DATABASES ON MEDICINE AND MOLECULAR BIOLOGY
|Austrian Breast & Colorectal Cancer Study Group" info|
Website and database provided by the Austrian Breast & Colorectal Cancer Study Group.
|Adam Health Illustrated Encyclopedia|
The Adam Health Illustrated Encyclopedia includes over 4,000 articles about diseases, tests, symptoms, injuries, and surgeries. It also contains an extensive library of medical photographs and illustrations.
|Literature on Adolescence Health|
Literature-database on Adolescence Health.
|X-linked Adrenoleukodystrophy Database|
Dtabase about adrenoleukodystrophy, a progressive, genetic disorder, which affects the adrenal glands and the white matter of the nervous system.
AgeLine abstracts the literature of social gerontology as well as aging-related research from psychology, sociology, social work, economics, public policy, and the health sciences.
|Agency for Healthcare Research and Quality - Evidence-based Medicine" info|
Collection of documents by the Agency for Healthcare Research and Quality>.
|AIDS: Clinical Guidelines|
AIDS Guidelines, provided by AIDSinfo - a service ofthe U.S.Department of HEalth and Human Services.
|African Index Medicus" info|
The Association for Health Information and Libraries in Africa (AHILA) with the technical support of the World Health Organization has produced an international index to African health literature and information sources.
|ALlele FREquency Database (alfred)|
ALFRED is designed to store and disseminate frequencies of alleles at human polymorphic sites for multiple populations, primarily for the population genetics and molecular anthropology communities.
Database of allergens.
|The Allergen Database|
Database on allergens and epitopes.
The I.U.I.S. Allergen Nomenclature Sub-committee operates under the auspices of the International Union of Immunological Societies (I.U.I.S.) and the World Health Organisation (W.H.O.). The objectives of the I.U.I.S. Allergen Nomenclature Sub-committee are to ...
|A Search Service for Abbreviation / Long Form|
Allie is a search service for abbreviations and long forms utilized in Lifesciences. It provides a solution to the issue that many abbreviations are used in the literature, and polysemous or synonymous abbreviations appear frequently, making it difficult to read and understand scientific papers that are not relevant to the reader's expertise. Allie searches for abbreviations and their corresponding long forms from titles and abstracts in the entire MEDLINE database.
|ALPORT Syndrome and COL4A5|
Alport Syndrome is a progressive renal disease with cochlear and ocular involvement. The most common form (~80%) is inherited in an X-linked pattern. X-linked Alport Syndrome (OMIM #301050) is caused by mutations in the type IV collagen alpha chain 5 (COL4A5).
The aim of this database is to record all known variants in the COL4A5 gene and their clinical significance. The GenBank sequence NC_000023.9 is used as the reference sequence. The Human Genome Variation Society nomenclature has been used to describe COL4A5 mutations, as well as original nomenclature described by Zhou et al (1994), which includes 202 nucleotides of 5' UTR.
ARUP offers full gene sequencing analysis (test 0051786) for classic X-linked Alport syndrome (80% of mutations) and targeted testing for p.C1564S (c.4692G>A), p.L1649R (c.4946T>G), p.R1677Q (c.5232G>A) mutations for adult type Alport syndrome (test 0051710).
|Autoimmune Lymphoproliferative Syndrome Database|
Autoimmune Lymphoproliferative Syndrome Database (ALPSbase):
Database of mutations causing human ALPS
This database is aimed at providing an unbiased, centralized, publicly available and regularly updated collection of genetic association studies performed on AD phenotypes.
The Alzheimer's Disease Clinical Trials Database is a joint project of the U.S. Food and Drug Administration (FDA) and the National Institute on Aging (NIA) maintained by the NIA's Alzheimer's Disease Education and Referral (ADEAR) Center.
|The Animal Ageing Database|
AnAge is a database dedicated to the comparative biology of ageing.
AntiJen is a database system focused on the integration of kinetic, thermodynamic, functional, and cellular data within the context of immunology and vaccinology.
|ARAMIS Information System for research and development projects in Switzerland|
The ARAMIS Information System for research and development projects in Switzerland is intended to provide information to interested parties about research which is financed or carried out by the Federal Government, to improve co-ordination and to increase transparency in this area. It has been implemented in response to a demand of the Swiss Parliament and the Government.
|Mutation Database - Autosomal Recessive Polycystic Kidney Disease (ARPKD / PKHD1)" info|
Autosomal Recessive Polycystic Kidney Disease (ARPKD) or Polycystic Kidney and Hepatic Disease 1 (PKHD1) is an important cause of childhood renal- and liver-related morbidity and mortality with a proposed incidence of 1:20,000 - 1:40,000 live births.
|OPRM - Atlas of Oral Pathology|
Atlas made by The University of Iowa / College of Dentistry & Dental Clinics. The goal of this atlas is to show multiple examples of important lesions of the oral cavity. One should never diagnose a lesion simply by visually inspecting it. The patient history and physical examination are critically important.
|The Autism Chromosome Rearrangement Database|
Database of chromosomal breakpoints and other genomic features related to autism, provided by the canadian Centre for Applied Genomics and The Hospital for Sick Children in Toronto.
|Brain Architecture Management System|
Database about the brain architecture.
|Database of B-Cell Epitopes" info|
Bcipep is a database of experimentally determined linear B-cell epitopes of varying immunogenicity collected from literature and other publicly available databases.
|British Committee for Standards in Haematology (BCSH) - Guidelines|
Guidelines on hematology
|Bioethics Database (BEKIS)|
BEKIS is an online database, which provides ready access to information about national and international institutions and activities in the area of bioethics research. Users can find information about: research institutions, research groups, research projects and events.
|Topics in Bioethics (BELIT)|
BELIT is an integrated online database developed by the German Reference Centre for Ethics in the Life Sciences (DRZE) and operated in cooperation with the Information and Documentation Centre for Ethics in Medicine (IDEM, Göttingen), the Interfaculty Centre for Ethics in the Sciences and Humanities (IZEW, Tübingen), the Kennedy Institute of Ethics (KIE, Washington) and the Centre de documentation en éthique des sciences de la vie et de la santé de l'INSERM (CDEI, Paris).
The Bioethics Database was created in 1998 and is being updated on a regular basis. It comprises more than 370 bioethics institutions (bioethics committees, commissions, training, research and documentation centres) in over 70 countries, including information on activities and publications. Information is based on replies obtained from a widely distributed questionnaire and has been gathered in cooperation with National Commissions and Permanent Delegations to UNESCO.
|Blood Group Antigen Gene Mutation Database|
The database is constructed under the aegis of the Human Genome Variation Society (HGVS); it is a Locus Specific Database (LSDB).. It deals with mutations in loci of allelic genes that specify the antigens of 28 blood group systems (includes all those for which the molecular basis is defined ) and the allelic variants of those genes. Orthologues of a number of genes are included.
|Botanical Dermatology Database" info|
Database about the influences of plants on the human skin.
The Bookshelf is a growing collection of biomedical books compiled by the NCBI (National Center for Biotechnology Information).
Mutation registry for X-linked agammaglobulinemia.
|Computer-Assisted Information Retrieval Service System for Music|
CAIRSS is a bibliographic database of music research literature in music education, music psychology, music therapy, and music medicine.
|CAIRSS for Music|
Database about the clinical aspects of music therapy.
|Complementary and Alternative Medicine (NCI)|
Scientific evaluation of complementary and alternative medicine by the National Cancer Institute.
