Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Junko, Seki"'
Autor:
Yosuke Sudo, Junko Seki-Nagasawa, Daigo Kajikawa, Gen Kuratsuji, Mitsuhiro Haga, Farhad Shokraneh, Noyuri Yamaji, Erika Ota, Fumihiko Namba
Publikováno v:
Neonatology. :1-8
Introduction: Because excessive physical stress is harmful, reducing pain and discomfort in premature neonates during mechanical ventilation is a major challenge for physicians. There are no consensus and systematic review on the use of fentanyl, the
Publikováno v:
Journal of Human Genetics. 68:321-327
Autor:
Junko, Yamanaka, Satoshi, Takasago, Akihisa, Horigome, Miho, Hayashi, Satoshi, Matsunashi, Shogo, Shioda, Mizue, Tanaka, Junko, Seki, Masao, Kaneshige, Tomohisa, Akamatsu, Hideko, Uryu, Shinji, Mochizuki, Keiji, Goishi, Hiroyuki, Shichino
Publikováno v:
Glob Health Med
The COVID-19 pandemic required our pediatric health care staff to adjust to many irregularities and solve serious issues in our routine clinical practice. In outpatient clinics, many children exhibited common cold symptoms that mimic COVID-19, thus w
Autor:
Tsubasa Kameyama, Kazuki Ohuchi, Michinori Funato, Shiori Ando, Satoshi Inagaki, Arisu Sato, Junko Seki, Chizuru Kawase, Kazuhiro Tsuruma, Ichizo Nishino, Shinsuke Nakamura, Masamitsu Shimazawa, Takashi Saito, Shin’ichi Takeda, Hideo Kaneko, Hideaki Hara
Publikováno v:
Frontiers in Pharmacology, Vol 9 (2018)
Duchenne muscular dystrophy (DMD) is a recessive X-linked form of muscular dystrophy characterized by progressive muscle degeneration. This disease is caused by the mutation or deletion of the dystrophin gene. Currently, there are no effective treatm
Externí odkaz:
https://doaj.org/article/0fb712442bbb401bb9f0fa17e684523c
Autor:
Kazuki Ohuchi, Michinori Funato, Hideo Kaneko, Arisu Sato, Chizuru Kawase, Satoshi Inagaki, Hideaki Hara, Shiori Ando, Shinsuke Nakamura, Junko Seki, Masamitsu Shimazawa
Publikováno v:
NeuroReport. 30:350-357
Survival motor neuron (SMN) deficiency indicates that various cellular processes are impaired in spinal muscular atrophy (SMA). Previous reports have shown that SMN deficiency causes motor neuron degeneration, whereas the numbers of astrocytes and mi
Autor:
Hideaki Hara, Hideo Kaneko, Toshio Saito, Chizuru Kawase, Arisu Sato, Shinsuke Nakamura, Kazuki Ohuchi, Junko Seki, Shiori Ando, Hisahide Nishio, Satoshi Inagaki, Yuta Yoshino, Michinori Funato, Masamitsu Shimazawa
Publikováno v:
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by the degeneration of spinal motor neurons and muscle atrophy. The disease is mainly caused by low level of the survival motor neuron (SMN) protein, which i
Autor:
Chizuru Kawase, Satoshi Inagaki, Masamitsu Shimazawa, Hideo Kaneko, Shiori Ando, Michinori Funato, Junko Seki, Kazuki Ohuchi, Shinsuke Nakamura, Hideaki Hara
Publikováno v:
Neuroscience and Medicine. 10:150-161
Glaucoma is a common neurodegenerative disease that can cause blindness and occurs worldwide. Currently, lowering intraocular pressure is the only therapy available to protect retinal ganglion cells (RGCs). However, this therapy does not prevent RGC
Autor:
Arisu Sato, Chizuru Kawase, Junko Seki, Hideaki Hara, Satoshi Inagaki, Kazuki Ohuchi, Michinori Funato, Shiori Ando, Shinsuke Nakamura, Toshio Saito, Hideo Kaneko, Masamitsu Shimazawa, Hisahide Nishio
Publikováno v:
Neurochemical research. 44(7)
Spinal muscular atrophy (SMA) is an inherited disease characterized by progressive motor neuron death and subsequent muscle weakness and is caused by deletion or mutation of survival motor neuron (SMN) 1 gene. Protecting spinal motor neuron is an eff
Autor:
Yoko Ono, Yuki Nagahara, Hideaki Hara, Chizuru Kawase, Kazuki Ohuchi, Kazuhiro Tsuruma, Zenichiro Kato, Hideo Kaneko, Yuya Tamai, Junko Seki, Michinori Funato, Yasuhiro Noda, Shiori Ando, Tsubasa Kameyama, Masamitsu Shimazawa
Publikováno v:
Stem Cells Translational Medicine. 5:152-163
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by the degeneration of spinal motor neurons. This disease is mainly caused by mutation or deletion of the survival motor neuron 1 (SMN1) gene. Currently, no
Autor:
Arisu Sato, Hideo Kaneko, Kazuhide Kawase, Takeshi Iwata, Daisuke Iejima, Kazuki Ohuchi, Hideaki Hara, Satoshi Inagaki, Shiori Ando, Tetsuya Yamamoto, Chizuru Kawase, Tsubasa Kameyama, Shinsuke Nakamura, Wataru Morozumi, Michinori Funato, Masamitsu Shimazawa, Junko Seki
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose To determine a chemical agent that can reduce the aggregation of optineurin (OPTN) in cells differentiated from induced pluripotent stem cells obtained from a patient with normal-tension glaucoma (NTG) caused by an E50K mutation in the OPTN g