The Jackson Laboratory (TJL) Cancer Center has 48 members organized into a single program, Gene Discovery and Analysis, Research focuses on genetic approaches for analyzing individual steps in the progression to cancer. In advancing this strategy, TJL researchers develop new tools for genetic analysis, which are used here and disseminated to the wider scientific community for work on the molecular and cellular bases of cancer. Virtually all TJL Cancer Center research uses genetically defined mice as the premier mammalian model for identifying and analyzing the genes that regulate these processes. Resources provided by the Cancer Center are the foundation of this research, supporting genome-scale gene discovery via QTL analysis, mutagenesis and positional cloning and functional analysis via gene targeting, transgenesis, phenotypic analyses, and expression arrays. The scientific leadership of TJL has direct oversight of the Cancer Center. Dr. Kenneth Paigen is the Director of TJL and the Cancer Center. Dr. Barbara Knowles, Associate Director of TJL and the Cancer Center, is also Director for Research at TJL and Program Leader at the Cancer Center. Support is requested for Scientific Resources and Services. Resources include the Mouse Models Resource, which provides spontaneous and induced mutant mice to Cancer Center staff, Cryopreservation and Rederivation Resource, for economical maintenance of strains at high health status, Veterinary Medicine Resource for ensuring animal health, the Diagnostic Laboratory Resource for consultation in clinical and anatomical pathology, and the Computational Biology Resource, which provides staff with access to expertise and analytical tools for advanced computational and statistical analysis. Scientific Services include Biological Imaging for complete histological analyses, Cell Biology and Microinjection for transgenic and targeted mutagenesis services, Flow Cytometry for a full suite of sorted and analysis services, and Microchemistry for molecular biological resources. Funds are requested for development of new techniques in these resources and services through a pilot program. Support is also requested for new investigators who will bring additional strength to the TJL Cancer Center's focus on mouse genomic and biological approaches to gene discovery in cancer research.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA034196-22S1
Application #
6943322
Study Section
Subcommittee G - Education (NCI)
Program Officer
Rosenfeld, Bobby
Project Start
1996-08-25
Project End
2006-07-31
Budget Start
2004-08-01
Budget End
2005-07-31
Support Year
22
Fiscal Year
2004
Total Cost
$68,445
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
Cho, Sung-Yup; Sung, Chang Ohk; Chae, Jeesoo et al. (2018) Alterations in the Rho pathway contribute to Epstein-Barr virus-induced lymphomagenesis in immunosuppressed environments. Blood 131:1931-1941
Pullagura, Sri Ramulu N; Buaas, Bill; Gray, Nichelle et al. (2018) Functional Redundancy of DICER Cofactors TARBP2 and PRKRA During Murine Embryogenesis Does Not Involve miRNA Biogenesis. Genetics 208:1513-1522
Kong, Yang; Naggert, Jürgen K; Nishina, Patsy M (2018) The Impact of Adherens and Tight Junctions on Physiological Function and Pathological Changes in the Retina. Adv Exp Med Biol 1074:545-551
Chang, Bo; FitzMaurice, Bernard; Wang, Jieping et al. (2018) Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele. Invest Ophthalmol Vis Sci 59:5127-5139
Sharma, Manju; Braun, Robert E (2018) Cyclical expression of GDNF is required for spermatogonial stem cell homeostasis. Development 145:
Shi, Jiayuan; Hua, Li; Harmer, Danielle et al. (2018) Cre Driver Mice Targeting Macrophages. Methods Mol Biol 1784:263-275
Hosur, Vishnu; Farley, Michelle L; Low, Benjamin E et al. (2018) RHBDF2-Regulated Growth Factor Signaling in a Rare Human Disease, Tylosis With Esophageal Cancer: What Can We Learn From Murine Models? Front Genet 9:233
Johnson, Kenneth R; Gagnon, Leona H; Tian, Cong et al. (2018) Deletion of a Long-Range Dlx5 Enhancer Disrupts Inner Ear Development in Mice. Genetics 208:1165-1179
Dominguez, Pilar M; Ghamlouch, Hussein; Rosikiewicz, Wojciech et al. (2018) TET2 Deficiency Causes Germinal Center Hyperplasia, Impairs Plasma Cell Differentiation, and Promotes B-cell Lymphomagenesis. Cancer Discov 8:1632-1653
Paigen, Kenneth; Petkov, Petko M (2018) PRDM9 and Its Role in Genetic Recombination. Trends Genet 34:291-300

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