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FH HUS Mutation Database Resource Report Resource Website 10+ mentions |
FH HUS Mutation Database (RRID:SCR_008512) | data or information resource, database | The database has now been updated to include ALL mutations found in HUS patients, including those in Factor I(FI) and Membrane (MCP). Homology models are available for the domains of FI and MCP and all analysis previously available for Factor H (FH) are now also available for FI and MCP. All SNP records for FH, FI and MCP are also now included in the database on the SNP pages. Only those SNPs within coding regions will be included in the full list of mutations and within the advanced search. For more information on the different versions of the database click here. We have also redesigned the site in order to display information more clearly. Please let us know what you think of the new design. Home Information Mutations Models References Links Submit Contact Us Help Collaborators NEWS !! SEP 2009 The database has now been recovered. Please report any bugs that you notice. NEWS !! MAY 2009 We have suffered from a complete server failure this month but these issues have been sorted out and work is being carried out to restore all the data within our FH-HUS database. Sorry for any inconvenience this may have caused. NEWS !! JAN 2007 Mutations within complement Factor B have also been associated with aHUS. (Goicoechea de Jorge et al., 2007) NEW !! Nov 2006 FH-HUS Database Version 2.1 The database has now been updated to include ALL mutations found in HUS patients, including those in Factor I(FI) and Membrane (MCP). Homology models are available for the domains of FI and MCP and all analysis previously available for Factor H (FH) are now also available for FI and MCP. All SNP records for FH, FI and MCP are also now included in the database on the SNP pages. Only those SNPs within coding regions will be included in the full list of mutations and within the advanced search. For more information on the different versions of the database click here. We have also redesigned the site in order to display information more clearly. Please let us know what you think of the new design. Quick Search Enter Codon No : Choose Protein : Advanced Search Have you or someone you know been diagnosed with aHUS? The information contained on this web site is provided for scientific research purposes only. We do not give medical advice or recommend any particular treatment for specific individuals. Here are several links for patient information on aHUS: http://renux.dmed.ed.ac.uk/ http://en.wikipedia.org/ http://kidney.niddk.nih.gov http://www.webmd.com HUS HUS (Haemolytic Uraemic Syndrome) is a disease associated with microangiopathic haemolytic anemia, thrombocytopenia and acute renal failure. A subgroup of the syndrome is strongly associated with abnormalities within the complement regulator factor H gene. To read information on HUS click here. To read information on Factor H (FH) click here. FH Mutations There are currently 74 Factor H mutations, 10 Factor I mutations and 25 MCP mutations linked with HUS patients within this database. There are also 5 mutations within FH that are associated with MPGN patients. . Following HGVS guidelines, mutations are numbered starting from the ATG initiation codon and include the 18-residue signal peptide. The number of the codon with respect to the mature FH protein and consistent with the RSCB PDB entry for secreted FH (1haq.pdb) is shown alongside in parenthesis. Type I and Type II Phenotype Type I indicates that the mutant protein is either absent from the plasma or present in lower amounts. This indicates the mutation has a structural effect on the mutant protein - ie reducing the stability Type II indicates that the mutant protein is present in normal amounts in plasma. This indicates that the mutation has a functional effect on the protein ie affecting substrate binding References There are three references you can use to reference this database Saunders et al, 2007. The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: update and integration of membrane cofactor protein and Factor I mutations with structural models. Hum Mutat. 2007 28:222-234. Saunders et al, 2006. An interactive web database of factor H-associated hemolytic uremic syndrome mutations: insights into the structural consequences of disease-associated mutations. Hum Mutat. 2006 27:21-30. Saunders & Perkins, 2006. A user''s guide to the interactive Web database of factor H-associated hemolytic uremic syndrome. Semin Thromb Hemost. 