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Repeat instability: mechanisms of dynamic mutations
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19960809)64:2<434::aid-ajmg40>3.0.co;2-dopenalex-snapshot
FRAXE mutation analysis in three spanish families
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19990528)84:3<233::aid-ajmg14>3.3.co;2-yopenalex-snapshot
Tissue heterogeneity of the FMR1 mutation in a high‐functioning male with fragile X syndrome
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19990528)84:3<240::aid-ajmg15>3.0.co;2-bopenalex-snapshot
Strong similarities of theFMR1 mutation in multiple tissues: Postmortem studies of a male with a full mutation and a male carrier of a premutation
inferredcites →https://doi.org/10.1002/(sici)1096-8628(19990528)84:3<245::aid-ajmg16>3.0.co;2-uopenalex-snapshot
Postmortem examination of two fragile X brothers with anFMR1 full mutation
inferredcites →https://doi.org/10.1002/(sici)1097-4598(200005)23:5<804::aid-mus19>3.0.co;2-eopenalex-snapshot
CTG triplet repeat expansion in a laryngeal carcinoma from a patient with myotonic dystrophy
inferredcites →https://doi.org/10.1002/(sici)1098-1004(1998)11:1<23::aid-humu4>3.0.co;2-mopenalex-snapshot
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph disease
inferredcites →https://doi.org/10.1002/ajmg.1320430134openalex-snapshot
Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development
inferredcites →https://doi.org/10.1002/ana.20207openalex-snapshot
Generalized brain and skin proteasome inhibition in Huntington's disease
inferredcites →https://doi.org/10.1002/ana.410350116openalex-snapshot
Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes
inferredcites →https://doi.org/10.1002/ana.410400211openalex-snapshot
Somatic mosaicism in the central nervous system in spinocerebellar ataxia type 1 and machado‐joseph disease
inferredcites →https://doi.org/10.1002/ana.410410414openalex-snapshot
Brain regional differences in the expansion of a CAG repeat in the spinocerebellar ataxias: Dentatorubral‐pallidoluysian atrophy, machado‐joseph disease, and spinocerebellar ataxia type 1
inferredcites →https://doi.org/10.1002/ana.410430305openalex-snapshot
Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado‐Joseph disease
inferredcites →https://doi.org/10.1002/pros.10333openalex-snapshot
In situ shortening of CAG repeat length within the androgen receptor gene in prostatic cancer and its possible precursors
inferredcites →https://doi.org/10.1006/jmbi.2000.3796openalex-snapshot
Length of CTG·CAG repeats determines the influence of mismatch repair on genetic instability 1 1Edited by M. Yaniv
inferredcites →https://doi.org/10.1006/jmbi.2000.4489openalex-snapshot
Modulation of transcription reveals a new mechanism of triplet repeat instability in Escherichia coli
inferredcites →https://doi.org/10.1007/bf00207386openalex-snapshot
Somatic stability in chorionic villi samples and other Huntington fetal tissues
inferredcites →https://doi.org/10.1007/s00438-001-0635-4openalex-snapshot
Most meiotic CAG repeat tract-length alterations in yeast are SPO11 dependent
inferredcites →https://doi.org/10.1007/s00439-002-0723-5openalex-snapshot
Timing of the absence of FMR1 expression in full mutation chorionic villi
inferredcites →https://doi.org/10.1007/s004390000400openalex-snapshot
Differential somatic CAG repeat instability in variable brain cell lineage in dentatorubral pallidoluysian atrophy (DRPLA): a laser-captured microdissection (LCM)-based analysis
inferredcites →https://doi.org/10.1007/s004390050179openalex-snapshot
Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines
inferredcites →https://doi.org/10.1016/0378-3782(79)90022-7openalex-snapshot
Comparative aspects of the brain growth spurt
inferredcites →https://doi.org/10.1016/j.dnarep.2004.06.006openalex-snapshot
Mismatch repair and DNA damage signalling
inferredcites →https://doi.org/10.1016/j.gene.2004.12.008openalex-snapshot
A SCA7 CAG/CTG repeat expansion is stable in Drosophila melanogaster despite modulation of genomic context and gene dosage
inferredcites →https://doi.org/10.1016/j.jmb.2003.12.038openalex-snapshot
DNA Double-strand Breaks Induce Deletion of CTG·CAG Repeats in an Orientation-dependent Manner in Escherichia coli
inferredcites →https://doi.org/10.1016/j.jsbmb.2004.10.012openalex-snapshot
Alterations of androgen receptor in prostate cancer
inferredcites →https://doi.org/10.1016/j.molmed.2003.08.006openalex-snapshot
Huntington's disease: a synaptopathy?
inferredcites →https://doi.org/10.1016/j.molmed.2003.09.006openalex-snapshot
Slipping while sleeping? Trinucleotide repeat expansions in germ cells
inferredcites →https://doi.org/10.1016/j.tig.2003.11.002openalex-snapshot
Alanine tracts: the expanding story of human illness and trinucleotide repeats
inferredcites →https://doi.org/10.1016/j.tig.2005.03.008openalex-snapshot
Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability
inferredcites →https://doi.org/10.1016/j.ygeno.2004.04.003openalex-snapshot
GAA repeat instability in Friedreich ataxia YAC transgenic mice
inferredcites →https://doi.org/10.1016/s0022-510x(01)00596-2openalex-snapshot
Single cell analysis of CAG repeat in brains of dentatorubral-pallidoluysian atrophy (DRPLA)
inferredcites →https://doi.org/10.1016/s0022-510x(99)00031-3openalex-snapshot
Neurodegeneration in Xeroderma Pigmentosum: a trinucleotide repeat mutation analysis
inferredcites →https://doi.org/10.1016/s0027-5107(02)00223-3openalex-snapshot
DNA repair during organogenesis
inferredcites →https://doi.org/10.1016/s0304-3940(00)01029-6openalex-snapshot
The expanded CAG repeat associated with juvenile Huntington disease shows a common origin of most or all neurons and glia in human cerebrum
inferredcites →https://doi.org/10.1016/s1097-2765(00)80236-1openalex-snapshot
Inhibition of FEN-1 Processing by DNA Secondary Structure at Trinucleotide Repeats
inferredcites →https://doi.org/10.1016/s1568-7864(01)00005-2openalex-snapshot
DNA repair in terminally differentiated cells
inferredcites →https://doi.org/10.1021/bi972546copenalex-snapshot
Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation
inferredcites →https://doi.org/10.1034/j.1399-0004.2001.590210.xopenalex-snapshot
The ‘flap’ endonuclease gene FEN1 is excluded as a candidate gene implicated in the CAG repeat expansion underlying Huntington disease
inferredcites →https://doi.org/10.1038/70598openalex-snapshot
Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice
inferredcites →https://doi.org/10.1038/72101openalex-snapshot
Polyglutamine expansion down-regulates specific neuronal genes before pathologic changes in SCA1
inferredcites →https://doi.org/10.1038/86906openalex-snapshot
Trinucleotide expansion in haploid germ cells by gap repair
inferredcites →https://doi.org/10.1038/emm.2002.44openalex-snapshot
Human FEN-1 can process the 5'-flap DNA of CTG/CAG triplet repeat derived from human genetic diseases by length and sequence dependent manner
inferredcites →https://doi.org/10.1038/ng0297-165openalex-snapshot
Characterization of the full fragile X syndrome mutation in fetal gametes
inferredcites →https://doi.org/10.1038/ng0297-190openalex-snapshot
Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice
inferredcites →https://doi.org/10.1038/ng0297-193openalex-snapshot
Hypermutable myotonic dystrophy CTG repeats in transgenic mice
inferredcites →https://doi.org/10.1038/ng0297-197openalex-snapshot
Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation
inferredcites →https://doi.org/10.1038/ng0795-344openalex-snapshot
Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1
inferredcites →https://doi.org/10.1038/ng1093-184openalex-snapshot
Reduced transcriptional regulatory competence of the androgen receptor in X–linked spinal and bulbar muscular atrophy
inferredcites →https://doi.org/10.1038/ng1197-298openalex-snapshot
Trinucleotide repeats affect DNA replication in vivo
inferredcites →https://doi.org/10.1038/ng570openalex-snapshot
CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus
inferredcites →https://doi.org/10.1038/ng870openalex-snapshot
Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells
inferredcites →https://doi.org/10.1038/nsmb959openalex-snapshot
Slipped (CTG)•(CAG) repeats can be correctly repaired, escape repair or undergo error-prone repair
inferredcites →https://doi.org/10.1038/nsmb965openalex-snapshot
(CAG)n-hairpin DNA binds to Msh2–Msh3 and changes properties of mismatch recognition
inferredcites →https://doi.org/10.1038/sj.onc.1207462openalex-snapshot
The mismatch DNA repair heterodimer, hMSH2/6, regulates BLM helicase
inferredcites →https://doi.org/10.1046/j.1365-2958.2000.01727.xopenalex-snapshot
Two opposing effects of mismatch repair on CTG repeat instability in Escherichia coli
inferredcites →https://doi.org/10.1073/pnas.040460297openalex-snapshot
Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast
inferredcites →https://doi.org/10.1073/pnas.1331390100openalex-snapshot
Huntington disease expansion mutations in humans can occur before meiosis is completed
inferredcites →https://doi.org/10.1073/pnas.1532244100openalex-snapshot
Increased cell proliferation and neurogenesis in the adult human Huntington's disease brain
inferredcites →https://doi.org/10.1073/pnas.92.12.5465openalex-snapshot
Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure.
