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Kinji Ohno

Showing results (211-220 of 245) with videos related to

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Applied Physiology, Nutrition, and Metabolism = Physiologie Appliquee, Nutrition Et Metabolisme|August 15, 2017
Interactions between genetic polymorphisms of glucose metabolizing genes and smoking and alcohol consumption in the risk of type 2 diabetes mellitusKaiping Gao, Yongcheng Ren, Jinjin Wang, et al.
NPJ Parkinson'S Disease|June 1, 2022
Short chain fatty acids-producing and mucin-degrading intestinal bacteria predict the progression of early Parkinson's diseaseHiroshi Nishiwaki, Mikako Ito, Tomonari Hamaguchi, et al.
Neuroscience Letters|April 10, 2009
Molecular hydrogen is protective against 6-hydroxydopamine-induced nigrostriatal degeneration in a rat model of Parkinson's diseaseYuan Fu, Mikako Ito, Yasunori Fujita, et al.
Biochemical and Biophysical Research Communications|July 18, 2024
A class of chemical compounds enhances clustering of muscle nicotinic acetylcholine receptor in cultured myogenic cellsYuichi Miyairi, Bisei Ohkawara, Ayato Sato, et al.
Disease Models & Mechanisms|June 21, 2024
Muscle-specific lack of Gfpt1 triggers ER stress to alleviate misfolded protein accumulationRuchen Zhang, Paniz Farshadyeganeh, Bisei Ohkawara, et al.
NPJ Parkinson'S Disease|May 21, 2024
Meta-analysis of shotgun sequencing of gut microbiota in Parkinson's diseaseHiroshi Nishiwaki, Jun Ueyama, Mikako Ito, et al.
Cell Reports|May 3, 2018
Loss of Sfpq Causes Long-Gene Transcriptopathy in the BrainAkihide Takeuchi, Kei Iida, Toshiaki Tsubota, et al.
JCI Insight|April 10, 2020
Congenital myasthenic syndrome-associated agrin variants affect clustering of acetylcholine receptors in a domain-specific mannerBisei Ohkawara, XinMing Shen, Duygu Selcen, et al.
Neuromuscular Disorders : NMD|June 3, 2015
A missense mutation in domain III in HSPG2 in Schwartz-Jampel syndrome compromises secretion of perlecan into the extracellular spaceSatoshi Iwata, Mikako Ito, Tomohiko Nakata, et al.
International Journal of Systematic and Evolutionary Microbiology|January 13, 2025
<i>Desulfovibrio falkowii</i> sp. nov., <i>Porphyromonas miyakawae</i> sp. nov., <i>Mediterraneibacter flintii</i> sp. nov. and <i>Owariibacterium komagatae</i> gen. nov., sp. nov., isolated from human faecesTomonari Hamaguchi, Misuzu Ohara, Atsushi Hisatomi, et al.
Pageof 25

Showing results (211-220 of 245) with videos related to

Sort By:
Pageof 25
Applied Physiology, Nutrition, and Metabolism = Physiologie Appliquee, Nutrition Et Metabolisme|August 15, 2017
Interactions between genetic polymorphisms of glucose metabolizing genes and smoking and alcohol consumption in the risk of type 2 diabetes mellitusKaiping Gao, Yongcheng Ren, Jinjin Wang, et al.
NPJ Parkinson'S Disease|June 1, 2022
Short chain fatty acids-producing and mucin-degrading intestinal bacteria predict the progression of early Parkinson's diseaseHiroshi Nishiwaki, Mikako Ito, Tomonari Hamaguchi, et al.
Neuroscience Letters|April 10, 2009
Molecular hydrogen is protective against 6-hydroxydopamine-induced nigrostriatal degeneration in a rat model of Parkinson's diseaseYuan Fu, Mikako Ito, Yasunori Fujita, et al.
Biochemical and Biophysical Research Communications|July 18, 2024
A class of chemical compounds enhances clustering of muscle nicotinic acetylcholine receptor in cultured myogenic cellsYuichi Miyairi, Bisei Ohkawara, Ayato Sato, et al.
Disease Models & Mechanisms|June 21, 2024
Muscle-specific lack of Gfpt1 triggers ER stress to alleviate misfolded protein accumulationRuchen Zhang, Paniz Farshadyeganeh, Bisei Ohkawara, et al.
NPJ Parkinson'S Disease|May 21, 2024
Meta-analysis of shotgun sequencing of gut microbiota in Parkinson's diseaseHiroshi Nishiwaki, Jun Ueyama, Mikako Ito, et al.
Cell Reports|May 3, 2018
Loss of Sfpq Causes Long-Gene Transcriptopathy in the BrainAkihide Takeuchi, Kei Iida, Toshiaki Tsubota, et al.
JCI Insight|April 10, 2020
Congenital myasthenic syndrome-associated agrin variants affect clustering of acetylcholine receptors in a domain-specific mannerBisei Ohkawara, XinMing Shen, Duygu Selcen, et al.
Neuromuscular Disorders : NMD|June 3, 2015
A missense mutation in domain III in HSPG2 in Schwartz-Jampel syndrome compromises secretion of perlecan into the extracellular spaceSatoshi Iwata, Mikako Ito, Tomohiko Nakata, et al.
International Journal of Systematic and Evolutionary Microbiology|January 13, 2025
<i>Desulfovibrio falkowii</i> sp. nov., <i>Porphyromonas miyakawae</i> sp. nov., <i>Mediterraneibacter flintii</i> sp. nov. and <i>Owariibacterium komagatae</i> gen. nov., sp. nov., isolated from human faecesTomonari Hamaguchi, Misuzu Ohara, Atsushi Hisatomi, et al.
Pageof 25