Physical and functional interaction of the Werner syndrome protein with poly-ADP ribosyl transferase
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/S0014-5793(03)01088-3/fullpdf
Reference41 articles.
1. Genetic Diagnosis of Werner's Syndrome, a Premature Aging Disease, by Mutant Allele Specific Amplification (MASA) and Oligomer Ligation Assay (OLA)
2. Chromosome breaks in Werner's syndrome and their prevention in vitro by radical-scavenging enzymes
3. Clonal structural chromosomal rearrangements in primary fibroblast cultures and in lymphocytes of patients with Werner's syndrome
4. Spontaneous and induced chromosomal instability in Werner syndrome
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2. Functions of ADP-ribose transferases in the maintenance of telomere integrity;Cellular and Molecular Life Sciences;2022-03-29
3. WRN is recruited to damaged telomeres via its RQC domain and tankyrase1-mediated poly-ADP-ribosylation of TRF1;Nucleic Acids Research;2017-02-01
4. Differential and Concordant Roles for Poly(ADP-Ribose) Polymerase 1 and Poly(ADP-Ribose) in Regulating WRN and RECQL5 Activities;Molecular and Cellular Biology;2015-12
5. RecQ helicases and PARP1 team up in maintaining genome integrity;Ageing Research Reviews;2015-09
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