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List of works by Robert Glanville Lloyd

A soluble RecN homologue provides means for biochemical and genetic analysis of DNA double-strand break repair in Escherichia coli

scientific article published on 20 October 2009

Avoiding and resolving conflicts between DNA replication and transcription

scientific article published on 30 March 2007

Avoiding chromosome pathology when replication forks collide

scientific article published on 28 July 2013

Cellular location and activity of Escherichia coli RecG proteins shed light on the function of its structurally unresolved C-terminus

scientific article

DNA binding by the meningococcal RdgC protein, associated with pilin antigenic variation.

scientific article published on February 2004

DNA binding by the substrate specificity (wedge) domain of RecG helicase suggests a role in processivity.

scientific article

DNA double strand break repair and crossing over mediated by RuvABC resolvase and RecG translocase

scientific article published on 7 July 2008

Direct rescue of stalled DNA replication forks via the combined action of PriA and RecG helicase activities.

scientific article

Holliday junction binding and processing by the RuvA protein of Mycoplasma pneumoniae

scientific article

Inhibiting translation elongation can aid genome duplication in Escherichia coli

scientific article published on 11 December 2016

Interplay between DNA replication, recombination and repair based on the structure of RecG helicase

scientific article published on January 2004

Is RecG a general guardian of the bacterial genome?

scientific article published on 25 January 2010

Localization of an accessory helicase at the replisome is critical in sustaining efficient genome duplication

scientific article published on 4 October 2010

Maintaining replication fork integrity in UV-irradiated Escherichia coli cells

scientific article

Modulation of DNA damage tolerance in Escherichia colirecG and ruv strains by mutations affecting PriB, the ribosome and RNA polymerase ⬇️

scientific article published on September 7, 2012

On the viability of Escherichia colicells lacking DNA topoisomerase I ⬇️

scientific article published on February 28, 2012

Pathological replication in cells lacking RecG DNA translocase

scientific article published on 16 June 2009

Promoting and avoiding recombination: contrasting activities of the Escherichia coli RuvABC Holliday junction resolvase and RecG DNA translocase

scientific article published on 15 February 2010

Protein-DNA complexes are the primary sources of replication fork pausing in Escherichia coli

scientific article published on 15 April 2013

RecG helicase promotes DNA double-strand break repair

scientific article published in April 2004

RecG protein and single-strand DNA exonucleases avoid cell lethality associated with PriA helicase activity in Escherichia coli

scientific article published on 20 July 2010

RecN protein and transcription factor DksA combine to promote faithful recombinational repair of DNA double-strand breaks

scientific article published in July 2005

Rep and PriA helicase activities prevent RecA from provoking unnecessary recombination during replication fork repair

scientific article published on August 2006

Rep provides a second motor at the replisome to promote duplication of protein-bound DNA.

scientific article

Replication fork collisions cause pathological chromosomal amplification in cells lacking RecG DNA translocase ⬇️

scientific article published on 8 October 2009

Replication fork stalling and cell cycle arrest in UV-irradiated Escherichia coli

scientific article

RusA proteins from the extreme thermophile Aquifex aeolicus and lactococcal phage r1t resolve Holliday junctions

scientific article published in April 2002

The Balance between Recombination Enzymes and Accessory Replicative Helicases in Facilitating Genome Duplication

scientific article published on 29 July 2016

The RdgC protein employs a novel mechanism involving a finger domain to bind to circular DNA.

scientific article published on 4 June 2010

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