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Attila Tóth

Researcher at Dresden University of Technology

Publications -  44
Citations -  4893

Attila Tóth is an academic researcher from Dresden University of Technology. The author has contributed to research in topics: Meiosis & Homologous chromosome. The author has an hindex of 27, co-authored 41 publications receiving 4261 citations. Previous affiliations of Attila Tóth include Research Institute of Molecular Pathology.

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Cohesin's Binding to Chromosomes Depends on a Separate Complex Consisting of Scc2 and Scc4 Proteins

TL;DR: It is shown that Scc2p forms a complex with a novel protein, Scc4p, which is also necessary for sister cohesion, suggesting that a major role for the SCC2p/SCC4p complex is to facilitate the loading of cohesin complexes onto chromosomes.
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Yeast cohesin complex requires a conserved protein, Eco1p(Ctf7), to establish cohesion between sister chromatids during DNA replication.

TL;DR: This and a previous study have identified six proteins essential for establishing or maintaining sister chromatid cohesion, four of which are subunits of a 'Cohesin' complex that binds chromosomes from late G1 until the onset of anaphase.
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Mouse HORMAD1 and HORMAD2, Two Conserved Meiotic Chromosomal Proteins, Are Depleted from Synapsed Chromosome Axes with the Help of TRIP13 AAA-ATPase

TL;DR: The behavior of two previously uncharacterized meiosis-specific mouse HORMA-domain proteins—HORMAD1 and HORMAD2—in wild-type mice and in mutants defective in DSB processing or SC formation are examined, raising the possibility that involvement of meiotic HORMA -domain proteins in the regulation of homologue interactions is conserved in mammals.
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APC Cdc20 promotes exit from mitosis by destroying the anaphase inhibitor Pds1 and cyclin Clb5

TL;DR: It is shown that APCCdc20 allows activation of Cdc14 and promotes exit from mitosis by mediating proteolysis of Pds1 and the S phase cyclin Clb5 in the yeast Saccharomyces cerevisiae.
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Functional Genomics Identifies Monopolin: A Kinetochore Protein Required for Segregation of Homologs during Meiosis I

TL;DR: It is concluded that monopolar attachment during meiosis I requires at least one meiosis-specific protein and is independent of the process that protects sister centromere cohesion.