The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence
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[1] C. Caskey,et al. Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy. , 1996, Genomics.
[2] D. Paslier,et al. Human Chromosomal Fragile Site FRA16B Is an Amplified AT-Rich Minisatellite Repeat , 1997, Cell.
[3] R. Gellibolian,et al. Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene. , 1996, Journal of molecular biology.
[4] I. Kanazawa,et al. A unique origin and multistep process for the generation of expanded DRPLA triplet repeats. , 1996, Human molecular genetics.
[5] J. Todd,et al. Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus , 1995, Nature Genetics.
[6] En Li,et al. De novo methylation of MMLV provirus in embryonic stem cells: CpG versus non-CpG methylation. , 2002, Gene.
[7] P. Hieter,et al. Increased Instability of Human CTG Repeat Tracts on Yeast Artificial Chromosomes during Gametogenesis , 1999, Molecular and Cellular Biology.
[8] Í. Lopes-Cendes,et al. Study of three intragenic polymorphisms in the Machado-Joseph disease gene (MJD1) in relation to genetic instability of the (CAG)n tract , 1999, European Journal of Human Genetics.
[9] G. P. Smith,et al. Evolution of repeated DNA sequences by unequal crossover. , 1976, Science.
[10] M. Nelen,et al. Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins. , 2002, Human molecular genetics.
[11] H. Smeets,et al. Normal phenotype in two brothers with a full FMR1 mutation. , 1995, Human molecular genetics.
[12] A. Oppenheim,et al. Initiation points for cellular deoxyribonucleic acid replication in human lymphoid cells converted by Epstein-Barr virus , 1981, Molecular and cellular biology.
[13] S. Pulst,et al. Analysis of the dynamic mutation in the SCA7 gene shows marked parental effects on CAG repeat transmission. , 1998, Human molecular genetics.
[14] D. Sillence,et al. Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population. , 1995, Human molecular genetics.
[15] M. Macias,et al. Fragile X syndrome and deletions in FMR1: new case and review of the literature. , 1997, American journal of medical genetics.
[16] Brooke L Heidenfelder,et al. Hairpin Formation in Friedreich's Ataxia Triplet Repeat Expansion* , 2003, The Journal of Biological Chemistry.
[17] W. Vogel,et al. Mitotic behavior of expanded CGG repeats studied on cultured cells: further evidence for methylation-mediated triplet repeat stability in fragile X syndrome. , 1999, American journal of medical genetics.
[18] M. Koenig,et al. Evolution of the Friedreich's ataxia trinucleotide repeat expansion: founder effect and premutations. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[19] C. Gunter,et al. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1. , 1998, Human molecular genetics.
[20] Alan P. Wolffe,et al. Transcription: In tune with the histones , 1994, Cell.
[21] C. Chetsanga,et al. Single-stranded regions in DNA of old mice , 1975, Nature.
[22] B. Trask,et al. Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability. , 1998, Human molecular genetics.
[23] R. Eritja,et al. NMR study of the conformation of the 2-aminopurine:cytosine mismatch in DNA. , 1996, Biochemistry.
[24] J E Hewitt,et al. Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy. , 1994, Human molecular genetics.
[25] B. V. van Oost,et al. Parental origin of the fra(X) gene is a major determinant of the cytogenetic expression and the CGG repeat length in female carriers. , 1992, American journal of medical genetics.
[26] A. Verkerk,et al. Segregation of the fragile X mutation from an affected male to his normal daughter. , 1992, Human molecular genetics.
[27] W. Greenough,et al. Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome. , 1999, American journal of medical genetics.
[28] Robin L. Bennett,et al. Laboratory Guidelines for Huntington Disease Genetic Testing , 1998 .
[29] B. Howard,et al. Nucleosome Positioning by Human Alu Elements in Chromatin (*) , 1995, The Journal of Biological Chemistry.
[30] R. Wells,et al. Tetracycline promoter mutations decrease non-B DNA structural transitions, negative linking differences and deletions in recombinant plasmids in Escherichia coli. , 1989, Journal of molecular biology.
[31] J. Gécz. FMR3 is a novel gene associated withFRAXE CpG island and transcriptionally silent in FRAXE full mutations , 2000, Journal of medical genetics.
[32] W Dean,et al. DNA methylation and mammalian epigenetics , 2001, Electrophoresis.
[33] R. Korneluk,et al. High resolution genetic analysis suggests one ancestral predisposing haplotype for the origin of the myotonic dystrophy mutation. , 1994, Human molecular genetics.
[34] C. Junien,et al. 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. , 1998, Human molecular genetics.
[35] D Riesner,et al. Mismatches in DNA double strands: thermodynamic parameters and their correlation to repair efficiencies. , 1986, Nucleic acids research.
[36] R. Wells,et al. GGA·TCC-interrupted Triplets in Long GAA·TTC Repeats Inhibit the Formation of Triplex and Sticky DNA Structures, Alleviate Transcription Inhibition, and Reduce Genetic Instabilities* , 2001, The Journal of Biological Chemistry.
[37] R. Sinden,et al. Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines , 1996, Human Genetics.
[38] I. V. Kovtun,et al. Gender of the embryo contributes to CAG instability in transgenic mice containing a Huntington's disease gene. , 2000, Human molecular genetics.
[39] R. Sinden,et al. Trinucleotide repeat DNA structures: dynamic mutations from dynamic DNA. , 1998, Current opinion in structural biology.
[40] E. Wilson,et al. Reduced androgen receptor gene expression with first exon CAG repeat expansion. , 1996, Molecular endocrinology.
[41] T. Bird,et al. SCA8 CTG repeat: en masse contractions in sperm and intergenerational sequence changes may play a role in reduced penetrance. , 2000, Human molecular genetics.
[42] S. Tapscott,et al. CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus , 2001, Nature Genetics.
[43] D. Crawford,et al. Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR. , 2000, Human molecular genetics.
[44] P. Henson. The presence of single-stranded regions in mammalian DNA. , 1978, Journal of molecular biology.
[45] S. Mirkin,et al. Replication and Expansion of Trinucleotide Repeats in Yeast , 2003, Molecular and Cellular Biology.
[46] H. Scher,et al. Androgen receptor CAG repeat lengths in prostate cancer: correlation with age of onset. , 1996, The Journal of clinical endocrinology and metabolism.
