g.oxfordjournals.org/ D ow nloaded from 2 More than 12 neurogenetic disorders are caused by unstable expansions of (CTG)•(CAG) repeats. The expanded repeats are unstable in germline and somatic cells, with potential consequences for disease severity. Previous studies have shown that contractions of (CAG)95 are more frequent when the repeat tract is transcribed. Here we determined whether transcription can promote repeat expansion, using (CTG)•(CAG) repeat tracts in the size range that is typical in myotonic dystrophy type 1 (DM1). We derived normal human fibroblasts having single-copy genomic integrations of 800 CTG repeats. The repeat tract showed modest instability when it was not transcribed, yielding an estimated mutation rate of 0.28 %...
More than 20 human hereditary diseases have been linked to expansions of unstable simple nucleotide ...
Contains fulltext : 208576.pdf (publisher's version ) (Open Access)CRISPR/Cas tech...
Polyglutamine (polyQ) disease is a group of neurodegenerative disorders caused by abnormal expansion...
More than 12 neurogenetic disorders are caused by unstable expansions of (CTG)†(CAG) repeats. The ex...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Contains fulltext : 52050.pdf ( ) (Open Access)BACKGROUND: Trinucleotide instabili...
Myotonic dystrophy type 1 (DM1) is a dominant human neuromuscular disorder caused by a CTG repeat ex...
There are many diseases associated with the expansion of DNA repeats in humans. Myotonic dystrophy t...
Contains fulltext : 174401.pdf (publisher's version ) (Closed access)Myotonic dyst...
There are many diseases associated with the expansion of DNA repeats in humans. Myotonic dystrophy t...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Myotonic dystrophy (DM) is an autosomal dominant genetic disease which affects approximately 1 in 80...
The discovery of expanded simple repeated sequences causing or associated with human disease has lea...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Trinucleotide repeats can be highly unstable, mutating far more frequently than point mutations. Rep...
More than 20 human hereditary diseases have been linked to expansions of unstable simple nucleotide ...
Contains fulltext : 208576.pdf (publisher's version ) (Open Access)CRISPR/Cas tech...
Polyglutamine (polyQ) disease is a group of neurodegenerative disorders caused by abnormal expansion...
More than 12 neurogenetic disorders are caused by unstable expansions of (CTG)†(CAG) repeats. The ex...
License, which permits unrestricted use, distribution, and reproduction in any medium, provided the ...
Contains fulltext : 52050.pdf ( ) (Open Access)BACKGROUND: Trinucleotide instabili...
Myotonic dystrophy type 1 (DM1) is a dominant human neuromuscular disorder caused by a CTG repeat ex...
There are many diseases associated with the expansion of DNA repeats in humans. Myotonic dystrophy t...
Contains fulltext : 174401.pdf (publisher's version ) (Closed access)Myotonic dyst...
There are many diseases associated with the expansion of DNA repeats in humans. Myotonic dystrophy t...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Myotonic dystrophy (DM) is an autosomal dominant genetic disease which affects approximately 1 in 80...
The discovery of expanded simple repeated sequences causing or associated with human disease has lea...
Myotonic dystrophy (DM), an autosomal dominant disorder mapping to human chromosome 19q13.3, is the ...
Trinucleotide repeats can be highly unstable, mutating far more frequently than point mutations. Rep...
More than 20 human hereditary diseases have been linked to expansions of unstable simple nucleotide ...
Contains fulltext : 208576.pdf (publisher's version ) (Open Access)CRISPR/Cas tech...
Polyglutamine (polyQ) disease is a group of neurodegenerative disorders caused by abnormal expansion...