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Margaret A Gustafson

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Molecular Biology of the Cell|October 6, 2017
Regulation of Arf activation occurs via distinct mechanisms at early and late Golgi compartmentsMargaret A Gustafson, J Christopher Fromme
DNA Repair|October 22, 2020
Consequences of compromised mitochondrial genome integrityMargaret A Gustafson, Eric D Sullivan, William C Copeland
Cell Reports|August 31, 2022
Structural basis for activation of Arf1 at the Golgi complexArnold J Muccini, Margaret A Gustafson, J Christopher Fromme
DNA Repair|August 31, 2021
Mechanisms of SSBP1 variants in mitochondrial disease: Molecular dynamics simulations reveal stable tetramers with altered DNA binding surfacesMargaret A Gustafson, Lalith Perera, Min Shi, et al.
The Journal of Biological Chemistry|December 24, 2011
Human mitochondrial DNA polymerase γ exhibits potential for bypass and mutagenesis at UV-induced cyclobutane thymine dimersRajesh Kasiviswanathan, Margaret A Gustafson, William C Copeland, et al.
Elife|January 15, 2016
The Sec7 N-terminal regulatory domains facilitate membrane-proximal activation of the Arf1 GTPaseBrian C Richardson, Steve L Halaby, Margaret A Gustafson, et al.
DNA Repair|September 11, 2012
In vivo repair of alkylating and oxidative DNA damage in the mitochondrial and nuclear genomes of wild-type and glycosylase-deficient Caenorhabditis elegansSenyene E Hunter, Margaret A Gustafson, Kathleen M Margillo, et al.
Biochemistry|November 16, 2011
Importance of the C2, N7, and C8 positions to the mutagenic potential of 8-Oxo-2'-deoxyguanosine with two A family polymerasesMichelle L Hamm, Kelly A Crowley, Michael Ghio, et al.
Plos One|September 4, 2019
Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromesMargaret A Gustafson, Elizabeth M McCormick, Lalith Perera, et al.
The Journal of Clinical Investigation|September 25, 2019
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, et al.
Pageof 1

Showing results (1-10 of 10) with videos related to

Sort By:
Pageof 1
Molecular Biology of the Cell|October 6, 2017
Regulation of Arf activation occurs via distinct mechanisms at early and late Golgi compartmentsMargaret A Gustafson, J Christopher Fromme
DNA Repair|October 22, 2020
Consequences of compromised mitochondrial genome integrityMargaret A Gustafson, Eric D Sullivan, William C Copeland
Cell Reports|August 31, 2022
Structural basis for activation of Arf1 at the Golgi complexArnold J Muccini, Margaret A Gustafson, J Christopher Fromme
DNA Repair|August 31, 2021
Mechanisms of SSBP1 variants in mitochondrial disease: Molecular dynamics simulations reveal stable tetramers with altered DNA binding surfacesMargaret A Gustafson, Lalith Perera, Min Shi, et al.
The Journal of Biological Chemistry|December 24, 2011
Human mitochondrial DNA polymerase γ exhibits potential for bypass and mutagenesis at UV-induced cyclobutane thymine dimersRajesh Kasiviswanathan, Margaret A Gustafson, William C Copeland, et al.
Elife|January 15, 2016
The Sec7 N-terminal regulatory domains facilitate membrane-proximal activation of the Arf1 GTPaseBrian C Richardson, Steve L Halaby, Margaret A Gustafson, et al.
DNA Repair|September 11, 2012
In vivo repair of alkylating and oxidative DNA damage in the mitochondrial and nuclear genomes of wild-type and glycosylase-deficient Caenorhabditis elegansSenyene E Hunter, Margaret A Gustafson, Kathleen M Margillo, et al.
Biochemistry|November 16, 2011
Importance of the C2, N7, and C8 positions to the mutagenic potential of 8-Oxo-2'-deoxyguanosine with two A family polymerasesMichelle L Hamm, Kelly A Crowley, Michael Ghio, et al.
Plos One|September 4, 2019
Mitochondrial single-stranded DNA binding protein novel de novo SSBP1 mutation in a child with single large-scale mtDNA deletion (SLSMD) clinically manifesting as Pearson, Kearns-Sayre, and Leigh syndromesMargaret A Gustafson, Elizabeth M McCormick, Lalith Perera, et al.
The Journal of Clinical Investigation|September 25, 2019
SSBP1 mutations cause mtDNA depletion underlying a complex optic atrophy disorderValentina Del Dotto, Farid Ullah, Ivano Di Meo, et al.
Pageof 1