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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Website Status Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Rocky Mountain MS Center Tissue Bank
 
Resource Report
Resource Website
Rocky Mountain MS Center Tissue Bank (RRID:SCR_004361) Rocky Mountain MS Center Tissue Bank brain bank, material resource, tissue bank, biomaterial supply resource Scientists throughout the world depend on the Rocky Mountain MS Center Tissue Bank to supply high quality human brain tissue and cerebral spinal fluid to support their research. Funded in part by the National MS Society, the Tissue Bank is one of only four MS-related tissue banks in the nation. The Tissue Bank has distributed specimens to more than 160 investigators worldwide and over 1,600 people have consented to be donors after death. Tissue banks provide a unique bridge between those who live with MS and the scientific community. Studies conducted with samples from the Center have led to several important discoveries and 130 publications. While deeply personal, the decision to donate has far-reaching effects as scientists unlock the mysteries of multiple sclerosis. If you would like to donate, arrangements must be made in advance because it is important that tissue is taken within a few hours of death. For more information on making a donation, visit the How To Donate section of this website and contact the Rocky Mountain MS Center Tissue Bank at 303.788.4030 x111. brain tissue, cerebral spinal fluid, research, multiple sclerosis, brain, tissue is listed by: One Mind Biospecimen Bank Listing
has parent organization: Rocky Mountain MS Center
Multiple Sclerosis National MS Society Public nlx_143691 SCR_004361 Rocky Mountain Multiple Sclerosis Center Tissue Bank, Tissue Bank: Rocky Mountain MS Center 2026-02-15 09:18:42 0
RIKEN Brain Science Institute
 
Resource Report
Resource Website
1+ mentions
RIKEN Brain Science Institute (RRID:SCR_004796) BSI topical portal, data or information resource, portal RIKEN Brain Science Institute (BSI) has a mission to produce innovative research and technology leading to scientific discoveries of the brain. In addition, BSI aims to develop domestic and international brain researchers by creating an environment that will integrate various intellectual disciplines and from that convergence find solutions that will ultimately benefit society in the realms of medicine, engineering, business, and education. In striving toward this goal, BSI has become a leading international center for brain research with a reputation for discovery, innovation, training, and globalization of the scientific enterprise. Brain science is valuable not only for the advancement of science but also because it can greatly impact our society and economy. To meet these expectations, the Brain Science Institute (BSI) was established in 1997 as part of RIKEN, an independent research institution supported by the Japanese government. brain, research has parent organization: RIKEN
is parent organization of: Functional Annotation of the Mammalian Genome
is parent organization of: Dynamic Brain Platform
is parent organization of: Concierge
is parent organization of: Expression Atlas of the Marmoset
is parent organization of: Cerebellar Development Transcriptome Database
is parent organization of: Samurai Graph: A highly functional and user-friendly graph plotter
is parent organization of: Cerebellar Platform
is parent organization of: Brain Machine Interface Platform
is parent organization of: Visiome Platform
is parent organization of: INCF Japan Node
nlx_143907 SCR_004796 Brain Science Institute, RIKEN BSI, RIKEN Brain Science Institute 2026-02-15 09:18:49 1
National Brain Tumor Society
 
Resource Report
Resource Website
1+ mentions
National Brain Tumor Society (RRID:SCR_004744) NBTS portal, funding resource, data or information resource, topical portal, disease-related portal National Brain Tumor Society (NBTS) is a nonprofit organization committed to finding a cure for brain tumors. We aggressively drive strategic research, advocate for public policies that meet the critical needs of the brain tumor community, and provide patient information. Headquartered in Watertown, Massachusetts, with offices in San Francisco, California and Wilmington, Delaware, we host activities throughout the United States. Formed in 2008 by the merger of two leading organizations that had served the brain tumor community, the National Brain Tumor Foundation and the Brain Tumor Society, the National Brain Tumor Society is now the largest brain tumor nonprofit organization in the country. Both legacy organizations had been formed in the 1980s by parents and other people who were committed to increasing both research funding and access to resources specific to brain tumors. In 2010, the Kelly Heinz-Grundner Foundation, a Delaware-based organization, joined NBTS as a wholly-owned subsidiary. Founded in 2005, after the death of Kelly Heinz-Grundner to a brain tumor, the group has contributed to NBTS''s efforts to pursue research and public policies that benefit the brain tumor community. NBTS grant programs are effective for academic researchers, inclusive of industry expertise, and promising for the patient community. All funding is open to both the domestic and international research communities. The Innovation Research Grant Program supports catalytic transformative projects that will significantly move the field forward. These may include out-of-the-box projects or research that is critical to move therapies down the pipeline. Research that represents an incremental advance is not considered innovative. NBTS will accept Innovation Letters of Intent throughout the year. Researchers in academic or industry labs and at all stages of their career may be funded through this program. brain, tumor, brain tumor, cancer, human, grant, child, pediatric, research nlx_143891 SCR_004744 2026-02-15 09:18:48 8
National Academy of Sciences Podcasts
 
