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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
National Hematologic Diseases Information Service
 
Resource Report
Resource Website
National Hematologic Diseases Information Service (RRID:SCR_006817) NHDIS resource, data or information resource, service resource, narrative resource, training material Information dissemination service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) providing information about certain hematologic diseases in easy-to-understand language: online, in booklets and fact sheets, by email, and over the phone to patients, health professionals and the public. The NHDIS provides the following informational products and services: * Response to inquiries about hematologic diseases, ranging from information about available patient and professional education materials to referrals to patient support organizations. Assistance is available by phone (8:30 a.m. to 5 p.m. eastern time, M-F), fax, mail, and email. * Publications about hematologic diseases, provided free of copyright, in varying reading levels. Available online or in hard copy. NHDIS also sends publications to health fairs and community events. * Referrals to health professionals through the National Library of Medicine''''s MEDLINEplus, which includes a consumer-friendly listing of organizations to assist in the search for physicians and other health professionals. hematology, statistics, publication, medical, nutrition is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
Hematologic disease NIDDK Free, Public nlx_152714 SCR_006817 2026-02-14 02:01:24 0
AASK Clinical Trial and Cohort Study
 
Resource Report
Resource Website
AASK Clinical Trial and Cohort Study (RRID:SCR_006985) AASK Cohort Study portal, clinical trial, resource, data or information resource, research forum portal, disease-related portal, topical portal Clinical trial investigating whether a specific class of antihypertensive drugs (beta-adrenergic blockers, calcium channel blockers, or angiotensin converting enzyme inhibitors) and/or the level of blood pressure would influence progression of hypertensive kidney disease in African Americans. The initiative consisting of 21 clinical centers and a data-coordinating center is followed by a Continuation of AASK Cohort Study to investigate the environmental, socio-economic, genetic, physiologic, and other co-morbid factors that influence progression of kidney disease in a well-characterized cohort of African Americans with hypertensive kidney disease. Only patients who were previously in the randomized trial are eligible for the cohort study. A significant discovery was made in the treatment strategy for slowing kidney disease caused by hypertension. Angiotensin-converting enzyme (ACE) inhibitors, compared with calcium channel blockers, were found to slow kidney disease progression by 36 percent, and they drastically reduced the risk of kidney failure by 48 percent in patients who had at least one gram of protein in the urine, a sign of kidney failure. ACE inhibitors have been the preferred treatment for hypertension caused by diabetes since 1994; however, calcium channel blockers have been particularly effective in controlling blood pressure in African Americans. The AASK study now recommends ACE inhibitors to protect the kidneys from the damaging effects of hypertension. The Continuation of AASK Cohort Study will be followed at the clinical centers. The patients will be provided with the usual clinical care given to all such patients at the respective centers. Baseline demographic information, selected laboratory tests, and other studies are being obtained at the initiation of the Continuation Study. The patients will be seen quarterly at the centers, and some selected studies done at these visits. Samples will be obtained and stored for additional studies and analyses at a later date. african american, blood pressure, beta-adrenergic blocker, calcium channel blocker, angiotensin converting enzyme inhibitor, environment, socio-economic, genetic, physiology, co-morbid factor, gene, adult human, antihypertensive drug, clinical, treatment, longitudinal, demographics, laboratory test, biospecimen, biomaterial supply resource is listed by: One Mind Biospecimen Bank Listing
is related to: NIDDK Information Network (dkNET)
is related to: Chronic Renal Insufficiency Cohort Study
End-stage renal disease, Kidney failure, Kidney disease, Hypertension, Hypertensive kidney disease NIDDK nlx_152750 SCR_006985 African American Study of Kidney Disease and Hypertension (AASK) Clinical Trial and Cohort Study, African American Study of Kidney Disease and Hypertension Clinical Trial and Cohort Study, Continuation of AASK Cohort Study, African American Study of Kidney Disease and Hypertension 2026-02-14 02:01:16 0
IntAct
 
