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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.
| Resource Name | Proper Citation | Abbreviations | Resource Type |
Description |
Keywords | Resource Relationships | ||||||||||||||
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University of Lorraine; Lorraine; France Resource Report Resource Website 1+ mentions |
University of Lorraine; Lorraine; France (RRID:SCR_005705) | UL | university | French public university. | is parent organization of: Suggested Ontology for Pharmacogenomics | Wikidata:Q4173330, Crossref funder ID:100008990, nlx_158101, ISNI:0000 0001 2194 6418, grid.29172.3f | https://ror.org/04vfs2w97 | SCR_005705 | SciCrunch Registry | Universit� de Lorraine, University of Lorraine, Universite de Lorraine | 2026-10-24 12:45:31 | 1 | ||||||||
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go-moose Resource Report Resource Website |
go-moose (RRID:SCR_005666) | go-moose | data analysis software, data processing software, software application, software resource | go-moose is intended as a replacement for the aging go-perl and go-db-perl Perl libraries. It is written using the object oriented Moose libraries. It can be used for performing a number of analyses on GO data, including the remapping of GO annotations to a selected subset of GO terms. Platform: Windows compatible, Mac OS X compatible, Linux compatible, Unix compatible | software library, slimmer-type tool, analysis, gene ontology, other analysis |
is listed by: Gene Ontology Tools is related to: Gene Ontology is related to: go-perl is related to: go-db-perl has parent organization: SourceForge has parent organization: Berkeley Bioinformatics Open-Source Projects has parent organization: Lawrence Berkeley National Laboratory |
Free for academic use | nlx_149189 | SCR_005666 | SciCrunch Registry | 2026-10-24 12:45:30 | 0 | ||||||||
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MolGen Resource Report Resource Website 10+ mentions |
MolGen (RRID:SCR_005700) | MolGen | data or information resource, portal, topical portal | The research of the group concentrates on the molecular biology of Gram-positive bacteria, with Bacillus subtilis and Lactococcus lactis as the main model organisms. A number of important (human) pathogens are also investigated: Bacillus cereus, Streptococcus pneumoniae and Enterococcus faecalis. The nature of the research is both fundamental and application-oriented. Transcript- and protein profiling by high-throughput technologies such as DNA microarrays and proteomics tools are being used. The very large data sets generated are analyzed by employing existing and novel bioinformatics tools. Major lines of research are in the field of functional genomics of these organisms, using systems- and synthetic biology approaches. | molecular biology, gram-positive bacteria, pathogen, transcript, protein, profile, high-throughput, dna microarray, proteomics, dna, microarray, functional genomics, bioinformatics, genetics, gene |
has parent organization: University of Groningen; Groningen; Netherlands is parent organization of: FIVA - Functional Information Viewer and Analyzer |
nlx_149166 | http://molgen.biol.rug.nl/molgen/index.php | SCR_005700 | SciCrunch Registry | Molecular Genetics | 2026-10-24 12:45:31 | 28 | |||||||
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KI Biobank Resource Report Resource Website |
KI Biobank (RRID:SCR_005664) | KI Biobank - Gallstone | biomaterial supply resource, material resource | THIS RESOURCE IS NO LONGER IN SERVICE, documented August 29, 2016. KI Biobank - Gallstone aims at investigating genetics of gallstone disease on Swedish Twins. Types of samples * EDTA whole blood * DNA * Plasma Number of sample donors: 82 | gene, genetics |
is listed by: One Mind Biospecimen Bank Listing is related to: Swedish Twin Registry has parent organization: Karolisnka Biobank |
Gallstone disease, Twin | THIS RESOURCE IS NO LONGER IN SERVICE | nlx_151297, nlx_151300, SCR_005796 | https://www.researchgate.net/publication/246710484_Gallstone_disease_in_Swedish_twins_is_linked_to_ABCG8_D19H_risk_genotype | SCR_005664 | SciCrunch Registry | KI Biobank - Gallstone, KI Biobank - KTS | 2026-10-24 12:45:30 | 0 | |||||
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NIDA Podcasts Resource Report Resource Website |
NIDA Podcasts (RRID:SCR_005660) | NIDA Podcasts | data or information resource, narrative resource, podcast | Audio clips that highlight research efforts at the National Institute on Drug Abuse and include interviews with prominent NIDA scientists. To listen to these clips, just click Listen Now under the clip summary. You must have Real Media Player or Windows Media Player installed to download these clips. To view a printable transcript of a clip, click View Transcript under the clip summary. | drug abuse, transcript | has parent organization: National Institute on Drug Abuse | NIDA | All of these clips are free from copyright and can be used for broadcast or other use with acknowledgement of the National Institute on Drug Abuse. | nlx_149377 | SCR_005660 | SciCrunch Registry | 2026-10-24 12:45:30 | 0 | |||||||