Resource Report
Resource Website
National Academy of Sciences Podcasts (RRID:SCR_005124) NAS Podcasts data or information resource, narrative resource, podcast Subscribe to the National Academy of Sciences podcasts to learn more about scientists and their work, the latest in research, and key findings of National Research Council reports. * InterViews: InterViews provides first-person accounts of the lives and work of National Academy of Sciences members. In this series of one-on-one conversations, scientists talk about what inspired them to pursue the careers they chose and describe some of the most fascinating aspects of their research. * Science Sessions: The Proceedings of the National Academy of Sciences offers brief, 5-minute, nontechnical conversations with cutting-edge researchers, including members of the National Academy of Sciences, and policymakers as they discuss topics relevant to today''s scientific community. Learn the behind-the-scenes story of work published in PNAS, plus a broad range of scientific news about discoveries that affect the world around us. * News from the National Academies: Listen to the latest news conferences and public briefings on National Research Council and Institute of Medicine reports. * Sounds of Science: This informative and entertaining series puts a spotlight on the high-impact work of the National Research Council. Focusing on a wide range of critical issues in science, engineering, and medicine, these short episodes are a quick and easy way to tune in our key findings and important recommendations. * Cultural Programs: The Cultural Programs of the National Academy of Sciences presents public exhibitions, lectures, and other programs exploring the intersections of art, science, and culture. The podcast features audio recordings of past lectures and other events. * Engineering Innovation: This weekly podcast from the National Academy of Engineering highlights exciting developments in engineering and provides technical context to stories in the news. The 40-second episodes demonstrate how engineers are making an impactin energy, health, the environment, sports, and more. science, culture, research, engineering, medicine, news, interview is used by: NIF Data Federation
is related to: Integrated Podcasts
has parent organization: National Academy of Sciences
nlx_144132 SCR_005124 2026-02-15 09:18:54 0
UCSF Laboratory for Visual Neuroscience
 
Resource Report
Resource Website
UCSF Laboratory for Visual Neuroscience (RRID:SCR_004913) Laboratory for Visual Neuroscience organization portal, portal, laboratory portal, video resource, image, data or information resource Devise better ways to prevent and treat vision loss due to amblyopia and strabismus, and to advance medical science by understanding the human visual system. Various Images, Videos and Talks related to the research are available. In the Laboratory for Visual Neuroscience at the University of California, San Francisco, we are seeking to discover how visual perception occurs in the human brain. The function of the visual system is to guide our behavior by providing an efficient means for the rapid assimilation of information from the environment. As we navigate through our surroundings, a continuous stream of light images impinges on our eyes. In the back of each eye a light-sensitive tissue, the retina, converts patterns of light energy into electrical discharges known as action potentials. These signals are conveyed along the axons of retinal ganglion cells to the lateral geniculate body, a relay nucleus in the thalamus. Most of the output of the lateral geniculate body is relayed directly to the primary visual cortex (striate cortex, V1), and then to surrounding visual association areas. To understand the function of the visual pathways, our research is focused on 5 major themes: * Organization of Primary Visual Cortex * Mapping of Extrastriate Visual Cortex * Amblyopia and Visual Development * Strabismus and Visual Suppression * The Human Visual Cortex amblyopia, strabismus, human, visual system, ophthalmology, monkey, eye, vision loss, patient, research, education, pediatric ophthalmology, neuro-ophthalmology, pediatric, primary visual cortex, vision is used by: NIF Data Federation
is used by: Integrated Videos
has parent organization: University of California at San Francisco; California; USA
PMID:17898211 nlx_143941 SCR_004913 University of California San Francisco Laboratory for Visual Neuroscience 2026-02-15 09:18:57 0
Cliniques Universitaires Saint-Luc Cancer Centre
 
