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Justin Courcelle

Department of Biological Sciences; Mississippi State University

39762

USA

[email]@*.msstate.edu

Name/email consistency: high

 
 
 
 
 
 
 

Affiliations

  • Department of Biological Sciences; Mississippi State University, 39762, USA. 2001 - 2004
  • Department of Biochemistry, Howard Hughes Medical Institute, Stanford University, Stanford, USA. 2001

References

  1. When replication travels on damaged templates: bumps and blocks in the road. Courcelle, J., Belle, J.J., Courcelle, C.T. Res. Microbiol. (2004) [Pubmed]
  2. DNA damage-induced replication fork regression and processing in Escherichia coli. Courcelle, J., Donaldson, J.R., Chow, K.H., Courcelle, C.T. Science (2003) [Pubmed]
  3. RecA-dependent recovery of arrested DNA replication forks. Courcelle, J., Hanawalt, P.C. Annu. Rev. Genet. (2003) [Pubmed]
  4. Comparative gene expression profiles following UV exposure in wild-type and SOS-deficient Escherichia coli. Courcelle, J., Khodursky, A., Peter, B., Brown, P.O., Hanawalt, P.C. Genetics (2001) [Pubmed]
  5. Therefore, what are recombination proteins there for?. Courcelle, J., Ganesan, A.K., Hanawalt, P.C. Bioessays (2001) [Pubmed]
  6. Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination. Courcelle, J., Hanawalt, P.C. Proc. Natl. Acad. Sci. U.S.A. (2001) [Pubmed]
 
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