This application is a request for funds to continue to support the training of graduate students in Cell and Developmental Biology (CDB) at Harvard Medical School. Support for 20 (of -120) first and second year students from the transdepartmental Biological and Biomedical Sciences Program [BBS]) is requested. The 82 faculty program in Cell and Developmental Biology of Harvard Medical School is one of the major components of the BBS program (with 379 graduate students and 245 faculty). Our goal is to provide students with a foundation in cell and developmental biological that is necessary develop sound scientific hypotheses, to think broadly and critically about their research and that of others, and to have a strong grounding in methodologies used by cell and developmental biologists. Our ultimate goal is to train our students to become independent and creative researchers and scholars. Our faculty are from the departments of Biological Chemistry and Molecular Pharmacology, Cell Biology, Genetics, Microbiology and Molecular Genetics, and Pathology at Harvard Medical School. The research activities of the program faculty on this training grant are concentrated in the following areas: basic cellular processes (29), developmental biology (37), cell cycle (28), tumorigenesis, and cancer (28), RNA and chromosome biology (15), biological machines and signaling networks (35), stem cell biology (5), technology development (11). Apart from """"""""traditional"""""""" teaching approaches that will cover broader topics in the form of courses, seminars and discussions we are initiating a few novel teaching approaches to provide a dynamic and integrative educational experience to our students. In addition, we have also included many formats to provide students with opportunities to interact with the faculty and to be exposed to career mentoring. Relevance: Research in the areas of Cell and Developmental Biology is a conduit to understanding the molecular underpinnings of human biology and pathology. Studies of model systems, such as yeast, worms, frogs, and mice, as well as in vitro models of human cells, have become an essential tool for medicine. ? ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
2T32GM007226-32
Application #
7066805
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Zatz, Marion M
Project Start
1975-07-01
Project End
2011-06-30
Budget Start
2006-07-01
Budget End
2007-06-30
Support Year
32
Fiscal Year
2006
Total Cost
$642,341
Indirect Cost
Name
Harvard University
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
047006379
City
Boston
State
MA
Country
United States
Zip Code
02115
Giacomelli, Andrew O; Yang, Xiaoping; Lintner, Robert E et al. (2018) Mutational processes shape the landscape of TP53 mutations in human cancer. Nat Genet 50:1381-1387
Najm, Fadi J; Strand, Christine; Donovan, Katherine F et al. (2018) Orthologous CRISPR-Cas9 enzymes for combinatorial genetic screens. Nat Biotechnol 36:179-189
Egusquiaguirre, Susana P; Yeh, Jennifer E; Walker, Sarah R et al. (2018) The STAT3 Target Gene TNFRSF1A Modulates the NF-?B Pathway in Breast Cancer Cells. Neoplasia 20:489-498
Jih, Gloria; Iglesias, Nahid; Currie, Mark A et al. (2017) Unique roles for histone H3K9me states in RNAi and heritable silencing of transcription. Nature 547:463-467
Jamuar, Saumya S; Schmitz-Abe, Klaus; D'Gama, Alissa M et al. (2017) Biallelic mutations in human DCC cause developmental split-brain syndrome. Nat Genet 49:606-612
Bezzerides, Vassilios J; Zhang, Aifeng; Xiao, Ling et al. (2017) Inhibition of serum and glucocorticoid regulated kinase-1 as novel therapy for cardiac arrhythmia disorders. Sci Rep 7:346
Huang, Julie; Iglesias, Nahid; Moazed, Danesh (2017) Evaluation of the Nucleolar Localization of the RENT Complex to Ribosomal DNA by Chromatin Immunoprecipitation Assays. Methods Mol Biol 1505:195-213
D'Gama, Alissa M; Woodworth, Mollie B; Hossain, Amer A et al. (2017) Somatic Mutations Activating the mTOR Pathway in Dorsal Telencephalic Progenitors Cause a Continuum of Cortical Dysplasias. Cell Rep 21:3754-3766
Lim, Elaine T; Uddin, Mohammed; De Rubeis, Silvia et al. (2017) Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder. Nat Neurosci 20:1217-1224
Ubellacker, Jessalyn M; Haider, Marie-Therese; DeCristo, Molly J et al. (2017) Zoledronic acid alters hematopoiesis and generates breast tumor-suppressive bone marrow cells. Breast Cancer Res 19:23

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