Resource Report
Resource Website
Cliniques Universitaires Saint-Luc Cancer Centre (RRID:SCR_004922) Cliniques Universitaires Saint-Luc Cancer Centre training resource, topical portal, data or information resource, portal An essential reference center in Europe and a leader in French-speaking Belgium that treats all types of adult and childhood cancer. They fight against cancer while giving patients comprehensive and humane care. Their quest for excellence is in three main academic fields: clinical care, research and teaching. cancer, adult human, child, clinical, oncology, research, young human is parent organization of: Saint-Luc Tumour Bank Cancer nlx_143961 http://www.centreducancer.be/en SCR_004922 Centre du Cancer Cliniques Universitaires St-Luc, Cliniques Universitaires Saint-Luc Cancer Center 2026-02-15 09:18:57 0
NIH Office of Science Education
 
Resource Report
Resource Website
NIH Office of Science Education (RRID:SCR_005603) OSE organization portal, portal, training material, knowledge environment, data or information resource, narrative resource The NIH Office of Science Education (OSE) coordinates science education activities at the NIH and develops and sponsors science education projects in house. These programs serve elementary, secondary, and college students and teachers and the public. Activities * Develop curriculum supplements and other educational materials related to medicine and research through collaborations with scientific experts at NIH * Maintain a website as a central source of information about NIH science education resources * Establish national model programs in public science education, such as the NIH Mini-Med School and Science in the Cinema * Promote science education reform as outlined in the National Science Education Standards and related guidelines The OSE was established in 1991 within the Office of Science Policy of the Office of the Director of the National Institutes of Health. The NIH is the world''s foremost biomedical research center and the U.S. federal government''s focal point for such research. It is one of the components of the Department of Health and Human Services (HHS). The Office of Science Education (OSE) plans, develops, and coordinates a comprehensive science education program to strengthen and enhance efforts of the NIH to attract young people to biomedical and behavioral science careers and to improve science literacy in both adults and children. The function of the Office is as follows: (1) develops, supports, and directs new program initiatives at all levels with special emphasis on targeting students in grades kindergarten to 16, their educators and parents, and the general public; (2) advises NIH leadership on science education issues; (3) examines and evaluates research and emerging trends in science education and literacy for policy making; (4) works closely with the NIH extramural, intramural, women''s health, laboratory animal research, and minority program offices on science education special issues and programs to ensure coordination of NIH efforts; (5) works with NIH institutes, centers, and divisions to enhance communication of science education activities; and (6) works cooperatively with other public- and private-sector organizations to develop and coordinate activities. science, education, high school, middle school, elementary school, animal, research, bioethics, blood, lymphatic system, bones, joints, muscle, brain, nervous system, cell biology, cancer, child, adolescent, complementary medicine, alternative medicine, digestive system, ears, nose, throat, endocrine system, environmental, toxicology, evolution, eye, vision, food, nutrition, metabolism, genomics, genetics, heart, circulation, history, immune system, injury, wound, kidney, urinary system, medical research, man, mental health, behavior, microbiology, infectious disease, mouth, teeth, therapy, reproductive system, respiratory system, safety, late adult human, sexual health, skin, hair, nail, sleep, social, family, substance abuse, technology, wellness, lifestyle, woman, health, human, lesson plan, supplemental curricula, book, image, multimedia, poster, k-12, adult, non-human animal has parent organization: National Institutes of Health
is parent organization of: NIH SciEd Blog
NIH nlx_146222 SCR_005603 NIH OSE, National Institutes of Health Office of Science Education 2026-02-15 09:19:00 0
CTSAconnect
 
