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| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | |||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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Cystic Fibrosis Research and Translation Centers Resource Report Resource Website |
Cystic Fibrosis Research and Translation Centers (RRID:SCR_015383) | resource, disease-related portal, data or information resource, organization portal, topical portal, portal | Research centers that provide support for basic, preclinical, and clinical research efforts to advance scientific knowledge and new therapies for cystic fibrosis. | cystic fibrosis, research, collaboration |
is listed by: NIDDK Information Network (dkNET) is affiliated with: NIDDK - National Institute of Diabetes and Digestive and Kidney Diseases has organization facet: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center has organization facet: Gregory Fleming James Cystic Fibrosis Research Center has organization facet: Cystic Fibrosis Center - University of California San Francisco has organization facet: Cystic Fibrosis Center University of Pittsburgh has organization facet: Cystic Fibrosis Center - University of Washington has organization facet: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis has organization facet: University of Iowa Center for Gene Therapy |
Cystic Fibrosis | NIDDK RFA-DK17-007 | Available to the research community | SCR_015383 | 2026-07-28 09:43:47 | 0 | ||||||||
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University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Resource Report Resource Website 1+ mentions |
University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis (RRID:SCR_015406) | service resource, resource, disease-related portal, data or information resource, access service resource, topical portal, portal | Research center whose focus is on developing effective gene vectors derived from recombinant viruses. Much of their research is in the development of new adeno-associated virus (AAV) vectors, although some of their research involves both adenoviruses and lentiviruses. | cystic fibrosis molecular therapy, adenovirus, viral vector |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Pennsylvania Perelman School of Medicine; Pennsylvania; USA is parent organization of: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Cell Morphology Core is parent organization of: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Immunology Core is parent organization of: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Vector Core Facility has organization facet: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Vector Core Facility has organization facet: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Cell Morphology Core has organization facet: University of Pennsylvania Center for Molecular Therapy for Cystic Fibrosis Immunology Core has organization facet: Cystic Fibrosis Center - University of Pennsylvania Animal Models Core is organization facet of: Cystic Fibrosis Research and Translation Centers |
Cystic Fibrosis | NIDDK P30DK047757 | Available to the research community | SCR_015406 | 2026-07-28 09:44:03 | 2 | ||||||||
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University of Iowa Center for Gene Therapy Resource Report Resource Website |
University of Iowa Center for Gene Therapy (RRID:SCR_015412) | service resource, resource, disease-related portal, data or information resource, access service resource, topical portal, portal | Research center which provides access to core facilities and services to aid gene therapy researchers. | gene therapy, gene therapy research center |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Iowa Carver College of Medicine; Iowa; USA is parent organization of: University of Iowa Center for Gene Therapy Vectore Core is parent organization of: University of Iowa Center for Gene Therapy Clinical Core is parent organization of: University of Iowa Center for Gene Therapy Animal Model Core is parent organization of: University of Iowa Center for Gene Therapy Comparative Pathology Core is parent organization of: University of Iowa Center for Gene Therapy Cell Tissue Core has organization facet: University of Iowa Center for Gene Therapy Animal Model Core has organization facet: University of Iowa Center for Gene Therapy Cell Tissue Core has organization facet: University of Iowa Center for Gene Therapy Comparative Pathology Core has organization facet: University of Iowa Center for Gene Therapy Clinical Core has organization facet: University of Iowa Center for Gene Therapy Vectore Core is organization facet of: Cystic Fibrosis Research and Translation Centers |
Cystic Fibrosis | NIDDK P30DK054759 | Available to the research community | SCR_015412 | 2026-07-28 09:44:03 | 0 | ||||||||
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Cystic Fibrosis Center University of Pittsburgh Resource Report Resource Website 1+ mentions |
