intravenous infusion of an antisense oligonucleotide results in exon skipping in muscle dystrophin mRNA of Duchenne muscular dystrophy.

  Yasuhiro Takeshima;Mariko Yagi;Hiroko Wada;Kazuto Ishibashi

  165
  Citations

• Oligonucleotides against a splicing enhancer sequence led to dystrophin production in muscle cells from a Duchenne muscular dystrophy patient

  Yasuhiro Takeshima;Hiroko Wada;Mariko Yagi;Yukitoshi Ishikawa

  156
  Citations

• Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity

  Yosuke Harada;Retno Sutomo;Ahmad Hamim Sadewa;Tomoko Akutsu

  150
  Citations

• Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphoma

  Hiroyuki Imanishi;Noboru Okamura;Mariko Yagi;Yukari Noro

  149
  Citations

• Circadian clock genes directly regulate expression of the Na(+)/H(+) exchanger NHE3 in the kidney.

  Mohammad Saifur Rohman;Noriaki Emoto;Hidemi Nonaka;Ryusuke Okura

  141
  Citations

• Chimeric RNA/ethylene-bridged nucleic acids promote dystrophin expression in myocytes of duchenne muscular dystrophy by inducing skipping of the nonsense mutation-encoding exon.

  Agus Surono;Tran Van Khanh;Yasuhiro Takeshima;Hiroko Wada

  126
  Citations

• Early pathogenesis of Duchenne muscular dystrophy modelled in patient-derived human induced pluripotent stem cells

  Emi Shoji;Hidetoshi Sakurai;Tokiko Nishino;Tatsutoshi Nakahata

  119
  Citations

• Molecular analysis of digenic inheritance in Bartter syndrome with sensorineural deafness

  K Nozu;T Inagaki;X J Fu;Y Nozu

  114
  Citations

• Chemical treatment enhances skipping of a mutated exon in the dystrophin gene.

  Atsushi Nishida;Naoyuki Kataoka;Yasuhiro Takeshima;Mariko Yagi

  107
  Citations