The Developmental Biology (DB) Training Program at Case Western Reserve University (CWRU) is entitled """"""""Normal and Abnormal Development"""""""". This program is in its 43rd year of existence as a funded NICHD training program. The proposed goal is to provide trainees with an understanding of fundamental biological processes underlying embryonic development as well as the means to analyze them at the molecular, cellular, and organismal levels. The developmental biologist today combines the perspectives of classical embryology and modern developmental biology with methods of genetics, biochemistry, cell and molecular biology. The DB Training Program couples didactic training with laboratory experience featuring multiple approaches in vertebrate and invertebrate systems. The training program has several components, including: (1) a wide range of research opportunities, (2) a curriculum in developmental genetics and neurobiology that is coupled with training in cell and molecular biology, (3) the longest running Journal Club in CWRU history, (4) a yearly Scientific Retreat, (5) a yearly Student Symposium, (6) a dinner meeting with the program director to discuss improvements to the program and implementation of new initiatives, and (7) an annual review of trainees progress. Trainees will be well equipped to address fundamental problems in Developmental Biology, allowing them to apply knowledge and skills to important questions of normal and abnormal development as well as repair of developmental disorders. Two program directors, Drs. Peter Harte of the Department of Genetics and Lynn Landmesser of the Department of Neurosciences, administer the DB Training Program. Predoctoral trainees are selected from those admitted through the interdepartmental Biomedical Sciences Training Program or through direct admission to individual departmental programs. Postdoctoral trainees apply directly to individual trainers. Applications for support by the DB Training Program are reviewed by the Steering Committee, consisting of trainers from participating departments. The most promising applicants, as judged by a variety of criteria, are selected for support for a maximum of three years, subject to successful yearly review by the Steering Committee. Training laboratories are located in several departments at CWRU, including Genetics, Neurosciences, Molecular Biology, Biochemistry, Pharmacology, Physiology and Biophysics and Biology. An extensive core infrastructure offers an outstanding research environment for trainees. ? ? ?

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Institutional National Research Service Award (T32)
Project #
5T32HD007104-32
Application #
7425902
Study Section
Pediatrics Subcommittee (CHHD)
Program Officer
Javois, Lorette Claire
Project Start
1977-07-01
Project End
2011-04-30
Budget Start
2008-05-01
Budget End
2009-04-30
Support Year
32
Fiscal Year
2008
Total Cost
$265,617
Indirect Cost
Name
Case Western Reserve University
Department
Genetics
Type
Schools of Medicine
DUNS #
077758407
City
Cleveland
State
OH
Country
United States
Zip Code
44106
Turk, Edward M; Das, Vaijayanti; Seibert, Ryan D et al. (2013) The mitochondrial RNA landscape of Saccharomyces cerevisiae. PLoS One 8:e78105
Guan, D; Factor, D; Liu, Yu et al. (2013) The epigenetic regulator UHRF1 promotes ubiquitination-mediated degradation of the tumor-suppressor protein promyelocytic leukemia protein. Oncogene 32:3819-28
Mason-Suares, Heather; Tie, Feng; Yan, Christopher M et al. (2013) Polycomb silencing of the Drosophila 4E-BP gene regulates imaginal disc cell growth. Dev Biol 380:111-24
Bernardo, G M; Bebek, G; Ginther, C L et al. (2013) FOXA1 represses the molecular phenotype of basal breast cancer cells. Oncogene 32:554-63
Aranjuez, George; Kudlaty, Elizabeth; Longworth, Michelle S et al. (2012) On the role of PDZ domain-encoding genes in Drosophila border cell migration. G3 (Bethesda) 2:1379-91
Stepanik, Vincent A; Harte, Peter J (2012) A mutation in the E(Z) methyltransferase that increases trimethylation of histone H3 lysine 27 and causes inappropriate silencing of active Polycomb target genes. Dev Biol 364:249-58
Chau, Johnnie; Kulnane, Laura Shapiro; Salz, Helen K (2012) Sex-lethal enables germline stem cell differentiation by down-regulating Nanos protein levels during Drosophila oogenesis. Proc Natl Acad Sci U S A 109:9465-70
Hector, Ronald E; Ray, Alo; Chen, Bo-Ruei et al. (2012) Mec1p associates with functionally compromised telomeres. Chromosoma 121:277-90
Fox, Stephanie R; Deneris, Evan S (2012) Engrailed is required in maturing serotonin neurons to regulate the cytoarchitecture and survival of the dorsal raphe nucleus. J Neurosci 32:7832-42
Majumder, Pralay; Aranjuez, George; Amick, Joseph et al. (2012) Par-1 controls myosin-II activity through myosin phosphatase to regulate border cell migration. Curr Biol 22:363-72

Showing the most recent 10 out of 78 publications