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Current Opinion in Genetics & Development|April 12, 2016
Human mitochondrial DNA replication machinery and diseaseMatthew J Young, William C CopelandMethods (San Diego, Calif.)|February 24, 2010
Purification and functional characterization of human mitochondrial DNA polymerase gamma harboring disease mutationsRajesh Kasiviswanathan, Matthew J Longley, Matthew J Young, et al.Human Molecular Genetics|July 1, 2015
POLG2 disease variants: analyses reveal a dominant negative heterodimer, altered mitochondrial localization and impaired respiratory capacityMatthew J Young, Margaret M Humble, Karen L DeBalsi, et al.Human Molecular Genetics|May 11, 2011
Biochemical analysis of human POLG2 variants associated with mitochondrial diseaseMatthew J Young, Matthew J Longley, Fang-Yuan Li, et al.Annual Review of Medicine|September 26, 2007
Inherited mitochondrial diseases of DNA replicationWilliam C CopelandSub-Cellular Biochemistry|December 17, 2009
The mitochondrial DNA polymerase in health and diseaseWilliam C CopelandCritical Reviews in Biochemistry and Molecular Biology|December 20, 2011
Defects in mitochondrial DNA replication and human diseaseWilliam C CopelandHuman Molecular Genetics|December 1, 2012
Polg2 is essential for mammalian embryogenesis and is required for mtDNA maintenanceMargaret M Humble, Matthew J Young, Julie F Foley, et al.Mitochondrion|December 14, 2011
A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunitsKate Craig, Matthew J Young, Emma L Blakely, et al.Pageof 15