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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
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Duke O'Brien Center for Kidney Research Resource Report Resource Website |
Duke O'Brien Center for Kidney Research (RRID:SCR_015268) | access service resource, resource, topical portal, portal, service resource, data or information resource, disease-related portal | Research center which investigates the mechanisms underlying the impact kidney disease has on cardiovascular morbidity and mortality using genetic and basic science approaches. | kidney disease, cardiovascular disease, kidney research |
is listed by: NIDDK Information Network (dkNET) has parent organization: Duke University School of Medicine; North Carolina; USA has parent organization: Duke University; North Carolina; USA is parent organization of: Duke O'Brien Center for Kidney Research Clinical and Translational Core is parent organization of: Duke O'Brien Center for Kidney Research Renal Genomics Core is parent organization of: Duke O'Brien Center for Kidney Research Animal Models Core has organization facet: Duke O'Brien Center for Kidney Research Animal Models Core has organization facet: Duke O'Brien Center for Kidney Research Renal Genomics Core has organization facet: Duke O'Brien Center for Kidney Research Clinical and Translational Core is organization facet of: O'Brien Kidney Centers |
kidney disease, heart disease, hypertension, muscle disease | NIDDK P30DK096493 | Available to the research community | SCR_015268 | 2026-02-16 09:48:53 | 0 | ||||||||
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Penn Diabetes Research Center Resource Report Resource Website |
Penn Diabetes Research Center (RRID:SCR_015123) | access service resource, resource, topical portal, portal, service resource, data or information resource, disease-related portal | Diabetes research center created to address the prevalence of diabetes and obesity. The goal of the center is to support and develop successful approaches to the prevention, treatment, and cure of diabetes mellitus and obesity. | cure for diabetes research, obesity, cardiovascular metabolism |
is listed by: NIDDK Information Network (dkNET) is affiliated with: Diabetes Research Centers has parent organization: University of Pennsylvania Perelman School of Medicine; Pennsylvania; USA is parent organization of: Penn Diabetes Research Center Metabolomics Core is parent organization of: Penn Diabetes Research Center Functional Genomics Core is parent organization of: Penn Diabetes Research Center Mouse Phenotyping Physiology and Metabolism Core is parent organization of: University of Pennsylvania School of Medicine Penn Diabetes Research Center Pancreatic Islet Cell Biology Core Facility is parent organization of: Penn Diabetes Research Center Radioimmunoassay and Biomarkers Core Facility is parent organization of: Penn Diabetes Research Center Transgenic and Chimeric Mouse Core Facility has organization facet: Penn Diabetes Research Center Functional Genomics Core has organization facet: Penn Diabetes Research Center Metabolomics Core has organization facet: University of Pennsylvania School of Medicine Penn Diabetes Research Center Pancreatic Islet Cell Biology Core Facility has organization facet: Penn Diabetes Research Center Mouse Phenotyping Physiology and Metabolism Core has organization facet: Penn Diabetes Research Center Radioimmunoassay and Biomarkers Core Facility has organization facet: Penn Diabetes Research Center Transgenic and Chimeric Mouse Core Facility has organization facet: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Vector Core Facility is organization facet of: Diabetes Research Centers |
Diabetes | NIDDK P30DK19525 | Available to the research community | SCR_015123 | 2026-02-16 09:48:48 | 0 | ||||||||
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Yale Liver Center Resource Report Resource Website |
Yale Liver Center (RRID:SCR_015255) | access service resource, resource, topical portal, portal, service resource, data or information resource, disease-related portal | Research center which supports investigation of liver structure, function and disease through access to its four core facilities (Administrative, Physiology, Clinical and Translational, and Morphology cores) and Pilot Feasability Projects. | liver research, liver research center, digestive disease, digestive disease research |
is listed by: NIDDK Information Network (dkNET) has parent organization: Yale School of Medicine; Connecticut; USA is parent organization of: Yale Liver Center Morphology Core is parent organization of: Yale Liver Center Clinical and Translational Core is parent organization of: Yale Liver Center Cellular and Molecular Physiology Core is parent organization of: Yale Liver Center Administrative Core has organization facet: Yale Liver Center Administrative Core has organization facet: Yale Liver Center Cellular and Molecular Physiology Core has organization facet: Yale Liver Center Clinical and Translational Core has organization facet: Yale Liver Center Morphology Core is organization facet of: Digestive Disease Centers |