2006 32:160-8. Abstract. BACKGROUND: cblC disease is a cause of hemolytic uremic syndrome (HUS), which has been primarily described in neonates and infants with severe renal and neurological lesions. PATIENTS: Two sisters aged 6 and 8.5 years presented with a latent hemolytic process characterized by undetectable or low plasma haptoglobin, respectively, associated with renal failure and gross proteinuria. Renal biopsies performed in both patients found typical findings of thrombotic microangiopathy suggesting the diagnosis of HUS. Both patients were free of neurologic signs. RESULTS: Biochemical investigations found a cobalamin processing deficiency of the cblC type. Search for additional factors susceptible to worsen endothelial damage revealed homozygosity 677C--> T mutation in the methylenetetrahydrofolate reductase gene as well as heterozygosity for a 3254T--> C mutation in factor H in the patient with the most severe clinical presentation. Long-term subcutaneous administration of hydroxocobalamin in combination with oral betaine and folic acid resulted in clinical and biological improvement in both patients. CONCLUSION: cblC disease may be a cause of chronic HUS with delayed onset in childhood. Superimposed mutation of factor H gene might influence clinical severity. | has parent organization: University College London; London; United Kingdom | nif-0000-30558 | SCR_008512 | SciCrunch Registry | FH HUS Mutation Database | 2026-10-17 01:34:01 | 25 | ||||||||||
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Zebrafish Models for Human Development and Disease Resource Report Resource Website 1+ mentions |
Zebrafish Models for Human Development and Disease (RRID:SCR_008595) | data or information resource, database | ZF-MODELS - Zebrafish Models for Human Development and Disease is an Integrated Project funded by the European Commission as part of its Sixth Framework Programme (EC Contract LSHG-CT-2003-503496). The project started on January 1, 2004 and is scheduled to run over a period of five years. The aim of this project is to exploit the advantages of the zebrafish to produce knowledge, technology and materials in the form of disease models, drug targets and insight into pathways of gene regulation applicable to human development and disease. | nif-0000-31929 | SCR_008595 | SciCrunch Registry | ZF-Models | 2026-10-17 01:34:02 | 5 | |||||||||||
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Zinc Resource Report Resource Website 1000+ mentions |
Zinc (RRID:SCR_008596) | data or information resource, database | Welcome to ZINC, a free database of commercially-available compounds for virtual screening. ZINC contains over 13 million purchasable compounds in ready-to-dock, 3D formats. ZINC is provided by the Shoichet Laboratory in the Department of Pharmaceutical Chemistry at the University of California, San Francisco (UCSF). To cite ZINC, please reference: Irwin and Shoichet, J. Chem. Inf. Model. 2005;45(1):177-82 PDF, DOI. We thank NIGMS for financial support (GM71896). There are release notes for ZINC 10. - We have a survey where you can give us feedback. | FASEB list | r3d100010372, nif-0000-31930 | https://doi.org/10.17616/R3JG77, https://doi.org/10.17616/R3JG77 | SCR_008596 | SciCrunch Registry | Zinc | 2026-10-17 01:33:27 | 1047 | |||||||||
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PolygenicBlog Resource Report Resource Website |
PolygenicBlog (RRID:SCR_008789) | blog, data or information resource, narrative resource | A blog concerning the relationships between genes, risk factors and immunity in Alzheimer's disease, autism, Bipolar disorder, multiple sclerosis, Parkinson's disease, schizophrenia and chronic fatigue. | gene, risk factor, immunity, alzheimer's disease, autism, bipolar disorder, multiple sclerosis, parkinson's disease, schizophrenia, chronic fatigue |
is used by: NIF Data Federation is used by: Integrated Blogs has parent organization: Polygenic Pathways |
Alzheimer's disease, Autism, Bipolar disorder, Multiple sclerosis, Parkinson's disease, Schizophrenia, Chronic fatigue | Public | nlx_144238 | SCR_008789 | SciCrunch Registry | Polygenic Blog | 2026-10-17 01:34:50 | 0 | |||||||
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Layton Center Clinical Data Resources Resource Report Resource Website |
Layton Center Clinical Data Resources (RRID:SCR_008822) | data or information resource, database | A database housing longitudinal relational research data from over 4,000 research subjects. The database includes the following types of data: physical and neurological exam findings, neurocognitive test scores, personal and family history of dementia, personal demographic genotypes (APOE, HLA), age at service evaluations, age at onset, age at death, clinical diagnosis, neuropathology diagnosis, tissue inventory information (when available), health status, medications, laboratory tests, and MRI data. | clinical data, alzheimer's disease, dementia, genotype, late adult human, longitudinal, clinical, mri |
is related to: Oregon Brain Bank has parent organization: OHSU Layton Aging and Alzheimer's Disease Center |
