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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Authority Synonyms Record Last Update Mentions Count
Type 1 Diabetes Genetics Consortium
 
Resource Report
Resource Website
1+ mentions
Type 1 Diabetes Genetics Consortium (RRID:SCR_001557) T1DGC data or information resource, disease-related portal, portal, research forum portal, resource, topical portal Data and biological samples were collected by this consortium organizing international efforts to identify genes that determine an individual risk of type 1 diabetes. It originally focused on recruiting families with at least two siblings (brothers and/or sisters) who have type 1 diabetes (affected sibling pair or ASP families). The T1DGC completed enrollment for these families in August 2009. They completed enrollment of trios (father, mother, and a child with type 1 diabetes), as well as cases (people with type 1 diabetes) and controls (people with no history of type 1 diabetes) from populations with a low prevalence of this disease in January 2010. T1DGC Data and Samples: Phenotypic and genotypic data as well as biological samples (DNA, serum and plasma) for T1DGC participants have been deposited in the NIDDKCentral Repositories for future research. gene, genetics, genotyping, analytic, dna, serum, plasma, data set, biomaterial supply resource, phenotypic, genotypic, autoantibody, hla, phenotype, genotype is listed by: One Mind Biospecimen Bank Listing
is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Central Repository
Type 1 diabetes, Diabetes NIDDK ;
NIAID ;
NHGRI ;
JDRF
PMID:17130525 Free, Freely available nlx_152867 SCR_001557 SciCrunch Registry Type 1 Diabetes Genetics Consortium (T1DGC) 2026-10-10 12:35:55 2
Intestinal Stem Cell Consortium
 
Resource Report
Resource Website
10+ mentions
Intestinal Stem Cell Consortium (RRID:SCR_001555) ISCC consortium, data or information resource, organization portal, portal THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 23,2022. Consortium to advance the understanding of intestinal epithelial stem cell biology during development, homeostasis, regeneration and disease. Its immediate goals are to isolate, characterize, culture and validate populations of intestinal stem cells; answer major questions in stem cell biology of the intestinal epithelium; and accelerate research by making information and resources available to the research community. Resources include data sets, protocols, and a resource catalog. Long-term goals include: 1) laying the ground work for therapeutic manipulation of the intestinal epithelium 2) contributing to the greater understanding of stem cell biology through knowledge of the intestine as a model stem cell-driven system. Research Projects are housed at 8 institutions across the nation: Oregon Health & Science University, Stanford University, Stowers Institute for Medical Research, University of California, Los Angeles School of Medicine (UCLA) (partnered with the VA Greater Los Angeles), University of North Carolina, Chapel Hill (UNC), University of Oklahoma, University of Pennsylvania, and University of Pittsburgh. intestinal, epithelial stem cell, development, homeostasis, regeneration, disease, intestine, stem cell, intestinal stem cell, intestinal epithelium, stem cell, antibody, epithelium, data set is used by: NIF Data Federation
is used by: NIDDK Information Network (dkNET)
is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
NIDDK U01DK085532 THIS RESOURCE IS NO LONGER IN SERVICE nlx_152862 SCR_001555 SciCrunch Registry ISCC - Intestinal Stem Cell Consortium 2026-10-10 12:36:02 19
Type 1 Diabetes Resource
 
Resource Report
Resource Website
1+ mentions
Type 1 Diabetes Resource (RRID:SCR_001475) T1DR biomaterial supply resource, material resource, organism supplier International repository for importation, curation, genotypic and phenotypic validation, cryopreservation, and distribution of mouse stocks of value to the type 1 diabetes scientific community holding over 250 genetically modified or congenic mouse stocks that are being used to dissect genetic and biologic features of T1D. They provide extensive genotypic and phenotypic quality control and genetic stabilization for these strains, as well as incidence studies when available. An added value of T1DR stocks is their ability to propel advances in related areas of science, including research in non-T1D autoimmunity and infectious diseases. The staff provides information and technical assistance regarding selection and use of existing T1DR models, and will provide limited support for development of new models considered to be of high-value for the T1D community. The resource includes strains generated at the Jackson Laboratory as well as strains donated by external scientists. Investigators are highly encouraged to donate a strain to ensure its preservation and availability to other researchers. genotype, phenotype, animal model is listed by: One Mind Biospecimen Bank Listing
is listed by: NIDDK Information Network (dkNET)
has parent organization: Jackson Laboratory
Type 1 diabetes, Diabetes NIDDK UC4DK097610 Free, Freely Available nlx_152730 SCR_001475 SciCrunch Registry 2026-10-10 12:36:03 1
Type 1 Diabetes TrialNet
 
