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EMBO Molecular Medicine|June 17, 2026
Activation of AMPK as a therapeutic strategy for FBXL4-related mitochondrial DNA depletion syndromeAniketh Bishnu, Juan Zapata-Muñoz, Robert W Taylor, et al.
British Journal of Pharmacology|August 1, 1992
Modulation of the pharmacological actions of nitrovasodilators by methylene blue and pyocyaninR J Gryglewski, A Zembowicz, D Salvemini, et al.
Journal of the Neurological Sciences|September 3, 2010
A novel mitochondrial tRNAGlu (MTTE) gene mutation causing chronic progressive external ophthalmoplegia at low levels of heteroplasmy in muscleCharlotte L Alston, James Lowe, Douglass M Turnbull, et al.
The New England Journal of Medicine|April 3, 1986
Determining optimal therapy--randomized trials in individual patientsG Guyatt, D Sackett, D W Taylor, et al.
Clinical Nutrition ESPEN|February 9, 2018
Association between nutrient patterns and bone mineral density among ageing adultsYohannes Adama Melaku, Tiffany K Gill, Anne W Taylor, et al.
Frontiers in Genetics|August 2, 2021
Epigenetic Markers Are Associated With Differences in Isocyanate Biomarker Levels in Exposed Spray-PaintersLaura W Taylor, John E French, Zachary G Robbins, et al.
Neuromuscular Disorders : NMD|January 22, 2004
A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysisRobert McFarland, Robert W Taylor, Patrick F Chinnery, et al.
Trends in Genetics : TIG|November 4, 2004
Assigning pathogenicity to mitochondrial tRNA mutations: when "definitely maybe" is not good enoughRobert McFarland, Joanna L Elson, Robert W Taylor, et al.
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