| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Haber JE | |
| P2860 | cites work | Requirement for Xist in X chromosome inactivation | Q29614509 |
| P921 | main subject | donor selection | Q22244427 |
| inactivation of recombination (HML) | Q22244428 | ||
| activation of recombination (HML) | Q22244524 | ||
| gene conversion at mating-type locus | Q22279515 | ||
| mating type switching | Q22280406 | ||
| Saccharomyces cerevisiae | Q719725 | ||
| P304 | page(s) | 561-599 | |
| P577 | publication date | 1998-01-01 | |
| P1433 | published in | Annual Review of Genetics | Q567358 |
| P1476 | title | Mating-type gene switching in Saccharomyces cerevisiae. | |
| P478 | volume | 32 |
| Q60154714 | 2 Yeast Genetics and Strain Construction |
| Q47804471 | A 72-base pair AT-rich DNA sequence element functions as a bacterial gene silencer |
| Q34368387 | A PIWI homolog is one of the proteins expressed exclusively during macronuclear development in the ciliate Stylonychia lemnae |
| Q42653271 | A Saccharomyces servazzii clone homologous to Saccharomyces cerevisiae chromosome III spanning KAR4, ARS 304 and SPB1 lacks the recombination enhancer but contains an unknown ORF. |
| Q35574396 | A genomic screen revealing the importance of vesicular trafficking pathways in genome maintenance and protection against genotoxic stress in diploid Saccharomyces cerevisiae cells |
| Q35558859 | A homolog of male sex-determining factor SRY cooperates with a transposon-derived CENP-B protein to control sex-specific directed recombination. |
| Q42958560 | A novel approach for the improvement of ethanol fermentation by Saccharomyces cerevisiae |
| Q34200585 | A novel engineered meganuclease induces homologous recombination in yeast and mammalian cells |
| Q33633991 | A pattern analysis of gene conversion literature |
| Q27933727 | A phosphatase complex that dephosphorylates gammaH2AX regulates DNA damage checkpoint recovery |
| Q40445788 | A role for RAD51 and homologous recombination in Trypanosoma brucei antigenic variation |
| Q73634170 | A selfish origin for recombination |
| Q34031504 | A single heterochromatin boundary element imposes position-independent antisilencing activity in Saccharomyces cerevisiae minichromosomes |
| Q40895699 | A strand invasion 3' polymerization intermediate of mammalian homologous recombination |
| Q45226582 | ATP-dependent and ATP-independent roles for the Rad54 chromatin remodeling enzyme during recombinational repair of a DNA double strand break |
| Q40419489 | Activation of the DNA damage checkpoint in yeast lacking the histone chaperone anti-silencing function 1. |
| Q24802780 | Activation-induced cytidine deaminase initiates immunoglobulin gene conversion and hypermutation by a common intermediate |
| Q42020243 | Alpha3, a transposable element that promotes host sexual reproduction |
| Q93054584 | An Evolutionary View of Trypanosoma Cruzi Telomeres |
| Q42081550 | An alternative DNA structure is necessary for pilin antigenic variation in Neisseria gonorrhoeae |
| Q27930768 | An auxiliary silencer and a boundary element maintain high levels of silencing proteins at HMR in Saccharomyces cerevisiae. |
| Q37401963 | Analysis of chromatin remodeling during formation of a DNA double-strand break at the yeast mating type locus |
| Q34492605 | Analysis of involvement of the RecF pathway in p44 recombination in Anaplasma phagocytophilum and in Escherichia coli by using a plasmid carrying the p44 expression and p44 donor loci |
| Q34594338 | Antigen-receptor genes of the agnathan lamprey are assembled by a process involving copy choice. |
| Q34335649 | Apparent ploidy effects on silencing are post-transcriptional at HML and telomeres in Saccharomyces cerevisiae. |
| Q35132557 | Arrest, adaptation, and recovery following a chromosome double-strand break in Saccharomyces cerevisiae |
| Q30503610 | Asymmetry in sexual pheromones is not required for ascomycete mating |