liver disease | NIDDK P30DK034989 | Available to the research community | SCR_015255 | 2026-02-16 09:48:44 | 0 | ||||||||
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Washington University School of Medicine Diabetes Research Center Resource Report Resource Website |
Washington University School of Medicine Diabetes Research Center (RRID:SCR_015138) | access service resource, resource, topical portal, portal, service resource, data or information resource, disease-related portal | University-affiliated center established to support and enhance research in diabetes and related metabolic diseases. Its long-term goal is the development of new preventive strategies and therapies aimed at improving the lives of Americans with or at risk for diabetes. | diabetes, metabolic disease, preventative care |
is listed by: NIDDK Information Network (dkNET) has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA is parent organization of: Washington University School of Medicine Diabetes Research Center Translational Diagnostics Core is parent organization of: Washington University School of Medicine Diabetes Research Center Diabetes Models Phenotyping Core Facility is parent organization of: Washington University School of Medicine Diabetes Research Center Immunology of Type 1 Diabetes Core is parent organization of: Washington University School of Medicine Diabetes Research Center Transgenic and ES Cell Core is parent organization of: Washington University School of Medicine Diabetes Research Center Cell and Tissue Imaging Core is parent organization of: Washington University School of Medicine Diabetes Research Center Mass Spectrometry Core is parent organization of: Washington University School of Medicine Diabetes Research Center Morphology and Metabolic Analysis Core has organization facet: Washington University School of Medicine Diabetes Research Center Diabetes Models Phenotyping Core Facility has organization facet: Washington University School of Medicine Diabetes Research Center Translational Diagnostics Core has organization facet: Washington University School of Medicine Diabetes Research Center Immunology of Type 1 Diabetes Core has organization facet: Washington University School of Medicine Diabetes Research Center Mass Spectrometry Core has organization facet: Washington University School of Medicine Diabetes Research Center Morphology and Metabolic Analysis Core has organization facet: Washington University School of Medicine Diabetes Research Center Transgenic and ES Cell Core has organization facet: Washington University School of Medicine Diabetes Research Center Cell and Tissue Imaging Core is organization facet of: Diabetes Research Centers |
Type 1 diabetes, Type 2 diabetes, Diabetes | NIDDK P30DK020579 | Available to the research community | SCR_015138 | 2026-02-16 09:48:42 | 0 | ||||||||
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Washington University Digestive Diseases Research Core Center Resource Report Resource Website |
Washington University Digestive Diseases Research Core Center (RRID:SCR_015252) | access service resource, resource, topical portal, portal, service resource, data or information resource, disease-related portal | Research center whose purpose is to advance research in digestive disease with a focus on interactions between host and environment. It provides research resources to basic and translational investigators through various core facilities. | digestive disease research, core facility access |
is listed by: NIDDK Information Network (dkNET) has parent organization: Washington University School of Medicine in St. Louis; Missouri; USA is parent organization of: Washington University Digestive Diseases Research Core Center Murine Models and Gnotobiotics Core is parent organization of: Washington University Digestive Diseases Research Core Center Biobank Core is parent organization of: Washington University Digestive Diseases Research Core Center Advanced Imaging and Tissue Analysis Core is parent organization of: Washington University Digestive Diseases Research Core Center Administrative and Resource Access Core has organization facet: Washington University Digestive Diseases Research Core Center Administrative and Resource Access Core has organization facet: Washington University Digestive Diseases Research Core Center Advanced Imaging and Tissue Analysis Core has organization facet: Washington University Digestive Diseases Research Core Center Biobank Core has organization facet: Washington University Digestive Diseases Research Core Center Murine Models and Gnotobiotics Core is organization facet of: Digestive Disease Centers |
digestive disease | NIDDK P30DK052574 | Available to the research community | SCR_015252 | 2026-02-16 09:48:53 | 0 | ||||||||
