Other names published for RAD50: YNL250W
RAD50 LITERATURE TOPICS
- Curated Literature
- Genetics/Cell Biology
- Cell Cycle Phase Involved
- Cellular Location
- Function/Process
- Genetic Interactions
- Mutants/Phenotypes
- Regulation of
- Regulatory Role
- Nucleic Acid Information
- Gene Product Information
- Related Genes/Proteins
- Research Aids
- Genome-wide Analysis
- Proteome-wide Analysis
- Other Topics
- Additional Information
RAD50 - Genetic Interactions (134)
| Reference | Other Genes Addressed |
|---|---|
| Kalifa L, et al. (2012) Mitochondrial genome maintenance: roles for nuclear nonhomologous end-joining proteins in Saccharomyces cerevisiae. Genetics 190(3):951-64 | |
| Addinall SG, et al. (2011) Quantitative Fitness Analysis Shows That NMD Proteins and Many Other Protein Complexes Suppress or Enhance Distinct Telomere Cap Defects. PLoS Genet 7(4):e1001362 | |
| Chang HY, et al. (2011) Genome-wide analysis to identify pathways affecting telomere-initiated senescence in budding yeast. G3 (Bethesda) 1(3):197-208 | |
| Foster SS, et al. (2011) Functional interplay of the mre11 nuclease and ku in the response to replication-associated DNA damage. Mol Cell Biol 31(21):4379-89 | |
| Houseley J and Tollervey D (2011) Repeat expansion in the budding yeast ribosomal DNA can occur independently of the canonical homologous recombination machinery. Nucleic Acids Res 39(20):8778-91 | |
| Huang Z, et al. (2011) Sampangine inhibits heme biosynthesis in both yeast and human. Eukaryot Cell 10(11):1536-44 | |
| Kelly MK, et al. (2011) Minisatellite alterations in ZRT1 mutants occur via RAD52-dependent and RAD52-independent mechanisms in quiescent stationary phase yeast cells. DNA Repair (Amst) 10(6):556-66 | |
| Leon Ortiz AM, et al. (2011) Srs2 overexpression reveals a helicase-independent role at replication forks that requires diverse cell functions. DNA Repair (Amst) 10(5):506-17 | |
| Li XC and Tye BK (2011) Ploidy Dictates Repair Pathway Choice under DNA Replication Stress. Genetics 187(4):1031-40 | |
| Ma W, et al. (2011) Alkylation Base Damage Is Converted into Repairable Double-Strand Breaks and Complex Intermediates in G2 Cells Lacking AP Endonuclease. PLoS Genet 7(4):e1002059 | |
| Merchan S, et al. (2011) Genetic alterations leading to increases in internal potassium concentrations are detrimental for DNA integrity in Saccharomyces cerevisiae. Genes Cells 16(2):152-65 | |
| Mischo HE, et al. (2011) Yeast sen1 helicase protects the genome from transcription-associated instability. Mol Cell 41(1):21-32 | |
| Nakai W, et al. (2011) Chromosome integrity at a double-strand break requires exonuclease 1 and MRX. DNA Repair (Amst) 10(1):102-10 | |
| Reid RJ, et al. (2011) Selective ploidy ablation, a high-throughput plasmid transfer protocol, identifies new genes affecting topoisomerase I-induced DNA damage. Genome Res 21(3):477-86 | |
| Ruiz-Gomez MJ (2011) Telomere instability caused by subtelomeric Y' amplification and rearrangements in Saccharomyces cerevisiae (ku70 tel1 and ku70 rad50) double mutants. Indian J Exp Biol 49(5):324-31 | |
| Zanders S, et al. (2011) Pch2 modulates chromatid partner choice during meiotic double-strand break repair in Saccharomyces cerevisiae. Genetics 188(3):511-21 | |
| Aggarwal M, et al. (2010) Delineation of WRN helicase function with EXO1 in the replicational stress response. DNA Repair (Amst) 9(7):765-76 | |
| Daley JM, et al. (2010) Genetic interactions between HNT3/Aprataxin and RAD27/FEN1 suggest parallel pathways for 5' end processing during base excision repair. DNA Repair (Amst) 9(6):690-9 | |
| Faucher D and Wellinger RJ (2010) Methylated H3K4, a transcription-associated histone modification, is involved in the DNA damage response pathway.LID - e1001082 [pii] PLoS Genet 6(8) | |
| Lee C, et al. (2010) Alternative mechanisms for coordinating polymerase alpha and MCM helicase. Mol Cell Biol 30(2):423-35 | |
| Meng FL, et al. (2010) Sua5p is required for telomere recombination in Saccharomyces cerevisiae. Cell Res 20(4):495-8 | |
| Moriel-Carretero M and Aguilera A (2010) A Postincision-Deficient TFIIH Causes Replication Fork Breakage and Uncovers Alternative Rad51- or Pol32-Mediated Restart Mechanisms. Mol Cell 37(5):690-701 | |
| Shim EY, et al. (2010) Saccharomyces cerevisiae Mre11/Rad50/Xrs2 and Ku proteins regulate association of Exo1 and Dna2 with DNA breaks. EMBO J 29(19):3370-80 | |
| Toussaint M, et al. (2010) Differential participation of homologous recombination and nucleotide excision repair in yeast survival to ultraviolet light radiation. Mutat Res 698(1-2):52-59 | |
| Enserink JM, et al. (2009) Cdc28/Cdk1 positively and negatively affects genome stability in S. cerevisiae. J Cell Biol 185(3):423-37 | |
| Galli A, et al. (2009) The pol3-t Hyperrecombination Phenotype and DNA Damage-Induced Recombination in Saccharomyces cerevisiae Is RAD50 Dependent. J Biomed Biotechnol 2009:312710 | |
| Grandin N and Charbonneau M (2009) Telomerase- and Rad52-independent immortalization of budding yeast by an inherited-long-telomere pathway of telomeric repeat amplification. Mol Cell Biol 29(4):965-85 | |
| Koehn DR, et al. (2009) Tethering Recombination Initiation Proteins in Saccharomyces cerevisiae Promotes Double Strand Break Formation. Genetics 182(2):447-58 | |
| Lebel C, et al. (2009) Telomere Maintenance and Survival in Saccharomyces cerevisiae in the Absence of Telomerase and RAD52. Genetics 182(3):671-84 | |
| Lin YH, et al. (2009) Recruitment of rad51 and rad52 to short telomeres triggers a mec1-mediated hypersensitivity to double-stranded DNA breaks in senescent budding yeast. PLoS One 4(12):e8224 |