inferredcites →https://doi.org/10.1073/pnas.92.24.11019openalex-snapshot
Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases.
inferredcites →https://doi.org/10.1073/pnas.95.21.12438openalex-snapshot
Orientation-dependent and sequence-specific expansions of CTG/CAG trinucleotide repeats in Saccharomyces cerevisiae
inferredcites →https://doi.org/10.1073/pnas.96.4.1504openalex-snapshot
Triplet repeats form secondary structures that escape DNA repair in yeast
inferredcites →https://doi.org/10.1074/jbc.270.45.27014openalex-snapshot
Pausing of DNA Synthesis in Vitro at Specific Loci in CTG and CGG Triplet Repeats from Human Hereditary Disease Genes
inferredcites →https://doi.org/10.1074/jbc.274.33.23468openalex-snapshot
Genetic Instabilities in (CTG·CAG) Repeats Occur by Recombination
inferredcites →https://doi.org/10.1074/jbc.274.33.23599openalex-snapshot
Efficient Processing of DNA Ends during Yeast Nonhomologous End Joining
inferredcites →https://doi.org/10.1074/jbc.275.24.18382openalex-snapshot
Base Stacking and Even/Odd Behavior of Hairpin Loops in DNA Triplet Repeat Slippage and Expansion with DNA Polymerase
inferredcites →https://doi.org/10.1074/jbc.m104697200openalex-snapshot
Involvement of the Nucleotide Excision Repair Protein UvrA in Instability of CAG·CTG Repeat Sequences in Escherichia coli
inferredcites →https://doi.org/10.1074/jbc.m304284200openalex-snapshot
Fidelity of Primate Cell Repair of a Double-strand Break within a (CTG)·(CAG) Tract
inferredcites →https://doi.org/10.1074/jbc.m313216200openalex-snapshot
On the Roles of Saccharomyces cerevisiae Dna2p and Flap Endonuclease 1 in Okazaki Fragment Processing
inferredcites →https://doi.org/10.1074/jbc.m412359200openalex-snapshot
Human Bloom Protein Stimulates Flap Endonuclease 1 Activity by Resolving DNA Secondary Structure
inferredcites →https://doi.org/10.1074/jbc.m413239200openalex-snapshot
Effect of CAT or AGG Interruptions and CpG Methylation on Nucleosome Assembly upon Trinucleotide Repeats on Spinocerebellar Ataxia, Type 1 and Fragile X Syndrome*
inferredcites →https://doi.org/10.1074/jbc.m500264200openalex-snapshot
Biochemical Analysis of the DNA Unwinding and Strand Annealing Activities Catalyzed by Human RECQ1*[boxs]
inferredcites →https://doi.org/10.1074/jbc.m500265200openalex-snapshot
RECQ1 Helicase Interacts with Human Mismatch Repair Factors That Regulate Genetic Recombination*[boxs]
inferredcites →https://doi.org/10.1074/jbc.m909635199openalex-snapshot
Inhibition of Flap Endonuclease 1 by Flap Secondary Structure and Relevance to Repeat Sequence Expansion
inferredcites →https://doi.org/10.1086/302578openalex-snapshot
Tissue-Specific Somatic Mosaicism in Spinal and Bulbar Muscular Atrophy Is Dependent on CAG-Repeat Length and Androgen Receptor–Gene Expression Level
inferredcites →https://doi.org/10.1086/302730openalex-snapshot
De Novo Facioscapulohumeral Muscular Dystrophy: Frequent Somatic Mosaicism, Sex-Dependent Phenotype, and the Role of Mitotic Transchromosomal Repeat Interaction between Chromosomes 4 and 10
inferredcites →https://doi.org/10.1086/379523openalex-snapshot
Replication Inhibitors Modulate Instability of an Expanded Trinucleotide Repeat at the Myotonic Dystrophy Type 1 Disease Locus in Human Cells
inferredcites →https://doi.org/10.1086/422175openalex-snapshot
Mechanism and Timing of Mitotic Rearrangements in the Subtelomeric D4Z4 Repeat Involved in Facioscapulohumeral Muscular Dystrophy
inferredcites →https://doi.org/10.1086/422762openalex-snapshot
Intergenerational Instability of the Expanded CTG Repeat in the DMPK Gene: Studies in Human Gametes and Preimplantation Embryos
inferredcites →https://doi.org/10.1086/427268openalex-snapshot
Extreme Heterogeneity in the Molecular Events Leading to the Establishment of Chiasmata during Meiosis I in Human Oocytes
inferredcites →https://doi.org/10.1086/427928openalex-snapshot
Role of Replication and CpG Methylation in Fragile X Syndrome CGG Deletions in Primate Cells
inferredcites →https://doi.org/10.1093/emboj/19.10.2381openalex-snapshot
Recombination‐induced CAG trinucleotide repeat expansions in yeast involve the MRE11–RAD50–XRS2 complex
inferredcites →https://doi.org/10.1093/emboj/cdg202openalex-snapshot
CTG repeat instability and size variation timing in DNA repair‐deficient mice
inferredcites →https://doi.org/10.1093/genetics/155.4.1657openalex-snapshot
The Impact of Lagging Strand Replication Mutations on the Stability of CAG Repeat Tracts in Yeast
inferredcites →https://doi.org/10.1093/hmg/1.6.397openalex-snapshot
DNA methylation represses FMR-1 transcription in fragile X syndrome
inferredcites →https://doi.org/10.1093/hmg/10.10.1039openalex-snapshot
Transgenic mice with an expanded CAG repeat controlled by the human AR promoter show polyglutamine nuclear inclusions and neuronal dysfunction without neuronal cell death
inferredcites →https://doi.org/10.1093/hmg/10.21.2425openalex-snapshot
Centrosome disorganization in fibroblast cultures derived from R6/2 Huntington's disease (HD) transgenic mice and HD patients
inferredcites →https://doi.org/10.1093/hmg/10.8.845openalex-snapshot
Mouse tissue culture models of unstable triplet repeats: in vitro selection for larger alleles, mutational expansion bias and tissue specificity, but no association with cell division rates
inferredcites →https://doi.org/10.1093/hmg/11.2.191openalex-snapshot
Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins
inferredcites →https://doi.org/10.1093/hmg/11.7.791openalex-snapshot
Age and insertion site dependence of repeat number instability of a human DM1 transgene in individual mouse sperm
inferredcites →https://doi.org/10.1093/hmg/12.3.273openalex-snapshot
Mismatch repair gene Msh2 modifies the timing of early disease in HdhQ111 striatum
inferredcites →https://doi.org/10.1093/hmg/2.10.1535openalex-snapshot
Molecular analysis of juvenile Huntington disease: the major influence on (CAG) n repeat length is the sex of the affected parent
inferredcites →https://doi.org/10.1093/hmg/3.10.1823openalex-snapshot
Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes
inferredcites →https://doi.org/10.1093/hmg/4.1.1openalex-snapshot
Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses
inferredcites →https://doi.org/10.1093/hmg/4.3.401openalex-snapshot
Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?
