Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mayu Ishiguro"'
Autor:
Toshiki Tezuka, Mayu Ishiguro, Daisuke Taniguchi, Ehoto Osogaguchi, Kahori Shiba-Fukushima, Jun Ogata, Ryota Ishii, Aya Ikeda, Yuanzhe Li, Hiroyo Yoshino, Taro Matsui, Kenichi Kaida, Manabu Funayama, Kenya Nishioka, Fumihisa Kumazawa, Tomoyasu Matsubara, Hitoshi Tsuda, Yuko Saito, Shigeo Murayama, Yuzuru Imai, Nobutaka Hattori
Publikováno v:
Neurobiology of Disease, Vol 199, Iss , Pp 106571- (2024)
Leucine-rich repeat kinase 2 (LRRK2) is the most common gene responsible for familial Parkinson's disease (PD). The gene product of LRRK2 contains multiple protein domains, including armadillo repeat, ankyrin repeat, leucine-rich repeat (LRR), Ras-of
Externí odkaz:
https://doaj.org/article/de656de5f6c04063a9a2a899476b1c7d
Autor:
Mayu Ishiguro, Manabu Funayama, Taku Hatano, Hiroshi Nishida, Yuko Wada, Kazuyuki Noda, Masahiko Tomiyama, Hiroyo Yoshino, Yuanzhe Li, Stephanie Ong, Ettore Cioffi, Kenya Nishioka, Nobutaka Hattori
Publikováno v:
Heliyon, Vol 10, Iss 15, Pp e35271- (2024)
Background: Biallelic variants in PARK7, which encodes protein-nucleic acid deglycase DJ-1, can cause early-onset Parkinson's disease (PD). Although many patients with PARK7 variants have been identified from European and Middle Eastern ethnic groups
Externí odkaz:
https://doaj.org/article/30fc1bb21b564f41b30e176752e1c380
Autor:
Genko Oyama, Maximilien Burq, Taku Hatano, William J. Marks, Ritu Kapur, Jovelle Fernandez, Keita Fujikawa, Yoshihiko Furusawa, Keisuke Nakatome, Erin Rainaldi, Chen Chen, King Chung Ho, Takashi Ogawa, Hikaru Kamo, Yutaka Oji, Haruka Takeshige-Amano, Daisuke Taniguchi, Ryota Nakamura, Fuyuko Sasaki, Shinichi Ueno, Kenta Shiina, Anri Hattori, Noriko Nishikawa, Mayu Ishiguro, Shinji Saiki, Ayako Hayashi, Masatoshi Motohashi, Nobutaka Hattori
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-13 (2023)
Abstract Continuous, objective monitoring of motor signs and symptoms may help improve tracking of disease progression and treatment response in Parkinson’s disease (PD). This study assessed the analytical and clinical validity of multi-sensor smar
Externí odkaz:
https://doaj.org/article/eca698ce76b243348283baa494b268d1
Autor:
Kei-ichi Ishikawa, Mayu Ishiguro, Yuanzhe Li, Kenya Nishioka, Nobutaka Hattori, Wado Akamatsu
Publikováno v:
Stem Cell Research, Vol 60, Iss , Pp 102739- (2022)
Approximately 10% of Parkinson's disease cases are familial and more than 20 disease-related genes have been identified. The VPS35 gene causes a rare type of Parkinson's disease called PARK17, which is inherited in an autosomal dominant manner. The V
Externí odkaz:
https://doaj.org/article/4785a1019fbb47a6b085fd1cef04ed5f
Autor:
Mayu Ishiguro, Yuji Ueno, Yuta Ishiguro, Masashi Takanashi, Kenji Murai, Guillaume Taieb, Kensuke Daida, Akimitsu Suda, Kazumasa Yokoyama, Toshio Naito, Nobutaka Hattori
Publikováno v:
BMC Neurology, Vol 20, Iss 1, Pp 1-5 (2020)
Abstract Background Diverse mechanisms including infections, autoimmune inflammatory reactions, neoplasms, and degeneration are involved in the central nervous system in cases of acquired immune deficiency syndrome. In such cases, it is difficult to
Externí odkaz:
https://doaj.org/article/644f9783d28b4a1c890fbdf502d1c57b
Autor:
Kenya Nishioka, Manabu Funayama, Aya Ikeda, Yuanzhe Li, Hiroyo Yoshino, Mayu Ishiguro, Nobutaka Hattori
Publikováno v:
Parkinsonism & Related Disorders. 88:10-12
Compound heterozygosity of ATP10B is thought to be a risk factor for young-onset Parkinson's disease (PD). We genetically screened 245 patients with young-onset sporadic PD and 33 patients with autosomal recessive PD for ATP10B. All 13 identified gen
Autor:
Maya Ando, Kazuyuki Noda, Takashi Ogawa, Kotaro Ogaki, Yasuyuki Okuma, Nobutaka Hattori, Mayu Ishiguro, Tomokatsu Yoshida
Publikováno v:
Mov Disord Clin Pract
Autor:
Yuanzhe Li, Genko Oyama, Nobutaka Hattori, Manabu Funayama, Kensuke Daida, Shinji Saiki, Kenya Nishioka, Yuta Ishiguro, Hiroyo Yoshino, Mayu Ishiguro
Publikováno v:
Parkinsonismrelated disorders. 84
Introduction To identify and investigate patients with Parkinson's disease (PD) harboring VPS35 variants in Japan. Methods Using targeted gene panel screening, we analyzed 393 familial, 294 young-onset, and 52 late-onset sporadic PD patients derived