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Nature Cell Biology, ISSN 1465-7392, 05/2012, Volume 14, Issue 5, pp. 510 - 517
Homologous recombination, an essential process for preserving genomic integrity, uses intact homologous sequences to repair broken chromosomes. To explore the... 
LOCALIZATION | REPAIR | CHROMATIN | SEQUENCES | BUDDING YEAST | DNA-DAMAGE RESPONSE | NUCLEAR ARCHITECTURE | DYNAMICS | DOUBLE-STRAND BREAKS | LIVING CELLS | CELL BIOLOGY | Chromosomes, Fungal | Gamma Rays | DNA Damage | DNA, Fungal - genetics | Recombination, Genetic | Saccharomyces cerevisiae - genetics | Physiological aspects | Research | Genetic recombination | Chromosomes | DNA damage | Index Medicus
Journal Article
2007, Topics in current genetics, ISBN 9783540710202, Volume 17
Web Resource
2007, Topics in current genetics, ISBN 9783540710202, Volume 17
Web Resource
2007, Topics in current genetics, ISBN 9783540710202, Volume 17
Web Resource
2007, Topics in current genetics, ISBN 3540710213, Volume 17
Web Resource
Journal Article
Nature, ISSN 0028-0836, 03/2011, Volume 471, Issue 7336, pp. 74 - 79
Protein acetylation is mediated by histone acetyltransferases (HATs) and deacetylases (HDACs), which influence chromatin dynamics, protein turnover and the DNA... 
YEAST | REPAIR | ACTIVATION | ACETYLATION | MULTIDISCIPLINARY SCIENCES | VALPROIC ACID | CHECKPOINT | HOMOLOGOUS RECOMBINATION | END RESECTION | HISTONE DEACETYLASE INHIBITORS | SACCHAROMYCES-CEREVISIAE | Autophagy-Related Proteins | Protein Kinases - genetics | Microtubule-Associated Proteins - metabolism | Saccharomyces cerevisiae - genetics | Intracellular Signaling Peptides and Proteins - metabolism | Endonucleases - metabolism | Valproic Acid - pharmacology | Autophagy - drug effects | DNA Breaks, Double-Stranded - drug effects | Protein Processing, Post-Translational - drug effects | Histone Acetyltransferases - metabolism | Endodeoxyribonucleases - metabolism | Protein-Serine-Threonine Kinases - antagonists & inhibitors | Aminopeptidases - metabolism | Chromosomal Instability | Protein-Serine-Threonine Kinases - metabolism | DNA Repair - drug effects | Histone Deacetylases - genetics | Saccharomyces cerevisiae Proteins - antagonists & inhibitors | Intracellular Signaling Peptides and Proteins - antagonists & inhibitors | Histone Deacetylases - metabolism | Saccharomyces cerevisiae Proteins - genetics | Endonucleases - chemistry | Saccharomyces cerevisiae - cytology | Autophagy-Related Protein 8 Family | Acetylation - drug effects | Signal Transduction - drug effects | Exodeoxyribonucleases - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Saccharomyces cerevisiae - enzymology | Histone Deacetylase Inhibitors - pharmacology | Saccharomyces cerevisiae Proteins - chemistry | Proteins | Physiological aspects | Causes of | Enzymes | Genetic aspects | DNA damage | Phosphorylation | Yeast | Kinases | DNA repair | Autophagy | Experiments | Recruitment | Cell cycle | Genetics | Influence | Apoptosis | Index Medicus
Journal Article
Journal Article
The EMBO Journal, ISSN 0261-4189, 04/2009, Volume 28, Issue 8, pp. 1121 - 1130
Recruitment of the homologous recombination machinery to sites of double‐strand breaks is a cell cycle‐regulated event requiring entry into S phase and CDK1... 
