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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 Synonyms Record Last Update Mentions Count
Glomerular Filtration Rate Calculators
 
Resource Report
Resource Website
Glomerular Filtration Rate Calculators (RRID:SCR_006443) GFR Calculators production service resource, data analysis service, resource, analysis service 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 Glomerular Filtration Rate Calculator, Glomerular Filtration Rate (GFR) Calculator 2026-08-03 09:33:04 0
United States Renal Data System
 
Resource Report
Resource Website
50+ mentions
United States Renal Data System (RRID:SCR_006699) USRDS database, narrative resource, resource, data or information resource, report Annual report, standard analysis files and an online query system from the national data registry on the end-stage renal disease (ESRD) population in the U.S., including treatments and outcomes. The Annual Data Report is divided into two parts. The Atlas section displays data using graphs and charts. Specific chapters address trends in ESRD patient populations, quality of ESRD care, kidney transplantation outcomes, costs of ESRD care, Healthy People 2010 objectives, chronic kidney disease, pediatric ESRD, and cardiovascular disease special studies. The Reference Tables are devoted entirely to the ESRD population. The RenDER (Renal Data Extraction and Referencing) online data query system allows users to build data tables and maps for the ESRD population. National, state, and county level data are available. USRDS staff collaborates with members of Centers for Medicare & Medicaid Services (CMS), the United Network for Organ Sharing (UNOS), and the ESRD networks, sharing datasets and actively working to improve the accuracy of ESRD patient information. renal, population, socio-demographic, treatment modality, treatment, kidney, trend, kidney transplantation, outcome, cost, pediatric, cardiovascular disease, incidence, prevalence, patient characteristic, clinical indicator, preventive care, hospitalization, survival, medicare, FASEB list is listed by: NIDDK Information Network (dkNET)
is listed by: NIDDK Research Resources
End-stage renal disease, Chronic kidney disease NIDDK PMID:23124788 Free, Public domain, Acknowledgement requested, Account required, For RenDER nlx_152716 SCR_006699 U.S. Renal Data System 2026-08-03 09:33:07 59
Nonhuman Primate Transplantation Tolerance Cooperative Study Group
 
Resource Report
Resource Website
Nonhuman Primate Transplantation Tolerance Cooperative Study Group (RRID:SCR_006847) NHPCSG portal, disease-related portal, resource, topical portal, research forum portal, data or information resource Cooperative program for research on nonhuman primate models of kidney, islet, heart, and lung transplantation evaluating the safety and efficacy of existing and new treatment regimens that promote the immune system''''s acceptance of a transplant and to understand why the immune system either rejects or does not reject a transplant. This program bridges the critical gap between small-animal research and human clinical trials. The program supports research into the immunological mechanisms of tolerance induction and development of surrogate markers for the induction, maintenance, and loss of tolerance. transplantation, clinical, kidney, islet, tolerance, heart, lung, treatment, immune system, tolerance induction is related to: NIDDK Information Network (dkNET) Kidney transplantation, Islet transplantation, Heart transplantation, Lung transplantation NIDDK ;
NIAID
nlx_152728 http://www.niddk.nih.gov/fund/diabetesspecialfunds/consortia/NHP.pdf SCR_006847 Non-human Primate Transplantation Tolerance Cooperative Study Group 2026-08-03 09:33:11 0
Diabetes in America
 