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Joslin Diabetes Center Resource Report Resource Website 1+ mentions |
Joslin Diabetes Center (RRID:SCR_009019) | Joslin, JDC | access service resource, resource, topical portal, portal, service resource, data or information resource, disease-related portal | Diabetes research center which provides patient care and performs diabetes research. Its primary aim is to provide a facilitating framework for conducting multi-disciplinary basic and clinical research and to encourage the scientific development of young investigators. | diabetes, patient, clinical, care, research, investigate, disease |
is listed by: NIDDK Information Network (dkNET) is affiliated with: Diabetes Research Centers is related to: Harvard Bioinformatics Core at Joslin Diabetes Center has parent organization: Harvard University; Cambridge; United States is parent organization of: TINSAL-T2D is parent organization of: Joslin Diabetes Center Advanced Genomics and Genetics Core Facility is parent organization of: Joslin Diabetes Center Advanced Microscopy Core Facility is parent organization of: Joslin Diabetes Center Animal Physiology Core Facility is parent organization of: JDC Computer Resource is parent organization of: Joslin Diabetes Center Flow Cytometry Core Facility is parent organization of: JDC Genetics Core is parent organization of: JDC Media Core is parent organization of: Joslin Diabets Center Proteomics Core Facility is parent organization of: JDC Specialized Assay Core is parent organization of: Joslin Diabetes Center Islet Isolation Core is parent organization of: Joslin Diabetes Center Genomics Core is parent organization of: Joslin Diabetes Center Induced Pluripotent Stem Cell Core is parent organization of: Joslin Diabetes Center Enrichment Core is parent organization of: Joslin Diabetes Center Bioinformatics and Biostatistics Core is parent organization of: Joslin Diabetes Center Molecular Phenotyping and Genotyping Core has organization facet: Joslin Diabetes Center Advanced Genomics and Genetics Core Facility has organization facet: Joslin Diabetes Center Advanced Microscopy Core Facility has organization facet: Joslin Diabetes Center Animal Physiology Core Facility has organization facet: Joslin Diabetes Center Bioinformatics and Biostatistics Core has organization facet: Joslin Diabetes Center Enrichment Core has organization facet: Joslin Diabetes Center Flow Cytometry Core Facility has organization facet: Joslin Diabetes Center Induced Pluripotent Stem Cell Core is organization facet of: Diabetes Research Centers |
Diabetes | NIDDK P30 DK036836 | Available to the research community | nlx_152856 | SCR_009019 | Joslin Diabetes Cntr | 2026-02-16 09:47:19 | 2 | |||||
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JDRF Artificial Pancreas Project Consortium Resource Report Resource Website |
JDRF Artificial Pancreas Project Consortium (RRID:SCR_004010) | Artificial Pancreas Consortium | data or information resource, organization portal, consortium, portal | Consortium aiming to accelerate the development of systems for automated control of blood glucose in patients with diabetes. Consortium investigators seek to research and develop strategies, which can be commercialized, that will confer the long-term benefits of improved glycemic control by combining novel automated control algorithms and hormone therapies with continuous glucose monitors and pump devices. The field of closed-loop artificial pancreas research requires expert diabetologists partnering with expert mathematicians and engineers. Consortium investigators include endocrinologists and control theorists at research institutions in the US and in Europe. Many of the diabetes device manufacturers have also participated, providing pumps and sensors with enhanced capabilities that allow for closed-loop experiments to be performed. The goals of the consortium include: * Design, optimization, and clinical testing of multiple algorithmic approaches to closed-loop control * An in silico simulation platform, accepted by the FDA, for validating candidate closed-loop control algorithms in place of animal trials * Reusable templates for constructing the Investigational Device Exemption regulatory documents that must be approved by the FDA prior to any in-clinic, computer-assisted, closed-loop control research involving people * A modular software platform-the Artificial Pancreas System-with a protocol-independent user interface and hooks to incorporate an arbitrary control algorithm and control various continuous glucose monitors and pump devices * A secure consortium Web site with a central repository for experimental data and interfaces to submit candidate control algorithms for centralized validation and to upload or download clinical data sets * the first outpatient studies of an overnight controller * the first outpatient studies of a hypoglycemia minimization strategy * the development and testing of a modular treat-to-range closed-loop approach * multiple studies of dual hormone (insulin and glucagon) devices and a means to improve insulin kinetics Ongoing and recently completed in-clinic studies at the end of 2011 include investigations into hypoglycemia prediction and avoidance as well as fully-automated closed-loop control investigations using MPC and PID/PD-based algorithms. The most recent developments include the first-ever feasibility trials of portable, outpatient-based closed-loop control systems. | device development, product development, device, blood glucose, hypoglycemia, glucose monitor, pump device, glycemic control, insulin, glucagon, closed-loop control, clinical |
