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Gökhan Tolun

Researcher at Illawarra Health & Medical Research Institute

Publications -  16
Citations -  1170

Gökhan Tolun is an academic researcher from Illawarra Health & Medical Research Institute. The author has contributed to research in topics: DNA replication & DNA. The author has an hindex of 12, co-authored 13 publications receiving 1015 citations. Previous affiliations of Gökhan Tolun include University of North Carolina at Chapel Hill & University of Miami.

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Journal ArticleDOI

Concerted Loading of Mcm2-7 Double Hexamers Around DNA during DNA Replication Origin Licensing

TL;DR: The loading of Mcm2-7 onto DNA requires the origin recognition complex (ORC), Cdc6, and Cdt1, and depends on ATP, and has significant implications for understanding how eukaryotic DNA replication origins are chosen and licensed, how replisomes assemble during initiation, and how unwinding occurs during DNA replication.
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The Killing of African Trypanosomes by Ethidium Bromide

TL;DR: It is concluded that minicircle replication initiation is likely EB's most vulnerable target, but the effect on nuclear replication may also contribute to cell killing.
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The Werner syndrome protein binds replication fork and holliday junction DNAs as an oligomer.

TL;DR: Using electron microscopy, it is shown that both wild-type WRN and a helicase-defective mutant bind with exceptionally high specificity to DNA secondary structures at the replication fork and at Holliday junctions, little or no binding is observed elsewhere on the DNA molecules.
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Structural Basis of Hat Transposon End Recognition by Hermes, an Octameric DNA Transposase from Musca Domestica.

TL;DR: The unusual assembly of the Hermes transposase-DNA complex reveals that Hermes forms an octameric ring organized as a tetramer of dimers, which explains the basis of bipartite DNA recognition at hAT transposon ends, provides a rationale for transPOSon end asymmetry, and suggests how the avidity provided by multiple sites of interaction could allow a transpos enzyme to locate its transposons ends amidst a sea of chromosomal DNA.
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A real‐time DNase assay (ReDA) based on PicoGreen ® fluorescence

TL;DR: A continuous DNase assay based on the differential fluorescence output of a DNA dye ligand called PicoGreen is described and appears to have general utility as it is also suitable for measuring the DNA digestion activities of a processive helicase/nuclease, RecBCD, a distributive exonuclease