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Slipping while sleeping? Trinucleotide repeat expansions in germ cells

Trends in molecular medicine, 2003-11, Vol.9 (11), p.490-495

Pearson, Christopher E

2003

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Repeat instability: mechanisms of dynamic mutations

Nature reviews. Genetics, 2005-10, Vol.6 (10), p.729-742

2005

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RNA-Mediated Neurodegeneration Caused by the Fragile X Premutation rCGG Repeats in Drosophila

Neuron (Cambridge, Mass.), 2003-08, Vol.39 (5), p.739-747

2003

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Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes

Human genetics, 2014-10, Vol.133 (10), p.1311-1318

2014

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Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability

Trends in genetics, 2005-05, Vol.21 (5), p.272-280

2005

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Evidence of cis -acting factors in replication-mediated trinucleotide repeat instability in primate cells

Nature genetics, 2002-05, Vol.31 (1), p.37-46

2002

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Interruptions in the Expanded ATTCT Repeat of Spinocerebellar Ataxia Type 10: Repeat Purity as a Disease Modifier?

American journal of human genetics, 2006-01, Vol.78 (1), p.125-129

2006

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The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence

Cytogenetic and Genome Research, 2003-01, Vol.100 (1-4), p.25-55

2003

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ACVRL1 germinal mosaic with two mutant alleles in hereditary hemorrhagic telangiectasia associated with pulmonary arterial hypertension

Clinical genetics, 2012-08, Vol.82 (2), p.173-179

2012

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Slipped-strand DNAs formed by long (CAG)(CTG) repeats: slipped-out repeats and slip-out junctions

Nucleic acids research, 2002-10, Vol.30 (20), p.4534

2002

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Trinucleotide repeat DNA structures: dynamic mutations from dynamic DNA

Current opinion in structural biology, 1998-06, Vol.8 (3), p.321-330

1998

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Mutagenic roles of DNA “repair” proteins in antibody diversity and disease-associated trinucleotide repeat instability

DNA repair, 2008-07, Vol.7 (7), p.1135-1154

2008

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Replication Inhibitors Modulate Instability of an Expanded Trinucleotide Repeat at the Myotonic Dystrophy Type 1 Disease Locus in Human Cells

American journal of human genetics, 2003-11, Vol.73 (5), p.1092-1105

2003

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Alternative Structures in Duplex DNA Formed within the Trinucleotide Repeats of the Myotonic Dystrophy and Fragile X Loci

Biochemistry (Easton), 1996-04, Vol.35 (15), p.5041-5053

1996

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CpG methylation modifies the genetic stability of cloned repeat sequences

Genome research, 2002-08, Vol.12 (8), p.1246-1256

2002

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Role of Replication and CpG Methylation in Fragile X Syndrome CGG Deletions in Primate Cells

American journal of human genetics, 2005-02, Vol.76 (2), p.302-311

2005

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Effect of CAT or AGG Interruptions and CpG Methylation on Nucleosome Assembly upon Trinucleotide Repeats on Spinocerebellar Ataxia, Type 1 and Fragile X Syndrome

The Journal of biological chemistry, 2005-02, Vol.280 (6), p.4498-4503

2005

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The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptions

Gene, 2009-04, Vol.434 (1), p.29-34

2009

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Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA

Journal of biosciences, 2002-02, Vol.27 (1 Suppl 1), p.53-65

2002

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Human MSH2 Binds to Trinucleotide Repeat DNA Structures Associated with Neurodegenerative Diseases

Human molecular genetics, 1997-07, Vol.6 (7), p.1117-1123

1997

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New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1)

Neurology, 2000-03, Vol.54 (6), p.1218-1221

The International Myotonic Dystrophy Consortium (IDMC)

2000

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Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation

Biochemistry (Easton), 1998-02, Vol.37 (8), p.2701-2708

1998

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DNA methylation and replication : Implications for the Deletion Hotspot region of FMR1

Human genetics, 2005-11, Vol.118 (2), p.301-304

2005

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Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice

Human molecular genetics, 2003-01, Vol.12 (1), p.41-50

2003

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Fidelity of Primate Cell Repair of a Double-strand Break within a (CTG) super(.)(CAG) Tract: Effect of Slipped DNA Structures

The Journal of biological chemistry, 2003-09, Vol.278 (36), p.33848-33856

2003

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Slipping while sleeping? Trinucleotide repeat expansions in germ cells

Repeat instability: mechanisms of dynamic mutations

RNA-Mediated Neurodegeneration Caused by the Fragile X Premutation rCGG Repeats in Drosophila

Modifiers of (CAG)(n) instability in Machado-Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes

Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability

Evidence of cis -acting factors in replication-mediated trinucleotide repeat instability in primate cells

Interruptions in the Expanded ATTCT Repeat of Spinocerebellar Ataxia Type 10: Repeat Purity as a Disease Modifier?

The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence

ACVRL1 germinal mosaic with two mutant alleles in hereditary hemorrhagic telangiectasia associated with pulmonary arterial hypertension

Slipped-strand DNAs formed by long (CAG)(CTG) repeats: slipped-out repeats and slip-out junctions

Trinucleotide repeat DNA structures: dynamic mutations from dynamic DNA

Mutagenic roles of DNA “repair” proteins in antibody diversity and disease-associated trinucleotide repeat instability

Replication Inhibitors Modulate Instability of an Expanded Trinucleotide Repeat at the Myotonic Dystrophy Type 1 Disease Locus in Human Cells

Alternative Structures in Duplex DNA Formed within the Trinucleotide Repeats of the Myotonic Dystrophy and Fragile X Loci

CpG methylation modifies the genetic stability of cloned repeat sequences

Role of Replication and CpG Methylation in Fragile X Syndrome CGG Deletions in Primate Cells

Effect of CAT or AGG Interruptions and CpG Methylation on Nucleosome Assembly upon Trinucleotide Repeats on Spinocerebellar Ataxia, Type 1 and Fragile X Syndrome

The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptions

Triplet repeat DNA structures and human genetic disease: dynamic mutations from dynamic DNA

Human MSH2 Binds to Trinucleotide Repeat DNA Structures Associated with Neurodegenerative Diseases

New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1)

Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation

DNA methylation and replication : Implications for the Deletion Hotspot region of FMR1

Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice

Fidelity of Primate Cell Repair of a Double-strand Break within a (CTG) super(.)(CAG) Tract: Effect of Slipped DNA Structures

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