Resource Report
Resource Website
10+ mentions
Type 1 Diabetes TrialNet (RRID:SCR_001508) TrialNet clinical trial, data or information resource, database, disease-related portal, portal, resource, topical portal International network of researchers who are exploring ways to prevent, delay and reverse the progression of type 1 diabetes. It is conducting clinical trials with researchers from 18 Clinical Centers in the United States, Canada, Finland, United Kingdom, Italy, Germany, Australia and New Zealand. In addition, more than 150 medical centers and physician offices are participating in the TrialNet network. Studies are available for people newly diagnosed with type 1 diabetes, as well as for relatives of people with type 1 diabetes who are at greater risk of developing the disease. This NIH-sponsored clinical trials network conducts studies designed to evaluate new approaches to prevent or ameliorate type 1 diabetes specifically by interdicting the type 1 diabetes disease process. These include interventions designed to decrease beta-cell destruction and/or enhance beta-cell survival. Studies are conducted in non-diabetic persons at risk of type 1 diabetes in an effort to delay the development of type 1 diabetes as a clinical disease; or (if initiated prior to appearance of autoimmunity) in an effort to delay the appearance of autoimmunity; or in individuals with type 1 diabetes who are either newly diagnosed or have evidence of sustained beta cell function. Studies include long-term follow-up of subjects developing type 1 diabetes. The TrialNet network also supports natural history and genetics studies in populations screened for or enrolled in studies conducted by the TrialNet study group. In addition, TrialNet will evaluate methodologies that enhance the conduct of clinical trials interdicting the type 1 diabetes disease process. intervention, beta-cell, clinical, child, young human, natural history, genetics, prevention, delay is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Central Repository
has parent organization: University of South Florida; Florida; USA
is parent organization of: Living Biobank
Diabetes, Type 1 diabetes NIDDK U01DK061058 Available to the research community nlx_152812 SCR_001508 SciCrunch Registry 2026-10-10 12:35:56 22
CKID A Prospective Cohort Study of Kidney Disease in Children
 
Resource Report
Resource Website
10+ mentions
CKID A Prospective Cohort Study of Kidney Disease in Children (RRID:SCR_001500) CKID bibliography, data or information resource, disease-related portal, portal, research forum portal, resource, topical portal Prospective, observational cohort study of children with mild to moderate chronic kidney disease (CKD) to: (1) determine risk factors for progression of pediatric chronic kidney disease (CKD); (2) examine the impact of CKD on neurocognitive development; (3) examine the impact of CKD on risk factors for cardiovascular disease, and; (4) examine the impact of CKD on growth. The CKiD study population will include a cohort of 540 children, age 1 16 years, expected to be enrolled over a 24-month period. child, young human, pediatric, risk factor, kidney function, neurodevelopment, cognitive ability, behavior, kidney, urologic problem, glomerular disease, adverse effect, cognition, growth, adolescent, infant, clinical is listed by: NIDDK Information Network (dkNET)
has parent organization: Johns Hopkins University; Maryland; USA
Chronic kidney disease, Renal disease, Cardiovascular disease NIDDK U01DK066174;
NCRR M01RR000052
Free, Freely available nlx_152790 SCR_001500 SciCrunch Registry CKID: A Prospective Cohort Study of Kidney Disease in Children, Chronic Kidney Disease in Children 2026-10-10 12:35:54 10
Collaborative Islet Transplant Registry
 
