The Gene Targeting and Transgenic Mouse (GTTM) Share Resource assists Cancer Center members who use animal models in constructing and managing genetically altered mouse strains. It is operated by Dr. Sang-Yong Kim, a microinjection expert, and is supervised by Dr. Jacek Skowronski (Associate Investigator). The GTTM Shared Resource is equipped with two microinjection stations and support equipment that allow for generation of transgenic mice by direct DNA injection into fertilized zygotes and construction of chimeric mice using Embryonic Stem (ES) cell technologies. Service provided by the GTTM Shared Resource will initially include generation of transgenic animal models by pro-nuclear injection, maintenance of ES cell line stocks capable of efficient germline contribution for use in gene targeting experiments, generation of chimeric mice with genetically altered ES cells, and mouse embryo cryopreservation services. Funds are requested for the equipment necessary to establish ES cell culture and embryo cryopreservation services. The GTTM Shared Resource was recently established to meet the rising demand for these services from the Cancer Center members that use animal models that use animal models in their research. We predict that the GTTM Shared Resource will become an important resource for cancer researchers at CSHL, further promoting scientific interactions between CSHL investigators, and at other research institutions around the world.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA045508-16
Application #
6617299
Study Section
Subcommittee G - Education (NCI)
Project Start
2002-08-01
Project End
2003-07-31
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
16
Fiscal Year
2002
Total Cost
$78,870
Indirect Cost
Name
Cold Spring Harbor Laboratory
Department
Type
DUNS #
065968786
City
Cold Spring Harbor
State
NY
Country
United States
Zip Code
11724
Arun, Gayatri; Diermeier, Sarah D; Spector, David L (2018) Therapeutic Targeting of Long Non-Coding RNAs in Cancer. Trends Mol Med 24:257-277
Giuliano, Christopher J; Lin, Ann; Smith, Joan C et al. (2018) MELK expression correlates with tumor mitotic activity but is not required for cancer growth. Elife 7:
Li, Jiahe; Wu, Connie; Wang, Wade et al. (2018) Structurally modulated codelivery of siRNA and Argonaute 2 for enhanced RNA interference. Proc Natl Acad Sci U S A 115:E2696-E2705
Tarumoto, Yusuke; Lu, Bin; Somerville, Tim D D et al. (2018) LKB1, Salt-Inducible Kinases, and MEF2C Are Linked Dependencies in Acute Myeloid Leukemia. Mol Cell 69:1017-1027.e6
Krishnan, Navasona; Konidaris, Konstantis F; Gasser, Gilles et al. (2018) A potent, selective, and orally bioavailable inhibitor of the protein-tyrosine phosphatase PTP1B improves insulin and leptin signaling in animal models. J Biol Chem 293:1517-1525
Borges, Filipe; Parent, Jean-Sébastien; van Ex, Frédéric et al. (2018) Transposon-derived small RNAs triggered by miR845 mediate genome dosage response in Arabidopsis. Nat Genet 50:186-192
Chen, Xiaoyin; Sun, Yu-Chi; Church, George M et al. (2018) Efficient in situ barcode sequencing using padlock probe-based BaristaSeq. Nucleic Acids Res 46:e22
Tonelli, Claudia; Chio, Iok In Christine; Tuveson, David A (2018) Transcriptional Regulation by Nrf2. Antioxid Redox Signal 29:1727-1745
Kumar, Vijay; Rosenbaum, Julie; Wang, Zihua et al. (2018) Partial bisulfite conversion for unique template sequencing. Nucleic Acids Res 46:e10
Lee, Je H (2018) Tracing single-cell histories. Science 359:521-522

Showing the most recent 10 out of 380 publications