Resource Report
Resource Website
CTSAconnect (RRID:SCR_005225) CTSAconnect source code, ontology, software resource, knowledge environment, service resource, data or information resource, controlled vocabulary, narrative resource, standard specification THIS RESOURCE IS NO LONGER IS SERVICE. Documented on December 5th, 2022. Semantic framework to integrate information about research activities, clinical activities, and scientific resources to facilitate the production and consumption of Linked Open Data about investigators, physicians, biomedical research resources, services, and clinical activities. The goal is to enable software to consume data from multiple sources and allow the broadest possible representation of researchers'''' and clinicians'''' activities and research products. Current research tracking and networking systems rely largely on publications, but clinical encounters, reagents, techniques, specimens, model organisms, etc., are equally valuable for representing expertise. CTSAConnect will provide linkage between semantic representations of a wide range of clinical and research data using controlled vocabularies mapped to the Unified Medical Language System (UMLS) as a bridge between the two subject areas. The data sources include data from Medicaid, hospital billing systems, CTSAShareCenter, and other CTSA resource data, eagle-i and VIVO. It allows institutions to leverage existing tools and data sources by making the information they contain more discoverable and easier to integrate. For instance, with the ISF, researchers can be characterized by organizational affiliations, grant and project participation, research resources that they have generated, and publications that they have (co)-authored. Clinicians can be characterized by training and credentials, by clinical research topic, and by the kinds of procedures and specialization that can be inferred from encounter data. LOD refers to data that has been given a specific Uniform Resource Identifier (URI), for the purpose of sharing and linking data and information on the Semantic Web. While a large amount of data is published as LOD, there remains a significant gap in the representation of research resources and clinical expertise. Researchers can be characterized by the organization to which they belong, the grants and research in which they have participated, the research topics and research resources (reagents, biospecimens, animal models) they have generated, as well as the publications they have (co)-authored. Clinician profiles on the other hand, can be defined by their credentials, clinical research topics, and the kinds of procedures and specialization that can be inferred from clinical encounter data. They believe that integrating and relating this diversity of information sources and platforms requires addressing the overlap between research resources and the attributes and activities of researchers and clinicians. CTSAconnect aims to promote integration and discovery of research activities, resources, and clinical expertise. To this end, they will publish their ontologies and LOD via their website, which will also illustrate repeatable methods and examples of how to extract, consume, and utilize this valuable new LOD using freely available tools like VIVO, eagle-i, and Google APIs. CTSAconnect is a collaboration between Oregon Health & Science University, Stony Brook University, Cornell University, Harvard University, University at Buffalo, and the University of Florida, and leverages the work of eagle-i (eagle-i.net), VIVO (vivoweb.org), and ShareCenter (ctsasharecenter.org). data sharing, clinical, research, semantic framework, linked open data, collaborate is related to: Eagle I
is related to: VIVO
is related to: CTSA ShareCenter
is related to: Clinical and Translational Science Awards Consortium
is related to: CTSA ShareCenter
has parent organization: Oregon Health and Science University; Oregon; USA
has parent organization: Harvard University; Cambridge; United States
Booz Allen Hamilton ;
National Center for Advancing Translational Sciences
THIS RESOURCE IS NO LONGER IS SERVICE nlx_144228 SCR_005225 CTSAconnect: A Linked Open Data approach to represent clinical and research expertise activities and resources, CTSA Connect, Clinical and Translational Science Awards Connect 2026-02-15 09:18:56 0
North Texas Traumatic Brain Injury Model System
 
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Resource Website
North Texas Traumatic Brain Injury Model System (RRID:SCR_005879) NT-TBIMS topical portal, data or information resource, portal The 16 affiliated Model System centers throughout the United States are responsible for gathering and submitting the core data set to the national database as well as conducting research studies on traumatic brain injury (TBI) both in collaboration with the other centers and within our own site. Through our research we hope to learn more about TBI and about the issues and concerns of people with TBI. Our goals are to improve the outcome and quality of life for people who have had brain injuries and for those who are caring for the person with a TBI. The North Texas Traumatic Brain Injury Model System (NT-TBIMS) pools the efforts and talents of individuals from the Departments of Neurosurgery, Neurology, Physical Medicine and Rehabilitation, Psychiatry (Neuropsychiatry), and Neuroradiology of the two leading medical institutions in the North Texas region. To be a patient involved in the research being conducted by the North Texas Traumatic Brain Injury Model System you must have suffered a TBI, be at least 16 years of age, have received initial treatment for the TBI at either Parkland Health and Hospital System or Baylor University Medical Center and then have received rehabilitative care at either Parkland, University Hospital Zale-Lipshy, or Baylor Institute for Rehabilitation. The patient must also be able to understand and sign an informed consent to participate or, if unable, have a family member or a legal guardian who understands the form sign the informed consent for the patient. brain injury, brain, injury, traumatic brain injury, clinical, research has parent organization: University of Texas Southwestern Medical Center; Texas; USA Traumatic Brain Injury National Institute on Disability and Rehabilitation Research H133A070027 nlx_149440 SCR_005879 North Texas TBI Model System, North Texas Traumatic Brain Injury Model System (NT-TBIMS) 2026-02-15 09:19:04 0
NIH Pain Consortium
 
