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Masato Mori

Showing results (11-20 of 62) with videos related to

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Journal of Human Genetics|May 29, 2002
Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1Hung Li, Takanori Yamagata, Masato Mori, et al.
Brain & Development|March 2, 2005
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patientsHong Li, Takanori Yamagata, Masato Mori, et al.
Brain & Development|January 26, 2005
RSK2 gene mutations in Coffin-Lowry syndrome with drop episodesMiki Nakamura, Takanori Yamagata, Masato Mori, et al.
Pediatric Neurology|May 7, 2005
Early-onset ataxia with oculomotor apraxia with a novel APTX mutationAya Ito, Takanori Yamagata, Masato Mori, et al.
Sensors (Basel, Switzerland)|October 16, 2024
Development of Assistance Level Adjustment Function for Variable Load on a Forearm-Supported Robotic WalkerYuto Mori, Soichiro Yokoyama, Tomohisa Yamashita, et al.
Cureus|May 24, 2021
Transient Pseudohypoaldosteronism Secondary to Group B Streptococcus PyelonephritisAtsuo Morisaki, Yuki Naruse, Yui Shibata, et al.
Springerplus|May 19, 2015
The protection mechanism of proline from D-galactosamine hepatitis involves the early activation of ROS-eliminating pathway in the liverYoko Obayashi, Harumi Arisaka, Shintaro Yoshida, et al.
Amino Acids|June 28, 2008
Adaptational modification of serine and threonine metabolism in the liver to essential amino acid deficiency in ratsKenji Nagao, Makoto Bannai, Shinobu Seki, et al.
Amino Acids|May 16, 2012
Proline protects liver from D-galactosamine hepatitis by activating the IL-6/STAT3 survival signaling pathwayYoko Obayashi, Harumi Arisaka, Shintaro Yoshida, et al.
Brain & Development|June 22, 2005
Mutation analysis of methyl-CpG binding protein family genes in autistic patientsHong Li, Takanori Yamagata, Masato Mori, et al.
Pageof 7

Showing results (11-20 of 62) with videos related to

Sort By:
Pageof 7
Journal of Human Genetics|May 29, 2002
Association of autism in two patients with hereditary multiple exostoses caused by novel deletion mutations of EXT1Hung Li, Takanori Yamagata, Masato Mori, et al.
Brain & Development|March 2, 2005
Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patientsHong Li, Takanori Yamagata, Masato Mori, et al.
Brain & Development|January 26, 2005
RSK2 gene mutations in Coffin-Lowry syndrome with drop episodesMiki Nakamura, Takanori Yamagata, Masato Mori, et al.
Pediatric Neurology|May 7, 2005
Early-onset ataxia with oculomotor apraxia with a novel APTX mutationAya Ito, Takanori Yamagata, Masato Mori, et al.
Sensors (Basel, Switzerland)|October 16, 2024
Development of Assistance Level Adjustment Function for Variable Load on a Forearm-Supported Robotic WalkerYuto Mori, Soichiro Yokoyama, Tomohisa Yamashita, et al.
Cureus|May 24, 2021
Transient Pseudohypoaldosteronism Secondary to Group B Streptococcus PyelonephritisAtsuo Morisaki, Yuki Naruse, Yui Shibata, et al.
Springerplus|May 19, 2015
The protection mechanism of proline from D-galactosamine hepatitis involves the early activation of ROS-eliminating pathway in the liverYoko Obayashi, Harumi Arisaka, Shintaro Yoshida, et al.
Amino Acids|June 28, 2008
Adaptational modification of serine and threonine metabolism in the liver to essential amino acid deficiency in ratsKenji Nagao, Makoto Bannai, Shinobu Seki, et al.
Amino Acids|May 16, 2012
Proline protects liver from D-galactosamine hepatitis by activating the IL-6/STAT3 survival signaling pathwayYoko Obayashi, Harumi Arisaka, Shintaro Yoshida, et al.
Brain & Development|June 22, 2005
Mutation analysis of methyl-CpG binding protein family genes in autistic patientsHong Li, Takanori Yamagata, Masato Mori, et al.
Pageof 7