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http://diabetesresearchcenter.dom.wustl.edu/transgenic-es-cell-core/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 7,2024. Core facility that provides services for efficient and cost-effective development of genetically altered mouse models to elucidate the pathogenesis of diabetes and related metabolic disorders.

Proper citation: Washington University School of Medicine Diabetes Research Center Transgenic and ES Cell Core (RRID:SCR_015141) Copy   

•   Source: SciCrunch Registry

https://ddrcc.wustl.edu/scientific-cores/murine-models-gnotobiotics-core/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on June 15,2026. Core facility that provides advice and technical services to DDRCC investigators that include production of transgenic and chimeric mice, derivation of speed congenics and assisted reproduction services for maintaining pedigrees via the Mouse Genetics Core, as well as gnotobiotic mouse provision, colonization and rederivation.

Proper citation: Washington University Digestive Diseases Research Core Center Murine Models and Gnotobiotics Core (RRID:SCR_015260) Copy   

•   Source: SciCrunch Registry

http://diabetesresearchcenter.dom.wustl.edu/cell-and-tissue-imaging-core/

Core facility which provides researchers access to and technological support for advanced cellular microscopy and tools.

Proper citation: Washington University School of Medicine Diabetes Research Center Cell and Tissue Imaging Core (RRID:SCR_015140) Copy   

•   Source: SciCrunch Registry

http://www.gcdtr.org/core-programs/disparities.html

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 30,2025. Core which facilitate combined diabetes-disparities translation research that can identify ways to improve engagement in evidence-based diabetes prevention and management interventions among vulnerable populations. Their services include methodological expertise, sociocultural competencies, access to populations in community, and clinical settings, and relevant databases, tools, and technologies that help diabetes investigators.

Proper citation: Georgia Center for Diabetes Translation Research Disparities Core (RRID:SCR_015157) Copy   

•   Source: SciCrunch Registry

http://www.gcdtr.org/core-programs/engagement-behavior-change.html

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on January 30,2025. Core which works to create more equitable health promotion and educational programs.

Proper citation: Georgia Center for Diabetes Translation Research Engagement and Behavior Change Core (RRID:SCR_015155) Copy   

•   Source: SciCrunch Registry

http://diabetestranslation.org/en/Cores/dop/

Research core for the prevention of diabetes and obesity in young women and children. The core works to collaborate on issues of translational interventions for diabetes and obesity prevention by research, evaluation and implementation studies.

Proper citation: Health Delivery Systems Center for Diabetes Translational Research Diabetes and Obesity Prevention Core (RRID:SCR_015159) Copy   

•   Source: SciCrunch Registry

https://www.vumc.org/vdrc/cores-hmpg

Core facility that provides a range of animal model systems to investigators working in the areas of diabetes and metabolism. It also offers surgical and experimental services, with limited analytical capacity in blood glucose and serology. The Human Metabolic Physiology and Genomics Core evolved from the Metabolic Physiology Shared Resource.

Proper citation: Vanderbilt Diabetes Research and Training Center Metabolic Physiology Shared Resource (RRID:SCR_015150) Copy   

•   Source: SciCrunch Registry

http://www.ucdenver.edu/academics/colleges/PublicHealth/research/centers/CAIANH/cdtr/Pages/National-Resource-Core.aspx

Purpose is to assemble, focus, mobilize, provide, monitor, and evaluate resources necessary to stimulate, carry out, and translate the outcomes of diabetes prevention and management research.

Proper citation: Center for American Indian and Alaska Native Diabetes Translational Research National Resource (RRID:SCR_015151) Copy   

•   Source: SciCrunch Registry

http://drtc.bsd.uchicago.edu/islet-cell-biology-core-about/

THIS RESOURCE IS NO LONGER IN SERVICE. Documented on November 7,2024. Core which provides services and hands-on training in the isolation and functional characterization of pancreatic islets from normal and diabetic humans and mice. It also maintains a repository of insulinoma cell lines for distribution. It puts emphasis on facilitating studies of primary islet cells and it has developed many unique tools and techniques for carrying such studies including novel animals models, biophysical methods and a library of adenovirus-based expression constructs for studying beta-cell function.

Proper citation: University of Chicago Diabetes Research and Training Center Islet Cell Biology Core (RRID:SCR_015132) Copy   

•   Source: SciCrunch Registry

http://livercenter.yale.edu/core-facilities/clinical-translational-core.aspx

Core facility which aims to develop an infrastructure for patient-oriented research by streamlining regulatory and compliance processes, obtaining and storing high-quality samples linked to clinical information, offering consultation in the design and implementation of clinical trials, and supplying statistical expertise for interpreting clinical and translational data.

Proper citation: Yale Liver Center Clinical and Translational Core (RRID:SCR_015259) Copy   

•   Source: SciCrunch Registry

https://diabetes.med.umich.edu/partners/michigan-diabetes-research-center-mdrc/cores/clinical

Clinical Core of the Michigan Diabetes Research Center (MDRC) provides expertise and services to support basic biomedical research, research focused on the translation of basic science findings into early phase clinical trials, and the testing of treatments related to diabetes in human subjects.