is listed by: Consortia-pedia is related to: Juvenile Diabetes Research Foundation is related to: Critical Path Initiative has parent organization: Jaeb Center for Health Research |
JDRF ; NIDDK |
nlx_158431 | SCR_004010 | Artificial Pancreas Project Consortium, JDRF/NIDDK Artificial Pancreas Project Consortium | 2026-02-16 09:46:18 | 0 | |||||||
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Nutrition and Obesity Research Centers Resource Report Resource Website 10+ mentions |
Nutrition and Obesity Research Centers (RRID:SCR_004131) | NORC | organization portal, resource, topical portal, portal, data or information resource, disease-related portal | Portal to research centers and core facilities specifically support obesity research and better understand the relationship between health and nutrition. | obesity core facility, obesity portal, obesity research center |
is listed by: NIDDK Information Network (dkNET) is listed by: Diabetes Research Centers is affiliated with: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases has organization facet: Boston Nutrition and Obesity Research Centers has organization facet: Nutrition and Obesity Research Centers at Harvard has organization facet: Mid-Atlantic Nutrition Obesity Research Center has organization facet: New York Obesity Nutrition Research Center has organization facet: Pennington Biomedical Research Center Nutrition and Obesity Research Center has organization facet: University of Alabama at Birmingham Nutrition and Obesity Research Center has organization facet: University of California San Francisco Nutrition and Obesity Research Center has organization facet: University of Colorado Anschutz Medical Campus Nutrition and Obesity Research Center has organization facet: University of Michigan Nutrition and Obesity Research Center has organization facet: University of North Carolina at Chapel Hill Nutrition and Obesity Research Center has organization facet: University of Washington Nutrition and Obesity Research Center has organization facet: Washington University St. Louis Nutrition Obesity Research Center |
Obesity, Nutrition-related disease, Eating disorder, Anorexia nervosa, AIDS, Cancer | NIDDK RFA-DK16-006 | Available to the research community | nlx_158684 | SCR_004131 | 2026-02-16 09:46:17 | 40 | ||||||
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Human Biological Data Interchange Resource Report Resource Website 100+ mentions |
Human Biological Data Interchange (RRID:SCR_004591) | HBDI | service resource, storage service resource, material storage repository, biospecimen repository | Database of medical history and genealogical data on over 6700 families who are affected by type 1 diabetes and a repository of DNA and immortalized cell lines collected from 500 families. This database and repository was originally created to help researchers uncover the genetic causes of type 1 diabetes but today, it is also used by researchers who study type 2 diabetes, diabetic complications, autoimmune diseases, kidney disease, and other disorders. The following resources and services are available to researchers through HBDI: * International Type 1 Diabetes Database: This database includes more than 6700 families with diabetes, related complications and other genetic diseases. There are extensive genealogical and medical histories for more than 90,000 individuals. NDRI conducts searches of the database for approved research requests. * HBDI Catalog: The catalog contains 503 family pedigrees with associated cell lines, DNA, and serum for research. Also available are HLA-typing and auto-antibody test results for diabetes families in the catalog. * HBDI Repository: The HBDI repository contains cell lines, DNA, and HLA typing information from 480 families, and frozen buffy coats from 23 families, all with Type 1 diabetes. They have recently expanded the repository to include specimens from individuals with rare diseases. * Customized Collections: NDRI will collect data from patients and physicians, conduct phone interviews and collect blood and other specimens for research on request., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | genetics, medical history, genealogical data, type 2 diabetes, diabetic complication, autoimmune disease, kidney disease, disorder, family pedigree, hla typing, frozen, buffy coat, catalog, demographic data, clinical data, autoantibody data, FASEB list |
