Integrated Islet Distribution Program (U24) - 2021

综合胰岛分布计划 (U24) - 2021

基本信息

项目摘要

PROJECT SUMMARY / ABSTRACT Human pancreatic islets are an essential research resource for research on the prevention, treatment, and pathophysiology of diabetes mellitus. Recent data have highlighted important differences between murine and human islets, substantiating the continued need for access to human islets, as the gold standard in diabetes research. City of Hope (COH) is applying for this U24 renewal to remain as the Integrated Islet Distribution Program Coordinating Center (IIDP CC) for the next 5 years, to continue to provide distribution of human cadaveric islets and ancillary tissue for biomedical research to researchers worldwide. Our proposal leverages the significant investment made by NIH over the last 19 years that has established and successfully maintained the IIDP at COH. From qualification and auditing of high-quality Islet Isolation Centers (IICs), to forecasting, tracking, and meeting the needs of investigators, since 2002 our experienced team has worked with 20 different islet isolation laboratories to coordinate the distribution of over 330 million islet equivalents to more than 400 investigators across 16 countries since 2002, supporting 767 peer reviewed publications. Through this renewal we will continue to subcontract with our 5 highly qualified IICs to isolate and distribute human islets and ancillary tissue via our advanced electronic Islet Allocation System (IAS). We will continue to manage the review process for islet receipt, pilot studies, and Opportunity Pool funding. We will further enhance our IAS to broadcast offers online and notify approved waiting researchers of islet availability, in a fair, equitable and time sensitive manner. IIDP will continue to maintain the existing cost recovery system through subscription fees collected from islet researchers, which has garnered a total of $9,303,950 since the implementation of subscription fees to offset the expenses of pancreatic processing for the IICs. We will continue to closely monitor and help to improve the quality of islets distributed, through the continuation of the Human Islet Phenotyping Program (HIPP) that conducts assays on a sample from each islet isolation. IIDP has just added a Human Islet Genotyping Initiative (HIGI) to genotype each isolation as well. Phenotyping and genotyping data, as well as UNOS data, extensive donor and islet isolation data, will be made available to approved investigators through online access to the IIDP Research Data Repository, with IIDP and NIDDK approval of applying scientists. Investigators can easily search the required data, select filter criteria, save their searches, and download the integrated IIDP data for exploratory analyses. Through our proven state-of-the-art administrative, business, technical, statistical, quality assurance, and informatics processes and tools, the accessibility of human islets for investigators conducting essential diabetes mellitus research will be secured. We will continue to provide an indispensable research resource for the diabetes research community by ensuring that the IIDP remains stable, technologically advanced, continually enhanced, and fully responsive to the islet needs of the research community, promoting the next generation of scientific experimentation toward the prevention and treatment of diabetes.
项目摘要/摘要

项目成果

期刊论文数量(0)
专著数量(0)
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会议论文数量(0)
专利数量(0)

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Carmella Evans-Molina其他文献

Carmella Evans-Molina的其他文献

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{{ truncateString('Carmella Evans-Molina', 18)}}的其他基金

β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes Pathogenesis
β 细胞 miRNA 作为 1 型糖尿病发病机制的分子中心
  • 批准号:
    10561855
  • 财政年份:
    2022
  • 资助金额:
    $ 299.11万
  • 项目类别:
β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes Pathogenesis
β 细胞 miRNA 作为 1 型糖尿病发病机制的分子中心
  • 批准号:
    10321295
  • 财政年份:
    2021
  • 资助金额:
    $ 299.11万
  • 项目类别:
Control of beta cell function and survival by RYR2-mediated calcium signals
通过 RYR2 介导的钙信号控制 β 细胞功能和存活
  • 批准号:
    10491304
  • 财政年份:
    2021
  • 资助金额:
    $ 299.11万
  • 项目类别:
β cell miRNAs Function as Molecular Hubs of Type 1 Diabetes Pathogenesis
β 细胞 miRNA 作为 1 型糖尿病发病机制的分子中心
  • 批准号:
    10615586
  • 财政年份:
    2021
  • 资助金额:
    $ 299.11万
  • 项目类别:
Control of beta cell function and survival by RYR2-mediated calcium signals
通过 RYR2 介导的钙信号控制 β 细胞功能和存活
  • 批准号:
    10689291
  • 财政年份:
    2021
  • 资助金额:
    $ 299.11万
  • 项目类别:
Control of beta cell function and survival by RYR2-mediated calcium signals
通过 RYR2 介导的钙信号控制 β 细胞功能和存活
  • 批准号:
    10375087
  • 财政年份:
    2021
  • 资助金额:
    $ 299.11万
  • 项目类别:
Indiana University clinical Center for acute pancreatitis and diabetes clinical research network
印第安纳大学急性胰腺炎和糖尿病临床中心临床研究网络
  • 批准号:
    10458720
  • 财政年份:
    2020
  • 资助金额:
    $ 299.11万
  • 项目类别:
Indiana University clinical Center for acute pancreatitis and diabetes clinical research network
印第安纳大学急性胰腺炎和糖尿病临床中心临床研究网络
  • 批准号:
    10673629
  • 财政年份:
    2020
  • 资助金额:
    $ 299.11万
  • 项目类别:
Indiana University clinical Center for acute pancreatitis and diabetes clinical research network
印第安纳大学急性胰腺炎和糖尿病临床中心临床研究网络
  • 批准号:
    10265585
  • 财政年份:
    2020
  • 资助金额:
    $ 299.11万
  • 项目类别:
Islet Core
胰岛核心
  • 批准号:
    9105738
  • 财政年份:
    2016
  • 资助金额:
    $ 299.11万
  • 项目类别:

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