Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Mariko Taniguchi-Ikeda"'
Autor:
Kenta Morita, Tomoko Moriwaki, Shunsuke Habe, Mariko Taniguchi-Ikeda, Tadao Hasegawa, Yusuke Minato, Takashi Aoi, Tatsuo Maruyama
Publikováno v:
JACS Au, Vol 4, Iss 6, Pp 2262-2266 (2024)
Externí odkaz:
https://doaj.org/article/467f9280f9f34aa3bce081c6e3fab871
Autor:
Miki Ikeda, Mariko Taniguchi-Ikeda, Takema Kato, Yasuko Shinkai, Sonoko Tanaka, Hiroki Hagiwara, Naomichi Sasaki, Toshihiro Masaki, Kiichiro Matsumura, Masahiro Sonoo, Hiroki Kurahashi, Fumiaki Saito
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss , Pp 131-144 (2020)
Myotonic dystrophy type 1 is the most common type of adult-onset muscular dystrophy. This is an autosomal dominant disorder and caused by the expansion of the CTG repeat in the 3′ untranslated region of the dystrophia myotonica protein kinase (DMPK
Externí odkaz:
https://doaj.org/article/023d7e99a665465ca9bfb584a02b1aa6
Autor:
Mariko Taniguchi-Ikeda, Michiyo Koyanagi-Aoi, Tatsuo Maruyama, Toru Takaori, Akiko Hosoya, Hiroyuki Tezuka, Shotaro Nagase, Takuma Ishihara, Taisuke Kadoshima, Keiko Muguruma, Keiko Ishigaki, Hidetoshi Sakurai, Akira Mizoguchi, Bennett G. Novitch, Tatsushi Toda, Momoko Watanabe, Takashi Aoi
Publikováno v:
iScience, Vol 24, Iss 10, Pp 103140- (2021)
Summary: Fukuyama congenital muscular dystrophy (FCMD) is a severe, intractable genetic disease that affects the skeletal muscle, eyes, and brain and is attributed to a defect in alpha dystroglycan (αDG) O-mannosyl glycosylation. We previously estab
Externí odkaz:
https://doaj.org/article/9e0187a4344d489cb9ee7920e4ea9915
Autor:
Shigefumi Morioka, Hirofumi Sakaguchi, Hiroaki Mohri, Mariko Taniguchi-Ikeda, Motoi Kanagawa, Toshiaki Suzuki, Yuko Miyagoe-Suzuki, Tatsushi Toda, Naoaki Saito, Takehiko Ueyama
Publikováno v:
PLoS Genetics, Vol 16, Iss 5, p e1008826 (2020)
Hearing loss (HL) is one of the most common sensory impairments and etiologically and genetically heterogeneous disorders in humans. Muscular dystrophies (MDs) are neuromuscular disorders characterized by progressive degeneration of skeletal muscle a
Externí odkaz:
https://doaj.org/article/e459f0bf0deb4f4bba4537cab949d556
Autor:
Ichiro Morioka, Naohiro Kamiyoshi, Masahiro Nishiyama, Tomohiko Yamamura, Shogo Minamikawa, Sota Iwatani, Hiroaki Nagase, Kandai Nozu, Noriyuki Nishimura, Mariko Taniguchi-Ikeda, Kazuto Ishibashi, Akihito Ishida, Kazumoto Iijima
Publikováno v:
Environmental Health and Preventive Medicine, Vol 22, Iss 1, Pp 1-7 (2017)
Abstract Background Acute gastroenteritis (AGE) is a major reason for presentation to pediatric primary emergency medical centers. Because rotavirus vaccines were introduced in November 2011 for voluntary vaccination in Japan, we analyzed the changes
Externí odkaz:
https://doaj.org/article/3efeba5e48e4475b80a86699adca6ce0
Autor:
Masahiro Nishiyama, Ichiro Morioka, Mariko Taniguchi-Ikeda, Takeshi Mori, Kazumi Tomioka, Keita Nakanishi, Junya Fujimura, Noriyuki Nishimura, Kandai Nozu, Hiroaki Nagase, Kazuto Ishibashi, Akihito Ishida, Kazumoto Iijima
