Center PI: Malenka, Robert C. Principal Investigator: Malenka, Robert C. Administrative Core Summary The Administrative Core will oversee and provide administrative support for all Conte Center activities. It will be run by the Conte Center director (Malenka) and consist of one full time Conte Center administrator who will be assisted by a departmental administrator with expertise in financial grants management. The administrators will manage budgets, order supplies, monitor inventory, arrange travel and meetings for Center investigators and the External Scientific Advisory Board, maintain the web site, assist in the dissemination of reagents and findings generated by the Conte Center, and provide general administrative and secretarial support. The Administrative Core will be located in the office suite shared by Dr.'s Malenka and Sudhof. Relevance To achieve its stated goals in the most efficient and cost-effective manner, the Conte Center will require an Administrative Core that will provide administrative support to all Center investigators and assist in the dissemination of reagents and findings generated by the Center.

Public Health Relevance

Center PI: Malenka, Robert C. Principal Investigator: Malenka, Robert C. Administrative Core Narrative To achieve its stated goals in the most efficient and cost-effective manner, the Conte Center will require an Administrative Core that will provide administrative support to all Center investigators and assist in the dissemination of reagents and findings generated by the Center.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Specialized Center (P50)
Project #
5P50MH086403-10
Application #
9635815
Study Section
Special Emphasis Panel (ZMH1)
Project Start
Project End
Budget Start
2019-02-01
Budget End
2020-01-31
Support Year
10
Fiscal Year
2019
Total Cost
Indirect Cost
Name
Stanford University
Department
Type
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Zhang, Zhenjie; Marro, Samuele G; Zhang, Yingsha et al. (2018) The fragile X mutation impairs homeostatic plasticity in human neurons by blocking synaptic retinoic acid signaling. Sci Transl Med 10:
Bhouri, Mehdi; Morishita, Wade; Temkin, Paul et al. (2018) Deletion of LRRTM1 and LRRTM2 in adult mice impairs basal AMPA receptor transmission and LTP in hippocampal CA1 pyramidal neurons. Proc Natl Acad Sci U S A 115:E5382-E5389
Südhof, Thomas C (2018) Towards an Understanding of Synapse Formation. Neuron 100:276-293
Li, Jie; Park, Esther; Zhong, Lei R et al. (2018) Homeostatic synaptic plasticity as a metaplasticity mechanism?-?a molecular and cellular perspective. Curr Opin Neurobiol 54:44-53
Sclip, Alessandra; Acuna, Claudio; Luo, Fujun et al. (2018) RIM-binding proteins recruit BK-channels to presynaptic release sites adjacent to voltage-gated Ca2+-channels. EMBO J 37:
Wu, Dick; Bacaj, Taulant; Morishita, Wade et al. (2017) Postsynaptic synaptotagmins mediate AMPA receptor exocytosis during LTP. Nature 544:316-321
Südhof, Thomas C (2017) Synaptic Neurexin Complexes: A Molecular Code for the Logic of Neural Circuits. Cell 171:745-769
Liu, Zhihui; Chen, Zijun; Shang, Congping et al. (2017) IGF1-Dependent Synaptic Plasticity of Mitral Cells in Olfactory Memory during Social Learning. Neuron 95:106-122.e5
Jiang, M; Polepalli, J; Chen, L Y et al. (2017) Conditional ablation of neuroligin-1 in CA1 pyramidal neurons blocks LTP by a cell-autonomous NMDA receptor-independent mechanism. Mol Psychiatry 22:375-383
Zhou, Qiangjun; Zhou, Peng; Wang, Austin L et al. (2017) The primed SNARE-complexin-synaptotagmin complex for neuronal exocytosis. Nature 548:420-425

Showing the most recent 10 out of 65 publications