inferredcites →https://doi.org/10.1093/hmg/4.7.1147openalex-snapshot
Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a causal involvement of methyl-directed DNA mismatch repair in triplet repeat stability
inferredcites →https://doi.org/10.1093/hmg/6.12.2135openalex-snapshot
Increased Trinucleotide Repeat Instability with Advanced Maternal Age
inferredcites →https://doi.org/10.1093/hmg/6.3.349openalex-snapshot
Destabilization of CAG Trinucleotide Repeat Tracts by Mismatch Repair Mutations in Yeast
inferredcites →https://doi.org/10.1093/hmg/6.6.877openalex-snapshot
Somatic Instability of the Myotonic Dystrophy (CTG)n Repeat during Human Fetal Development
inferredcites →https://doi.org/10.1093/hmg/6.7.1117openalex-snapshot
Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases
inferredcites →https://doi.org/10.1093/hmg/6.7.971openalex-snapshot
Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic
inferredcites →https://doi.org/10.1093/hmg/7.1.69openalex-snapshot
Expansions of CAG Repeat Tracts are Frequent in a Yeast Mutant Defective in Okazaki Fragment Maturation
inferredcites →https://doi.org/10.1093/hmg/7.12.1901openalex-snapshot
Parental gender, age at birth and expansion length influence GAA repeat intergenerational instability in the X25 gene: pedigree studies and analysis of sperm from patients with Friedreich's Ataxia
inferredcites →https://doi.org/10.1093/hmg/7.2.307openalex-snapshot
Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients
inferredcites →https://doi.org/10.1093/hmg/7.6.959openalex-snapshot
Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability
inferredcites →https://doi.org/10.1093/hmg/7.8.1285openalex-snapshot
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
inferredcites →https://doi.org/10.1093/hmg/8.1.99openalex-snapshot
Transgenic mice harboring a full-length human mutant DRPLA gene exhibit age-dependent intergenerational and somatic instabilities of CAG repeats comparable with those in DRPLA patients
inferredcites →https://doi.org/10.1093/hmg/8.12.2293openalex-snapshot
Fully Expanded FMR1CGG Repeats Exhibit a Length-and Differentiation-Dependent Instability in Cell Hybrids That is Independent of DNA Methylation
inferredcites →https://doi.org/10.1093/hmg/8.6.1061openalex-snapshot
Cis-acting modifiers of expanded CAG/CTG triplet repeat expandability: associations with flanking GC content and proximity to CpG islands
inferredcites →https://doi.org/10.1093/hmg/9.14.2125openalex-snapshot
SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance
inferredcites →https://doi.org/10.1093/hmg/9.17.2539openalex-snapshot
Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
inferredcites →https://doi.org/10.1093/hmg/9.3.439openalex-snapshot
Dramatic, expansion-biased, age-dependent, tissue-specific somatic mosaicism in a transgenic mouse model of triplet repeat instability
inferredcites →https://doi.org/10.1093/hmg/9.5.713openalex-snapshot
Allele diversity and germline mutation at the insulin minisatellite
inferredcites →https://doi.org/10.1093/hmg/9.8.1185openalex-snapshot
Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability
inferredcites →https://doi.org/10.1093/hmg/ddg006openalex-snapshot
Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice
inferredcites →https://doi.org/10.1093/hmg/ddg111openalex-snapshot
Candidate DNA replication initiation regions at human trinucleotide repeat disease loci
inferredcites →https://doi.org/10.1093/hmg/ddg300openalex-snapshot
Regional differences of somatic CAG repeat instability do not account for selective neuronal vulnerability in a knock-in mouse model of SCA1
inferredcites →https://doi.org/10.1093/hmg/ddg352openalex-snapshot
Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis
inferredcites →https://doi.org/10.1093/hmg/ddh186openalex-snapshot
Pms2 is a genetic enhancer of trinucleotide CAG{middle dot}CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion
inferredcites →https://doi.org/10.1093/hmg/ddh317openalex-snapshot
Genome-wide demethylation destabilizes CTG·CAG trinucleotide repeats in mammalian cells
inferredcites →https://doi.org/10.1093/nar/22.15.3181openalex-snapshot
The length and location of CAG trinucleotide repeats in the androgen receptor N-terminal domain affect transactivation function
inferredcites →https://doi.org/10.1093/nar/25.14.2861openalex-snapshot
Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli
inferredcites →https://doi.org/10.1093/nar/27.2.616openalex-snapshot
Nucleotide excision repair affects the stability of long transcribed (CTG*CAG) tracts in an orientation-dependent manner in Escherichia coli
inferredcites →https://doi.org/10.1093/nar/30.3.711openalex-snapshot
hMutSalpha forms an ATP-dependent complex with hMutLalpha and hMutLbeta on DNA
inferredcites →https://doi.org/10.1093/nar/gkh170openalex-snapshot
YB-1 promotes strand separation in vitro of duplex DNA containing either mispaired bases or cisplatin modifications, exhibits endonucleolytic activities and binds several DNA repair proteins
inferredcites →https://doi.org/10.1093/nar/gkh933openalex-snapshot
Replication-mediated instability of the GAA triplet repeat mutation in Friedreich ataxia
inferredcites →https://doi.org/10.1093/nar/gkh976openalex-snapshot
Chemotherapeutic deletion of CTG repeats in lymphoblast cells from DM1 patients
inferredcites →https://doi.org/10.1093/nar/gki712openalex-snapshot
The Bloom's syndrome helicase promotes the annealing of complementary single-stranded DNA
inferredcites →https://doi.org/10.1101/gr.74502openalex-snapshot
CpG Methylation Modifies the Genetic Stability of Cloned Repeat Sequences
inferredcites →https://doi.org/10.1111/j.1399-0004.1998.tb03718.xopenalex-snapshot
Spinal and bulbar muscular atrophy (SBMA): Somatic stability of an expanded CAG repeat in fetal tissues
inferredcites →https://doi.org/10.1126/science.279.5352.853openalex-snapshot
Expansion and Length-Dependent Fragility of CTG Repeats in Yeast
inferredcites →https://doi.org/10.1126/science.8036515openalex-snapshot
Preferential Nucleosome Assembly at DNA Triplet Repeats from the Myotonic Dystrophy Gene
inferredcites →https://doi.org/10.1126/science.8094260openalex-snapshot
Reduction in Size of the Myotonic Dystrophy Trinucleotide Repeat Mutation During Transmission
