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This is a proposal to continue NINDS funding of a Core Facility at Brandeis University. This will allow us to fully exploit the three subcomponents that are now firmly established: a microarray and FACS facility, an imaging facility and a mouse/transgenic facility. They are the underpinnings of a large number of NINDS- funded and other neuroscience-relevant research projects on campus. We also propose major expansions of all three existing cores and the establishment of a fourth core. The microarray/FACS facility will be expanded to encompass proteomics thereby becoming the Genomics/Proteomics Core Facility. The imaging facility will be expanded to include Correlated Light and Electron Microscopy (CLEM) and ultra high- resolution cryo-fluorescence imaging thereby become the Imaging/CLEM Core Facility. The mouse/transgenic facility has recently added the capacity to produce Lentiviral vectors for transfection and transgenesis, and is now referred to as the Transgenic Mouse and Viral Transfection Core Facility. Finally, we will establish a new Computational Core Facility to support large scale neural simulations and computational biology projects as part of a large high-performance computing cluster. These additions will allow the Brandeis community to remain at the cutting edge technologically, and ensure that we can continue to generate exciting and ground-breaking new science. The projects supported by the cores are joined together through the shared interests of multiple neuroscience faculty members in basic as well disease- related aspects of brain and neuron function: cell identity, synaptic transmission and circuits, plasticity, behavior and its modulation. The proposed studies will exploit vertebrate and invertebrate model systems, with a strong emphasis on transgenic animals. They address basic and applied problems that are pertinent to a wide range of neurological and psychiatric diseases including disturbances of excitability, such as epilepsy, disturbances of sleep, waking and mood, neurodevelopmental disorders such as Autism and Rett Syndrome, neurodegenerative disorders, like Amyotrophic Lateral Sclerosis, and disturbances of long and short -term memory such as those that accompany Alzheimer's Disease and Schizophrenia.
期刊论文(20)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1093/nar/gkv1193
发表时间: 2015-12-15
期刊: Nucleic acids research
影响因子: 14.9
作者: [Rahman R, Chirn GW, Kanodia A, Sytnikova YA, Brembs B, Bergman CM, Lau NC]
通讯作者: Lau NC
DOI: 10.1371/journal.pgen.1005652
发表时间: 2015-11
期刊: PLoS genetics
影响因子: 4.5
作者: [Chirn GW, Rahman R, Sytnikova YA, Matts JA, Zeng M, Gerlach D, Yu M, Berger B, Naramura M, Kile BT, Lau NC]
通讯作者: Lau NC
DOI: 10.1523/jneurosci.3503-08.2009
发表时间: 2009-04-29
期刊: The Journal of neuroscience : the official journal of the Society for Neuroscience
影响因子: --
作者: [Luther JA, Birren SJ]
通讯作者: Birren SJ
DOI: 10.1016/j.neuron.2014.10.046
发表时间: 2014-12-03
期刊: NEURON
影响因子: 16.2
作者: [Yu, Yanxun V., Bell, Harold W., Glauser, Dominique A., Van Hooser, Stephen D., Goodman, Miriam B., Sengupta, Piali]
通讯作者: Sengupta, Piali
11
    2013 Chronobiology GRC/GRS
    • 批准号:
      8529855
    • 项目类别:
    • 资助金额:
      $2.8万
    • 财政年份:
      2013
    • 负责人:
      MICHAEL ROSBASH
    • 依托单位:
    A new tool for the cell-specific identification of RNA binding protein targets
    • 批准号:
      8640299
    • 项目类别:
    • 资助金额:
      $28.12万
    • 财政年份:
      2013
    • 负责人:
      MICHAEL ROSBASH
    • 依托单位:
    A new tool for the cell-specific identification of RNA binding protein targets
    • 批准号:
      8735924
    • 项目类别:
    • 资助金额:
      $28.21万
    • 财政年份:
      2013
    • 负责人:
      MICHAEL ROSBASH
    • 依托单位:
    Addressing Protein Synthesis Regulation within Small Numbers of Discrete Neurons
    • 批准号:
      10586226
    • 项目类别:
    • 资助金额:
      $40.63万
    • 财政年份:
      2013
    • 负责人:
      MICHAEL ROSBASH
    • 依托单位: