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Page 1
Role of the mitochondrial DNA replication machinery in mitochondrial DNA mutagenesis, aging and age-related diseases.
Ageing Res Rev. 2017 Jan;33:89-104. doi: 10.1016/j.arr.2016.04.006. Epub 2016 Apr 30.
Ageing Res Rev. 2017.
PMID: 27143693
Free PMC article.
Review.
Crystal structure of an Escherichia coli Hfq Core (residues 2-69)-DNA complex reveals multifunctional nucleic acid binding sites.
Orans J, Kovach AR, Hoff KE, Horstmann NM, Brennan RG.
Orans J, et al. Among authors: hoff ke.
Nucleic Acids Res. 2020 Apr 17;48(7):3987-3997. doi: 10.1093/nar/gkaa149.
Nucleic Acids Res. 2020.
PMID: 32133526
Free PMC article.
Item in Clipboard
Structure-specific roles for PolG2-DNA complexes in maintenance and replication of mitochondrial DNA.
Wojtaszek JL, Hoff KE, Longley MJ, Kaur P, Andres SN, Wang H, Williams RS, Copeland WC.
Wojtaszek JL, et al. Among authors: hoff ke.
Nucleic Acids Res. 2023 Oct 13;51(18):9716-9732. doi: 10.1093/nar/gkad679.
Nucleic Acids Res. 2023.
PMID: 37592734
Free PMC article.
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Characterization of the human homozygous R182W POLG2 mutation in mitochondrial DNA depletion syndrome.
Hoff KE, DeBalsi KL, Sanchez-Quintero MJ, Longley MJ, Hirano M, Naini AB, Copeland WC.
Hoff KE, et al.
PLoS One. 2018 Aug 29;13(8):e0203198. doi: 10.1371/journal.pone.0203198. eCollection 2018.
PLoS One. 2018.
PMID: 30157269
Free PMC article.
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Synergistic Effects of the in cis T251I and P587L Mitochondrial DNA Polymerase γ Disease Mutations.
DeBalsi KL, Longley MJ, Hoff KE, Copeland WC.
DeBalsi KL, et al. Among authors: hoff ke.
J Biol Chem. 2017 Mar 10;292(10):4198-4209. doi: 10.1074/jbc.M116.773341. Epub 2017 Feb 2.
J Biol Chem. 2017.
PMID: 28154168
Free PMC article.
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Recognition of U-rich RNA by Hfq from the Gram-positive pathogen Listeria monocytogenes.
Kovach AR, Hoff KE, Canty JT, Orans J, Brennan RG.
Kovach AR, et al. Among authors: hoff ke.
RNA. 2014 Oct;20(10):1548-59. doi: 10.1261/rna.044032.113. Epub 2014 Aug 22.
RNA. 2014.
PMID: 25150227
Free PMC article.
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Whole exome sequencing identifies a homozygous POLG2 missense variant in an infant with fulminant hepatic failure and mitochondrial DNA depletion.
Varma H, Faust PL, Iglesias AD, Lagana SM, Wou K, Hirano M, DiMauro S, Mansukani MM, Hoff KE, Nagy PL, Copeland WC, Naini AB.
Varma H, et al. Among authors: hoff ke.
Eur J Med Genet. 2016 Oct;59(10):540-5. doi: 10.1016/j.ejmg.2016.08.012. Epub 2016 Aug 31.
Eur J Med Genet. 2016.
PMID: 27592148
Free PMC article.
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