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Biochemical and Biophysical Research Communications|March 27, 1996
A novel mitochondrial DNA point mutation in the tRNA(Ile) gene is associated with progressive external ophtalmoplegiaG Silvestri, S Servidei, M Rana, et al.Langmuir : the ACS Journal of Surfaces and Colloids|June 12, 2024
Dynamic Drop Penetration of Horizontally Oriented Fiber ArraysGene Patrick S Rible, Michael A Spinazzola, Robert E Jones, et al.The Journal of Biological Chemistry|March 27, 1999
Oligomycin induces a decrease in the cellular content of a pathogenic mutation in the human mitochondrial ATPase 6 geneG Manfredi, N Gupta, M E Vazquez-Memije, et al.Neurology|August 15, 2001
Coenzyme Q10 reverses pathological phenotype and reduces apoptosis in familial CoQ10 deficiencyS Di Giovanni, M Mirabella, A Spinazzola, et al.Journal of Inherited Metabolic Disease|January 7, 2009
Clinical and molecular features of mitochondrial DNA depletion syndromesA Spinazzola, F Invernizzi, F Carrara, et al.Biochimica Et Biophysica Acta|September 15, 2009
Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1)J Poulton, M Hirano, A Spinazzola, et al.Neurology|September 17, 1999
A distinctive autosomal dominant vacuolar neuromyopathy linked to 19p13S Servidei, F Capon, A Spinazzola, et al.Nucleic Acids Research|March 29, 2012
Mitochondrial nucleoid interacting proteins support mitochondrial protein synthesisJ He, H M Cooper, A Reyes, et al.ESMO Open|February 3, 2026
Impact of ECOG performance status 2 participants on outcomes of pivotal cancer clinical trials: a meta-analysis and meta-regressionG M Iannantuono, T Giovagnoli, L Mastrantoni, et al.European Journal of Neurology|March 20, 2010
EFNS guidelines on the molecular diagnosis of channelopathies, epilepsies, migraine, stroke, and dementiasJ-M Burgunder, J Finsterer, Z Szolnoki, et al.Pageof 3