Resource Report
Resource Website
1+ mentions
NIH Pain Consortium (RRID:SCR_006767) NIH Pain Consortium topical portal, data or information resource, portal The NIH Pain Consortium was established to enhance pain research and promote collaboration among researchers across the many NIH Institutes and Centers that have programs and activities addressing pain. To this end, the following goals have been identified for the Pain Consortium: * To develop a comprehensive and forward-thinking pain research agenda for the NIH - one that builds on what we have learned from our past efforts. * To identify key opportunities in pain research, particularly those that provide for multidisciplinary and trans-NIH participation. * To increase visibility for pain research - both within the NIH intramural and extramural communities, as well as outside the NIH. The latter audiences include our various pain advocacy and patient groups who have expressed their interests through scientific and legislative channels. * To pursue the pain research agenda through Public-Private partnerships, wherever applicable. This underscores a key dynamic that has been reinforced and encouraged through the Roadmap process. pain, clinical trial, research has parent organization: National Institutes of Health nif-0000-00400 SCR_006767 Pain Consortium, PainConsortium 2026-02-15 09:19:21 6
Thompson Center for Autism and Neurodevelopmental Disorders
 
Resource Report
Resource Website
Thompson Center for Autism and Neurodevelopmental Disorders (RRID:SCR_006812) Thompson Center portal, training resource, data or information resource, topical portal, disease-related portal The mission of the Thompson Center is to improve the lives of individuals and families affected by autism and neurodevelopmental disorders through world class programs that integrate research, clinical service delivery, education and public policy. The Thompson Center''s vision is to become a recognized national center of excellence that serves as a model of interdisciplinary practice, research and training in the field of autism and neurodevelopmental disorders. At the MU Thompson Center, education and training activities are a key part of our mission. Our goal is to teach others about the needs of persons with autism and other neurodevelopmental disorders and their families. In addition, we strive to help learners acquire skills needed to improve the outcomes of individuals with developmental differences. These skills include evidence-based assessment and intervention strategies, interdisciplinary approaches to service delivery, research methods, and policy development. The Thompson Center offers a range of health, educational and behavioral services in one location for individuals with autism and other developmental concerns. Professionals from different disciplines strive to deliver family-centered care that is comprehensive and coordinated. Autism recently has been recognized as a national public health concern, and federal research funding in this area has increased substantially. Faculty members engage in research that will lead to early identification, treatment and ultimately prevention of autism spectrum disorders (ASD). How findings may eventually translate into improved outcomes in clinical and community settings is a primary goal of our research. research, training, service, resource has parent organization: University of Missouri; Missouri; USA Autism, Neurodevelopmental disease, Autism spectrum disorder nlx_151589 SCR_006812 MU Thompson Center, Thompson Center for Autism Neurodevelopmental Disorders, MU Thompson Center for Autism and Neurodevelopmental Disorders 2026-02-15 09:19:22 0
Stanford Center for Narcolepsy
 