[47] J. Grootegoed,et al. DNA repair mechanisms and gametogenesis. , 2001, Reproduction.
[48] M. DePamphilis,et al. Review: nuclear structure and DNA replication. , 2000, Journal of structural biology.
[49] S. Thibodeau,et al. High functioning fragile X males: demonstration of an unmethylated fully expanded FMR-1 mutation associated with protein expression. , 1994, American journal of medical genetics.
[50] G. Neri,et al. Significance of linkage disequilibrium between the fragile X locus and its flanking markers. , 1996, American journal of medical genetics.
[51] K. Mathews,et al. The DNA rearrangement associated with facioscapulohumeral muscular dystrophy involves a heterochromatin-associated repetitive element: Implications for a role of chromatin structure in the pathogenesis of the disease , 1994, Chromosome Research.
[52] W. Brown,et al. In situ nick translation of the fragile X region. , 1988, American journal of medical genetics.
[53] D. Averbeck,et al. Characterisation of homologous recombination induced by replication inhibition in mammalian cells , 2020 .
[54] J. Griffith,et al. Methylation of Expanded CCG Triplet Repeat DNA from Fragile X Syndrome Patients Enhances Nucleosome Exclusion* , 1996, The Journal of Biological Chemistry.
[55] S. Warren,et al. Characterization of the full fragile X syndrome mutation in fetal gametes , 1997, Nature Genetics.
[56] N. Tommerup,et al. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene , 1999, Nature.
[57] Mika Nakamoto,et al. Unequal crossing-over in unique PABP2 mutations in Japanese patients: a possible cause of oculopharyngeal muscular dystrophy. , 2002, Archives of neurology.
[58] M. Kinoshita,et al. CTG triplet repeat expansion in a laryngeal carcinoma from a patient with myotonic dystrophy , 2000, Muscle & nerve.
[59] B. Migeon,et al. DNA methylation of the fragile X locus in somatic and germ cells during fetal development: Relevance to the fragile X syndrome and X inactivation , 1993, Somatic cell and molecular genetics.
[60] I. Kanazawa,et al. 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 , 1997, Annals of neurology.
[61] Takanori Yamagata,et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10 , 2000, Nature Genetics.
[62] M. Ruberg,et al. De novo expansion of intermediate alleles in spinocerebellar ataxia 7. , 1998, Human molecular genetics.
[63] J. J. Breen,et al. BORIS, a novel male germ-line-specific protein associated with epigenetic reprogramming events, shares the same 11-zinc-finger domain with CTCF, the insulator protein involved in reading imprinting marks in the soma , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[64] W. Brown,et al. Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes. , 1996, American journal of medical genetics.
[65] M. Linsenmeyer,et al. Asymmetric Methylation in the Hypermethylated CpG Promoter Region of the Human L1 Retrotransposon* , 1997, The Journal of Biological Chemistry.
[66] D. Crawford,et al. Prevalence of the fragile X syndrome in African-Americans. , 2002, American journal of medical genetics.
[67] H. Paulson,et al. Genetic Instabilities and Hereditary Neurological Diseases , 1998 .
[68] C. Caskey,et al. Hypermutable myotonic dystrophy CTG repeats in transgenic mice , 1997, Nature Genetics.
[69] A. Delacourte,et al. Dysregulation of human brain microtubule-associated tau mRNA maturation in myotonic dystrophy type 1. , 2001, Human molecular genetics.
[70] H. Zoghbi,et al. Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I , 1993, Nature Genetics.
[71] J. Squire,et al. The role of Alu repeat clusters as mediators of recurrent chromosomal aberrations in tumors , 2002, Genes, chromosomes & cancer.
[72] M. Mitas,et al. The purine-rich trinucleotide repeat sequences d(CAG)15 and d(GAC)15 form hairpins. , 1995, Nucleic acids research.
[73] J. Drost,et al. Biological basis of germline mutation: Comparisons of spontaneous germline mutation rates among drosophila, mouse, and human , 1995, Environmental and molecular mutagenesis.
[74] H. Cann,et al. The gene for spinal cerebellar ataxia 1 (SCA1) is flanked by two closely linked highly polymorphic microsatellite loci. , 1993, Human molecular genetics.
[75] B. Keats,et al. Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations: a variant nucleotide is associated with the number of CAG repeats. , 1996, Human molecular genetics.
[76] D. M. Livingston,et al. Mapping the Polarity of Changes That Occur in Interrupted CAG Repeat Tracts in Yeast , 1998, Molecular and Cellular Biology.
[77] M. Lieber,et al. Developmental stage specificity of the lymphoid V(D)J recombination activity. , 1987, Genes & development.
[78] M. Dixon,et al. Mismatch repair blocks expansions of interrupted trinucleotide repeats in yeast. , 2000, Molecular cell.
[79] R. Favier,et al. Co-localisation of CCG repeats and chromosome deletion breakpoints in Jacobsen syndrome: evidence for a common mechanism of chromosome breakage. , 2000, Human molecular genetics.
[80] T. Komori,et al. A patient with myotonic dystrophy type 1 (DM 1) accompanied by laryngeal and renal cell carcinomas had a small CTG triplet repeat expansion but no somatic instability in normal tissues. , 2002, Internal medicine.
[81] M. Lieber. The biochemistry and biological significance of nonhomologous DNA end joining: an essential repair process in multicellular eukaryotes , 1999, Genes to cells : devoted to molecular & cellular mechanisms.
[82] C. Junien,et al. Characteristics of intergenerational contractions of the CTG repeat in myotonic dystrophy. , 1994, American journal of human genetics.
[83] N. Morton,et al. The role of size, sequence and haplotype in the stability of FRAXA and FRAXE alleles during transmission. , 1997, Human Molecular Genetics.
[84] S. Choudhry,et al. CAG repeat instability at SCA2 locus: anchoring CAA interruptions and linked single nucleotide polymorphisms. , 2001, Human molecular genetics.
[85] T. Ashizawa,et al. Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses. , 1995, Human molecular genetics.
[86] W. Vogel,et al. Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats. , 1998, Journal of medical genetics.
[87] R. Roos,et al. Somatic expansion of the (CAG)n repeat in Huntington disease brains , 1995, Human Genetics.
[88] B. Oostra,et al. The full mutation in the FMR–1 gene of male fragile X patients is absent in their sperm , 1993, Nature Genetics.