Aging, Alzheimer's disease | Researchers must submit a request | nlx_144446 | SCR_008822 | SciCrunch Registry | Layton Aging and Alzheimer's Disease Center Clinical Data Resources | 2026-10-17 01:34:50 | 0 | |||||||
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Neuron-Restrictive Silencer Factor Resource Report Resource Website 1+ mentions |
Neuron-Restrictive Silencer Factor (RRID:SCR_008546) | data or information resource, database | THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 15, 2013. A database containing all genomic human and mouse binding sites of the Repressor Element 1 Silencing Transcription factor (REST), identified by PSSM. The RE1 silencing transcription factor (REST; also known as the neuron-restrictive silencer factor), is a nine zinc-finger transcription factor, related to the Gli-Kruppel family. REST binds to a conserved 21-nucleotide element, known as repressor element 1 (RE1; also known as the neuron-restrictive silencer element). REST was proposed to be a ''master'' silencer of neuron specific gene expression in non-neuronal tissues and undifferentiated neuroepithelium (precursor of neuronal cells), preventing the default expression of the neuronal phenotype during embryogenesis. It has been shown to function independently of orientation and distance from a gene promoter. REST has an important role during embryonic development, as homozygous gene knockout mice (Rest-/-) die by embryonic day 11.5. The constitutive expression of REST has also been shown to disrupt neuronal gene expression and cause axon path finding errors in chicken embryos (Paquette et al. 2000). RE1 sequences that are known to bind REST have also been found near to non-neuronal genes, including keratin and cytochrome P450 genes. | molecular neuroanatomy resource | has parent organization: University of Leeds; West Yorkshire; United Kingdom | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-31400 | SCR_008546 | SciCrunch Registry | RE1 | 2026-10-17 01:34:02 | 1 | ||||||||
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Discover Magazine Resource Report Resource Website 10+ mentions |
Discover Magazine (RRID:SCR_008787) | Discover | blog, data or information resource, narrative resource | Popular science magazine which includes news and blogs on topics including Health & Medicine, Mind & Brain, Technology, Space, Human origins, Living World, Environment, and Physics & Math. NIF Indexes include: The Brain: DISCOVER blogger, columnist, and contributing editor Carl Zimmer''s monthly column will make your brain happy. Discover Interview: The magazine''s signature in-depth discussion with the leading lights of the world of science Vital Signs: A medical mystery, as written by the doctor involved. | health, medicine, mind, brain, technology, magazine |
is used by: NIF Data Federation is used by: Integrated Blogs is parent organization of: Neuroskeptic is parent organization of: The Loom |
nlx_144214 | SCR_008787 | SciCrunch Registry | 2026-10-17 01:33:28 | 15 | |||||||||
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Alizadehlab: MeeboChip and HeeboChip Open Source Project Resource Report Resource Website 1+ mentions |
Alizadehlab: MeeboChip and HeeboChip Open Source Project (RRID:SCR_008384) | data or information resource, database | This is an open-source Mouse Exonic Evidence-Based Oligonucleotide Chip (MEEBOChip), and are in the process of building the human counterpart, HEEBOChip. The set of 70mers for MEEBOChip is already available from Illumina, Inc., with synthesis of HEEBOChip 70mers in progress. Both arrays are based on a novel selection of exonic long-oligonucleotides (70-mers) from a genomic annotation of the corresponding complete genome sequences, using a transcriptome-based annotation of exon structure for each genomic locus. Using a combination of existing and custom-tailored tools and datasets (including millions of mRNA and EST sequences), we built and performed a systematic examination of transcript-supported exon structure for each genomic locus at the base-pair level (i.e., exonic evidence). This strategy allowed them to select both constitutive and in many cases alternative exons for nearly every gene in the corresponding genome (e.g., protocadherin locus), allowing an unprecedented exploration of human and mouse biology. Furthermore, they used experimentally derived data to hone the selection of these 70mers, helping maximize their performance under typical fluorescent labeling and hybridization conditions. Specifically, they applied and refined the ArrayOligoSelector algorithm from Joe DeRisis laboratory to select 70mers, considering not only their uniqueness (i.e., hybridization specificity) within the content of the entire genome, but also to overcome the known biases of labeling and hybridization methods (e.g., 3-biased reverse transcription and in vitro transcription reactions). | mouse, exonic, evidence, oligonucleotide, chip, human, array, genomic, annoation, sequence, transcriptome, annotation, dataset, mrna, est, systematic, transcript, exon, locus, biology | has parent organization: Stanford University; Stanford; California | Stanford University ; UCSF ; Stowers-Institute ; Rockefeller University ; Basel University |