inferredcites →https://doi.org/10.1128/mcb.18.4.2045openalex-snapshot
Expansions and Contractions in a Tandem Repeat Induced by Double-Strand Break Repair
inferredcites →https://doi.org/10.1128/mcb.19.6.4153openalex-snapshot
Increased Instability of Human CTG Repeat Tracts on Yeast Artificial Chromosomes during Gametogenesis
inferredcites →https://doi.org/10.1128/mcb.23.17.6063-6074.2003openalex-snapshot
Nuclease-Deficient FEN-1 Blocks Rad51/BRCA1-Mediated Repair and Causes Trinucleotide Repeat Instability
inferredcites →https://doi.org/10.1128/mcb.23.21.7849-7860.2003openalex-snapshot
Mutations in Yeast Replication Proteins That Increase CAG/CTG Expansions Also Increase Repeat Fragility
inferredcites →https://doi.org/10.1128/mcb.23.4.1349-1357.2003openalex-snapshot
Replication and Expansion of Trinucleotide Repeats in Yeast
inferredcites →https://doi.org/10.1128/mcb.23.9.3152-3162.2003openalex-snapshot
Long CTG Tracts from the Myotonic Dystrophy Gene Induce Deletions and Rearrangements during Recombination at the APRT Locus in CHO Cells
inferredcites →https://doi.org/10.1128/mcb.24.2.629-637.2004openalex-snapshot
MSH2-Dependent Germinal CTG Repeat Expansions Are Produced Continuously in Spermatogonia from DM1 Transgenic Mice
inferredcites →https://doi.org/10.1128/mcb.24.6.2286-2295.2004openalex-snapshot
Replication Stalling at Friedreich's Ataxia (GAA)n Repeats In Vivo
inferredcites →https://doi.org/10.1128/mcb.24.9.4049-4064.2004openalex-snapshot
Saccharomyces cerevisiae Flap Endonuclease 1 Uses Flap Equilibration To Maintain Triplet Repeat Stability
inferredcites →https://doi.org/10.1136/jmg.32.8.593openalex-snapshot
Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period.
inferredcites →https://doi.org/10.1136/jmg.35.2.103openalex-snapshot
Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats.
inferredcites →https://doi.org/10.1136/jmg.37.11.842openalex-snapshot
Increase of FMRP expression, raised levels ofFMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations?
inferredcites →https://doi.org/10.1136/jnnp.60.1.78openalex-snapshot
Neuropathological diagnosis and CAG repeat expansion in Huntington's disease.
inferredcites →https://doi.org/10.1136/jnnp.74.7.968openalex-snapshot
Genetically confirmed clinical Huntington's disease with no observable cell loss
inferredcites →https://doi.org/10.1158/0008-5472.can-03-2957openalex-snapshot
An Msh2 Point Mutation Uncouples DNA Mismatch Repair and Apoptosis
inferredcites →https://doi.org/10.1159/000072837openalex-snapshot
The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence
inferredcites →https://doi.org/10.1212/wnl.49.2.606openalex-snapshot
Somatic mosaicism for Friedreich's ataxia GAA triplet repeat expansions in the central nervous system
inferredcites →https://doi.org/10.1212/wnl.51.5.1442openalex-snapshot
Larger CAG expansions in skeletal muscle compared with lymphocytes in Kennedy disease but not in Huntington disease
inferredcites →https://doi.org/10.1677/jme.0.0250085openalex-snapshot
Effect of the androgen receptor CAG repeat polymorphism on transcriptional activity: specificity in prostate and non-prostate cell lines
inferredcites →https://doi.org/10.2169/internalmedicine.41.312openalex-snapshot
A Patient with Myotonic Dystrophy Type 1 (DM1) Accompanied by Laryngeal and Renal Cell Carcinomas Had a Small CTG Triplet Repeat Expansion But No Somatic Instability in Normal Tissues.
inferredcites →https://doi.org/10.4161/cc.3.11.1246openalex-snapshot
Structure-Forming CAG/CTG Repeat Sequences are Sensitive to Breakage in the Absence of Mrc1 Checkpoint Function and S-Phase Checkpoint Signaling: Implications for Trinucleotide Repeat Expansion Diseases
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Fragile X full mutation alleles composed of few alleles: Implications for CGG repeat expansion
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inferred← citeshttps://doi.org/10.1002/ajmg.b.30624openalex-snapshot
Cis‐acting factors promoting the CAG intergenerational instability in Machado–Joseph disease
inferred← citeshttps://doi.org/10.1002/ajmg.b.30970openalex-snapshot
Unstable familial transmissions of Huntington disease alleles with 27–35 CAG repeats (intermediate alleles)
inferred← citeshttps://doi.org/10.1002/alz.13168openalex-snapshot
Bioinformatics pipeline to guide post‐GWAS studies in Alzheimer's: A new catalogue of disease candidate short structural variants
inferred← citeshttps://doi.org/10.1002/ana.21052openalex-snapshot
Progressive gaa expansions in dorsal root ganglia of Friedreich's ataxia patients
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DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases
inferred← citeshttps://doi.org/10.1002/ana.25488openalex-snapshot
A hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism
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The rise, fall and renaissance of microsatellites in eukaryotic genomes
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inferred← citeshttps://doi.org/10.1002/biof.1060openalex-snapshot
Expanded complexity of unstable repeat diseases
inferred← citeshttps://doi.org/10.1002/bip.21343openalex-snapshot
Energetic coupling between clustered lesions modulated by intervening triplet repeat bulge loops: Allosteric implications for DNA repair and triplet repeat expansion
inferred← citeshttps://doi.org/10.1002/bip.22236openalex-snapshot
Impact of bulge loop size on DNA triplet repeat domains: Implications for DNA repair and expansion
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Stable recombinant production of codon‐scrambled lubricin and mucin in human cells
inferred← citeshttps://doi.org/10.1002/cbic.200800062openalex-snapshot
Identification of Trinucleotide Repeat Ligands with a FRET Melting Assay
inferred← citeshttps://doi.org/10.1002/chem.201602741openalex-snapshot
A Ligand That Targets CUG Trinucleotide Repeats
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Design and Synthesis of Cyclic Mismatch‐Binding Ligands (CMBLs) with Variable Linkers by Ring‐Closing Metathesis and their Photophysical and DNA Repeat Binding Properties
inferred← citeshttps://doi.org/10.1002/chem.201804368openalex-snapshot
