Transgenic and knockout technologies are an extremely powerful set of tools used increasingly to investigate normal development and physiological processes, as well as a variety of disease processes, including cancer. Rapid progress in molecular epidemiology and genomic approaches to cancer now promise an explosive increase in the rate of identification of genetic loci associated with cancer. Any understanding of how such loci function in normal and pathological processes will depend heavily on experiments in genetically altered mice. The Transgenic Core Facility was established in April 1993 with Developmental Funds from the Cancer Center Support Grant. The primary services provided by the technical staff of the Transgenic Core Facility are the production of transgenic mice by pro-nuclear injection and the production of knockout by ES cell injection into blastocysts. The Core can also assist with genotyping of mice, and proposes to expand this service in a joint venture with the Genomics Core Facility. Finally, the Core provides advice and expert consultation on vector preparation, mouse developmental biology, and methods and approaches to testing gene function in mice. Dr. Robert Maxson, Professor of Biochemistry and Molecular Biology, directs the Transgenic Core Facility and has extensive experience with transgenic and knockout mice. The facility is staffed by Frank Sangiorgi, Ph.D., who manages the facility. Dr. Nancy Wu. Who performs most of the DNA injections and egg manipulations and Ms. Youzhen Yan, who monitors the mice and performs various technical services. The facility is located on the 7th floor of the Norris building in Cancer Center Vivarium space and consists of a microinjection room and two dedicated mouse holding rooms.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
3P30CA014089-27S1
Application #
6577717
Study Section
Project Start
2002-04-02
Project End
2002-11-30
Budget Start
Budget End
Support Year
27
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of Southern California
Department
Type
DUNS #
041544081
City
Los Angeles
State
CA
Country
United States
Zip Code
90033
Suenaga, Mitsukuni; Schirripa, Marta; Cao, Shu et al. (2018) Potential role of PIN1 genotypes in predicting benefit from oxaliplatin-based and irinotecan-based treatment in patients with metastatic colorectal cancer. Pharmacogenomics J 18:623-632
Singh, Hardeep P; Wang, Sijia; Stachelek, Kevin et al. (2018) Developmental stage-specific proliferation and retinoblastoma genesis in RB-deficient human but not mouse cone precursors. Proc Natl Acad Sci U S A 115:E9391-E9400
Tsai, Yuan-Li; Ha, Dat P; Zhao, He et al. (2018) Endoplasmic reticulum stress activates SRC, relocating chaperones to the cell surface where GRP78/CD109 blocks TGF-? signaling. Proc Natl Acad Sci U S A 115:E4245-E4254
Rodrigues, Luana L S; Morgado, Mariza G; Sahasrabuddhe, Vikrant V et al. (2018) Cervico-vaginal self-collection in HIV-infected and uninfected women from Tapajós region, Amazon, Brazil: High acceptability, hrHPV diversity and risk factors. Gynecol Oncol 151:102-110
Valentin-Torres, Alice; Savarin, Carine; Barnett, Joslyn et al. (2018) Blockade of sustained tumor necrosis factor in a transgenic model of progressive autoimmune encephalomyelitis limits oligodendrocyte apoptosis and promotes oligodendrocyte maturation. J Neuroinflammation 15:121
Ricker, Charité N; Koff, Rachel B; Qu, Chenxu et al. (2018) Patient communication of cancer genetic test results in a diverse population. Transl Behav Med 8:85-94
Jayne, Jordanna G; Bensman, Timothy J; Schaal, Justin B et al. (2018) Rhesus ?-Defensin-1 Attenuates Endotoxin-induced Acute Lung Injury by Inhibiting Proinflammatory Cytokines and Neutrophil Recruitment. Am J Respir Cell Mol Biol 58:310-319
Tobin, Jessica; Miller, Kimberly A; Baezconde-Garbanati, Lourdes et al. (2018) Acculturation, Mental Health, and Quality of Life among Hispanic Childhood Cancer Survivors: A Latent Class Analysis. Ethn Dis 28:55-60
Harris, Holly R; Babic, Ana; Webb, Penelope M et al. (2018) Polycystic Ovary Syndrome, Oligomenorrhea, and Risk of Ovarian Cancer Histotypes: Evidence from the Ovarian Cancer Association Consortium. Cancer Epidemiol Biomarkers Prev 27:174-182
Lee, Brian H; Stallcup, Michael R (2018) Different chromatin and DNA sequence characteristics define glucocorticoid receptor binding sites that are blocked or not blocked by coregulator Hic-5. PLoS One 13:e0196965

Showing the most recent 10 out of 842 publications