nif-0000-30030 | SCR_008384 | SciCrunch Registry | MeeboChip and HeeboChip | 2026-10-17 01:33:27 | 7 | ||||||||
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HIV Brain Sequence Database Resource Report Resource Website 1+ mentions |
HIV Brain Sequence Database (RRID:SCR_008819) | HIVBrainSeqDB | data or information resource, database | The HIV Brain Sequence Database (HIVBrainSeqDB) is a public database of HIV envelope sequences, directly sequenced from brain and other tissues from the same patients. For inclusion in the database, sequences must: (i) be deposited in Genbank; (ii) include some portion of the HIV env region; (iii) be clonal, amplified directly from tissue; and (iv) be sampled from the brain, or sampled from a patient for which the database already contains brain sequence. Sequences are annotated with clinical data including viral load, CD4 count, antiretroviral status, neurocognitive impairment, and neuropathological diagnosis, all curated from the original publication. Tissue source is coded using an anatomical ontology, the Foundational Model of Anatomy, to capture the maximum level of detail available, while maintaining ontological relationships between tissues and their subparts. 44 tissue types are represented within the database, grouped into 4 categories: (i) brain, brainstem, and spinal cord; (ii) meninges, choroid plexus, and CSF; (iii) blood and lymphoid; and (iv) other (bone marrow, colon, lung, liver, etc). Currently, the database contains 2517 envelope sequences from 90 patients, obtained from 22 published studies. 1272 sequences are from brain; the remaining 1245 are from blood, lymph node, spleen, bone marrow, colon, lung and other non-brain tissues. The database interface utilizes a faceted interface, allowing real-time combination of multiple search parameters to assemble a meta-dataset, which can be downloaded for further analysis. This online resource will greatly facilitate analysis of the genetic aspects of HIV macrophage tropism, HIV compartmentalization and evolution within the brain and other tissue reservoirs, and the relationship of these findings to HIV-associated neurological disorders and other clinical consequences of HIV infection. | human immunodeficiency virus, hiv, brain, sequence, hiv envelope sequence, brain sequence, clone, tissue, brainstem, spinal cord, meninges, choroid plexus, csf, blood, lymphoid, bone marrow, colon, lung, liver, aids |
is related to: FMA has parent organization: Harvard University; Cambridge; United States |
Human immunodeficiency virus | ARRA ; NIMH 3ROI MH83588-12S1; NIMH MH83588 |
PMID:21156070 | nlx_149217 | SCR_008819 | SciCrunch Registry | The HIV Brain Sequence Database | 2026-10-17 01:33:28 | 1 | |||||
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OMICS! OMICS! Resource Report Resource Website |
OMICS! OMICS! (RRID:SCR_008533) | OMICS! OMICS! | blog, data or information resource, narrative resource | A computational biologist''s personal views on new technologies & publications on genomics & proteomics and their impact on drug discovery. | is listed by: OMICtools | OMICS_01719 | SCR_008533 | SciCrunch Registry | 2026-10-17 01:33:27 | 0 | ||||||||||
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Human Embryogenesis at a glance Resource Report Resource Website |
Human Embryogenesis at a glance (RRID:SCR_008499) | data or information resource, database | THIS RESOURCE IS NO LONGER IN SERVICE, documented on July 17, 2013. During the embryogenesis of human embryo, the development of each organ may be impaired during specific time periods. As illustrated, such impairment leads to congenital anomalies. After such critical periods, the environmental factors cause either minor congenital anomalies or lead to functional abnormalities. True beginning of gestation starts with the fertilization of the ovum which normally occurs one to several days after ovulation. By convention, however, due the fact that the day of the last menstrual period is easily defined, gestation starts on such day. During the first two weeks of pregnancy the embryo does not exist and endometrium is undergoing its normal menstrual and then proliferative phases. Stage one of the development starts with the fertilization of the ovum and stage 2 is initiated by the cleavage of the fertilized ovum. It is during the 4th and 5th stages of development that blastocyst starts its implantation process. By the end of the second week after fertilization, the stage 6 is initiated. During this stage, the primary chorionic villi and embryonic disc are formed. | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-30514 | SCR_008499 | SciCrunch Registry | Embryogenesis | 2026-10-17 01:33:27 | 0 | ||||||||||
