Relationships between putative G-quadruplex-forming sequences, RecQ helicases, and transcription (Q38829444)

6 September 2017

Relationships between putative G-quadruplex-forming sequences, RecQ helicases, and transcription (English)

1 reference

6 September 2017

John A Smestad

1

0 references

author name string

L James Maher

series ordinal

2

1 reference

6 September 2017

8 October 2015

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6 September 2017

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6 September 2017

16

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6 September 2017

91

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Creative Commons Attribution 4.0 International

6 September 2017

start time

8 October 2015

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

describes a project that uses

limma

1 reference

22 June 2022

https://europepmc.org/article/PMC/4599794

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Regulation of gene expression by the BLM helicase correlates with the presence of G-quadruplex DNA motifs.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Telomerase protects Werner syndrome lineage-specific stem cells from premature aging.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Spectrum and risk of neoplasia in Werner syndrome: a systematic review

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Modeling gene expression using chromatin features in various cellular contexts

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Altered gene expression in the Werner and Bloom syndromes is associated with sequences having G-quadruplex forming potential

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Genome-wide analysis reveals regulatory role of G4 DNA in gene transcription

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Telomere dysfunction as a cause of genomic instability in Werner syndrome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

G-quadruplex formation within the promoter of the KRAS proto-oncogene and its effect on transcription.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

POT1 stimulates RecQ helicases WRN and BLM to unwind telomeric DNA substrates

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Prevalence of quadruplexes in the human genome

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Stabilization of the c-myc gene promoter quadruplex by specific ligands' inhibitors of telomerase.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Congenital telangiectatic erythema resembling lupus erythematosus in dwarfs; probably a syndrome entity.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Positional cloning of the Werner's syndrome gene

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Werner's syndrome a review of its symptomatology, natural history, pathologic features, genetics and relationship to the natural aging process

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Bloom's Syndrome. VII. Progress report for 1978

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Defective telomere lagging strand synthesis in cells lacking WRN helicase activity.

9 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

RecQ helicase and topoisomerase III comprise a novel DNA strand passage function: a conserved mechanism for control of DNA recombination

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Bloom syndrome: a mendelian prototype of somatic mutational disease.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

Regulation of WRN helicase activity in human base excision repair

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4599794

A Review of its Symptomatology, Natural History, Pathologic Features, Genetics And Relationship to the Natural Aging Process

22 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FS12881-015-0236-4

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2FS12881-015-0236-4

Self-Organized Formation of Topologically Correct Feature Maps

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1186%2FS12881-015-0236-4

The Bloom's syndrome helicase unwinds G4 DNA

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26449372

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/26449372

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12881-015-0236-4

1 reference

PMC publication ID

4599794

Dimensions Publication ID

6 September 2017

0 references

1 reference

PMC publication ID

4599794

6 September 2017

PubMed publication ID

26449372

1 reference

PMC publication ID

4599794