is listed by: One Mind Biospecimen Bank Listing is related to: NIDDK Information Network (dkNET) has parent organization: National Disease Research Interchange |
Type 1 diabetes, Rare disease, Type 2 diabetes, Diabetic complication, Autoimmune disease, Kidney disease, Diabetes | NIDDK | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_143829 | SCR_004591 | Human Biological Data Interchange (HBDI) | 2026-02-16 09:46:27 | 107 | |||||
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DGAP Resource Report Resource Website 1+ mentions |
DGAP (RRID:SCR_003036) | DGAP | narrative resource, experimental protocol, resource, database, data or information resource | Produce resources to unravel the interface between insulin action, insulin resistance and the genetics of type 2 diabetes including an annotated public database, standardized protocols for gene expression and proteomic analysis, and ultimately diabetes-specific and insulin action-specific DNA chips for investigators in the field. The project aims to identify the sets of the genes involved in insulin action and the predisposition to type 2 diabetes, as well as the secondary changes in gene expression that occur in response to the metabolic abnormalities present in diabetes. There are five major and one pilot project involving human and rodent tissues that are designed to: * Create a database of the genes expressed in insulin-responsive tissues, as well as accessible tissues, that are regulated by insulin, insulin resistance and diabetes. * Assess levels and patterns of gene expression in each tissue before and after insulin stimulation in normal and genetically-modified rodents; normal, insulin resistant and diabetic humans, and in cultured and freshly isolated cell models. * Correlate the level and patterns of expression at the mRNA and/or protein level with the genetic and metabolic phenotype of the animal or cell. * Generate genomic sequence from a panel of humans with type 2 diabetes focusing on the genes most highly regulated by insulin and diabetes to determine the range of sequence and expression variation in these genes and the proteins they encode, which might affect the risk of diabetes or insulin resistance. The DGAP project will define: * the normal anatomy of gene expression, i.e. basal levels of expression and response to insulin. * the morbid anatomy of gene expression, i.e., the impact of diabetes on expression patterns and the insulin response. * the extent to which genetic variability might contribute to the alterations in expression or to diabetes itself. | gene, insulin action, predisposition, gene expression, metabolic abnormality, diabetes, insulin resistance, genetics, insulin, genetic variation, proteomics, genomics, affymetrix oligonucleotide array, microarray, protein, genomic sequence, data set |
is related to: NIDDK Information Network (dkNET) has parent organization: Harvard Medical School; Massachusetts; USA has parent organization: Broad Institute has parent organization: Dana-Farber Cancer Institute has parent organization: University of Massachusetts Medical School; Massachusetts; USA has parent organization: University of Southern Denmark; Odense; Denmark |
Type 2 diabetes, Normal, Insulin resistance | NIDDK | PMID:19786482 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-30414 | SCR_003036 | The Diabetes Genome Anatomy Project, Diabetes Genome Anatomy Project | 2026-02-16 09:45:54 | 9 | ||||
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BMAP cDNA Resources Resource Report Resource Website 1+ mentions |
BMAP cDNA Resources (RRID:SCR_002973) | BMAP Resources | material service resource, resource, biomaterial manufacture, topical portal, portal, production service resource, service resource, data or information resource | As part of BMAP gene discovery efforts, mouse brain cDNA libraries and Expressed Sequence Tags (ESTs) have been generated. Through this project a BMAP mouse brain UniGene set consisting of over 24,000 non-redundant members of unique clusters has been developed from EST sequencing of more than 50,000 cDNA clones from 10 regions of adult mouse brain, spinal cord, and retina (http://brainEST.eng.uiowa.edu/). In 2001, NIMH along with NICHD, NIDDK, and NIDA, awarded a contract to the University of Iowa ( M.B. Soares, PI) to isolate full-length cDNA clones corresponding to genes expressed in the developing mouse nervous system and determine their full-coding sequences. The BMAP mouse brain EST sequences can be accessed at NCBI's dbEST database (http://www.ncbi.nlm.nih.gov/dbEST/). Arrayed sets of BMAP mouse brain UniGenes and cDNA libraries, and individual BMAP cDNA clones can be purchased from Open Biosystems, Huntsville, AL (http://www.openbiosystems.com | brain, spinal cord, retina, gene, cdna, library, est, cluster, clone, nervous system, dbest, database, gene discovery, cdna library, expressed sequence tag, coding sequence, adult |