A Dimeric 2,9‐Diamino‐1,10‐phenanthroline Derivative Improves Alternative Splicing in Myotonic Dystrophy Type 1 Cell and Mouse Models
inferred← citeshttps://doi.org/10.1002/chir.22064openalex-snapshot
Circular Dichroism Spectroscopy of DNA: From Duplexes to Quadruplexes
inferred← citeshttps://doi.org/10.1002/ece3.1305openalex-snapshot
Challenges in analysis and interpretation of microsatellite data for population genetic studies
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Modulation of mutagenesis in eukaryotes by DNA replication fork dynamics and quality of nucleotide pools
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Diverse chromosome breakage mechanisms underlie subtelomeric rearrangements, a common cause of mental retardation
inferred← citeshttps://doi.org/10.1002/humu.20466openalex-snapshot
CAG and CTG repeat polymorphism in exons of human genes shows distinct features at the expandable loci
inferred← citeshttps://doi.org/10.1002/humu.20600openalex-snapshot
Closely linkedcis‐acting modifier of expansion of the CGG repeat in high riskFMR1haplotypes
inferred← citeshttps://doi.org/10.1002/humu.22495openalex-snapshot
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
inferred← citeshttps://doi.org/10.1002/humu.23023openalex-snapshot
The SSV Evaluation System: A Tool to Prioritize Short Structural Variants for Studies of Possible Regulatory and Causal Variants
inferred← citeshttps://doi.org/10.1002/humu.23531openalex-snapshot
Unusual association of a unique CAG interruption in 5′ of DM1 CTG repeats with intergenerational contractions and low somatic mosaicism
inferred← citeshttps://doi.org/10.1002/jcb.23075openalex-snapshot
The mouse mismatch repair protein, MSH3, is a nucleoplasmic protein that aggregates into denser nuclear bodies under conditions of stress
inferred← citeshttps://doi.org/10.1002/jdn.70054openalex-snapshot
Clinical, Genetic and Molecular Divergences Between Full Mutation and Premutation in Fragile X Syndrome: A Systematic Review
inferred← citeshttps://doi.org/10.1002/jnr.22551openalex-snapshot
Perspectives on gene therapy in myotonic dystrophy type 1
inferred← citeshttps://doi.org/10.1002/mc.20488openalex-snapshot
Transcription destabilizes triplet repeats
inferred← citeshttps://doi.org/10.1002/mc.20534openalex-snapshot
Genetic instabilities of (CCTG)·(CAGG) and (ATTCT)·(AGAAT) disease‐associated repeats reveal multiple pathways for repeat deletion
inferred← citeshttps://doi.org/10.1002/mdc3.13165openalex-snapshot
Challenges in Clinicogenetic Correlations: One Gene – Many Phenotypes
inferred← citeshttps://doi.org/10.1002/mds.27595openalex-snapshot
Sample enrichment for clinical trials to show delay of onset in huntington disease
inferred← citeshttps://doi.org/10.1002/pmic.202300235openalex-snapshot
Effects of genetic variation on the structure of RNA and protein
inferred← citeshttps://doi.org/10.1002/qua.22834openalex-snapshot
Coherent states as consequences of keto‐amino→ enol‐imine hydrogen bond arrangements driven by quantum uncertainty limits on amino DNA protons
inferred← citeshttps://doi.org/10.1007/978-0-387-87429-6_69openalex-snapshot
Genetics of Familial and Idiopathic Pulmonary Arterial Hypertension
inferred← citeshttps://doi.org/10.1007/978-1-0716-2357-2_5openalex-snapshot
Long-Read Sequencing and Analysis of Variable Number Tandem Repeats
inferred← citeshttps://doi.org/10.1007/978-1-4419-7104-3_11openalex-snapshot
Trinucleotide-Expansion Diseases
inferred← citeshttps://doi.org/10.1007/978-1-4614-6280-4_7openalex-snapshot
Microsatellite Repeats: Canaries in the Coalmine
inferred← citeshttps://doi.org/10.1007/978-1-4614-6567-6_59openalex-snapshot
The Myotonic Dystrophies
inferred← citeshttps://doi.org/10.1007/978-1-4939-3070-8_7openalex-snapshot
Mini- and Micro-Satellite Markers in Health, Disease and Evolution
inferred← citeshttps://doi.org/10.1007/978-1-4939-3509-3_9openalex-snapshot
Engineered Nucleases and Trinucleotide Repeat Diseases
inferred← citeshttps://doi.org/10.1007/978-1-4939-9784-8_1openalex-snapshot
Experimenting with Trinucleotide Repeats: Facts and Technical Issues
inferred← citeshttps://doi.org/10.1007/978-1-4939-9784-8_4openalex-snapshot
Quantifying Replication Fork Progression at CTG Repeats by 2D Gel Electrophoresis
inferred← citeshttps://doi.org/10.1007/978-1-60327-367-1_16openalex-snapshot
Short Tandem Repeats and Genetic Variation
inferred← citeshttps://doi.org/10.1007/978-1-62703-514-9_7openalex-snapshot
Profiling Short Tandem Repeats from Short Reads
inferred← citeshttps://doi.org/10.1007/978-3-030-23810-0_101openalex-snapshot
Autosomal Dominant Spinocerebellar Ataxias and Episodic Ataxias
inferred← citeshttps://doi.org/10.1007/978-3-030-41283-8_7openalex-snapshot
Mystery of Expansion: DNA Metabolism and Unstable Repeats
inferred← citeshttps://doi.org/10.1007/978-3-031-82990-1_12openalex-snapshot
Proteostasis as a Sentry for Sperm Quality and Male Fertility
inferred← citeshttps://doi.org/10.1007/978-3-319-20796-4_24-1openalex-snapshot
DNA Methylation in Eukaryotes: Regulation and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-25159-2_75openalex-snapshot
Prediction of Single Nucleotide Mutation Patterns in Microsatellites
inferred← citeshttps://doi.org/10.1007/978-3-319-48838-7_6openalex-snapshot
Mechanisms of Global and Region-Specific Control of Mutagenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-50542-8_24openalex-snapshot
DNA Methylation in Eukaryotes: Regulation and Function
inferred← citeshttps://doi.org/10.1007/978-3-319-71815-6_13openalex-snapshot
Defective DNA Repair in Spermiogenesis
inferred← citeshttps://doi.org/10.1007/978-3-319-76768-0_13openalex-snapshot
Echinodermata: The Complex Immune System in Echinoderms
inferred← citeshttps://doi.org/10.1007/978-3-540-29678-2_6122openalex-snapshot
Trinucleotide Repeat Disease
inferred← citeshttps://doi.org/10.1007/978-3-540-37654-5_12openalex-snapshot
Human Gene Mutation: Mechanisms and Consequences
inferred← citeshttps://doi.org/10.1007/978-3-540-69414-4_17openalex-snapshot
DNA-Reparatur und Mutagenese
inferred← citeshttps://doi.org/10.1007/978-3-642-02481-8_159openalex-snapshot
Analysing the Evolution of Repetitive Strands in Genomes
inferred← citeshttps://doi.org/10.1007/978-3-642-04298-0_9openalex-snapshot
