N
Naomi Kondo
Researcher at Gifu University
Publications - 385
Citations - 9254
Naomi Kondo is an academic researcher from Gifu University. The author has contributed to research in topics: Zellweger syndrome & Peroxisome. The author has an hindex of 47, co-authored 384 publications receiving 8807 citations. Previous affiliations of Naomi Kondo include Heisei College of Health Sciences.
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Journal ArticleDOI
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,Kazunaga Agematsu,Shigeru Tsuchiya,Hidetoshi Takada,Toshiro Hara,Nobuaki Kawamura,Tadashi Ariga,Hideo Kaneko,Naomi Kondo,Ikuya Tsuge,Akihiro Yachie,Yukio Sakiyama,Tsutomu Iwata,Fumio Bessho,Tsutomu Oh-ishi,Kosuke Joh,Kohsuke Imai,Kazuhiro Kogawa,Miwa Shinohara,Mikiya Fujieda,Hiroshi Wakiguchi,Srdjan Pasic,Mario Abinun,Hans D. Ochs,Eleonore D. Renner,Eleonore D. Renner,Annette Jansson,Bernd H. Belohradsky,Ayse Metin,Norio Shimizu,Shuki Mizutani,Toshio Miyawaki,Shigeaki Nonoyama,Hajime Karasuyama +36 more
TL;DR: It is demonstrated that Tyk2 plays obligatory roles in multiple cytokine signals involved in innate and acquired immunity of humans, which differs substantially fromTyk2 function in mice.
Journal ArticleDOI
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,Maho Hamasaki,Kamran Ghaedi,Ronald J.A. Wanders,Yasuyuki Suzuki,Naomi Kondo,Yukio Fujiki +9 more
TL;DR: It is suggested that the C-terminal part, including the CAAX homology box, is required for the biological function of Pex19p, which is apparently involved at the initial stage in peroxisome membrane assembly, before the import of matrix protein.
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Selective utilization of nonhomologous end-joining and homologous recombination DNA repair pathways during nervous system development.
TL;DR: Different tissue- and cell-type requirements for each DNA DSB repair pathway during neural development are revealed and insights for understanding the contributions of DNA D SB responses to disease are provided.
Journal ArticleDOI
Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
Masanori Honsho,Shigehiko Tamura,Nobuyuki Shimozawa,Yasuyuki Suzuki,Naomi Kondo,Yukio Fujiki +5 more
TL;DR: Results demonstrate that mutation in PEX16 is the genetic cause of CG-D PBDs, and expression morphologically and biochemically restored peroxisome biogenesis only in fibroblasts from a patient with ZS in Japan.
Journal ArticleDOI
Molecular cloning of cdna encoding rat very long-chain acyl-coa synthetase
Atsushi Uchiyama,Toshifumi Aoyama,Keiju Kamijo,Yasushi Uchida,Naomi Kondo,Tadao Orii,Takashi Hashimoto +6 more
TL;DR: The cDNA encoding rat very long-chain acyl-CoA synthetase (VLACS) was cloned, using degenerative primers synthesized according to the partial amino acid sequences of the peptide fragments of the purified rat liver enzyme to characterize the cDNA and the enzyme.