[89] D. Roth,et al. Unequal Access Regulating V(D)J Recombination through Chromatin Remodeling , 2000, Cell.
[90] M. Baiget,et al. Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development. , 1997, Human molecular genetics.
[91] B. Stillman,et al. Anatomy of a DNA replication fork revealed by reconstitution of SV40 DNA replication in vitro , 1994, Nature.
[92] M. Cerone,et al. In vitro low propensity to form nucleosomes of four telomeric sequences , 1997, FEBS letters.
[93] Dmitry A. Gordenin,et al. Repeat expansion — all in flap? , 1997, Nature Genetics.
[94] S. Tavaré,et al. Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. , 1995, Human molecular genetics.
[95] T. Lindahl,et al. Long regions of single-stranded DNA in human cells , 1979, Nature.
[96] Keiichi Ohshima,et al. Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli , 1995, Nature Genetics.
[97] Yuri Dubrova,et al. Influences of array size and homogeneity on minisatellite mutation , 1998, The EMBO journal.
[98] E. van Marck,et al. Postmortem examination of two fragile X brothers with an FMR1 full mutation. , 1999, American journal of medical genetics.
[99] M. Savontaus,et al. Clinical and genetic findings in Finnish ataxia patients with the spinocerebellar ataxia 8 repeat expansion , 2000, Annals of neurology.
[100] T. Makinodan,et al. Age-Associated Changes in the DNA of Mouse Tissue , 1971, Science.
[101] H. Hameister,et al. Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells. , 2001, American journal of human genetics.
[102] S Kobayashi,et al. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? , 1999, Human molecular genetics.
[103] D. Monckton,et al. 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. , 2001, Human molecular genetics.
[104] M. Dichgans,et al. Spinocerebellar ataxia type 6: Evidence for a strong founder effect among German families , 1999, Neurology.
[105] N. Carson,et al. Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature. , 2002, American journal of medical genetics.
[106] S. Detera-Wadleigh,et al. Mutation analysis of oculopharyngeal muscular dystrophy in Hispanic American families. , 1999, Archives of neurology.
[107] P. Wieacker,et al. The size of the CAG repeat in exon 1 of the androgen receptor gene shows no significant relationship to impaired spermatogenesis in an infertile Caucasoid sample of German origin. , 2000, Molecular human reproduction.
[108] M. Baiget,et al. Frequency and stability of the myotonic dystrophy type 1 premutation , 2001, Neurology.
[109] R. Richards,et al. Association of a chromosome deletion syndrome with a fragile site within the proto-oncogene CBL2 , 1995, Nature.
[110] C. E. Pearson,et al. Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells , 2002, Nature Genetics.
[111] T. Tahira,et al. Polar alteration of short tandem repeats (STRs) in mammalian cells. , 2001, Mutation research.
[112] H. Hobbs,et al. A high frequency of length polymorphisms in repeated sequences adjacent to Alu sequences. , 1990, American journal of human genetics.
[113] D. Livingston,et al. Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation. , 1998, Human molecular genetics.
[114] L. Peltonen,et al. Ancestral differences in the distribution of the delta 2642 glutamic acid polymorphism is associated with varying CAG repeat lengths on normal chromosomes: insights into the genetic evolution of Huntington disease. , 1995, Human molecular genetics.
[115] A. Messer,et al. Instability of the CAG repeat in immortalized fibroblast cell cultures from Huntington's Disease transgenic mice 1 Published on the World Wide Web on 15 April 1999. 1 , 1999, Brain Research.
[116] M. Siciliano,et al. Dramatic, expansion-biased, age-dependent, tissue-specific somatic mosaicism in a transgenic mouse model of triplet repeat instability. , 2000, Human molecular genetics.
[117] Complex gene conversion events in germline mutation at human minisatellites , 1994 .
[118] S. Mirkin,et al. Trinucleotide repeats affect DNA replication in vivo , 1997, Nature Genetics.
[119] Unexpected formation of parallel duplex in GAA and TTC trinucleotide repeats of Friedreich's ataxia. , 2000 .
[120] Elena Komissarova,et al. Transcription-coupled DNA Repair Is Genomic Context-dependent* , 2002, The Journal of Biological Chemistry.
[121] A. Duval,et al. Comparative analysis of mutation frequency of coding and non coding short mononucleotide repeats in mismatch repair deficient colorectal cancers , 2002, Oncogene.
[122] Asad Umar,et al. Meiotic Pachytene Arrest in MLH1-Deficient Mice , 1996, Cell.
[123] D. Crawford,et al. Paternally transmitted FMR1 alleles are less stable than maternally transmitted alleles in the common and intermediate size range. , 2002, American journal of human genetics.
[124] M. Fukuda,et al. Age associated increase of single-stranded regions in the DNA of mouse brain and liver cells , 1979, Mechanisms of Ageing and Development.
[125] M. Shimizu,et al. Destabilization of nucleosomes by an unusual DNA conformation adopted by poly(dA) small middle dotpoly(dT) tracts in vivo. , 2000, The EMBO journal.
[126] J. Emparanza,et al. Influence of the sex of the transmitting grandparent in congenital myotonic dystrophy. , 1995, Journal of medical genetics.
[127] J. Gécz,et al. Identification of the gene FMR2, associated with FRAXE mental retardation , 1996, Nature Genetics.
[128] K. Usdin,et al. Tetraplex formation by the progressive myoclonus epilepsy type‐1 repeat: implications for instability in the repeat expansion diseases , 2001, FEBS letters.
[129] Yun Zhang,et al. Age and insertion site dependence of repeat number instability of a human DM1 transgene in individual mouse sperm. , 2002, Human molecular genetics.
[130] S. Blumen,et al. Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene , 2000, Neurology.
[131] G. Richard,et al. Mini‐ and microsatellite expansions: the recombination connection , 2000, EMBO reports.
[132] C. L. Warner,et al. Meiotic stability and genotype – phenotype correlation of the trinucleotide repeat in X–linked spinal and bulbar muscular atrophy , 1992, Nature Genetics.
[133] A. Hunter,et al. Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission. , 1993, Science.
[134] T. Bestor,et al. Sex-specific exons control DNA methyltransferase in mammalian germ cells. , 1998, Development.
[135] I. Kanazawa,et al. Unstable transmission of the RS447 human megasatellite tandem repetitive sequence that contains the USP17 deubiquitinating enzyme gene , 2002, Human Genetics.
