Showing 1 - 7 results of 7 for search 'William C. Copeland', query time: 0.03s Refine Results
  1. 1
    MMS exposure promotes increased MtDNA mutagenesis in the presence of replication-defective disease-associated DNA polymerase γ variants.

    MMS exposure promotes increased MtDNA mutagenesis in the presence of replication-defective disease-associated DNA polymerase γ variants. by Jeffrey D Stumpf, William C Copeland

    Published 2014-10-01
    Get full text
    Article
  2. 2
    A new pathogenic POLG variant

    A new pathogenic POLG variant by S. Nicholas Russo, Ekta G. Shah, William C. Copeland, Mary Kay Koenig

    Published 2022-09-01
    Get full text
    Article
  3. 3
    Corrigendum to “A new pathogenic POLG variant” [Molecular Genetics and Metabolism Reports 32 (2022) 100890]

    Corrigendum to “A new pathogenic POLG variant” [Molecular Genetics and Metabolism Reports 32 (2022) 100890] by S. Nicholas Russo, Ekta G. Shah, William C. Copeland, Mary Kay Koenig

    Published 2023-03-01
    Get full text
    Article
  4. 4
    Automated systematic evaluation of cryo-EM specimens with SmartScope

    Automated systematic evaluation of cryo-EM specimens with SmartScope by Jonathan Bouvette, Qinwen Huang, Amanda A Riccio, William C Copeland, Alberto Bartesaghi, Mario J Borgnia

    Published 2022-08-01
    Get full text
    Article
  5. 5
    Recent insights into the structure and function of coronavirus ribonucleases

    Recent insights into the structure and function of coronavirus ribonucleases by Meredith N. Frazier, Amanda A. Riccio, Isha M. Wilson, William C. Copeland, Robin E. Stanley

    Published 2022-09-01
    Get full text
    Article
  6. 6
    Characterization of the human homozygous R182W POLG2 mutation in mitochondrial DNA depletion syndrome.

    Characterization of the human homozygous R182W POLG2 mutation in mitochondrial DNA depletion syndrome. by Kirsten E Hoff, Karen L DeBalsi, Maria J Sanchez-Quintero, Matthew J Longley, Michio Hirano, Ali B Naini, William C Copeland

    Published 2018-01-01
    Get full text
    Article
  7. 7
    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 syndromes.

    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-S... by Margaret A Gustafson, Elizabeth M McCormick, Lalith Perera, Matthew J Longley, Renkui Bai, Jianping Kong, Matthew Dulik, Lishuang Shen, Amy C Goldstein, Shana E McCormack, Benjamin L Laskin, Bart P Leroy, Xilma R Ortiz-Gonzalez, Meredith G Ellington, William C Copeland, Marni J Falk

    Published 2019-01-01
    Get full text
    Article

Search Tools: