Naomi Kondo

Overview

Best Publications

• Human Tyrosine Kinase 2 Deficiency Reveals Its Requisite Roles in Multiple Cytokine Signals Involved in Innate and Acquired Immunity

  Yoshiyuki Minegishi;Masako Saito;Tomohiro Morio;Ken Watanabe

  804
  Citations

• Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

  Yuji Matsuzono;Naohiko Kinoshita;Shigehiko Tamura;Nobuyuki Shimozawa

  284
  Citations

• Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.

  Kenji E. Orii;Youngsoo Lee;Naomi Kondo;Peter J. McKinnon

  239
  Citations

• Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

  Masanori Honsho;Shigehiko Tamura;Nobuyuki Shimozawa;Yasuyuki Suzuki

  227
  Citations

• MOLECULAR CLONING OF CDNA ENCODING RAT VERY LONG-CHAIN ACYL-COA SYNTHETASE

  Atsushi Uchiyama;Toshifumi Aoyama;Keiju Kamijo;Yasushi Uchida

  221
  Citations

• Enzymes of ketone body utilization in human tissues: protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases.

  Fukao T;Song Xq;Mitchell Ga;Yamaguchi S

  202
  Citations

• STXBP1 mutations in early infantile epileptic encephalopathy with suppression‐burst pattern

  Hirotomo Saitsu;Mitsuhiro Kato;Ippei Okada;Kenji E. Orii

  164
  Citations

• Functional link between BLM defective in Bloom's syndrome and the ataxia-telangiectasia-mutated protein, ATM.

  Heather Beamish;Padmini Kedar;Hideo Kaneko;Philip Chen

  154
  Citations

• d-3-Hydroxyacyl-CoA Dehydratase/d-3-Hydroxyacyl-CoA Dehydrogenase Bifunctional Protein Deficiency: A Newly Identified Peroxisomal Disorder

  Yasuyuki Suzuki;Ling Ling Jiang;Masayoshi Souri;Shoko Miyazawa

  150
  Citations

• Roles of anti-hemagglutinin IgA and IgG antibodies in different sites of the respiratory tract of vaccinated mice in preventing lethal influenza pneumonia

  Reiko Ito;Yasuko Asahi Ozaki;Tomoki Yoshikawa;Hideki Hasegawa

  148
  Citations

• The structural basis for receptor recognition of human interleukin-18

  Naotaka Tsutsumi;Takeshi Kimura;Kyohei Arita;Mariko Ariyoshi

  146
  Citations

• Mutations in PEX10 Is the Cause of Zellweger Peroxisome Deficiency Syndrome of Complementation Group B

  Kanji Okumoto;Ryota Itoh;Nobuyuki Shimozawa;Yasuyuki Suzuki

  140
  Citations

• PEX12, the Pathogenic Gene of Group III Zellweger Syndrome: cDNA Cloning by Functional Complementation on a CHO Cell Mutant, Patient Analysis, and Characterization of Pex12p

  Kanji Okumoto;Nobuyuki Shimozawa;Atsusi Kawai;Shigehiko Tamura

  140
  Citations

• Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

  Shigehiko Tamura;Kanji Okumoto;Ryusuke Toyama;Nobuyuki Shimozawa

  130
  Citations

• Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.

  S. Fukuda;N. Shimozawa;Y. Suzuki;Z. Zhang

  130
  Citations

• Succinyl-CoA: 3-ketoacid CoA transferase (SCOT): Cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations

  Toshiyuki Fukao;Grant A. Mitchell;Xiang-Qian Song;Haruki Nakamura

  127
  Citations

• Mouse model of N-acetylgalactosamine-6-sulfate sulfatase deficiency (Galns−/−) produced by targeted disruption of the gene defective in Morquio A disease

  Shunji Tomatsu;Koji O. Orii;Carole Vogler;Jun Nakayama

  127
  Citations

• Lymphocyte responses to food antigens in patients with atopic dermatitis who are sensitive to foods

  Naomi Kondo;Hiroatsu Agata;Osamu Fukutomi;Fumiaki Motoyoshi

  123
  Citations

• The clinical phenotype and outcome of mitochondrial acetoacetyl-CoA thiolase deficiency (beta-ketothiolase or T2 deficiency) in 26 enzymatically proved and mutation-defined patients.

  Toshiyuki Fukao;Charles R. Scriver;Naomi Kondo

  123
  Citations

• Autoantibodies and cell-mediated autoimmunity to NMDA-type GluRepsilon2 in patients with Rasmussen's encephalitis and chronic progressive epilepsia partialis continua.

  Yukitoshi Takahashi;Hisashi Mori;Masayoshi Mishina;Masahiko Watanabe

  122
  Citations