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Stanford Center for Biomedical Informatics Research Resource Report Resource Website |
Stanford Center for Biomedical Informatics Research (RRID:SCR_005698) | BMIR | data or information resource, laboratory portal, organization portal, portal | Mark Musen''s laboratory studies components for building knowledge-based systems, controlled terminologies and ontologies, and technology for the Semantic Web. For more than two decades, Musen''s group has worked to elucidate reusable building blocks of intelligent systems, and to develop scalable computational architectures for systems with significant applications in biomedicine. Informatics is the study of information: its structure, its communication, and its use. As society becomes increasingly information intensive, the need to understand, create, and apply new methods for modeling, managing, and acquiring information has never been greater especially in biomedicine. BMIR is home to world class scientists and trainees developing cutting-edge ways to acquire, represent, process, and manage knowledge and data related to health, health care, and the biomedical sciences. Our faculty, students, and staff are committed to ensuring the biomedical community is properly equipped for the information age, and believe our efforts will provide the structure for the burgeoning revolution of health care and the biomedical sciences. | biomedicine, informatics |
has parent organization: Stanford University; Stanford; California is parent organization of: CLENCH is parent organization of: BioPortal is parent organization of: Center for Expanded Data Annotation and Retrieval is parent organization of: Protege is parent organization of: WebProtege |
nlx_149147 | SCR_005698 | SciCrunch Registry | Stanford Medical Informatics | 2026-10-24 12:45:31 | 0 | ||||||||
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Science of Mental Illness: Grades 6- 8 Resource Report Resource Website |
Science of Mental Illness: Grades 6- 8 (RRID:SCR_005612) | data or information resource, narrative resource, training material, video resource | A set of lessons for students used to gain insight into the biological basis of mental illnesses and how scientific evidence and research can help us understand its causes and lead to treatments and, ultimately, cures. Both the Web version and the free supplement are available. It is a creative, inquiry-based instruction program designed to promote active learning and stimulate student interest in medical topics. This curriculum supplement aims to help students experience the process of scientific inquiry and develop an enhanced understanding of the nature and methods of science. | mental disease, treatment, human, curriculum, student, adolescent, teacher, teacher's guide, lesson plan, k-12, training resource | has parent organization: NIMH Educational Resources | National Institute of Mental Health | nlx_146230 | http://science.education.nih.gov/customers.nsf/MSMental | SCR_005612 | SciCrunch Registry | Science of Mental Illness | 2026-10-24 12:45:29 | 0 | |||||||
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Virtual Biology Lab Resource Report Resource Website |
Virtual Biology Lab (RRID:SCR_005694) | Virtual Biology | data or information resource, laboratory portal, organization portal, portal, software resource | Virtual Biology Lab portal from the University of Nice Sophia Antipolis; Nice; France. Offered are a variety of software including: * GenBank2Treedyn: Extract annotations from GenBank files for: ** More convenient alignments and phylogeny (replace def line of fasta file by GI number) ** Extremely powerful annotations of phylogenetic trees with TreeDyn. * THEA: Analyses of DNA chip data with ontologies * Blast2Tree: Blast server for the identification of procaryotes * Dashboard: e-Tool for data exchanges among partners, DNA chips design and developement * Oligo Heat Map: Check thermodynamical parameters for PCR primers and compute graphical representation to show specificity of target sequences * EmblEx: A cgi tool to parse and extract data from EMBL entries to various formats * Miscellaneous software ** Jane plugin: Add a small panel to Jane server to retrieve PMID of publications ** EtBlast plugin: Add a small panel to EtBlast server to retrieve PMID of publications ** Oligo Builder: Get the oligomers from a set of target sequences by avoiding non-target sequences | biodiversity, ontology, bioinformatics, thea, ontology |