[136] M. Baiget,et al. Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1 , 2000, European Journal of Human Genetics.
[137] M. Smerdon,et al. Nucleotide excision repair in a constitutive and inducible gene of a yeast minichromosome in intact cells. , 1999, Nucleic acids research.
[138] J. Vincent,et al. Polyglutamine-containing proteins in schizophrenia: an effect of lymphoblastoid cells? , 2000, Molecular Psychiatry.
[139] P. Hanawalt,et al. DNA repair in terminally differentiated cells. , 2002, DNA repair.
[140] T. Petes,et al. Triplet repeats form secondary structures that escape DNA repair in yeast. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[141] R. Sinke,et al. Spinocerebellar ataxias in the Netherlands: Prevalence and age at onset variance analysis , 2002, Neurology.
[142] C. E. Pearson,et al. Slipped-strand DNAs formed by long (CAG)*(CTG) repeats: slipped-out repeats and slip-out junctions. , 2002, Nucleic acids research.
[143] T. Petes,et al. Stabilization of microsatellite sequences by variant repeats in the yeast Saccharomyces cerevisiae. , 1997, Genetics.
[144] W Zacharias,et al. Methylation of cytosine influences the DNA structure. , 1993, EXS.
[145] Y. Clermont,et al. KINETICS OF THE GERMINAL EPITHELIUM IN MAN. , 1964, Recent progress in hormone research.
[146] F. Hazama,et al. Somatic mosaicism of CAG repeat in dentatorubral-pallidoluysian atrophy (DRPLA). , 1995, Human molecular genetics.
[147] B. Oostra,et al. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities , 1999, Journal of medical genetics.
[148] T. Mori,et al. Destabilization of nucleosomes by an unusual DNA conformation adopted by poly(dA)·poly(dT) tracts in vivo , 2000 .
[149] A. Niveleau,et al. DNA global hypomethylation in EBV-transformed interphase nuclei. , 1999, Experimental cell research.
[150] I. Kennerknecht,et al. Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stability. , 1995, Human molecular genetics.
[151] T. Kamp,et al. Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15. , 1995, Nucleic acids research.
[152] B. Stillman,et al. Histone Acetyltransferase HBO1 Interacts with the ORC1 Subunit of the Human Initiator Protein* , 1999, The Journal of Biological Chemistry.
[153] K. Fischbeck,et al. Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy , 1991, Nature.
[154] J. Penney,et al. Trinucleotide repeat length instability and age of onset in Huntington's disease , 1993, Nature Genetics.
[155] R. Edwards,et al. Genetics and human conception DNA repair by oocytes , 1996 .
[156] D. Dash,et al. Origin and Instability of GAA Repeats: Insights from Alu Elements , 2002, Journal of biomolecular structure & dynamics.
[157] D. Nelson,et al. High resolution methylation analysis of the FMR1 gene trinucleotide repeat region in fragile X syndrome. , 1993, Human molecular genetics.
[158] Mikael Kubista,et al. Nucleosome Structural Features and Intrinsic Properties of the TATAAACGCC Repeat Sequence* , 1999, The Journal of Biological Chemistry.
[159] Richard R. Sinden,et al. Neurodegenerative diseases: Origins of instability , 2001, Nature.
[160] Georg Auburger,et al. Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2 , 1996, Nature Genetics.
[161] A. Razin,et al. DNA methylation in early development. , 1995, Human molecular genetics.
[162] S Srivastava,et al. A National Cancer Institute Workshop on Microsatellite Instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. , 1998, Cancer research.
[163] J. Stavenhagen,et al. Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome , 1997, Molecular and cellular biology.
[164] S. Warren,et al. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus. , 1997, Journal of medical genetics.
[165] J. Rommens,et al. Unstable insertion in the 5′ flanking region of the cystatin B gene is the most common mutation in progressive myoclonus epilepsy type 1, EPM1 , 1997, Nature Genetics.
[166] F. Ledeist,et al. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome. , 1993, Human molecular genetics.
[167] H. Widlund,et al. TGGA repeats impair nucleosome formation. , 1998, Journal of molecular biology.
[168] P. Andersen,et al. Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the world , 2001, European Journal of Human Genetics.
[169] E. Nieschlag,et al. Inverse correlation between sperm concentration and number of androgen receptor CAG repeats in normal men. , 2001, The Journal of clinical endocrinology and metabolism.
[170] H. Smeets,et al. Brief report: reverse mutation in myotonic dystrophy. , 1993, The New England journal of medicine.
[171] A. Sano,et al. Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p , 1994, Nature Genetics.
[172] J.. Neurodegenerative Diseases , 1996, GWUMC Department of Biochemistry and Molecular Biology Annual Spring Symposia.
[173] C. E. Pearson,et al. In Vitro (CTG)·(CAG) Expansions and Deletions by Human Cell Extracts* , 2002, The Journal of Biological Chemistry.
[174] Milovan Krnjajic,et al. Active Alu elements are passed primarily through paternal germlines. , 2002, Theoretical population biology.
[175] J. Mandel,et al. Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset. , 1994, Journal of medical genetics.
[176] W. Brown,et al. FMR1 CGG-repeat instability in single sperm and lymphocytes of fragile-X premutation males. , 1999, American journal of human genetics.
[177] R. Sinden,et al. Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci. , 1996, Biochemistry.
[178] P. Fraser,et al. Intergenic transcription and developmental remodeling of chromatin subdomains in the human beta-globin locus. , 2000, Molecular cell.
[179] L. Pianese,et al. The effect of parental gender on the GAA dynamic mutation in the FRDA gene. , 1997, American journal of human genetics.
[180] M. Bichara,et al. Expansion of CTG repeats from human disease genes is dependent upon replication mechanisms in Escherichia coli: the effect of long patch mismatch repair revisited. , 1998, Journal of molecular biology.
[181] M. Ramsay,et al. New founder haplotypes at the myotonic dystrophy locus in southern Africa. , 1995, American journal of human genetics.
[182] J. Miret,et al. Instability of CAG and CTG trinucleotide repeats in Saccharomyces cerevisiae , 1997, Molecular and cellular biology.
[183] H. Zoghbi,et al. Increased trinucleotide repeat instability with advanced maternal age. , 1997, Human molecular genetics.
[184] E. Hirsch,et al. Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado‐Joseph disease , 1998, Human mutation.
[185] S. Tsujino,et al. Small increase in triplet repeat length of cerebellum from patients with myotonic dystrophy , 1996, Human Genetics.
[186] R. Gibbs,et al. Somatic sequence variation at the Friedreich ataxia locus includes complete contraction of the expanded GAA triplet repeat, significant length variation in serially passaged lymphoblasts and enhanced mutagenesis in the flanking sequence. , 1999, Human molecular genetics.
[187] C. Schmid,et al. Genome-wide chromatin remodeling modulates the Alu heat shock response. , 2001, Gene.
[188] S. Tapscott,et al. Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[189] R. Sinden,et al. Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[190] R. Winqvist,et al. Unstable DNA may be responsible for the incomplete penetrance of the myotonic dystrophy phenotype. , 1992, Human molecular genetics.
[191] D. Goldgaber,et al. Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[192] I. Kanazawa,et al. 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. , 1999, Human molecular genetics.
[193] A. Jeffreys,et al. Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphism , 1994, Nature Genetics.
[194] G. Almouzni,et al. When repair meets chromatin , 2002, EMBO reports.
[195] M. DePamphilis,et al. Initiation of SV40 DNA replication in vivo: Location and structure of 5′ ends of DNA synthesized in the ori region , 1982, Cell.
[196] B. Michel. Replication fork arrest and DNA recombination. , 2000, Trends in biochemical sciences.
[197] Absence of chromosome fragility at 19q13.3 in patients with myotonic dystrophy. , 1993, American journal of medical genetics.
[198] R. Korneluk,et al. Intergenerational stability of the myotonic dystrophy protomutation. , 1993, Human molecular genetics.
[199] Y. Itoyama,et al. Reduction of CAG expansions in cerebellar cortex and spinal cord of DRPLA , 1996, Clinical genetics.
[200] G. Coetzee,et al. The CAG and GGC microsatellites of the androgen receptor gene are in linkage disequilibrium in men with prostate cancer. , 1995, Cancer research.
[201] D. Rubinsztein,et al. Analysis of the huntingtin gene reveals a trinucleotide-length polymorphism in the region of the gene that contains two CCG-rich stretches and a correlation between decreased age of onset of Huntington's disease and CAG repeat number. , 1993, Human molecular genetics.
[202] N. Risch,et al. An association between the risk of cancer and mutations in the HRAS1 minisatellite locus. , 1993, The New England journal of medicine.
[203] T. Ashizawa,et al. The GAA triplet-repeat sequence in Friedreich ataxia shows a high level of somatic instability in vivo, with a significant predilection for large contractions. , 2002, Human molecular genetics.
[204] E. Hoffman,et al. Unique PABP2 mutations in "Cajuns" suggest multiple founders of oculopharyngeal muscular dystrophy in populations with French ancestry. , 1999, American journal of medical genetics.
[205] C. Junien,et al. Transgenic mice carrying large human genomic sequences with expanded CTG repeat mimic closely the DM CTG repeat intergenerational and somatic instability. , 2000, Human molecular genetics.
[206] B. Bardoni,et al. 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? , 2000, Journal of medical genetics.
[207] S. Warren,et al. Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus , 1996, Somatic cell and molecular genetics.
[208] D. Nelson,et al. Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes. , 1994, Human molecular genetics.
[209] Mika Nakamoto,et al. A CAG/CTG expansion in the normal population , 1997, Nature Genetics.
[210] Shigenobu Nakamura,et al. CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 , 1994, Nature Genetics.
[211] M. Batzer,et al. Alu repeats and human disease. , 1999, Molecular genetics and metabolism.
[212] P. Sadowski. Bacteriophage T7 endonuclease. I. Properties of the enzyme purified from T7 phage-infected Escherichia coli B. , 1971, The Journal of biological chemistry.
[213] M. Hayden,et al. Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm , 1994, Nature Genetics.
[214] F. Thépot,et al. Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range. , 1996, Human molecular genetics.
[215] Stephen Neidle,et al. Crystal structure of parallel quadruplexes from human telomeric DNA , 2002, Nature.
[216] R. Gellibolian,et al. Long CCG triplet repeat blocks exclude nucleosomes: a possible mechanism for the nature of fragile sites in chromosomes. , 1996, Journal of molecular biology.
[217] J. Puymirat,et al. Decreased levels of myotonic dystrophy protein kinase (DMPK) and delayed differentiation in human myotonic dystrophy myoblasts , 2001, Neuromuscular Disorders.
[218] J. Jurka,et al. Inverted Alu repeats unstable in yeast are excluded from the human genome , 2000, The EMBO journal.
[219] B. Alberts,et al. Head-on collision between a DNA replication apparatus and RNA polymerase transcription complex , 1995, Science.
[220] N. Gregersen,et al. One short well conserved region of Alu-sequences is involved in human gene rearrangements and has homology with prokaryotic chi. , 1995, Nucleic acids research.
[221] I. V. Kovtun,et al. Trinucleotide expansion in haploid germ cells by gap repair , 2001, Nature Genetics.
[222] C. Richards,et al. Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent. , 1995, American journal of human genetics.
[223] E. Eichler,et al. Interruptions in the triplet repeats of SCA1 and FRAXA reduce the propensity and complexity of slipped strand DNA (S-DNA) formation. , 1998, Biochemistry.
[224] P. Hagerman,et al. Cytosine methylation can induce local distortions in the structure of duplex DNA. , 1992, Biochemistry.
[225] Tetsuo Ashizawa,et al. Somatic instability of CTG repeat in myotonic dystrophy , 1993, Neurology.
[226] B. Popovich,et al. Fully expanded FMR1 CGG repeats exhibit a length- and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. , 1999, Human molecular genetics.
[227] N H Terry,et al. "Mitotic drive" of expanded CTG repeats in myotonic dystrophy type 1 (DM1). , 2001, Human molecular genetics.
[228] R. Wells,et al. Pausing of DNA Synthesis in Vitro at Specific Loci in CTG and CGG Triplet Repeats from Human Hereditary Disease Genes (*) , 1995, The Journal of Biological Chemistry.
[229] Margarita Salas,et al. Bacteriophage φ29 DNA replication arrest caused by codirectional collisions with the transcription machinery , 1997, The EMBO journal.