Drosophila as a Model for Neurodegenerative Disease: Roles of RNA Pathways in Pathogenesis
inferred← citeshttps://doi.org/10.1007/978-3-642-13214-8_14openalex-snapshot
An Application for Studying Tandem Repeats in Orthologous Genes
inferred← citeshttps://doi.org/10.1007/978-3-642-29627-7_7openalex-snapshot
lobSTR: A Short Tandem Repeat Profiler for Personal Genomes
inferred← citeshttps://doi.org/10.1007/978-4-431-56603-8_7openalex-snapshot
CNVs and Microsatellite DNA Polymorphism
inferred← citeshttps://doi.org/10.1007/978-81-322-2110-4_4openalex-snapshot
Stem Cell Therapy for Neurological Disorders: From Bench to Bedside
inferred← citeshttps://doi.org/10.1007/978-94-007-1333-8_101openalex-snapshot
Autosomal Dominant Spinocerebellar Ataxias and Episodic Ataxias
inferred← citeshttps://doi.org/10.1007/978-981-13-0508-5_12openalex-snapshot
Disease Modeling and Drug Development with DM1 Patient-Derived iPS Cells
inferred← citeshttps://doi.org/10.1007/978-981-13-0508-5_7openalex-snapshot
Molecular Defects in the DM Central Nervous System
inferred← citeshttps://doi.org/10.1007/978-981-13-0529-0_5openalex-snapshot
Repeat Expansion Disease Models
inferred← citeshttps://doi.org/10.1007/978-981-16-1313-5_68-1openalex-snapshot
Small Molecules Targeting Repeat Sequences Causing Neurological Disorders
inferred← citeshttps://doi.org/10.1007/978-981-19-9776-1_68openalex-snapshot
Small Molecules Targeting Repeat Sequences Causing Neurological Disorders
inferred← citeshttps://doi.org/10.1007/s00018-009-0131-2openalex-snapshot
Non-B DNA structure-induced genetic instability and evolution
inferred← citeshttps://doi.org/10.1007/s00018-016-2284-0openalex-snapshot
Modeling simple repeat expansion diseases with iPSC technology
inferred← citeshttps://doi.org/10.1007/s00109-020-01885-zopenalex-snapshot
Exploring the role of high-mobility group box 1 (HMGB1) protein in the pathogenesis of Huntington’s disease
inferred← citeshttps://doi.org/10.1007/s00122-008-0831-2openalex-snapshot
Development of microsatellite markers specific for the short arm of rye (Secale cereale L.) chromosome 1
inferred← citeshttps://doi.org/10.1007/s00239-010-9328-0openalex-snapshot
Unstable DNA Repair Genes Shaped by Their Own Sequence Modifying Phenotypes
inferred← citeshttps://doi.org/10.1007/s00239-010-9425-0openalex-snapshot
Role of Everlasting Triplet Expansions in Protein Evolution
inferred← citeshttps://doi.org/10.1007/s00294-016-0619-xopenalex-snapshot
Are all repeats created equal? Understanding DNA repeats at an individual level
inferred← citeshttps://doi.org/10.1007/s00381-015-2993-yopenalex-snapshot
Congenital myotonic dystrophy: ventriculomegaly and shunt considerations for the pediatric neurosurgeon
inferred← citeshttps://doi.org/10.1007/s00401-014-1286-yopenalex-snapshot
C9orf72 hypermethylation protects against repeat expansion-associated pathology in ALS/FTD
inferred← citeshttps://doi.org/10.1007/s00401-015-1445-9openalex-snapshot
Semi-automated quantification of C9orf72 expansion size reveals inverse correlation between hexanucleotide repeat number and disease duration in frontotemporal degeneration
inferred← citeshttps://doi.org/10.1007/s00438-008-0370-1openalex-snapshot
The pattern of insertion/deletion polymorphism in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1007/s00439-006-0164-7openalex-snapshot
Msh3 is a limiting factor in the formation of intergenerational CTG expansions in DM1 transgenic mice
inferred← citeshttps://doi.org/10.1007/s00439-014-1467-8openalex-snapshot
Modifiers of (CAG)n instability in Machado–Joseph disease (MJD/SCA3) transmissions: an association study with DNA replication, repair and recombination genes
inferred← citeshttps://doi.org/10.1007/s00439-016-1691-5openalex-snapshot
Gene correction in patient-specific iPSCs for therapy development and disease modeling
inferred← citeshttps://doi.org/10.1007/s00439-024-02644-7openalex-snapshot
Novel genotype–phenotype correlations, differential cerebellar allele-specific methylation, and a common origin of the (ATTTC)n insertion in spinocerebellar ataxia type 37
inferred← citeshttps://doi.org/10.1007/s00702-021-02454-5openalex-snapshot
Proteinopathies associated to repeat expansion disorders
inferred← citeshttps://doi.org/10.1007/s10038-007-0197-3openalex-snapshot
De novo polyalanine expansion of PHOX2B in congenital central hypoventilation syndrome: unequal sister chromatid exchange during paternal gametogenesis
inferred← citeshttps://doi.org/10.1007/s10048-007-0088-yopenalex-snapshot
Identification of the porcine homologous of human disease causing trinucleotide repeat sequences
inferred← citeshttps://doi.org/10.1007/s10048-017-0523-7openalex-snapshot
Molecular genetic and clinical characterization of myotonic dystrophy type 1 patients carrying variant repeats within DMPK expansions
inferred← citeshttps://doi.org/10.1007/s10048-018-0546-8openalex-snapshot
Toward deciphering the mechanistic role of variations in the Rep1 repeat site in the transcription regulation of SNCA gene
inferred← citeshttps://doi.org/10.1007/s10072-023-06677-0openalex-snapshot
Current advances in neuronal intranuclear inclusion disease
inferred← citeshttps://doi.org/10.1007/s10535-008-0031-6openalex-snapshot
Limited variability of CTG/CAG repeats in Lycopersicon nuclear DNA
inferred← citeshttps://doi.org/10.1007/s10549-006-9411-9openalex-snapshot
The GH1/IGF-1 axis polymorphisms and their impact on breast cancer development
inferred← citeshttps://doi.org/10.1007/s10549-014-2908-8openalex-snapshot
Microsatellite genotyping reveals a signature in breast cancer exomes
inferred← citeshttps://doi.org/10.1007/s10681-010-0286-9openalex-snapshot
Microsatellite markers: an overview of the recent progress in plants
inferred← citeshttps://doi.org/10.1007/s10815-016-0663-yopenalex-snapshot
Effects of aging on the male reproductive system
inferred← citeshttps://doi.org/10.1007/s11033-010-0235-7openalex-snapshot
Distribution of CTG repeats at the DMPK gene in myotonic distrophy patients and healthy individuals from the Mexican population
inferred← citeshttps://doi.org/10.1007/s11033-014-3432-yopenalex-snapshot
Convergent transcription through microsatellite repeat tracts induces cell death