Resource Report
Resource Website
1+ mentions
Collaborative Islet Transplant Registry (RRID:SCR_001466) CITR data or information resource, data repository, database, narrative resource, report, resource, service resource, storage service resource Collect, analyze, and communicate on comprehensive and current data on all islet/beta cell transplants in human recipients performed in North America, as well as some European and Australian centers to expedite progress and promote safety in islet/beta cell transplantation. This site serves as a repository for general information concerning protocols, clinical transplantation sites, publications, and other information of interest to the general community. Annual Reports are available. Islet/beta cell transplantation is a complex procedure with many factors contributing to the outcome. Compiling and analyzing data from all transplant centers in the US, Canada, as well as some European and Australian centers will accelerate the identification of both critical risk factors and key determinants of success and thereby guide transplant centers in developing and refining islet/beta cell transplant protocols. The inclusion of the term collaborative in the name of the Registry emphasizes the importance of collaboration in fulfilling the CITR mission and goals. Close collaboration with the transplant centers will ensure that relevant questions are addressed, that data submitted are accurate and complete, and that the needs of the transplant community are served. Information on how to participate as a CITR Transplant Center and to receive a transplant center application is available through the website. Progress in islet transplantation depends entirely on complete, high-quality medical data, including the information patients consented to report to the Collaborative Islet Transplant Registry. To make it as easy as possible to provide updated information about patient's health, an on-line questionnaire is available or patients can mail it to their transplant center. This information is very important in the continuing search for a cure for Type 1 diabetes. transplant center, transplant, islet, beta cell, clinical, islet transplantation, beta cell transplantation, outcome, metadata standard, adverse event report, diabetes, data element, bibliography, questionnaire, protocol, risk factor, case report form, allograft, pancreatectomy, autograft, islet processing is listed by: NIDDK Information Network (dkNET) Type 1 diabetes, Diabetes NIDDK N01-DK6-2868;
NIDDK N01-DK1-2472
PMID:15387102 Free, Freely Available nlx_152693 SCR_001466 SciCrunch Registry 2026-10-10 12:35:56 9
Teen-Longitudinal Assessment of Bariatric Surgery
 
Resource Report
Resource Website
Teen-Longitudinal Assessment of Bariatric Surgery (RRID:SCR_001492) consortium, data or information resource, organization portal, portal THIS RESOURCE IS NO LONGER IN SERVICE. Documented on June 29,2023. Consortium made up of five clinical centers and a data coordinating center. The goal of Teen-LABS is to conduct clinical, epidemiological, and behavioral research in adolescent bariatric surgery, through an observational prospective study protocol. Teen-LABS is an ancillary study to LABS, an observational study of adult bariatric surgery. Research staff, certified in standardized uniform data collection according to the protocol, collect data at pre-operative research visits, at surgery, 30 days and six months post-operative, and annual post-operative research visits at the five participating centers. adolescent human, bariatrics, pre-operative, at surgery, post-operative, clinical, epidemiology, behavior, surgical outcome, metadata standard, observational study, clinical, experimental protocol, evidence-based recommendation, patient evaluation, follow-up care is listed by: NIDDK Information Network (dkNET) Bariatric surgery, Obesity NIDDK R01DK080020 THIS RESOURCE IS NO LONGER IN SERVICE SCR_014388, nlx_152747 SCR_001492 SciCrunch Registry Teen-LABS, Adolescent Bariatrics: Assessing Health Benefits and Risks, Teen-Longitudinal Assessment of Bariatric Surgery, Adolescent Bariatrics: Assessing Health Benefits and Risks (Teen-LABS) 2026-10-10 12:36:04 0
Globin Gene Server
 
Resource Report
Resource Website
10+ mentions
Globin Gene Server (RRID:SCR_001480) Globin Gene Server analysis service resource, data analysis service, data or information resource, database, narrative resource, production service resource, resource, service resource, software resource, source code, training material Data and tools for studying the function of DNA sequences, with an emphasis on those involved in the production of hemoglobin. It includes information about naturally-occurring human hemoglobin mutations and their effects, experimental data related to the regulation of the beta-like globin gene cluster, and software tools for comparing sequences with one another to discover regions that are likely to play significant roles. dna sequence, hemoglobin, mutation, globin gene cluster, sequence comparison, functional genomics, gene, alignment, genetic analysis, variant, gene expression, protein, thalassemia, globin gene, genome, pairwise alignment, multiple alignment, annotation, sequence analysis, dna is listed by: NIDDK Information Network (dkNET)
has parent organization: Pennsylvania State University
NLM R01LM05773;
NLM R01LM05110;
NIDDK DK27635
PMID:11857738
PMID:11480780
PMID:9799599
PMID:9576329
PMID:8088828
Free, Freely available nlx_152723 SCR_001480 SciCrunch Registry 2026-10-10 12:35:56 30
Nonalcoholic Steatohepatitis Clinical Research Network
 