Resource Report
Resource Website
Stanford Center for Narcolepsy (RRID:SCR_007021) Stanford Center for Narcolepsy brain bank, material resource, tissue bank, biomaterial supply resource The Stanford Center for Narcolepsy was established in the 1980s as part of the Department of Psychiatry and Behavioral Sciences. Today, it is the world leader in narcolepsy research with more than 100 articles on narcolepsy to its name. The Stanford Center for Narcolepsy was the first to report that narcolepsy-cataplexy is caused by hypocretin (orexin) abnormalities in both animal models and humans. Under the direction of Drs. Emmanuel Mignot and Seiji Nishino, the Stanford Center for Narcolepsy today treats several hundred patients with the disorder each year, many of whom participate in various research protocols. Other research protocols are conducted in animal models of narcolespy. We are always looking for volunteers in our narcolepsy research studies. We are presently recruiting narcoleptic patients for genetic studies, drug clinical trials, hypocretin measurement studies in the CSF and functional MRI studies. Monetary gifts to the Center for Narcolepsy are welcome. If you wish to make the ultimate gift, please consider participating in our Brain Donation Program. To advance our understanding of the cause, course, and treatment of narcolepsy, in 2001 Stanford University started a program to obtain human brain tissue for use in narcolepsy research. Donated brains provide an invaluable resource and we have already used previously donated brains to demonstrate that narcolepsy is caused by a lack of a very specific type of cell in the brain, the hypocretin (orexin) neuron. While the brain donations do not directly help the donor, they provide an invaluable resource and a gift to others. The real answers as to what causes or occurrs in the brain when one has narcolepsy will only be definitively understood through the study of brain tissue. Through these precious donations, narcolepsy may eventually be prevented or reversible. We currently are seeking brains from people with narcolepsy (with cataplexy and without), idiopathic hypersomnia and controls or people without a diagnosed sleep disorder of excessive sleepiness. Control brains are quite important to research, as findings must always be compared to tissue of a non-affected person. Friends and loved ones of people who suffer with narcoleps may wish to donate to our program to help fill this very important need. Refer to the Movies tab for movies of Narcolepsy / Cataplexy. brain tissue, brain, tissue, hypocretin, orexin, narcolepsy, sleep disorder, cataplexy, idiopathic hypersomnia, normal control, kleine-levin syndrome, dog, zebrafish, research, therapy is listed by: One Mind Biospecimen Bank Listing
has parent organization: Stanford University School of Medicine; California; USA
Narcolepsy, Sleep disorder, Cataplexy, Idiopathic hypersomnia, Normal control, Kleine-Levin Syndrome Individual gifts ;
NIH
Private: not stated but looks that way nlx_144254 http://med.stanford.edu/school/Psychiatry/narcolepsy/ SCR_007021 Stanford University Center for Narcolepsy 2026-02-15 09:19:26 0
European Xenopus Resource Center
 
Resource Report
Resource Website
50+ mentions
European Xenopus Resource Center (RRID:SCR_007164) EXRC organism supplier, material resource, biomaterial supply resource Supports researchers using Xenopus models. Researchers are encouraged to deposit Xenopus transgenic and mutant lines, Xenopus in situ hybridization probes, Xenopus specific antibodies and Xenopus expression clones with the Centre. EXRC staff perform quality assurance testing on these reagents and then make them available to researchers at cost. Supplies wild-type Xenopus, embryos, oocytes and Xenopus tropicalis fosmids. RIN, Resource Information Network, Xenopus, Resouce, Distributor, Supplier, Researcher, Research, Model, Hybridization, Probe, Antibody, Expression, Clone, Reagent, Embryo, Oocyte, Fosmid, Xenopus tropicalis, RRID Community Authority is listed by: Resource Information Network Wellcome Trust ;
BBSRC ;
NC3Rs
nif-0000-38111 SCR_007164 2026-02-15 09:19:28 54
Professor Anne Chaos Website
 
Resource Report
Resource Website
10+ mentions
Professor Anne Chaos Website (RRID:SCR_007205) data or information resource, topical portal, portal, software resource This portal takes you to the website of Professor Anne Chao of the National Tsing Hua University, China. She studies birds. The portal offers Software, course information, publications and teaching. There are about 458 bird species in Taiwan. We have observed 155 species in our neighboring Ker-Yar estuary. We would estimate the total number of species in this area to be 180 including those unobserved. The more we discover about birds, the more we realize how intimately and closely our lives are entwined with those of birds. When the habitats of birds are destroyed and birds become extinct, we human beings are losing the land.... bird, research, collection, speciation, speciman has parent organization: National Tsing Hua University; Hsinchu; Taiwan nif-0000-30106 SCR_007205 Professor Anne Chao''s Website 2026-02-15 09:19:30 13
Arizona Center for Education and Research on Therapeutics
 