| Q27930012 | Binding of the Fkh1 Forkhead Associated Domain to a Phosphopeptide within the Mph1 DNA Helicase Regulates Mating-Type Switching in Budding Yeast. |
| Q64389008 | Biochemical attributes of mitotic and meiotic presynaptic complexes |
| Q34596215 | Braking the silence: how heterochromatic gene repression is stopped in its tracks. |
| Q38847818 | Break dosage, cell cycle stage and DNA replication influence DNA double strand break response |
| Q33879775 | Cell and nuclear recognition mechanisms mediated by mating type in filamentous ascomycetes |
| Q39393309 | Characterization of the complex involved in regulating V-ATPase activity of the vacuolar and endosomal membrane |
| Q33887311 | Chipping away at gamma-H2AX foci |
| Q37078952 | Chromatin assembly factors Asf1 and CAF-1 have overlapping roles in deactivating the DNA damage checkpoint when DNA repair is complete |
| Q36736550 | Chromatin disassembly and reassembly during DNA repair. |
| Q37760043 | Chromatin dynamics during repair of chromosomal DNA double-strand breaks |
| Q37049853 | Chromatin structure mapping in Saccharomyces cerevisiae in vivo with DNase I. |
| Q34572390 | Chromosome loss followed by duplication is the major mechanism of spontaneous mating-type locus homozygosis in Candida albicans |
| Q33866590 | Class V myosins. |
| Q35003595 | Clustering heterochromatin: Sir3 promotes telomere clustering independently of silencing in yeast |
| Q34365634 | Co-evolution of transcriptional silencing proteins and the DNA elements specifying their assembly |
| Q27940019 | Colocalization of multiple DNA double-strand breaks at a single Rad52 repair centre |
| Q35233999 | Communication in fungi |
| Q33948459 | Completion of replication map of Saccharomyces cerevisiae chromosome III. |
| Q27932385 | Complex chromosomal rearrangements mediated by break-induced replication involve structure-selective endonucleases |
| Q41077128 | Conservative inheritance of newly synthesized DNA in double-strand break-induced gene conversion |
| Q86182622 | Construction of ploidy series of Saccharomyces cerevisiae by the plasmid YCplac33-GHK |
| Q45345101 | Control of cross-over by single-strand DNA resection |
| Q33963951 | Corepressor-directed preacetylation of histone H3 in promoter chromatin primes rapid transcriptional switching of cell-type-specific genes in yeast |
| Q39023900 | Cycling through developmental decisions: how cell cycle dynamics control pluripotency, differentiation and reprogramming. |
| Q37361939 | DNA double-strand break processing: the beginning of the end. |
| Q34525927 | DNA double-strand break repair from head to tail |
| Q35126429 | DNA loss at the Ceratocystis fimbriata mating locus results in self-sterility |
| Q33969023 | DNA replication forks pause at silent origins near the HML locus in budding yeast |
| Q74307721 | DNA replication origins: from sequence specificity to epigenetics |
| Q33582128 | Defective resection at DNA double-strand breaks leads to de novo telomere formation and enhances gene targeting |
| Q33905811 | Degradation or maintenance: actions of the ubiquitin system on eukaryotic chromatin |
| Q27932022 | Dephosphorylation of gamma H2A by Glc7/protein phosphatase 1 promotes recovery from inhibition of DNA replication. |
| Q33824700 | Development: the natural history of genes |
| Q39647149 | Directional bias during mating type switching in Saccharomyces is independent of chromosomal architecture |
| Q50455994 | Display of heterologous proteins on the Saccharomyces cerevisiae surface display system using a single constitutive expression vector. |
| Q34685615 | Diversity of mating-type chromosome structures in the yeast Zygosaccharomyces rouxii caused by ectopic exchanges between MAT-like loci |
| Q27934176 | Double-strand break repair in yeast requires both leading and lagging strand DNA polymerases |
| Q42516363 | Dual chromatin remodeling roles for RSC during DNA double strand break induction and repair at the yeast MAT locus |
| Q35620454 | Dynamics of homology searching during gene conversion in Saccharomyces cerevisiae revealed by donor competition. |
