This is the competitive renewal application of The Children's Hospital of Philadelphia (CHOP) MAPS/CHRC Grant. During the past granting period, we supported molecular research training and research of 16 MAPS Scholars during their transition from pediatric fellowship to faculty appointments (a total of 24 years on funding). At the date of preparation of this renewal application (11/96), each of these 16 holds an academic appointment in a department of pediatrics, and 12 have already been successful in obtaining additional extramural research support, including 2RO1s, 2 R29s, 5K08s, and a RW Johnson Minority Faculty K08 equivalent. Of the 4 who have not yet received additional extramural research support, 3 became MAPS Scholars only 5 months ago. Our MAPS/CHRC is based largely in the CHOP Abramson Research Building, a facility providing 138,000 square feet of wet lab space. The CHOP MAPS/CHRC Molecular Core is in this building, as are the laboratories of 23 of the 28 Established Investigators who will provide mentoring to our MAPS Scholars. We have also reached out to the University of Pennsylvania (U of P), immediately adjacent to CHOP, for Established Investigators--1 at the Wistar Institute, 2 at the Hughes Institute, and 2 in U of P Medical School basic science departments. Our renewal application requests New Program Development funds to support 5 MAPS Scholars/year. In order to amplify the effects of this important program, CHOP will waive all indirect cost recovery, and will match MAPS/CHRC support to the Molecular Core provided for MAPS Scholar usage. In addition, as during the previous granting period, the Department of Pediatrics of the University of Pennsylvania will provide internally generated funds to substantially supplement MAPS/CHRC New Program Development funds, in order to permit us to select and support a large proportion of our outstanding pool of MAPS Scholarship applicants.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Center Core Grants (P30)
Project #
5P30HD028815-10
Application #
6476768
Study Section
Special Emphasis Panel (ZHD1-DRG-H (03))
Program Officer
Grave, Gilman D
Project Start
1992-04-01
Project End
2002-11-30
Budget Start
2001-12-01
Budget End
2002-11-30
Support Year
10
Fiscal Year
2002
Total Cost
$337,796
Indirect Cost
Name
Children's Hospital of Philadelphia
Department
Type
DUNS #
073757627
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Shaikh, Tamim H; O'Connor, Ronald J; Pierpont, Mary Ella et al. (2007) Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms. Genome Res 17:482-91
Saitta, Sulagna C; Harris, Stacy E; McDonald-McGinn, Donna M et al. (2004) Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome. Am J Med Genet A 124A:313-7
Saitta, Sulagna C; Harris, Stacy E; Gaeth, Ann P et al. (2004) Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion. Hum Mol Genet 13:417-28
Cron, Randy Q (2003) CD154 transcriptional regulation in primary human CD4 T cells. Immunol Res 27:185-202
Ming, J E; Elkan, M; Tang, K et al. (2002) Type I bone morphogenetic protein receptors are expressed on cerebellar granular neurons and a constitutively active form of the type IA receptor induces cerebellar abnormalities. Neuroscience 114:849-57
Maris, J M; Guo, C; White, P S et al. (2001) Allelic deletion at chromosome bands 11q14-23 is common in neuroblastoma. Med Pediatr Oncol 36:24-7
Maris, J M; Guo, C; Blake, D et al. (2001) Comprehensive analysis of chromosome 1p deletions in neuroblastoma. Med Pediatr Oncol 36:32-6
McVeigh, K E; Mallee, J J; Lucente, A et al. (2000) Murine chromosome 16 telomeric region, homologous with human chromosome 21q22, contains the osmoregulatory Na(+)/myo-inositol cotransporter (SLC5A3) gene. Cytogenet Cell Genet 88:153-8
Korimilli, A; Gonzales, L W; Guttentag, S H (2000) Intracellular localization of processing events in human surfactant protein B biosynthesis. J Biol Chem 275:8672-9
Guttentag, S H; Beers, M F; Bieler, B M et al. (1998) Surfactant protein B processing in human fetal lung. Am J Physiol 275:L559-66

Showing the most recent 10 out of 39 publications