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1.

[Classification and Diagnostics of Pediatric Brain Tumors].

Kanemura, Yonehiro.

No Shinkei Geka ; 51(5): 778-788, 2023 Sep.

Artículo en Japonés | MEDLINE | ID: mdl-37743329

2.

JNK1-Dependent Phosphorylation of GAP-43 Serine 142 is a Novel Molecular Marker for Axonal Growth.

Okada, Masayasu; Kawagoe, Yosuke; Takasugi, Toshiyuki; Nozumi, Motohiro; Ito, Yasuyuki; Fukusumi, Hayato; Kanemura, Yonehiro; Fujii, Yukihiko; Igarashi, Michihiro.

Neurochem Res ; 47(9): 2668-2682, 2022 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-35347634

3.

Four pedigrees with aminoacyl-tRNA synthetase abnormalities.

Okamoto, Nobuhiko; Miya, Fuyuki; Tsunoda, Tatsuhiko; Kanemura, Yonehiro; Saitoh, Shinji; Kato, Mitsuhiro; Yanagi, Kumiko; Kaname, Tadashi; Kosaki, Kenjiro.

Neurol Sci ; 43(4): 2765-2774, 2022 Apr.

Artículo en Inglés | MEDLINE | ID: mdl-34585293

4.

Prenatal clinical manifestations in individuals with COL4A1/2 variants.

Itai, Toshiyuki; Miyatake, Satoko; Taguri, Masataka; Nozaki, Fumihito; Ohta, Masayasu; Osaka, Hitoshi; Morimoto, Masafumi; Tandou, Tomoko; Nohara, Fumikatsu; Takami, Yuichi; Yoshioka, Fumitaka; Shimokawa, Shoko; Okuno-Yuguchi, Jiu; Motobayashi, Mitsuo; Takei, Yuko; Fukuyama, Tetsuhiro; Kumada, Satoko; Miyata, Yohane; Ogawa, Chikako; Maki, Yuki; Togashi, Noriko; Ishikura, Teruyuki; Kinoshita, Makoto; Mitani, Yusuke; Kanemura, Yonehiro; Omi, Tsuyoshi; Ando, Naoki; Hattori, Ayako; Saitoh, Shinji; Kitai, Yukihiro; Hirai, Satori; Arai, Hiroshi; Ishida, Fumihiko; Taniguchi, Hidetoshi; Kitabatake, Yasuji; Ozono, Keiichi; Nabatame, Shin; Smigiel, Robert; Kato, Mitsuhiro; Tanda, Koichi; Saito, Yoshihiko; Ishiyama, Akihiko; Noguchi, Yushi; Miura, Mazumi; Nakano, Takaaki; Hirano, Keiko; Honda, Ryoko; Kuki, Ichiro; Takanashi, Jun-Ichi; Takeuchi, Akihito.

J Med Genet ; 58(8): 505-513, 2021 08.

Artículo en Inglés | MEDLINE | ID: mdl-32732225

5.

Quantitative measurement of peritumoral concentrations of glutamate, N-acetyl aspartate, and lactate on magnetic resonance spectroscopy predicts glioblastoma-related refractory epilepsy.

Nakamura, Yawara; Inoue, Akihiro; Nishikawa, Masahiro; Ohnishi, Takanori; Yano, Hajime; Kanemura, Yonehiro; Ohtsuka, Yoshihiro; Ozaki, Saya; Kusakabe, Kosuke; Suehiro, Satoshi; Yamashita, Daisuke; Shigekawa, Seiji; Watanabe, Hideaki; Kitazawa, Riko; Tanaka, Junya; Kunieda, Takeharu.

Acta Neurochir (Wien) ; 164(12): 3253-3266, 2022 12.

Artículo en Inglés | MEDLINE | ID: mdl-36107232

6.

[Medulloblastoma].

Kanemura, Yonehiro.

No Shinkei Geka ; 50(1): 73-90, 2022 Jan.

Artículo en Japonés | MEDLINE | ID: mdl-35169088

7.

TERT promoter mutation status is necessary and sufficient to diagnose IDH-wildtype diffuse astrocytic glioma with molecular features of glioblastoma.