| Q52550164 | Efficient sporulation in Clostridium difficile requires disruption of the σK gene |
| Q42702326 | Evidence that MEK1 positively promotes interhomologue double-strand break repair |
| Q36160831 | Evolution of the MAT locus and its Ho endonuclease in yeast species |
| Q37324326 | Evolution of uni- and bifactorial sexual compatibility systems in fungi |
| Q22066305 | Evolutionary erosion of yeast sex chromosomes by mating-type switching accidents |
| Q35008390 | Evolutionary maintenance of selfish homing endonuclease genes in the absence of horizontal transfer. |
| Q37260157 | Formation, maintenance and consequences of the imprint at the mating-type locus in fission yeast |
| Q37672042 | Fungal sex and pathogenesis |
| Q35088993 | Gain- and loss-of-function of Rhp51, a Rad51 homolog in fission yeast, reveals dissimilarities in chromosome integrity |
| Q36579390 | GammaH2AX and its role in DNA double-strand break repair |
| Q34335541 | Gene conversion occurs within the mating-type locus of Cryptococcus neoformans during sexual reproduction |
| Q50492151 | Genetic characterization and construction of an auxotrophic strain of Saccharomyces cerevisiae JP1, a Brazilian industrial yeast strain for bioethanol production |
| Q27935054 | Genetically engineered transvestites reveal novel mating genes in budding yeast |
| Q40977223 | Genome evolution in the eremothecium clade of the Saccharomyces complex revealed by comparative genomics. |
| Q28477286 | Genome-wide mapping of DNA strand breaks |
| Q37598813 | Global chromatin structure of 45,000 base pairs of chromosome III in a- and alpha-cell yeast and during mating-type switching |
| Q24617585 | Heterothallism in Saccharomyces cerevisiae isolates from nature: effect of HO locus on the mode of reproduction |
| Q33960526 | High-resolution structural analysis of chromatin at specific loci: Saccharomyces cerevisiae silent mating-type locus HMRa |
| Q34286591 | Histone H3 and the histone acetyltransferase Hat1p contribute to DNA double-strand break repair |
| Q41825478 | Histone dosage regulates DNA damage sensitivity in a checkpoint-independent manner by the homologous recombination pathway |
| Q34067489 | Home and away- the evolutionary dynamics of homing endonucleases |
| Q49236959 | Homologous pairing promoted by the human Rad52 protein |
| Q35845326 | Homothallism: an umbrella term for describing diverse sexual behaviours |
| Q27939283 | In vivo assembly and disassembly of Rad51 and Rad52 complexes during double-strand break repair |
| Q43993843 | Inactivation of Mre11 does not affect VSG gene duplication mediated by homologous recombination in Trypanosoma brucei. |
| Q27934880 | Increased mutagenesis and unique mutation signature associated with mitotic gene conversion |
| Q34572744 | Increased virulence and competitive advantage of a/alpha over a/a or alpha/alpha offspring conserves the mating system of Candida albicans |
| Q27929905 | Inhibition of proteasomal degradation of rpn4 impairs nonhomologous end-joining repair of DNA double-strand breaks |
| Q64389313 | Initiation of homologous recombination at DNA nicks |
| Q41878613 | Interhaplotypic heterogeneity and heterochromatic features may contribute to recombination suppression at the S locus in apple (Malusxdomestica). |
| Q41194763 | Involvement of Sir2/4 in silencing of DNA breakage and recombination on mouse YACs during yeast meiosis |
| Q24564918 | It infects me, it infects me not: phenotypic switching in the fungal pathogen Cryptococcus neoformans |
| Q58052030 | Kinetics of Diffusing Polymer Encounter in Confined Cellular Microdomains |
| Q37167774 | Kinetochore asymmetry defines a single yeast lineage |
| Q51821277 | Lattice model of diffusion-limited bimolecular chemical reactions in confined environments. |
| Q38330605 | LeuO protein delimits the transcriptionally active and repressive domains on the bacterial chromosome |
| Q33885431 | Links between replication, recombination and genome instability in eukaryotes |