Reliable information on complementary and alternative medicines relating to cancer provided by the European Union (EU).
|CAM on PubMed|
More than 700.000 CAM-articles in MEDLINE (PubMed). One can find these with the subset
The NHS Priorities/CAMEOL Project is a joint project between the Research Council for Complementary Medicine (RCCM) and the School of Integrated Health, University of Westminster (UoW), London and University of Plymouth, UK.
|Cancer Chromosomes" info|
Three databases, the NCI/NCBI SKY/M-FISH & CGH Database, the NCI Mitelman Database of Chromosome Aberrations in Cancer, and the NCI Recurrent Aberrations in Cancer, are now integrated into NCBI's Entrez system as Cancer Chromosomes.
|Cancer Immunome Database|
Database about the human immune response to cancer.
|Cancer Statistics, 2018" info|
Each year, the American Cancer Society estimates the number of new cancer cases and deaths expected in the United States in the current year and compiles the most recent data on cancer incidence, mortality, and survival rates based on incidence data from the National Cancer Institute and mortality data from the National Center for Health Statistics.
|Familial Hypertrophic Cardiomyopathy / DNA Mutation Database" info|
This database contains information on familial hypertrophic cardiomyopathy (FHC)-associated mutations and related data.
CardioSignal was designed for integration of regulatory information on the transcriptional regulation involved in heart development and cardiac hypertrophy.
|Computer Access to Research on Dietary Supplements (CARDS)" info|
CARDS stands for Computer Access to Research on Dietary Supplements. It is a database of federally funded research projects pertaining to dietary supplements. Currently, CARDS contains projects funded by the United States Department of Agriculture (USDA) and the Institutes and Centers (ICs) of the National Institutes of Health (NIH) beginning with fiscal year 1999, the first year that NIH ICs began reporting research related to dietary supplements.
CarpeDB is a epilepsy genetics database. It profiles some 400 genes linked to epilepsy in humans, mice, nematodes, and other organisms.
|Calcium Sensing Receptor Databases|
CASR mutations causing hypercalcemia and/or hyperparathyroidism.
|Collecting Duct Phosphoprotein Database|
This database of renal inner medullary collecting duct (IMCD) phosphoproteins is based on protein mass spectrometry data from the NHLBI Laboratory of Kidney and Electrolyte Metabolism. All data are from IMCD cells freshly purified from rat inner medullas.
Cellular Properties Database provides a simple repository for data regarding membrane channels, receptor and neurotransmitters that are expressed in specific types of cells. The database is presently focused on neurons but will eventually include other cell types, such as glia, muscle, and gland cells.
|Clinical Trials Listing Service|
Information about more than 41,000 active industry and government-sponsored clinical trials, as well as new drug therapies in research and those recently approved by the FDA.
|Cancer Gene Expression Database|
CGED (Cancer Gene Expression Database) is a database of gene expression profile and accompanying clinical information. The data of CGED were obtained through collaborative efforts of Nara Institute of Science and Technology and Osaka University School of Medicine to identify genes of clinical importance. This database offers graphical presentation of expression and clinical data with similarity search and sorting functions. Currently, data of breast, colorectal, and hepatocellular cancers are available.
Genes in CGED can be searched by 1) gene names or identifiers, or 2) gene ontology terms or keywords in functional annotations in the SwissProt.
|Center for International Rehabilitation Research Information and Exchange Database" info|
The CIRRIE Database currently contains over 24,000 citations of international rehabilitation research published between 1990 and the present.
|Images from the Clendening Library|
This exhibit displays hundreds of images from medical and natural history texts, most of which were printed before 1800. They are organized by theme: diagnostics, human body, imaging, instruments, physician-patient culture, portraits, public health, reproduction, reproduction instruments, therapeutics.
|Clinical Trials" info|
ClinicalTrials provides regularly updated information about federally and privately supported clinical research in human volunteers. ClinicalTrials gives you information about a trial's purpose, who may participate, locations, and phone numbers for more details.
Collection of canadian guidelines.
|Annotated List of Onlince Continuing Medical Education (Bernard Sklar)|
The Annotated List of Online Continuing Medical Education, with inks to, and descriptions of, more than 285 Web Sites offering more than 13,000 courses and more than 23,000 hours of CME credit.
|COCHRANE CAM FIELD|
The CAM-related Cochrane reviews and protocols are also available in The Cochrane Library.
|COCHRANE LIBRARY" info|
The Cochrane Library is a collection of six databases that contain different types of high-quality, independent evidence to inform healthcare decision-making, and a seventh database that provides information about Cochrane groups.
|Collation of Cortical [cell + microcircuitry] Data|
CoCoDat contains data about morphology, firing properties, ionic currents, ionic conductances, synaptic currents, and connectivity from published experimental reports along with brain structures, methods, bibliographic references and PubMed IDs.
|Collations of Connectivity data on the Macaque brain" info|
Database about the wiring of the primate brain. The main database contains details of hundreds of tracing studies in their original descriptions.
|Database of Human Type I and Type III Collagen Mutations|
This database aims to record all published accounts of mutations in the genes encoding human collagen types I and III. Mutations of these collagen types result predominantly in osteogenesis imperfecta and Ehlers-Danlos syndrome type IV respectively.
|A COMmon DataBASE on Microbial Responses to Food Environments (ComBase)" info|
ComBase is a database protocol that encompasses observations of bacterial responses to food environments.
|Cytokines Online Pathfinder Encyclopaedia (cope)|
Encyclopaedia of cytokines.
|Central Research Infrastructure for molecular Pathology|
CRIP provides anonymized data on and from human biospecimen available for basic, preclinical and clinical research projects in its database partners’ institutes. Web-based query requires prior user’s registration and is for free for researchers both from academia and industry. CRIP covers data from all disease areas for R&D in molecular and clinical medicine.
|Comparative Toxicogenomics Database (CTD)" info|
The Comparative Toxicogenomics Database (CTD) identifies interactions between chemicals and genes/proteins in diverse organisms to elucidate the molecular mechanisms by which environmental chemicals affect human health.
|Clinical Trials Registry- India|
The Clinical Trials Registry- India (CTRI), hosted at the ICMRs National Institute of Medical Statistics, is a free and online public record system for registration of clinical trials being conducted in India that was launched on 20th July 2007
|Cystic Fibrosis Mutation Database|
This database is devoted to the collection of mutations in the CFTR gene and is currently maintained by the laboratory of Lap-Chee Tsui on behalf of the international Cystic Fibrosis genetics research community. It was initiated by the Cystic Fibrosis Genetic Analysis Consortium in 1989 to increase and facilitate communications among CF researchers. The specific aim of the database is to provide CF researchers and other related professionals with up to date information about individual mutations in the CFTR gene.
|Database of Abstracts of Reviews of Effects (DARE)" info|
DARE is a high quality database with structured abstracts of reviews published in the world wide literature, including otherwise difficultly accessible grey literature.
|Developmental & Reproductive Toxicology" info|
Developmental and Reproductive Toxicology - Current and older literature on developmental and reproductive toxicology.
|database of Genotypes and Phenotypes (dbGaP)|
The database of Genotypes and Phenotypes (dbGaP) was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype. Such studies include genome-wide association studies, medical sequencing, molecular diagnostic assays, as well as association between genotype and non-clinical traits.
The dbMHC database provides an open, publicly accessible platform for DNA and clinical data related to the human Major Histocompatibility Complex (MHC).
|Database for Preterm Birth" info|
The Database for Preterm Birth (dbPTB) is a web-based aggregation tool to organize the genes, genetic variations and pathways involved in preterm birth, dbPTB. We used semantic data mining to extract all published articles related to preterm birth. All articles were reviewed by a team of curators. Genes identified from public databases and archives of expression arrays were aggregated with genes curated from the literature.
|Database of Highly Similar and Duplicate Citations" info|
Deja vu is a database of extremely similar Medline citations. Many, but not all, of which contain instances of duplicate publication and potential plagiarism.
|Atlas of Dermatology" info|
Excellent atlas of dermatology.
Diagnosaurus allows you to search 1000+ differential diagnoses by:
Facts about dietary supplements, provided by the NIH, National Institutes of Health.
Registry of austrian dissertations.
|Registry of German Dissertations|
Registry of Dissertations from Germany.
|Dissertations from Karolinska Institutet|
Dissertations from the Karolinska Institute.
|Database of Quantitative Cellular Signaling|
The Database of Quantitative Cellular Signaling is a repository of models of signaling pathways.
|Food Additive Database|
EAFUS is a database maintained by the U.S. Food and Drug Administration (FDA) Center for Food Safety and Applied Nutrition (CFSAN) under an ongoing program known as the Priority-based Assessment of Food Additives (PAFA).
|A Digital Warehouse of Auditory Models and Data|
Auditory models and data, provided by Boston's University.
|NIH Human Embryonic Stem Cell Registry|
The NIH Human Embryonic Stem Cell Registry lists the derivations of stem cells that are eligible for federal funding. The purpose of the Registry is to provide investigators with:
|Environmental Mutagenesis Information Center" info|
EMIC is prepared by the Environmental Mutagen Information Center, Oak Ridge National Laboratory, Oak Ridge, Tennessee (EMIC/ORNL) for the federal government. EMIC covers environmental mutation literature from 1950. The records contain CAS Registry Numbers.
|Index Medicus for the Eastern Mediterranean Region (EMR)|
Literature database for the Eastern Mediterranean Region, including countries such as: Afghanistan, Bahrain, Cyprus, Djibouti, Egypt, Iran, Iraq, Jordan, Kuwait, Lebanon, Libya, Morocco, Oman, The Occupied Territories, Pakistan, Qatar, Saudi Arabia, Somalia, Sudan, Syria, Tunisia, U.A.E., and Yemen Arab Republic has long been felt by researchers, development agencies, health administrators and planners both inside and outside the Eastern Mediterranean Region. Eastern Mediterranean Regional health and biomedical information sources are not always included in the world's leading bibliographic databases.
|United States Environmental Protection Agency (EPA)|
EPA provides on this site Informations about Methods, Models, Tools, and Databases about the following fields:
> CLIMATE CHANGE
> HOMELAND SECURITY
> LAND AND WASTE MANAGEMENT
> SAFER CHEMICALS
|Database of MHC Ligands" info|
EPIMHC is a relational database of MHC-binding peptides and T cell epitopes that are observed in real proteins. Currently, the database contains 4867 distinct peptide sequences from various sources, including 84 tumor-associated antigens.
|Database of Structurally inferred Antigenic Epitopes in Proteins" info|
Epitome is a database of all known antigenic residues and the antibodies that interact with them, including a detailed description of residues involved in the interaction and their sequence / structure environments. Additionally, Interactions can be visualized using an interface into Jmol.
ETHMED is a literature database in German and English language in the field of biomedical ethics with an emphasis on ethics in medicine. It contains mainly information from Germany, Austria, and Switzerland.
|Bibliographic Database on Bioethics and Professional Ethics|
A literature database made by the Georgetown University.
|Alcohol and Alcohol Problems Science Database (ETOH)|
The Alcohol and Alcohol Problems Science Database, commonly referred to as ETOH, is the most comprehensive online resource covering all aspects of alcohol abuse and alcoholism. Produced by the National Institute on Alcohol Abuse and Alcoholism (NIAAA), ETOH contains over 110,000 records and is accessed by both researchers and clinicians worldwide. Included in ETOH are abstracts and bibliographic references to journal articles, books, dissertation abstracts, conference papers and proceedings, reports and studies, and chapters in edited works. Updated monthly, ETOH contains research findings from the late 1960s to the present, as well as historical research literature.
|EURAXESS - Researchers in Motion|
EURAXESS - Researchers in Motion is a unique pan-European initiative providing access to a complete range of information and support services to researchers wishing to pursue their research careers in Europe or stay connected to it.
The EyeSite database is an information and modelling resource for families of proteins that function in the eye. Homologues are collected from all species and clustered according to tissue type, function and sequence similarity.
|Factor H Associated HUS - Mutation Database" info|
Database about the HUS (Haemolytic Uraemic Syndrome); this 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.
|Food Allergy Research and Resource Program / Allergen Database|
FARRP offers ...
|Factor H Associated HUS Mutation Database" info|
The Factor H Associated HUS Mutation Database is a database of mutations within the human complement Factor H protein that are associated with Haemolytic Uraemic Syndrome (HUS).
|The Frequency of Inherited Disorders Database|
The Frequency of Inherited Disorders Database (FIDD) has been established by the University of Wales College of Medicine for use in a clinical context, in medical research, for epidemiological studies and in planning for genetic services.
Meta search-engine for orphan diseases / rare diseases.
|Finnish heritage disease|
A Finnish heritage disease is a genetic disease or disorder that is significantly more common in people whose ancestors were ethnic Finns, natives of Finland and Sweden. About 40 rare diseases are regarded as Finnish heritage diseases. The diseases are not restricted to Finns; they are genetic diseases with far wider distribution in the world, but due to founder effects and genetic isolation they are more common in Finns. (WIKIPEDIA)
|Freebooks 4 Doctors|
Online library with more then 600 medical textbooks.
|Low-Complexity Peptides of Forming Amyloid Plaques|
Database about Peptides, which are capable of forming amyloid plaques.
|Genetic and Rare Diseases Information Center|
The database GARD is a service by ORDR (Office of Rare Diseases Research) and by NHGRI (National Human Genome Research Institute) - both belong to the NIH.
|Global Disaster Alert and Coordination System|
The Global Disaster Alert and Coordination System provides near real-time alerts about natural disasters around the world and tools to facilitate response coordination, including media monitoring, map catalogues and Virtual On-Site Operations Coordination Centre
|Genetic Modification Clinical Research Information System|
The NIH/FDA Genetic Modification Clinical Research Information System (GeMCRIS) is a comprehensive information resource and analytical tool for scientists, research participants, sponsors, institutional oversight committees, federal officials, and others with an interest in human gene transfer research.
|NIH Genetic Modification Clinical Research Information System (GeMCRIS) - Clinical Trials|
Clinical trials, provided by the NIH Genetic Modification Clinical Research Information System (GeMCRIS).
|The Human Ageing Genes Database" info|
GenAge ia a database of genes related to human ageing.
|Gene Connection for the Heart|
This database is a repository of the genetic variations identified and published in the field of inherited arrhythmogenic diseases and cardiac ion channels.
|Gene Therapy Clinical Trials Worldwide|
Overview about clinical trials on the field of gene therapy, provided by the Journal of Gene Medicine.
Genes and Disease is a collection of articles that discuss genes and the diseases that they cause.
GeneSeeker is a database for the identification of genes underlying human genetic disorders. This requires the combination of data related to cytogenetic localization, phenotypes and expression patterns, to generate a list of candidate genes.
Citations to literature on ethics and public policy issues in genetics.
|Genetic Association Database" info|
The Genetic Association Database is an archive of human genetic association studies of complex diseases and disorders. The aim of this database is to identify medically relevant polymorphism from the large volume of polymorphism and mutational data.
|Genetics Home Reference" info|
The Genetics Home Reference is the National Library of Medicine's web site about genetic conditions and the genes responsible for those conditions.
|Global Ethics Observatory|
The observatory is a system of databases with worldwide coverage in bioethics and other areas of applied ethics in science and technology such as environmental ethics, science ethics, and technology ethics.