has parent organization: University of Nice Sophia Antipolis; Nice; France is parent organization of: THEA - Tools for High-throughput Experiments Analysis |
nlx_149144 | SCR_005694 | SciCrunch Registry | Virtual Biology Laboratory | 2026-10-24 12:45:31 | 0 | ||||||||
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BIIT - Bioinformatics Algorithmics and Data Mining Group Resource Report Resource Website 10+ mentions |
BIIT - Bioinformatics Algorithmics and Data Mining Group (RRID:SCR_005690) | BIIT Research group | data or information resource, department portal, organization portal, portal, software application, software resource, text-mining software | The Bioinformatics, Algorithmics, and Data Mining group BIIT lead by prof. Jaak Vilo is a joint research group between the Department of Computer Science (University of Tartu), Quretec, and the Estonian Biocenter. Our main research topics and capabilities include the gene regulation, gene expression data analysis, biological data mining, systems biology, combinatorial pattern matching, developing software for biomedical research databases, as well as partnering in stem cell and cancer related projects. Software * MEM - Multi-Experiment-Matrix -- large-scale gene expression data queries and mining (Genome Biology 2009) * g:Profiler family of tools for functional assessment of gene groups, gene ID mappings, orthology and expression similarity searches. (NAR web server issue 2007) * KEGGanim - visualisation of high-throughput data on biological pathway charts (Bioinformatics, 2007) * GraphWeb - a tool for mining large biological networks (NAR Web server issue 2008) * FunGenES data atlas * More software tools | gene regulation, gene expression, data analysis, biological, data mining, systems biology, combinatorial pattern matching, software, biomedical research, stem cell, cancer |
has parent organization: University of Tartu; Tartu; Estonia is parent organization of: GraphWeb is parent organization of: g:Profiler |
nlx_149141 | http://biit.cs.ut.ee/about/main | SCR_005690 | SciCrunch Registry | BIIT - Bioinformatics Algorithmics Data Mining Group, BIIT Group - Institute of Computer Science | 2026-10-24 12:45:31 | 10 | |||||||
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Principe Felipe Research Centre; Valencia; Spain Resource Report Resource Website 1+ mentions |
Principe Felipe Research Centre; Valencia; Spain (RRID:SCR_005691) | CIPF | institution | The Pr��ncipe Felipe Research Centre (CIPF), which was inaugurated by their Royal Highnesses the Prince and Princess of Asturias on 17th March 2005, is a centre dedicated to biomedical research, with the aim of taking on new challenges in the field of basic research and encouraging scientific works of excellence. The construction of the Centre was carried out thanks to the Regional Development Funds from the European Union, and from the Regional Government (Generalitat Valenciana) through its Ministry of Health. The current financing of the CIPF comes mainly from the investment made by the Generalitat Valenciana through the Ministry of Health, as well as the Regenerative Medicine Programme, the fruit of an agreement between the Institute of Health Carlos III and the Ministry of Health for basic and translation research in this field. The CIPF takes the research tradition from the then Valencian Cytological Research Institute and the Valencian Biomedical Research Foundation, with the aim of consolidating and expanding this research. Therefore the activity in the CIPF can be divided into three main strategic work areas: The Regenerative Medicine area focuses its research on cellular therapy and interdisciplinary research in human embryonic and adult stem cells, with the aim of regenerating damaged organs to improve human health. The Chemical and Quantative Biology area aims to understand, through the application of (bio) chemical, genetic, and bioinformatic methods, to understand the molecular mechanisms that control the biological processes and alterations that lead to pathological conditions. The Biomedicine area focuses on understanding the molecular bases of human pathologies that require new diagnostic and clinical procedures for their identification and treatment, pathologies such as cancer, neurological pathologies and rare illnesses. |
is parent organization of: QualiMap is parent organization of: VARIANT is parent organization of: CIPF Bioinformatics and Genomics Department is parent organization of: Blast2GO is parent organization of: Gene Expression Profile Analysis Suite |