Resource Report
Resource Website
Diabetes in America (RRID:SCR_006754) Diabetes in America narrative resource, data or information resource, resource, book A compilation and assessment of epidemiologic, public health, and clinical data on diabetes and its complications in the United States. Published by the National Diabetes Data Group of the National Institute of Diabetes and Digestive and Kidney Diseases, the book contains 36 chapters organized in five areas: * the descriptive epidemiology of diabetes in the United States based on national surveys and community-based studies, including prevalence, incidence, sociodemographic and metabolic characteristics, risk factors for developing diabetes, and mortality * the myriad complications that affect patients with diabetes * characteristics of therapy and medical care for diabetes * economic aspects, including health insurance and health care costs * diabetes in special populations, including African Americans, Hispanics, Asian and Pacific Islanders, Native Americans, and pregnant women. Diabetes in America, 2nd Edition, has been designed to serve as a reliable scientific resource for assessing the scope and impact of diabetes and its complications, determining health policy and priorities in diabetes, and identifying areas of need in research. The intended audience includes health policy makers at the local and Federal levels who need a sound quantitative base of knowledge to use in decision making; clinicians who need to know the probability that their patients will develop diabetes and the prognosis of the disease for complications and premature mortality; persons with diabetes and their families who need sound information on which to make decisions about their life with diabetes; and the research community which needs to identify areas where important scientific knowledge is lacking. epidemiology, prevalence, incidence, sociodemographic, metabolic, risk factor, mortality, complication, therapy, medical care, economic, health insurance, health care cost, african american, hispanic, asian, pacific islander, native american, pregnant, clinical, pdf, medical care is related to: NIDDK Information Network (dkNET)
has parent organization: National Diabetes Information Clearinghouse
Diabetes NIDDK Public, Not copyrighted. The Clearinghouse encourages users of this publication to duplicate and distribute as many copies as desired. nlx_152695 SCR_006754 Diabetes in America 2nd Edition 2026-08-03 09:33:09 0
PeptideAtlas
 
Resource Report
Resource Website
100+ mentions
PeptideAtlas (RRID:SCR_006783) PeptideAtlas data repository, data or information resource, database, storage service resource, service resource Multi-organism, publicly accessible compendium of peptides identified in a large set of tandem mass spectrometry proteomics experiments. Mass spectrometer output files are collected for human, mouse, yeast, and several other organisms, and searched using the latest search engines and protein sequences. All results of sequence and spectral library searching are subsequently processed through the Trans Proteomic Pipeline to derive a probability of correct identification for all results in a uniform manner to insure a high quality database, along with false discovery rates at the whole atlas level. The raw data, search results, and full builds can be downloaded for other uses. All results of sequence searching are processed through PeptideProphet to derive a probability of correct identification for all results in a uniform manner ensuring a high quality database. All peptides are mapped to Ensembl and can be viewed as custom tracks on the Ensembl genome browser. The long term goal of the project is full annotation of eukaryotic genomes through a thorough validation of expressed proteins. The PeptideAtlas provides a method and a framework to accommodate proteome information coming from high-throughput proteomics technologies. The online database administers experimental data in the public domain. You are encouraged to contribute to the database. proteomics, peptide, mass spectrometry, annotation, eukaryotic, genome, peptide sequence, high-throughput mass spectrometry, ensembl, peptideprophet, protein sequence, blood plasma, protein, eukaryotic cell, dna, bio.tools, FASEB list is used by: NIF Data Federation
is used by: ProteomeXchange
is recommended by: NIDDK Information Network (dkNET)
is recommended by: National Library of Medicine
is recommended by: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is listed by: Biositemaps
is listed by: re3data.org
is listed by: bio.tools
is listed by: Debian
is related to: Ensembl
is related to: ProteomeXchange
is related to: NIH Data Sharing Repositories
is related to: Integrated Manually Extracted Annotation
has parent organization: Institute for Systems Biology; Washington; USA
NCI ;
NHGRI ;
NIGMS
PMID:20013378
PMID:23215161
PMID:16381952
PMID:15642101
Public, The community can contribute to this resource, Acknowledgement requested nif-0000-03266, r3d100010889, biotools:peptideatlas https://bio.tools/peptideatlas, https://doi.org/10.17616/R3BK61 SCR_006783 Peptide Atlas, PeptideAtlas 2026-08-03 09:33:14 479
National Kidney and Urologic Diseases Information Clearinghouse
 