[230] D. Nag,et al. Meiotic instability of CAG repeat tracts occurs by double-strand break repair in yeast. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[231] B. Suter,et al. Poly(dA.dT) sequences exist as rigid DNA structures in nucleosome-free yeast promoters in vivo. , 2000, Nucleic acids research.
[232] S. Mirkin,et al. Positioned to expand , 2002, Nature Genetics.
[233] M. Hayden,et al. The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease , 1993, Nature Genetics.
[234] R. Wells,et al. Long CTG·CAG Repeats from Myotonic Dystrophy Are Preferred Sites for Intermolecular Recombination* , 2002, The Journal of Biological Chemistry.
[235] T. Ashizawa,et al. De novo myotonic dystrophy mutation in a Nigerian kindred. , 1995, American journal of human genetics.
[236] C. E. Pearson,et al. CpG methylation modifies the genetic stability of cloned repeat sequences. , 2002, Genome research.
[237] L. Edström,et al. Larger expansions of the CTG repeat in muscle compared to lymphocytes from patients with myotonic dystrophy. , 1993, Human molecular genetics.
[238] N. E. Morton,et al. Further segregation analysis of the fragile X syndrome with special reference to transmitting males , 2004, Human Genetics.
[239] R M Winter,et al. Synpolydactyly phenotypes correlate with size of expansions in HOXD13 polyalanine tract. , 1997, Proceedings of the National Academy of Sciences of the United States of America.
[240] S. Lumbroso,et al. Mutations of androgen receptor gene in androgen insensitivity syndromes , 1993, The Journal of Steroid Biochemistry and Molecular Biology.
[241] A. S. Krasilnikov,et al. Transcription through a simple DNA repeat blocks replication elongation , 1998, The EMBO journal.
[242] D. Leach,et al. Secondary structures in d(CGG) and d(CCG) repeat tracts. , 1998, Journal of molecular biology.
[243] A. Simpson,et al. Microsatellite instability in tumors as a model to study the process of microsatellite mutations. , 2000, Human molecular genetics.
[244] E. Eichler,et al. Length of uninterrupted CGG repeats determines instability in the FMR1 gene , 1994, Nature Genetics.
[245] J. Weissenbach,et al. Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeat. , 1996, Human molecular genetics.
[246] J. Herman,et al. CpG island methylator phenotype in colorectal cancer. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[247] A. Marquis Gacy,et al. Trinucleotide repeats that expand in human disease form hairpin structures in vitro , 1995, Cell.
[248] T. Haaf,et al. The effects of 5-azacytidine and 5-azadeoxycytidine on chromosome structure and function: implications for methylation-associated cellular processes. , 1995, Pharmacology & therapeutics.
[249] M. Shoji,et al. Analysis of spinocerebellar ataxia type 2 gene and haplotype analysis: (CCG)1- 2 polymorphism and contribution to founder effect , 1999, Journal of medical genetics.
[250] W. Brown,et al. Familial transmission of the FMR1 CGG repeat. , 1996, American journal of human genetics.
[251] R. Sinden,et al. Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases. , 1997, Human molecular genetics.
[252] M. Pandolfo,et al. The Friedreich ataxia GAA triplet repeat: premutation and normal alleles. , 1997, Human molecular genetics.
[253] J. Weber,et al. Alu repeats: a source for the genesis of primate microsatellites. , 1995, Genomics.
[254] T. Bird,et al. An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8) , 1999, Nature Genetics.
[255] J. Mandel,et al. Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development. , 1992, American journal of medical genetics.
[256] G. Sobue,et al. Differential pattern in tissue-specific somatic mosaicism of expanded CAG trinucleotide repeat in dentatorubral-pallidoluysian atrophy, Machado-Joseph disease, and X-linked recessive spinal and bulbar muscular atrophy , 1996, Journal of the Neurological Sciences.
[257] C. Mathew,et al. A multicenter study on genotype-phenotype correlations in the fragile X syndrome, using direct diagnosis with probe StB12.3: the first 2,253 cases. , 1994, American journal of human genetics.
[258] Robert I. Richards,et al. Simple repeat DNA is not replicated simply , 1994, Nature Genetics.
[259] C. Amemiya,et al. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene. , 1992, Science.
[260] M. Krangel,et al. A role for histone acetylation in the developmental regulation of VDJ recombination. , 2000, Science.
[261] D. Lilley,et al. A dominant influence of flanking sequences on a local structural transition in DNA , 1986, Cell.
[262] C. Junien,et al. Moderate intergenerational and somatic instability of a 55-CTG repeat in transgenic mice , 1997, Nature Genetics.
[263] W. Brown,et al. Reverse mutations in the fragile X syndrome. , 1994, American journal of medical genetics.
[264] J. Haber,et al. Recombination‐induced CAG trinucleotide repeat expansions in yeast involve the MRE11–RAD50–XRS2 complex , 2000, The EMBO journal.
[265] A. Wolffe,et al. Nucleosome Assembly on Methylated CGG Triplet Repeats in the Fragile X Mental Retardation Gene 1 Promoter* , 1996, The Journal of Biological Chemistry.
[266] J. Rüschoff,et al. Diagnostic microsatellite instability: definition and correlation with mismatch repair protein expression. , 1997, Cancer research.
[267] A. Smit. Interspersed repeats and other mementos of transposable elements in mammalian genomes. , 1999, Current opinion in genetics & development.
[268] A. Razin,et al. Demethylation of CpG islands in embryonic cells , 1991, Nature.
[269] Y. Agid,et al. Multiple origins of the spinocerebellar ataxia 7 (SCA7) mutation revealed by linkage disequilibrium studies with closely flanking markers, including an intragenic polymorphism (G3145TG/A3145TG) , 1999, European Journal of Human Genetics.
[270] M. Pandolfo,et al. Sticky DNA: self-association properties of long GAA.TTC repeats in R.R.Y triplex structures from Friedreich's ataxia. , 1999, Molecular cell.
[271] B. Oostra,et al. Trinucleotide (GGN) repeat polymorphism in the human androgen receptor (AR) gene. , 1993, Human molecular genetics.
[272] R. Wells,et al. Long CTG·CAG Repeat Sequences Markedly Stimulate Intramolecular Recombination* , 2002, The Journal of Biological Chemistry.
[273] J. Haber. DNA recombination: the replication connection. , 1999, Trends in biochemical sciences.
[274] J. Trasler. Origin and roles of genomic methylation patterns in male germ cells. , 1998, Seminars in cell & developmental biology.