Resource Report
Resource Website
1000+ mentions
IntAct (RRID:SCR_006944) IntAct data repository, storage service resource, data or information resource, service resource, database Open source database system and analysis tools for molecular interaction data. All interactions are derived from literature curation or direct user submissions. Direct user submissions of molecular interaction data are encouraged, which may be deposited prior to publication in a peer-reviewed journal. The IntAct Database contains (Jun. 2014): * 447368 Interactions * 33021 experiments * 12698 publications * 82745 Interactors IntAct provides a two-tiered view of the interaction data. The search interface allows the user to iteratively develop complex queries, exploiting the detailed annotation with hierarchical controlled vocabularies. Results are provided at any stage in a simplified, tabular view. Specialized views then allows "zooming in" on the full annotation of interactions, interactors and their properties. IntAct source code and data are freely available. protein domain, motif, protein interaction, molecular interaction, interaction, protein, binary interaction, complex, data set, protein-protein interaction, pathway, small molecule-protein, nucleic acid-protein, small molecule, nucleic acid, protein binding, chromatin, cancer, apoptosis, molecular biology, virus, source code, isoform, gold standard is used by: ChannelPedia
is used by: MINT
is used by: Pathway Analysis Tool for Integration and Knowledge Acquisition
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: 3DVC
is listed by: re3data.org
is listed by: OMICtools
is related to: 3D-Interologs
is related to: IMEx - The International Molecular Exchange Consortium
is related to: MPIDB
is related to: TissueNet - The Database of Human Tissue Protein-Protein Interactions
is related to: InteroPorc
is related to: Interaction Reference Index
is related to: Pathway Commons
is related to: ConsensusPathDB
is related to: FlyMine
is related to: IMEx - The International Molecular Exchange Consortium
is related to: Integrated Molecular Interaction Database
is related to: VirHostNet: Virus-Host Network
is related to: PSICQUIC Registry
is related to: UniProt
is related to: SIB Swiss Institute of Bioinformatics
is related to: I2D
is related to: InnateDB
is related to: MatrixDB
is related to: MBInfo
is related to: AgBase
is related to: Cardiovascular Gene Ontology Annotation Initiative
is related to: PSI-MI
is related to: Agile Protein Interactomes DataServer
has parent organization: European Bioinformatics Institute
works with: IMEx - The International Molecular Exchange Consortium
European Union contract FP7-HEALTH-2007-223411;
European Union contract FP7-HEALTH-2007-200767
PMID:24234451
PMID:22121220
PMID:19850723
PMID:17145710
PMID:14681455
Apache License, v2, (software), Creative Commons Attribution License, (data), The community can contribute to this resource OMICS_01918, r3d100010671, nif-0000-03026 https://doi.org/10.17616/R3QS4R SCR_006944 IntAct 2026-02-14 02:01:18 1892
Boston Area Community Health Survey
 
Resource Report
Resource Website
Boston Area Community Health Survey (RRID:SCR_007115) BACH Survey, BACH portal, resource, data or information resource, research forum portal, disease-related portal, topical portal An epidemiologic study being conducted in the Boston metropolitan area to examine the prevalence of symptoms for health problems such as interstitial cystitis, urinary incontinence, benign prostatic hyperplasia, prostatitis, hypogonadism, and sexual function. Of interest to the survey are health disparities and inequalities. BACH is especially concerned with lack of adequate health insurance, lack of access to adequate medical care, and how these problems influence patterns of disease. The study also focuses on social determinants of disease that are over and above the contribution of individual characteristics and risk factors. To achieve a randomly sampled population, four neighborhoods were divided into 12 strata and from them investigators selected census blocks. Households were then randomly selected from the census blocks and sampled to identify eligible study participants. Investigators conduct a two-hour, in-home, bilingual field interview of all eligible participants, looking at symptoms and asking questions about lifestyle, physical activity, alcohol use, nutrition, demographics, and morbidity. They also conduct a detailed inventory of medications, both prescribed and over-the-counter, and take two non-fasting blood samples for hormone, cholesterol, and lipid levels that will be stored for future studies. By the time the study ends, approximately 6,000 men and women, ages 30 to 79, from four Boston area neighborhoods that have density levels proportionate with minority populations will have been interviewed in their homes. One third of the randomly sampled population will be African American; one third, Hispanic; and one third, Caucasian. prevalence, symptom, epidemiology, health problem, disparity, inequality, health insurance, medical care, disease, social determinant, risk factor, male, female, adult human, middle adult human, late adult human, interview, african-american, hispanic, caucasian, epidemiological study, lifestyle, physical activity, alcohol use, nutrition, demographics, morbidity, medication, blood, hormone, cholesterol, lipid level, biomaterial supply resource is listed by: One Mind Biospecimen Bank Listing
is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
Urological problem, Interstitial cystitis, Urinary incontinence, Benign prostatic hyperplasia, Prostatitis, Hypogonadism, Sexual dysfunction NIDDK nlx_152753 SCR_007115 Boston Area Community Health (BACH) Survey 2026-02-14 02:01:28 0
Knockout Mouse Project Repository
 