Resource Report
Resource Website
1+ mentions
National Kidney and Urologic Diseases Information Clearinghouse (RRID:SCR_006842) NKUDIC service resource, narrative resource, resource, data or information 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 diseases of the kidneys and urologic system among people with these conditions and their families, health care professionals, and the general public: online, in booklets and fact sheets, by email, and over the phone. To carry out this mission, NKUDIC works closely with a coordinating panel of representatives from Federal agencies; voluntary organizations on the national level; professional groups; and State health departments to identify and respond to informational needs about kidney and urologic diseases. NKUDIC provides the following informational products and services: * Response to inquiries about kidney and urologic diseases-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 specific kidney and urologic diseases, provided free of copyright, in varying reading levels. Available online or as booklets and brochures. (See our Publications Catalog.) NKUDIC also sends publications to health fairs and community events. Please contact us for more information. * 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 kidney and urologic diseases, as well as cross-cutting professional meetings. NKUDIC exhibits at 11 professional meetings, each year, including Society of Urologic Nurses and Associates, American Urologic Association, American Society of Nephrology, National Kidney Foundation, Polycystic Kidney Disease Research Foundation, American Academy of Family Physicians, American Academy of Physician Assistants, American Nurses Association, and the National Conference for Nurse Practitioners. statistics, publication, kidney, urologic system, bladder, renal health, renal disease is related to: NIDDK Information Network (dkNET)
has parent organization: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases
is parent organization of: Urologic Diseases in America
Kidney disease, Urologic disease NIDDK Free, Public nlx_152711 SCR_006842 National Kidney and Urologic Diseases Information Clearinghouse (NKUDIC) 2026-08-03 09:33:11 1
National Addiction and HIV Data Archive Program (NAHDAP)
 
Resource Report
Resource Website
National Addiction and HIV Data Archive Program (NAHDAP) (RRID:SCR_000636) NAHDAP data repository, portal, disease-related portal, service resource, topical portal, storage service resource, data or information resource Archive that acquires, preserves and disseminates data relevant to drug addiction and HIV research. Collection of data on drug addiction and HIV infection in United States. Most of datasets are raw data from surveys, interviews, and administrative records. They were originally gathered in research projects and for administrative purposes. Some datasets have been used in published studies. Bibliographies of these studies are available . Provides access to research data and technical assistance for data depositors. Provides e-workshops on data preparation and data systems. drug addiction data, HIV infection data, uses: DataCite
is used by: NIH Heal Project
is recommended by: National Library of Medicine
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: Inter-university Consortium for Political and Social Research (ICPSR)
Addiction, Human immunodeficiency virus, HIV NIDA ;
Office of Behavioral and Social Sciences Research
Restricted nif-0000-06713, r3d100010261, DOI:10.3886 https://doi.org/10.3886/, https://dx.doi.org/10.3886/, https://doi.org/10.17616/R3PK64 SCR_000636 , National Addiction & HIV DATA Archive Program, National Addiction HIV Data Archive Program, National Addiction and HIV DATA Archive Program, NAHDAP, National Addiction and HIV DATA Archive Program (NAHDAP), National Addiction & HIV DATA Archive Program (NAHDAP), ICPSR/NAHDP 2026-08-03 09:31:06 0
Type 1 Diabetes Genetics Consortium
 
Resource Report
Resource Website
1+ mentions
Type 1 Diabetes Genetics Consortium (RRID:SCR_001557) T1DGC portal, disease-related portal, resource, topical portal, research forum portal, data or information resource 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 Type 1 Diabetes Genetics Consortium (T1DGC) 2026-08-03 09:31:22 2
Intestinal Stem Cell Consortium
 
Resource Report
Resource Website
10+ mentions
Intestinal Stem Cell Consortium (RRID:SCR_001555) ISCC consortium, organization portal, data or information resource, 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 ISCC - Intestinal Stem Cell Consortium 2026-08-03 09:31:26 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 2026-08-03 09:31:23 1
Type 1 Diabetes TrialNet
 
Resource Report
Resource Website
10+ mentions
Type 1 Diabetes TrialNet (RRID:SCR_001508) TrialNet portal, disease-related portal, database, resource, topical portal, clinical trial, data or information resource 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 2026-08-03 09:31:21 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 portal, disease-related portal, resource, topical portal, research forum portal, data or information resource, bibliography 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 CKID: A Prospective Cohort Study of Kidney Disease in Children, Chronic Kidney Disease in Children 2026-08-03 09:31:24 10
Collaborative Islet Transplant Registry
 
Resource Report
Resource Website
1+ mentions
Collaborative Islet Transplant Registry (RRID:SCR_001466) CITR data repository, data or information resource, database, narrative resource, resource, storage service resource, service resource, report 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 2026-08-03 09:31:23 9
Teen-Longitudinal Assessment of Bariatric Surgery
 
