(prepared by applicant): The objectives of the proposed UCLA Child Health Research Career Development Award (CHRCDA) include: l) To increase the number and effectiveness of pediatric scientists engaged in human and molecular development research applied to child health problems through mentoring by the CHRCDA Faculty Member, the Principal Investigator/Core Laboratory Director, the Program Director, Core Laboratory Staff, the CHRCDA Scientific Advisory Board, the External Advisory Board, the Department of Pediatrics promotion and tenure mentor, the annual workshops (How to Succeed in Academics, Leadership and Grants), and the weekly research sessions (Translational Course, Work in Progress Seminars, Human and Molecular Development Research Seminars, and Developmental Biology Journal Club); 2) To facilitate the research activities of the CHRCDA Scholars and Faculty Mentors by providing the Human and Molecular Development Core Laboratory to complement and extend their research capabilities in a cost-effective manner; and 3) To provide increased opportunities for creative interdisciplinary approaches to pediatric disease by bringing together investigators interested in human and molecular development applications to clinical medicine through the use of the Core Laboratory and the monthly research seminars. To accomplish these objectives, the proposed UCLA CHRCDA has recruited 56 Faculty Mentors from 14 departments and 24 potential CHRCDA Scholars and continued the Human and Molecular Development Core Laboratory, the three annual workshops and the weekly research sessions. This application represents a competitive renewal of the UCLA Child Health Research Center (1996-2001) that supported 11 Scholars. The UCLA CHRC Scholars currently hold three R01s, two P0l projects, one R21, three K08s, and private foundation grants. They have seven R0l and two K08 applications pending. Since the inception of their CHRC support, their publications have increased from 103 to 178.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Physician Scientist Award (Program) (PSA) (K12)
Project #
5K12HD034610-07
Application #
6620962
Study Section
Special Emphasis Panel (ZHD1-MCHG-B (20))
Program Officer
Winer, Karen
Project Start
2002-02-15
Project End
2006-11-30
Budget Start
2002-12-01
Budget End
2003-11-30
Support Year
7
Fiscal Year
2003
Total Cost
$432,000
Indirect Cost
Name
University of California Los Angeles
Department
Pediatrics
Type
Schools of Medicine
DUNS #
092530369
City
Los Angeles
State
CA
Country
United States
Zip Code
90095
Calkins, Kara L; Thamotharan, Shanthie; Dai, Yun et al. (2018) Early dietary restriction in rats alters skeletal muscle tuberous sclerosis complex, ribosomal s6 and mitogen-activated protein kinase. Nutr Res 54:93-104
Kuo, Caroline Y; Long, Joseph D; Campo-Fernandez, Beatriz et al. (2018) Site-Specific Gene Editing of Human Hematopoietic Stem Cells for X-Linked Hyper-IgM Syndrome. Cell Rep 23:2606-2616
Chen, Pao-Yang; Chu, Alison; Liao, Wen-Wei et al. (2018) Prenatal Growth Patterns and Birthweight Are Associated With Differential DNA Methylation and Gene Expression of Cardiometabolic Risk Genes in Human Placentas: A Discovery-Based Approach. Reprod Sci 25:523-539
Gell, Joanna J; Zhao, Jasmine; Chen, Di et al. (2018) PRDM14 is expressed in germ cell tumors with constitutive overexpression altering human germline differentiation and proliferation. Stem Cell Res 27:46-56
Kuo, Caroline Y; Garcia-Lloret, Maria I; Slev, Patricia et al. (2017) Profound T-cell lymphopenia associated with prenatal exposure to purine antagonists detected by TREC newborn screening. J Allergy Clin Immunol Pract 5:198-200
Williams, Carmen J; Chu, Alison; Jefferson, Wendy N et al. (2017) Epithelial membrane protein 2 (EMP2) deficiency alters placental angiogenesis, mimicking features of human placental insufficiency. J Pathol 242:246-259
Truscott, Laurel; Gell, Joanna; Chang, Vivian Y et al. (2017) Novel association of familial testicular germ cell tumor and autosomal dominant polycystic kidney disease with PKD1 mutation. Pediatr Blood Cancer 64:100-102
Ha, V L; Luong, A; Li, F et al. (2017) The T-ALL related gene BCL11B regulates the initial stages of human T-cell differentiation. Leukemia 31:2503-2514
Hanudel, Mark R; Salusky, Isidro B (2017) Treatment of Pediatric Chronic Kidney Disease-Mineral and Bone Disorder. Curr Osteoporos Rep 15:198-206
Upadhyay, Shivani Y; De Oliveira, Satiro N; Moore, Theodore B (2017) Use of Rapamycin in a Patient With Juvenile Myelomonocytic Leukemia: A Case Report. J Investig Med High Impact Case Rep 5:2324709617728528

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