Publikováno v:
Journal of International Medical Research, Vol 46 (2018)
Objectives To identify clinical features that predict Group A streptococcal (GAS) pharyngitis in a Japanese paediatric primary emergency medical centre. Methods The prevalence of GAS pharyngitis according to age and body temperature (BT) was calculat
Externí odkaz:
https://doaj.org/article/f62980cb9b684db2b680fc2472891ab4
Autor:
Sota Iwatani, Nur Imma Fatimah Harahap, Dian Kesumapramudya Nurputra, Shinya Tairaku, Akemi Shono, Daisuke Kurokawa, Keiji Yamana, Khin Kyae Mon Thwin, Makiko Yoshida, Masami Mizobuchi, Tsubasa Koda, Kazumichi Fujioka, Mariko Taniguchi-Ikeda, Hideto Yamada, Ichiro Morioka, Kazumoto Iijima, Hisahide Nishio, Noriyuki Nishimura
Publikováno v:
Frontiers in Pediatrics, Vol 5 (2017)
BackgroundSpinal muscular atrophy (SMA) is the most common genetic neurological disease leading to infant death. It is caused by loss of survival motor neuron (SMN) 1 gene and subsequent reduction of SMN protein in motor neurons. Because SMN is ubiqu
Externí odkaz:
https://doaj.org/article/ee97f9d837ea4bda83b1bd25ce6dba28
Autor:
Sota Iwatani, Akemi Shono, Makiko Yoshida, Keiji Yamana, Khin Kyae Mon Thwin, Jumpei Kuroda, Daisuke Kurokawa, Tsubasa Koda, Kosuke Nishida, Toshihiko Ikuta, Kazumichi Fujioka, Masami Mizobuchi, Mariko Taniguchi-Ikeda, Ichiro Morioka, Kazumoto Iijima, Noriyuki Nishimura
Publikováno v:
Stem Cells International, Vol 2017 (2017)
Mesenchymal stem cells (MSCs) are a heterogeneous cell population that is isolated initially from the bone marrow (BM) and subsequently almost all tissues including umbilical cord (UC). UC-derived MSCs (UC-MSCs) have attracted an increasing attention
Externí odkaz:
https://doaj.org/article/35b4c97013164b818646295d10e1b6bc
Autor:
Sarantuya Enkhjargal, Kana Sugahara, Behnoush Khaledian, Miwako Nagasaka, Hidehito Inagaki, Hiroki Kurahashi, Hisatsugu Koshimizu, Tatsushi Toda, Mariko Taniguchi-Ikeda
Publikováno v:
Human molecular genetics.
Fukuyama congenital muscular dystrophy (FCMD) is an autosomal recessive disorder caused by fukutin (FKTN) gene mutations. FCMD is the second most common form of childhood muscular dystrophy in Japan, and the most patients possess a homozygous retrotr
Autor:
Hiroki Kurahashi, Hiroki Hagiwara, Naomichi Sasaki, Sonoko Tanaka, Miki Ikeda, Yasuko Shinkai, Kiichiro Matsumura, Mariko Taniguchi-Ikeda, Fumiaki Saito, Toshihiro Masaki, Takema Kato, Masahiro Sonoo
Publikováno v:
Molecular Therapy: Methods & Clinical Development, Vol 18, Iss, Pp 131-144 (2020)
Molecular Therapy. Methods & Clinical Development
Molecular Therapy. Methods & Clinical Development
Myotonic dystrophy type 1 is the most common type of adult-onset muscular dystrophy. This is an autosomal dominant disorder and caused by the expansion of the CTG repeat in the 3′ untranslated region of the dystrophia myotonica protein kinase (DMPK