is related to: Nucleotide database is related to: Open Biosystems has parent organization: BMAP - Brain Molecular Anatomy Project |
NINDS ; NICHD ; NIDDK ; NIDA ; NIMH N01 MH80014 |
THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-30154 | SCR_002973 | Brain Molecular Anatomy Project cDNA Resources | 2026-02-16 09:46:04 | 2 | ||||||
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HumanIslets Resource Report Resource Website 1+ mentions |
HumanIslets (RRID:SCR_025719) | data or information resource, project portal, portal | Data visualization portal for HumanIslets project. Integrated platform for human islet data access and analysis. Includes data on human islet donors, allows users to access linked datasets describing molecular profiles, islet function and donor phenotypes, and to perform various statistical and functional analyses at donor, islet and single-cell levels. Provides set of resources and tools to support metabolism and diabetes research community. | human islet data, data access and analysis, molecular profiles, islet function, donor phenotypes, metabolism, diabetes | Canadian Institutes of Health Research ; BCCHRI Child Health Integrative Partnership Strategy Funding ; NIDDK U01 DK 120447; NIDDK U01-DK-123716; NIDDK U01-DK105535; NIDDK U01-DK085545; NIDDK UM-1DK126185; Wellcome Trust ; UBC Life Sciences Institute ; Canada Foundation for Innovation ; BC Knowledge Development Fund ; Genome Canada |
PMID:38948734 | Free, Freely available | SCR_025719 | 2026-02-15 09:23:58 | 9 | |||||||||
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HiCDCPlus Resource Report Resource Website 1+ mentions |
HiCDCPlus (RRID:SCR_025317) | software toolkit, software resource | Software package for Hi-C/HiChIP interaction calling and differential analysis using efficient implementation of HiC-DC statistical framework. Enables principled statistical analysis of Hi-C and HiChIP data sets. Enables systematic 3D interaction calls and differential analysis for Hi-C and HiChIP | Hi-C/HiChIP interaction calling, differential analysis, statistical analysis of Hi-C and HiChIP data sets, systematic 3D interaction calls, | NHGRI U01 HG009395; NIDDK U01 DK128852 |
PMID:34099725 | Free, Available for download, Freely available | https://bitbucket.org/leslielab/hicdcplus/src/master/ | SCR_025317 | , HiC-DC+, Hi-C Direct Caller Plus, HiCDCPlus (HiC-DC+) | 2026-02-15 09:23:49 | 1 | |||||||
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Cistrome Resource Report Resource Website 10+ mentions |
Cistrome (RRID:SCR_000242) | data access protocol, software resource, web service | Web based integrative platform for transcriptional regulation studies. | Transcriptional, regulation, Chip, data, analysis, genome, gene, expression, motif, mining, bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools is related to: Galaxy has parent organization: Harvard University; Cambridge; United States |
Dana-Farber Cancer Institute High Tech and Campaign Technology Fund ; National Basic Research Program of China ; NHGRI HG004069; NIDDK DK074967; NIDDK DK062434 |
PMID:21859476 | Free, Freely available | SCR_017663, biotools:cistrome, OMICS_02173 | http://cistrome.org/ap/root https://bio.tools/cistrome |
SCR_000242 | Galaxy Cistrome | 2026-02-16 09:45:13 | 16 | |||||
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MTOPS Prostate Samples Analysis Consortium Resource Report Resource Website |
MTOPS Prostate Samples Analysis Consortium (RRID:SCR_000041) | MPSA Consortium | organization portal, data or information resource, consortium, portal | THIS RESOURCE IS NO LONGER IN SERVICE. Documented on August 16,2023. Cross-disciplinary, multi-institutional network with wide range of experts to analyze serum and tissue samples collected in the Medical Therapy of Prostatic Symptoms (MTOPS) trial. Consortium aims to discover and validate biomarkers for the detection, risk assessment, and disease progression assessment of benign prostatic hyperplasia (BPH). | prostate, male, adult human, biomarker, serum, tissue, microarray |
is affiliated with: Medical Therapy of Prostatic Symptoms is related to: NIDDK Information Network (dkNET) has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases |
Benign Prostatic Hyperplasia | NIDDK 1U01DK063661 | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_152864 | SCR_000041 | MTOPS Prostate Samples Analysis (MPSA) Consortium | 2026-02-16 09:45:10 | 0 | |||||
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Epidemiology of Diabetes Interventions and Complications Resource Report Resource Website 1+ mentions |
