(Q40263704)

English

Non-B DNA conformations formed by long repeating tracts of myotonic dystrophy type 1, myotonic dystrophy type 2, and Friedreich's ataxia genes, not the sequences per se, promote mutagenesis in flanking regions

scientific article published on 21 June 2006

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Non-B DNA conformations formed by long repeating tracts of myotonic dystrophy type 1, myotonic dystrophy type 2, and Friedreich's ataxia genes, not the sequences per se, promote mutagenesis in flanking regions (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Friedreich ataxia

1 reference

based on heuristic

inferred from title

myotonic dystrophy

1 reference

based on heuristic

inferred from title

Jacquelynn E Larson

3

object named as

Jacquelynn E Larson

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

author name string

Marzena Wojciechowska

1

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Marek Napierala

2

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Robert D Wells

4

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

language of work or name

0 references

publication date

21 June 2006

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Journal of Biological Chemistry

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

281

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

34

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

24531-24543

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

Advances in mechanisms of genetic instability related to hereditary neurological diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Mechanisms of transcription-replication collisions in bacteria

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Transcription influences the types of deletion and expansion products in an orientation-dependent manner from GAC*GTC repeats

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Cloning, characterization, and properties of seven triplet repeat DNA sequences.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Breakpoints of gross deletions coincide with non-B DNA conformations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

The myotonic dystrophy type 1 triplet repeat sequence induces gross deletions and inversions.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Z-DNA-forming sequences generate large-scale deletions in mammalian cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Naturally occurring H-DNA-forming sequences are mutagenic in mammalian cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Long CTG Tracts from the Myotonic Dystrophy Gene Induce Deletions and Rearrangements during Recombination at the APRT Locus in CHO Cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Non-B DNA conformations, genomic rearrangements, and human disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Increased negative superhelical density in vivo enhances the genetic instability of triplet repeat sequences.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Supercoiling of the DNA template during transcription

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Stabilization of Z DNA in vivo by localized supercoiling.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Recombination-induced CAG trinucleotide repeat expansions in yeast involve the MRE11-RAD50-XRS2 complex

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Triplet repeats form secondary structures that escape DNA repair in yeast

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

The SbcCD nuclease of Escherichia coli is a structural maintenance of chromosomes (SMC) family protein that cleaves hairpin DNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

DNA cleavage and degradation by the SbcCD protein complex from Escherichia coli

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Hairpin structure-forming propensity of the (CCTG.CAGG) tetranucleotide repeats contributes to the genetic instability associated with myotonic dystrophy type 2.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

RNA structure of trinucleotide repeats associated with human neurological diseases

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Elevated unconstrained supercoiling of plasmid DNA generated by transcription and translation of the tetracycline resistance gene in eubacteria.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Inhibition of FEN-1 processing by DNA secondary structure at trinucleotide repeats

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Replication Inhibitors Modulate Instability of an Expanded Trinucleotide Repeat at the Myotonic Dystrophy Type 1 Disease Locus in Human Cells

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Sticky DNA: effect of the polypurine.polypyrimidine sequence.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Instability of repetitive DNA sequences: the role of replication in multiple mechanisms

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Repeat instability: mechanisms of dynamic mutations

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Biological implications of the DNA structures associated with disease-causing triplet repeats

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

DNA structure, mutations, and human genetic disease

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Occurrence of potential cruciform and H-DNA forming sequences in genomic DNA

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Long homopurine*homopyrimidine sequences are characteristic of genes expressed in brain and the pseudoautosomal region

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

DNA structural transitions within the PKD1 gene.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Repair of site-specific double-strand breaks in a mammalian chromosome by homologous and illegitimate recombination

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M603888200

21 January 2018

Identifiers

10.1074/JBC.M603888200

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 September 2017

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