DNA secondary structure: a common and causative factor for expansion in human disease (Q33537493)

27 July 2017

1 reference

title

DNA secondary structure: a common and causative factor for expansion in human disease (English)

1 reference

27 July 2017

C T McMurray

1

1 reference

27 July 2017

language of work or name

English

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publication date

1 March 1999

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Proceedings of the National Academy of Sciences of the United States of America

27 July 2017

published in

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27 July 2017

volume

96

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27 July 2017

issue

5

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27 July 2017

page(s)

1823-1825

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Triplet repeats form secondary structures that escape DNA repair in yeast

27 July 2017

cites work

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21 June 2018

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Expansions and contractions in a tandem repeat induced by double-strand break repair

21 June 2018

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21 June 2018

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Dynamic mutation: possible mechanisms and significance in human disease

21 June 2018

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21 June 2018

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Stability of a CTG/CAG trinucleotide repeat in yeast is dependent on its orientation in the genome

21 June 2018

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Hypermutability of homonucleotide runs in mismatch repair and DNA polymerase proofreading yeast mutants.

21 June 2018

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Different mechanisms underlie DNA instability in Huntington disease and colorectal cancer

21 June 2018

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The FEN-1 family of structure-specific nucleases in eukaryotic DNA replication, recombination and repair

21 June 2018

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The effect of parental gender on the GAA dynamic mutation in the FRDA gene

21 June 2018

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Genetically unstable CXG repeats are structurally dynamic and have a high propensity for folding. An NMR and UV spectroscopic study

21 June 2018

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Trinucleotide repeats in neurogenetic disorders

21 June 2018

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Molecular basis of genetic instability of triplet repeats

21 June 2018

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Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion

21 June 2018

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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

21 June 2018

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Destabilization of tracts of simple repetitive DNA in yeast by mutations affecting DNA mismatch repair

21 June 2018

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DNA loop repair by human cell extracts

21 June 2018

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Hairpins are formed by the single DNA strands of the fragile X triplet repeats: structure and biological implications

21 June 2018

1 reference

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Trinucleotide repeats that expand in human disease form hairpin structures in vitro

21 June 2018

1 reference

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Hairpin properties of single-stranded DNA containing a GC-rich triplet repeat: (CTG)15.

21 June 2018

1 reference

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Expansion and deletion of CTG repeats from human disease genes are determined by the direction of replication in E. coli

21 June 2018

1 reference

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Pausing of DNA synthesis in vitro at specific loci in CTG and CGG triplet repeats from human hereditary disease genes.

21 June 2018

1 reference

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Mechanisms of DNA expansion

21 June 2018

1 reference

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Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases

21 June 2018

1 reference

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Preferential DNA secondary structure mutagenesis in the lagging strand of replication in E. coli

21 June 2018

1 reference

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Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

21 June 2018

1 reference

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Characterization of the full fragile X syndrome mutation in fetal gametes

21 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.96.5.1823

Increased trinucleotide repeat instability with advanced maternal age.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.96.5.1823

Instability of highly expanded CAG repeats in mice transgenic for the Huntington's disease mutation.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1073%2FPNAS.96.5.1823

Greater susceptibility to mutations in lagging strand of DNA replication in Escherichia coli than in leading strand.

21 January 2018

1 reference

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Long CCG triplet repeat blocks exclude nucleosomes: a possible mechanism for the nature of fragile sites in chromosomes

31 October 2018

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12 December 2020

A novel mutation avoidance mechanism dependent on S. cerevisiae RAD27 is distinct from DNA mismatch repair

1 reference

12 December 2020

Repeat expansion--all in a flap?

1 reference

12 December 2020

Human MSH2 binds to trinucleotide repeat DNA structures associated with neurodegenerative diseases

1 reference

12 December 2020

Cystosine-rich strands of the insulin minisatellite adopt hairpins with intercalated cytosine+.cytosine pairs

1 reference

12 December 2020

Preferential nucleosome assembly at DNA triplet repeats from the myotonic dystrophy gene

1 reference

12 December 2020

Trinucleotide repeats affect DNA replication in vivo

1 reference

12 December 2020

Expansion and length-dependent fragility of CTG repeats in yeast

1 reference

12 December 2020

DNA mismatch repair and cancer

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12 December 2020

Influence of hairpins on template reannealing at trinucleotide repeat duplexes: a model for slipped DNA

1 reference

12 December 2020

GAA instability in Friedreich's Ataxia shares a common, DNA-directed and intraallelic mechanism with other trinucleotide diseases

1 reference

12 December 2020

Evolution of simple repeats in DNA and their relation to human disease

1 reference

12 December 2020

CAG repeat length variation in sperm from a patient with Kennedy's disease

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.96.5.1823

1 reference

27 July 2017

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1 reference

27 July 2017

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