Core A functions to provide the leadership, interaction and co-ordination between the different projects of thePPG in order to facilitate them in meeting their scientific goals. It can be divided into two sections: scientificsupport and administrative support. Important functions of the scientific support will be: to organize and holdweekly meetings of the project leaders and key personnel, to hold executive meetings of the project leadersalone to review progress and scientific direction, and to hold annual reviews with an external advisory boardto review progress on the overall goals of the PPG as a whole.Important aspects of administrative support will be to monitor the dispersion of financial resources, monitorresearch allocations. The steering committee composed of all four project leaders will meet twice a year toreview expenditures and resource allocations for the projects and cores. The administrative core will also beresponsible for writing and transmitting the yearly progress report on the PPG, including the written report ofthe External Advisory Committee.An additional function of the administrative core will be to disseminate a program for seminars at Stanfordthat are broadly related to the scientific directions of the PPG. A final aspect of the scientific support will beto ensure that all investigators are using common reagents and cell strains to maintain uniformity inexperimental protocols.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA067166-12
Application #
7558957
Study Section
Special Emphasis Panel (ZCA1)
Project Start
Project End
Budget Start
2008-02-01
Budget End
2009-01-31
Support Year
12
Fiscal Year
2008
Total Cost
$112,127
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Saiki, Julie P; Cao, Hongbin; Van Wassenhove, Lauren D et al. (2018) Aldehyde dehydrogenase 3A1 activation prevents radiation-induced xerostomia by protecting salivary stem cells from toxic aldehydes. Proc Natl Acad Sci U S A 115:6279-6284
Olcina, Monica M; Kim, Ryan K; Melemenidis, Stavros et al. (2018) The tumour microenvironment links complement system dysregulation and hypoxic signalling?. Br J Radiol :20180069
Vilalta, Marta; Brune, Jourdan; Rafat, Marjan et al. (2018) The role of granulocyte macrophage colony stimulating factor (GM-CSF) in radiation-induced tumor cell migration. Clin Exp Metastasis 35:247-254
Tandon, Neha; Thakkar, Kaushik N; LaGory, Edward L et al. (2018) Generation of Stable Expression Mammalian Cell Lines Using Lentivirus. Bio Protoc 8:
Yang, Zhifen; Zhang, Jing; Jiang, Dadi et al. (2018) A Human Genome-Wide RNAi Screen Reveals Diverse Modulators that Mediate IRE1?-XBP1 Activation. Mol Cancer Res 16:745-753
Benej, Martin; Hong, Xiangqian; Vibhute, Sandip et al. (2018) Papaverine and its derivatives radiosensitize solid tumors by inhibiting mitochondrial metabolism. Proc Natl Acad Sci U S A 115:10756-10761
Rafat, Marjan; Aguilera, Todd A; Vilalta, Marta et al. (2018) Macrophages Promote Circulating Tumor Cell-Mediated Local Recurrence following Radiotherapy in Immunosuppressed Patients. Cancer Res 78:4241-4252
Castellini, Laura; Moon, Eui Jung; Razorenova, Olga V et al. (2017) KDM4B/JMJD2B is a p53 target gene that modulates the amplitude of p53 response after DNA damage. Nucleic Acids Res 45:3674-3692
VandeKopple, Matthew J; Wu, Jinghai; Baer, Lisa A et al. (2017) Stress-responsive HILPDA is necessary for thermoregulation during fasting. J Endocrinol 235:27-38
Peinado, Héctor; Zhang, Haiying; Matei, Irina R et al. (2017) Pre-metastatic niches: organ-specific homes for metastases. Nat Rev Cancer 17:302-317

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