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Items: 10

1.

DNA Polymerase III, but Not Polymerase IV, Must Be Bound to a τ-Containing DnaX Complex to Enable Exchange into Replication Forks.

Yuan Q, Dohrmann PR, Sutton MD, McHenry CS.

J Biol Chem. 2016 May 27;291(22):11727-35. doi: 10.1074/jbc.M116.725358. Epub 2016 Apr 7.

2.

The DNA polymerase III holoenzyme contains γ and is not a trimeric polymerase.

Dohrmann PR, Correa R, Frisch RL, Rosenberg SM, McHenry CS.

Nucleic Acids Res. 2016 Feb 18;44(3):1285-97. doi: 10.1093/nar/gkv1510. Epub 2016 Jan 18.

3.

DNA Polymerase α Subunit Residues and Interactions Required for Efficient Initiation Complex Formation Identified by a Genetic Selection.

Lindow JC, Dohrmann PR, McHenry CS.

J Biol Chem. 2015 Jul 3;290(27):16851-60. doi: 10.1074/jbc.M115.661090. Epub 2015 May 18.

4.

The rate of polymerase release upon filling the gap between Okazaki fragments is inadequate to support cycling during lagging strand synthesis.

Dohrmann PR, Manhart CM, Downey CD, McHenry CS.

J Mol Biol. 2011 Nov 18;414(1):15-27. doi: 10.1016/j.jmb.2011.09.039. Epub 2011 Oct 1.

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RAD53 regulates DBF4 independently of checkpoint function in Saccharomyces cerevisiae.

Dohrmann PR, Oshiro G, Tecklenburg M, Sclafani RA.

Genetics. 1999 Mar;151(3):965-77.

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Parallel pathways of gene regulation: homologous regulators SWI5 and ACE2 differentially control transcription of HO and chitinase.

Dohrmann PR, Butler G, Tamai K, Dorland S, Greene JR, Thiele DJ, Stillman DJ.

Genes Dev. 1992 Jan;6(1):93-104.

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