Resource Report
Resource Website
10+ mentions
Nonalcoholic Steatohepatitis Clinical Research Network (RRID:SCR_001519) NASH CRN clinical trial, data or information resource, disease-related portal, portal, research forum portal, resource, topical portal Clinical research network to focus on the etiology, contributing factors, natural history, complications, and therapy of nonalcoholic steatohepatitis. They research the nature and underlying cause of Nonalcoholic Steatohepatitis (NASH) and conduct clinical studies on prevention and treatment. Approximately 1,500 pediatric and adult participants throughout the United States and Canada with nonalcoholic fatty liver disease (NAFLD) have enrolled into a database. The NASH CRN has recently reopened the database to enroll additional pediatric and adult participants with NAFLD. Serum, liver tissue, and genomic DNA samples are being collected and stored in the NIDDKrepository for ongoing as well as future studies. A three-arm randomized, placebo-controlled clinical trial of pioglitazone versus vitamin E completed enrollment in 2009. In addition to this adult trial, a similar trial in pediatric NASH patients randomized 180 children to receive treatment with vitamin E, metformin, or placebo. prevention, treatment, pediatric, child, adult human, serum, liver tissue, dna, placebo, pioglitazone, vitamin e, metformin, etiology, contributing factor, natural history, complication, therapy, young human, database, clinical trial, bibliography, patient registry is listed by: One Mind Biospecimen Bank Listing
is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Central Repository
has parent organization: Johns Hopkins University; Maryland; USA
Nonalcoholic steatohepatitis, Nonalcoholic fatty liver disease NIDDK 1ZIADK075013 Free, Freely available nlx_152845 https://www.nashcrn.com SCR_001519 SciCrunch Registry Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN), Clinical Research Network in Nonalcoholic Steatohepatitis 2026-10-10 12:36:04 21
Pediatric Acute Liver Failure Study
 
Resource Report
Resource Website
Pediatric Acute Liver Failure Study (RRID:SCR_001478) PALF data or information resource, disease-related portal, portal, research forum portal, resource, topical portal Study group and network for a 2008 longitudinal study for the etiology, diagnosis, treatment, and outcome of acute liver failure in infants, children, and adolescents. Data from patients include urine, bile, serum, liver tissue, cell lines derived from fibroblast culture, and DNA. management strategy, infant, child, adolescent, clinical, liver, patient care, rare disease, blood, tissue, longitudinal, urine, bile, serum, liver tissue, cell line, fibroblast culture, dna, etiology, diagnosis, treatment, outcome is listed by: NIDDK Information Network (dkNET)
is related to: Acute Liver Failure Study Group
has parent organization: University of Pittsburgh; Pennsylvania; USA
Acute liver failure NIDDK U01DK072146 Free, Freely available nlx_152715 http://www.palfstudy.org/ SCR_001478 SciCrunch Registry Pediatric Acute Liver Failure (PALF) Study, Pediatric Acute Liver Failure (PALF) Study Group 2026-10-10 12:36:01 0
GenitoUrinary Development Molecular Anatomy Project
 
Resource Report
Resource Website
100+ mentions
GenitoUrinary Development Molecular Anatomy Project (RRID:SCR_001554) GUDMAP biomaterial supply resource, material resource, organism supplier Project aggregates and provides experimental gene expression data from genito-urinary system. International consortium providing molecular atlas of gene expression for developing organs of GenitoUrinary (GU) tract. Mouse strains to facilitate developmental and functional studies within GU system. Experimental protocols and standard specifications. Tutorials describing GU organogenesis and primary data via database. Data are from large-scale in situ hybridization screens (wholemount and section) and microarray gene expression data of microdissected, laser-captured and FACS-sorted components of developing mouse genitourinary (GU) system. gene expression, genitourinary tract, molecular anatomy, genitourinary system, organogenesis, genitourinary, in situ hybridization, immunohistochemistry, microarray, mutant mouse strain, development, rna, protein, theiler stage, gene, anatomy, male, female, embryonic mouse, kidney, urogenital tract, urinary, reproductive, disease, molecule, cell, gene, phenotype, functional annotation, protein interaction, transgenic transgene, image, rna extraction, sample preparation, fluorescent immunohistochemistry, rna isolation, rna amplification, labeling, fluorescent in situ-hybridization, riboprobe synthesis, cellular localization, tissue isolation, embedding, cryostat sectioning, laser capture microdissection, paraffin, whole mount, optimal cutting temperature, riboprobe synthesis, target amplification, sectioning, FASEB list is used by: NIDDK Information Network (dkNET)
is listed by: One Mind Biospecimen Bank Listing
is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
is listed by: Collaborating for the Advancement of Interdisciplinary Research in Benign Urology
is related to: ToppCluster
is related to: One Mind Biospecimen Bank Listing
is parent organization of: GUDMAP Ontology
is parent organization of: GATACA GUDMAP Gene Explorer
NIDDK DK070136;
NIDDK DK070181;
NIDDK DK070200
PMID:21652655
PMID:18287559
THIS RESOURCE IS NO LONGER IN SERVICE nlx_152871, nif-0000-33426 SCR_001554 SciCrunch Registry Murine Atlas for Genitourinary Development 2026-10-10 12:36:05 289
TOMUS
 