replication | checkpoints | recombination | DNA damage | Replication | Recombination | DNAdamage | Checkpoints | BUDDING YEAST | PROTEIN-KINASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | UBIQUITIN-LIGASE COMPLEX | DOUBLE-STRAND BREAKS | SACCHAROMYCES-CEREVISIAE | NUCLEOTIDE EXCISION-REPAIR | CELL BIOLOGY | CYCLIN-DEPENDENT KINASES | S-PHASE | CELL-CYCLE | HOMOLOGOUS RECOMBINATION | Saccharomyces cerevisiae - genetics | CDC2 Protein Kinase - metabolism | Saccharomyces cerevisiae - metabolism | Rad52 DNA Repair and Recombination Protein - metabolism | Recombination, Genetic | Cell Cycle Proteins - genetics | CDC28 Protein Kinase, S cerevisiae - metabolism | Protein-Serine-Threonine Kinases - metabolism | Caffeine - metabolism | CDC2 Protein Kinase - genetics | Enzyme Inhibitors - metabolism | F-Box Proteins - metabolism | Cell Cycle Proteins - metabolism | Protein-Serine-Threonine Kinases - genetics | Ubiquitin-Protein Ligases - metabolism | Intracellular Signaling Peptides and Proteins | CDC28 Protein Kinase, S cerevisiae - genetics | DNA Replication | Saccharomyces cerevisiae Proteins - genetics | Rad52 DNA Repair and Recombination Protein - genetics | Saccharomyces cerevisiae Proteins - metabolism | Cell Cycle - physiology | Checkpoint Kinase 2 | DNA Damage | Ubiquitin-Protein Ligases - genetics | F-Box Proteins - genetics | Hydroxyurea - metabolism | Genetic recombination | Kinases | Molecular biology | Genomics | Cell cycle | Index Medicus
Journal Article
11/2010, Topics in Current Genetics Ser., ISBN 9783642090059, Volume 17
Annotation This work offers a fascinating insight into a crucial genetic process. Recombination is, quite simply, one of the most important topics in... 
Molecular Genetics | Dna | Science | Recombinant Dna
Web Resource
11/2010, Topics in Current Genetics Ser., ISBN 9783642090059, Volume 17
Annotation This work offers a fascinating insight into a crucial genetic process. Recombination is, quite simply, one of the most important topics in... 
Molecular Genetics | Dna | Science | Recombinant Dna
Web Resource
by Southey, Melissa C and Goldgar, David E and Winqvist, Robert and Pylkäs, Katri and Couch, Fergus and Tischkowitz, Marc and Foulkes, William D and Dennis, Joe and Michailidou, Kyriaki and van Rensburg, Elizabeth J and Heikkinen, Tuomas and Nevanlinna, Heli and Hopper, John L and Dörk, Thilo and Claes, Kathleen BM and Reis-Filho, Jorge and Teo, Zhi Ling and Radice, Paolo and Catucci, Irene and Peterlongo, Paolo and Tsimiklis, Helen and Odefrey, Fabrice A and Dowty, James G and Schmidt, Marjanka K and Broeks, Annegien and Hogervorst, Frans B and Verhoef, Senno and Carpenter, Jane and Clarke, Christine and Scott, Rodney J and Fasching, Peter A and Haeberle, Lothar and Ekici, Arif B and Beckmann, Matthias W and Peto, Julian and dos-Santos-Silva, Isabel and Fletcher, Olivia and Johnson, Nichola and Bolla, Manjeet K and Sawyer, Elinor J and Tomlinson, Ian and Kerin, Michael J and Miller, Nicola and Marme, Federik and Burwinkel, Barbara and Yang, Rongxi and Guénel, Pascal and Truong, Thérèse and Menegaux, Florence and Sanchez, Marie and Bojesen, Stig and Nielsen, Sune F and Flyger, Henrik and Benitez, Javier and Zamora, M Pilar and Perez, Jose Ignacio Arias and Menéndez, Primitiva and Anton-Culver, Hoda and Neuhausen, Susan and Ziogas, Argyrios and Clarke, Christina A and Brenner, Hermann and Arndt, Volker and Stegmaier, Christa and Brauch, Hiltrud and Brüning, Thomas and Ko, Yon-Dschun and Muranen, Taru A and Aittomäki, Kristiina and Blomqvist, Carl and Bogdanova, Natalia V and Antonenkova, Natalia N and Lindblom, Annika and Margolin, Sara and Mannermaa, Arto and Kataja, Vesa and Kosma, Veli-Matti and Hartikainen, Jaana M and Spurdle, Amanda B and Investigators, kConFab and Wauters, Els and Smeets, Dominiek and Beuselinck, Benoit and Floris, Giuseppe and Chang-Claude, Jenny and Rudolph, Anja and Seibold, Petra and Flesch-Janys, Dieter and Olson, Janet E and Vachon, Celine and Pankratz, Vernon S and McLean, Catriona and Haiman, Christopher A and Henderson, Brian E and Schumacher, Fredrick and Le Marchand, Loic and Kristensen, Vessela and Alnæs, Grethe Grenaker and Zheng, Wei and Hunter, David J and ... and Australian Ovarian Canc Study Grp and kConFab Investigators and Australian Ovarian Cancer Study Group
Journal of Medical Genetics, ISSN 0022-2593, 12/2016, Volume 53, Issue 12, pp. 800 - 811
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