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http://www.med.upenn.edu/idom/drc/cores/metacore.html

Core which aims to develop and validate metabolomic methods and data analysis software and provide high quality routine metabolomic services. Its services include quantitation of selected water-soluble metabolites, fatty acids, and lipids, quantitation of metabolic fluxes using stable isotope tracers, and identification of novel metabolites involved in diabetes pathophysoiology.

Proper citation: Penn Diabetes Research Center Metabolomics Core (RRID:SCR_015122) Copy   

•   Source: SciCrunch Registry

https://www.iths.org/resources/directory/listing/drc-human-studies-core-university-of-washington

Core facility that provides specialized technical resources and expertise to enhance the efficiency, productivity and multidisciplinary nature of clinical research performed by Diabetes Research Center (DRC)-affiliated investigators.

Proper citation: University of Washington Diabetes Research Center Human Studies Core Facility (RRID:SCR_015127) Copy   

•   Source: SciCrunch Registry

http://depts.washington.edu/diabetes/cell-function-analysis-core/

Core facility that supports the Diabetes Research Center affiliates by offering precise real time functional analysis of intact cells and primary tissue. The Cell Function Analysis Core also provides an islet isolation service, which gives affiliates easy access to primary tissue/cells ex vivo.

Proper citation: University of Washington Diabetes Research Center Cell Function Analysis Core Facility (RRID:SCR_015128) Copy   

•   Source: SciCrunch Registry

http://drtc.bsd.uchicago.edu/molecular-biology-and-genetics-core-laboratory-about/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 7,2024. Molecular biology and genetics core which helps independently funded investigators with an interest in diabetes mellitus and other metabolic disorders to clone, sequence and characterize cDNAs and genes of interest. It also provides research tools and expertise to enable investigators to discover how genetic variation in diabetes genes leads to hyperglycemia.

Proper citation: University of Chicago Diabetes Research and Training Center Molecular Biology and Genetics Core Laboratory (RRID:SCR_015129) Copy   

•   Source: SciCrunch Registry

http://drtc.bsd.uchicago.edu/physiology-core-about/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 7,2024. Core whose goal is to facilitate the use of model organisms in diabetes and metabolism-related research. The Core provides access to resources, technology, equipment and services for the generation and study of genetically modified mice and other model organisms; consultation on experimental design and analysis; technology development; and opportunities for collaboration and training.

Proper citation: University of Chicago Diabetes Research and Training Center Animal Models and Physiology Core (RRID:SCR_015134) Copy   

•   Source: SciCrunch Registry

http://www.uab.edu/shp/drc/interventions-translational-core-links

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 7,2024. Core which provides expertise and services that range from methods of intervention development, basic study design and data analysis, and cutting-edge methodologies in measurement, to subject recruitment and retention strategies with an emphasis on increasing minority participation.

Proper citation: University of Alabama at Birmingham Diabetes Research Center Interventions and Translation Core (RRID:SCR_015135) Copy   

•   Source: SciCrunch Registry

https://diabetescenters.org/cores/ucsd-ucla-human-genetics-core

Core provides services such as assistance in the development and successful completion of well-designed genetic studies, establishment and storage of EBV-transformed lymphoblastoid cell lines (LCLs), as well as PAXgene tubes, and specialized (e.g., the exome chip) single nucleotide polymorphism (SNP) testing, candidate gene sequencing, whole exome sequencing (WES), whole genome sequencing (WGS), and large-scale gene methylation analysis.

Proper citation: University of California San Diego - University of California Los Angeles Diabetes Research Center Human Genetics Core Facility (RRID:SCR_015099) Copy   

•   Source: SciCrunch Registry

http://diabetesresearch.med.umich.edu/Core_MDRC_Animal.php

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 6,2024. Fee-for-service laboratory that provides consultation and utilizes specialized skills and equipment to assess the metabolic state and related endocrine and behavioral phenotypes of rats and mice. The labs include Rat Metabolic Phenotyping Lab, Optogenetics and Behavioral Phenotyping Lab, Islet Laboratory, and Continuous Glucose Monitoring Lab.

Proper citation: Michigan Diabetes Research Center Animal Studies Core (RRID:SCR_015133) Copy   

•   Source: SciCrunch Registry

http://diabetesresearchcenter.dom.wustl.edu/metabolic-tissue-function-core/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 7,2024. Core facility with the goal of assisting Diabetes Research Core investigators in obtaining metabolic tissues and conducting functional and metabolic analysis of cells and tissues relevant to the pathogenesis of diabetes.

Proper citation: Washington University School of Medicine Diabetes Research Center Morphology and Metabolic Analysis Core (RRID:SCR_015136) Copy   

•   Source: SciCrunch Registry

https://joslinresearch.org/drc-cores/Enrichment-Core

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 9,2024. Six component core which facilitates the exchange of research information and discussions among investigators, fellows and students within the Joslin Diabetes Center, as well as between Joslin Staff and outside researchers with similar interests.

