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Matthew J Longley

Showing results (31-40 of 43) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
DNA precursor asymmetries in mammalian tissue mitochondria and possible contribution to mutagenesis through reduced replication fidelityShiwei Song, Zachary F Pursell, William C Copeland, et al.
Eukaryotic Cell|August 13, 2003
POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNAMicheline K Strand, Gregory R Stuart, Matthew J Longley, 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.
Plos One|August 30, 2018
Characterization of the human homozygous R182W POLG2 mutation in mitochondrial DNA depletion syndromeKirsten E Hoff, Karen L DeBalsi, Maria J Sanchez-Quintero, et al.
Nucleic Acids Research|August 18, 2023
Structure-specific roles for PolG2-DNA complexes in maintenance and replication of mitochondrial DNAJessica L Wojtaszek, Kirsten E Hoff, Matthew J Longley, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 2022
Structural insight and characterization of human Twinkle helicase in mitochondrial diseaseAmanda A Riccio, Jonathan Bouvette, Lalith Perera, et al.
Nucleic Acids Research|June 27, 2026
Persistence of large mtDNA rearrangements linked to premature aging in Pol γ exonuclease-deficient miceShilan Wu, Scott A Lujan, Adam B Burkholder, et al.
Nucleic Acids Research|October 4, 2017
Complementation of aprataxin deficiency by base excision repair enzymes in mitochondrial extractsMelike Çaglayan, Rajendra Prasad, Rachel Krasich, et al.
American Journal of Human Genetics|May 11, 2006
Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegiaMatthew J Longley, Susanna Clark, Cynthia Yu Wai Man, et al.
Archives of Neurology|January 16, 2008
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Proceedings of the National Academy of Sciences of the United States of America|March 24, 2005
DNA precursor asymmetries in mammalian tissue mitochondria and possible contribution to mutagenesis through reduced replication fidelityShiwei Song, Zachary F Pursell, William C Copeland, et al.
Eukaryotic Cell|August 13, 2003
POS5 gene of Saccharomyces cerevisiae encodes a mitochondrial NADH kinase required for stability of mitochondrial DNAMicheline K Strand, Gregory R Stuart, Matthew J Longley, 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.
Plos One|August 30, 2018
Characterization of the human homozygous R182W POLG2 mutation in mitochondrial DNA depletion syndromeKirsten E Hoff, Karen L DeBalsi, Maria J Sanchez-Quintero, et al.
Nucleic Acids Research|August 18, 2023
Structure-specific roles for PolG2-DNA complexes in maintenance and replication of mitochondrial DNAJessica L Wojtaszek, Kirsten E Hoff, Matthew J Longley, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 1, 2022
Structural insight and characterization of human Twinkle helicase in mitochondrial diseaseAmanda A Riccio, Jonathan Bouvette, Lalith Perera, et al.
Nucleic Acids Research|June 27, 2026
Persistence of large mtDNA rearrangements linked to premature aging in Pol γ exonuclease-deficient miceShilan Wu, Scott A Lujan, Adam B Burkholder, et al.
Nucleic Acids Research|October 4, 2017
Complementation of aprataxin deficiency by base excision repair enzymes in mitochondrial extractsMelike Çaglayan, Rajendra Prasad, Rachel Krasich, et al.
American Journal of Human Genetics|May 11, 2006
Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegiaMatthew J Longley, Susanna Clark, Cynthia Yu Wai Man, et al.
Archives of Neurology|January 16, 2008
Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1Silvio Ferraris, Susanna Clark, Emanuela Garelli, et al.
Pageof 5