Resource Report
Resource Website
TOMUS (RRID:SCR_001549) TOMUS bibliography, clinical trial, data or information resource, resource Study that compared the outcomes of two minimally invasive surgical procedures to treat stress urinary incontinence in women. These procedures are called mid-urethral slings. The procedures insert a mesh sling or hammock to support the bladder neck so that urine does not leak. Both procedures have been approved by the FDA and have been shown to be safe and successful in treating stress urinary incontinence. However, it is not known if one is better than the other. This study answers that question. The secondary aims of the trial are to compare other outcomes for the two surgical procedures, including quality of life, sexual function, satisfaction with treatment outcomes, complications, and the need for other treatments(s) after surgery. Follow-up will be a minimum of two years. Stress urinary incontinence is the accidental leakage of urine during activities such as coughing, laughing, sneezing, or lifting heavy objects. surgical procedure, female, mid-urethral sling, treatment, outcome, quality of life, sexual function, complication, retropubic mid-urethral sling, transobturator mid-urethral sling, adult human is listed by: ClinicalTrials.gov
is listed by: NIDDK Information Network (dkNET)
has parent organization: Urinary Incontinence Treatment Network
Stress urinary incontinence, Urinary incontinence NIDDK U01DK060401;
NIDDK U01DK060379;
NIDDK U01DK060397;
NIDDK U01DK058234;
NIDDK U01DK060393;
NIDDK U01DK058229;
NIDDK U01DK058225
PMID:20479459
PMID:22378483
PMID:21422865
PMID:21925636
PMID:23635737
Free, Freely available nlx_152859 SCR_001549 SciCrunch Registry Trial Of Mid-Urethral Slings, TOMUS-Trial Of Mid-Urethral Slings 2026-10-10 12:36:02 0
SISTEr
 
Resource Report
Resource Website
100+ mentions
SISTEr (RRID:SCR_001542) SISTEr clinical trial, data or information resource, data set, resource Clinical trial under the Urinary Incontinence Treatment Network to compare the treatment success for two surgical procedures that are frequently used and have similar cure rates, yet have not been compared directly to each other in a large, rigorously conducted randomized trial. The secondary aims of the trial are to compare other outcomes for the two surgical procedures, including quality of life, sexual function, satisfaction with treatment outcomes, complications, and need for other treatment(s) after surgery. Follow-up will be a minimum of two years and up to four years. urinary, incontinence, dataset, surgical procedure, outcome, quality of life, sexual function, satisfaction, treatment, complication, burch procedure, sling procedure, female, surgery is listed by: NIDDK Information Network (dkNET)
has parent organization: Urinary Incontinence Treatment Network
Urinary incontinence, Stress, Stress urinary incontinence NIDDK ;
NICHD
Free, Freely available nlx_152852 http://www.uitn.net/sister.asp SCR_001542 SciCrunch Registry Stress Incontinence Surgical Treatment Efficacy Trial 2026-10-10 12:36:05 151
HALT-C Trial
 
