description): The candidate is a neonatology sub specialist in the field of pediatrics who has sought to develop a career in academic medicine since the outset of his pediatric training. The goal during this period will be to generate more skills necessary to enable the candidate to become a productive independent investigator. Recently in mice, the investigators have generated a series of mutations at the Fgf8 gene locus utilizing transgenic cre and Flp recombinase technology. Using this strategy they have created a null allele, a hypomorphic allele as well as an allele of Fgf8 that can be used in tissue specific gene elimination experiments. The experiments proposed are designed to examine the role of Fgf8 in LR axis determination and cardiac development. Particular attention will be paid to interactions between Fgf8 and Tgf-beta family members in the generation of LR asymmetry and to define the range of abnormalities seen in the compound heterozygous mutants. Experiments will be performed to analyze this phenotype and the molecular pathways involved in the generation of LR asymmetry and cardiac defects associated with abnormalities of LR axis determination. These cardiac defects include transposition of the great vessels, the most common congenital cyanotic heart disease in humans.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Clinical Investigator Award (CIA) (K08)
Project #
5K08HD001216-06
Application #
6520608
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Javois, Lorette Claire
Project Start
1998-08-01
Project End
2004-06-30
Budget Start
2002-07-01
Budget End
2004-06-30
Support Year
6
Fiscal Year
2002
Total Cost
$79,380
Indirect Cost
Name
Duke University
Department
Pediatrics
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
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Sun, X; Lewandoski, M; Meyers, E N et al. (2000) Conditional inactivation of Fgf4 reveals complexity of signalling during limb bud development. Nat Genet 25:83-6
Sun, X; Meyers, E N; Lewandoski, M et al. (1999) Targeted disruption of Fgf8 causes failure of cell migration in the gastrulating mouse embryo. Genes Dev 13:1834-46
Meyers, E N; Martin, G R (1999) Differences in left-right axis pathways in mouse and chick: functions of FGF8 and SHH. Science 285:403-6