Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Noriko, Nomura"'
Autor:
Yohei Takenobu, Noriko Nomura, Yoshito Sugita, Akihiro Okada, Takeshi Kawauchi, Tao Yang, Kenji Hashimoto
Publikováno v:
Stroke: Vascular and Interventional Neurology, Vol 4, Iss 2 (2024)
Objective Carotid artery stenting for heavily calcified lesions is challenging for interventionists. A calcium burden is associated with suboptimal dilatation, periprocedural complications, high rates of restenosis, and poor outcomes. We describe the
Externí odkaz:
https://doaj.org/article/2ffa0d4120a04c98b52b73f16a7ef3e1
Autor:
Yohei Takenobu, Noriko Nomura, Yoshito Sugita, Akihiro Okada, Takeshi Kawauchi, Tao Yang, Kenji Hashimoto
Publikováno v:
Stroke: Vascular and Interventional Neurology, Vol 3, Iss S2 (2023)
Introduction In carotid artery stenting (CAS), a guiding catheter (GC) placement to the appropriate position is the first step of the successful procedure. In normal settings, GC is navigated along with stable support of guidewire and inner‐cathete
Externí odkaz:
https://doaj.org/article/4df4dd97ca8c49ac98364dc15c4f8acb
Autor:
Kenichiro Yamada, Misako Naiki, Shin Hoshino, Yasuyuki Kitaura, Yusuke Kondo, Noriko Nomura, Reiko Kimura, Daisuke Fukushi, Yasukazu Yamada, Nobuyuki Shimozawa, Seiji Yamaguchi, Yoshiharu Shimomura, Kiyokuni Miura, Nobuaki Wakamatsu
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 1, Iss C, Pp 455-460 (2014)
3-Hydroxyisobutyryl-CoA hydrolase (HIBCH) deficiency is an autosomal recessive disorder characterized by episodes of ketoacidosis and a Leigh-like basal ganglia disease, without high concentrations of pyruvate and lactate in the cerebrospinal fluid.
Externí odkaz:
https://doaj.org/article/aa771066eebf4225b498f08ee01ae9f9
Autor:
Noriko Nomura, Daisuke Fukushi, Kimiko Katoh, Yoshihito Tokita, Yasushi Enokido, Mie Inaba, Nobuaki Wakamatsu, Seiji Mizuno, Shin Hayashi, Yasuyo Suzuki, Kenichiro Yamada
Publikováno v:
American Journal of Medical Genetics Part A. 185:1776-1786
R3HDM1 (R3H domain containing 1) is an uncharacterized RNA-binding protein that is highly expressed in the human cerebral cortex. We report the first case of a 12-year-old Japanese male with haploinsufficiency of R3HDM1. He presented with mild intell
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5587c4de92d6ac9647cbd057800c865c
https://doi.org/10.1002/ajmg.a.62173
https://doi.org/10.1002/ajmg.a.62173
Autor:
Daisuke Motooka, Shota Nakamura, Koji Tominaga, Nobuhiko Okamoto, Jun Natsume, Yoshiko Murakami, Junpei Tanigawa, Haruka Mimatsu, Taroh Kinoshita, Keiichi Ozono, Seiji Mizuno, Yukako Muramatsu, Eriko Nishi, Nobuaki Wakamatsu, Shin Nabatame, Tetsuya Niihori, Yoko Aoki, Masahiro Hayakawa, Daisuke Fukushi, Noriko Nomura, Hiroyuki Kidokoro, Kiyoshi Hayasaka
Publikováno v:
Human Mutation. 38:805-815
Inherited GPI (glycosylphosphatidylinositol) deficiencies (IGDs), a recently defined group of diseases, show a broad spectrum of symptoms. Hyperphosphatasia mental retardation syndrome, also known as Mabry syndrome, is a type of IGDs. There are at le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::751b42146c97a85285ae92c7fe06862f
https://doi.org/10.1002/humu.23219
https://doi.org/10.1002/humu.23219
Autor:
Naohito Hato, Yui Kirino, Kentaro Ohara, Haruna Yaguchi, Kohei Shiota, Toru Ugumori, Junya Tanaka, Noriko Nomura, Hajime Yano, Issei Tetsumura, Teppei Kaminota, Tomoyoshi Sanada
Publikováno v:
Biochemical and Biophysical Research Communications. 486:101-107