[275] J. Mandel,et al. Origin of the expansion mutation in myotonic dystrophy , 1993, Nature Genetics.
[276] I. Kanazawa,et al. DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence. , 1994, Human molecular genetics.
[277] M. Passos-Bueno,et al. Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur? , 1995, Human molecular genetics.
[278] F Vogel,et al. Spontaneous mutation in man. , 1975, Advances in human genetics.
[279] K. Fischbeck,et al. CAG repeat length variation in sperm from a patient with Kennedy's disease. , 1995, Human molecular genetics.
[280] H. Zoghbi,et al. Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations. , 1998, American journal of human genetics.
[281] G. Felsenfeld,et al. Chromatin Unfolds , 1996, Cell.
[282] A J Jeffreys,et al. Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variability. , 1993, Human molecular genetics.
[283] R. Bambara,et al. Inhibition of Flap Endonuclease 1 by Flap Secondary Structure and Relevance to Repeat Sequence Expansion* , 2000, The Journal of Biological Chemistry.
[284] T. Nethanel,et al. Two DNA polymerases may be required for synthesis of the lagging DNA strand of simian virus 40 , 1990, Journal of virology.
[285] A. Taylor,et al. Strong similarities of the FMR1 mutation in multiple tissues: postmortem studies of a male with a full mutation and a male carrier of a premutation. , 1999, American journal of medical genetics.
[286] R. G. Lloyd,et al. Modulation of RNA Polymerase by (p)ppGpp Reveals a RecG-Dependent Mechanism for Replication Fork Progression , 2000, Cell.
[287] G. Yvert,et al. Variation on a trinucleotide theme , 1999, Nature Network Boston.
[288] M. DePamphilis,et al. Metabolism of Okazaki fragments during simian virus 40 DNA replication. , 1979, The Journal of biological chemistry.
[289] M. Hayden,et al. Different mechanisms underlie DNA instability in Huntington disease and colorectal cancer. , 1997, American journal of human genetics.
[290] R. Albin,et al. Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues , 1993, Nature Genetics.
[291] A. de la Chapelle,et al. Genetics of hereditary colon cancer. , 1995, Annual review of genetics.
[292] R. Meek,et al. Establishment of mouse embryo cells in vitro. Relationship of DNA synthesis, senescence and malignant transformation. , 1977, Experimental cell research.
[293] V. Sheffield,et al. Characterization of Alu repeats that are associated with trinucleotide and tetranucleotide repeat microsatellites. , 1997, Genome research.
[294] Rudolf Jaenisch,et al. DNA hypomethylation leads to elevated mutation rates , 1998, Nature.
[295] J. Rommens,et al. Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy , 1998, Nature Genetics.
[296] H. Zoghbi,et al. Gametic and somatic tissue–specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1 , 1995, Nature Genetics.
[297] J. Carpten,et al. Polymorphic GGC repeats in the androgen receptor gene are associated with hereditary and sporadic prostate cancer risk , 2002, Human Genetics.
[298] D. J. Driscoll,et al. Programmed demethylation in CpG islands during human fetal development , 1991, Somatic cell and molecular genetics.
[299] B. Stillman,et al. Reconstitution of complete SV40 DNA replication with purified replication factors. , 1994, The Journal of biological chemistry.
[300] Í. Lopes-Cendes,et al. Ancestral origins of the Machado-Joseph disease mutation: a worldwide haplotype study. , 2001, American journal of human genetics.
[301] E. Eichler,et al. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome. , 1996, Human molecular genetics.
[302] R. Wells,et al. Gene Conversion (Recombination) Mediates Expansions of CTG·CAG Repeats* , 2000, The Journal of Biological Chemistry.
[303] M. Radman,et al. Structures of mismatched base pairs in DNA and their recognition by the Escherichia coli mismatch repair system. , 1986, The EMBO journal.
[304] J. Mandel,et al. Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic. , 1997, Human molecular genetics.
[305] D. Labuda,et al. Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion , 2000, Neurology.
[306] S. Warren,et al. Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells , 1999, Nature Genetics.
[307] R. Moxley,et al. Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes , 1994, Annals of neurology.
[308] W. Wilcox,et al. Trinucleotide expansion mutations in the cartilage oligomeric matrix protein (COMP) gene. , 1999, Human molecular genetics.
[309] N. Hecht,et al. DNA methylation and demethylation events during meiotic prophase in the mouse testis , 1990, Molecular and cellular biology.
[310] S. Tavaré,et al. Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism. , 1999, Human molecular genetics.
[311] M. Baiget,et al. Comparison of CTG repeat length expansion and clinical progression of myotonic dystrophy over a five year period. , 1995, Journal of medical genetics.
[312] W. Vogel,et al. Mitotic stability of fragile X mutations in differentiated cells indicates early post–conceptional trinucleotide repeat expansion , 1993, Nature Genetics.
[313] Satoshi Tanaka,et al. Epigenetic marks by DNA methylation specific to stem, germ and somatic cells in mice , 2002, Genes to cells : devoted to molecular & cellular mechanisms.
[314] L. Richardson,et al. Expression of Deoxyribonucleic Acid Repair Enzymes During Spermatogenesis in Mice1 , 2000, Biology of reproduction.
[315] T. Bestor. Cytosine methylation and the unequal developmental potentials of the oocyte and sperm genomes. , 1998, American journal of human genetics.
[316] M. V. Katti,et al. Differential distribution of simple sequence repeats in eukaryotic genome sequences. , 2001, Molecular biology and evolution.
[317] R I Richards,et al. Simple tandem DNA repeats and human genetic disease. , 1995, Proceedings of the National Academy of Sciences of the United States of America.
[318] J. Herman,et al. Incidence and functional consequences of hMLH1 promoter hypermethylation in colorectal carcinoma. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[319] V. Sgaramella,et al. Triplet repeats, over-expanded in neuromuscular diseases, are under-represented in mammalian DNA: a survey of models , 2001, Brain Research Bulletin.
[320] D. Livingston,et al. The effect of DNA replication mutations on CAG tract stability in yeast. , 1999, Genetics.
[321] S. Antonarakis,et al. The polydeoxyadenylate tract of Alu repetitive elements is polymorphic in the human genome. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[322] H. Smeets,et al. Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm. , 1994, American journal of human genetics.
[323] Brooks Jd. Retreat of the triplet repeat , 1993 .