Cystic Fibrosis Center University of Pittsburgh (RRID:SCR_015400) | service resource, resource, disease-related portal, data or information resource, access service resource, topical portal, portal | Research center whose goal is to understand and translate the basic mechanisms of cystic fibrosis. It uses the molecular and cell biology of CFTR, CFTR mutants, infection, and inflammation with the overall theme of translating preclinical science into clinical investigations. | cystic fibrosis mechanism, cystic fibrosis translational research, cystic fibrosis research |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Pittsburgh; Pennsylvania; USA is organization facet of: Cystic Fibrosis Research and Translation Centers |
Cystic Fibrosis | NIDDK P30DK072506; Cystic Fibrosis Foundation Research Development Program R883-CR07 |
Available to the research community | SCR_015400 | 2026-07-28 09:44:03 | 1 | ||||||||
|
CFTR2 Resource Report Resource Website 100+ mentions |
CFTR2 (RRID:SCR_019078) | disease-related portal, data or information resource, database, topical portal, portal | International initiative led by team of researchers and clinicians and supported by the US Cystic Fibrosis Foundation that seeks to provide complete, advanced and expert reviewed functional and clinical information on CFTR mutations. Provides information for patients, researchers, and general public about specific variants. For each variant or variant combination included in database, website will provide information about whether variant or variant combination is CF-causing, and information about sweat chloride, lung function, pancreatic status, and Pseudomonas infection rate in patients in CFTR2 database with this variant or variant combination. | CF gene, cystic fibrosis gene, functional testing, CFTR2 variant, data, CFTR mutations, clinical information, , FASEB list | is related to: Cystic Fibrosis Mutation Database | cystic fibrosis | Free, Freely available | SCR_019078 | Clinical and Functional TRanslation of CFTR, cftr2, Clinical and Functional TRanslation 2 | 2026-07-28 09:45:02 | 127 | ||||||||
|
Cystic Fibrosis Mutation Database Resource Report Resource Website 10+ mentions |
Cystic Fibrosis Mutation Database (RRID:SCR_000685) | CFTR1, CFMDB | service resource, data or information resource, data repository, database, storage service resource | Collection of mutations in CFTR gene for international cystic fibrosis genetics research community. Provides up to date information about individual mutations in CFTR gene. All known CFTR mutations and sequence variants have been converted to standard nomenclature recommended by Human Genome Variation Society. On line process for submission of new mutations has been added.While they continue to ensure quality of data, they urge international community to give them feedback and suggestions. Clinical information in this database relates only to details of discovery of specific mutations. As part of 2010 upgrade, CFTR1 joined new project called CFTR2 - Clinical and Functional TRanslation of CFTR. Links to CFTR2 for many mutations in CFTR1 will provide up-to-date summaries of genotype-phenotype information from patient registries around the world. | Gene, genetic, amino acid, clinical, cystic fibrosis, mutation, phenotype, genotype-phenotype, genotype, dna sequence, mouse, sequence, genetic variation, polymorphism, translation, function, sequence variation, metadata standard, cftr2, FASEB list | is related to: CFTR2 | Cystic fibrosis | Free, Freely available | nif-0000-21105, r3d100012093 | https://doi.org/10.17616/R38356 | SCR_000685 | 2026-07-28 09:40:03 | 42 | ||||||
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TCAG Resource Report Resource Website 50+ mentions |
TCAG (RRID:SCR_001840) | TCAG | service resource, biomaterial analysis service, material service resource, data or information resource, database, production service resource, material analysis service, biomaterial manufacture, analysis service resource, topical portal, portal, training service resource | Service and training support for academic, government, and private sector scientists worldwide in genomics, including laboratory experimentation, statistical analysis, and comprehensive bioinformatics support, including large-scale genome comparisons, algorithm and tools development, and database curation, annotation and hosting. The Centre for Applied Genomics hosts a variety of databases related to ongoing supported projects: *Autism Chromosome Rearrangement Database *Cystic Fibrosis Mutation Database *The Lafora Progressive Myoclonus Epilepsy Mutation and Polymorphism Database *Database of Genomic Variants *The Chromosome 7 Annotation Project *Human Genome Segmental Duplication Database *Non-Human Segmental Duplication Database Healthy control DNA samples from the Ontario Population Genomics Platform are available. The Biobanking and Databasing Facility