(Taken directly from the application) The techniques of modern mouse genetics have provided extremely important tools in biomedical research. The generation of transgenic mice has allowed investigators to examine the roles of genes involved in a wide variety of disease processes. The ability to generate specific mutations in genes of interest, including both knockouts and knock-ins, has expanded the power of this approach, allowing the identification of gene regulating immune responses and autoimmunity, as well as genes involved in susceptibility to disease. In addition, these techniques have provided a straightforward means to generate mouse models of important human diseases. The Transgenic/Knockout Mouse Core facility at UMMS currently generates transgenic mice for the analysis of gene function and regulation in intact animals. Transgenic animals are generated by pronuclear injection of DNA constructs into fertilized one-cell mouse embryos, followed by oviduct transfer of the injected embryos into foster mothers. The facility is currently expanding to provide gene targeting (knockout and knock-in) services. As of July 1998, the facility began providing the services of embryonic stem cell injections into 2.5 day mouse blastocysts, followed by uterine transfer of injected embryos into foster mothers. In the near future (by July 1999), the facility will begin providing embryonic stem cell culture services, assisting investigators in growing, transfecting, selecting, and cloning embryonic stem cells for gene targeting purposes.

Project Start
2001-04-01
Project End
2002-03-31
Budget Start
Budget End
Support Year
18
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Massachusetts Medical School Worcester
Department
Type
DUNS #
660735098
City
Worcester
State
MA
Country
United States
Zip Code
01655
Desai, Paurav B; San Agustin, Jovenal T; Stuck, Michael W et al. (2018) Ift25 is not a cystic kidney disease gene but is required for early steps of kidney development. Mech Dev 151:10-17
Ly, Socheata; Navaroli, Deanna M; Didiot, Marie-Cécile et al. (2017) Visualization of self-delivering hydrophobically modified siRNA cellular internalization. Nucleic Acids Res 45:15-25
Wang, Feng; McCannell, Kurtis N; Boškovi?, Ana et al. (2017) Rlim-Dependent and -Independent Pathways for X Chromosome Inactivation in Female ESCs. Cell Rep 21:3691-3699
Watkin, Levi B; Mishra, Rabinarayan; Gil, Anna et al. (2017) Unique influenza A cross-reactive memory CD8 T-cell receptor repertoire has a potential to protect against EBV seroconversion. J Allergy Clin Immunol 140:1206-1210
LeBlanc, Scott E; Wu, Qiong; Lamba, Pallavi et al. (2016) Promoter-enhancer looping at the PPAR?2 locus during adipogenic differentiation requires the Prmt5 methyltransferase. Nucleic Acids Res 44:5133-47
Wang, Feng; Shin, JongDae; Shea, Jeremy M et al. (2016) Regulation of X-linked gene expression during early mouse development by Rlim. Elife 5:
Kincaid, Eleanor Z; Murata, Shigeo; Tanaka, Keiji et al. (2016) Specialized proteasome subunits have an essential role in the thymic selection of CD8(+) T cells. Nat Immunol 17:938-45
Townsley, E; O'Connor, G; Cosgrove, C et al. (2016) Interaction of a dengue virus NS1-derived peptide with the inhibitory receptor KIR3DL1 on natural killer cells. Clin Exp Immunol 183:419-30
Wyss, Lena; Stadinski, Brian D; King, Carolyn G et al. (2016) Affinity for self antigen selects Treg cells with distinct functional properties. Nat Immunol 17:1093-101
Delong, Thomas; Wiles, Timothy A; Baker, Rocky L et al. (2016) Pathogenic CD4 T cells in type 1 diabetes recognize epitopes formed by peptide fusion. Science 351:711-4

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