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Kinji Ohno

Showing results (161-170 of 245) with videos related to

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Genes & Development|May 22, 2015
Position-specific binding of FUS to nascent RNA regulates mRNA lengthAkio Masuda, Jun-ichi Takeda, Tatsuya Okuno, et al.
American Journal of Human Genetics|January 16, 2002
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndromeKinji Ohno, Andrew G Engel, Xin-Ming Shen, et al.
Redox Biology|December 2, 2025
The Rieske iron-sulfur protein is a primary target of molecular hydrogenShuto Negishi, Mikako Ito, Tomoya Hasegawa, et al.
Parkinsonism & Related Disorders|November 26, 2010
Urinary 8-hydroxydeoxyguanosine correlate with hallucinations rather than motor symptoms in Parkinson's diseaseMasaaki Hirayama, Tomohiko Nakamura, Hirohisa Watanabe, et al.
Scientific Reports|October 24, 2024
Sacubitril/valsartan improves diastolic left ventricular stiffness with increased titin phosphorylation via cGMP-PKG activation in diabetic miceNozomi Furukawa, Hiroki Matsui, Hiroaki Sunaga, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 27, 2003
Myasthenic syndrome caused by mutation of the SCN4A sodium channelAkira Tsujino, Chantal Maertens, Kinji Ohno, et al.
Journal of Neuromuscular Diseases|March 28, 2025
Painful muscle stiffness with markedly elevated serum creatine kinase (CK) levels after twenty weeks of gestation in four patients with myotonic dystrophy type 1 (DM1) and a patient with paramyotonia congenita (PMC)Masanobu Kinoshita, Masaomi Yamamoto, Ryuichi Machida, et al.
JBMR Plus|March 28, 2024
Long-term oral meclozine administration improves survival rate and spinal canal stenosis during postnatal growth in a mouse model of achondroplasia in both sexesHiroto Funahashi, Masaki Matsushita, Ryusaku Esaki, et al.
Human Mutation|July 5, 2016
Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel GatingXin-Ming Shen, Tatsuya Okuno, Margherita Milone, et al.
Nucleic Acids Research|February 10, 2017
Competitive regulation of alternative splicing and alternative polyadenylation by hnRNP H and CstF64 determines acetylcholinesterase isoformsMohammad Nazim, Akio Masuda, Mohammad Alinoor Rahman, et al.
Pageof 25

Showing results (161-170 of 245) with videos related to

Sort By:
Pageof 25
Genes & Development|May 22, 2015
Position-specific binding of FUS to nascent RNA regulates mRNA lengthAkio Masuda, Jun-ichi Takeda, Tatsuya Okuno, et al.
American Journal of Human Genetics|January 16, 2002
Rapsyn mutations in humans cause endplate acetylcholine-receptor deficiency and myasthenic syndromeKinji Ohno, Andrew G Engel, Xin-Ming Shen, et al.
Redox Biology|December 2, 2025
The Rieske iron-sulfur protein is a primary target of molecular hydrogenShuto Negishi, Mikako Ito, Tomoya Hasegawa, et al.
Parkinsonism & Related Disorders|November 26, 2010
Urinary 8-hydroxydeoxyguanosine correlate with hallucinations rather than motor symptoms in Parkinson's diseaseMasaaki Hirayama, Tomohiko Nakamura, Hirohisa Watanabe, et al.
Scientific Reports|October 24, 2024
Sacubitril/valsartan improves diastolic left ventricular stiffness with increased titin phosphorylation via cGMP-PKG activation in diabetic miceNozomi Furukawa, Hiroki Matsui, Hiroaki Sunaga, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 27, 2003
Myasthenic syndrome caused by mutation of the SCN4A sodium channelAkira Tsujino, Chantal Maertens, Kinji Ohno, et al.
Journal of Neuromuscular Diseases|March 28, 2025
Painful muscle stiffness with markedly elevated serum creatine kinase (CK) levels after twenty weeks of gestation in four patients with myotonic dystrophy type 1 (DM1) and a patient with paramyotonia congenita (PMC)Masanobu Kinoshita, Masaomi Yamamoto, Ryuichi Machida, et al.
JBMR Plus|March 28, 2024
Long-term oral meclozine administration improves survival rate and spinal canal stenosis during postnatal growth in a mouse model of achondroplasia in both sexesHiroto Funahashi, Masaki Matsushita, Ryusaku Esaki, et al.
Human Mutation|July 5, 2016
Mutations Causing Slow-Channel Myasthenia Reveal That a Valine Ring in the Channel Pore of Muscle AChR is Optimized for Stabilizing Channel GatingXin-Ming Shen, Tatsuya Okuno, Margherita Milone, et al.
Nucleic Acids Research|February 10, 2017
Competitive regulation of alternative splicing and alternative polyadenylation by hnRNP H and CstF64 determines acetylcholinesterase isoformsMohammad Nazim, Akio Masuda, Mohammad Alinoor Rahman, et al.
Pageof 25