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Times Cited: 143
Times Cited
Times Co-cited
Similarity
37
Somatic and gonadal mosaicism of the Huntington disease gene CAG repeat in brain and sperm.
H Telenius, B Kremer, Y P Goldberg, J Theilmann, S E Andrew, J Zeisler, S Adam, C Greenberg, E J Ives, L A Clarke. Nat Genet 1994
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M Duyao, C Ambrose, R Myers, A Novelletto, F Persichetti, M Frontali, S Folstein, C Ross, M Franz, M Abbott. Nat Genet 1993
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Analysis of germline mutation spectra at the Huntington's disease locus supports a mitotic mutation mechanism.
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I V Kovtun, C T McMurray. Nat Genet 2001
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K Manley, T L Shirley, L Flaherty, A Messer. Nat Genet 1999
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Somatic expansion behaviour of the (CTG)n repeat in myotonic dystrophy knock-in mice is differentially affected by Msh3 and Msh6 mismatch-repair proteins.
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Contribution of DNA sequence and CAG size to mutation frequencies of intermediate alleles for Huntington disease: evidence from single sperm analyses.
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Somatic mosaicism, germline expansions, germline reversions and intergenerational reductions in myotonic dystrophy males: small pool PCR analyses.
D G Monckton, L J Wong, T Ashizawa, C T Caskey. Hum Mol Genet 1995
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Trinucleotide repeats that expand in human disease form hairpin structures in vitro.
A M Gacy, G Goellner, N Juranić, S Macura, C T McMurray. Cell 1995
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C H Freudenreich, S M Kantrow, V A Zakian. Science 1998
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Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor gene.
L Zhang, E P Leeflang, J Yu, N Arnheim. Nat Genet 1994
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Dramatic, expansion-biased, age-dependent, tissue-specific somatic mosaicism in a transgenic mouse model of triplet repeat instability.
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Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum.
Vanessa C Wheeler, Lori-Anne Lebel, Vladimir Vrbanac, Allison Teed, Hein te Riele, Marcy E MacDonald. Hum Mol Genet 2003
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Increased instability of intermediate alleles in families with sporadic Huntington disease compared to similar sized intermediate alleles in the general population.
Y P Goldberg, C T McMurray, J Zeisler, E Almqvist, D Sillence, F Richards, A M Gacy, J Buchanan, H Telenius, M R Hayden. Hum Mol Genet 1995
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Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome.
C H Freudenreich, J B Stavenhagen, V A Zakian. Mol Cell Biol 1997
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Sex-dependent mechanisms for expansions and contractions of the CAG repeat on affected Huntington disease chromosomes.
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Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.
L Mangiarini, K Sathasivam, A Mahal, R Mott, M Seller, G P Bates. Nat Genet 1997
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Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli.
S Kang, A Jaworski, K Ohshima, R D Wells. Nat Genet 1995
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Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I.
M Y Chung, L P Ranum, L A Duvick, A Servadio, H Y Zoghbi, H T Orr. Nat Genet 1993
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Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae.
D J Maurer, B L O'Callaghan, D M Livingston. Mol Cell Biol 1996
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Length-dependent gametic CAG repeat instability in the Huntington's disease knock-in mouse.
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The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease.
S E Andrew, Y P Goldberg, B Kremer, H Telenius, J Theilmann, S Adam, E Starr, F Squitieri, B Lin, M A Kalchman. Nat Genet 1993
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Trinucleotide repeats affect DNA replication in vivo.
G M Samadashwily, G Raca, S M Mirkin. Nat Genet 1997
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Expansions of CAG repeat tracts are frequent in a yeast mutant defective in Okazaki fragment maturation.
J K Schweitzer, D M Livingston. Hum Mol Genet 1998
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Dramatic mutation instability in HD mouse striatum: does polyglutamine load contribute to cell-specific vulnerability in Huntington's disease?
L Kennedy, P F Shelbourne. Hum Mol Genet 2000
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Mitotic stability and meiotic variability of the (CAG)n repeat in the Huntington disease gene.
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Triplet repeats form secondary structures that escape DNA repair in yeast.
H Moore, P W Greenwell, C P Liu, N Arnheim, T D Petes. Proc Natl Acad Sci U S A 1999
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Gametic but not somatic instability of CAG repeat length in Huntington's disease.
M E MacDonald, G Barnes, J Srinidhi, M P Duyao, C M Ambrose, R H Myers, J Gray, P M Conneally, A Young, J Penney. J Med Genet 1993
M E MacDonald, G Barnes, J Srinidhi, M P Duyao, C M Ambrose, R H Myers, J Gray, P M Conneally, A Young, J Penney. J Med Genet 1993
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Cis-acting modifiers of expanded CAG/CTG triplet repeat expandability: associations with flanking GC content and proximity to CpG islands.
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Recombination-induced CAG trinucleotide repeat expansions in yeast involve the MRE11-RAD50-XRS2 complex.
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Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells.
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CTG repeat instability and size variation timing in DNA repair-deficient mice.
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Pms2 is a genetic enhancer of trinucleotide CAG.CTG repeat somatic mosaicism: implications for the mechanism of triplet repeat expansion.
Mário Gomes-Pereira, M Teresa Fortune, Laura Ingram, John P McAbney, Darren G Monckton. Hum Mol Genet 2004
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Dramatic tissue-specific mutation length increases are an early molecular event in Huntington disease pathogenesis.
Laura Kennedy, Elizabeth Evans, Chiung-Mei Chen, Lyndsey Craven, Peter J Detloff, Margaret Ennis, Peggy F Shelbourne. Hum Mol Genet 2003
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OGG1 initiates age-dependent CAG trinucleotide expansion in somatic cells.
Irina V Kovtun, Yuan Liu, Magnar Bjoras, Arne Klungland, Samuel H Wilson, Cynthia T McMurray. Nature 2007
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Molecular analysis of new mutations for Huntington's disease: intermediate alleles and sex of origin effects.
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Inherited CAG.CTG allele length is a major modifier of somatic mutation length variability in Huntington disease.
Nicola J Veitch, Margaret Ennis, John P McAbney, Peggy F Shelbourne, Darren G Monckton. DNA Repair (Amst) 2007
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Relationship between trinucleotide repeat expansion and phenotypic variation in Huntington's disease.
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Gametic and somatic tissue-specific heterogeneity of the expanded SCA1 CAG repeat in spinocerebellar ataxia type 1.
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Destabilization of CAG trinucleotide repeat tracts by mismatch repair mutations in yeast.
J K Schweitzer, D M Livingston. Hum Mol Genet 1997
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De novo expansion of a (CAG)n repeat in sporadic Huntington's disease.
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Molecular analysis of juvenile Huntington disease: the major influence on (CAG)n repeat length is the sex of the affected parent.
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Huntington disease expansion mutations in humans can occur before meiosis is completed.
Song-Ro Yoon, Louis Dubeau, Margot de Young, Nancy S Wexler, Norman Arnheim. Proc Natl Acad Sci U S A 2003
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15
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.