Resource Report
Resource Website
100+ mentions
Knockout Mouse Project Repository (RRID:SCR_007318) KOMP Repository biomaterial supply resource, organism supplier, material resource Repository of mouse vectors, ES cells, mice, embryos, and sperm generated by NIH KOMP Mutagenesis Project. In addition, KOMP Repository offers services in support of KOMP products, including ES cell microinjection, vector cloning, post-insertional modification of cloned ES cells, cryopreservation, assisted reproduction techniques (IVF, ICSI) and mouse breeding, pathology services, phenotyping services, etc. KOMP Repository is final component of more than $50 million trans-NIH initiative to increase availability of genetically altered mice and related materials. The University of California, Davis (UC Davis) and Children''s Hospital Oakland Research Institute (CHORI) in Oakland, Calif., are collaborating to preserve, protect, and make available about 8,500 types of knockout mice and related products available to research community. Products are generated by two KOMP mutagenesis teams (CSD consortium and Regeneron Inc). All KOMP products generated by CSD consortium and Regeneron are available through KOMP Repository. Notice as of December 19, 2019: Materials from KOMP Repository have been deposited into MMRRC, including all mouse models and mouse embryonic stem cell lines. Eventually www.komp.org will be sunsetting, and IMSR will remove KOMP Repository listings, since they were double listed in MMRRC. MMRRC will contain the most accurate and up to date resource models. vector, embryonic stem cell, embryo, sperm, germplasm, gene, breeding, mutagenesis, mutation, frozen, cryopreserved, knockout mouse, germline transmission testing, genotyping, in vitro fertilization, intracytoplasmic sperm injection, pathology, pathology service, phenotyping service, phenotype, phenotyping, FASEB list is listed by: One Mind Biospecimen Bank Listing
is listed by: NIDDK Information Network (dkNET)
has parent organization: University of California at Davis; California; USA
has parent organization: Childrens Hospital Oakland Research Institute
has parent organization: Knockout Mouse Project
is provided by: International Mouse Phenotyping Consortium (IMPC)
is provided by: Mutant Mouse Resource and Research Center
is provided by: CMMR - Canadian Mouse Mutant Repository
is provided by: Jackson Laboratory
Knock out mouse For research purposes only nif-0000-00185 SCR_007318 UCDavis KOMP Repository Knockout Mouse Project, KOMP Repository Knockout Mouse Project, UC Davis KOMP Repository Knockout Mouse Project 2026-02-14 02:01:29 282
National Library of Medicine
 
