Pages that link to "Q24561996"
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The following pages link to Saccharomyces cerevisiae Ku70 potentiates illegitimate DNA double-strand break repair and serves as a barrier to error-prone DNA repair pathways (Q24561996):
Displaying 50 items.
- Alternative end-joining mechanisms: a historical perspective (Q21131241) (← links)
- DNA end-joining catalyzed by human cell-free extracts (Q22008041) (← links)
- Ku binds telomeric DNA in vitro (Q22010395) (← links)
- Ku is associated with the telomere in mammals (Q22010717) (← links)
- The 3' to 5' exonuclease activity of Mre 11 facilitates repair of DNA double-strand breaks (Q24311761) (← links)
- Mammalian DNA double-strand break repair protein XRCC4 interacts with DNA ligase IV (Q24323238) (← links)
- CDK targets Sae2 to control DNA-end resection and homologous recombination (Q24328867) (← links)
- KARP-1: a novel leucine zipper protein expressed from the Ku86 autoantigen locus is implicated in the control of DNA-dependent protein kinase activity (Q24532230) (← links)
- Components of the Ku-dependent non-homologous end-joining pathway are involved in telomeric length maintenance and telomeric silencing (Q24533190) (← links)
- Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae (Q24548535) (← links)
- The Rad51 paralog Rad51B promotes homologous recombinational repair (Q24551864) (← links)
- RAD51 is required for the repair of plasmid double-stranded DNA gaps from either plasmid or chromosomal templates (Q24554318) (← links)
- The SIR2/3/4 complex and SIR2 alone promote longevity in Saccharomyces cerevisiae by two different mechanisms (Q24597989) (← links)
- Nbs1 potentiates ATP-driven DNA unwinding and endonuclease cleavage by the Mre11/Rad50 complex (Q24604459) (← links)
- A newly identified DNA ligase of Saccharomyces cerevisiaeinvolved in RAD52-independent repair of DNA double-strand breaks (Q24609020) (← links)
- Robust chromosomal DNA repair via alternative end-joining in the absence of X-ray repair cross-complementing protein 1 (XRCC1) (Q24629508) (← links)
- MRE11 and RAD50, but not NBS1, are essential for gene targeting in the moss Physcomitrella patens (Q24633971) (← links)
- Screening the yeast genome for new DNA-repair genes (Q24791574) (← links)
- Ku and the Stability of the Genome (Q24793684) (← links)
- The RING finger ATPase Rad5p of Saccharomyces cerevisiae contributes to DNA double-strand break repair in a ubiquitin-independent manner (Q24813831) (← links)
- Genome wide distribution of illegitimate recombination events in Kluyveromyces lactis (Q25255793) (← links)
- Linking replication stress with heterochromatin formation (Q26778138) (← links)
- Homologous Recombination Deficiency: Exploiting the Fundamental Vulnerability of Ovarian Cancer (Q26783551) (← links)
- Structure of the Ku heterodimer bound to DNA and its implications for double-strand break repair (Q27634006) (← links)
- Mitochondrial genome maintenance: roles for nuclear nonhomologous end-joining proteins in Saccharomyces cerevisiae (Q27929976) (← links)
- NEJ1 controls non-homologous end joining in Saccharomyces cerevisiae (Q27930222) (← links)
- Distinct roles of two separable in vitro activities of yeast Mre11 in mitotic and meiotic recombination (Q27930776) (← links)
- Yeast DNA ligase IV mediates non-homologous DNA end joining (Q27931843) (← links)
- Distinct roles for the RSC and Swi/Snf ATP-dependent chromatin remodelers in DNA double-strand break repair (Q27933564) (← links)
- New function of CDC13 in positive telomere length regulation (Q27933597) (← links)
- Acetylation of histone H4 by Esa1 is required for DNA double-strand break repair. (Q27935926) (← links)
- Microarray-based genetic screen defines SAW1, a gene required for Rad1/Rad10-dependent processing of recombination intermediates (Q27936561) (← links)
- The nuclease activity of Mre11 is required for meiosis but not for mating type switching, end joining, or telomere maintenance (Q27937328) (← links)
- Saccharomyces cerevisiae LIF1: a function involved in DNA double-strand break repair related to mammalian XRCC4. (Q27938296) (← links)
- Nuclear pore complexes in the organization of silent telomeric chromatin (Q27939276) (← links)
- Homologous recombination via synthesis-dependent strand annealing in yeast requires the Irc20 and Srs2 DNA helicases (Q27939787) (← links)
- Differential requirement for SUB1 in chromosomal and plasmid double-strand DNA break repair (Q27939893) (← links)
- Saccharomyces cerevisiae Sin3p facilitates DNA double-strand break repair (Q27940284) (← links)
- Balancing self-renewal against genome preservation in stem cells: How do they manage to have the cake and eat it too? (Q28070584) (← links)
- DNA Polymerase θ: A Unique Multifunctional End-Joining Machine (Q28073133) (← links)
- Noncanonical views of homology-directed DNA repair (Q28080032) (← links)
- Microhomology-Mediated End Joining: A Back-up Survival Mechanism or Dedicated Pathway? (Q28083182) (← links)
- Ku, a DNA repair protein with multiple cellular functions? (Q28137885) (← links)
- Exo1 roles for repair of DNA double-strand breaks and meiotic crossing over in Saccharomyces cerevisiae (Q28140402) (← links)
- ERCC1-XPF endonuclease facilitates DNA double-strand break repair (Q28283273) (← links)
- Novel functional requirements for non-homologous DNA end joining in Schizosaccharomyces pombe. (Q28354272) (← links)
- Microhomology-mediated end joining: new players join the team (Q28468576) (← links)
- DNA ligases I and III cooperate in alternative non-homologous end-joining in vertebrates (Q28489091) (← links)
- Interaction of Ku protein and DNA-dependent protein kinase catalytic subunit with nucleic acids (Q28608946) (← links)
- Trypanosoma brucei homologous recombination is dependent on substrate length and homology, though displays a differential dependence on mismatch repair as substrate length decreases (Q28757482) (← links)