Pages that link to "Q69041738"
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The following pages link to Spontaneous and induced chromosomal instability in Werner syndrome (Q69041738):
Displayed 50 items.
- Cloning of two new human helicase genes of the RecQ family: biological significance of multiple species in higher eukaryotes (Q22008619) (← links)
- Ku complex interacts with and stimulates the Werner protein (Q22253994) (← links)
- Characterization of the human and mouse WRN 3'-->5' exonuclease (Q22254412) (← links)
- Physical and functional interaction of the Werner syndrome protein with poly‐ADP ribosyl transferase (Q24299153) (← links)
- Identification and biochemical characterization of a Werner's syndrome protein complex with Ku70/80 and poly(ADP-ribose) polymerase-1 (Q24305550) (← links)
- WRN controls formation of extrachromosomal telomeric circles and is required for TRF2DeltaB-mediated telomere shortening (Q24307499) (← links)
- Werner syndrome protein interacts functionally with translesion DNA polymerases (Q24309639) (← links)
- The Werner syndrome protein is a DNA helicase (Q24310486) (← links)
- The human Werner syndrome protein stimulates repair of oxidative DNA base damage by the DNA glycosylase NEIL1 (Q24316909) (← links)
- Identification of RecQL1 as a Holliday junction processing enzyme in human cell lines (Q24536291) (← links)
- Requirement for three novel protein complexes in the absence of the Sgs1 DNA helicase in Saccharomyces cerevisiae (Q24548169) (← links)
- The Werner syndrome protein: linking the replication checkpoint response to genome stability (Q24596050) (← links)
- Roles of Werner syndrome protein in protection of genome integrity (Q24643050) (← links)
- A conserved and species-specific functional interaction between the Werner syndrome-like exonuclease atWEX and the Ku heterodimer in Arabidopsis (Q24810688) (← links)
- Role of SGS1 and SLX4 in maintaining rDNA structure in Saccharomyces cerevisiae (Q27936801) (← links)
- Werner's syndrome lymphoblastoid cells are hypersensitive to topoisomerase II inhibitors in the G2 phase of the cell cycle (Q28373681) (← links)
- Mutations in the WRN gene in mice accelerate mortality in a p53-null background (Q28510148) (← links)
- Telomere instability in a human tumor cell line expressing a dominant-negative WRN protein (Q30953207) (← links)
- Requirements for the nucleolytic processing of DNA ends by the Werner syndrome protein-Ku70/80 complex (Q31816061) (← links)
- WRN helicase expression in Werner syndrome cell lines (Q33613095) (← links)
- The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases (Q33899444) (← links)
- Functional interaction between the Werner Syndrome protein and DNA polymerase delta (Q33899465) (← links)
- Werner's syndrome protein is required for correct recovery after replication arrest and DNA damage induced in S-phase of cell cycle (Q33944087) (← links)
- Acetylation of Werner syndrome protein (WRN): relationships with DNA damage, DNA replication and DNA metabolic activities (Q34004402) (← links)
- Homologous recombination resolution defect in werner syndrome (Q34150355) (← links)
- The Werner syndrome protein stimulates DNA polymerase beta strand displacement synthesis via its helicase activity (Q34187025) (← links)
- Telomeres, replicative senescence and human ageing (Q34224763) (← links)
- Comparison of proliferation and genomic instability responses to WRN silencing in hematopoietic HL60 and TK6 cells (Q34498808) (← links)
- Telomeres, chromosome instability and cancer (Q34595437) (← links)
- Evolution of the RECQ family of helicases: A drosophila homolog, Dmblm, is similar to the human bloom syndrome gene (Q34606438) (← links)
- Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN gene (Q34608450) (← links)
- Bipartite structure of the SGS1 DNA helicase in Saccharomyces cerevisiae (Q34608894) (← links)
- Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence and stimulation by replication protein A (Q34669156) (← links)
- RecQ family helicases: roles as tumor suppressor proteins (Q35026401) (← links)
- Possible association of BLM in decreasing DNA double strand breaks during DNA replication (Q35115298) (← links)
- Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group (Q35238400) (← links)
- The Werner Syndrome Helicase-Nuclease--One Protein, Many Mysteries (Q35577695) (← links)
- The Progerias (Q35582519) (← links)
- Telomere dysfunction as a cause of genomic instability in Werner syndrome (Q35629126) (← links)
- From cells to ageing: a review of models and mechanisms of cellular senescence and their impact on human ageing. (Q35895097) (← links)
- TLK1B mediated phosphorylation of Rad9 regulates its nuclear/cytoplasmic localization and cell cycle checkpoint (Q35918497) (← links)
- A novel Werner Syndrome mutation: pharmacological treatment by read-through of nonsense mutations and epigenetic therapies (Q36214442) (← links)
- Werner syndrome protein, WRN, protects cells from DNA damage induced by the benzene metabolite hydroquinone (Q37091544) (← links)
- Progeroid syndromes: probing the molecular basis of aging? (Q37229309) (← links)
- Risks at the DNA Replication Fork: Effects upon Carcinogenesis and Tumor Heterogeneity (Q37628288) (← links)
- Werner Syndrome-specific induced pluripotent stem cells: recovery of telomere function by reprogramming (Q38358089) (← links)
- Bloom's syndrome: Why not premature aging?: A comparison of the BLM and WRN helicases (Q38847700) (← links)
- The Werner's Syndrome protein collaborates with REV1 to promote replication fork progression on damaged DNA (Q39670254) (← links)
- The human WRN and BLM RecQ helicases differentially regulate cell proliferation and survival after chemotherapeutic DNA damage (Q39675082) (← links)
- Displacement of DNA-PKcs from DNA ends by the Werner syndrome protein (Q39688137) (← links)