nlx_149142, grid.418274.c, ISNI: 0000 0004 0399 600X | https://ror.org/05xr2yq54 | SCR_005691 | SciCrunch Registry | Centro de Investigaci��n Pr��ncipe Felipe, Centro de Investigacion Principe Felipe, Principe Felipe Research Center, Pr��ncipe Felipe Research Centre | 2026-10-24 12:45:30 | 2 | ||||||||
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CIPF Bioinformatics and Genomics Department Resource Report Resource Website 1+ mentions |
CIPF Bioinformatics and Genomics Department (RRID:SCR_005692) | CIPF Bioinformatics and Genomics | data or information resource, department portal, institution, organization portal, portal | Biomedicine can only be understood in the context of genomics and with the concourse of bioinformatics. Our department aims to tackle biomedical problems from a system's biology perspective. Following this, the general objective we seek through the main lines of research is to relate the mutations (Pharmacogenomics and Comparative Genomics) to their effect at cellular and phenotypic level (Functional Genomics) trying to understand the mechanism of action (Structural Genomics). Systems Biology Genes operate within an intricate network of interactions that we have only recently started to envisage. Many higher-order levels of interaction are continuously being discovered. In this scenario we are interested in developing methods and tools which can help to understand large-scale experiments from a systems biology perspective. Comparative genomics We are interested in the analysis of patterns and processes occurred during the evolution of our genome, and in the application of the evolutionary thought in human health and disease. * Adaptive Human Evolution * Evolutionary Pharmacogenetics * SNP's and Human Disease Structural genomics Our Unit aims to develop and apply computational methods for understanding the molecular mechanisms of cell regulation beyond proteins. In particular, we apply our methods to study the interaction of small chemical compounds with proteins and to characterize their molecular actions. We are also developing methods for RNA 3D structure prediction with the aim of applying them to understand the effects of non-coding RNA molecules. Finally, in collaboration with experimentalists, we are working in determining the first ever 3D structure of a genomic domain in human. | genomics, bioinformatics |
has parent organization: Principe Felipe Research Centre; Valencia; Spain is parent organization of: Babelomics |
nlx_149143 | SCR_005692 | SciCrunch Registry | CIPF Department of Bioinformatics, CIPF Bioinformatics Genomics | 2026-10-24 12:45:31 | 5 | ||||||||
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VAGUE Resource Report Resource Website 1+ mentions |
VAGUE (RRID:SCR_005607) | VAGUE | software resource | An open-source de novo genome assembly software tool, which is run from the Unix command line, providing a multi-platform graphical front-end for the Velvet de novo assembler. VAGUE is implemented in JRuby and targets the Java Virtual Machine. | command line, assembler |
is listed by: OMICtools has parent organization: Monash University; Melbourne; Australia |
PMID:23162059 | GNU General Public License, v2, Acknowledgement requested | OMICS_00897 | SCR_005607 | SciCrunch Registry | Velvet Assembler Graphical Front End | 2026-10-24 12:45:29 | 5 | ||||||
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DBD - Slim Gene Ontology Resource Report Resource Website |
DBD - Slim Gene Ontology (RRID:SCR_005728) | Slim Gene Ontology | data or information resource, database, software application, software resource | Db for Dummies! is a small database that imports the Generic GO Slim. It allows data to be viewed in a tree. The Gene Ontology describes gene products in terms of their associated biological processes, cellular components and molecular functions. The Generic Slim Gene Ontology is a subset of the whole Gene Ontology. The slim version gives a broad overview and leaves out specific/fine grained terms. This example stores the slim version of the Gene Ontology (goslim_generic_obo) that can be downloaded from www.geneontology.org/GO.slims.shtml. Platform: Windows compatible | gene ontology, gene, hierarchy, visualization, database or data warehouse |
is listed by: Gene Ontology Tools is related to: Gene Ontology has parent organization: Db for Dummies! |
Free for academic use | nlx_149185 | SCR_005728 | SciCrunch Registry | Db for Dummies! - Slim Gene Ontology, Db for Dummies - Slim Gene Ontology | 2026-10-24 12:45:31 | 0 | |||||||
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NIH Office of Science Education Resource Report Resource Website |