Resource Report
Resource Website
100+ mentions
National Library of Medicine (RRID:SCR_011446) NLM government granting agency NLM collects, organizes, and makes available biomedical science information to scientists, health professionals, and the public. The Library's Web-based databases, including PubMed/Medline and MedlinePlus, are used extensively around the world. NLM conducts and supports research in biomedical communications; creates information resources for molecular biology, biotechnology, toxicology, and environmental health; and provides grant and contract support for training, medical library resources, and biomedical informatics and communications research. Celebrating its 175th anniversary in 2011, the National Library of Medicine (NLM), in Bethesda, Maryland, is a part of the National Institutes of Health, U.S. Department of Health and Human Services (HHS). Since its founding in 1836 as the library of the U.S. Army Surgeon General, NLM has played a pivotal role in translating biomedical research into practice. It is the world's largest biomedical library and the developer of electronic information services that deliver trillions of bytes of data to millions of users every day. Scientists, health professionals, and the public in the United States and around the globe search the Library's online information resources more than 1 billion times each year. The Library is open to all and has many services and resources for scientists, health professionals, historians, and the general public. NLM has over 17 million books, journals, manuscripts, audiovisuals, and other forms of medical information on its shelves, making it the largest health-science library in the world. In today's increasingly digital world, NLM carries out its mission of enabling biomedical research, supporting health care and public health, and promoting healthy behavior by: * Acquiring, organizing, and preserving the world's scholarly biomedical literature; * Providing access to biomedical and health information across the country in partnership with the 5,800-member National Network of Libraries of Medicine (NN/LM); * Serving as a leading global resource for building, curating and providing sophisticated access to molecular biology and genomic information, including those from the Human Genome Project and NIH Common Fund; * Creating high-quality information services relevant to toxicology and environmental health, health services research, and public health; * Conducting research and development on biomedical communications systems, methods, technologies, and networks and information dissemination and utilization among health professionals, patients, and the general public; * Funding advanced biomedical informatics research and serving as the primary supporter of pre- and post-doctoral research training in biomedical informatics at 18 U.S. universities. is used by: DisGeNET
recommends: Brain Image Library
recommends: Data Archive BRAIN Initiative
recommends: OpenNeuro
recommends: Brain Observatory Storage Service and Database (BossDB)
recommends: CRCNS
recommends: NCBI database of Genotypes and Phenotypes (dbGap)
recommends: NIMH Data Archive
recommends: ENCODE
recommends: Genotype-Tissue Expression
recommends: HMP Data Analysis and Coordination Center
recommends: Illuminating the Druggable Genome
recommends: Kids First Data Resource Portal
recommends: HMS LINCS Database
recommends: Metabolomics Workbench
recommends: Patient-Reported Outcomes Measurement Information System
recommends: Cancer Nanotechnology Laboratory (caNanoLab)
recommends: Cancer Imaging Archive (TCIA)
recommends: Network Data Exchange (NDEx)
recommends: eyeGENE
recommends: National Eye Institute (NEI) Commons
recommends: National Sleep Research Resource (NSRR)
recommends: CardioVascular Research Grid (CVRG)
recommends: AMP-AD Knowledge Portal
recommends: National Archive of Computerized Data on Aging (NACDA)