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GOstat Resource Report Resource Website 100+ mentions |
GOstat (RRID:SCR_008535) | GOstat | analysis service resource, data analysis service, production service resource, service resource | GOstat is a tool that allows you to find statistically overrepresented Gene Ontologies within a group of genes. The Gene-Ontology database (GO: http://www.geneontology.org) provides a useful tool to annotate and analyze the function of large numbers of genes. Modern experimental techniques, as e.g. DNA microarrays, often result in long lists of genes. To learn about the biology in this kind of data it is desirable to find functional annotation or Gene-Ontology groups which are highly represented in the data. This program (GOstat) should help in the analysis of such lists and will provide statistics about the GO terms contained in the data and sort the GO annotations giving the most representative GO terms first. Run GOstat: * Go to search form - Computes GO statistics of a list of genes selected from a microarray. * GOstat Display - You can store results from a previously run and view them here, either by uploading them as a file or putting them on a selected URL. * Upload Custom GO Annotations - This allows you to upload your own GO annotation database and use it with GOstat. Variants of GOstat: * Rank GOstat - Takes input from all genes on microarray instead of using a fixed cutoff and uses ranks using a Wilcoxon test or either ranks or pvalues to score GOs using Kolmogorov-Smirnov statistics. * Gene Abundance GOstats - Takes input from all genes on microarray and sums up the gene abundances for each GO to compute statistics. * Two list GOstat - Compares GO statistics in two independent lists of genes, not necessarily one of them being the complete list the other list is sampled from. Platform: Online tool, THIS RESOURCE IS NO LONGER IN SERVICE. Documented on September 16,2025. | gene, gene ontology, annotation, statistical analysis, FASEB list |
is listed by: Gene Ontology Tools is related to: Gene Ontology has parent organization: Walter and Eliza Hall Institute of Medical Research; Victoria; Australia |
DFG | PMID:14962934 | THIS RESOURCE IS NO LONGER IN SERVICE | nif-0000-30625 | SCR_008535 | SciCrunch Registry | 2026-10-17 01:34:47 | 159 | ||||||
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Aquatic Animal Health Code - 2008 Resource Report Resource Website |
Aquatic Animal Health Code - 2008 (RRID:SCR_008413) | data or information resource, database |
For the purposes of the Aquatic Code, spring viraemia of carp (SVC) means infection with the viral species SVC virus (SVCV) tentatively placed in the genus Vesiculovirus of the family Rhabdoviridae. Methods for surveillance and diagnosis are provided in the Aquatic Manual. The recommendations in this Chapter apply to: common carp (Cyprinus carpio carpio) and koi carp (Cyprinus carpio koi), crucian carp (Carassius carassius), sheatfish (also known as European catfish or wels) (Silurus glanis), silver carp (Hypophthalmichthys molitrix), bighead carp (Aristichthys nobilis), grass carp (white amur) (Ctenopharyngodon idellus), goldfish (Carassius auratus), orfe (Leuciscus idus), and tench (Tinca tinca). These recommendations also apply to any other susceptible species referred to in the Aquatic Manual when traded internationally. 1) Periodicals *Scientific and Technical Review (available on the Online Bookshop and Website); *Bulletin (available on the Online Bookshop and Website); *Disease Information (available on the WAHID interface); *World Animal Health (available on the Online Bookshop and on the WAHID interface); Health standards *Terrestrial Animal Health Code (available on the Online Bookshop and Website); *Aquatic Animal Health Code (available on the Online Bookshop and Website); *OIE Quality Standard and Guidelines for Veterinary Laboratories: Infectious Diseases (available on the Online Bookshop); *Manual of Diagnostic Tests and Vaccines for Terrestrial Animals (available on the Online Bookshop and Website); *Manual of Diagnostic Tests for Aquatic Animals (available on the Online Bookshop in English only (2009 version) and also on the Website). |
nif-0000-30119 | http://www.oie.int/eng/normes/fcode/en_chapitre_2.1.4.htm | SCR_008413 | SciCrunch Registry | Aquatic Animal Health Code | 2026-10-17 01:33:27 | 0 | ||||||||||
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Embase Biomedical Answers Resource Report Resource Website 1000+ mentions |
