Gene conversion (recombination) mediates expansions of CTG[middle dot]CAG repeats (Q73004193)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

title

Gene conversion (recombination) mediates expansions of CTG[middle dot]CAG repeats (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

author name string

Jakupciak JP

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

Wells RD

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

language of work or name

English

0 references

publication date

1 December 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

Journal of Biological Chemistry

31 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

volume

275

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

issue

51

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

page(s)

40003-40013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

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

31 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Relationship between Escherichia coli growth and deletions of CTG.CAG triplet repeats in plasmids.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Flexible DNA: genetically unstable CTG.CAG and CGG.CCG from human hereditary neuromuscular disease genes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Transcription increases the deletion frequency of long CTG.CAG triplet repeats from plasmids in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

CTG triplet repeats from the myotonic dystrophy gene are expanded in Escherichia coli distal to the replication origin as a single large event.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Nucleotide excision repair affects the stability of long transcribed (CTG*CAG) tracts in an orientation-dependent manner in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Small slipped register genetic instabilities in Escherichia coli in triplet repeat sequences associated with hereditary neurological diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Hairpin formation during DNA synthesis primer realignment in vitro in triplet repeat sequences from human hereditary disease genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

DNA polymerase III proofreading mutants enhance the expansion and deletion of triplet repeat sequences in Escherichia coli

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Expansion and length-dependent fragility of CTG repeats in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Destabilization of CAG trinucleotide repeat tracts by mismatch repair mutations in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Destabilization of yeast micro- and minisatellite DNA sequences by mutations affecting a nuclease involved in Okazaki fragment processing (rad27) and DNA polymerase delta (pol3-t).

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Repeat expansion--all in a flap?

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Triplet repeats form secondary structures that escape DNA repair in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Orientation dependence of trinucleotide CAG repeat instability in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Stability of an expanded trinucleotide repeat in the androgen receptor gene in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Hypermutable myotonic dystrophy CTG repeats in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Ataxin-1 nuclear localization and aggregation: role in polyglutamine-induced disease in SCA1 transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Progress in pathogenesis studies of spinocerebellar ataxia type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Trinucleotide repeats affect DNA replication in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Expansion of CTG repeats from human disease genes is dependent upon replication mechanisms in Escherichia coli: the effect of long patch mismatch repair revisited

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Abasic sites induce triplet-repeat expansion during DNA replication in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Double-strand break repair can lead to high frequencies of deletions within short CAG/CTG trinucleotide repeats

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Correlation between CTG trinucleotide repeat length and frequency of severe congenital myotonic dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Reduction in size of the myotonic dystrophy trinucleotide repeat mutation during transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Loss of mutation at the FMR1 locus through multiple exchanges between maternal X chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Reverse mutations in the fragile X syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Fragile X founder effects and new mutations in Finland

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Heritable unstable DNA sequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Bovine Alu-like sequences mediate transposition of a new site-specific retroelement

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Double-strand break repair by interchromosomal recombination: suppression of chromosomal translocations

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Multiple pathways for repair of DNA double-strand breaks in mammalian chromosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Genetic instabilities in (CTG.CAG) repeats occur by recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Plasmid transformation of Escherichia coli and other bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

High efficiency transformation of E. coli by high voltage electroporation

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

21 January 2018

Left-handed DNA in vivo.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Expansion and deletion of triplet repeat sequences in Escherichia coli occur on the leading strand of DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Instability of the expanded (CTG)n repeats in the myotonin protein kinase gene in cultured lymphoblastoid cell lines from patients with myotonic dystrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Cryptic and polar variation of the fragile X repeat could result in predisposing normal alleles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Length of uninterrupted CGG repeats determines instability in the FMR1 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

The double-strand-break repair model for recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

A broadening view of recombinational DNA repair in bacteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Enzymes and molecular mechanisms of genetic recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

RecQ helicase, in concert with RecA and SSB proteins, initiates and disrupts DNA recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Analysis of DNA replication forks encountering a pyrimidine dimer in the template to the leading strand

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

CGG repeats associated with DNA instability and chromosome fragility form structures that block DNA synthesis in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

The trinucleotide repeat sequence d(CGG)15 forms a heat-stable hairpin containing Gsyn. Ganti base pairs

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

DNA recombination: the replication connection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

DNA double-strand breaks caused by replication arrest

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Lethality of rep recB and rep recC double mutants of Escherichia coli.

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Instability of CAG and CTG trinucleotide repeats in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Increased instability of human CTG repeat tracts on yeast artificial chromosomes during gametogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

Gene conversion tracts from double-strand break repair in mammalian cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1074%2FJBC.M007153200

21 January 2018

Identifiers

DOI

10.1074/JBC.M007153200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11005819%20AND%20SRC:MED&resulttype=core&format=json

31 October 2019

1 reference