Fujimoto, Kenji; Arita, Hideyuki; Satomi, Kaishi; Yamasaki, Kai; Matsushita, Yuko; Nakamura, Taishi; Miyakita, Yasuji; Umehara, Toru; Kobayashi, Keiichi; Tamura, Kaoru; Tanaka, Shota; Higuchi, Fumi; Okita, Yoshiko; Kanemura, Yonehiro; Fukai, Junya; Sakamoto, Daisuke; Uda, Takehiro; Machida, Ryunosuke; Kuchiba, Aya; Maehara, Taketoshi; Nagane, Motoo; Nishikawa, Ryo; Suzuki, Hiroyoshi; Shibuya, Makoto; Komori, Takashi; Narita, Yoshitaka; Ichimura, Koichi.

Acta Neuropathol ; 142(2): 323-338, 2021 08.

Artículo en Inglés | MEDLINE | ID: mdl-34148105

8.

Infrequent RAS mutation is not associated with specific histological phenotype in gliomas.

Makino, Yasuhide; Arakawa, Yoshiki; Yoshioka, Ema; Shofuda, Tomoko; Minamiguchi, Sachiko; Kawauchi, Takeshi; Tanji, Masahiro; Kanematsu, Daisuke; Nonaka, Masahiro; Okita, Yoshiko; Kodama, Yoshinori; Mano, Masayuki; Hirose, Takanori; Mineharu, Yohei; Miyamoto, Susumu; Kanemura, Yonehiro.

BMC Cancer ; 21(1): 1025, 2021 Sep 15.

Artículo en Inglés | MEDLINE | ID: mdl-34525976

9.

Homozygous ADCY5 mutation causes early-onset movement disorder with severe intellectual disability.

Okamoto, Nobuhiko; Miya, Fuyuki; Kitai, Yukihiro; Tsunoda, Tatsuhiko; Kato, Mitsuhiro; Saitoh, Shinji; Kanemura, Yonehiro; Kosaki, Kenjiro.

Neurol Sci ; 42(7): 2975-2978, 2021 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-33704598

10.

A case of medulloblastoma in a patient with fetal ventricular enlargement.

Li, Yi; Nonaka, Masahiro; Kanemura, Yonehiro; Kodama, Yoshinori; Mano, Masayuki; Asai, Akio.

Childs Nerv Syst ; 37(3): 977-982, 2021 03.

Artículo en Inglés | MEDLINE | ID: mdl-32556458

11.

Grip and slip of L1-CAM on adhesive substrates direct growth cone haptotaxis.

Abe, Kouki; Katsuno, Hiroko; Toriyama, Michinori; Baba, Kentarou; Mori, Tomoyuki; Hakoshima, Toshio; Kanemura, Yonehiro; Watanabe, Rikiya; Inagaki, Naoyuki.

Proc Natl Acad Sci U S A ; 115(11): 2764-2769, 2018 03 13.

Artículo en Inglés | MEDLINE | ID: mdl-29483251

12.

Concise Review: Laying the Groundwork for a First-In-Human Study of an Induced Pluripotent Stem Cell-Based Intervention for Spinal Cord Injury.

Tsuji, Osahiko; Sugai, Keiko; Yamaguchi, Ryo; Tashiro, Syoichi; Nagoshi, Narihito; Kohyama, Jun; Iida, Tsuyoshi; Ohkubo, Toshiki; Itakura, Go; Isoda, Miho; Shinozaki, Munehisa; Fujiyoshi, Kanehiro; Kanemura, Yonehiro; Yamanaka, Shinya; Nakamura, Masaya; Okano, Hideyuki.

Stem Cells ; 37(1): 6-13, 2019 01.

Artículo en Inglés | MEDLINE | ID: mdl-30371964

13.

Relationships between recurrence patterns and subventricular zone involvement or CD133 expression in glioblastoma.

Yamaki, Tetsu; Shibahra, Ichiyo; Matsuda, Ken-Ichiro; Kanemura, Yonehiro; Konta, Tsuneo; Kanamori, Masayuki; Yamakawa, Mitsunori; Tominaga, Teiji; Sonoda, Yukihiko.

J Neurooncol ; 146(3): 489-499, 2020 Feb.

Artículo en Inglés | MEDLINE | ID: mdl-32020479

14.

MYCN de novo gain-of-function mutation in a patient with a novel megalencephaly syndrome.

Kato, Kohji; Miya, Fuyuki; Hamada, Nanako; Negishi, Yutaka; Narumi-Kishimoto, Yoko; Ozawa, Hiroshi; Ito, Hidenori; Hori, Ikumi; Hattori, Ayako; Okamoto, Nobuhiko; Kato, Mitsuhiro; Tsunoda, Tatsuhiko; Kanemura, Yonehiro; Kosaki, Kenjiro; Takahashi, Yoshiyuki; Nagata, Koh-Ichi; Saitoh, Shinji.

