Edwin Haghnazari

1994 - B.S. Molecular Biology - San Jose State University (CA)

1998 - M.S. Molecular Biology - San Jose State University (CA)


e-Mail address: ehaghnazari@ucdavis.edu

Positions and experience:

1990-1994 - B.S. Molecular Biology, San Jose State University (CA)

1996-1998 - M.S. Molecular Biology, San Jose State University (CA)
with Dr. David Matthes

1998- present - BMB Graduate Student, Section of Microbiology,
University of California, Davis (CA)

Publications:

Herzberg, K., Bashkirov, V.I., Rolfsmeier, M., Haghnazari, E., McDonald, W.H., Anderson, S., Bashkirova, E.V., Yates, J.R. 3rd, and Heyer, W.-D. (2006) Phosphorylation of Rad55 on serines 2, 8, and 14 is required for efficient homologous recombination in the recovery of stalled replication forks Mol. Cell. Biol. 26, 8396-8409. [PDF file]

Bashkirov, V.I., Herzberg, K., Haghnazari, E., Vlasenko, A., and Heyer, W.-D. (2005) DNA damage-induced phosphorylation of Rad55 protein as a sentinel for DNA damage checkpoint activation in S. cerevisiae. Meth. Enzymol. 409, 166-182. [PDF file]

Haghnazari, E. and Heyer, W.-D. (2004a)
The Hog1 MAP kinase pathway and the Mec1 DNA damage checkpoint pathway
independently control the cellular responses to hydrogen peroxide.
DNA Repair 3, 769-776. [PDF file]

Haghnazari, E. and Heyer, W.-D. (2004b)
The DNA damage checkpoint pathways exert multiple controls on the efficiency
and outcome of the repair of a double stranded DNA gap.
Nucleic Acids Res. 32, 4257-4268. [PDF file]

Bashkirov, V.I., Bashkirova, E.V., Haghnazari, E., and Heyer, W.-D. (2003)
Direct kinase-to-kinase signaling mediated by the FHA phosphoprotein recognition domain of the Dun1 DNA damage checkpoint kinase.
Mol Cell Biol. 23, 1441-1452. [PDF file]