recommends: National Institute on Aging Genetics of Alzheimer’s Disease Data Storage Site (NIAGADS)
recommends: Immune Tolerance Network TrialShare
recommends: The Immunology Database and Analysis Portal (ImmPort)
recommends: VectorBase
recommends: Virus Pathogen Resource (ViPR)
recommends: LONI Image and Data Archive
recommends: NeuroImaging Tools and Resources Collaboratory (NITRC)
recommends: Child Language Data Exchange System (CHILDES)
recommends: Data and Specimen Hub (NICHD DASH)
recommends: National Children's Study (NCS) Archive
recommends: PhonBank
recommends: Archive of Data on Disability to Enable Policy (ADDEP)
recommends: National Addiction and HIV Data Archive Program (NAHDAP)
recommends: Neuroscience Information Framework
recommends: National Institute on Drug Abuse Center for Genetic Studies
recommends: NIDA Data Share
recommends: AphasiaBank
recommends: FluencyBank
recommends: NIDDK Central Repository
recommends: NIDDK Information Network (dkNET)
recommends: Nuclear Receptor Signaling Atlas
recommends: Chemical Effects in Biological Systems (CEBS)
recommends: Cell Image Library (CIL)
recommends: PhysioNet
recommends: Transporter Classification Database
recommends: Biological General Repository for Interaction Datasets (BioGRID)
recommends: Federal Interagency Traumatic Brain Injury Research Informatics System
recommends: NeuroMorpho.Org
recommends: Parkinson’s Disease Biomarkers Program Data Management Resource (PDBP DMR)
recommends: The NINDS Human Cell and Data Repository (NHCDR)
recommends: ClinicalTrials.gov
recommends: dbSNP
recommends: dbVar
recommends: GenBank
recommends: Gene Expression Omnibus (GEO)
recommends: NCBI Sequence Read Archive (SRA)
recommends: 1000 Functional Connectomes Project
recommends: exRNA Atlas
recommends: Accelerating Medicines Partnership Type 2 Diabetes Knowledge Portal (AMP-T2D)
recommends: PeptideAtlas
recommends: Zebrafish Information Network (ZFIN)
recommends: FlyBase
recommends: Database of Interacting Proteins (DIP)
recommends: Mouse Genome Informatics (MGI)
recommends: UniProt
recommends: Research Collaboratory for Structural Bioinformatics Protein Data Bank (RCSB PDB)
recommends: European Nucleotide Archive (ENA)
recommends: Analysis, Visualization, and Informatics Lab-space (AnVIL)
recommends: DNA DataBank of Japan (DDBJ)
recommends: UniProtKB
recommends: SPARC Portal
is related to: CureHunter
is related to: Entrez
has parent organization: National Institutes of Health
is parent organization of: MalariaWorld
is parent organization of: GenNav
is parent organization of: NIH Common Data Element Repository
is parent organization of: MEDLINE
is parent organization of: ClinicalTrials.gov
is parent organization of: Developmental and Reproductive Toxicology Database
is parent organization of: Directory of Health Organizations Online
is parent organization of: Haz-Map: Occupational Exposure to Hazardous Agents
is parent organization of: Hazardous Substances Data Bank
is parent organization of: Drug Information Portal
is parent organization of: NIH Data Sharing Repositories
is parent organization of: MeSH
is parent organization of: Unified Medical Language System
is parent organization of: NCBI
is parent organization of: MedlinePlus
is parent organization of: RxNorm
is parent organization of: Bibliography on Alternatives to the Use of Live Vertebrates in Biomedical Research and Testing
is parent organization of: Chemical Carcinogenesis Research Information System
is parent organization of: International Toxicity Estimates for Risk
is parent organization of: BLAST Assembled RefSeq Genomes
is parent organization of: Cross-Sectional and Longitudinal Aging Study
is parent organization of: OrbitProject
is parent organization of: Household Products Database
is parent organization of: Entrez Utilities
is parent organization of: Epidemiology of Chronic Disease in the Oldest Old
nlx_inv_1005117 SCR_011446 U.S. National Library of Medicine 2026-02-14 02:02:19 391
Network of Minority Health Research Investigators
 