Embase Biomedical Answers (RRID:SCR_008498) | data or information resource, database | You can begin your search immediately using the Quick form on the home page or you can access the other specialized search forms in Embase. You can choose any section from the options on the top menu bar: Search, Emtree, Journals, Authors, or Help. You can start to search without logging in but if you would like to set up an email alert or save a search, then you may Login or Register from the upper-right part of the screen. Note: if you are outside your institution IP range, you will first be directed to the info site before accessing the Embase Home page. For more information on remote access, please see Login section. Search Forms Search is at the core of Embase and all search forms are designed to allow you to look for biomedical and pharmaceutical clinical and research information easily and quickly, whether you are a new or experienced searcher. The Embase search engine allows Boolean searching with wildcard and truncation features, as well as many predefined search limits. Search is divided into five options: Quick, Advanced, Drug, Disease and Article. Quick lets you perform easy yet powerful searches without having to learn a complex search language. It is perfect if you are starting your research and looking for an overview of the literature or good terms to include in your search strategy. Autocomplete will help you to search using the bext terminology. Advanced incorporates options from Emtree term mapping including explosion searching for maximum precision in subject searching (see Emtree) and Drug and Disease provide access to specialized features useful to search these topics, such as ''Adverse Drug Reaction''''Drug Combination''. Generally speaking, drug searches are best carried out in the Drug form, diseases in the Disease form and non-drug and disease searches in the Advanced form. Article allows you to pinpoint individual articles. Embase is owned and operated by Elsevier B.V., Radarweg 29, 1043 NX Amsterdam, The Netherlands, Reg. No. 33156677, BTW No. 002967455B65 (Elsevier). | FASEB list | nif-0000-30513 | SCR_008498 | SciCrunch Registry | Embase | 2026-10-17 01:34:47 | 1135 | ||||||||||
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Emsdiasum Resource Report Resource Website 50+ mentions |
Emsdiasum (RRID:SCR_008497) | data or information resource, database | A complete online Product Catalog of chemicals, supplies, accessories, and equipment for Electron and Light Microscopy, Histology, Cell Biology, Neuroscience, and all biological related research fields. At the site, you can find technical tips and recommended articles of interest, technical and product data sheets, Material Safety Data Sheets, and many revolutionary new products and exclusive items. A complete product catalog of the entire Diatome collection of Diamond knives, tools, and accessories for Electron and Light microscopy for Biological and Materials Science at room and cryo temperatures. Available on-line as well is information on our services, programs, specials, and policies. The complete handling and use technical manual as well as troubleshooting can also be found at our site. The Summers Optical on-line catalog including a complete line of optical cements and adhesives, decementing agents, hardness testers, ultrasonic baths and UV lights as well as technical and transmission data and problem solving can be found at this site. As well as, our unique bonding manual including troubleshooting and charts for how to choose a cement for specific applications and a complete set of MSDS on all of our products can be seen here. EMS Contract Packaging is a total service contract manufacturer, packager, and formulator with over 40 years experience in drug and cosmetic formulating and packaging. Negafile furniture quality wood filing systems and storage cases for grids, negatives, film and microscope glass slides. And a full line of shipping and packaging solutions for all your traditional or digital media. | FASEB list | nif-0000-30510 | SCR_008497 | SciCrunch Registry | Emsdiasum | 2026-10-17 01:33:27 | 54 | ||||||||||
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3D Macromolecular Analysis and Kinemage Home Page Resource Report Resource Website 1+ mentions |
3D Macromolecular Analysis and Kinemage Home Page (RRID:SCR_008569) | data or information resource, database | Resources for macromolecular X-ray crystallography from the Richardson Laboratory, including kinemages (a scientific illustration presented as an interactive computer display), databases, software, training materials and images | x-ray crystallography | has parent organization: Duke University; North Carolina; USA | nif-0000-31460 | SCR_008569 | SciCrunch Registry | Richardson Lab and Kinemage | 2026-10-17 01:33:27 | 1 | |||||||||