provides DNA extraction from lymphoblasts, fibroblasts and other cell types, archiving of white cell pellets, preparation and immortalization of cell lines, and comprehensive databasing and tracking of samples and/or cell lines within the facility. | genomics, publication, link, bioinformatics, genome, research, microarray analysis, gene expression, genotyping, biobanking, statistical analysis, genetic analysis, cytogenomics, dna sequencing, dna synthesis, comparative genomic hybridization, karyotyping, fish mapping, human, mouse, gene expression, biobanking, dna, mutation, genomic variant, chromosome 7, FASEB list | is listed by: One Mind Biospecimen Bank Listing | Healthy control, Autism, Cystic fibrosis, Epilepsy, Polymorphism | Free, Freely available | nif-0000-12519 | SCR_001840 | Centre for Applied Genomics, The Centre for Applied Genomics | 2026-07-28 09:40:26 | 80 | ||||||
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Ontological Knowledge Base Model for Cystic Fibrosis Resource Report Resource Website |
Ontological Knowledge Base Model for Cystic Fibrosis (RRID:SCR_010382) | ONTOKBCF | controlled vocabulary, data or information resource, ontology | An ontological knowledge base model for cystic fibrosis. There are molecular genetic information (i.e. gene mutations) and health information included in OntoKBCF. The purposes of OntoKBCF include management of molecular genetic information and health information and embedding OntoKBCF into EHR settings. | owl | is listed by: BioPortal | Cystic fibrosis | nlx_157513 | SCR_010382 | 2026-07-28 09:42:49 | 0 | ||||||||
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Polygenic Pathways Resource Report Resource Website 1+ mentions |
Polygenic Pathways (RRID:SCR_006962) | data or information resource, database | Database of disease genes and risk factors and of host pathogen/interactomes. Lists genes, pathways and environmental risk factors positively associated with diseases and conditions such as Alzheimer's disease, schizophrenia, multiple sclerosis, childhood obesity, anorexia nervosa, HIV-1/AIDS, and helicobacter pylori. Details of polymorphisms as well as negative/positive association data can be found via Useful links. Throughout the site are links to Entrez Gene and Pubmed. | genetic disease, risk factor, host pathogen, interactome, polygenic pathway, bio.tools |
is listed by: bio.tools is listed by: Debian is parent organization of: Polygenic Pathways Jobs is parent organization of: PolygenicBlog |
Alzheimer's disease, Schizophrenia, Bipolar disorder, depression, Parkinson's disease, Huntington's disease, Multiple sclerosis, Cystic fibrosis, Childhood obesity, Chronic fatigue syndrome, Autism, Anorexia nervosa, Attention deficit hyperactivity disorder, HIV-1/AIDS | Google ; Amazon |
Free, Freely available | nif-0000-00514, biotools:polygenicpathways, SCR_015716 | https://bio.tools/polygenicpathways | SCR_006962 | PolygenicPathways, Polygenic Signaling Pathways | 2026-07-28 09:41:39 | 4 | |||||
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University of Iowa Center for Gene Therapy Clinical Core Resource Report Resource Website |
University of Iowa Center for Gene Therapy Clinical Core (RRID:SCR_015415) | access service resource, service resource, resource, core facility | Core facility which aims to provide cystic fibrosis researchers with a biobank of archived biosamples collected during routine clinical visits and research-related visits. Biospecimens include normal and CF specimens including DNA, bronchoalveolar lavage fluid, whole blood, plasma, feces, urine, and bacterial isolates. It also aims to facilitate patient recruitment and enrollment in clinical trials. | cystic fibrosis biobank, cystic fibrosis sample, clinical sample |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Iowa Carver College of Medicine; Iowa; USA has parent organization: University of Iowa Center for Gene Therapy is organization facet of: University of Iowa Center for Gene Therapy |
Cystic Fibrosis | NIDDK P30DK054759 | Available to the research community | SCR_015415 | 2026-07-28 09:44:03 | 0 | ||||||||
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Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Pre-Clinical Core Resource Report Resource Website |
Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Pre-Clinical Core (RRID:SCR_015387) | access service resource, service resource, resource, core facility | Core whose objectives include evaluation of pre-clinical drug candidates in vitro, pre-clinical drug candidates ex vivo, and pre-clinical drug candidates in vivo. | pre-clinical drug analysis, cystic fibrosis research, cftr function |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA has parent organization: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center is organization facet of: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center |