| Q36917558 | Long-range heterochromatin association is mediated by silencing and double-strand DNA break repair proteins |
| Q33984265 | Lucky breaks: analysis of recombination in Saccharomyces |
| Q35862243 | MRE11/RAD50/NBS1: complex activities |
| Q49186289 | Mate choice among yeast gametes can purge deleterious mutations |
| Q53642117 | Mating type regulation of cellular tolerance to DNA damage is specific to the DNA post-replication repair and mutagenesis pathway. |
| Q36322219 | Mating type-dependent constraints on the mobility of the left arm of yeast chromosome III. |
| Q35917385 | Mating-type genes and MAT switching in Saccharomyces cerevisiae |
| Q27931077 | Mcm10 is required for the maintenance of transcriptional silencing in Saccharomyces cerevisiae |
| Q34040940 | Mechanisms and principles of homology search during recombination |
| Q35623181 | Mechanisms of insulator function in gene regulation and genomic imprinting |
| Q33947315 | Mitotic recombination in yeast: elements controlling its incidence |
| Q33552321 | Molecular and cellular dissection of mating-type switching steps in Schizosaccharomyces pombe |
| Q40744256 | Molecular basis for anaerobic growth of Saccharomyces cerevisiae on xylose, investigated by global gene expression and metabolic flux analysis |
| Q33914220 | Molecular characterization of KU70 and KU80 homologues and exploitation of a KU70-deficient mutant for improving gene deletion frequency in Rhodosporidium toruloides |
| Q24548535 | Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae |
| Q36836982 | Mutants defective in Rad1-Rad10-Slx4 exhibit a unique pattern of viability during mating-type switching in Saccharomyces cerevisiae |
| Q27930222 | NEJ1 controls non-homologous end joining in Saccharomyces cerevisiae |
| Q39312205 | Non-homologous DNA end joining and alternative pathways to double-strand break repair |
| Q33799984 | Nucleosome resection at a double-strand break during Non-Homologous Ends Joining in mammalian cells - implications from repressive chromatin organization and the role of ARTEMIS. |
| Q34471544 | Nucleosome-positioning sequence repeats impact chromatin silencing in yeast minichromosomes |
| Q24544014 | Opaque cells signal white cells to form biofilms in Candida albicans |
| Q35744530 | Organelle segregation during mitosis: lessons from asymmetrically dividing cells. |
| Q53589396 | PUF protein-mediated deadenylation is catalyzed by Ccr4p. |
| Q33362303 | Pathogen corruption and site-directed recombination at a plant disease resistance gene cluster |
| Q37542238 | Predicting complex phenotype-genotype interactions to enable yeast engineering: Saccharomyces cerevisiae as a model organism and a cell factory. |
| Q33959039 | Predominance of duplicative VSG gene conversion in antigenic variation in African trypanosomes |
| Q37941514 | Propagation of histone marks and epigenetic memory during normal and interrupted DNA replication |
| Q27929938 | Proteomic and genomic characterization of chromatin complexes at a boundary |
| Q47445796 | Proteomic identification of histone post-translational modifications and proteins enriched at a DNA double-strand break |
| Q51053390 | Purification of native, defined chromatin segments |
| Q35780104 | Quality control of MATa1 splicing and exon skipping by nuclear RNA degradation |
| Q38955829 | RAS/cyclic AMP and transcription factor Msn2 regulate mating and mating-type switching in the yeast Kluyveromyces lactis. |
| Q35602957 | RNA asymmetric distribution and daughter/mother differentiation in yeast |
| Q24536343 | RNA polymerase III and RNA polymerase II promoter complexes are heterochromatin barriers in Saccharomyces cerevisiae |
| Q37417045 | RNase-sensitive DNA modification(s) initiates S. pombe mating-type switching |
| Q47336460 | Rapid and Efficient CRISPR/Cas9-Based Mating-Type Switching of Saccharomyces cerevisiae |
| Q27674642 | RecA-Binding pilE G4 Sequence Essential for Pilin Antigenic Variation Forms Monomeric and 5′ End-Stacked Dimeric Parallel G-Quadruplexes |