Epidemiology of Diabetes Interventions and Complications (RRID:SCR_001468) | EDIC | clinical trial, resource, database, data or information resource, bibliography | Publications from a multi-center, longitudinal, observational study examining the risk factors associated with the long-term complications of type 1 diabetes. The study began in 1994 and follows the 1441 participants previously enrolled in the Diabetes Control and Complications Trial (DCCT), http://diabetes.niddk.nih.gov/dm/pubs/control/index.aspx. The primary aim of EDIC is to examine the long-term effects of conventional vs. intensive diabetes treatment received during the DCCT on the subsequent development and progression of microvascular, neuropathic and cardiovascular complications. This involves studying the influence of genetic factors and other factors such as HbA1c, blood pressure, lipid levels, and treatment modalities on the development and progression of these complications. Annual or biennial measurements (using DCCT methods, standardized protocols and central laboratories) of vascular events, albumin excretion, GFR, ECG, ankle-brachial BP index, serum lipids and HbA1c allows the following analyses: 1) continuation of intention-to-treat analyses to determine long-term effects of prior separation of glycemic levels; 2) risk factors for macrovascular outcomes; 3) correlation of progression of micro- and macrovascular outcomes. The current updated version of the EDIC Protocol is available for download. EDIC is made up of 28 clinical centers, one data coordinating center and one clinical coordinating center. | longitudinal, observational, nephropathy, macrovascular, complication, risk factor, clinical, genetic factor, hba1c, blood pressure, lipid level, treatment modality, complication |
is listed by: ClinicalTrials.gov is listed by: NIDDK Information Network (dkNET) is listed by: NIDDK Central Repository is related to: Diabetes Control and Complications Trial is related to: Diabetes Control and Complications Trial has parent organization: George Washington University; Washington D.C.; USA |
Type 1 diabetes, Diabetes | NIDDK 4U01DK094157 | Free, Freely Available | nlx_152698 | SCR_001468 | 2026-02-16 09:45:30 | 1 | ||||||
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Adult to Adult Living Donor Liver Transplantation Cohort Study Resource Report Resource Website |
Adult to Adult Living Donor Liver Transplantation Cohort Study (RRID:SCR_001494) | A2ALL | research forum portal, resource, topical portal, portal, data or information resource, disease-related portal | Study consisting of nine liver transplant centers with expertise in adult living-donor liver transplantation (LDLT) and a central data coordinating center to provide valuable information on the outcomes of adult to adult living donor liver transplantation (AALDLT) to aid decisions made by physicians, patients, and potential donors. The study will establish and maintain the infrastructure required to accrue and follow sufficient numbers of patients being considered for and undergoing AALDLT to provide generalizable data from adequately powered studies. The major aims of A2ALL are as follows: * Quantify the impact of choosing LDLT on the candidate for transplantation * Characterize the difference between LDLT and deceased donor liver transplant (DDLT) in terms of post-transplant outcomes, including patient and graft survival, surgical morbidity, and resource utilization on the recipient of a transplant * Determine the short- and long-term health and quality of life (QOL) impact of donation, including (a) morbidity after liver donation and (b) long-term health-related QOL of donors. * Standardize and assess the role of informed consent in affecting the decision to donate and satisfaction after living liver donation * Other aims include comparison of the severity of recurrence of hepatocellular carcinoma for DDLT versus LDLT, the systematic characterization of liver regeneration and function in donors and recipients, the evaluation of the differences in the immune response to LDLT versus DDLT, and the establishment of a robust data and sample repository on liver transplantation that may be used to study clinical and biological questions as new technologies and resources become available. Patients enrolled in the study will be followed and managed in a standardized fashion. | transplant, liver, adult human, risk factor, surgery, outcome, quality of life, clinical |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Michigan; Ann Arbor; USA |
Liver transplant, Liver disease | NIDDK 1U01DK62498 | PMID:18976306 PMID:18756453 PMID:16135918 |
Free, Freely available | nlx_152749 | http://www.nih-a2all.org/ | SCR_001494 | A2ALL: The Adult to Adult Living Donor Liver Transplantation Cohort Study | 2026-02-16 09:45:30 | 0 | |||
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Behavior Enhances Drug Reduction of Incontinence Resource Report Resource Website |