Proper citation: Michigan Diabetes Research Center Clinical Core Facility (RRID:SCR_015139) Copy   

•   Source: SciCrunch Registry

http://diabetesresearchcenter.dom.wustl.edu/metabolomics-core/

Core facility which provides mass spectrometry analyses to Diabetes Research Center investigators that includes quantification as well as structural characterization of diabetes-related biomolecules.

Proper citation: Washington University School of Medicine Diabetes Research Center Mass Spectrometry Core (RRID:SCR_015137) Copy   

•   Source: SciCrunch Registry

http://livercenter.yale.edu/core-facilities/cellular-molecular-physiology-core-facility.aspx

Core facility that provides technical expertise, equipment and personnel to Liver Center Investigators who wish to work with animal models of liver disease, isolated liver cells, or gene expression in liver tissue. The Cell Isolation sub-core isolates hepatocytes and non-parenchymal liver cells primarily from rat and mouse, while the Molecular Biology sub-core provides equipment and expertise to Liver Center members in a centralized facility.

Proper citation: Yale Liver Center Cellular and Molecular Physiology Core (RRID:SCR_015258) Copy   

•   Source: SciCrunch Registry

http://depts.washington.edu/diabetes/viral-vector-and-transgenic-mouse/

Core facility that provides Diabetes Research Center affiliates with vectors necessary to overexpress, knockdown, knockout, or alter expression of RNAs and proteins of interest in cultured cells, isolated tissues, and animals.

Proper citation: University of Washington Diabetes Research Center Vector and Transgenic Mouse Core (RRID:SCR_015130) Copy   

•   Source: SciCrunch Registry

https://ww2.mc.vanderbilt.edu/DDRC/19909

Core facility whose services include training, acquisition and analysis on cytometers for experiments that include different fluorochromes, imaging cytometry, and mass cytometry.

Proper citation: Vanderbilt Digestive Disease Research Center Flow Cytometry Core (RRID:SCR_015251) Copy   

•   Source: SciCrunch Registry

https://www.iths.org/resources/directory/listing/drc-quantitative-and-functional-proteomics-core-university-of-washington

Core facility that provides the powerful tools of modern mass spectrometry and complex data set analysis to Diabetes Research Center investigators to permit structural identification and quantitation of proteins involved in diabetes and its complications.

Proper citation: University of Washington Diabetes Research Center Quantitative and Functional Proteomics Core Facility (RRID:SCR_015131) Copy   

•   Source: SciCrunch Registry

https://ww2.mc.vanderbilt.edu/DDRC/6914

Core facility whose goals include furnishing professional guidance in experimental design and data interpretation and providing access to optical and electron microscopy. Its services include confocal microscopy, wide-field microscopy, transmission electron microscopy, and processing and embedment of tissue or cells for EM.

Proper citation: Vanderbilt Digestive Disease Research Center Cellular Imaging Core (RRID:SCR_015250) Copy   

•   Source: SciCrunch Registry

https://scicrunch.org/

Community portal for researchers and content management system for data and databases. Intended to provide common source of data to research community and data about Research Resource Identifiers (RRIDs), which can be used in scientific publications. Central service where RRIDs can be searched and created. Designed to help communities of researchers create their own portals to provide access to resources, databases and tools of relevance to their research areas. Adds value to existing scientific resources by increasing their discoverability, accessibility, visibility, utility and interoperability, regardless of their current design or capabilities and without need for extensive redesign of their components or information models. Resources can be searched and discovered at multiple levels of integration, from superficial discovery based on limited description of resource at SciCrunch Registry, to deep content query at SciCrunch Data Federation.

Proper citation: SciCrunch (RRID:SCR_003115) Copy   

•   Source: SciCrunch Registry

http://www.mmrrc.org/

National public repository system for mutant mice. Archives and distributes scientifically valuable spontaneous and induced mutant mouse strains and ES cell lines for use by biomedical research community. Includes breeding/distribution facilities and information coordinating center. Mice strains are cryopreserved, unless live colony must be established. Live mice are supplied from production colony, from colony recovered from cryopreservation, or via micro-injection of cell line into host blastocysts. MMRRC member facilities also develop technologies to improve handling of mutant mice, including advances in assisted reproductive techniques, cryobiology, genetic analysis, phenotyping and infectious disease diagnostics.

Proper citation: Mutant Mouse Resource and Research Center (RRID:SCR_002953) Copy   

•   Source: SciCrunch Registry

https://www.ddbj.nig.ac.jp/jga/index-e.html

A service for permanent archiving and sharing of all types of personally identifiable genetic and phenotypic data resulting from biomedical research projects. The JGA contains exclusive data collected from individuals whose consent agreements authorize data release only for specific research use or to bona fide researchers. Strict protocols govern how information is managed, stored and distributed by the JGA. Once processed, all data are encrypted. The JGA accepts only de-identified data approved by JST-NBDC. The JGA implements access-granting policy whereby the decisions of who will be granted access to the data resides with the JST-NBDC. After data submission the JGA team will process the data into databases and archive the original data files. The accepted data types include manufacturer-specific raw data formats from the array-based and new sequencing platforms. The processed data such as the genotype and structural variants or any summary level statistical analyses from the original study authors are stored in databases. The JGA also accepts and distributes any phenotype data associated with the samples. For other human biological data, please contact the NBDC human data ethical committee.

Proper citation: Japanese Genotype-phenotype Archive (JGA) (RRID:SCR_003118) Copy   

•   Source: SciCrunch Registry