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Biochemical and Biophysical Research Communications|April 24, 2012
Cadmium activates extracellular signal-regulated kinase 5 in HK-2 human renal proximal tubular cellsMio Kondo, Hisako Inamura, Ken-ichi Matsumura, et al.Bioorganic & Medicinal Chemistry|November 5, 2002
A novel class of endothelin-A receptor antagonists, (R)-2-(benzo[1,3]dioxol-5-yl)-6-isopropyloxy-2H-chromene-3-carboxylic acids (S-1255). Conformational analysis of basic structure, crucial for ET(A) antagonism, in solution and solid statesNatsuki Ishizuka, Ken-ichi Matsumura, Junko Kikuchi, et al.Neurologia Medico-Chirurgica|February 9, 2005
Intracranial localized Castleman's disease. Case reportKen-ichi Matsumura, Satoshi Nakasu, Toshiki Tanaka, et al.Neurologia Medico-Chirurgica|January 29, 2019
CT Hounsfield Unit Is a Good Predictor of Growth in MeningiomasSatoshi Nakasu, Takeshi Onishi, Sawako Kitahara, et al.Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association|August 11, 2007
Circumstances, activities, and events precipitating aneurysmal subarachnoid hemorrhageMasayuki Matsuda, Kazuyoshi Watanabe, Akira Saito, et al.The Journal of Organic Chemistry|October 26, 2002
Practical enantioselective synthesis of endothelin antagonist S-1255 by dynamic resolution of 4-methoxychromene-3-carboxylic acid intermediateToshiro Konoike, Ken-Ichi Matsumura, Tadahiko Yorifuji, et al.Journal of Medicinal Chemistry|May 3, 2002
Structure-activity relationships of a novel class of endothelin-A receptor antagonists and discovery of potent and selective receptor antagonist, 2-(benzo[1,3]dioxol-5-yl)-6-isopropyloxy-4-(4-methoxyphenyl)-2H-chromene-3-carboxylic acid (S-1255). 1. Study on structure-activity relationships and basic structure crucial for ET(A) antagonismNatsuki Ishizuka, Ken-ichi Matsumura, Katsunori Sakai, et al.Plos One|August 18, 2025
Sex and age differences in the association between routine suicide newspaper reporting and change in admissions of suicidal patients: An investigation at an emergency and critical care center in TokyoYasushi Emura, Sho Kanata, Naoki Hayashi, et al.Journal of Medicinal Chemistry|August 8, 2023
Design, Synthesis, and Anti-Inflammatory Evaluation of a Novel PPARδ Agonist with a 4-(1-Pyrrolidinyl)piperidine StructureTerukazu Kato, Keita Fukao, Takafumi Ohara, et al.Bioorganic & Medicinal Chemistry Letters|January 22, 2022
Discovery and structure-based design of a new series of potent and selective PPARδ agonists utilizing a virtual screening methodTerukazu Kato, Takafumi Ohara, Naoyuki Suzuki, et al.Pageof 2