[324] H. Cederberg,et al. Cis-regulation of inter-allelic exchanges in mutation at human minisatellite MS205 in yeast. , 1999, Gene.
[325] M. Baiget,et al. Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients. , 1998, Human molecular genetics.
[326] I. Lerer,et al. Negative expansion of the myotonic dystrophy unstable sequence. , 1993, American journal of human genetics.
[327] R. Wells,et al. Genetic Instabilities in (CTG·CAG) Repeats Occur by Recombination* , 1999, The Journal of Biological Chemistry.
[328] S. Warren,et al. The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing , 2005 .
[329] K. Friend,et al. Dynamic mutation loci: allele distributions in different populations , 1996, Annals of human genetics.
[330] R. Bambara,et al. Enzymes and Reactions at the Eukaryotic DNA Replication Fork* , 1997, The Journal of Biological Chemistry.
[331] Robert I. Richards,et al. Dynamic mutations: A new class of mutations causing human disease , 1992, Cell.
[332] C. Ware,et al. Genomic context drives SCA7 CAG repeat instability, while expressed SCA7 cDNAs are intergenerationally and somatically stable in transgenic mice. , 2003, Human molecular genetics.
[333] J. Griffith,et al. Expanded CTG triplet blocks from the myotonic dystrophy gene create the strongest known natural nucleosome positioning elements. , 1995, Genomics.
[334] J. Weber. Informativeness of human (dC-dA)n.(dG-dT)n polymorphisms. , 1990, Genomics.
[335] P. de Knijff,et al. Using a roster and haplotyping is useful in risk assessment for persons with intermediate and reduced penetrance alleles in Huntington disease. , 2001, American journal of medical genetics.
[336] K K Kidd,et al. A global haplotype analysis of the myotonic dystrophy locus: implications for the evolution of modern humans and for the origin of myotonic dystrophy mutations. , 1998, American journal of human genetics.
[337] M. Bichara,et al. Modulation of transcription reveals a new mechanism of triplet repeat instability in Escherichia coli. , 2001, Journal of molecular biology.
[338] P. Andersen,et al. Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia , 2000, European Journal of Human Genetics.
[339] G. Almouzni,et al. First in series on chromatin dynamics , 2002 .
[340] A. Messer,et al. Msh2 deficiency prevents in vivo somatic instability of the CAG repeat in Huntington disease transgenic mice , 1999, Nature Genetics.
[341] M. Dixon,et al. Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats. , 1999, Molecular cell.
[342] M. Owen,et al. Mutations Involving the Transcription Factor CBFA1 Cause Cleidocranial Dysplasia , 1997, Cell.
[343] Jian Yu,et al. Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene , 1994, Nature Genetics.
[344] Benjamin Tycko,et al. Creation of genomic methylation patterns , 1996, Nature Genetics.
[345] P. D. de Jong,et al. Genomic analysis of human chromosome 10q and 4q telomeres suggests a common origin. , 2002, Genomics.
[346] M. Wabl,et al. Mismatch repair co-opted by hypermutation. , 1998, Science.
[347] W. Vogel,et al. (CAG)nCAA and GGN repeats in the human androgen receptor gene are not associated with prostate cancer in a French–German population , 1999, European Journal of Human Genetics.
[348] R. Wells,et al. Hairpin Formation during DNA Synthesis Primer Realignmentin Vitro in Triplet Repeat Sequences from Human Hereditary Disease Genes* , 1997, The Journal of Biological Chemistry.
[349] W. Doerfler,et al. The Human 20-kDa 5′-(CGG) n -3′-binding Protein Is Targeted to the Nucleus and Affects the Activity of the FMR1Promoter* , 2000, The Journal of Biological Chemistry.
[350] J. Longshore,et al. Instability of the FMR2 trinucleotide repeat region associated with expanded FMR1 alleles. , 1997, American journal of medical genetics.
[351] S. Farrington,et al. Sequence interruptions confer differential stability at microsatellite alleles in mismatch repair-deficient cells. , 2000, Human molecular genetics.
[352] R. Richards,et al. Fragile sites-cytogenetic similarity with molecular diversity. , 1999, American journal of human genetics.
[353] Yuh-Hwa Wang,et al. Human Fragile Site FRA16B DNA Excludes Nucleosomes in the Presence of Distamycin* , 2002, The Journal of Biological Chemistry.
[354] M. Pandolfo,et al. A nonpathogenic GAAGGA repeat in the Friedreich gene: Implications for pathogenesis , 1999, Neurology.
[355] Len A. Pennacchio,et al. Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 , 1997, Nature Genetics.
[356] I Berger,et al. In vitro generated antibodies specific for telomeric guanine-quadruplex DNA react with Stylonychia lemnae macronuclei , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[357] D. Monckton,et al. Cis-acting modifiers of expanded CAG/CTG triplet repeat expandability: associations with flanking GC content and proximity to CpG islands. , 1999, Human molecular genetics.
[358] R. Wells,et al. Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli. , 1997, Nucleic acids research.
[359] R. Osman,et al. Role of DNA flexibility in sequence-dependent activity of uracil DNA glycosylase. , 2002, Biochemistry.
[360] A. Aiyar,et al. The plasmid replicon of EBV consists of multiple cis‐acting elements that facilitate DNA synthesis by the cell and a viral maintenance element , 1998, The EMBO journal.
[361] A. Bird,et al. Methylation-Induced Repression— Belts, Braces, and Chromatin , 1999, Cell.
[362] J. Miret,et al. Orientation-dependent and sequence-specific expansions of CTG/CAG trinucleotide repeats in Saccharomyces cerevisiae. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[363] R I Richards,et al. FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. , 1998, Molecular cell.
[364] R. Mott,et al. Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation , 1997, Nature Genetics.
[365] V. Zakian,et al. Expansion and length-dependent fragility of CTG repeats in yeast. , 1998, Science.
[366] J. Sutcliffe,et al. DNA methylation represses FMR-1 transcription in fragile X syndrome. , 1992, Human molecular genetics.
[367] B. Michel,et al. Impairment of lagging strand synthesis triggers the formation of a RuvABC substrate at replication forks , 2001, The EMBO journal.
[368] D. Livingston,et al. Destabilization of CAG trinucleotide repeat tracts by mismatch repair mutations in yeast. , 1997, Human molecular genetics.