Resource Report
Resource Website
1+ mentions
Network of Minority Health Research Investigators (RRID:SCR_006589) NMRI data or information resource, portal, community building portal, resource Communication network of current and potential biomedical research investigators and technical personnel from traditionally under-served communities: African American, Hispanic American, American Indian, Alaskan Native, Native Hawaiian, and other Pacific Islanders. The major objective of the network is to encourage and facilitate participation of members of underrepresented racial and ethnic minority groups in the conduct of biomedical research in the fields of diabetes, endocrinology, metabolism, digestive diseases, nutrition, kidney, urologic and hematologic diseases. A second objective is to encourage and enhance the potential of the underrepresented minority investigators in choosing a biomedical research career in these fields. An important component of this network is promotion of two-way communications between network members and the NIDDK. african-american, hispanic american, american indian, alaskan native, native hawaiian, pacific islander, minority, endocrinology, metabolism, nutrition, kidney, urology, hematology, digestion, minority health, race, ethnicity is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
Diabetes, Digestive disease, Kidney disease, Urologic disease, Hematologic disease NIDDK nlx_152865 SCR_006589 Network of Minority Health Research Investigators (NMRI) 2026-02-14 02:01:12 5
LIPID Metabolites And Pathways Strategy
 
Resource Report
Resource Website
1000+ mentions
LIPID Metabolites And Pathways Strategy (RRID:SCR_006579) LIPID MAPS data or information resource, narrative resource, database, standard specification Multi-institutional supported website and database that provides access to large number of globally used lipidomics resources. Internationally led the field of lipid curation, classification, and nomenclature since 2003. Produces new open-access databases, informatics tools and lipidomics-focused training activities will be generated and made publicly available for researchers studying lipids in health and disease. lipid, pathway, classification, metabolomics, metabolite, FASEB list is listed by: NIDDK Information Network (dkNET)
has parent organization: University of California at San Diego; California; USA
is parent organization of: LIPID MAPS Proteome Database
is parent organization of: LIPID MAPS Structure Database
NIGMS ;
Glue Grant
Free, Freely available nif-0000-00368, SCR_026208, r3d100012315 https://doi.org/10.17616/R3WW7G SCR_006579 , LIPID Maps database, LIPID Metabolites And Pathways Strategy database, LIPID Maps 2026-02-14 02:01:19 1266
Kidney and Urinary Pathway Ontology
 
Resource Report
Resource Website
Kidney and Urinary Pathway Ontology (RRID:SCR_006690) KUPO data or information resource, ontology, controlled vocabulary Ontology describing kidney and urinary pathways cell, anatomy, and disease. kidney, urinary, pathway, urine, cell, anatomy, disease, owl is related to: NIDDK Information Network (dkNET) Public domain nlx_154154 SCR_006690 2026-02-14 02:01:11 0
Urologic Diseases in America
 
Resource Report
Resource Website
Urologic Diseases in America (RRID:SCR_006644) UDA human subject report A report incorporating current and retrospective data on all aspects of the epidemiology, practice patterns, costs, and impact of urologic diseases in the United States and is intended for use by public officials, nongovernment organizations, the media, academic researchers, health professionals, and the public. The UDA compendium consists of data tables annotated in chapters that amplify the data analyses. The objectives of the UDA project include: secondary data analyses of: changes in the overall healthcare burden for individual urologic diseases, in physician practice patterns for each urologic disease, and in demographics of persons with urologic disease, the impact of specific urologic diseases, especially diseases of the prostate, on the minority populations of the U.S., and documentation of new and evolving therapies for urologic disease and their cost. epidemiology, urology, diagnosis, risk factor, prevalence, treatment, urological disease, report, practice pattern, data table, data analysis, prostate is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
has parent organization: National Kidney and Urologic Diseases Information Clearinghouse
Urologic disease National Institute of Diabetes and Digestive and Kidney Diseases Public, Acknowledgement requested nlx_152720 SCR_006644 Urologic Diseases in America Compendium, UDA Compendium 2026-02-14 02:01:20 0
National Diabetes Information Clearinghouse
 
Resource Report
Resource Website
National Diabetes Information Clearinghouse (RRID:SCR_006702) NDIC resource, data or information resource, service resource, narrative resource, training material Information dissemination service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) established to increase knowledge and understanding about diabetes among patients, health care professionals, and the general public: online, in booklets and fact sheets, by email, and over the phone. To carry out this mission, NDIC works closely with NIDDK''''s Diabetes Research and Training Centers; the National Diabetes Education Program (NDEP); professional, patient, and voluntary associations; Government agencies; and State health departments to identify and respond to informational needs about diabetes and its management. NDIC provides the following informational products and services: * Response to inquiries about diabetes, ranging from information about available patient and professional education materials to statistical data. By phone (8:30 a.m. to 5 p.m. eastern time, M-F), fax, mail, and email. * Publications about diabetes, provided free of copyright, in varying reading levels. Available online or as booklets and brochures. NDIC also sends publications to health fairs and community events. * Referrals to health professionals through the National Library of Medicine''''s MEDLINEplus includes a consumer-friendly listing of organizations that will assist you in your search for physicians and other health professionals. * Exhibits at professional meetings specific to diabetes, as well as cross-cutting professional meetings. NDIC exhibits at 12 professional meetings, each year, including American Diabetes Association Postgraduate Course, American College of Physicians, CDC Diabetes Translation Conference, American Academy of Physician Assistants, American Diabetes Association, American Association of Diabetes Educators, and American Dietetic Association. medical, nutrition, disease-related portal, statistics, digestive, kidney, urologic, publication, medicine, health, treatment is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is parent organization of: Diabetes in America
is parent organization of: Diabetes Control and Complications Trial
Diabetes NIDDK Public, Free nlx_152709 SCR_006702 National Diabetes Information Clearinghouse (NDIC) 2026-02-14 02:01:21 0
National Endocrine and Metabolic Diseases Information Service
 
