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Tomoko Nagase

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Sachi Kozawa; Tomoko Nagase; Shigeru Nakashima; Hideki Nikami; Yukio Okano; Ayako Honda; Naomi Kajiwara; Yasuhiko Takemoto; Nobuyuki Shimozawa
Induction of peroxisomal lipid metabolism in mice fed a high-fat diet.
Nobuyuki Shimozawa; Ayako Honda; Naomi Kajiwara; Sachi Kozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki
X-linked adrenoleukodystrophy: diagnostic and follow-up system in Japan.
Hiroko Horikoshi; Zenichiro Kato; Mitsuo Masuno; Takahiko Asano; Tomoko Nagase; Yuka Yamagishi; Ryo Kozawa; Takahiro Arai; Minako Aoki; Takahide Teramoto; Kentaro Omoya; Naomichi Matsumoto; Naohiro Kurotaki; Osamu Shimokawa; Kenji Kurosawa; Naomi Kondo
Neuroradiologic findings in Sotos syndrome.

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2011: Sachi Kozawa; Tomoko Nagase; Shigeru Nakashima; Hideki Nikami; Yukio Okano; Ayako Honda; Naomi Kajiwara; Yasuhiko Takemoto; Nobuyuki Shimozawa
Induction of peroxisomal lipid metabolism in mice fed a high-fat diet.
Molecular medicine reports 2011;4(6):1157-62.
2011: Nobuyuki Shimozawa; Ayako Honda; Naomi Kajiwara; Sachi Kozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki
X-linked adrenoleukodystrophy: diagnostic and follow-up system in Japan.
Journal of human genetics 2011;56(2):106-9.
2006: Hiroko Horikoshi; Zenichiro Kato; Mitsuo Masuno; Takahiko Asano; Tomoko Nagase; Yuka Yamagishi; Ryo Kozawa; Takahiro Arai; Minako Aoki; Takahide Teramoto; Kentaro Omoya; Naomichi Matsumoto; Naohiro Kurotaki; Osamu Shimokawa; Kenji Kurosawa; Naomi Kondo
Neuroradiologic findings in Sotos syndrome.
Journal of child neurology 2006;21(7):614-8.
2006: Michinori Funato; Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki; Yoshihiko Imamura; Tadashi Matsumoto; Toshiro Tsukamoto; Tomoko Kojidani; Takashi Osumi; Toshiyuki Fukao; Naomi Kondo
Aberrant peroxisome morphology in peroxisomal beta-oxidation enzyme deficiencies.
Brain & development 2006;28(5):287-92.
2005: Kazuyuki Hashimoto; Zenichiro Kato; Tomoko Nagase; Nobuyuki Shimozawa; Kazuo Kuwata; Kentaro Omoya; Ailian Li; Eiji Matsukuma; Yutaka Yamamoto; Hidenori Ohnishi; Hidehito Tochio; Masahiro Shirakawa; Yasuyuki Suzuki; Ronald J A Wanders; Naomi Kondo
Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder.
Pediatric research 2005;58(2):263-9.
2005: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Michinori Funato; Naomi Kondo; Yasuyuki Suzuki
Molecular and neurologic findings of peroxisome biogenesis disorders.
Journal of child neurology 2005;20(4):326-9.
2004: Nobuyuki Shimozawa; Toshiro Tsukamoto; Tomoko Nagase; Yasuhiko Takemoto; Naoki Koyama; Yasuyuki Suzuki; Masayuki Komori; Takashi Osumi; Gootjes Jeannette; Ronald J A Wanders; Naomi Kondo
Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene.
Human mutation 2004;23(6):552-8.
2004: Tomoko Nagase; Nobuyuki Shimozawa; Yasuhiko Takemoto; Yasuyuki Suzuki; Masayuki Komori; Naomi Kondo
Peroxisomal localization in the developing mouse cerebellum: implications for neuronal abnormalities related to deficiencies in peroxisomes.
Biochimica et biophysica acta 2004;1671(1-3):26-33.
2003: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Toshihiro Ohura; Yasuyuki Suzuki; Naomi Kondo
Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation.
American journal of medical genetics. Part A 2003;120A(1):40-3.
2003: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki; Naomi Kondo
Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene.
Advances in experimental medicine and biology 2003;544():71.
2002: Naomi Kondo; Takahide Teramoto; Ryosuke Inoue; Osamu Fukutomi; Eiko Matsui; Shinji Shinoda; Mizuho Watanabe; Heima Sakaguchi; Minako Aoki; Wataru Morimoto; Kiyotaka Suzuki; Hidenori Ohnishi; Yasuhiko Takemoto; Yoko Tanaka; Tsutomu Asano; Kaori Yoshikawa; Tomoko Nagase; Kazuyuki Hashimoto; Yukiko Fujita; Yutaka Yamamoto; Airen Ri; Khoichirou Hirayama
[Evaluation before and after pranlukast administration with the QOL questionnaire (revised version 2001) for pediatric patients with bronchial asthma and their parents or caregivers].
Arerugī = [Allergy] 2002;51(5):421-9.
2002: Nobuyuki Shimozawa; Tomoko Nagase; Yasuhiko Takemoto; Yasuyuki Suzuki; Yukio Fujiki; Ronald J A Wanders; Naomi Kondo
A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.
Biochemical and biophysical research communications 2002;292(1):109-12.