Proper citation: Joslin Diabetes Center Enrichment Core (RRID:SCR_015094) Copy   

•   Source: SciCrunch Registry

http://www.hopkinsmedicine.org/diabetes-research-center/research-cores/gene-editing.html

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 9,2024. Core that provides services in Gene Editing Expertise Using CRISPR/CAS9, Conventional Transgenic Mouse Generation, Conventional Knockout, Knock-In Mouse Generation, and Cryopereservation of Sperm, Oocytes and Embryos.

Proper citation: Johns Hopkins University - University of Maryland Diabetes Research Center Gene Editing Core (RRID:SCR_015091) Copy   

•   Source: SciCrunch Registry

https://www.joslin.org/research/diabetes-research-centercore-laboratories/bioinformatics-biostatistics-core

Core that offers support for data-driven projects related to basic, clinical and translational research, with a particular emphasis on diabetes. The core aims to ensure that researchers take advantage of the most modern and robust methods available in the field of Bioinformatics and Biostatistics.

Proper citation: Joslin Diabetes Center Bioinformatics and Biostatistics Core (RRID:SCR_015092) Copy   

•   Source: SciCrunch Registry

https://medschool.ucsd.edu/som/medicine/divisions/endocrinology/research/diabetes-research-center/Cores/Pages/Targeted-Pathway-Analysis-Core.aspx

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on October 8, 2024. Core with main goal to steer investigators through introductory discovery lipidomics and proteomics experiments toward statistically powered, targeted experiments aimed at measuring biological pathways relevant to diabetes and metabolism.

Proper citation: University of California San Diego - University of California Los Angeles Diabetes Research Center Targeted Pathway Analysis Core Facility (RRID:SCR_015098) Copy   

•   Source: SciCrunch Registry

https://diabetescenters.org/cores/ucsd-ucla-transgenic-and-knockout-mouse-core

Core that provides and produces transgenic mice. Services and methodologies include pronuclear microinjection and blastocyst microinjection for creation of new mouse cell lines as well as archival services like embryo and sperm freezing.

Proper citation: University of California San Diego - University of California Los Angeles Diabetes Research Center Transgenic and Knockout Mouse Core Facility (RRID:SCR_015096) Copy   

•   Source: SciCrunch Registry

http://chicagodiabetesresearch.org/cores/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on June 30,2023. Core facility that provides support to investigators in designing and carrying out translational studies assessing outcomes for patients with diabetes, or populations at risk.

Proper citation: Chicago Center for Diabetes Translation Research Outcomes Improvement Core (RRID:SCR_015221) Copy   

•   Source: SciCrunch Registry

https://cdtr.wustl.edu/our-cores/dissemination-and-implementation/

Core facility whose services include consultion for further dissemination of diabetes research and assistance with design methods for early dissemination of results.

Proper citation: Washington University Center for Diabetes Translation Research Dissemination and Implementation in Diabetes Research Core (RRID:SCR_015230) Copy   

•   Source: SciCrunch Registry

http://mmpc.ucdavis.edu/core.php?coreID=29

Core that provides phenotyping services for the assessment of endocrine function and metabolic pathways in mouse models of obesity, diabetes, and related metabolic diseases including dyslipidemia and fatty liver disease.

Proper citation: MMPC-University of California Davis Endocrinology and Metabolism Core (RRID:SCR_015359) Copy   

•   Source: SciCrunch Registry

Ratings or validation data are available for this resource

http://www.jdrfnpod.org

A collaborative research project that supports nPOD approved diabetes investigators by freely providing rare and difficult-to-obtain tissues from type 1 and type 2 diabetes donors. Interested researchers are encouraged to apply to obtain nPOD tissues, or to request access to analyze cases in the nPOD Online Pathology site. Interested donors can contact nPOD directly for more information.

Proper citation: Network for Pancreatic Organ Donors with Diabetes (RRID:SCR_014641) Copy   

•   Source: SciCrunch Registry

https://repository.niddk.nih.gov/study/36

Data set and biosepecimens of a multi-center clinical trial to determine if treatment with beta-cell antigens can delay the onset of Type 1 Diabetes Mellitus (Type 1 DM) in non-diabetic relatives of persons with Type 1 DM. Insulin is a well characterized antigen specifically produced by beta-cells, and it was used for this purpose in the initial DPT-1 studies. The protocol for high risk subjects uses daily subcutaneous insulin injections and an annual course of intravenous insulin treatment, while the protocol for intermediate risk subjects uses daily doses of insulin administered orally. Neither injected nor oral insulin at the doses used were observed to delay or prevent diabetes, although further studies are needed to test whether oral insulin can delay diabetes in people in the intermediate risk group with high titers of insulin autoantibodies.

Proper citation: Diabetes Prevention Type 1 (RRID:SCR_001467) Copy   

•   Source: SciCrunch Registry

https://www.pbcconsortium.org/

Portal to provide a repository for beta-cell data, to connect researchers from different backgrounds interested in contributing data, models and/or ideas for new insights into beta-cell biology. Used to understand beta-cell biology and diabetes through a cross-disciplinary approach for the assembly of spatiotemporal multi-scale whole cell models of human pancreatic beta-cells.

Proper citation: The Pancreatic Beta-Cell Consortium (RRID:SCR_016328) Copy   

•   Source: SciCrunch Registry