(Q33700188)

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DNA structure and the Werner protein modulate human DNA polymerase delta-dependent replication dynamics within the common fragile site FRA16D.

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Europe PubMed Central

PubMed publication ID

28 July 2017

DNA structure and the Werner protein modulate human DNA polymerase delta-dependent replication dynamics within the common fragile site FRA16D. (English)

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Europe PubMed Central

PubMed publication ID

28 July 2017

Kristin A. Eckert

5

object named as

Kristin A Eckert

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Europe PubMed Central

PubMed publication ID

28 July 2017

author name string

Sandeep N Shah

1

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Europe PubMed Central

PubMed publication ID

28 July 2017

Patricia L Opresko

2

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Europe PubMed Central

PubMed publication ID

28 July 2017

Xiao Meng

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Marietta Y W T Lee

4

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Europe PubMed Central

PubMed publication ID

28 July 2017

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publication date

6 December 2009

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Europe PubMed Central

PubMed publication ID

28 July 2017

Nucleic Acids Research

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Europe PubMed Central

PubMed publication ID

28 July 2017

38

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Europe PubMed Central

PubMed publication ID

28 July 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1149-1162

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Europe PubMed Central

PubMed publication ID

28 July 2017

describes a project that uses

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2831333/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation

1 reference

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21 June 2018

Human postmeiotic segregation 2 exhibits biased repair at tetranucleotide microsatellite sequences

1 reference

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21 June 2018

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1 reference

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21 June 2018

The Bloom's syndrome helicase (BLM) interacts physically and functionally with p12, the smallest subunit of human DNA polymerase delta

1 reference

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21 June 2018

Stably transfected common fragile site sequences exhibit instability at ectopic sites

1 reference

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21 June 2018

Mechanism and substrate specificity of telomeric protein POT1 stimulation of the Werner syndrome helicase

1 reference

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21 June 2018

Genome instability: a mechanistic view of its causes and consequences

1 reference

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21 June 2018

DNA polymerase kappa produces interrupted mutations and displays polar pausing within mononucleotide microsatellite sequences

1 reference

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21 June 2018

Human chromosome fragility

1 reference

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1 reference

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21 June 2018

An AT-rich sequence in human common fragile site FRA16D causes fork stalling and chromosome breakage in S. cerevisiae

1 reference

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21 June 2018

Chromosome fragile sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Werner syndrome protein interacts functionally with translesion DNA polymerases

1 reference

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21 June 2018

Replication fork stalling at natural impediments

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

A novel DNA damage response: rapid degradation of the p12 subunit of dna polymerase delta

1 reference

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21 June 2018

Large common fragile site genes and cancer

1 reference

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21 June 2018

MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias

1 reference

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21 June 2018

BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function

1 reference

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21 June 2018

The role of late/slow replication of the FRA16D in common fragile site induction

1 reference

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21 June 2018

Molecular basis for expression of common and rare fragile sites

1 reference

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21 June 2018

ATR Regulates Fragile Site Stability

1 reference

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21 June 2018

Reconstitution and characterization of the human DNA polymerase delta four-subunit holoenzyme

1 reference

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21 June 2018

Identification of unstable sequences within the common fragile site at 3p14.2: implications for the mechanism of deletions within fragile histidine triad gene/common fragile site at 3p14.2 in tumors

1 reference

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21 June 2018

Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

ATR and ATRIP: partners in checkpoint signaling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Replication slippage involves DNA polymerase pausing and dissociation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Werner protein recruits DNA polymerase delta to the nucleolus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

A-Tract bending: insights into experimental structures by computational models

1 reference

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21 June 2018

Common chromosomal fragile site FRA16D sequence: identification of the FOR gene spanning FRA16D and homozygous deletions and translocation breakpoints in cancer cells

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21 June 2018

WWOX, a novel WW domain-containing protein mapping to human chromosome 16q23.3-24.1, a region frequently affected in breast cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Functional interaction between the Werner Syndrome protein and DNA polymerase delta

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

A 700-kb physical map of a region of 16q23.2 homozygously deleted in multiple cancers and spanning the common fragile site FRA16D.

1 reference

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1 reference

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21 June 2018

Cancer-specific chromosome alterations in the constitutive fragile region FRA3B.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis.

1 reference

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21 June 2018

Molecular characterization of a common fragile site (FRA7H) on human chromosome 7 by the cloning of a simian virus 40 integration site.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

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1 reference

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21 June 2018

Identification of eukaryotic DNA replication proteins using simian virus 40 in vitro replication system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

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Template-directed pausing in in vitro DNA synthesis by DNA polymerase a from Drosophila melanogaster embryos

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Site-specific pausing of deoxyribonucleic acid synthesis catalyzed by four forms of Escherichia coli DNA polymerase III

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

DNA bending at adenine . thymine tracts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Induction of sister chromatid exchanges at common fragile sites

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Sequence dependence of DNA conformational flexibility

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

21 June 2018

Seven-base-pair inverted repeats in DNA form stable hairpins in vivo in Saccharomyces cerevisiae

1 reference

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1 reference

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30 October 2018

Werner syndrome helicase activity is essential in maintaining fragile site stability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

30 October 2018

Functional role of the Werner syndrome RecQ helicase in human fibroblasts.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

30 October 2018

Werner syndrome protein contains three structure-specific DNA binding domains

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2831333

30 October 2018

Replication dynamics of the yeast genome.

1 reference

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30 October 2018

Analysis of replication timing at the FRA10B and FRA16B fragile site loci

1 reference

https://pubmed.ncbi.nlm.nih.gov/19969545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Interactions between the Werner syndrome helicase and DNA polymerase delta specifically facilitate copying of tetraplex and hairpin structures of the d(CGG)n trinucleotide repeat sequence

1 reference

https://pubmed.ncbi.nlm.nih.gov/19969545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular characterization of FRAXB and comparative common fragile site instability in cancer cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19969545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA bend direction by phase sensitive detection

1 reference

https://pubmed.ncbi.nlm.nih.gov/19969545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Replication of a common fragile site, FRA3B, occurs late in S phase and is delayed further upon induction: implications for the mechanism of fragile site induction

1 reference

https://pubmed.ncbi.nlm.nih.gov/19969545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Common chromosomal fragile site FRA16D mutation in cancer cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19969545

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/GKP1131

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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