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Resource Website
10+ mentions
Arizona Center for Education and Research on Therapeutics (RRID:SCR_007201) portal, research forum portal, data or information resource, topical portal, disease-related portal Arizona CERT is an independent research and education center whose mission is to improve therapeutic outcomes and reduce adverse events caused by drug interactions and drugs that prolong the QT interval, especially those affecting women. The CERTs mission is to conduct research and provide education that will advance the optimal use of drugs, medical devices, and biological products The Arizona CERT is a program of the Critical Path Institute in collaboration with the Center for Health Outcomes and PharmacoEconomic Research at The University of Arizona College of Pharmacy. It is one of 14 national CERTs funded by the U.S. Agency for Healthcare Research and Quality (AHRQ). education, research, therapeutics, biological, medical, drug, interaction, woman, device has parent organization: University of Arizona; Arizona; USA U.S. Agency for Healthcare Research and Quality nif-0000-30121 SCR_007201 Arizona CERT 2026-02-15 09:19:29 11
Vision Public Information Network
 
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Resource Website
Vision Public Information Network (RRID:SCR_007340) topical portal, data or information resource, portal The National Eye Institute (NEI) created the VISION Public Information Network for the purpose of communicating with public information officers at NEI grantee institutions. The Network''s primary mission is to work with the NEI in disseminating research results to the national and local media. The Network also works to inform the public of the mission of the National Institutes of Health (NIH) to improve the health of America through medical research. The NEI is part of the NIH, U.S. Department of Health and Human Services (DHHS). General information portal for eye and vision related resources for the public. Sponsors: This resource is supported by the National Eye Institute. eye, grant, health, human, information, media, medical, network, research, vision has parent organization: National Eye Institute (NEI) Commons nif-0000-00236 SCR_007340 Vision Network 2026-02-15 09:19:33 0
Gladstone Institute of Neurological Disease
 
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1+ mentions
Gladstone Institute of Neurological Disease (RRID:SCR_008072) organization portal, portal, training resource, job resource, data or information resource GIND provides a highly interactive academic environment and state-of-the-art research facilities that are ideal for training in neuroscience and biomedical research. GIND Investigators hold university appointments at UCSF and participate in educational activities, including the teaching and training of graduate students and postdoctoral fellows. Additionally, GIND is actively engaged in efforts to translate scientific discoveries into better treatments for major diseases of the nervous system. Sponsors: Support for GIND comes from the University of California at San Francisco. biomedical, disease, nervous system, neuroscience, research, treatment is related to: Collaboratory of AIDS Researchers for Eradciation (CARE) nif-0000-10522 SCR_008072 GIND 2026-02-15 09:19:48 2
Buzsaki Lab
 
Resource Report
Resource Website
10+ mentions
Buzsaki Lab (RRID:SCR_008020) Buzsaki Lab organization portal, software application, portal, data processing software, software resource, laboratory portal, data or information resource, data analysis software Lab interested in understanding how neuronal circuitries of the brain support its cognitive capacities. Its goal is to provide rational, mechanistic explanations of cognitive functions at a descriptive level. In the lab''s view, the most promising area of cognitive faculties for scientific inquiry is memory, since it is a well-circumscribed term, can be studied in animals and substantial knowledge has accumulated on the molecular mechanisms of synaptic plasticity. Available software: * NeuroScope: NeuroScope can display local field potentials (EEG), neuronal spikes, behavioral events, as well as the position of the animal in the environment. It also features limited editing capabilities. * Klusters: Klusters is a powerful and easy-to-use cluster cutting application designed to help neurophysiologists sort action potentials from multiple neurons on groups of electrodes (e.g., tetrodes or multisite silicon probes). * KlustaKwik: KlustaKwik is a program for automatic cluster analysis, specifically designed to run fast on large data sets. * MATLAB m-files: A selection of MATLAB files developed in the lab., THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. eeg, electrode, environment, funtion, animal, application, behavioral, brain, capacity, circuit, cluster, cognitive, hippocampal, hippocampus, laboratory, local field potential, mechanism, memory, molecular, neuron, neuronal, plasticity, research, scientific, spike, synaptic, tetrode has parent organization: Rutgers University; New Jersey; USA
is parent organization of: NeuroScope
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-10182 http://osiris.rutgers.edu/frontmid/indexmid.html SCR_008020 Buzsaki''s Lab 2026-02-15 09:19:47 15
Induced Mutant Resource
 
