Training Program in the Genetic Basis of Pediatric Gastrointestinal Disorders

儿科胃肠道疾病遗传基础培训计划

基本信息

  • 批准号:
    8883521
  • 负责人:
  • 金额:
    $ 13.64万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2014
  • 资助国家:
    美国
  • 起止时间:
    2014-07-01 至 2019-06-30
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Training in the genetic basis of pediatric gastrointestinal disorders: The revolutions in genetics and genomics have led to discoveries in a range of GI diseases, many of which affect the health of children. Pediatric gastroenterologists who are trained in genetic research will be essential in the effort to identify novel genetic cause of GI disease, reveal their molecular mechanisms, and translate them into therapy. The outstanding laboratory, translational, and clinical research at CHOP and the Perelman School of Medicine (PSOM) present an ideal environment for research career development in the genetics of pediatric GI disease. The overarching goals of the this training program are to: Train a cadre of committed researchers to investigate the genetic basis of pediatric GI disease and to use this knowledge to improve the health of children and adults. Provide these individuals with the skill sets and foundation for career advancement. Encourage innovation and leadership in academic pediatric GI. The Specific Aims of this training program are to: Identify, recruit and foster the career development of post-doctoral research trainees from the pool of CHOP GI fellows, PSOM GI fellows, and other scientists committed to training and career development in the genetics of pediatric gastrointestinal disease. Match trainee strengths and interests with mentoring teams. Provide intensive mentored research experience and training with dedicated faculty. Provide career mentoring, including training on successful grant and manuscript preparation. Bring together faculty and fellows through seminar series and other academic activities to create a collaborative community of physician-scientists. Provide guidance for structured learning opportunities on the principles of genetic research, including research ethics and the protection of animal and human subjects. To achieve these goals, we have designed a training program comprising: Two years of support per trainee, with a total of 4 training slots each year (2 slots in the first year). Mentored independent research with a team approach and scholarship oversight. Career mentoring including individualized independent development plans (IDP), seminars and workshops focusing on professional development and career advancement skills. Didactic opportunities designed to provide specific research skills. Seminars, workshops and journal clubs focusing on research and progress in the field.
描述(由申请人提供):儿科胃肠道疾病遗传基础的培训:遗传学和基因组学的革命导致了一系列胃肠道疾病的发现,其中许多影响儿童的健康。在遗传研究方面受过训练的儿科胃肠病学家将在确定GI疾病的新遗传原因,揭示其分子机制并将其转化为治疗方面发挥重要作用。CHOP和Perelman医学院(PSOM)的杰出实验室,转化和临床研究为儿科GI疾病遗传学的研究职业发展提供了理想的环境。该培训计划的总体目标是:培养一批忠诚的研究人员,以调查儿科GI疾病的遗传基础,并利用这些知识来改善儿童和成人的健康。 为这些人提供职业发展的技能和基础。 鼓励创新和领导学术儿科GI。该培训计划的具体目标是:从CHOP GI研究员,PSOM GI研究员和其他致力于儿科胃肠道疾病遗传学培训和职业发展的科学家中识别,招募和培养博士后研究学员的职业发展。 将学员的优势和兴趣与指导团队相匹配。 提供密集的指导研究经验和专门的教师培训。 提供职业指导,包括关于成功获得资助和撰写论文的培训。通过系列研讨会和其他学术活动将教师和研究员聚集在一起,创建一个医生科学家的协作社区。 提供遗传研究原则(包括研究伦理)的结构化学习机会指导 以及保护动物和人类受试者。为了实现这些目标,我们设计了一个培训计划,包括:每名学员两年的支持,每年共有4个培训名额(第一年2个名额)。 指导独立研究与团队的方法和奖学金监督。 职业指导,包括个性化的独立发展计划(IDP),侧重于专业发展和职业发展技能的研讨会和讲习班。 旨在提供特定研究技能的教学机会。 研讨会、讲习班和期刊俱乐部,重点关注该领域的研究和进展。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Nancy Bettina Spinner其他文献

Nancy Bettina Spinner的其他文献

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{{ truncateString('Nancy Bettina Spinner', 18)}}的其他基金

Resolving Uncertainty in Alagille Syndrome Diagnostics
解决阿拉吉尔综合征诊断中的不确定性
  • 批准号:
    10734881
  • 财政年份:
    2023
  • 资助金额:
    $ 13.64万
  • 项目类别:
Training Program in the Genetic Basis of Pediatric Gastrointestinal Disorders
儿科胃肠道疾病遗传基础培训计划
  • 批准号:
    8666845
  • 财政年份:
    2014
  • 资助金额:
    $ 13.64万
  • 项目类别:
Genetic Modifiers of Liver Disease Severity in Alagille Syndrome
阿拉吉尔综合征肝病严重程度的基因修饰
  • 批准号:
    7883529
  • 财政年份:
    2009
  • 资助金额:
    $ 13.64万
  • 项目类别:
Genetic Modifiers of Liver Disease Severity in Alagille Syndrome
阿拉吉尔综合征肝病严重程度的基因修饰
  • 批准号:
    7661203
  • 财政年份:
    2009
  • 资助金额:
    $ 13.64万
  • 项目类别:
Genetic Modifiers of Liver Disease Severity in Alagille Syndrome
阿拉吉尔综合征肝病严重程度的基因修饰
  • 批准号:
    8502652
  • 财政年份:
    2009
  • 资助金额:
    $ 13.64万
  • 项目类别:
Genetic Modifiers of Liver Disease Severity in Alagille Syndrome
阿拉吉尔综合征肝病严重程度的基因修饰
  • 批准号:
    8097573
  • 财政年份:
    2009
  • 资助金额:
    $ 13.64万
  • 项目类别:
Genetic Modifiers of Liver Disease Severity in Alagille Syndrome
阿拉吉尔综合征肝病严重程度的基因修饰
  • 批准号:
    8306850
  • 财政年份:
    2009
  • 资助金额:
    $ 13.64万
  • 项目类别:
Genetic Modifiers of Liver Disease Severity in Alagille Syndrome
阿拉吉尔综合征肝病严重程度的基因修饰
  • 批准号:
    8090799
  • 财政年份:
    2009
  • 资助金额:
    $ 13.64万
  • 项目类别:
NOTCH SIGNALING PATHWAY LIGANDS IN CARDIOVASCULAR DISEASE
心血管疾病中的 NOTCH 信号通路配体
  • 批准号:
    6565108
  • 财政年份:
    2002
  • 资助金额:
    $ 13.64万
  • 项目类别:
NOTCH SIGNALING PATHWAY LIGANDS IN CARDIOVASCULAR DISEASE
心血管疾病中的 NOTCH 信号通路配体
  • 批准号:
    6302546
  • 财政年份:
    2000
  • 资助金额:
    $ 13.64万
  • 项目类别:

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