(Q24810688)

English

A conserved and species-specific functional interaction between the Werner syndrome-like exonuclease atWEX and the Ku heterodimer in Arabidopsis

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scholarly article

1 reference

Europe PubMed Central

5 July 2017

A conserved and species-specific functional interaction between the Werner syndrome-like exonuclease atWEX and the Ku heterodimer in Arabidopsis (English)

1 reference

Europe PubMed Central

5 July 2017

author name string

Baomin Li

1

1 reference

Europe PubMed Central

5 July 2017

Nathan Conway

2

1 reference

Europe PubMed Central

5 July 2017

Sonia Navarro

3

1 reference

Europe PubMed Central

5 July 2017

Luca Comai

4

1 reference

Europe PubMed Central

5 July 2017

Lucio Comai

5

1 reference

Europe PubMed Central

5 July 2017

language of work or name

0 references

publication date

7 December 2005

1 reference

Europe PubMed Central

5 July 2017

Nucleic Acids Research

1 reference

Europe PubMed Central

5 July 2017

33

1 reference

Europe PubMed Central

5 July 2017

6861-6867

1 reference

Europe PubMed Central

5 July 2017

21

1 reference

Europe PubMed Central

5 July 2017

Mammalian Ku86 mediates chromosomal fusions and apoptosis caused by critically short telomeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

Ku complex interacts with and stimulates the Werner protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

Mutator phenotype of Werner syndrome is characterized by extensive deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

Current advances in unraveling the function of the Werner syndrome protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

The Werner syndrome protein at the crossroads of DNA repair and apoptosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

Werner syndrome protein--unwinding function to explain disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

DNA ligase IV-dependent NHEJ of deprotected mammalian telomeres in G1 and G2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

Functional interaction between Ku and the werner syndrome protein in DNA end processing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

Positional cloning of the Werner's syndrome gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

7 April 2017

A means to a DNA end: the many roles of Ku.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Mechanism and regulation of human non-homologous DNA end-joining

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Large-scale discovery of induced point mutations with high-throughput TILLING.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Ku is required for telomeric C-rich strand maintenance but not for end-to-end chromosome fusions in Arabidopsis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Telomere length deregulation and enhanced sensitivity to genotoxic stress in Arabidopsis mutants deficient in Ku70.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Molecular characterisation of RecQ homologues in Arabidopsis thaliana.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Mut-7 of C. elegans, required for transposon silencing and RNA interference, is a homolog of Werner syndrome helicase and RNaseD.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

SV40 large T antigen binds to the TBP-TAF(I) complex SL1 and coactivates ribosomal RNA transcription

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

28 September 2017

Biochemical characterization of an exonuclease from Arabidopsis thaliana reveals similarities to the DNA exonuclease of the human Werner syndrome protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1310904

30 May 2018

Analysis of the Role of RecQ Helicases in RNAi in Mammals

1 reference

https://pubmed.ncbi.nlm.nih.gov/16396834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Spontaneous and induced chromosomal instability in Werner syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/16396834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A gene encoding an RNase D exonuclease-like protein is required for post-transcriptional silencing in Arabidopsis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16396834

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/NAR/GKI984

1 reference

Europe PubMed Central

5 July 2017

1 reference

Europe PubMed Central

5 July 2017

1 reference

Europe PubMed Central

5 July 2017

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