Database of gerontological literature.
|Genetics Home Reference|
Genetics Home Reference provides consumer-friendly information about the effects of genetic variations on human health.
|Globin Gene Server|
This site provides data and tools for studying the function of DNA sequences, with an emphasis on those involved in the production of hemoglobin. It includes information about naturally-occurring human hemoglobin mutations and their effects, experimental data related to the regulation of the beta-like globin gene cluster, and software tools for comparing sequences with one another to discover regions that are likely to play significant roles.
GOOGLE's bibliographic tool for scientists and other researchers.
|Austrian database for scholarships and research grants|
The Austrian database for scholarships and research grants is the most comprehensive online database in Austria concerning all research areas. Inner-Austrian grant options for students, graduates and researchers as well as incoming (to Austria) and outgoing (from Austria to ...) grants are offered in this database. Moreover, research allowances, prizes and other funding opportunities can be found. Information is given including details of application conditions (application deadline and place) as well as on duration, allocation and financing of each grant.
|Haemophilia A Mutation Database|
The Database covers the following three main classes of mutant:
Point Mutations, Insertions, Deletions
|Haemophilia B Mutation Database|
A database of point mutations and short additions and deletions in the factor IX gene.
|Human Ageing Genomic Resources" info|
The Human Ageing Genomic Resources (HAGR) are a collection of databases and tools designed to help researchers understand the genetics of human ageing. A major resource in HAGR is the core gene database GenAge, a database of genes related to human ageing. Featuring over 2,000 species, AnAge provides a basis for the comparative biology of ageing.
|Human Brain Project Database|
The Human Brain Project is multi-agency initiative to construct databases of neuroscience data, and to provide tools for searching and retrieving that data to support research, teaching and education of the public into normal and abnormal functions of the nervous system.
|Database of Human Hemoglobin Variants and Thalassemias" info|
Database about human hemoglobin variants and thalassemias.
|Heart and Calcium Functional Network (HCNet) Database|
The Heart and Calcium functional Network (HCNet) database is a collection of functional gene modules calculated from the microarray data compendium available from the GEO database. It is a specialized database designed to assist experimentalists for cardiac calcium signaling research by providing the pre-calculated gene clusters and their potential correlation network in heart.
|Heart and Calcium functional Network|
Heart and Calcium functional Network (HCNet) is a specialized database for mouse heart and calcium signaling toolkit genes. It contains the functional gene modules pre-calculated from the microarray data compendium using various algorithms for genetic network analyses. First of all, it could relieve the burden of wet-scientists in the related fields from the complex and tedious analyses of the high-throughput genetic data. Eventually, it will serve as a good vehicle for setting up an interesting hypothesis by reviewing the dynamic compilation of functional genetic modules.
|HEI Air Quality Database|
The HEI Air Quality Database, prepared and maintained by Atmospheric and Environmental Research (AER) Inc, focuses on levels of PM2.5 components and gaseous pollutants at and near sites in the EPA's PM2.5 Chemical Speciation Trends Network (STN) and State, Local and Tribal air monitoring stations (SLAMS).
|Hematopoiesis Promoter Database (HemoPDB)" info|
The Hematopoiesis Promoter Database (HemoPDB) has been developed as a information resource focused on transcriptional regulation in hematopoiesis. HemoPDB is composed of integral, experimentally defined regulatory information, including TFs, cis-regulatory elements, their target gene promoters and corresponding annotations, with links to supporting published references. Accordingly, the database may be searched by Gene Symbol, GenBank Accession Number, UniGene ID, TF (binding site) Name and lineage or cell type within which a gene is expressed.
|European Human Embryonic Stem Cell Registry" info|
The European Human Embryonic Stem Cell Registry (hESCreg) is funded as a Specific Support Action under the ‘Life Sciences, Genomics, and Biotechnology for Human Health’ Priority within the 6th Framework Programme for Research and Technological Development of the European Commission.
hESCreg was created to offer the research community, legislators, regulators and the general public at large an in-depth overview on the current status of hESC research in Europe. Its present content is the result of a survey by the project team, its partners and the input from numerous hESC line providers. The database has now entered its first public evaluation stage and will be continually developed.
This database of some 650 hESC lines that have been derived in Europe and beyond (as of August 2009) is freely accessible. Providers of hESC lines and researchers who work with these cell lines are invited to register - also free of charge - and provide detailed characteristics on their cell lines or information on their research.
|Human Gene Mutation Database at the Intitute of Medical Genetics in Cardiff" info|
The Human Gene Mutation Database (HGMD) represents an attempt to collate known (published) gene lesions responsible for human inherited disease. This database, whilst originally established for the study of mutational mechanisms in human genes (Cooper and Krawczak 1993), has now acquired a much broader utility in that it embodies an up-to-date and comprehensive reference source to the spectrum of inherited human gene lesions. Thus, HGMD provides information of practical diagnostic importance to (i) researchers and diagnosticians in human molecular genetics, (ii) physicians interested in a particular inherited condition in a given patient or family, and (iii) genetic counsellors.
List of human genome variation databases. This list was compiled by Rania Horaitis at the Genomic Disorders Research Centre, Melbourne.
|HIV - Molecular Immunology Database|
The HIV Molecular Immunology Database is an annotated, searchable collection of HIV-1 cytotoxic and helper T-cell epitopes and antibody binding sites. These data are also printed in the HIV Molecular Immunology compendium which is updated yearly and provided free of charge to scientific researchers. The goal of this database is to provide a comprehensive listing of defined HIV epitopes.
HIV-Guide provided by the John Hopkins University.
|HIV / SIV VACCINE TRIALS DATABASE|
The HIV/SIV Vaccine Trials Database was developed as a tool for compilation, search and comparison of published studies on SIV, HIV and SHIV vaccine trials in nonhuman primates.
Database about the HLA-system.
|Database of hormones and their receptors|
HMRbase is a manually curated database of Hormones and their Receptors. It is a compilation of sequence data after extensive manual literature search and from publicly available databases. HMRbase can be searched on the basis of a variety of data types such as hormone and receptor description and their names, molecular weight, molecular formula, IUPAC name, smiles, physiochemical properties, post-translational modification, developmental stage, subcellular location, length of the protein sequence, organism name etc. This database has been developed by Dr. GPS Raghava's group at Institute of Microbial Technology, Chandigarh, INDIA.
|Human Oral Microbiome Database (HOMD)|
The goal of creating the Human Oral Microbiome Database (HOMD) is to provide the scientific community with comprehensive information on the approximately 600 prokaryote species that are present in the human oral cavity. The majority of these species are uncultivated and unnamed, recognized primarily by their 16S rRNA sequences. The HOMD presents a provisional naming scheme for the currently unnamed species so that strain, clone, and probe data from any laboratory can be directly linked to a stably named reference entity. The HOMD links sequence data with phenotypic, phylogenetic, clinical, and bibliographic information. Full and partial oral bacterial genome sequences determined as part of this project and the Human Microbiome Project, are being added to the HOMD as they become available. HOMD offers easy to used tools for viewing all publically available oral bacterial genomes
|Hazardous Substances Data Bank" info|
HSDB (Hazardous Substances Data Bank) is a scientifically reviewed, factual database containing records for about 4500 toxic chemicals. It contains extensive information in areas as toxicity, environmental fate, human exposure, chemical safety, waste disposal, emergency handling, and regulatory requirements.