| Q37139999 | Recombination at DNA replication fork barriers is not universal and is differentially regulated by Swi1 |
| Q33262629 | Recombination hotspots flank the Cryptococcus mating-type locus: implications for the evolution of a fungal sex chromosome |
| Q27935713 | Recombinational repair within heterochromatin requires ATP-dependent chromatin remodeling |
| Q31151107 | Recruitment of the recombinational repair machinery to a DNA double-strand break in yeast |
| Q27935905 | Recruitment of the type B histone acetyltransferase Hat1p to chromatin is linked to DNA double-strand breaks |
| Q35214947 | Recurrent duplication-driven transposition of DNA during hominoid evolution |
| Q27936144 | Regulation of budding yeast mating-type switching donor preference by the FHA domain of Fkh1 |
| Q37072120 | Regulation of nuclear positioning and dynamics of the silent mating type loci by the yeast Ku70/Ku80 complex |
| Q34005133 | Reiterative Recombination for the in vivo assembly of libraries of multigene pathways. |
| Q35149529 | Relationship between switching and mating in Candida albicans |
| Q53616221 | Repair of DNA double strand breaks: in vivo biochemistry. |
| Q36755308 | Replication fork stalling at natural impediments |
| Q42174262 | Replicon dynamics, dormant origin firing, and terminal fork integrity after double-strand break formation |
| Q38166297 | Revisiting Mortimer's Genome Renewal Hypothesis: heterozygosity, homothallism, and the potential for adaptation in yeast. |
| Q36701282 | Role of DNA replication proteins in double-strand break-induced recombination in Saccharomyces cerevisiae |
| Q40643647 | Role of Dot1 in the response to alkylating DNA damage in Saccharomyces cerevisiae: regulation of DNA damage tolerance by the error-prone polymerases Polzeta/Rev1. |
| Q33869149 | Role of yeast SIR genes and mating type in directing DNA double-strand breaks to homologous and non-homologous repair paths. |
| Q27938903 | SCFCdc4 enables mating type switching in yeast by cyclin-dependent kinase-mediated elimination of the Ash1 transcriptional repressor. |
| Q27931613 | SMC1 coordinates DNA double-strand break repair pathways |
| Q27937947 | Saccharomyces forkhead protein Fkh1 regulates donor preference during mating-type switching through the recombination enhancer |
| Q36052343 | Schizosaccharomyces pombe switches mating type by the synthesis-dependent strand-annealing mechanism |
| Q24791574 | Screening the yeast genome for new DNA-repair genes |
| Q34067457 | Secondary metabolism in fungi: does chromosomal location matter? |
| Q35928892 | Selective gene expression in multigene families from yeast to mammals |
| Q34694887 | Separation of mother and daughter cells |
| Q38315392 | Sequence homology and microhomology dominate chromosomal double-strand break repair in African trypanosomes |
| Q22122502 | Sequencing and comparison of yeast species to identify genes and regulatory elements |
| Q38003708 | Sex, outcrossing and mating types: unsolved questions in fungi and beyond |
| Q33784919 | Sex-determination system in the diploid yeast Zygosaccharomyces sapae |
| Q38970515 | Sexual Reproduction in Dermatophytes |
| Q38060808 | Sexual selection in fungi. |
| Q30434650 | Shared forces of sex chromosome evolution in haploid-mating and diploid-mating organisms: Microbotryum violaceum and other model organisms |
| Q35802372 | Skin facilitates Candida albicans mating |
| Q27931113 | Smc5-Smc6 mediate DNA double-strand-break repair by promoting sister-chromatid recombination. |
| Q27681202 | Structure of Mre11–Nbs1 complex yields insights into ataxia-telangiectasia–like disease mutations and DNA damage signaling |
| Q36416262 | Subtelomeric elements influence but do not determine silencing levels at Saccharomyces cerevisiae telomeres |
| Q34569369 | Swi5 acts in meiotic DNA joint molecule formation in Schizosaccharomyces pombe |
| Q41790568 | Switching the mechanism of mating type switching: a domesticated transposase supplants a domesticated homing endonuclease |
