The Technology Core will play a major role in the Stanford Systems Biology Center by providing center researchers with the latest technology, training them in proper usage, and helping with experimental design. In addition, this core will be a very valuable asset to the national and international Systems Biology community since it will be a central place for disseminating knowledge, technology, and reagents from the Pis associated with this core who are all leaders in developing new cutting-edge approaches to monitor and perturb the signaling and transcriptional networks that control cell decision processes.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Specialized Center (P50)
Project #
5P50GM107615-02
Application #
8743225
Study Section
Special Emphasis Panel (ZGM1)
Project Start
Project End
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
City
Stanford
State
CA
Country
United States
Zip Code
94304
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Saldivar, Joshua C; Hamperl, Stephan; Bocek, Michael J et al. (2018) An intrinsic S/G2 checkpoint enforced by ATR. Science 361:806-810
Dobens, Leonard L; Shipman, Anna; Axelrod, Jeffrey D (2018) FijiWingsPolarity: An open source toolkit for semi-automated detection of cell polarity. Fly (Austin) 12:23-33
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Cheng, Xianrui; Ferrell Jr, James E (2018) Apoptosis propagates through the cytoplasm as trigger waves. Science 361:607-612
Breslow, David K; Hoogendoorn, Sascha; Kopp, Adam R et al. (2018) A CRISPR-based screen for Hedgehog signaling provides insights into ciliary function and ciliopathies. Nat Genet 50:460-471
Cappell, Steven D; Mark, Kevin G; Garbett, Damien et al. (2018) EMI1 switches from being a substrate to an inhibitor of APC/CCDH1 to start the cell cycle. Nature 558:313-317
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Bahrami-Nejad, Zahra; Zhao, Michael L; Tholen, Stefan et al. (2018) A Transcriptional Circuit Filters Oscillating Circadian Hormonal Inputs to Regulate Fat Cell Differentiation. Cell Metab 27:854-868.e8
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