Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Artificial Organs|July 29, 2014
Liposome-encapsulated hemoglobin enhances chemotherapy to suppress metastasis in miceChieko Murayama, Akira T Kawaguchi, Akemi Kamijo, et al.
Microscopy Research and Technique|November 1, 2011
MRT letter: Expression of ATP sensor protein in Caenorhabditis elegansJun-ichi Kishikawa, Makoto Fujikawa, Hiromi Imamura, et al.
Mechanisms of Ageing and Development|August 9, 2006
Age-related changes of mitochondrial structure and function in Caenorhabditis elegansKayo Yasuda, Takamasa Ishii, Hitoshi Suda, et al.
The Biochemical Journal|June 9, 2007
Mutant alpha-galactosidase A enzymes identified in Fabry disease patients with residual enzyme activity: biochemical characterization and restoration of normal intracellular processing by 1-deoxygalactonojirimycinSatoshi Ishii, Hui-Hwa Chang, Kunito Kawasaki, et al.
Journal of Clinical Biochemistry and Nutrition|January 24, 2022
Streptococcus thermophilus extends lifespan through activation of DAF-16-mediated antioxidant pathway in Caenorhabditis elegansNatsumi Desaka, Chinatsu Ota, Hitomi Nishikawa, et al.
Investigative Ophthalmology & Visual Science|July 13, 2012
Mitochondrial superoxide anion overproduction in Tet-mev-1 transgenic mice accelerates age-dependent corneal cell dysfunctionsHiromi Onouchi, Takamasa Ishii, Masaki Miyazawa, et al.
Plos One|October 17, 2012
Oxidative stress induced inflammation initiates functional decline of tear productionYuichi Uchino, Tetsuya Kawakita, Masaki Miyazawa, et al.
Journal of Natural Products|December 28, 2002
New polyhydroxylated pyrrolidine, piperidine, and pyrrolizidine alkaloids from Scilla sibiricaToru Yamashita, Kayo Yasuda, Haruhisa Kizu, et al.
Redox Biology|June 18, 2014
Genetically induced oxidative stress in mice causes thrombocytosis, splenomegaly and placental angiodysplasia that leads to recurrent abortionTakamasa Ishii, Masaki Miyazawa, Yumi Takanashi, et al.
Mitochondrion|September 28, 2010
Mitochondrial reactive oxygen species generation by the SDHC V69E mutation causes low birth weight and neonatal growth retardationTakamasa Ishii, Masaki Miyazawa, Akira Onodera, et al.
Pageof 5