Affiliation |
Graduate School of Medicine Doctorial Course in Medicine Bioregulatory Medicine Department of Cell Physiology |
OKAMOTO Yousuke
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Graduating School 【 display / non-display 】
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-2006.03
Akita University Faculty of Medicine Graduated
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-2000.03
Aoyama Gakuin University Faculty of Humanities Graduated
Graduate School 【 display / non-display 】
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-2012.09
Akita University Graduate School, Division of Medicine Doctor's Course Completed
Studying abroad experiences 【 display / non-display 】
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2012.11-2015.03
National Institute of Health Visiting fellow (postdoc)
Campus Career 【 display / non-display 】
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2020.06-Now
Akita University Graduate School of Medicine Doctorial Course in Medicine Bioregulatory Medicine Lecturer
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2017.11-2020.05
Akita University Graduate School of Medicine Doctorial Course in Medicine Bioregulatory Medicine Assistant Professor
Research Areas 【 display / non-display 】
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Life Science / Clinical pharmacy
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Life Science / Physiology
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Life Science / Pharmacology
Thesis for a degree 【 display / non-display 】
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Arrhythmogenic coupling between the Na+ -Ca2+ exchanger and inositol 1,4,5-triphosphate receptor in rat pulmonary vein cardiomyocytes.
Okamoto Y, Takano M, Ohba T, Ono K.
Journal of Molecular Cellular Cardiology 52 988 - 997 2012.09 [Refereed]
Domestic Co-author
Research Achievements 【 display / non-display 】
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Molecular characteristics of catecholamine-induced arrhythmia in pulmonary vein
Yosuke Okamoto
40 ( 3 ) 141 - 148 2020.10 [Refereed] [Invited]
Research paper (journal) Single author
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Takagi D, Okamoto Y, Ohba T, Yamamoto H, Ono K
Journal of Physiological Sciences 70 ( 1 ) 2020.02 [Refereed]
Research paper (journal) Domestic Co-author
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Okamoto Y, Nagasawa Y, Obara Y, Ishii I, Takagi D, Ono K
Journal of Biological Chemistry 294 ( 44 ) 16049 - 16061 2019.11 [Refereed]
Research paper (journal) Domestic Co-author
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Umehara S, Tan X, Okamoto Y, Ono K, Noma A, Amano A, Himeno Y
International Journal of Molecular Sciences 20 ( 12 ) 2019.06 [Refereed]
Research paper (journal) Domestic Co-author
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ERK5 Phosphorylates Kv4.2 and Inhibits Inactivation of the A-Type Current in PC12 Cells.
Kashino Y, Obara Y, Okamoto Y, Saneyoshi T, Hayashi Y, Ishii K.
International journal of molecular science 2018.07 [Refereed]
Research paper (journal) Domestic Co-author
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Fundamental research on on atrial fibrillation in the post-genomic age
BIO Clinica 35 ( 14 ) 56 - 60 2020.12
Introduction and explanation (scientific journal) Single author
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New strategies to characterize molecular pathophysiology of atrial fibrillation
BIO Clinica ( Hokuryukan ) 35 ( 9 ) 86 - 91 2020.08
Introduction and explanation (scientific journal) Single author
◆Original paper【 display / non-display 】
◆Introduction and explanation【 display / non-display 】
Books 【 display / non-display 】
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Molecular Pathogenesis of Cardiac Arrhythmia
Okamoto Y, Ono K.
MDPI 2022.11 ISBN: 978-3-0365-5614-7
Grant-in-Aid for Scientific Research 【 display / non-display 】
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Grant-in-Aid for Scientific Research(C)
Project Year: 2022.04 - 2025.03
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Grant-in-Aid for Early-Career Scientists
Project Year: 2020.04 - 2023.03
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Grant-in-Aid for Young Scientists(B)
Project Year: 2017.04 - 2020.03
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Cloning of the Cl- channel unique to pulmonary vein cardiomyocytes in rat
Grant-in-Aid for Research Activity start-up
Project Year: 2015.08 - 2017.03 Investigator(s): Yosuke Okamoto
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Grant-in-Aid for Young Scientists (Start-up)
Project Year: 2015.04 - 2017.03
Presentations 【 display / non-display 】
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Comparative Study of Transcriptome in the Hearts Isolated from Mice, Rats, and Humans
Okamoto Yosuke, Okada Daigo, Kobayashi Daiki, Ono Kyoichi, Ishii Kuniaki
Proceedings for Annual Meeting of The Japanese Pharmacological Society 2022 - 2022 Japanese Pharmacological Society
<p>The heart is a critical organ for maintaining life in mammals and has long been one of the most important targets of scientific research, and the basic molecular mechanisms of heart beat appear to have already been established. However, few studies have focused on species differences, and challenges remain in studying genes that have universal functions across species and genes that determine species differences. Here, we analyzed transcriptome data from mouse, rat, and human atria, ventricles, and sinus node (SA) and calculated and compared specificity measure (SPM) values that account for species differences among the three cardiac regions. SA has the largest species differences and we searched for a gene, which by our criteria was SHOX2; the SPM value for SHOX2 was prominently high across species. Similarly, SPM values identified 3 atrial-specific markers, 11 ventricular-specific markers, and 17 SA-specific markers. Ontology analysis identified 70 cardiac region- and species-specific ontologies. These results suggest that reanalysis of existing data by calculating SPM values may identify novel tissue-specific and species-dependent gene expression. This study demonstrates that SHOX2 is an SA-specific transcription factor, a novel cardiac region marker, and that species-dependent ontology is important. No COI.</p>
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シンポジウム:不整脈発症のメカニズムに迫る - 基礎と臨床の立場から -
岡本 洋介,永澤 悦伸,ナイン イエイ アウン,姫野 友紀子,野間 昭典,天野 晃,高木 大地,石井 邦明,尾野 恭一
第97回 日本生理学会大会 2020.03 - 2020.03