Masayuki Nakamori, Christopher E Pearson, Charles A Thornton. Hum Mol Genet 2011
Times Cited: 67
Times Cited: 67
Times Cited
Times Co-cited
Similarity
Transcription promotes contraction of CAG repeat tracts in human cells.
Yunfu Lin, Vincent Dion, John H Wilson. Nat Struct Mol Biol 2006
Yunfu Lin, Vincent Dion, John H Wilson. Nat Struct Mol Biol 2006
43
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
Arturo López Castel, John D Cleary, Christopher E Pearson. Nat Rev Mol Cell Biol 2010
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R loops stimulate genetic instability of CTG.CAG repeats.
Yunfu Lin, Sharon Y R Dent, John H Wilson, Robert D Wells, Marek Napierala. Proc Natl Acad Sci U S A 2010
Yunfu Lin, Sharon Y R Dent, John H Wilson, Robert D Wells, Marek Napierala. Proc Natl Acad Sci U S A 2010
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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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Transcription-induced CAG repeat contraction in human cells is mediated in part by transcription-coupled nucleotide excision repair.
Yunfu Lin, John H Wilson. Mol Cell Biol 2007
Yunfu Lin, John H Wilson. Mol Cell Biol 2007
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Convergent transcription through a long CAG tract destabilizes repeats and induces apoptosis.
Yunfu Lin, Mei Leng, Ma Wan, John H Wilson. Mol Cell Biol 2010
Yunfu Lin, Mei Leng, Ma Wan, John H Wilson. Mol Cell Biol 2010
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Determinants of R-loop formation at convergent bidirectionally transcribed trinucleotide repeats.
Kaalak Reddy, Mandy Tam, Richard P Bowater, Miriam Barber, Matthew Tomlinson, Kerrie Nichol Edamura, Yuh-Hwa Wang, Christopher E Pearson. Nucleic Acids Res 2011
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Transcription destabilizes triplet repeats.
Yunfu Lin, Leroy Hubert, John H Wilson. Mol Carcinog 2009
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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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Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice.
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OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells.
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Mechanisms of trinucleotide repeat instability during human development.
Cynthia T McMurray. Nat Rev Genet 2010
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(CAG)(n)-hairpin DNA binds to Msh2-Msh3 and changes properties of mismatch recognition.
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Repeat expansion disease: progress and puzzles in disease pathogenesis.
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Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice.
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Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1.
Leroy Hubert, Yunfu Lin, Vincent Dion, John H Wilson. Hum Mol Genet 2011
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Stoichiometry of base excision repair proteins correlates with increased somatic CAG instability in striatum over cerebellum in Huntington's disease transgenic mice.
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DNA instability in postmitotic neurons.
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Diverse effects of individual mismatch repair components on transcription-induced CAG repeat instability in human cells.
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Antisense transcription and heterochromatin at the DM1 CTG repeats are constrained by CTCF.
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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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Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.
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Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissues.
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MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic mice.
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Isolated short CTG/CAG DNA slip-outs are repaired efficiently by hMutSbeta, but clustered slip-outs are poorly repaired.
Gagan B Panigrahi, Meghan M Slean, Jodie P Simard, Opher Gileadi, Christopher E Pearson. Proc Natl Acad Sci U S A 2010
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Targeting nuclear RNA for in vivo correction of myotonic dystrophy.
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Myotonic dystrophy in transgenic mice expressing an expanded CUG repeat.
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Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy.
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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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Replication-dependent instability at (CTG) x (CAG) repeat hairpins in human cells.
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Slipped (CTG)*(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair.
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CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination.
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Trinucleotide repeats that expand in human disease form hairpin structures in vitro.
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A novel approach to investigate tissue-specific trinucleotide repeat instability.
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