To train predoctoral students in Neurobiology, 60 cooperating faculty propose continuation of broad, interdisciplinary predoctoral training program with approximately 90 total students in fall, 2005. These faculty members have research interests in molecular, cellular, developmental, systems, and medical neurobiology. They have appointments in several basic science and clinical departments with fully equipped, funded laboratories, mostly on the main U.C.S.F. campus at Parnassus Heights. We anticipate approximately 10 additional faculty will join our graduate program during the next five years. Interactions benefiting trainees will be promoted by an annual retreat, a weekly seminar series, a weekly student-faculty journal club, and student journal/pizza club meetings. Neuroscience training will be conducted within the broader context of the Boyer Program in Biological Sciences (P.I.B.S.), a consortium of 7 graduate programs with 185 total faculty. A weekly P.I.B.S. journal club, plus seminar series and retreats sponsored by the other P.I.B.S. programs will promote the broader education of our students and their interactions with the faculty and students of these programs. During the next 5 years, the number of our students at the beginning of each academic year is anticipated to be 80-to-95, approximately the same size as at present. We will continue major efforts to recruit under-represented minorities, the major selection criteria for all trainees will be originality, commitment and scientific potential. In the 1st year, students will take a three quarter core course which covers a span of topics ranging from membrane biophysics to systems and cognitive neuroscience. Students will rotate in 3 laboratories that will introduce them to different areas of neuroscience investigation. After these students will take at least 4 advanced seminar/discussion courses, exploring in depth subjects of particular importance. These will provide students will analytical skills, current knowledge and experience in making formal and informal scientific presentations. Near the end of the first year, trainees will choose Ph.D. thesis research mentors. During the 2 year, the proposed thesis project will be described in a written proposal. During a qualifying examination, the importance, scope and feasibility of this project will be defended. The exam will also test knowledge and analytical abilities in broader areas of Neuroscience. Training in later years will focus on the research required for a Ph.D. thesis, but will be supplemented by seminars, conferences, and journal clubs. Our goal is to facilitate the intellectual growth and development of scientific skills of new investigators committed to solving major problems in Neuroscience and to making positive contributions to education in the 21st Century.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Institutional National Research Service Award (T32)
Project #
5T32GM007449-35
Application #
8091389
Study Section
National Institute of General Medical Sciences Initial Review Group (BRT)
Program Officer
Maas, Stefan
Project Start
1977-09-01
Project End
2012-06-30
Budget Start
2011-07-01
Budget End
2012-06-30
Support Year
35
Fiscal Year
2011
Total Cost
$453,538
Indirect Cost
Name
University of California San Francisco
Department
Physiology
Type
Schools of Medicine
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94143
Clemente-Perez, Alexandra; Makinson, Stefanie Ritter; Higashikubo, Bryan et al. (2017) Distinct Thalamic Reticular Cell Types Differentially Modulate Normal and Pathological Cortical Rhythms. Cell Rep 19:2130-2142
Silberberg, Shanni N; Taher, Leila; Lindtner, Susan et al. (2016) Subpallial Enhancer Transgenic Lines: a Data and Tool Resource to Study Transcriptional Regulation of GABAergic Cell Fate. Neuron 92:59-74
Silbereis, John C; Nobuta, Hiroko; Tsai, Hui-Hsin et al. (2014) Olig1 function is required to repress dlx1/2 and interneuron production in Mammalian brain. Neuron 81:574-87
Yuen, Tracy J; Silbereis, John C; Griveau, Amelie et al. (2014) Oligodendrocyte-encoded HIF function couples postnatal myelination and white matter angiogenesis. Cell 158:383-396
Gorczyca, David A; Younger, Susan; Meltzer, Shan et al. (2014) Identification of Ppk26, a DEG/ENaC Channel Functioning with Ppk1 in a Mutually Dependent Manner to Guide Locomotion Behavior in Drosophila. Cell Rep 9:1446-58
Pattabiraman, Kartik; Golonzhka, Olga; Lindtner, Susan et al. (2014) Transcriptional regulation of enhancers active in protodomains of the developing cerebral cortex. Neuron 82:989-1003
McKinsey, Gabriel L; Lindtner, Susan; Trzcinski, Brett et al. (2013) Dlx1&2-dependent expression of Zfhx1b (Sip1, Zeb2) regulates the fate switch between cortical and striatal interneurons. Neuron 77:83-98
Visel, Axel; Taher, Leila; Girgis, Hani et al. (2013) A high-resolution enhancer atlas of the developing telencephalon. Cell 152:895-908
Seybold, Bryan A; Stanco, Amelia; Cho, Kathleen K A et al. (2012) Chronic reduction in inhibition reduces receptive field size in mouse auditory cortex. Proc Natl Acad Sci U S A 109:13829-34
Peterson, B E; Merzenich, M M (1995) EXP: a Macintosh program for automating data acquisition and analysis applied to neurophysiology. J Neurosci Methods 57:121-31

Showing the most recent 10 out of 15 publications