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SUMMARY Oklahoma is one of the states in the US with the highest prevalence of diabetes, with 10% of the population affected. Diabetes is particularly prevalent among Native American communities, where it affects up to 40% of older individuals in some tribes. Thus, diabetes and its complications constitute a major threat to the working- age and older population, and confer an immense social and economic burden on Oklahoma. The goal of this COBRE is to enhance diabetes research in Oklahoma. In Phase I and Phase II, our COBRE achieved its milestones. All of the COBRE-supported Junior Investigators have received independent grants, including eight NIH R01 grants, two R21 grants, and multiple grants from foundations such as the American Diabetes Association and the American Heart Association. Five of our Junior Investigators have been promoted to Associate Professor, and three of them have received tenure thus far. In addition, because of their success in research, two of them received endowed chair positions. Between them, the Junior Investigators have published 207 peer-reviewed papers, 135 of which received support from COBRE-funded Cores. In collaboration with the College of Medicine, the COBRE has recruited three NIH R01-funded and 1 K99/R00-funded diabetes researchers into The University of Oklahoma Health Sciences Center (OUHSC). The COBRE-funded Cores have provided support and service to multiple PIs and supported their publications and NIH-funded grants, which enhanced diabetes research in Oklahoma. In Phase III of the COBRE program, we plan to sustain and augment these successes. We will continue supporting and mentoring Junior Investigators who graduated from the COBRE. We will expand and improve Core facilities to serve diabetes research in Oklahoma and complete transition of the COBRE-funded facilities into institutional research Cores. We will further increase the critical mass of diabetes research in Oklahoma by promoting recruitment of diabetes researchers into OUHSC. Moreover, we will continue promoting collaborative and translational research. These efforts should contribute to continuous growth of diabetes research to achieve our goal of becoming a NIH P30-funded Diabetes Research Center (DRC). This Center should greatly improve prevention and treatment of diabetes.
期刊论文(10)
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会议论文
DOI: 10.1167/iovs.17-22107
发表时间: 2017-08-01
期刊: Investigative ophthalmology & visual science
影响因子: 4.4
作者: [Du M, Phelps E, Balangue MJ, Dockins A, Moiseyev G, Shin Y, Kane S, Otalora L, Ma JX, Farjo R, Farjo KM]
通讯作者: Farjo KM
DOI: 10.1161/hypertensionaha.117.10560
发表时间: 2018-05
期刊: Hypertension (Dallas, Tex. : 1979)
影响因子: --
作者: [Chen J, Fan J, Wang S, Sun Z]
通讯作者: Sun Z
DOI: 10.3390/biom11050712
发表时间: 2021-05-10
期刊: Biomolecules
影响因子: 5.5
作者: [Le YZ, Xu B, Chucair-Elliott AJ, Zhang H, Zhu M]
通讯作者: Zhu M
Critical Role of VEGF as a Direct Regulator of Photoreceptor Function.
VEGF 作为光感受器功能直接调节剂的关键作用。
DOI: 10.1007/978-3-031-27681-1_71
发表时间: 2023
期刊: Advances in experimental medicine and biology
影响因子: --
作者: [Hu,Jianyan, Zhu,Meili, Li,Dai, Wu,Qiang, Le,Yun-Zheng]
通讯作者: Le,Yun-Zheng
6
    Müller glia in disease and stress
    Müller glia in disease and stress
    Müller glia in disease and stress
    ROLE OF VEGF SIGNALING IN CONE AND ROD PHOTORECEPTOR SURVIVAL
    国内基金
    海外基金
    补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
    靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
    • 批准号:
      JCZRQN202500010
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
    • 依托单位:
    对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
    • 批准号:
      2025JJ70209
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2025
    • 负责人:
      雷芬芳
    • 依托单位:
    AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
    • 批准号:
      --
    • 项目类别:
      面上项目
    • 资助金额:
      --
    • 批准年份:
      2024
    • 负责人:
      万荣
    • 依托单位: