Child Health Research Career Development Award (CHRCDA) Program (K12)

儿童健康研究职业发展奖 (CHRCDA) 计划 (K12)

基本信息

  • 批准号:
    10598237
  • 负责人:
  • 金额:
    $ 37.34万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2007
  • 资助国家:
    美国
  • 起止时间:
    2007-03-01 至 2027-11-30
  • 项目状态:
    未结题

项目摘要

PROJECT SUMMARY / ABSTRACT The goal of the Boston Children's Hospital K12 CHRCDA Program is to develop independent pediatrician physician-scientists who will decipher the pathobiology of childhood disease and develop transformative new therapies. Our Scholars will perform laboratory-based basic and translational research under the mentorship of outstanding scientists at Boston Children's Hospital and other affiliated institutions. Our program has been established to ensure the continued development of outstanding independent pediatrician-scientists in the field. In this proposal, we describe a program that includes intensive mentoring, a comprehensive didactic program, and appropriate supervision and support to ensure that our Scholars reach their maximum scientific potential. Programmatic oversight will be provided by an External Advisory Committee and an Internal Steering Committee. Plans are in place for programmatic self-evaluation and for review of Scholar Progress. We propose to continue the funding of three Scholar positions. Scholars will be funded for a minimum of two years, contingent on satisfactory progress on research and career development activities, and the overall pool of Scholar candidates. Scholars will be faculty members most often at the rank of Instructor, but Assistant Professors who are early in the development of their independent careers will also be eligible to apply. Scholars will be considered at any point from the beginning of their Instructorship until they are considered to be two years away from submitting their first R-level NIH grant or equivalent, though no more than four years beyond the end of fellowship training. Scholars will work in broad areas of scientific investigation relevant to child health. Past and present Scholars have studied the genomics of rare childhood disease, developmental biology, mucosal immunology, host- microbe interactions, monogenic kidney diseases, genetics of epilepsy, and environmental effects on early brain development. Our Scholars are expected to elucidate molecular mechanisms of disease, leading to the development of transformative new therapies for a broad range of diseases of childhood.
项目摘要/摘要

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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Wendy K Chung其他文献

Recent advances in understanding neurodevelopmental outcomes in congenital heart disease
先天性心脏病神经发育结局理解方面的最新进展

Wendy K Chung的其他文献

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{{ truncateString('Wendy K Chung', 18)}}的其他基金

Fair Phenotype Annotation and Genomic Reinterpretation
公平表型注释和基因组重新解释
  • 批准号:
    10675315
  • 财政年份:
    2023
  • 资助金额:
    $ 37.34万
  • 项目类别:
Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in Autism
自闭症的前瞻性遗传风险评估(PROGRESS)
  • 批准号:
    10531728
  • 财政年份:
    2022
  • 资助金额:
    $ 37.34万
  • 项目类别:
Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in Autism
自闭症的前瞻性遗传风险评估(PROGRESS)
  • 批准号:
    10698037
  • 财政年份:
    2022
  • 资助金额:
    $ 37.34万
  • 项目类别:
Project 1: Identifying and optimizing monogenetic risk prediction for autism in newborns
项目 1:识别和优化新生儿自闭症单基因风险预测
  • 批准号:
    10698081
  • 财政年份:
    2022
  • 资助金额:
    $ 37.34万
  • 项目类别:
Core A: Administrative Core
核心A:行政核心
  • 批准号:
    10698072
  • 财政年份:
    2022
  • 资助金额:
    $ 37.34万
  • 项目类别:
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease
识别和应用与先天性心脏病患者临床结果相关的遗传变异
  • 批准号:
    10028016
  • 财政年份:
    2020
  • 资助金额:
    $ 37.34万
  • 项目类别:
Role of the Kinesin KIF1A in Neurological Disease
驱动蛋白 KIF1A 在神经系统疾病中的作用
  • 批准号:
    10328907
  • 财政年份:
    2020
  • 资助金额:
    $ 37.34万
  • 项目类别:
Molecular Biology/Molecular Genetics (Core C)
分子生物学/分子遗传学(核心 C)
  • 批准号:
    9901512
  • 财政年份:
    2020
  • 资助金额:
    $ 37.34万
  • 项目类别:
Role of the Kinesin KIF1A in Neurological Disease
驱动蛋白 KIF1A 在神经系统疾病中的作用
  • 批准号:
    10543786
  • 财政年份:
    2020
  • 资助金额:
    $ 37.34万
  • 项目类别:
Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart disease
识别和应用与先天性心脏病患者临床结果相关的遗传变异
  • 批准号:
    10226278
  • 财政年份:
    2020
  • 资助金额:
    $ 37.34万
  • 项目类别:

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