Peter 
Stambrook
, Ph.D.
Professor

There are three major areas of research interests in my laboratory. We have developed a "knockout" mouse that will be useful for detecting mutagenic environments using an endogenous gene as a reporter. As a second direction, we are examining signal transduction events mediated by leading the ras oncogene leading to genomic instability. Lastly, we have formed a collaboration with a clinical group to develop novel cancer gene therapy approaches.


Selected Publications:
  • Tichey ED and Stambrook PJ. (2008) DNA repair in murine embryonic stem cells and differentiated cells. Exp Cell Res, June, 314(9): 1929-36.
  • Bahassi EM, Ovesen JL, Riesenberg AL, Bernstein WZ, Hasty PE, and Stambrook PJ. (2008) The checkpoint kinases Chk1 and Chk2 regulate the functional associations between hBRCA2 and Rad51 in response to DNA damage. Oncogene, June, 27(28): 3977-85.
  • Bahassi el M, Penner CG, Robbins SB, Tichy E, Feliciano E, Yin M, Liang L, Deng L, Tischfield JA, and Stambrook PJ. (2007) The breast cancer susceptibility allele CHEK2*1100delC promotes genomic instability in a knock-in mouse model. Mutat Res, Mar, 616(1-2): 201-9.
  • Hong Y, Cervantes RB, Tichy E, Tischfield JA, and Stambrook PJ. (2007) Protecting genomic integrity in somatic cells and embryonic stem cells. Mutat Res, Jan, 614(1-2): 48-55.


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