Resource Report
Resource Website
HALT-C Trial (RRID:SCR_001534) HALT-C Trial, HALT-C bibliography, clinical trial, data or information resource, resource Multi-center, randomized controlled study designed to determine if continuing interferon long term over several years will suppress the Hepatitis C virus, prevent progression to cirrhosis, prevent liver cancer and reduce the need for liver transplantation. Patient enrollment began in 2000 and was completed in 2003 at 10 clinical centers, which were supported by a data coordinating center, virological testing center, and central sample repository. Patients with chronic hepatitis C and advanced fibrosis or cirrhosis on liver biopsy who failed to respond to a previous course of interferon alfa were enrolled in this study. Patients were initially treated with a 24-week course of peginterferon alfa-2a and ribavirin. Patients who remained hepatitis C virus RNA positive were then randomized to receive maintenance, low-dose peginterferon or to be followed on no treatment. Liver biopsies were done before enrollment and after 2 and 4 years of treatment or follow-up. The endpoints were development of cirrhosis, hepatic decompensation, hepatocellular carcinoma, death, or liver transplantation. 1050 patients were randomized and followed through the 4 year randomized phase of the trial and as long as 4 years off treatment. Serum samples collected at multiple time points, DNA and liver tissue are available for scientific investigation. interferon, progression, cirrhosis, prevention, liver cancer, liver transplantation, liver, pegylated interferon, clinical, outcome, adult human, dna, liver tissue, serum, blood, b lymphoblastoid cell-line, epstein-barr virus infection in peripheral blood mononuclear cell, peripheral blood mononuclear cell, biomaterial supply resource, formalin fixed, histology, frozen, stained liver slide, unstained liver slide, advanced fibrosis, liver biopsy, peginterferon alfa-2a, ribavirin is listed by: One Mind Biospecimen Bank Listing
is listed by: ClinicalTrials.gov
is listed by: NIDDK Central Repository
is listed by: NIDDK Research Resources
is listed by: NIDDK Information Network (dkNET)
Hepatitis C virus, Chronic hepatitis C NIDDK Free, Freely available nlx_152835 http://archives.niddk.nih.gov/haltctrial/displaypage.aspx?pagename=haltctrial/index.htm http://www.haltctrial.org/ SCR_001534 SciCrunch Registry Hepatitis C Antiviral Long-term Treatment against Cirrhosis, Hepatitis C Antiviral Long-term Treatment against Cirrhosis (HALT-C) Trial, Hepatitis C Antiviral Long-term Treatment against Cirrhosis Trial 2026-10-10 12:35:54 0
TEDDY
 
Resource Report
Resource Website
1+ mentions
TEDDY (RRID:SCR_000383) TEDDY clinical trial, consortium, data or information resource, database, organization portal, portal International consortium of six centers assembled to participate in the development and implementation of studies to identify infectious agents, dietary factors, or other environmental agents, including psychosocial factors, that trigger type 1 diabetes in genetically susceptible people. The coordinating centers recruit and enroll subjects, obtaining informed consent from parents prior to or shortly after birth, genetic and other types of samples from neonates and parents, and prospectively following selected neonates throughout childhood or until development of islet autoimmunity or T1DM. The study tracks child diet, illnesses, allergies and other life experiences. A blood sample is taken from children every 3 months for 4 years. After 4 years, children will be seen every 6 months until the age of 15 years. Children are tested for 3 different autoantibodies. The study will compare the life experiences and blood and stool tests of the children who get autoantibodies and diabetes with some of those children who do not get autoantibodies or diabetes. In this way the study hopes to find the triggers of T1DM in children with higher risk genes. consortium, gene, infectious agent, dietary factor, environmental factor, young human, insulin, child, pediatric, autoantibody, blood, stool, biomaterial supply resource, longitudinal, neonate, parent, genetic risk, genetic factor, observation, prospective, serum, plasma, peripheral blood mononuclear cell, saliva, nasal swab, nail clipping, water, dna, virus, nutrition, toxic agent, socioeconomic, psychosocial, male, female, environment, exposure, diet, toxin, infectious agent, bacterial, viral, immunization is listed by: One Mind Biospecimen Bank Listing
is listed by: ClinicalTrials.gov
is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Central Repository
is related to: Teddy study IA prediction
has parent organization: University of South Florida; Florida; USA
Type 1 diabetes, Diabetes NIDDK 2UC4DK063829 PMID:21564455 nlx_152857 SCR_000383 SciCrunch Registry The Environmental Determinants of Diabetes in the Young, TEDDY study 2026-10-10 12:35:36 3
Trans-Institute Angiogenesis Research Program
 
