High-dose thiamine prevents brain lesions and prolongs survival of Slc19a3-deficient mice
Suzuki, Kaoru, Yamada, Kenichiro, Fukuhara, Yayoi, Tsuji, Ai, Shibata, Katsumi, Wakamatsu, Nobuaki
Published in PloS one (30.06.2017)
Published in PloS one (30.06.2017)
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Journal Article
Lateral neck pain as a symptom of severe sinusitis: A case report
Asano, Satoshi, Fukushima, Naoya, Tsuzuki, Nobuyoshi, Nakamura, Akiyoshi, Yamada, Kenichiro
Published in Pediatrics international (01.05.2021)
Published in Pediatrics international (01.05.2021)
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Journal Article
Lipidomics analysis revealed the phospholipid compositional changes in muscle by chronic exercise and high-fat diet
Goto-Inoue, Naoko, Yamada, Kenichiro, Inagaki, Akiko, Furuichi, Yasuro, Ogino, Shinya, Manabe, Yasuko, Setou, Mitsutoshi, Fujii, Nobuharu L.
Published in Scientific reports (20.11.2013)
Published in Scientific reports (20.11.2013)
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Journal Article
Isozyme-Specific Role of SAD-A in Neuronal Migration During Development of Cerebral Cortex
Nakanishi, Keiko, Niida, Hiroyuki, Tabata, Hidenori, Ito, Tsuyoshi, Hori, Yuki, Hattori, Madoka, Johmura, Yoshikazu, Yamada, Chisato, Ueda, Takashi, Takeuchi, Kosei, Yamada, Kenichiro, Nagata, Koh-Ichi, Wakamatsu, Nobuaki, Kishi, Masashi, Pan, Y Albert, Ugawa, Shinya, Shimada, Shoichi, Sanes, Joshua R, Higashi, Yujiro, Nakanishi, Makoto
Published in Cerebral cortex (New York, N.Y. 1991) (14.08.2019)
Published in Cerebral cortex (New York, N.Y. 1991) (14.08.2019)
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Journal Article
The effect of rapamycin, NVP-BEZ235, aspirin, and metformin on PI3K/AKT/mTOR signaling pathway of PIK3CA-related overgrowth spectrum (PROS)
Suzuki, Yasuyo, Enokido, Yasushi, Yamada, Kenichiro, Inaba, Mie, Kuwata, Kumiko, Hanada, Naoki, Morishita, Tsuyoshi, Mizuno, Seiji, Wakamatsu, Nobuaki
Published in Oncotarget (11.07.2017)
Published in Oncotarget (11.07.2017)
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Journal Article
Identification of B.1.346 Lineage of SARS-CoV-2 in Japan: Genomic Evidence of Re-entry of Clade 20C
Abe, Kodai, Shimura, Takako, Takenouchi, Toshiki, Iwasaki, Yuka W., Ishizu, Hirotsugu, Uwamino, Yoshifumi, Uno, Shunsuke, Gotoh, Jun, Tachikawa, Natsuo, Takeuchi, Yuriko, Katayama, Junpei, Nozaki, Hiroyuki, Fujii, Susumu, Seki, Shikou, Nakamura, Morio, Uda, Kazuhiro, Misumi, Takahiko, Ishihara, Jun, Yamada, Kenichiro, Kanai, Toshio, Murai, Shinji, Araki, Kazuhiro, Ebihara, Tamotsu, Siomi, Haruhiko, Hasegawa, Naoki, Kitagawa, Yuko, Amagai, Masayuki, Suematsu, Makoto, Kosaki, Kenjiro
Published in Keio journal of medicine (01.01.2021)
Published in Keio journal of medicine (01.01.2021)
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Journal Article
Identification and characterization of splicing variants of PLEKHA5 (Plekha5) during brain development
Yamada, Kenichiro, Nomura, Noriko, Yamano, Arisa, Yamada, Yasukazu, Wakamatsu, Nobuaki
Published in Gene (15.01.2012)
Published in Gene (15.01.2012)
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Journal Article
Analysis of Effective Field Gradient in Microwave-Assisted Magnetic Recording
Narita, Naoyuki, Yamada, Kenichiro, Taguchi, Tomoko, Matsumoto, Takuya, Koi, Katsuhiko, Takeo, Akihiko
Published in IEEE transactions on magnetics (01.11.2014)
Published in IEEE transactions on magnetics (01.11.2014)
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Journal Article
A wide spectrum of clinical and brain MRI findings in patients with SLC19A3 mutations
