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Christopher E Pearson

Showing results (41-50 of 98) with videos related to

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Plos Genetics|May 14, 2009
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic miceStéphanie Tomé, Ian Holt, Winfried Edelmann, et al.
Journal of Molecular Biology|September 10, 2003
Slipped (CTG).(CAG) repeats of the myotonic dystrophy locus: surface probing with anti-DNA antibodiesMandy Tam, S Erin Montgomery, Mariana Kekis, et al.
Gene|January 28, 2009
The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptionsKatharine A Hagerman, Haihe Ruan, Kerrie Nichol Edamura, et al.
Human Molecular Genetics|October 12, 2010
Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiationAnna Seriola, Claudia Spits, Jodie P Simard, et al.
Biochimica Et Biophysica Acta. General Subjects|March 19, 2018
Stress-induced acidification may contribute to formation of unusual structures in C9orf72-repeatsBita Zamiri, Mila Mirceta, Rashid Abu-Ghazalah, et al.
Human Molecular Genetics|November 4, 2010
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissuesArturo López Castel, Masayuki Nakamori, Stephanie Tomé, et al.
Human Mutation|August 31, 2006
Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase alpha sitesJohn Christodoulou, Hugh J Craig, David C Walker, et al.
Plos Genetics|December 25, 2013
Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissuesMichelle M Axford, Yuh-Hwa Wang, Masayuki Nakamori, et al.
American Journal of Human Genetics|December 31, 2005
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?Tohru Matsuura, Ping Fang, Christopher E Pearson, et al.
Neuron|September 2, 2003
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in DrosophilaPeng Jin, Daniela C Zarnescu, Fuping Zhang, et al.
Pageof 10

Showing results (41-50 of 98) with videos related to

Sort By:
Pageof 10
Plos Genetics|May 14, 2009
MSH2 ATPase domain mutation affects CTG*CAG repeat instability in transgenic miceStéphanie Tomé, Ian Holt, Winfried Edelmann, et al.
Journal of Molecular Biology|September 10, 2003
Slipped (CTG).(CAG) repeats of the myotonic dystrophy locus: surface probing with anti-DNA antibodiesMandy Tam, S Erin Montgomery, Mariana Kekis, et al.
Gene|January 28, 2009
The ATTCT repeats of spinocerebellar ataxia type 10 display strong nucleosome assembly which is enhanced by repeat interruptionsKatharine A Hagerman, Haihe Ruan, Kerrie Nichol Edamura, et al.
Human Molecular Genetics|October 12, 2010
Huntington's and myotonic dystrophy hESCs: down-regulated trinucleotide repeat instability and mismatch repair machinery expression upon differentiationAnna Seriola, Claudia Spits, Jodie P Simard, et al.
Biochimica Et Biophysica Acta. General Subjects|March 19, 2018
Stress-induced acidification may contribute to formation of unusual structures in C9orf72-repeatsBita Zamiri, Mila Mirceta, Rashid Abu-Ghazalah, et al.
Human Molecular Genetics|November 4, 2010
Expanded CTG repeat demarcates a boundary for abnormal CpG methylation in myotonic dystrophy patient tissuesArturo López Castel, Masayuki Nakamori, Stephanie Tomé, et al.
Human Mutation|August 31, 2006
Deletion hotspot in the argininosuccinate lyase gene: association with topoisomerase II and DNA polymerase alpha sitesJohn Christodoulou, Hugh J Craig, David C Walker, et al.
Plos Genetics|December 25, 2013
Detection of slipped-DNAs at the trinucleotide repeats of the myotonic dystrophy type I disease locus in patient tissuesMichelle M Axford, Yuh-Hwa Wang, Masayuki Nakamori, et al.
American Journal of Human Genetics|December 31, 2005
Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?Tohru Matsuura, Ping Fang, Christopher E Pearson, et al.
Neuron|September 2, 2003
RNA-mediated neurodegeneration caused by the fragile X premutation rCGG repeats in DrosophilaPeng Jin, Daniela C Zarnescu, Fuping Zhang, et al.
Pageof 10