Resource Report
Resource Website
1+ mentions
Induced Mutant Resource (RRID:SCR_008366) IMR organism supplier, material resource, biomaterial supply resource THIS RESOURCE IS NO LONGER IN SERVICE, documented on June 08, 2012. The function of the IMR is to select, import, cryopreserve, maintain, and distribute these important strains of mice to the research community. To improve their value for research, the IMR also undertakes genetic development of stocks, such as transferring mutant genes or transgenes to defined genetic backgrounds and combining transgenes and/or targeted mutations to create new mouse models for research. The function of the IMR is to: * select biomedically important stocks of transgenic, chemically induced, and targeted mutant mice * import these stocks into the Jackson Laboratory by rederivation procedures that rid them of any pathogens they might carry * cryopreserve embryos from these stocks to protect them against accidental loss and genetic contamination * backcross the mutation onto an inbred strain, if necessary * distribute them to the scientific community More than 1000 mutant stocks have been accepted by the IMR from 1992 through December 2006. Current holdings include models for research on cancer; breast cancer; immunological and inflammatory diseases; neurological diseases; behavioral, cardiovascular and heart diseases; developmental, metabolic and other diseases; reporter (e.g., GFP) and recombinase (e.g., cre/loxP) strains. About eight strains a month are being added to the IMR holdings. Research is being conducted on improved methods for assisted reproduction and speed congenic production. Most of the targeted mutants arrive on a mixed 129xC57BL/6 genetic background, and as many of these as possible are backcrossed onto an inbred strain (usually C57BL/6J). In addition, new mouse models are being created by intercrossing carriers of specific transgenes and/or targeted mutations. Simple sequence length polymorphism DNA markers are being used to characterize and evaluate differences between inbred strains, substrains, and embryonic stem cell lines. embryo, genetic, behavioral, biomedical, breast cancer, cancer, cardiovascular, chemical, cre, cryopreserved, developmental, disease, distribution, dna, gfp, heart, immunological, inflammatory, loxp, marker, metabolic, model, mouse, mutation, neurological, pathogen, polymorphism, recombinase, research, stock, targeting, transgene has parent organization: Jackson Laboratory March of Dimes Birth Defects Foundation ;
American Cancer Society ;
American Heart Association ;
Cystic Fibrosis Foundation ;
National Multiple Sclerosis Society ;
Amyotrophic Lateral Sclerosis Association ;
NIAID ;
NIAMS ;
Howard Hughes Medical Institute ;
Department of the Army Breast Cancer Research Initiative. ;
NCRR P40 RR009781
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-25566 SCR_008366 2026-02-15 09:19:50 3
Australian Medical Bioinformatics Resource
 
Resource Report
Resource Website
1+ mentions
Australian Medical Bioinformatics Resource (RRID:SCR_008385) portal, research forum portal, data or information resource, topical portal, disease-related portal THIS RESOURCE IS NO LONGER IN SERVICE, documented September 6, 2016. AMBeR's aim is to bring together Australia's unique resources for genetic epidemiology and genomics with high level expertise in bioinformatics and statistical science, conduct advanced methodological research, develop new research capacity and competitiveness in cutting-edge techniques, bring them to bear on important medical research problems, train young Australians in bioinformatics and advanced biostatistics, and transfer this expertise to the medical research community. medical, bioinformatics, statistical, science, genomics, epidemiology, research, methodological, techniques, biostatistics has parent organization: University of Western Australia; Perth; Australia Medical Bioinformatics ;
National Health ;
MRC ;
Genomics and Proteomics Program
THIS RESOURCE IS NO LONGER IN SERVICE nif-0000-30032 SCR_008385 AMBeR 2026-02-15 09:19:50 1

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