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Satoshi Endo

Showing results (301-310 of 395) with videos related to

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IEEE Transactions on Bio-Medical Engineering|February 23, 2019
A Multi-Layer Gaussian Process for Motor Symptom Estimation in People With Parkinson's DiseaseMuriel Lang, Franz M J Pfister, Jakob Frohner, et al.
Biological & Pharmaceutical Bulletin|October 3, 2017
Enhancement of Endothelial Barrier Permeability by MitragynineToshiyuki Matsunaga, Yoshifumi Morikawa, Kyoko Kamase, et al.
Chemico-Biological Interactions|July 16, 2016
Aldo-keto reductase 1B10 promotes development of cisplatin resistance in gastrointestinal cancer cells through down-regulating peroxisome proliferator-activated receptor-γ-dependent mechanismToshiyuki Matsunaga, Ayaka Suzuki, Chihiro Kezuka, et al.
The Plant Cell|April 23, 2009
Identifying new components participating in the secondary cell wall formation of vessel elements in zinnia and ArabidopsisSatoshi Endo, Edouard Pesquet, Masatoshi Yamaguchi, et al.
Biochemical Pharmacology|September 3, 2013
Rabbit 3-hydroxyhexobarbital dehydrogenase is a NADPH-preferring reductase with broad substrate specificity for ketosteroids, prostaglandin D₂, and other endogenous and xenobiotic carbonyl compoundsSatoshi Endo, Toshiyuki Matsunaga, Atsuko Matsumoto, et al.
Bioorganic & Medicinal Chemistry|September 28, 2013
Synthesis and structure-activity relationship of 2-phenyliminochromene derivatives as inhibitors for aldo-keto reductase (AKR) 1B10Satoshi Endo, Dawei Hu, Miho Suyama, et al.
Scientific Reports|July 4, 2023
ARL-17477 is a dual inhibitor of NOS1 and the autophagic-lysosomal system that prevents tumor growth in vitro and in vivoTeiko Komori Nomura, Satoshi Endo, Takuma Kuwano, et al.
Journal of Medicinal Chemistry|June 11, 2011
Discovery of 1-{4-[1-(2,6-difluorobenzyl)-5-[(dimethylamino)methyl]-3-(6-methoxypyridazin-3-yl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl]phenyl}-3-methoxyurea (TAK-385) as a potent, orally active, non-peptide antagonist of the human gonadotropin-releasing hormone receptorKazuhiro Miwa, Takenori Hitaka, Takashi Imada, et al.
The Journal of Biological Chemistry|June 18, 2017
The RING finger- and PDZ domain-containing protein PDZRN3 controls localization of the Mg<sup>2+</sup> regulator claudin-16 in renal tube epithelial cellsKana Marunaka, Chisa Furukawa, Naoko Fujii, et al.
Current Oncology (Toronto, Ont.)|March 27, 2026
Concurrent Chemoradiotherapy with Daily Low-Dose Carboplatin in Older Patients with Unresectable Locally Advanced Non-Small-Cell Lung Cancer: Clinical Outcomes and Prognostic Significance of Systemic Inflammation MarkersYu Miura, Hisao Imai, Satoshi Endo, et al.
Pageof 40

Showing results (301-310 of 395) with videos related to

Sort By:
Pageof 40
IEEE Transactions on Bio-Medical Engineering|February 23, 2019
A Multi-Layer Gaussian Process for Motor Symptom Estimation in People With Parkinson's DiseaseMuriel Lang, Franz M J Pfister, Jakob Frohner, et al.
Biological & Pharmaceutical Bulletin|October 3, 2017
Enhancement of Endothelial Barrier Permeability by MitragynineToshiyuki Matsunaga, Yoshifumi Morikawa, Kyoko Kamase, et al.
Chemico-Biological Interactions|July 16, 2016
Aldo-keto reductase 1B10 promotes development of cisplatin resistance in gastrointestinal cancer cells through down-regulating peroxisome proliferator-activated receptor-γ-dependent mechanismToshiyuki Matsunaga, Ayaka Suzuki, Chihiro Kezuka, et al.
The Plant Cell|April 23, 2009
Identifying new components participating in the secondary cell wall formation of vessel elements in zinnia and ArabidopsisSatoshi Endo, Edouard Pesquet, Masatoshi Yamaguchi, et al.
Biochemical Pharmacology|September 3, 2013
Rabbit 3-hydroxyhexobarbital dehydrogenase is a NADPH-preferring reductase with broad substrate specificity for ketosteroids, prostaglandin D₂, and other endogenous and xenobiotic carbonyl compoundsSatoshi Endo, Toshiyuki Matsunaga, Atsuko Matsumoto, et al.
Bioorganic & Medicinal Chemistry|September 28, 2013
Synthesis and structure-activity relationship of 2-phenyliminochromene derivatives as inhibitors for aldo-keto reductase (AKR) 1B10Satoshi Endo, Dawei Hu, Miho Suyama, et al.
Scientific Reports|July 4, 2023
ARL-17477 is a dual inhibitor of NOS1 and the autophagic-lysosomal system that prevents tumor growth in vitro and in vivoTeiko Komori Nomura, Satoshi Endo, Takuma Kuwano, et al.
Journal of Medicinal Chemistry|June 11, 2011
Discovery of 1-{4-[1-(2,6-difluorobenzyl)-5-[(dimethylamino)methyl]-3-(6-methoxypyridazin-3-yl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl]phenyl}-3-methoxyurea (TAK-385) as a potent, orally active, non-peptide antagonist of the human gonadotropin-releasing hormone receptorKazuhiro Miwa, Takenori Hitaka, Takashi Imada, et al.
The Journal of Biological Chemistry|June 18, 2017
The RING finger- and PDZ domain-containing protein PDZRN3 controls localization of the Mg<sup>2+</sup> regulator claudin-16 in renal tube epithelial cellsKana Marunaka, Chisa Furukawa, Naoko Fujii, et al.
Current Oncology (Toronto, Ont.)|March 27, 2026
Concurrent Chemoradiotherapy with Daily Low-Dose Carboplatin in Older Patients with Unresectable Locally Advanced Non-Small-Cell Lung Cancer: Clinical Outcomes and Prognostic Significance of Systemic Inflammation MarkersYu Miura, Hisao Imai, Satoshi Endo, et al.
Pageof 40