Resource Report
Resource Website
National Endocrine and Metabolic Diseases Information Service (RRID:SCR_006681) NEMDIS resource, data or information resource, service resource, narrative resource, training material Information dissemination service of the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) providing information about endocrine and metabolic diseases in easy-to-understand language: online, in booklets and fact sheets, by email, and over the phone to patients, health professionals and the public. The NEMDIS provides the following informational products and services: * Response to inquiries about endocrine and metabolic diseases, ranging from information about available patient and professional education materials to referrals to patient support organizations. Assistance is available by phone (8:30 a.m. to 5 p.m. eastern time, M-F), fax, mail, and email. * Publications about endocrine and metabolic diseases, provided free of copyright, in varying reading levels. Available online or in hard copy. NEMDIS also sends publications to health fairs and community events. * Referrals to health professionals through the National Library of Medicine''''s MEDLINEplus, which includes a consumer-friendly listing of organizations to assist in the search for physicians and other health professionals. endocrine, metabolic, statistics, publication is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
Endocrine disease, Metabolic disease NIDDK Free, Public nlx_152713 SCR_006681 2026-02-14 02:01:22 0
Gastroparesis Clinical Research Consortium
 
Resource Report
Resource Website
Gastroparesis Clinical Research Consortium (RRID:SCR_006673) GpCRC portal, clinical trial, resource, data or information resource, research forum portal, disease-related portal, topical portal Perform clinical, epidemiological, and therapeutic research in gastroparesis and provide an infrastructure that can rapidly and efficiently design and conduct clinical trials for effective medical, surgical, or other interventions to improve treatment of patients with gastroparesis. The GpCRC studies comprise well characterized individuals with diabetic, surgical, and idiopathic gastroparesis. etiology, natural history, therapy, treatment is listed by: ClinicalTrials.gov
is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
has parent organization: Johns Hopkins University; Maryland; USA
Gastroparesis NIDDK nlx_152831 SCR_006673 Gastroparesis Clinical Research Consortium (GpCRC) 2026-02-14 02:01:20 0
Crystallography Open Database (COD)
 
Resource Report
Resource Website
10+ mentions
Crystallography Open Database (COD) (RRID:SCR_005874) COD data repository, storage service resource, data or information resource, service resource, database Database of crystal structures of organic, inorganic, metal-organic compounds and minerals, excluding biopolymers. It currently contains ~291204 entries (July 2014) in crystallographic information file format, with nearly full coverage of the International Union of Crystallography publications, and is growing in size and quality. Deposit your data: An interface allows you to upload, validate and edit CIF files before submitting them for deposition. inorganic, metal-organic, organic, molecule, structure, small molecule, compound, mineral, crystal structure, crystallography, polymorphism, crystal, organic compound is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: re3data.org
has parent organization: Vilnius University; Vilnius; Lithuania
Research Council of Lithuania contract MIP-124/2010 PMID:22070882
PMID:22477773
Public domain, The community can contribute to this resource, Acknowledgement requested r3d100010213, nlx_149430 https://doi.org/10.17616/R37S31 SCR_005874 COD - Crystallography Open Database, Crystallography Open Database, Crystallography Open Database (COD), COD 2026-02-14 02:01:10 17
Dryad Digital Repository
 
