Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats. (Q34470663)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21088112%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

title

Bidirectional transcription stimulates expansion and contraction of expanded (CTG)*(CAG) repeats (English)

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16 January 2020

1

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16 January 2020

author name string

Christopher E Pearson

series ordinal

2

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16 January 2020

Charles A Thornton

series ordinal

3

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publication date

18 November 2010

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16 January 2020

published in

Human Molecular Genetics

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16 January 2020

volume

20

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issue

3

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16 January 2020

page(s)

580-588

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describes a project that uses

16 January 2020

ImageQuant

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11 June 2022

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inferred from PubMed Central ID database lookup

cites work

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Transcriptional abnormality in myotonic dystrophy affects DMPK but not neighboring genes

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Gonosomal mosaicism in myotonic dystrophy patients: involvement of mitotic events in (CTG)n repeat variation and selection against extreme expansion in sperm.

6 July 2018

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Somatic heterogeneity of the CTG repeat in myotonic dystrophy is age and size dependent.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

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

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Supercoiling of the DNA template during transcription

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Antisense transcription and heterochromatin at the DM1 CTG repeats are constrained by CTCF.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

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

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Altered mRNA splicing of the skeletal muscle ryanodine receptor and sarcoplasmic/endoplasmic reticulum Ca2+-ATPase in myotonic dystrophy type 1.

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Antisense intergenic transcription in V(D)J recombination

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Germline mutational dynamics in myotonic dystrophy type 1 males: allele length and age effects.

27 October 2018

1 reference

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Mismatch repair gene Msh2 modifies the timing of early disease in Hdh(Q111) striatum

27 October 2018

1 reference

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Bifunctional protein conferring enhanced green fluorescence and puromycin resistance.

27 October 2018

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Z/AP, a double reporter for cre-mediated recombination.

27 October 2018

1 reference

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Relationship between parental trinucleotide GCT repeat length and severity of myotonic dystrophy in offspring.

27 October 2018

1 reference

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Myotonic dystrophy patients have larger CTG expansions in skeletal muscle than in leukocytes

27 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3016912

Defective satellite cells in congenital myotonic dystrophy

27 October 2018

1 reference

12 December 2020

Analysis of Unstable Triplet Repeats Using Small-Pool Polymerase Chain Reaction

1 reference

12 December 2020

Analysis of the CTG repeat in skeletal muscle of young and adult myotonic dystrophy patients: when does the expansion occur?

1 reference

12 December 2020

Effect of Myotonic Dystrophy Trinucleotide Repeat Expansion on DMPK Transcription and Processing

1 reference

12 December 2020

Heterogeneity of DM kinase repeat expansion in different fetal tissues and further expansion during cell proliferation in vitro: evidence for a casual involvement of methyl-directed DNA mismatch repair in triplet repeat stability

1 reference

12 December 2020

CTG repeat analysis in lymphocytes, muscles and fibroblasts in patients with myotonic dystrophy

1 reference

12 December 2020

Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal development

1 reference

12 December 2020

Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patients

1 reference

12 December 2020

Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons

1 reference

12 December 2020

Identifiers

DOI

10.1093/HMG/DDQ501

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21088112%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21088112%20AND%20SRC:MED&resulttype=core&format=json

16 January 2020

PubMed publication ID

21088112

1 reference