Cystic Fibrosis, pulmonary disease | NIDDK P30DK065988 | Available to the research community | SCR_015387 | 2026-07-28 09:43:50 | 0 | ||||||||
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Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Molecular Biology Core Resource Report Resource Website |
Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Molecular Biology Core (RRID:SCR_015384) | access service resource, service resource, resource, core facility | Core facility that provides expertise, equipment, training, and reagents to serve the molecular biology needs for cystic fibrosis research. | cystic fibrosis, molecular biology, lung disease |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA has parent organization: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center is organization facet of: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center |
Cystic Fibrosis, pulmonary disease | NIDDK P30DK065988 | Available to the research community | SCR_015384 | 2026-07-28 09:43:50 | 0 | ||||||||
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Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Michael Hooker Microscopy Core Facility Resource Report Resource Website 1+ mentions |
Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Michael Hooker Microscopy Core Facility (RRID:SCR_015390) | MHMF | access service resource, service resource, core facility | Core that provides advanced digital light microscopy, image processing and analysis resources for users from the UNC Chapel Hill campus. It also offers instrumentation and instruction to enable users to acquire, process and analyze images from a wide variety of sample types. | microscopy, light, cell, imaging, processing, core |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA has parent organization: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center is organization facet of: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center |
Cystic Fibrosis, pulmonary disease | NIDDK P30 DK065988 | Available to the research community | SCR_015390 | The Michael Hooker Microscopy Core Facility, Michael Hooker Microscopy Core Facility | 2026-07-28 09:43:51 | 1 | ||||||
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Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Clinical Translational Core Resource Report Resource Website |
Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Clinical Translational Core (RRID:SCR_015391) | access service resource, service resource, resource, core facility | Core whose services include biospecimen collection and storage, development of lung imaging outcomes, imaging training, and biostatical analysis. | cystic fibrosis, lung imaging, lung biospecimen |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA has parent organization: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center is organization facet of: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center |
Cystic Fibrosis, pulmonary disease | NIDDK P30DK065988 | Available to the research community | SCR_015391 | 2026-07-28 09:44:03 | 0 | ||||||||
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Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Tissue Procurement and Cell Culture Core Resource Report Resource Website |
Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Tissue Procurement and Cell Culture Core (RRID:SCR_015394) | access service resource, service resource, resource, core facility | Core that provides standardized cell cultures for cystic fibrosis research, notably normal, cystic fibrosis and disease control cells, tissues and fluids. Its functions include tissue procurement, airway epithelial cell isolation and culture, collecting airway surface liquid from in vivo and in vitro samples, genetic manipulation of cell cultures, creating and characterizing novel cell lines, and translation of technology and reagents to the greater cystic fibrosis research community. | cystic fibrosis, cf cell culture, cf biospecimen |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA has parent organization: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center is organization facet of: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center |
Cystic Fibrosis, pulmonary disease | NIDDK P30DK065988 | Available to the research community | SCR_015394 | 2026-07-28 09:44:03 | 0 | ||||||||
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Gregory Fleming James Cystic Fibrosis Research Center Cell Model and Evaluation Core Resource Report Resource Website |
Gregory Fleming James Cystic Fibrosis Research Center Cell Model and Evaluation Core (RRID:SCR_015395) | access service resource, service resource, resource, core facility | Core that assists with patch clamp and single channel analysis relevant to ion channel gating. The core also provides primary murine airway epithelial cells. | ion channel dysfunction, epithelial cells, cell model, cell evaluation, cystic fibrosis research |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Alabama at Birmingham School of Medicine; Alabama; USA has parent organization: Gregory Fleming James Cystic Fibrosis Research Center is organization facet of: Gregory Fleming James Cystic Fibrosis Research Center |