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Molecular Brain: Transcription Profiles of Mouse and Human Brains Resource Report Resource Website 1+ mentions |
Molecular Brain: Transcription Profiles of Mouse and Human Brains (RRID:SCR_008689) | data or information resource, database | MolecularBrain is an attempt to collect, collates, analyze and present the microarray derived gene expression data from various brain regions side by side. Transcription Profile of any gene in Mouse (online) and Human Brain (not yet) can be accessed as a histogram along with links to access various aspects of that gene. The expression levels were calculated from microarray data deposited at GEO (Gene expression omnibus). The molecular brain database could be searched using the built in search tool with the terms Entrez GeneID, gene symbol, synonym or description. Gene information along with their expression values can be also accessed from the alphabetical list of gene symbols on the footer. The protocol and GEO sample information is available. | molecular, molecule, brain, transcription, mouse, human, gene, microarray, data, expression, database, tool, expression, molecular neuroanatomy resource | has parent organization: National Institutes of Health | nif-0000-37035 | SCR_008689 | SciCrunch Registry | Molecular Brain | 2026-10-17 01:34:03 | 3 | |||||||||
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Classic Articles in Visual Perception Resource Report Resource Website |
Classic Articles in Visual Perception (RRID:SCR_008325) | data or information resource, database | This website contains a list of classic articles in visual perception. They are listed alphabetically by the last name if the article''s author. | article, perception, visual | has parent organization: Johns Hopkins University; Maryland; USA | nif-0000-24689 | http://www.psy.jhu.edu/~yantis/classics.html | SCR_008325 | SciCrunch Registry | Classic Articles in Visual Perception | 2026-10-17 01:34:00 | 0 | ||||||||
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ADAPT: A Database of Affymetrix Probesets and Transcripts Resource Report Resource Website |
ADAPT: A Database of Affymetrix Probesets and Transcripts (RRID:SCR_008688) | data or information resource, database | Library of many-to-many relationships between Affymetrix probesets transcripts and genes, by directly mapping every probe against publicly available mRNAs/cDNA sequences from RefSeq and Ensembl. You can search the database by AffymetrixProbeset ID, Transcript Accession, Gene Symbol or Gene Accession. Currently, the ADAPT database holds information on 23 Array Types containing 255771 unique Probesets, that themselves map onto 252788 entries in both RefSeq and Ensembl. ADAPT is clusterable, cross platform, runs on any Java Virtual machine after version 1.4, and utilises the following software: :- Apache Tomcat :- Apache Struts :- JBoss Application Server :- Postgresql Sponsors: ADAPT has been written with funding by Cancer Research UK. Keywords: Database, Gene, Transcript, Mapping, Probe, mRNA, cDNA, Sequence, Association, Array, Probeset, | has parent organization: University of Manchester; Manchester; United Kingdom | nif-0000-36878 | SCR_008688 | SciCrunch Registry | ADAPT | 2026-10-17 01:33:27 | 0 | ||||||||||
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Biomedical Search: Medical Research and Health Resources Resource Report Resource Website 1+ mentions |
Biomedical Search: Medical Research and Health Resources (RRID:SCR_008683) | data or information resource, database | BioMedSearch is a biomedical search engine that contains NIH/PubMed documents, plus a large collection of theses, dissertations, and other publications not found anywhere else for free, making it the most comprehensive free search on the web. :Besides free-form search, users can search based on Author, Journal Title, Publication Date, the Language in which the article was published (many non-English articles have English language abstracts), MeSH (Medical Subject Headings) and more. : The goal of BioMedSearch.com is to provide free access to a massive collection of authoritative documents relating to the biomedical field. Our mission is to make these important works available to the community in a way that is fast and easy, while still offering the advanced features demanded by power users such as portfolios, collaboration features, bibliographical citation export, alerts, and more. Whether you are doctor, scientist, or someone interested in researching a medical topic out of personal interest, BioMedSearch aggregates a vast number of authoritative documents in one place to make finding medical information easy, fast and free. | biomedical, doctor, health, medical, research, scientist, search engine | nif-0000-33767 | SCR_008683 | SciCrunch Registry | BioMedSearch | 2026-10-17 01:33:27 | 4 |
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