| Q40619582 | The CDK regulates repair of double-strand breaks by homologous recombination during the cell cycle |
| Q36376474 | The Conformation of Yeast Chromosome III Is Mating Type Dependent and Controlled by the Recombination Enhancer |
| Q27939248 | The DNA repair protein yKu80 regulates the function of recombination enhancer during yeast mating type switching |
| Q33960277 | The Mre11-Rad50-Xrs2 protein complex facilitates homologous recombination-based double-strand break repair in Saccharomyces cerevisiae |
| Q35209458 | The RING finger/B-box factor TAM-1 and a retinoblastoma-like protein LIN-35 modulate context-dependent gene silencing in Caenorhabditis elegans |
| Q24545654 | The Saccharomyces cerevisiae recombination enhancer biases recombination during interchromosomal mating-type switching but not in interchromosomal homologous recombination |
| Q33879831 | The Sir proteins of Saccharomyces cerevisiae: mediators of transcriptional silencing and much more. |
| Q33247457 | The dynamics of homologous pairing during mating type interconversion in budding yeast |
| Q37337415 | The establishment of gene silencing at single-cell resolution |
| Q28751643 | The evolution of sex: a perspective from the fungal kingdom |
| Q33698033 | The new field of epigenomics: implications for cancer and other common disease research. |
| Q33340248 | The pathway to detangle a scrambled gene |
| Q33835884 | The processive kinetics of gene conversion in bacteria. |
| Q42159764 | The sole introduction of two single-point mutations establishes glycerol utilization in Saccharomyces cerevisiae CEN.PK derivatives. |
| Q30657308 | The ste3 pheromone receptor gene of Pneumocystis carinii is surrounded by a cluster of signal transduction genes |
| Q40395489 | The tail-module of yeast Mediator complex is required for telomere heterochromatin maintenance |
| Q34168539 | The two different isoforms of the RSC chromatin remodeling complex play distinct roles in DNA damage responses |
| Q27934796 | The yeast chromatin remodeler RSC complex facilitates end joining repair of DNA double-strand breaks |
| Q34578729 | Transcriptional silencing in Saccharomyces cerevisiae and Schizosaccharomyces pombe |
| Q64251185 | Translatome and transcriptome analysis of TMA20 (MCT-1) and TMA64 (eIF2D) knockout yeast strains |
| Q42845280 | Transposon mutagenesis identifies sites upstream of the Neisseria gonorrhoeae pilE gene that modulate pilin antigenic variation |
| Q33195775 | Two different Swi5-containing protein complexes are involved in mating-type switching and recombination repair in fission yeast |
| Q46247501 | Two pathways of homologous recombination in Trypanosoma brucei |
| Q33984271 | Tying up loose ends: nonhomologous end-joining in Saccharomyces cerevisiae |
| Q35971167 | Ubiquitin-dependent degradation of the yeast Mat(alpha)2 repressor enables a switch in developmental state |
| Q37130505 | Understanding and re-engineering nucleoprotein machines to cure human disease |
| Q42591966 | Unique aspects of gene expression during Candida albicans mating and possible G(1) dependency |
| Q58323739 | Uses and abuses of HO endonuclease |
| Q37024699 | Using homologous recombination to manipulate the genome of human somatic cells |
| Q35342673 | What do you mean, "epigenetic"? |
| Q38001053 | What uses are mating types? The "developmental switch" model |
| Q34042795 | Yeast recombination enhancer is stimulated by transcription activation |
| Q33576944 | Yeast sex: surprisingly high rates of outcrossing between asci. |
| Q37168902 | Yeast silent mating type loci form heterochromatic clusters through silencer protein-dependent long-range interactions |
| Q27938890 | Yph1p, an ORC-interacting protein: potential links between cell proliferation control, DNA replication, and ribosome biogenesis. |
| Q42217424 | Zygomycetes, microsporidia, and the evolutionary ancestry of sex determination |
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