David A Claassen, Robert S Lahue. Hum Mol Genet 2007
Times Cited: 26
Times Cited: 26
Times Cited
Times Co-cited
Similarity
OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells.
Irina V Kovtun, Yuan Liu, Magnar Bjoras, Arne Klungland, Samuel H Wilson, Cynthia T McMurray. Nature 2007
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Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice.
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Trinucleotide expansion in haploid germ cells by gap repair.
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CTG repeat instability and size variation timing in DNA repair-deficient mice.
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(CAG)(n)-hairpin DNA binds to Msh2-Msh3 and changes properties of mismatch recognition.
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Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.
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Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
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Mário Gomes-Pereira, M Teresa Fortune, Laura Ingram, John P McAbney, Darren G Monckton. Hum Mol Genet 2004
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Repeat instability as the basis for human diseases and as a potential target for therapy.
Arturo López Castel, John D Cleary, Christopher E Pearson. Nat Rev Mol Cell Biol 2010
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Saccharomyces cerevisiae Srs2 DNA helicase selectively blocks expansions of trinucleotide repeats.
Saumitri Bhattacharyya, Robert S Lahue. Mol Cell Biol 2004
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Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.
Laurent Foiry, Li Dong, Cédric Savouret, Laurence Hubert, Hein te Riele, Claudine Junien, Geneviève Gourdon. Hum Genet 2006
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Repeat instability: mechanisms of dynamic mutations.
Christopher E Pearson, Kerrie Nichol Edamura, John D Cleary. Nat Rev Genet 2005
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Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair.
Gagan B Panigrahi, Rachel Lau, S Erin Montgomery, Michelle R Leonard, Christopher E Pearson. Nat Struct Mol Biol 2005
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Histone deacetylase complexes promote trinucleotide repeat expansions.
Kim Debacker, Aisling Frizzell, Olive Gleeson, Lucy Kirkham-McCarthy, Tony Mertz, Robert S Lahue. PLoS Biol 2012
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MutSβ and histone deacetylase complexes promote expansions of trinucleotide repeats in human cells.
Anne-Marie M Gannon, Aisling Frizzell, Evan Healy, Robert S Lahue. Nucleic Acids Res 2012
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Trinucleotide repeats that expand in human disease form hairpin structures in vitro.
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Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum.
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Mechanisms of trinucleotide repeat instability during human development.
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Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells.
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MSH2-dependent germinal CTG repeat expansions are produced continuously in spermatogonia from DM1 transgenic mice.
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Orientation-dependent and sequence-specific expansions of CTG/CAG trinucleotide repeats in Saccharomyces cerevisiae.
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Dnmt1 deficiency promotes CAG repeat expansion in the mouse germline.
Vincent Dion, Yunfu Lin, Leroy Hubert, Robert A Waterland, John H Wilson. Hum Mol Genet 2008
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CAG*CTG repeat instability in cultured human astrocytes.
Brian T Farrell, Robert S Lahue. Nucleic Acids Res 2006
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Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes.
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Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability.
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Expansion and length-dependent fragility of CTG repeats in yeast.
C H Freudenreich, S M Kantrow, V A Zakian. Science 1998
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Triplet repeat mutation length gains correlate with cell-type specific vulnerability in Huntington disease brain.
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Transcription-induced CAG repeat contraction in human cells is mediated in part by transcription-coupled nucleotide excision repair.
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CREB-binding protein modulates repeat instability in a Drosophila model for polyQ disease.
Joonil Jung, Nancy Bonini. Science 2007
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Somatic instability of the CTG repeat in mice transgenic for the myotonic dystrophy region is age dependent but not correlated to the relative intertissue transcription levels and proliferative capacities.
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Mechanistic features of CAG*CTG repeat contractions in cultured cells revealed by a novel genetic assay.
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Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired.
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Reconstitution of 5'-directed human mismatch repair in a purified system.
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Selectable system for monitoring the instability of CTG/CAG triplet repeats in mammalian cells.
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Genetic assays for triplet repeat instability in yeast.
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Double-strand break repair can lead to high frequencies of deletions within short CAG/CTG trinucleotide repeats.
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CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination.
Randell T Libby, Katharine A Hagerman, Victor V Pineda, Rachel Lau, Diane H Cho, Sandy L Baccam, Michelle M Axford, John D Cleary, James M Moore, Bryce L Sopher,[...]. PLoS Genet 2008
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Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.