Resource Report
Resource Website
Trans-Institute Angiogenesis Research Program (RRID:SCR_000384) TARP data or information resource, portal, resource, topical portal Trans-NIH program encouraging and facilitating the study of the underlying mechanisms controlling blood vessel growth and development. Other aims include: to identify specific targets and to develop therapeutics against pathologic angiogenesis in order to reduce the morbidity due to abnormal blood vessel proliferation in a variety of disease states; to better understand the process of angiogenesis and vascularization to improve states of decreased vascularization; to encourage and facilitate the study of the processes of lymphangiogenesis; and to achieve these goals through a multidisciplinary approach, bringing together investigators with varied backgrounds and varied interests. blood vessel, growth, development, target, therapeutic, vascularization, angiogenesis, lymphangiogenesis is listed by: NIDDK Information Network (dkNET)
has parent organization: National Institutes of Health
Angiogenesis, Lymphangiogenesis JDRF ;
NEI ;
NHLBI ;
NCI ;
NICHD ;
NIDDK ;
NINDS
THIS RESOURCE IS NO LONGER IN SERVICE nlx_152866 SCR_000384 SciCrunch Registry Trans-Institute Angiogenesis Research Program (TARP) 2026-10-10 12:35:37 0
ToppGene Suite
 
Resource Report
Resource Website
1000+ mentions
ToppGene Suite (RRID:SCR_005726) analysis service resource, data analysis service, data or information resource, database, portal, production service resource, resource, service resource ToppGene Suite is a one-stop portal for gene list enrichment analysis and candidate gene prioritization based on functional annotations and protein interactions network. ToppGene Suite is a one-stop portal for (i) gene list functional enrichment, (ii) candidate gene prioritization using either functional annotations or network analysis and (iii) identification and prioritization of novel disease candidate genes in the interactome. Functional annotation-based disease candidate gene prioritization uses a fuzzy-based similarity measure to compute the similarity between any two genes based on semantic annotations. The similarity scores from individual features are combined into an overall score using statistical meta-analysis. gene portal, enrichment analysis, functional annotation, gene prioritization, protein interaction, bio.tools, FASEB list is listed by: Gene Ontology Tools
is listed by: NIDDK Information Network (dkNET)
is listed by: GUDMAP Ontology
is listed by: Debian
is listed by: bio.tools
is related to: Gene Ontology
is related to: ToppCluster
State of Ohio Computational Medicine Center ODD TECH 04-042;
NIDDK 1U01DK70219;
NIDDK P30DK078392
PMID:19465376 Free for academic use nlx_149183, biotools:toppgene_suite https://bio.tools/toppgene_suite SCR_005726 SciCrunch Registry ToppGene 2026-10-10 12:37:11 1131
Glomerular Filtration Rate Calculators
 
Resource Report
Resource Website
Glomerular Filtration Rate Calculators (RRID:SCR_006443) GFR Calculators analysis service resource, data analysis service, production service resource, resource, service resource Glomerular Filtration Rate (GFR) calculators to estimate kidney function for adults (MDRD GFR Calculator) and children (Schwartz GFR Calculator). In adults, the recommended equation for estimating glomerular filtration rate (GFR) from serum creatinine is the Modification of Diet in Renal Disease (MDRD) Study equation. The IDMS-traceable version of the MDRD Study equation is used. Currently the best equation for estimating glomerular filtration rate (GFR) from serum creatinine in children is the Bedside Schwartz equation for use with creatinine methods with calibration traceable to IDMS. Using the original Schwartz equation with a creatinine value from a method with calibration traceable to IDMS will overestimate GFR. adult human, child, glomerular filtration rate, estimate, kidney function, serum creatinine is related to: Creatinine Standardization Program
is related to: NIDDK Information Network (dkNET)
has parent organization: National Kidney Disease Education Program
Chronic kidney disease NIDDK PMID:16908915 nlx_152733 SCR_006443 SciCrunch Registry Glomerular Filtration Rate Calculator, Glomerular Filtration Rate (GFR) Calculator 2026-10-10 12:37:31 0
Creatinine Standardization Program
 
