Gender and Cell-Type-Specific Effects of the Transcription-Coupled Repair Protein, ERCC6/CSB, on Repeat Expansion in a Mouse Model of the Fragile X-Related Disorders

Cockayne Syndrome B protein antagonizes OGG1 in modulating CAG repeat length in vivo

(2016) Irina V. Kovtun et al.   Aging-US

The Mismatch Repair Protein MSH2 is Rate Limiting for Repeat Expansion in a Fragile X Premutation Mouse Model

(2013) Rachel Adihe Lokanga et al.   HUMAN MUTATION

17β-Estradiol increases expression of the oxidative stress response and DNA repair protein apurinic endonuclease (Ape1) in the cerebral cortex of female mice following hypoxia

(2013) Alicia K. Dietrich et al.   JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY

Multiple interaction partners for Cockayne syndrome proteins: Implications for genome and transcriptome maintenance

(2013) Maria D. Aamann et al.   MECHANISMS OF AGEING AND DEVELOPMENT

MSH3 Polymorphisms and Protein Levels Affect CAG Repeat Instability in Huntington's Disease Mice

(2013) Stéphanie Tomé et al.   PLoS Genetics

Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice

(2012) L. Mollersen et al.   HUMAN MOLECULAR GENETICS

Somatic Expansion in Mouse and Human Carriers of Fragile X Premutation Alleles

(2012) Rachel Adihe Lokanga et al.   HUMAN MUTATION

p53, a Target of Estrogen Receptor (ER) α, Modulates DNA Damage-induced Growth Suppression in ER-positive Breast Cancer Cells

(2012) Crystal E. Berger et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

DNA Mismatch Repair Complex MutSβ Promotes GAA·TTC Repeat Expansion in Human Cells

(2012) Anasheh Halabi et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Nucleotide excision repair–initiating proteins bind to oxidative DNA lesions in vivo

(2012) Hervé Menoni et al.   JOURNAL OF CELL BIOLOGY

CGG repeat in the FMR1 gene: size matters

(2011) R Willemsen et al.   CLINICAL GENETICS

Xpa deficiency reduces CAG trinucleotide repeat instability in neuronal tissues in a mouse model of SCA1

(2011) Leroy Hubert et al.   HUMAN MOLECULAR GENETICS

DNA slip-outs cause RNA polymerase II arrest in vitro : potential implications for genetic instability

(2011) Viviana Salinas-Rios et al.   NUCLEIC ACIDS RESEARCH

ERα-associated protein networks

(2011) Jennifer R. Schultz-Norton et al.   TRENDS IN ENDOCRINOLOGY AND METABOLISM

A novel approach to investigate tissue-specific trinucleotide repeat instability

(2010) Jong-Min Lee et al.   BMC Systems Biology

Estrogen Stimulates the Expression of Mismatch Repair Gene hMLH1 in Colonic Epithelial Cells

(2010) P. Jin et al.   Cancer Prevention Research

Transcriptional activation of DNA-dependent protein kinase catalytic subunit gene expression by oestrogen receptor-α

(2010) Senad Medunjanin et al.   EMBO REPORTS

Cockayne Syndrome Group B Protein Stimulates Repair of Formamidopyrimidines by NEIL1 DNA Glycosylase

(2009) Meltem Muftuoglu et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

ATM and ATR protect the genome against two different types of tandem repeat instability in Fragile X premutation mice

(2009) A. Entezam et al.   NUCLEIC ACIDS RESEARCH

The biological effects of simple tandem repeats: Lessons from the repeat expansion diseases

(2008) K. Usdin   GENOME RESEARCH

CGG-repeat length and neuropathological and molecular correlates in a mouse model for fragile X-associated tremor/ataxia syndrome

(2008) Judith R. Brouwer et al.   JOURNAL OF NEUROCHEMISTRY

Transcription destabilizes triplet repeats

(2008) Yunfu Lin et al.   MOLECULAR CARCINOGENESIS

Intergenerational and striatal CAG repeat instability in Huntington's disease knock-in mice involve different DNA repair genes

(2008) Ella Dragileva et al.   NEUROBIOLOGY OF DISEASE