A program is proposed to provide advanced training to pre-doctoral and postdoctoral fellows in the fundamentals of neuronal plasticity in the aging nervous system. The program has three key features. The first of these is Academic Bridging, whereby a principal focus will be to provide the students and fellows with concepts and research experience which address problems at the interface of basic and clinical problems in aging. This bridging will be reflected in the faculty participating in the program, the students and fellows admitted to the program, and the structure of the training program itself. Seminars and co-sponsorships by basic scientists and clinical researchers of students and fellows will assure that bridging concepts and practice will be emphasized. The second feature is Life Span Development. We believe that the aging process is part of a life span process, which should and can be investigated as part of a continuum from birth to death. Many conceptual and practical problems presently being addressed in early development are translatable to late stage aging. This translation of ideas and approaches from studies of development and adult plasticity will be a feature of the program. In general we believe that investigations of neuronal plasticity are at the very core of understanding late stage aging, since age-related decline often reflects a decrease in neuronal and functional plasticity. Thus understanding the limits and mechanisms of neuronal plasticity will clearly contribute to an understanding of aging and functional decline. In this program we will encourage the participants to address these age-related aspects of plasticity. The third key feature is that the program will be Multidisciplinary. By their very nature Neuroscience and Aging are multidisciplinary fields of investigation. The modern neuroscientist is required to understand and use methods and techniques from the full range of biological disciplines. The faculty in this program represent technical expertise in the fields of Molecular Genetics, Protein Chemistry, Cell Biology, Neurophysiology, Systems Analysis, Behavioral Pharmacology, Computational Neuroscience, and Clinical Neurology. Our goal is to train students to be able to work and think effectively in several of these areas, and this will be achieved by choosing the correct faculty, students, and fellows, and providing them a forum for discussion and interaction.
Hsu, Cynthia L; Lee, Elian X; Gordon, Kara L et al. (2018) MAP4K3 mediates amino acid-dependent regulation of autophagy via phosphorylation of TFEB. Nat Commun 9:942 |
Lake, Blue B; Chen, Song; Sos, Brandon C et al. (2018) Integrative single-cell analysis of transcriptional and epigenetic states in the human adult brain. Nat Biotechnol 36:70-80 |
Urgolites, Zhisen J; Smith, Christine N; Squire, Larry R (2018) Eye movements support the link between conscious memory and medial temporal lobe function. Proc Natl Acad Sci U S A 115:7599-7604 |
Lee, Ming-Hsiang; Siddoway, Benjamin; Kaeser, Gwendolyn E et al. (2018) Somatic APP gene recombination in Alzheimer's disease and normal neurons. Nature 563:639-645 |
Devarajan, Priyadharshini; Jones, Michael C; Kugler-Umana, Olivia et al. (2018) Pathogen Recognition by CD4 Effectors Drives Key Effector and Most Memory Cell Generation Against Respiratory Virus. Front Immunol 9:596 |
Meves, Jessica M; Geoffroy, Cédric G; Kim, Noah D et al. (2018) Oligodendrocytic but not neuronal Nogo restricts corticospinal axon sprouting after CNS injury. Exp Neurol 309:32-43 |
Daugherty, Daniel J; Marquez, Alexandra; Calcutt, Nigel A et al. (2018) A novel curcumin derivative for the treatment of diabetic neuropathy. Neuropharmacology 129:26-35 |
Cheng, Weiwei; Wang, Shaopeng; Mestre, Alexander A et al. (2018) C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2? phosphorylation. Nat Commun 9:51 |
Urgolites, Zhisen J; Hopkins, Ramona O; Squire, Larry R (2017) Medial temporal lobe and topographical memory. Proc Natl Acad Sci U S A 114:8626-8630 |
Ngolab, Jennifer; Trinh, Ivy; Rockenstein, Edward et al. (2017) Brain-derived exosomes from dementia with Lewy bodies propagate ?-synuclein pathology. Acta Neuropathol Commun 5:46 |
Showing the most recent 10 out of 109 publications