Resource Report
Resource Website
1+ mentions
Creatinine Standardization Program (RRID:SCR_006441) Creatinine Standardization Program data or information resource, experimental protocol, international standard specification, narrative resource, resource, standard specification Standard specification to reduce inter-laboratory variation in creatinine assay calibration and therefore enable more accurate estimates of glomerular filtration rate (eGFR). Created by NKDEP''''s Laboratory Working Group in collaboration with the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) and the European Communities Confederation of Clinical Chemistry (now called the European Federation of Clinical Chemistry and Laboratory Medicine), the effort is part of a larger NKDEP initiative to help health care providers better identify and treat chronic kidney disease in order to prevent or delay kidney failure and improve patient outcomes. Recommendations are intended for the USA and other countries or regions that have largely completed standardization of creatinine calibration to be traceable to an isotope dilution mass spectrometry (IDMS) reference measurement procedure. The program''''s focus is to facilitate the sharing of information to assist in vitro diagnostic manufacturers, clinical laboratories, and others in the laboratory community with calibrating their serum creatinine measurement procedures to be traceable to isotope dilution mass spectrometry (IDMS). The program also supports manufacturers'''' efforts to encourage their customers in the laboratory to coordinate use of standardized creatinine methods with implementation of a revised GFR estimating equation appropriate for use with standardized creatinine methods. Communication resources and other information for various segments of the laboratory community are available in the Creatinine Standardization Recommendations section of the website. Also available is a protocol for calibrating creatinine measurements using whole blood devices. The National Institute for Standards and Technology (NIST) released a standard reference material (SRM 967 Creatinine in Frozen Human Serum) for use in establishing calibrations for routine creatinine measurement procedures. SRM 967 was validated to be commutable with native serum samples for many routine creatinine procedures and is useful to establish or verify traceability to an IDMS reference measurement procedure. Establishing calibrations for serum creatinine methods using SRM 967 not only provides a mechanism for ensuring more accurate measurement of serum creatinine, but also enables more accurate estimates of GFR. For clinical laboratories interested in independently checking the calibration supplied by their creatinine reagent suppliers/manufacturers, periodic measurement of NIST SRM 967 should be considered for inclusion in the lab''''s internal quality assurance program. To learn more about SRM 967, including how to purchase it, visit the NIST website, https://www-s.nist.gov/srmors/quickSearch.cfm creatinine, estimate, glomerular filtration rate, kidney, isotope dilution mass spectrometry, whole blood, calibration, serum, serum creatinine, clinical is related to: Glomerular Filtration Rate Calculators
is related to: NIDDK Information Network (dkNET)
is related to: NIST - National Institute of Standards and Technology
has parent organization: National Kidney Disease Education Program
Chronic kidney disease NIDDK nlx_152736 SCR_006441 SciCrunch Registry 2026-10-10 12:38:03 2
Autoimmunity Centers of Excellence
 
Resource Report
Resource Website
Autoimmunity Centers of Excellence (RRID:SCR_006510) ACE data or information resource, disease-related portal, portal, research forum portal, resource, topical portal Nine centers that conduct clinical trials and basic research on new immune-based therapies for autoimmune diseases. This program enhances interactions between scientists and clinicians in order to accelerate the translation of research findings into medical applications. By promoting better coordination and communication, and enabling limited resources to be pooled, ACEs is one of NIAID''''s primary vehicles for both expanding our knowledge and improving our ability to effectively prevent and treat autoimmune diseases. This coordinated approach incorporates key recommendations of the NIH Autoimmune Diseases Research Plan and will ensure progress in identifying new and highly effective therapies for autoimmune diseases. ACEs is advancing the search for effective treatments through: * Diverse Autoimmunity Expertise Medical researchers at ACEs include rheumatologists, neurologists, gastroenterologists, and endocrinologists who are among the elite in their respective fields. * Strong Mechanistic Foundation ACEs augment each clinical trial with extensive basic studies designed to enhance understanding of the mechanisms responsible for tolerance initiation, maintenance, or loss, including the role of cytokines, regulatory T cells, and accessory cells, to name a few. * Streamlined Patient Recruitment The cooperative nature of ACEs helps scientists recruit patients from distinct geographical areas. The rigorous clinical and basic science approach of ACEs helps maintain a high level of treatment and analysis, enabling informative comparisons between patient groups. immune system, infection, clinical trial, clinical, basic research is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
Type 1 diabetes, Diabetes, Autoimmune disease, Systematic lupus erythematosus, Rheumatoid arthritis, Sjogren's syndrome, Multiple sclerosis, Chronic inflammatory bowel disease, Pemphigus vulgaris, Scleroderma NIAID ;
NIDDK ;
NIH Office of Research on Womens Health
nlx_152751 SCR_006510 SciCrunch Registry 2026-10-10 12:37:27 0

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