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Postdoctoral Program in Functional Neurogenomics

Postdoctoral Program in Functional Neurogenomics
功能神经基因组学博士后项目
批准号:
10621290
负责人:
ROGER J COLBRAN
金额:
$33.02万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
未结题
起止时间:
2002-07-15 至 2025-06-30

项目摘要

项目成果

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PROJECT SUMMARY The genetic inheritance of specific risk alleles is widely accepted as a major contributing factor to many, if not all, mental illnesses. Moreover, recent studies found that the precise epigenetic regulation of gene expression is critical for normal learning and memory processes and is often disrupted in the diseased brain. However, despite recent concerted efforts of numerous neuroscientists and physicians, the links between precise molecular and synaptic defects resulting from (epi)genetic variation and specific brain circuit abnormalities that result in particular behavioral disorders remain rather poorly understood. Given the ongoing avalanche of new genetic/genomic data associated with neuropsychiatric disorders, there is a rapidly expanding need to train the next generation of neuroscientists to be facile in both modern molecular genetic approaches in different model systems, as well as in cutting edge molecular bioinformatics techniques that are required to link individual genes to normal brain functions and disease processes. The over-arching goal of this multi-disciplinary postdoctoral Training Program in Functional Neurogenomics is to support a training pipeline that fosters the development of new investigators with these skills. This competing renewal application will demonstrate an advancement and evolution in both the available training mentors and in cutting edge inter-disciplinary technical capabilities that builds on the substantial prior successes of this long-running program. Our efforts are supported by significant ongoing investments by Vanderbilt in new neuroscience leadership, faculty, educational programs, technological expertise and core facilities. Taken together, this provides a robust and rigorous environment for trainees to gain expertise in opportunities afforded by genetic model systems, the translation of human genetic findings into construct-valid animal models, in vivo manipulations of molecules, cells and circuits using advanced approaches, and in capturing the epigenetic, physiological, and behavioral consequences of such manipulations. The Program Director is Roger J. Colbran, Ph.D., Professor and Interim Chair of the Department of Molecular Physiology & Biophysics. Dr. Colbran has a long-standing, well-funded program investigating molecular mechanisms involved in synaptic plasticity using multi-disciplinary approaches from biochemical structure-function to mouse genetics and behavior. The Co-Director, J. David Sweatt, Ph.D., was recently recruited to Vanderbilt as the Chair of the Department of Pharmacology and has previously served on both the NIMH Advisory Council and the NIMH intramural program Board of Scientific Councilors. Dr. Sweatt has made numerous highly-cited contributions to understanding mechanisms underlying learning and memory in previous positions at Baylor College of Medicine and UAB, with a particular recent focus on the role of epigenetics in cognition and neural plasticity. The program leadership has a long-standing commitment to mentoring the next generation of neuroscientists, with a strong track record of facilitating the establishment of enduring and productive research careers for their trainees.
期刊论文(95)
专著(0)
科研奖励(0)
会议论文
Sensitivity to outcome devaluation in operant tasks is better predicted by food restriction level than reinforcement training schedule in mice.
与小鼠的强化训练计划相比,通过食物限制水平可以更好地预测操作任务中对结果贬值的敏感性。
DOI: 10.1101/2023.02.23.529699
发表时间: 2023
期刊: bioRxiv : the preprint server for biology
影响因子: --
作者: [Chevée,Maxime, Kim,CourtneyJ, Crow,Nevin, Follman,EmmaG, Calipari,ErinS]
通讯作者: Calipari,ErinS
Tepsin binds LC3B to promote ATG9A export and delivery at the cell periphery.
Tepsin 结合 LC3B 以促进 ATG9A 在细胞外周的输出和递送。
DOI: 10.1101/2023.07.18.549521
发表时间: 2023
期刊: bioRxiv : the preprint server for biology
影响因子: --
作者: [Wallace,NatalieS, Gadbery,JohnE, Cohen,CameronI, Kendall,AmyK, Jackson,LaurenP]
通讯作者: Jackson,LaurenP
DOI: 10.1002/0471142905.hg0109s64
发表时间: 2010-01-01
期刊: Current protocols in human genetics
影响因子: --
作者: [Bush, William S, Haines, Jonathan]
通讯作者: Haines, Jonathan
Directed evolution of a sphingomyelin flippase reveals mechanism of substrate backbone discrimination by a P4-ATPase.
鞘磷脂翻转酶的定向进化揭示了 P4-ATP 酶区分底物主链的机制。
DOI: 10.1073/pnas.1525730113
发表时间: 2016
期刊: Proceedings of the National Academy of Sciences of the United States of America
影响因子: 11.1
作者: [Roland,BartholomewP, Graham,ToddR]
通讯作者: Graham,ToddR
47
    Molecular Neuropharmacology and Signaling of Histone H2A.Z
    • 批准号:
      9626431
    • 项目类别:
    • 资助金额:
      $39.25万
    • 财政年份:
      2017
    • 负责人:
      ROGER J COLBRAN
    • 依托单位:
    Molecular Neuropharmacology and Signaling of Histone H2A.Z
    • 批准号:
      9480880
    • 项目类别:
    • 资助金额:
      $39.25万
    • 财政年份:
      2017
    • 负责人:
      ROGER J COLBRAN
    • 依托单位:
    Molecular Neuropharmacology and Signaling of Histone H2A.Z
    • 批准号:
      10115117
    • 项目类别:
    • 资助金额:
      $39.25万
    • 财政年份:
      2017
    • 负责人:
      ROGER J COLBRAN
    • 依托单位:
    Postdoctoral Program in Functional Neurogenomics
    • 批准号:
      9386221
    • 项目类别:
    • 资助金额:
      $1.08万
    • 财政年份:
      2016
    • 负责人:
      ROGER J COLBRAN
    • 依托单位:
    海外基金