|Health Technology Assessment Database|
The HTA database contains information on healthcare technology assessments and is produced in collaboration with the INAHTA Secretariat, based at SBU, Sweden.
|Human Life - Table Database|
Epidemiologic database, which provides life tables.
|International Bibliographic Information on Dietary Supplements (IBIDS) Database|
The International Bibliographic Information on Dietary Supplements (IBIDS) database provides access to bibliographic citations and abstracts from published, international, scientific literature on dietary supplements.
|Internet Brain Volume Database|
The Internet Brain Volume Database is a database of neuroanatomic volume measurements spanning various species, diagnoses, and structures for both individual and group results.
|International Classification of Diseases, Tenth Revision|
You can download the whole text under ...
|International Chemical Safety Cards|
An ICSC summarizes essential health and safety information on chemicals for their use at the "shop floor" level by workers and employers in factories, agriculture, construction and other work places.
|International Clinical Trials Registry Platform" info|
Database, maintained by the WHO, about clinical trials.
|Immediately Dangerous to Life or Health Concentration|
Toxic concentrations of chemicals.
|X-linked SCID Mutation Database|
X-linked severe combined immunodeficiency (XSCID or X-SCID) is an immune disorder caused by mutations in the X-linked gene IL2RG, which encodes the common gamma chain (c) of the lymphocyte receptors for interleukin-2 (IL-2) and many other cytokines. A database of human XSCID mutations (IL2RGbase) has been assembled. Information on new mutations may be submitted online.
|ImMunoGene Tics Database" info|
The international ImMunoGeneTics information system (IMGT; http://imgt.cines.fr), is a high quality integrated information system specialized in immunoglobulins (IG), T cell receptors (TR), major histocompatibility complex (MHC), and related proteins of the immune system (RPI) of human and other vertebrates, created in 1989, by the Laboratoire d'ImmunoGenetique Moleculaire (LIGM; Universite Montpellier II and CNRS) at Montpellier, France
|IMGT/3Dstructure Database" info|
IMGT/3Dstructure-DB and IMGT/Structural-Query are a 3D structure database and a tool for immunological proteins. They are part of IMGT, the international ImMunoGenetics information system, a high-quality integrated knowledge resource specializing in immunoglobulins (IG), T cell receptors (TR), major histocompatibility complex (MHC) and related proteins of the immune system (RPI) of human and other vertebrate species, which consists of databases, Web resources and interactive on-line tools.
Informations about vertebrate immunoglobulin and T cell receptor genes.
|IMGT/HLA - Sequence Database|
The IMGT/HLA Sequence Database is a database for sequences of the human major histocompatibility complex (HLA) and includes the official sequences for the WHO HLA Nomenclature Committee for factors of the HLA System. The IMGT/HLA Sequence Database is part of the international ImMunoGeneTics project (IMGT).
|The Index of Medieval Medical Images (IMMI) and the Graphic IMMI|
The Index of Medieval Medical Images (IMMI) was a project funded by the National Library of Medicine and by The Ahmanson Foundation. The mission of the IMMI project was to describe and index the contents of all medieval manuscript images with medical components presently held in North American collections.
|Repertory of Familial Mediterranean Fever and Hereditary Autoinflammatory Disorders Mutations" info|
Informations about the Familial Mediterranean Fever and hereditary autoinflammatory diseases.
|Database on Allergenic Foods" info|
Database on allergens in foods.
|Inner Ear Protein Database" info|
Database about the Proteom of the inner ear.
|The Discovery and Early Development of Insulin|
This site documents the initial period of the discovery and development of insulin, 1920-1925, by presenting over seven thousand page images reproducing original documents ranging from laboratory notebooks and charts, correspondence, writings, and published papers to photographs, awards, clippings, scrapbooks, printed ephemera and artifacts. Drawing mainly on the Banting, Best and related collections housed at the Thomas Fisher Rare Book Library and the Archives and Records Management Services at the University of Toronto, it also includes significant holdings from the Aventis Pasteur (formerly Connaught) Archives, and the personal collection of Dr. Henry Best.
|Immuno Polymorphism Database|
The Immuno Polymorphism Database (IPD), was developed in 2003 to provide a system for the study of polymorphism in genes of the immune system. The IPD project was established by the HLA Informatics Group of the Anthony Nolan Research Institute in close collaboration with the European Bioinformatics Institute.
IPD consists of the following databases:
|International Standard Randomised Controlled Trial Number Register|
The ISRCTN is a simple numeric system for the identification of randomised controlled clinical trials worldwide. The ISRCTN Register will also accept registration of other forms of studies designed to assess the efficacy of healthcare interventions. The ISRCTN scheme simplifies the identification of trials and provides a unique number that can be used to track all publications and reports resulting from each trial.
|International Toxicity Estimates|
A product of the Cincinnati based Toxicology Excellence for Risk Assessment, ITER presents chemical risk information from authoritative groups worldwide, including the U.S. Environmental Protection Agency, the U.S. Agency for Toxic Substances and Disease Registry, Health Canada, the Dutch National Institute of Public Health and the Environment, the International Agency for Research on Cancer, as well as independent parties whose risk values have undergone peer review.
|Japanese SNP Database" info|
JSNP is a repository of Japanese Single Nucleotide Polymorphism (SNP) data, begun in 2000 and developed through the Prime Minister’s Millennium Project. The aim of this undertaking is to identify and collate up to 150.000 SNPs from the Japanese population, located in genes or in adjacent regions that might influence the coding sequence of the genes. The project has been carried out by a collaboration between the Human Genome Center (HGC) in the Institute of Medical Science (IMS) at the University of Tokyo and the Japan Science and Technology Corporation (JST).
|Drugs and Lactation Database (LactMed)" info|
The Drugs and Lactation Database (LactMed) is a database of drugs to which breastfeeding mothers may be exposed. Among the data included are maternal and infant levels of drugs, possible effects on breastfed infants and on lactation, and alternate drugs to consider.
|The Lafora Progressive Myoclonus Epilepsy Mutation and Polymorphism Database|
Database about mutations and polymorphisms associated with Lafora progressive
|Lafora Progressive Myoclonus Epilepsy Mutation and Polymorphism Database" info|
Database about genes involved in the pathogenesis of Progressive Myoclonus Epilepsy (PME) of the Lafora type.
|Leukemia Gene Atlas|
The Leukemia Gene Atlas (LGA) is a public platform that supports the research and analysis of molecular data of leukemias. In addition to the molecular data the LGA stores the corresponding clinical and laboratory data. The LGA supports comprehensive queries of data, the visualization and analysis as well as download and upload. Currently, there are gene expression, methylation, sequencing data and genotypes of over 6000 samples in the LGA. To analyze data the user may choose between a set of tools: cluster analyses, statistical tests, data distribution plots and the Integrative Genomics Viewer (IGV).
|Literatura Latino Americana e do Caribe em Ciências da Saúde (LILACS)" info|
Database of latin-american and caribbean literature on health sciences.
|Databases & E-Resources at the Library of Congress|
Collection of databases and e-resources at the Library of Congress.
|Lowe Syndrome Mutation Database|
Lowe oculocerebrorenal syndrome is an X-linked disorder caused by mutations in the OCRL1 gene, which encodes a 105-kDa Golgi protein with phosphatidylinositol (4,5) bisphosphate 5-phosphatase activity. A database of mutations causing Lowe syndrome has been established. Information on new mutations may be submitted online.
|NASA's Life Sciences Data Archive|
NASA's Life Sciences Data Archive (LSDA) contains information and data from space flight experiments funded by the National Aeronautics and Space Administration (NASA).
|MalaCards - Human Disease Database" info|
MalaCards is an integrated database of human maladies and their annotations, modeled on the architecture and richness of the popular GeneCards database of human genes.
The MalaCards disease and disorders database is organized into "disease cards", each integrating prioritized information, and listing numerous known aliases for each disease, along with a variety of annotations, as well as inter-disease connections, empowered by the GeneCards relational database, searches, and GeneAnalytics set-analyses. Annotations include: symptoms, drugs, articles, genes, clinical trials, related diseases/disorders and more. An automatic computational information retrieval engine populates the disease cards, using remote data, as well as information gleaned using the GeneCards platform to compile the disease database. The MalaCards disease database integrates both specialized and general disease lists, including rare diseases, genetic diseases, complex disorders and more.
|Comparative Mammalian Brain Collections|
This database, made by the University of Wisconsin, Michigan State University and The National Museum of Health and Medicine contains images and information from one of the world's largest collection of well-preserved, sectioned and stained brains of mammals. Viewers can see and download photographs of brains of over 100 different species of mammals (including humans) representing 17 mammalian orders.
|Manufacturer and User Facility Device Experience Database - (maude)|
MAUDE data represents reports of adverse events involving medical devices. The data consists of all voluntary reports since June, 1993, user facility reports since 1991, distributor reports since 1993, and manufacturer reports since August, 1996.
|Multiple Congenital Anomaly / Mental Retardation" info|
This database has been developed to facilitate the identification and differentiation of syndromic entities. Special attention is given to the type of information which, because of space the limitations of the printed form, is usually limited or completely omitted in the existing reference sources.
|Caribbean Health Sciences Literature|
Medical literature-database from the Caribbean.
MedHist offers free access to a searchable catalogue of Internet sites and resources covering the history of medicine.
|Merriam-Webster's Medical Dictionary|
Merriam-Webster's Medical Dictionary - 60,000 terms, definitions and spelling
PubMed, a service of the National Library of Medicine, includes over 14 million citations for biomedical articles back to the 1950's.
|Gulf War Medical Research Library|
The Departments of Defense, Health and Human Services, and Veterans Affairs have worked together to create this library of government-sponsored Gulf War-related research.
|The Merck Manual of Geriatrics|
Basics about geriatrics.
MeSH is the National Library of Medicine's controlled vocabulary thesaurus. It consists of sets of terms naming descriptors in a hierarchical structure that permits searching at various levels of specificity.
|The MHC Haplotype Project" info|
The MHC Haplotype Project is a framework and resource for association studies of all MHC-linked diseases. It will provide the complete genomic sequences of at least 8 different HLA-homozygous typing haplotypes, their resulting variations (SNPs and indels) and ancestral relationships.
|The Microbial Rosetta Stone Database" info|
The Microbial Rosetta Stone Database provides access to up-to-date taxonomic classifications of organisms that cause human diseases, improves the consistency of nomenclature in disease reporting, and provides useful links between different public genomic and public health databases.
|Microsoft Academic" info|
Microsoft Academic (academic.microsoft.com) is an online destination that helps researchers to connect with the most personally relevant papers, research news, conferences, people, and ideas, powered by artificial intelligence (AI) bots that read, understand, and deliver the scientific information to further your work. It helps you stay abreast of developments, discover new ideas, and collaborate with others in the academic community, propelling your research—and your reputation—further, faster.
|Mitelman Database of Chromosome Aberrations in Cancer" info|
The information in the Mitelman Database of Chromosome Aberrations in Cancer relates chromosomal aberrations to tumor characteristics, based either on individual cases or associations. All the data have been manually culled from the literature by Felix Mitelman, Bertil Johansson, and Fredrik Mertens.
|Medicinal Materials DNA Barcode Database - MMDBD|
Medicinal materials from natural sources have been used for centuries in China and other countries. They have been recognized as particularly suitable for treating modern diseases such as cardiovascular diseases, asthma and other long-term illnesses. Substitutes and adulterants are often introduced intentionally or accidentally, thus seriously interfering with their therapeutic effects, even leading to life-threatening poisoning.
Medicinal materials are traditionally identified by their organoleptic characteristics and other physical properties. However, the differences among related species are sometimes too minute. Chemical analyses may be affected by the physiological and the storage conditions. With the advancement of molecular biology, DNA barcoding has now become a popular means for identification and authentication of plant and animal species. We have established this DNA barcode database for users to retrieve and analyze DNA sequences of medicinal materials. This website includes DNA sequences and information and key references of the medicinal materials recorded in the Pharmacopoeia of the People’s Republic of China, American Herbal Pharmacopoeia and other related references. Relevant information of common adulterants and substitutes are also listed. This database provides a web-based platform for storage, retrieval, comparison and analysis of DNA sequences, for distinguishing medicinal materials from their common substitutes and adulterants.
ModelDB provides an accessible location for storing and efficiently retrieving compartmental neuron models. ModelDB is tightly coupled with NeuronDB. Models can be coded in any language for any environment, though ModelDB has been initially constructed for use with NEURON and GENESIS. Model code can be viewed before downloading and browsers can be set to auto-launch the models.
|MHC-Peptide Interaction Database (MPID)" info|
MHC-Peptide Interaction Database (MPID) provides structural information and characterization of MHC peptide interaction on major histocompatibility complex of both class I and class II.
|Material Safety Data Sheets (MSDS)|
Material Safety Data Sheets (MSDS), regulated under Workplace Hazardous Materials Information System (WHMIS) legislation, for chemical products have been available to workers for many years. However because many laboratory workers, whether in research, public health, teaching, etc., are exposed to not only chemicals but infectious substances as well, there was a large gap in the readily available safety literature for employees. These MSDS are produced for personnel working in the life sciences as quick safety reference material relating to infectious micro-organisms.
|Mouse Tumor Biology Database|
The Mouse Tumor Biology (MTB) Database supports the use of the mouse as a model system of hereditary cancer by providing electronic access to:
|My Cancer Genome. Genetically Informed Cancer Medicine." info|
My Cancer Genome is a precision cancer medicine knowledge resource for physicians, patients, caregivers and researchers.
My Cancer Genome gives up-to-date information on what mutations make cancers grow and related therapeutic implications, including available clinical trials.
My Cancer Genome is a one-stop tool that matches tumor mutations to therapies, making information accessible and convenient for busy clinicians.
|National Center for Complementary and Alternative Medicine" info|
Informations about complementary remedies.
|NCCAM Clinical Trials|
Database on clinical trials, compiled by the National Center for Complementary and Alternative Medicine (NCCAM).
|NCI-Supported Clinical Trials|
NCI-supported clinical trials are those sponsored or otherwise financially supported by NCI.
|Neuronal Ceroid Lipofuscinoses Mutation Database|
The database contains published mutations and polymorphisms in the NCL genes together with unpublished data included with permission.
|The NeSys Database on Brain Map Transformations in Cerebellar Systems|
The database provides structure and structure-function data about brain map transformations in cerebellar systems.
Database about microelectrode recordings from cortex and other neurophysiological preparations.
Neuromice.org is a consortium of three projects established by NIH to enhance genomic and genetic tools for neuroscience research, by creating new mutant mouse models for neurological/behavioral disorders.
|Neuromuscular Disease Center|
Extensive informations about neurouscular diseases, made by the Neuromuscular Disease Center, Washington University, St. Louis, MO, USA.
