Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Takuya Morikawa"'
Autor:
Shiroh Miura, Emina Watanabe, Kensuke Senzaki, Shigeyoshi Hiruki, Sayaka Matsumoto, Takuya Morikawa, Yusuke Uchiyama, Seiji Kurata, Masayuki Ochi, Yasumasa Ohyagi, Hiroki Shibata
Publikováno v:
Human Genome Variation, Vol 11, Iss 1, Pp 1-3 (2024)
Abstract Autosomal dominant episodic ataxia type 2 (EA2) is caused by variants in CACNA1A. We examined a 20-year-old male with EA symptoms from a Japanese family with hereditary EA. Cerebellar atrophy was not evident, but single photon emission compu
Externí odkaz:
https://doaj.org/article/a1d8e99ecb164101ac3002e4d1d6beab
Publikováno v:
Journal of Wood Science, Vol 68, Iss 1, Pp 1-12 (2022)
Abstract The leaves and twigs of Lindera spp. have long been used as a herbal medicine and toothpicks in Japan. However, little is known about individual variations in the extractives of these species, because many previous studies have not distingui
Externí odkaz:
https://doaj.org/article/f1e8b8bf711d4575a5c214b9c572fd1d
Autor:
Eri Tabata, Ikuto Kobayashi, Takuya Morikawa, Akinori Kashimura, Peter O. Bauer, Fumitaka Oyama
Publikováno v:
iScience, Vol 26, Iss 8, Pp 107254- (2023)
Summary: Placental mammals' ancestors were insectivores, suggesting that modern mammals may have inherited the ability to digest insects. Acidic chitinase (Chia) is a crucial enzyme hydrolyzing significant component of insects' exoskeleton in many sp
Externí odkaz:
https://doaj.org/article/9fb2dd4b297a47de897af4261532ec99
Autor:
Takuya Morikawa, Shiroh Miura, Luoming Fan, Emina Watanabe, Ryuta Fujioka, Hiromichi Motooka, Shingo Yasumoto, Yusuke Uchiyama, Hiroki Shibata
Publikováno v:
Human Genome Variation, Vol 9, Iss 1, Pp 1-3 (2022)
Abstract Dystonia (DYT) is a heterogeneous neurological disorder, and there are many types of DYT depending on the responsible genes. DYT11 is an autosomal dominant DYT caused by functional variants in the SGCE gene. We examined a Japanese patient wi
Externí odkaz:
https://doaj.org/article/1241a7c11c5b43969a0d66c0cda05e80
Autor:
Takuya Morikawa, Masatomo Takahashi, Yoshihiro Izumi, Takeshi Bamba, Kosei Moriyama, Gohsuke Hattori, Ryuta Fujioka, Shiroh Miura, Hiroki Shibata
Publikováno v:
Biomedicines, Vol 11, Iss 4, p 1092 (2023)
Hereditary spastic paraplegia is a genetic neurological disorder characterized by spasticity of the lower limbs, and spastic paraplegia type 28 is one of its subtypes. Spastic paraplegia type 28 is a hereditary neurogenerative disorder with an autoso
Externí odkaz:
https://doaj.org/article/508eeeb5063f4cd4809863476cf1804c
Autor:
Marohito Nakata, Naoko Yokota, Kazuhiko Tabata, Takuya Morikawa, Hiroki Shibata, Tsuneaki Kenzaka
Publikováno v:
Medicina, Vol 59, Iss 3, p 615 (2023)
Background: Cardiopulmonary disorders are the most common cause of central cyanosis, and methemoglobinemia is often overlooked in the differential diagnosis of patients with central cyanosis. In most cases, methemoglobinemia is acquired and hereditar
Externí odkaz:
https://doaj.org/article/d9bc5b332f8a44eba445f2e42f5fd56b
Publikováno v:
Human Genome Variation, Vol 8, Iss 1, Pp 1-3 (2021)
Abstract Spastic paraplegia (SPG) type 4 is an autosomal dominant SPG caused by functional variants in the SPAST gene. We examined a Japanese family with three autosomal dominant SPG patients. These patients presented with typical symptoms of SPG, su
Externí odkaz:
https://doaj.org/article/e920c3d765784b88a2ba7552076bc6b7
Publikováno v:
Journal of Pharmaceutical Health Care and Sciences, Vol 3, Iss 1, Pp 1-8 (2017)
Abstract Background The accuracy, safety and feasibility of, the compounding robot APOTECAchemo were evaluated in the clinical practice of Japan. Methods Accuracy and precision of robotic preparations by APOTECAchemo was evaluated in 20 preparations
Externí odkaz:
https://doaj.org/article/677fdbce0eda4ffda5c3dbb8e86cfd9a
Publikováno v:
Holzforschung. 77:378-382
The Japanese longhorn beetle, Anaglyptus subfasciatus, infests coniferous trees resulting in stained wood and low-value discolored lumber. In this study, the discolored Hinoki (Chamaecyparis obtusa) wood was analysed by GC-MS for n-hexane extract, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8ce64291a3b62dd3465ee13b70388afd
https://doi.org/10.1515/hf-2022-0183
https://doi.org/10.1515/hf-2022-0183
Autor:
Akihiro Nagano, Shiroh Miura, Hiroaki Ohishi, Takuya Morikawa, Motoko Unoki, Kengo Kosaka, Hiroyuki Sasaki, Kosei Moriyama, Motonao Nakao, Takeshi Bamba, Yoshihiro Izumi, Masatomo Takahashi, Itsuki Taniguchi, Tomofumi Shimojo, Ryuta Fujioka, Hiroki Shibata
Publikováno v:
Bioscience Reports
We have previously reported a novel homozygous 4-bp deletion in DDHD1 as the responsible variant for spastic paraplegia type 28 (SPG28; OMIM#609340). The variant causes a frameshift, resulting in a functionally null allele in the patient. DDHD1 encod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83d52e818085dec0a19aa09cd32ab81a
https://pubmed.ncbi.nlm.nih.gov/33600578
https://pubmed.ncbi.nlm.nih.gov/33600578