Resource Report
Resource Website
Teen-Longitudinal Assessment of Bariatric Surgery (RRID:SCR_001492) consortium, organization portal, data or information resource, 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 Teen-LABS, Adolescent Bariatrics: Assessing Health Benefits and Risks, Teen-Longitudinal Assessment of Bariatric Surgery, Adolescent Bariatrics: Assessing Health Benefits and Risks (Teen-LABS) 2026-08-03 09:31:24 0
Globin Gene Server
 
Resource Report
Resource Website
10+ mentions
Globin Gene Server (RRID:SCR_001480) Globin Gene Server production service resource, data analysis service, service resource, database, narrative resource, resource, source code, analysis service resource, data or information resource, software resource, 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 2026-08-03 09:31:21 27
Nonalcoholic Steatohepatitis Clinical Research Network
 
Resource Report
Resource Website
10+ mentions
Nonalcoholic Steatohepatitis Clinical Research Network (RRID:SCR_001519) NASH CRN portal, disease-related portal, clinical trial, resource, topical portal, research forum portal, data or information resource 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 Nonalcoholic Steatohepatitis Clinical Research Network (NASH CRN), Clinical Research Network in Nonalcoholic Steatohepatitis 2026-08-03 09:31:25 21
Pediatric Acute Liver Failure Study
 
Resource Report
Resource Website
Pediatric Acute Liver Failure Study (RRID:SCR_001478) PALF portal, disease-related portal, resource, topical portal, research forum portal, data or information resource 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 Pediatric Acute Liver Failure (PALF) Study, Pediatric Acute Liver Failure (PALF) Study Group 2026-08-03 09:31:24 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 DK070200;
NIDDK DK070181
PMID:21652655
PMID:18287559
THIS RESOURCE IS NO LONGER IN SERVICE nlx_152871, nif-0000-33426 SCR_001554 Murine Atlas for Genitourinary Development 2026-08-03 09:31:21 287
TOMUS
 
Resource Report
Resource Website
TOMUS (RRID:SCR_001549) TOMUS resource, clinical trial, data or information resource, bibliography 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 Trial Of Mid-Urethral Slings, TOMUS-Trial Of Mid-Urethral Slings 2026-08-03 09:31:21 0
Integrated Animals
 
Resource Report
Resource Website
Integrated Animals (RRID:SCR_001421) biomaterial supply resource, material resource, organism supplier Integrated Animals is a virtual database currently indexing available animal strains and mutants from: AGSC (Ambystoma), BCBC (mice), BDSC (flies), CWRU Cystic Fibrosis Mouse Models (mice), DGGR (flies), FlyBase (flies), IMSR (mice), MGI (mice), MMRRC (mice), NSRRC (pig), NXR (Xenopus), RGD (rats), Sperm Stem Cell Libraries for Biological Research (rats), Tetrahymena Stock Center (Tetrahymena), WormBase (worms), XGSC (Xiphophorus), ZFIN (zebrafish), and ZIRC (zebrafish). non human animal, mutant, database, integrated, nif, FASEB list uses: Mouse Genome Informatics (MGI)
uses: Beta Cell Biology Consortium
uses: Zebrafish Information Network (ZFIN)
uses: International Mouse Strain Resource
uses: Bloomington Drosophila Stock Center
uses: Rat Genome Database (RGD)
uses: Zebrafish International Resource Center
uses: Ambystoma Genetic Stock Center
uses: Kyoto Stock Center
uses: FlyBase
uses: Mutant Mouse Resource and Research Center
uses: National Swine Resource and Research Center
uses: National Xenopus Resource
uses: CWRU In Vivo Animal Facilities
uses: Sperm Stem Cell Libraries for Biological Research
uses: Tetrahymena Stock Center
uses: WormBase
uses: Xiphophorus Genetic Stock Center
is used by: NIF Data Federation
is used by: NIDDK Information Network (dkNET)
has parent organization: Integrated
Free, Freely Available nif-0000-08137 https://legacy.neuinfo.org/mynif/search.php?q=*&t=indexable&nif=nlx_154697-1 http://neuinfo.org/nif/nifgwt.html?query=nif-0000-08137, https://www.neuinfo.org/mynif/search.php?q=*&t=indexable&nif=nif-0000-08137-1 SCR_001421 NIF Animals, NIF Integrated Animals, Integrated Animal 2026-08-03 09:31:19 0

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