Yamada, Kenichiro, Miura, Kiyokuni, Hara, Kenju, Suzuki, Motomasa, Nakanishi, Keiko, Kumagai, Toshiyuki, Ishihara, Naoko, Yamada, Yasukazu, Kuwano, Ryozo, Tsuji, Shoji, Wakamatsu, Nobuaki
Published in BMC medical genetics (22.12.2010)
Published in BMC medical genetics (22.12.2010)
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Journal Article
Ultra-narrow interval angular control signal for holographic data storage system
Yamazaki, Kazuyoshi, Hosaka, Makoto, Yamada, Kenichiro, Ogata, Takeshi, Shimada, Kenichi
Published in Optical review (Tokyo, Japan) (01.10.2016)
Published in Optical review (Tokyo, Japan) (01.10.2016)
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Journal Article
The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations
Yamada, Yasukazu, Nomura, Noriko, Yamada, Kenichiro, Matsuo, Mari, Suzuki, Yuka, Sameshima, Kiyoko, Kimura, Reiko, Yamamoto, Yuto, Fukushi, Daisuke, Fukuhara, Yayoi, Ishihara, Naoko, Nishi, Eriko, Imataka, George, Suzumura, Hiroshi, Hamano, Shin-Ichiro, Shimizu, Kenji, Iwakoshi, Mie, Ohama, Kazunori, Ohta, Akira, Wakamoto, Hiroyuki, Kajita, Mitsuharu, Miura, Kiyokuni, Yokochi, Kenji, Kosaki, Kenjiro, Kuroda, Tatsuo, Kosaki, Rika, Hiraki, Yoko, Saito, Kayoko, Mizuno, Seiji, Kurosawa, Kenji, Okamoto, Nobuhiko, Wakamatsu, Nobuaki
Published in American journal of medical genetics. Part A (01.08.2014)
Published in American journal of medical genetics. Part A (01.08.2014)
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Journal Article
MBTPS2 mutation causes BRESEK/BRESHECK syndrome
Naiki, Misako, Mizuno, Seiji, Yamada, Kenichiro, Yamada, Yasukazu, Kimura, Reiko, Oshiro, Makoto, Okamoto, Nobuhiko, Makita, Yoshio, Seishima, Mariko, Wakamatsu, Nobuaki
Published in American journal of medical genetics. Part A (01.01.2012)
Published in American journal of medical genetics. Part A (01.01.2012)
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Journal Article
Chronic exercise enhances insulin secretion ability of pancreatic islets without change in insulin content in non-diabetic rats
Tsuchiya, Miho, Manabe, Yasuko, Yamada, Kenichiro, Furuichi, Yasuro, Hosaka, Masahiro, Fujii, Nobuharu L.
Published in Biochemical and biophysical research communications (11.01.2013)
Published in Biochemical and biophysical research communications (11.01.2013)
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Journal Article
Mutations in SIP1 , encoding Smad interacting protein-1, cause a form of Hirschsprung disease
Wakamatsu, Nobuaki, Yamada, Yasukazu, Yamada, Kenichiro, Ono, Takao, Nomura, Noriko, Taniguchi, Hiroko, Kitoh, Hiroshi, Mutoh, Norihiro, Yamanaka, Tsutomu, Mushiake, Kyosuke, Kato, Kanefusa, Sonta, Shin-ichi, Nagaya, Masahiro
Published in Nature genetics (01.04.2001)
Published in Nature genetics (01.04.2001)
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Journal Article
The first case of recurrent ultra late onset group B streptococcal sepsis in a 3-year-old child
Hosoda, Ai, Gatayama, Ryohei, Moriyama, Shiori, Ishii, Noriyuki, Yamada, Kenichiro, Matsuzaki, Youhei, Shinjoh, Masayoshi
Published in IDCases (01.01.2017)
Published in IDCases (01.01.2017)
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Journal Article
Clinical and biochemical characterization of 3-hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency that causes Leigh-like disease and ketoacidosis
Yamada, Kenichiro, Naiki, Misako, Hoshino, Shin, Kitaura, Yasuyuki, Kondo, Yusuke, Nomura, Noriko, Kimura, Reiko, Fukushi, Daisuke, Yamada, Yasukazu, Shimozawa, Nobuyuki, Yamaguchi, Seiji, Shimomura, Yoshiharu, Miura, Kiyokuni, Wakamatsu, Nobuaki
Published in Molecular genetics and metabolism reports (01.01.2014)
Published in Molecular genetics and metabolism reports (01.01.2014)
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Journal Article