Behavior Enhances Drug Reduction of Incontinence (RRID:SCR_001495) | BE-DRI | data or information resource, clinical trial, resource, bibliography | Multi-center randomized clinical trial to determine if the addition of behavioral treatment to drug therapy for the treatment of urge incontinence will make it possible to discontinue the drug and still maintain a reduced number of accidents. The most popular treatments for urge incontinence are drug therapy and behavior therapy, each with its own limitations. In this clinical study, the Urinary Incontinence Treatment Network (UITN) aims to determine differences with the addition of behavioral treatment to drug therapy alone. | drug therapy, behavioral therapy, female, urinary incontinence, overactive bladder, combined modality therapy, quality of life, pelvic floor muscle exercise, tolterodine, clinical |
is listed by: ClinicalTrials.gov is listed by: NIDDK Information Network (dkNET) has parent organization: Urinary Incontinence Treatment Network |
Urge incontinence, Urinary Incontinence | NIDDK U01DK58225; NIDDK U01DK58234; NIDDK U01DK58229; NIDDK U01DK58231; NIDDK U01DK60397; NIDDK U01DK60401; NIDDK U01DK60395; NIDDK U01DK60393; NIDDK U01DK60380; NIDDK U01DK60379 |
PMID:16919506 | Free, Freely available | nlx_152752 | http://www.uitn.net/bedri.asp | SCR_001495 | 2026-02-16 09:45:30 | 0 | ||||
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Standardization of C-peptide measurements Resource Report Resource Website |
Standardization of C-peptide measurements (RRID:SCR_001499) | Standardization of c-peptide | data or information resource, standard specification, resource, narrative resource | Standardization of c-peptide by calibrating C-peptide measurement to a reference method can increase comparability between laboratories. The C-peptide standardization program is supported to establish reliability in results and facilitate the conduct of international clinical trials. For c-peptide, purified or processed material shows significant matrix effects and cannot be used for calibration. The C-peptide program has evaluated the use of single donor and pooled specimens for use by manufacturers in the calibration of these assays and determined that this strategy will reduce C-peptide variability among different assay methods. The standardization process through manufacturer re-calibration is ongoing. | c-peptide, insulin secretion, clinical, calibration |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Missouri School of Medicine; Missouri; USA |
Diabetes | NIDDK 200200409985 | PMID:18420730 | Free, Freely available | nlx_152766 | SCR_001499 | C-peptide Standardization | 2026-02-16 09:45:30 | 0 | ||||
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trackViewer Resource Report Resource Website |
trackViewer (RRID:SCR_027743) | software toolkit, software resource | Software R package to visualize mapped reads along with annotation as track layers for NGS dataset such as ChIP-seq, RNA-seq, miRNA-seq, DNA-seq, SNPs and methylation data. | annotation as track layers for NGS dataset, ChIP-seq, DNA-seq, SNP, methylation, data, visualize mapped reads, annotation as track layers, | NIDDK R01DK076118 | PMID:31133757 | Free, Available for download, Freely available | SCR_027743 | 2026-02-15 09:24:16 | 0 |
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We recommend that you click next to the search bar to check some helpful tips on searches and refine your search firstly. Alternatively, please register your tool with the SciCrunch Registry by adding a little information to a web form, logging in will enable users to create a provisional RRID, but it not required to submit.
Welcome to the NIF Resources search. From here you can search through a compilation of resources used by NIF and see how data is organized within our community.
You are currently on the Community Resources tab looking through categories and sources that NIF has compiled. You can navigate through those categories from here or change to a different tab to execute your search through. Each tab gives a different perspective on data.
If you have an account on NIF then you can log in from here to get additional features in NIF such as Collections, Saved Searches, and managing Resources.
Here is the search term that is being executed, you can type in anything you want to search for. Some tips to help searching:
If you are logged into NIF you can add data records to your collections to create custom spreadsheets across multiple sources of data.
Here are the facets that you can filter the data by.
If you have any further questions please check out our FAQs Page to ask questions and see our tutorials. Click this button to view this tutorial again.
Welcome to the Neuroscience Information Framework Project, designed to serve the biomedical research community. NIF maintains the largest searchable collection of neuroscience data, the largest catalog of biomedical resources, and the largest ontology for neuroscience on the web. We welcome all feedback and suggestions and are actively looking for resource providers to make their resources accessible through NIF. Learn about the tools available to help you share your data and discover a dynamic inventory of Web-based neuroscience resources.