Cystic Fibrosis | NIDDK P30DK072482; Cystic Fibrosis Foundation |
Available to the research community | SCR_015395 | 2026-07-28 09:43:48 | 0 | ||||||||
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Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Mucus and Mucin Biochemistry and Biophysics Core Resource Report Resource Website |
Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center Mucus and Mucin Biochemistry and Biophysics Core (RRID:SCR_015393) | access service resource, service resource, resource, core facility | Core that provides a service to quantify the concentration of given mucus samples for both total mucus concentration and the absolute relative contributions of each secreted mucin. It also provides quantitation of extracellular DNA. The mucus biphysics subcore component, provides core users with information on the biophysical properties of the mucus layer and its interaction with the cell surface. | mucus research, mucus biophysics, mucin biochemistry, cystic fibrosis |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of North Carolina at Chapel Hill School of Medicine; North Carolina; USA has parent organization: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center is organization facet of: Cystic Fibrosis and Pulmonary Diseases Research and Treatment Center |
Cystic Fibrosis, pulmonary disease | NIDDK P30DK065988 | Available to the research community | SCR_015393 | 2026-07-28 09:43:51 | 0 | ||||||||
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Cystic Fibrosis Center - University of Washington Clinical Core Resource Report Resource Website 1+ mentions |
Cystic Fibrosis Center - University of Washington Clinical Core (RRID:SCR_015402) | access service resource, service resource, resource, core facility | Core that aims to provide preclinical support for novel therapeutics, work with other biomedical cores to enhance and support bacterial and human specimen repositories, and support developmental research and training. | clinical core, cystic fibrosis translational research, cystic fibrosis therpeutics, cystic fibrosis specimen repository |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Washington; Seattle; USA has parent organization: Cystic Fibrosis Center - University of Washington is organization facet of: Cystic Fibrosis Center - University of Washington |
Cystic Fibrosis | NIDDK P30DK89507 | Available to the research community | SCR_015402 | 2026-07-28 09:43:51 | 1 | ||||||||
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Gregory Fleming James Cystic Fibrosis Research Center Assay Core Resource Report Resource Website |
Gregory Fleming James Cystic Fibrosis Research Center Assay Core (RRID:SCR_015407) | access service resource, service resource, resource, core facility | Core that provides Ussing chamber capabilities and expertise for testing vectoral anion transport in polarized airway epithelial monolayers, and florescent dye-based methods for evaluating CFTR activity in cells grown on coverslips. The core also performs immunolocalization for proteins relevant to cystic fibrosis pathogenesis. | ussing chamber, cystic fibrosis research, cystic fibrosis assay, cystic fibrosis core |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Alabama at Birmingham School of Medicine; Alabama; USA has parent organization: Gregory Fleming James Cystic Fibrosis Research Center is organization facet of: Gregory Fleming James Cystic Fibrosis Research Center |
Cystic Fibrosis | NIDDK P30DK072482; Cystic Fibrosis Foundation |
Available to the research community | SCR_015407 | 2026-07-28 09:43:48 | 0 | ||||||||
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Cystic Fibrosis Center - University of Washington Host Response Core Resource Report Resource Website |
Cystic Fibrosis Center - University of Washington Host Response Core (RRID:SCR_015405) | access service resource, service resource, resource, core facility | Core whose objective is to obtain information on relevant parameters of the host response that is unique to cystic fibrosis using a variety of techniques, including in vivo and in vitro imaging, immunohistochemistry, imaging and image analysis, cells and bacteria in tissues, and quantification of chemokines, cytokines, and other factors with ELISA. | cystic fibrosis host response, host response |
is listed by: NIDDK Information Network (dkNET) has parent organization: University of Washington; Seattle; USA has parent organization: Cystic Fibrosis Center - University of Washington is organization facet of: Cystic Fibrosis Center - University of Washington |
Cystic Fibrosis | NIDDK P30DK89507 | Available to the research community | SCR_015405 | 2026-07-28 09:43:51 | 0 |
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