Resource Report
Resource Website
1000+ mentions
Dryad Digital Repository (RRID:SCR_005910) data repository, storage service resource, data or information resource, service resource, database International, curated, digital repository that makes the data underlying scientific publications discoverable, freely reusable, and citable. Particularly data for which no specialized repository exists. Provides the infrastructure for, and promotes the re-use of, data underlying the scholarly literature. Governed by a nonprofit membership organization. Membership is open to any stakeholder organization, including but not limited to journals, scientific societies, publishers, research institutions, libraries, and funding organizations. Most data are associated with peer-reviewed articles, although data associated with non-peer reviewed publications from reputable academic sources, such as dissertations, are also accepted. Used to validate published findings, explore new analysis methodologies, repurpose data for research questions unanticipated by the original authors, and perform synthetic studies.UC system is member organization of Dryad general subject data repository. international, digital, repository, curated, data, collection, scientific, medical, publication, dataset, FASEB list is used by: NIH Heal Project
is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: CINERGI
is listed by: re3data.org
is listed by: Connected Researchers
is listed by: DataCite
is listed by: FAIRsharing
is related to: ImpactStory
is related to: Connected Researchers
has parent organization: NESCent - National Evolutionary Synthesis Center
has parent organization: University of North Carolina at Chapel Hill; North Carolina; USA
has parent organization: University of California; California; USA
Institute for Museum and Library Services ;
JISC ;
NSF ;
European Commission
DOI:10.25504/FAIRsharing.wkggtx, DOI:10.5061, r3d100000044, DOI:10.15146, DOI:10.17616/R34S33, nlx_149486 https://doi.org/10.17616/R34S33
https://doi.org/10.5061/
https://doi.org/10.15146
https://dx.doi.org/10.5061/
https://dx.doi.org/10.15146
https://fairsharing.org/10.25504/FAIRsharing.wkggtx
https://api.datacite.org/dois?prefix=10.18736
https://api.datacite.org/dois?prefix=10.6076

https://doi.org/10.17616/R34S33
http://www.datadryad.org/ SCR_005910 , The Dryad Digital Repository, Dryad Digital Repository, Dryad 2026-02-14 02:01:00 2535
PubChem BioAssay
 
Resource Report
Resource Website
100+ mentions
PubChem BioAssay (RRID:SCR_010734) PubChem BioAssay data repository, storage service resource, data or information resource, service resource, database Data and information collection and repository for biological activities of small molecules and small interfering RNAs (siRNAs) hosted by the US National Institutes of Health (NIH). Used to select and summarize the bioactivities of tested substances. collection, compound, substance, bioassay, chemical, structure, biological, activity is recommended by: NIDDK Information Network (dkNET)
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is affiliated with: Entrez
is related to: PubChem
has parent organization: NCBI
Intramural Research program of the National Institutes of Health PMID:19933261
PMID:22140110
nlx_93939 http://pubchem.ncbi.nlm.nih.gov/
https://www.ncbi.nlm.nih.gov/pcassay
SCR_010734 NCBI PubChem BioAssay, PubChem BioAssay Database 2026-02-14 02:01:48 255
NIH Division of Nutrition Research Coordination
 
Resource Report
Resource Website
NIH Division of Nutrition Research Coordination (RRID:SCR_001469) DNRC data or information resource, portal, topical portal, training resource Coordinates nutritional sciences-related research and research training across the National Institutes of Health (NIH) and among Federal Agencies by providing mechanisms to communicate research, research training, policy, and education initiatives. The DNRC facilitates the exchange of information, coordinates workshops and seminars on critical issues, encourages national and international research collaborations, and serves as the NIH primary point of contact for the Department of Health and Human Services (DHHS) and other agencies, departments, and organizations in matters pertaining to nutritional sciences and physical activity. Through its dedicated efforts to promote scientific policy reviews, innovative research, interagency collaboration, and technical advancements, the DNRC strives to define the increasing roles of nutritional sciences and physical activity in health promotion and disease prevention and treatment. nutrition, adult human, child, nutritional sciences, physical activity, health promotion, disease prevention, treatment is listed by: NIDDK Information Network (dkNET)
has parent organization: National Institutes of Health
is parent organization of: Human Nutrition Research Information Management
NIH Free, Freely Available nlx_152699 http://dnrc.nih.gov/ SCR_001469 Division of Nutrition Research Coordination 2026-02-14 02:00:04 0
Epidemiology of Diabetes Interventions and Complications
 
Resource Report
Resource Website
1+ mentions
Epidemiology of Diabetes Interventions and Complications (RRID:SCR_001468) EDIC bibliography, clinical trial, resource, data or information resource, database 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 2026-02-14 02:00:09 1
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 portal, resource, data or information resource, research forum portal, disease-related portal, topical 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 2026-02-14 02:00:04 0
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, bibliography, resource 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 2026-02-14 02:00:01 0

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