NeuronDB provides a dynamically searchable database of three types of neuronal properties: voltage gated conductances, neurotransmitter receptors, and neurotransmitter substances. It contains tools that provide for integration of these properties in a given type of neuron and compartment, and for comparison of properties across different types of neurons and compartments.
|National Health and Medical Research Council (Australia)|
Collection of Guidelines from Australia. Many of them are outdated, but some of the newer ones are excellent.
|National Institute for Health and Clinical Excellence|
Collection of Guidelines from Great Britain.
|National Information Center on Health Services Research and Health Care Technology|
This page provides specialized PubMed searches on healthcare quality and costs.
|Neuroscience Information Framework" info|
The Neuroscience Information Framework (NIF) is an initiative of the NIH Blueprint for Neuroscience Research, which was established in 2004 by the National Institutes of Health. NIF is a repository of global neuroscience web resources, including experimental, clinical, and translational neuroscience databases, knowledge bases, atlases, and genetic/genomic resources and provides many authoritative links throughout the neuroscience portal of Wikipedia.
|NIPH Clinical Trials Search - Japan|
This website can be used to cross-search the content of three national clinical research information registries:
The University Hospital Medical Information Network Center (UMIN-CTR),
The Japan Medical Association Center (JMACCT),
The Japan Pharmaceutical Information Center (JAPIC).
|National Library of Guidelines|
Excellent structured directory of guidelines.
The National Library of Guidelines is a collection of guidelines for the NHS. It is based on the guidelines produced by NICE and other national agencies. The main focus of the Library is on guidelines produced in the UK, but where no UK guideline is available, guidelines from other countries are included in the collection.
NICE issues guidelines of very high quality. They are based on a systematic review of the evidence and have extensive consultation not only with clinicians but also with patients and, where relevant, industry.
|The Nobel Prize in Physiology or Medicine|
All laureates of the nobel prize in physiology or medicine.
|National Organization for Rare Disorders|
This site provides a database about rare diseases.
|Novartis Clinical Trials|
Clinical Trials by Novartis.
|Nuclide Safety Data Sheets|
Nuclide Safety Data Sheets provided by the North Carolina State University.
Collection of nutrition databases, scheduled by the Food Safety Risk Analysis Clearinghouse.
|Odor Molecules Database|
OdorDB is a database of odor molecules.
|Olfactory Bulb Odor Map Database" info|
OdorMapDB is designed to be a database to support the experimental analysis of the molecular and functional organization of the olfactory bulb and its basis for the perception of smell.
|Ovarian Kaleidoscope Database" info|
The Ovarian Kaleidoscope database (OKdb) is a collaborative online resource for scientists investigating the ovary. It provides information regarding the biological function, expression pattern, and regulation of genes expressed in the ovary, as well as for the phenotypes associated with their mutation.
|Online Mendelian Inheritance in Man" info|
Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders, with links to literature references, sequence records, maps, and related databases. It is based on the book, Mendelian Inheritance in Man. The online version is updated daily.
|Vienna Ophthalmic Case Studies|
Excellent ophthalmic case studies.
|Vienna Ophthalmic Case Studies|
Excellent ophthalmic case studies.
|Oral Pathogen Sequence Databases|
The scope of the project includes molecular information pertaining to oral pathogens, bacterial and viral.
|Olfactory Receptor Database|
Olfactory receptors (ORs) are the largest family in the genome, and the first of a widening range of chemosensory receptors (CRs) in other chemosensory organs. ORDB began as a database of vertebrate OR genes and proteins and continues to support sequencing and analysis of these receptors by providing a comprehensive archive with search tools for this expanding family. Because of the associated growth of interest in other CRs, the database has grown over the years to include a broad range of chemosensory genes and proteins, that includes in addition to ORs the taste papilla receptors (TPRs), vomeronasal organ receptors (VNRs), insect olfaction receptors (IORs), Caenorhabditis elegans chemosensory receptors (CeCRs), fungal pheromone receptors (FPRs) [these are informal abbreviations for tracking in ORDB, pending development of consensus nomenclature by the field].
Compilation of information on orphan diseases.
|Occupational Safety and Health|
The Occupational Safety and Health Review Commission (OSHRC) is an
independent Federal agency created to decide contests of citations or
penalties resulting from OSHA inspections of American work places.
|OTseeker - Occupational Therapy|
OTseeker is a database that contains abstracts of systematic reviews and randomised controlled trials relevant to occupational therapy.
Panteleimon is a database of medical-biological, chemical-pharmaceutical and chemical publications printed in scientific and scientific-practical journals in Ukraine and Russian Federation since 1998.
Free, regularly updated surgical pathology outlines with links to journal articles, gross and microscopic images, as well as extensive listings of pathology related jobs, fellowships and conferences.
PediatricEducation.org is a Pediatric Digital Library and Learning Collaboratory intended to serve as a source of continuing pediatric education
|Physiotherapy Evidence Database" info|
PEDro is the Physiotherapy Evidence Database. It gives access to bibliographic details and abstracts of randomised controlled trials, systematic reviews and evidence-based clinical practice guidelines in physiotherapy.
|Prostate Epigenetic Database|
Prostate cancer (PC) develops in the prostate (a male sex gland) and is a common malignancy and a leading cause of cancer death among men. In addition to genetic alteration, epigenetic aberration plays key roles in progression of PC. Studies in epigenetic changes in PC have accumulated vast amount of useful data that could shed light on the development of PC and include potential epigenetic markers as diagnosis and prognosis for PC. Therefore, we constructed PEpiD to store the curated epigenetic data retrieved by literature mining, which previous studies indicated as involved in PC of human, mouse, and rat. A user-friendly interface is implemented for easy and flexible query. PEpiD can serve as an important resource for epigenetic research in PC.
|Pesticide Fact Sheets|
Pesticide Fact Sheets - NPIC fact sheets are designed to answer questions that are commonly asked by the general public about pesticides and pesticide related topics. These documents are intended to be educational in nature and helpful to consumers making decisions about pesticide use.
|Human Prostate Gene DataBase" info|
PGDB is a database of human genes related to the prostate and prostatic diseases.
|Phylogeny of sleep|
This database contains what are known as sleep quotas for 178 separate references, on 127 different species (as of June 29, 2007), in 46 families, across 17 orders, with additional sleep data on other species being added to the database as they become available. Sleep quotas are essentially time spent in each of the two major sleep states (REM and NREM) per day. There are several lines of evidence that point to the fundamental importance of sleep quotas for an analysis of sleep state function.
|Pub Med Central" info|
PubMed Central (PMC) is the U.S. National Library of Medicines digital archive of life sciences journal literature. Access to the full text of articles in PMC is free, except where a journal requires a subscription for access to recent articles.
|Drug-Induced Respiratory Disease Website" info|
Pneumotox is an aid to the diagnosis of DIRD
POPLINE® (POPulation information onLINE), the world's largest database on reproductive health, provides more than 300,000 citations with abstracts to scientific articles, reports, books, and unpublished reports in the field of population, family planning, and related health issues.
PsiTri is a database on published and unpublished controlled clinical trials, reporting on treatments and interventions for a wide range of conditions within the field of mental health.
|PTCH1 Mutation Database|
Database about mutations and polymorphisms in the PTCH1 gene.
|Visual Culture and Public Health Posters|
Database made by the NLM, History of Medicine Division.
|QT Drug List|
Database of drugs that prolong the Qt interval
|Rare Metabolic Diseases Database" info|
The RAMEDIS system is a platform independent, web-based information system for rare metabolic diseases based on filed case reports. It was developed in close cooperation with clinical partners to allow them to collect information on rare metabolic diseases with extensive details, e.g. about occurring symptoms, laboratory findings, therapy and molecular data.
|RARE BLEEDING DISORDERS|
Compilation of rare bleeding and coagulation disorders.
|RARE DISEASE (ORPHAN) DESIGNATIONS|
Database - provided by EMA (European Medicines Agency) about drugs for orphan diseases.
|Rare diseases in Ashkenazi Jews|
Compilation of Genetic disorders in Ashkenazi Jews. (WIKIPEDIA)
Collection of approximately 7000 rare diseases that affect more than 300 million people worldwide.
|Retinoblastoma Gene Mutation Database|
Database about mutations in the RB1-gene.
|Rare Diseases Human Biospecimens / Biorepositories|
Rare Disease-HUB (RD-HuB) of the Office of Rare Diseases Research (ORDR). This Website contains a searchable database of biospecimens collected, stored, and distributed by biorepositories in the United States and around the globe.
