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DCB - DNA and Chromosome Aberrations Branch (DCAB)


The DNA and Chromosome Aberrations Branch (DCAB) plans and administers a broadly-based extramural program of grants on the cancer-related mechanisms of DNA damage/repair, and related molecular, cytogenetic, and chromosomal effects during induction and progression to malignancy. The scientific scope encompasses a number of disciplines, including: DNA damage detection, repair, and response mechanisms, as well as the molecular basis for spontaneous and heritable defects in DNA repair and chromosome stability.


Program Announcements and Request for Application

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STAFF
NameTitle
 Mietz, Judy, Ph.D. Chief
 Okano, Paul, Ph.D. Program Director
 Pelroy, Richard, Ph.D. Program Director
 Kim, Kelly Program Administrator
 Graham, Renee International Program Asst.




Biochemistry, Molecular Biology, Genetics, and Structural Biology of carcinogen
Biochemistry, molecular biology, genetics, and structural biology of carcinogen (e.g., radiation, chemicals, etc.)-induced and endogenous DNA repair mechanisms (e.g., nucleotide and base excision, recombination, mismatch repair pathways)

Cytogenetic and Molecular Structure/Function Analysis
Cytogenetic and molecular structure/function analysis of induced and spontaneous chromosome aberrations that are associated with genomic instability and cancer induction (e.g., translocations, deletions, fragile sites)

Discovery
Discovery, molecular mapping and characterization of new cancer genes

Epigenetic Mechanisms
Epigenetic mechanisms involved in gene silencing and cancer induction

Mechanisms of DNA damage
Mechanisms of DNA damage-inducible signaling, resulting perturbations to the cell-cycle, and regulation of apoptosis or other mechanisms of programmed cell death.



 

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