inferred← citeshttps://doi.org/10.1007/s11262-012-0802-1openalex-snapshot
Differential distribution and occurrence of simple sequence repeats in diverse geminivirus genomes
inferred← citeshttps://doi.org/10.1007/s11427-017-9186-7openalex-snapshot
DNA mismatch repair in trinucleotide repeat instability
inferred← citeshttps://doi.org/10.1007/s11626-010-9284-4openalex-snapshot
Derivation, culture, and characterization of VUB hESC lines
inferred← citeshttps://doi.org/10.1007/s11910-016-0643-8openalex-snapshot
New Genetic Approaches to AD: Lessons from APOE-TOMM40 Phylogenetics
inferred← citeshttps://doi.org/10.1007/s11940-016-0434-1openalex-snapshot
Myotonic Dystrophy Type 1 Management and Therapeutics
inferred← citeshttps://doi.org/10.1007/s12031-021-01850-6openalex-snapshot
STRs: Ancient Architectures of the Genome beyond the Sequence
inferred← citeshttps://doi.org/10.1007/s12033-009-9230-4openalex-snapshot
Mutational Dynamics of Microsatellites
inferred← citeshttps://doi.org/10.1007/s12035-012-8348-8openalex-snapshot
Spinocerebellar Ataxia Type 2: Clinical Presentation, Molecular Mechanisms, and Therapeutic Perspectives
inferred← citeshttps://doi.org/10.1007/s12035-014-8724-7openalex-snapshot
Antisense Oligonucleotide Therapy for the Treatment of C9ORF72 ALS/FTD Diseases
inferred← citeshttps://doi.org/10.1007/s12035-018-1160-3openalex-snapshot
Tissue-Specific Upregulation of Drosophila Insulin Receptor (InR) Mitigates Poly(Q)-Mediated Neurotoxicity by Restoration of Cellular Transcription Machinery
inferred← citeshttps://doi.org/10.1007/s12038-007-0053-9openalex-snapshot
Polyglutamine expansion in Drosophila: thermal stress and Hsp70 as selective agents
inferred← citeshttps://doi.org/10.1007/s12041-010-0072-4openalex-snapshot
Modifiers and mechanisms of multi-system polyglutamine neurodegenerative disorders: lessons from fly models
inferred← citeshttps://doi.org/10.1007/s12041-016-0704-4openalex-snapshot
Chromosomal structural changes and microsatellite variations in newly synthesized hexaploid wheat mediated by unreduced gametes
inferred← citeshttps://doi.org/10.1007/s12149-014-0901-2openalex-snapshot
Detailed assessment of gene activation levels by multiple hypoxia-responsive elements under various hypoxic conditions
inferred← citeshttps://doi.org/10.1007/s12264-019-00360-1openalex-snapshot
Effect of Apolipoprotein E Genotypes on Huntington’s Disease Phenotypes in a Han Chinese Population
inferred← citeshttps://doi.org/10.1007/s12311-011-0315-9openalex-snapshot
Infantile Childhood Onset of Spinocerebellar Ataxia Type 2
inferred← citeshttps://doi.org/10.1007/s12311-026-01980-wopenalex-snapshot
Rare but Instructive: Pediatric-Onset Spinocerebellar Ataxia Type 2 and Its Clinical and Genetic Insights
inferred← citeshttps://doi.org/10.1007/s12539-011-0065-xopenalex-snapshot
The molecular clock in terms of quantum information processing of coherent states, entanglement and replication of evolutionarily selected decohered isomers
inferred← citeshttps://doi.org/10.1007/s13148-010-0017-zopenalex-snapshot
Epigenetic mechanisms and genome stability
inferred← citeshttps://doi.org/10.1007/s13237-016-0189-9openalex-snapshot
Cytogenetic investigation of Cyprinus carpio (Linnaeus, 1758) using giemsa, silver nitrate, CMA3 staining and fluorescence in situ hybridization
inferred← citeshttps://doi.org/10.1007/s43538-025-00578-wopenalex-snapshot
Expansion of human disease causing triplet repeats in vertebrate genomes: an evolutionary perspective
inferred← citeshttps://doi.org/10.1016/b978-0-08-045031-5.00015-3openalex-snapshot
Myotonic dystrophy types 1 and 2
inferred← citeshttps://doi.org/10.1016/b978-0-12-381510-1.00068-5openalex-snapshot
Myotonic Dystrophy
inferred← citeshttps://doi.org/10.1016/b978-0-12-383834-6.00007-0openalex-snapshot
Human Gene Mutation in Inherited Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-387003-2.00008-2openalex-snapshot
Modeling Human Trinucleotide Repeat Diseases in Drosophila
inferred← citeshttps://doi.org/10.1016/b978-0-12-404748-8.00009-5openalex-snapshot
Insertions and Deletions (Indels)
inferred← citeshttps://doi.org/10.1016/b978-0-12-410529-4.00001-2openalex-snapshot
Mendelian, Non-Mendelian, Multigenic Inheritance, and Epigenetics
inferred← citeshttps://doi.org/10.1016/b978-0-12-801238-3.04605-5openalex-snapshot
Genomic Disorder and Gene Expression in the Developing CNS☆
inferred← citeshttps://doi.org/10.1016/b978-0-12-801942-9.00008-2openalex-snapshot
Huntington Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-809324-5.23794-2openalex-snapshot
Genetic Disorders: Single Gene
inferred← citeshttps://doi.org/10.1016/b978-0-12-812537-3.00006-8openalex-snapshot
Human Genomic Variants and Inherited Disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-813955-4.00001-5openalex-snapshot
Mendelian, non-Mendelian, multigenic inheritance, and epigenetics
inferred← citeshttps://doi.org/10.1016/b978-0-12-819715-8.00005-7openalex-snapshot
Genome mapping tools: current research and future prospects
inferred← citeshttps://doi.org/10.1016/b978-0-323-85679-9.00018-0openalex-snapshot
DNA mismatch repair in mammals
inferred← citeshttps://doi.org/10.1016/b978-0-323-89778-5.00026-xopenalex-snapshot
Bioinformatics intervention in identification and development of molecular markers: an overview
inferred← citeshttps://doi.org/10.1016/b978-0-323-95502-7.00066-xopenalex-snapshot
Repeats in Genomes
inferred← citeshttps://doi.org/10.1016/b978-0-323-95672-7.00002-9openalex-snapshot
Mechanisms of somatic CAG-repeat expansions in Huntington's disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-13550-7.00009-4openalex-snapshot
Genetic modifiers of age-related penetrance in X-linked dystonia-parkinsonism
inferred← citeshttps://doi.org/10.1016/b978-0-443-15702-8.00011-7openalex-snapshot
The pathophysiology of neurodegenerative diseases: The back effects of oxidative stress and antioxidants system
inferred← citeshttps://doi.org/10.1016/b978-0-443-19041-4.00019-4openalex-snapshot
Mendelian, non-Mendelian, multigenic inheritance, and epigenetics
inferred← citeshttps://doi.org/10.1016/b978-0-443-27333-9.00009-9openalex-snapshot
Molecular mechanisms of reactive oxygen species in neurodegenerative diseases (Alzheimer, Parkinson, etc.)