The REHABDATA database spans almost 50 years of disability and rehabilitation research. More than 65,000 abstracts are available through this database. The database is provided by the National Rehabilitation Information Center for Independence.
Rehabilitation information system.
|Mouse Retroviral Tagged Cancer Gene Database" info|
Retroviral insertional mutagenesis in mouse hematopoietic tumors provides a potent cancer gene discovery tool in the post-genome-sequence era. To manage multiple high-throughput insertional mutagenesis screening projects, the Retroviral Tagged Cancer Gene Database was developed.
|Science of Aging Database" info|
This database includes genes and interventions that have been studied with respect to their effects on life-span or age-related neurological diseases.
|Sarcomere Protein Gene Mutation Database|
Mutations in sarcomere protein genes are known to cause hypertrophic cardiomyopathy, dilated cardiomyopathy, and other diseases.
|SARS (Severe Acute Respiratory Syndrome ) Reference|
SARS Reference is a medical textbook that provides a comprehensive and up-to-date overview of severe acute respiratory syndrome (SARS).
|Database for Repeat Prioritization" info|
Satellog provides the ability to dynamically prioritize repeats based on any of their characteristics (i.e. repeat unit, class, period, length, repeat length percentile rank, genomic co-ordinates), polymorphism profile within UniGene, proximity to or presence within gene regions (i.e. cds, UTR, 15 kb upstream etc.), metadata of the genes they are detected within and gene expression profiles within normal human tissues. Unstable repeats associated with 31 diseases were analyzed in Satellog to evaluate their common repeat properties. The utility of Satellog was highlighted by prioritizing repeats for Huntington's disease and schizophrenia.
|ISBT Human Blood Group Systems|
Informations about the human blood group system.
|Structural Database of Allergenic Proteins" info|
SDAP is a Web server that integrates a database of allergenic proteins with various bioinformatics tools for performing structural studies related to allergens and characterization of their epitopes.
|Surveillance, Epidemiology and End Results" info|
Epidemiologic database by the NCI, USA.
|Scottish Intercollegiate Guidelines Network|
Collection of Scottish Guidelines, many of them are outdated.
|Stanley Medical Research Institute Online Genomics Database" info|
The Stanley Medical Research Institute online genomics database (SMRIDB) is a web-based system for understanding the genetic effects of human brain disease (i.e. bipolar, schizophrenia, and depression). This database contains fully annotated clinical metadata and gene expression patterns.
|Short Tandem Repeat DNA|
While the use of STRs for genetic mapping and identity testing has become widespread among DNA typing laboratories, there is no single place where information may be found regarding STR systems. This web site is an attempt to bring together the abundant literature on the subject in a cohesive fashion to make future work in this field easier. Facts and sequence information on each STR system, population data, commonly used multiplex STR systems, PCR primers and conditions, and a review of various technologies for analysis of STR alleles have been included in this database. Addresses for scientists and organizations working in this area have also been included as well as a comprehensive reference listing of material on STRs used for DNA typing purposes.
|Stromal Cell Database|
The Stromal Cell Database is a joint project of the laboratories of Kateri Moore and Ihor Lemischka in the Department of Molecular Biology at Princeton University, and Christian J. Stoeckert, Jr. at the Center for Bioinformatics at the University of Pennsylvania.
|Rare Disease Database of the Swedish National Board of Health and Welfare|
Database about rare diseases, provided by The Swedish Information Centre for Rare Diseases
|Swiss Life Sciences Database|
The Swiss Life Sciences Database provides access to a very comprehensive directory and information platform comprising data of Life Sciences and Biotechnology companies and institutes in Switzerland including company description, additional information and categorization.
This Database contains information on:
|The Language of the Nucleus|
|The Merck Manual of Diagnosis and Therapy" info|
Comprehensive high quality medical encyclopedia.
Extensive array of references to literature on biochemical, pharmacological, physiological, and toxicological effects of drugs and other chemicals.
TOXNET is a cluster of databases on toxicology, hazardous chemicals, and related areas. Provided by the NLM, National Library of Medicine:
|Toxics Release Inventory" info|
TRI contains data on the estimated annual releases of toxic chemicals to the environment – air, water, soil, underground injection; amounts transferred off-site for waste treatment; and source reduction and recycling data.
|Turning Research Into Practice|
This database contains evidence based medical material from more than 60 EBM sites.
Extensive assemblage of guidelines, collected by the National Guideline Clearinghouse.
|Atlas of Ultrastructural Neurocytology|
The Atlas of Ultrastructural Neurocytology was created by Josef Spacek, MUDr., DrSc.
|The Urbana Atlas of Pathology|
The Urbana Atlas of Pathology, produced by the University of Illinois College of Medicine at Urbana-Champaign. Legends by Patricia J. O'Morchoe, M.D. Images from material collected by Donald R. Thursh, M.D. and Dr. P. J. O'Morchoe.
|U.S. Database of Completed Regulatory Agency Reviews|
The database contains information on genetically engineered crop plants intended for food or feed that have completed all recommended or required reviews for planting, food, or feed use in the United States.
VBASE2 is a database of germ-line V genes from the immunoglobulin loci of human and mouse. It presents V gene sequences extracted from the EMBL nucleotide sequence database and Ensembl together with links to the respective source sequences.
|Virtual Naval Hospital|
Virtual Naval Hospital is a digital library of naval medicine and military medicine and humanitarian medicine.
|The Internet Pathology Laboratory|
This popular web resource includes over 1900 images along with text, tutorials, laboratory exercises, and examination items for self-assessment that demonstrate gross and microscopic pathologic findings associated with human disease conditions.
|Who Named It ?|
Whonamedit.com is a biographical dictionary of medical eponyms. It presents a complete survey of all medical phenomena named for a person, with a biography of that person. Eventually, this will include more than 15.000 eponyms and more than 6.000 persons.
|World Health Organization Library Database|
WHOLIS is the World Health Organization library database available on the web. WHOLIS indexes all WHO publications from 1948 onwards and articles from WHO-produced journals and technical documents from 1985 to the present. An on-site card catalogue provides access to the pre-1986 technical documents.
|WIKIPEDIA CATEGORY: Rare diseases|
Overview in Wikipedia about rare diseases.
|The Y-Chromosome Haplotype Reference Database" info|
The ability to identify male-specific DNA renders polymorphic Y-chromosomal sequences an invaluable addition to the standard panel of autosomal loci used in forensic genetics (Roewer 2009). Y-STR haplotyping is particularly important for sensitive typing of male DNA in mixed stains as well as for rapid assortment of biological crime scene evidence. Moreover, Y chromosomal profiling can trace back paternal lineages into the past and has thus been proven a useful tool in genealogical and kinship testing. The individuality of the male-specific part of the Y chromosome can be optimally explored by the Y-STR haplotype analysis using a set of highly variable short tandem repeat markers approved by the forensic and scientific community.