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Nature Genetics|March 6, 2007
Mitochondrial point mutations do not limit the natural lifespan of miceMarc Vermulst, Jason H Bielas, Gregory C Kujoth, et al.
Journal of Medical Primatology|April 30, 2005
Assessment of nutritional status in rhesus monkeys: comparison of dual-energy X-ray absorptiometry and stable isotope dilutionStéphane Blanc, Ricki Colman, Joseph Kemnitz, et al.
Annals of Clinical and Translational Neurology|December 26, 2014
Heterozygous Polg mutation causes motor dysfunction due to mtDNA deletionsSatoshi Fuke, Mizue Kametani, Kazuyuki Yamada, et al.
Neurobiology of Aging|June 4, 2016
Sirt1 deficiency protects cochlear cells and delays the early onset of age-related hearing loss in C57BL/6 miceChul Han, Paul Linser, Hyo-Jin Park, et al.
Free Radical Biology & Medicine|February 5, 2003
The selenoprotein GPX4 is essential for mouse development and protects from radiation and oxidative damage insultsLevi J Yant, Qitao Ran, Lin Rao, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 11, 2011
Mitochondrial DNA polymerase editing mutation, PolgD257A, reduces the diabetic phenotype of Akita male mice by suppressing appetiteRaymond Fox, Hyung-Suk Kim, Robert L Reddick, et al.
The Oncologist|September 28, 2014
Novel approaches in anaplastic thyroid cancer therapyKun-Tai Hsu, Xiao-Min Yu, Anjon W Audhya, et al.
Experimental Gerontology|November 6, 2008
Longitudinal analysis of early stage sarcopenia in aging rhesus monkeysSusan H McKiernan, Ricki Colman, Marisol Lopez, et al.
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