J Med Genet ; 56(6): 388-395, 2019 06.

Artículo en Inglés | MEDLINE | ID: mdl-30573562

15.

Author Correction: A missense mutation in the HECT domain of NEDD4L identified in a girl with periventricular nodular heterotopia, polymicrogyria, and cleft palate.

Kato, Koji; Miya, Fuyuki; Hori, Ikumi; Ieda, Daisuke; Ohashi, Kei; Negishi, Yutaka; Hattori, Ayako; Okamoto, Nobuhiko; Kato, Mitsuhiro; Tsunoda, Tatsuhiko; Yamasaki, Mami; Kanemura, Yonehiro; Kosaki, Kenjiro; Saitoh, Shinji.

J Hum Genet ; 64(7): 701-702, 2019 Jul.

Artículo en Inglés | MEDLINE | ID: mdl-31028281

16.

Evaluation of the susceptibility of neurons and neural stem/progenitor cells derived from human induced pluripotent stem cells to anticancer drugs.

Fukusumi, Hayato; Handa, Yukako; Shofuda, Tomoko; Kanemura, Yonehiro.

J Pharmacol Sci ; 140(4): 331-336, 2019 Aug.

Artículo en Inglés | MEDLINE | ID: mdl-31501056

17.

A novel homozygous missense mutation in the SH3-binding motif of STAMBP causing microcephaly-capillary malformation syndrome.

Hori, Ikumi; Miya, Fuyuki; Negishi, Yutaka; Hattori, Ayako; Ando, Naoki; Boroevich, Keith A; Okamoto, Nobuhiko; Kato, Mitsuhiro; Tsunoda, Tatsuhiko; Yamasaki, Mami; Kanemura, Yonehiro; Kosaki, Kenjiro; Saitoh, Shinji.

J Hum Genet ; 63(9): 957-963, 2018 Sep.

Artículo en Inglés | MEDLINE | ID: mdl-29907875

18.

Characteristics and outcomes of elderly patients with diffuse gliomas: a multi-institutional cohort study by Kansai Molecular Diagnosis Network for CNS Tumors.

Sasaki, Takahiro; Fukai, Junya; Kodama, Yoshinori; Hirose, Takanori; Okita, Yoshiko; Moriuchi, Shusuke; Nonaka, Masahiro; Tsuyuguchi, Naohiro; Terakawa, Yuzo; Uda, Takehiro; Tomogane, Yusuke; Kinoshita, Manabu; Nishida, Namiko; Izumoto, Shuichi; Nakajima, Yoshikazu; Arita, Hideyuki; Ishibashi, Kenichi; Shofuda, Tomoko; Kanematsu, Daisuke; Yoshioka, Ema; Mano, Masayuki; Fujita, Koji; Uematsu, Yuji; Nakao, Naoyuki; Mori, Kanji; Kanemura, Yonehiro.

J Neurooncol ; 140(2): 329-339, 2018 Nov.

Artículo en Inglés | MEDLINE | ID: mdl-30076584

19.

Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability.

Hamada, Nanako; Negishi, Yutaka; Mizuno, Makoto; Miya, Fuyuki; Hattori, Ayako; Okamoto, Nobuhiko; Kato, Mitsuhiro; Tsunoda, Tatsuhiko; Yamasaki, Mami; Kanemura, Yonehiro; Kosaki, Kenjiro; Tabata, Hidenori; Saitoh, Shinji; Nagata, Koh-Ichi.

J Neurochem ; 140(1): 82-95, 2017 01.

Artículo en Inglés | MEDLINE | ID: mdl-27787898

20.

A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly.

Negishi, Yutaka; Miya, Fuyuki; Hattori, Ayako; Johmura, Yoshikazu; Nakagawa, Motoo; Ando, Naoki; Hori, Ikumi; Togawa, Takao; Aoyama, Kohei; Ohashi, Kei; Fukumura, Shinobu; Mizuno, Seiji; Umemura, Ayako; Kishimoto, Yoko; Okamoto, Nobuhiko; Kato, Mitsuhiro; Tsunoda, Tatsuhiko; Yamasaki, Mami; Kanemura, Yonehiro; Kosaki, Kenjiro; Nakanishi, Makoto; Saitoh, Shinji.

BMC Med Genet ; 18(1): 4, 2017 Jan 13.

Artículo en Inglés | MEDLINE | ID: mdl-28086757

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