inferred← citeshttps://doi.org/10.1016/b978-008045046-9.00184-4openalex-snapshot
Genomic Disorder and Gene Expression in the Developing CNS
inferred← citeshttps://doi.org/10.1016/b978-012369462-1/50042-9openalex-snapshot
Error-Prone Repair of Slipped (CTG)·(CAG) Repeats and Disease-Associated Expansions
inferred← citeshttps://doi.org/10.1016/b978-1-4160-2973-1.50010-7openalex-snapshot
10.1016/b978-1-4160-2973-1.50010-7
inferred← citeshttps://doi.org/10.1016/b978-1-4160-3080-5.50009-2openalex-snapshot
Patterns of Single-Gene Inheritance
inferred← citeshttps://doi.org/10.1016/b978-1-4160-3080-5.50011-0openalex-snapshot
Genetic Variation in Individuals and Populations: Mutation and Polymorphism
inferred← citeshttps://doi.org/10.1016/b978-1-4160-3080-5.50015-8openalex-snapshot
The Molecular, Biochemical, and Cellular Basis of Genetic Disease
inferred← citeshttps://doi.org/10.1016/j.ajhg.2009.02.003openalex-snapshot
CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup
inferred← citeshttps://doi.org/10.1016/j.ajhg.2009.11.006openalex-snapshot
Response to Falush: A Role for cis-Element Polymorphisms in HD
inferred← citeshttps://doi.org/10.1016/j.ajhg.2013.04.017openalex-snapshot
Hypermethylation of the CpG Island Near the G4C2 Repeat in ALS with a C9orf72 Expansion
inferred← citeshttps://doi.org/10.1016/j.ajhg.2020.07.004openalex-snapshot
Evolution of a Human-Specific Tandem Repeat Associated with ALS
inferred← citeshttps://doi.org/10.1016/j.ajhg.2021.03.011openalex-snapshot
30 years of repeat expansion disorders: What have we learned and what are the remaining challenges?
inferred← citeshttps://doi.org/10.1016/j.ajhg.2023.12.019openalex-snapshot
The shared ancestry between the C9orf72 hexanucleotide repeat expansion and intermediate-length alleles using haplotype sharing trees and HAPTK
inferred← citeshttps://doi.org/10.1016/j.bbadis.2006.05.013openalex-snapshot
Myotonic dystrophy: Emerging mechanisms for DM1 and DM2
inferred← citeshttps://doi.org/10.1016/j.bbadis.2013.03.002openalex-snapshot
RNA toxicity in human disease and animal models: From the uncovering of a new mechanism to the development of promising therapies
inferred← citeshttps://doi.org/10.1016/j.bbadis.2015.09.007openalex-snapshot
Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1)
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.12.037openalex-snapshot
Expanded [CCTG]n repetitions are not associated with abnormal methylation at the CNBP locus in myotonic dystrophy type 2 (DM2) patients
inferred← citeshttps://doi.org/10.1016/j.bbamcr.2007.10.014openalex-snapshot
Functional characterisation of the Schizosaccharomyces pombe homologue of the leukaemia-associated translocation breakpoint binding protein translin and its binding partner, TRAX
inferred← citeshttps://doi.org/10.1016/j.bbrc.2018.01.083openalex-snapshot
Drastic stability change of X-X mismatch in d(CXG) trinucleotide repeat disorders under molecular crowding condition
inferred← citeshttps://doi.org/10.1016/j.bbrc.2019.04.171openalex-snapshot
The human Exonuclease-1 interactome and phosphorylation sites
inferred← citeshttps://doi.org/10.1016/j.bcp.2025.117438openalex-snapshot
Inhibiting Cytosine-Adenine-Guanine (CAG) repeat expansions as a therapeutic strategy for Huntington’s disease
inferred← citeshttps://doi.org/10.1016/j.bios.2017.07.052openalex-snapshot
Neutralized chimeric DNA probe for detection of single nucleotide polymorphism on surface plasmon resonance biosensor
inferred← citeshttps://doi.org/10.1016/j.bmc.2019.05.022openalex-snapshot
Development of novel macrocyclic small molecules that target CTG trinucleotide repeats
inferred← citeshttps://doi.org/10.1016/j.bmc.2022.116897openalex-snapshot
Junctions in DNA: underexplored targets for therapeutic intervention
inferred← citeshttps://doi.org/10.1016/j.bmc.2023.117580openalex-snapshot
A new small molecule DoNA binding to CAG repeat RNA
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.05.062openalex-snapshot
Synthesis of 1H-pyrrolo[3,2-h]quinoline-8-amine derivatives that target CTG trinucleotide repeats
inferred← citeshttps://doi.org/10.1016/j.bmcl.2016.10.037openalex-snapshot
Development of pharmacophore models for small molecules targeting RNA: Application to the RNA repeat expansion in myotonic dystrophy type 1
inferred← citeshttps://doi.org/10.1016/j.bmcl.2017.06.067openalex-snapshot
AuNP-CTG based probing system targeting CAG repeat DNA and RNA sequences
inferred← citeshttps://doi.org/10.1016/j.bmcl.2022.129082openalex-snapshot
A small molecule binding to TGGAA pentanucleotide repeats that cause spinocerebellar ataxia type 31
inferred← citeshttps://doi.org/10.1016/j.bpj.2017.05.041openalex-snapshot
Structure and Dynamics of DNA and RNA Double Helices of CAG and GAC Trinucleotide Repeats
inferred← citeshttps://doi.org/10.1016/j.brainres.2014.03.039openalex-snapshot
RNA–protein interactions in unstable microsatellite diseases
inferred← citeshttps://doi.org/10.1016/j.brainres.2015.10.004openalex-snapshot
Epigenetic modifications in human fragile X pluripotent stem cells; Implications in fragile X syndrome modeling
inferred← citeshttps://doi.org/10.1016/j.bse.2016.05.023openalex-snapshot
Genome-wide distribution and organization of microsatellites in six species of birds
inferred← citeshttps://doi.org/10.1016/j.cbd.2010.01.002openalex-snapshot
EST analysis and identification of gonad-related genes from the normalized cDNA library of large yellow croaker, Larimichthys crocea
inferred← citeshttps://doi.org/10.1016/j.cbpb.2006.11.029openalex-snapshot
Stable minihairpin structures forming at minisatellite DNA isolated from yellow fin sea bream Acanthopagrus latus
inferred← citeshttps://doi.org/10.1016/j.ccr.2009.01.004openalex-snapshot
Metal complexes as structure-selective binding agents for nucleic acids
inferred← citeshttps://doi.org/10.1016/j.cdp.2007.10.001openalex-snapshot
Polymorphisms in the insulin like growth factor 1 and IGF binding protein 3 genes and risk of colorectal cancer
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.03.024openalex-snapshot
Nucleoporins and chromatin metabolism
inferred← citeshttps://doi.org/10.1016/j.cell.2011.02.012openalex-snapshot
Double-Strand Breaks in Heterochromatin Move Outside of a Dynamic HP1a Domain to Complete Recombinational Repair
inferred← citeshttps://doi.org/10.1016/j.cell.2018.01.012openalex-snapshot
Rescue of Fragile X Syndrome Neurons by DNA Methylation Editing of the FMR1 Gene
inferred← citeshttps://doi.org/10.1016/j.cell.2018.06.044openalex-snapshot
RNA-Dependent Epigenetic Silencing Directs Transcriptional Downregulation Caused by Intronic Repeat Expansions
inferred← citeshttps://doi.org/10.1016/j.cell.2018.08.005openalex-snapshot
Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries
inferred← citeshttps://doi.org/10.1016/j.cell.2023.09.008openalex-snapshot
Antagonistic roles of canonical and Alternative-RPA in disease-associated tandem CAG repeat instability
inferred← citeshttps://doi.org/10.1016/j.celrep.2014.10.048openalex-snapshot
Coupling Transcriptional State to Large-Scale Repeat Expansions in Yeast
inferred← citeshttps://doi.org/10.1016/j.celrep.2015.08.084openalex-snapshot
Reversion of FMR1 Methylation and Silencing by Editing the Triplet Repeats in Fragile X iPSC-Derived Neurons
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.110078openalex-snapshot
FAN1 exo- not endo-nuclease pausing on disease-associated slipped-DNA repeats: A mechanism of repeat instability
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