Cancer cells can migrate as collectives during invasion and/or metastasis; however, the precise molecular mechanisms of this form of migration are less clear compared with single cell migration following epithelial-mesenchymal transition. Elevated Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::084cc73a70ee579f1af5053593235265
https://doi.org/10.1016/j.bbrc.2017.03.007
https://doi.org/10.1016/j.bbrc.2017.03.007
Autor:
Kenichiro Yamada, Daisuke Fukushi, Kaori Aiba, Seiji Yamaguchi, Nobuaki Wakamatsu, Yasuyuki Kitaura, Yuji Nakamura, Kenji Yokochi, Kei Murayama, Noriko Nomura, Yusuke Kondo, Yoshiharu Shimomura, James Pitt
Publikováno v:
Journal of Medical Genetics. 52:691-698
Background Short-chain enoyl-CoA hydratase—ECHS1—catalyses many metabolic pathways, including mitochondrial short-chain fatty acid β-oxidation and branched-chain amino acid catabolic pathways; however, the metabolic products essential for the di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb0e6e55018a0d3fa0af5dfb5ad23a9f
https://doi.org/10.1136/jmedgenet-2015-103231
https://doi.org/10.1136/jmedgenet-2015-103231
Autor:
Teppei, Kaminota, Hajime, Yano, Kohei, Shiota, Noriko, Nomura, Haruna, Yaguchi, Yui, Kirino, Kentaro, Ohara, Issei, Tetsumura, Tomoyoshi, Sanada, Toru, Ugumori, Junya, Tanaka, Naohito, Hato
Publikováno v:
Biochemical and biophysical research communications. 486(1)
Cancer cells can migrate as collectives during invasion and/or metastasis; however, the precise molecular mechanisms of this form of migration are less clear compared with single cell migration following epithelial-mesenchymal transition. Elevated Na
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b8aaded3bbb5e8c7722e8cd7bd8dccf7
https://pubmed.ncbi.nlm.nih.gov/28268168
https://pubmed.ncbi.nlm.nih.gov/28268168
Autor:
Junpei, Tanigawa, Haruka, Mimatsu, Seiji, Mizuno, Nobuhiko, Okamoto, Daisuke, Fukushi, Koji, Tominaga, Hiroyuki, Kidokoro, Yukako, Muramatsu, Eriko, Nishi, Shota, Nakamura, Daisuke, Motooka, Noriko, Nomura, Kiyoshi, Hayasaka, Tetsuya, Niihori, Yoko, Aoki, Shin, Nabatame, Masahiro, Hayakawa, Jun, Natsume, Keiichi, Ozono, Taroh, Kinoshita, Nobuaki, Wakamatsu, Yoshiko, Murakami
Publikováno v:
Human mutation. 38(7)
Inherited GPI (glycosylphosphatidylinositol) deficiencies (IGDs), a recently defined group of diseases, show a broad spectrum of symptoms. Hyperphosphatasia mental retardation syndrome, also known as Mabry syndrome, is a type of IGDs. There are at le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::895c096aafa83c099cc93ac4180ff22f
https://pubmed.ncbi.nlm.nih.gov/28337824
https://pubmed.ncbi.nlm.nih.gov/28337824
Autor:
Kazunori Ohama, Mitsuharu Kajita, Kenichiro Yamada, Naoko Ishihara, Mie Iwakoshi, Kenji Kurosawa, Kiyokuni Miura, Daisuke Fukushi, Yayoi Fukuhara, Kenjiro Kosaki, Reiko Kimura, Eriko Nishi, Yuto Yamamoto, Tatsuo Kuroda, Mari Matsuo, Kiyoko Sameshima, Akira Ohta, Nobuhiko Okamoto, Seiji Mizuno, Rika Kosaki, Kenji Yokochi, Shin ichiro Hamano, Hiroshi Suzumura, Yasukazu Yamada, Nobuaki Wakamatsu, Hiroyuki Wakamoto, Kayoko Saito, George Imataka, Yuka Suzuki, Yoko Hiraki, Noriko Nomura, Kenji Shimizu
Publikováno v:
American Journal of Medical Genetics Part A. 164:1899-1908
Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by moderate or severe intellectual disability, a characteristic facial appearance, microcephaly, epilepsy, agenesis or hypoplasia of the corpus callosum, congenital h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::647ebb4c6d3babe959bc5b56b388363f
https://doi.org/10.1002/ajmg.a.36551
https://doi.org/10.1002/ajmg.a.36551