NIH Office of Science Education (RRID:SCR_005603) | OSE | data or information resource, knowledge environment, narrative resource, organization portal, portal, training material | The NIH Office of Science Education (OSE) coordinates science education activities at the NIH and develops and sponsors science education projects in house. These programs serve elementary, secondary, and college students and teachers and the public. Activities * Develop curriculum supplements and other educational materials related to medicine and research through collaborations with scientific experts at NIH * Maintain a website as a central source of information about NIH science education resources * Establish national model programs in public science education, such as the NIH Mini-Med School and Science in the Cinema * Promote science education reform as outlined in the National Science Education Standards and related guidelines The OSE was established in 1991 within the Office of Science Policy of the Office of the Director of the National Institutes of Health. The NIH is the world''s foremost biomedical research center and the U.S. federal government''s focal point for such research. It is one of the components of the Department of Health and Human Services (HHS). The Office of Science Education (OSE) plans, develops, and coordinates a comprehensive science education program to strengthen and enhance efforts of the NIH to attract young people to biomedical and behavioral science careers and to improve science literacy in both adults and children. The function of the Office is as follows: (1) develops, supports, and directs new program initiatives at all levels with special emphasis on targeting students in grades kindergarten to 16, their educators and parents, and the general public; (2) advises NIH leadership on science education issues; (3) examines and evaluates research and emerging trends in science education and literacy for policy making; (4) works closely with the NIH extramural, intramural, women''s health, laboratory animal research, and minority program offices on science education special issues and programs to ensure coordination of NIH efforts; (5) works with NIH institutes, centers, and divisions to enhance communication of science education activities; and (6) works cooperatively with other public- and private-sector organizations to develop and coordinate activities. | science, education, high school, middle school, elementary school, animal, research, bioethics, blood, lymphatic system, bones, joints, muscle, brain, nervous system, cell biology, cancer, child, adolescent, complementary medicine, alternative medicine, digestive system, ears, nose, throat, endocrine system, environmental, toxicology, evolution, eye, vision, food, nutrition, metabolism, genomics, genetics, heart, circulation, history, immune system, injury, wound, kidney, urinary system, medical research, man, mental health, behavior, microbiology, infectious disease, mouth, teeth, therapy, reproductive system, respiratory system, safety, late adult human, sexual health, skin, hair, nail, sleep, social, family, substance abuse, technology, wellness, lifestyle, woman, health, human, lesson plan, supplemental curricula, book, image, multimedia, poster, k-12, adult, non-human animal |
has parent organization: National Institutes of Health is parent organization of: NIH SciEd Blog |
NIH | nlx_146222 | SCR_005603 | SciCrunch Registry | NIH OSE, National Institutes of Health Office of Science Education | 2026-10-24 12:45:29 | 0 | |||||||
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SeqGSEA Resource Report Resource Website 10+ mentions |
SeqGSEA (RRID:SCR_005724) | SeqGSEA | data analysis software, data processing software, software application, software resource | Software package that provides methods for gene set enrichment analysis of high-throughput RNA-Seq data by integrating differential expression and splicing. It uses negative binomial distribution to model read count data, which accounts for sequencing biases and biological variation. Based on permutation tests, statistical significance can also be achieved regarding each gene''s differential expression and splicing, respectively. | differential expression, gene expression, gene set enrichment, rna-seq, sequencing, splicing |
is listed by: OMICtools has parent organization: Bioconductor |
GNU General Public License, v3 or newer | OMICS_02251 | SCR_005724 | SciCrunch Registry | SeqGSEA - Gene Set Enrichment Analysis (GSEA) of RNA-Seq Data: integrating differential expression and splicing | 2026-10-24 12:45:31 | 36 | |||||||
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Bismark Resource Report Resource Website 1000+ mentions |
Bismark (RRID:SCR_005604) | Bismark | software resource | Software tool to map bisulfite converted sequence reads and determine cytosine methylation states. Flexible aligner and methylation caller for Bisulfite-Seq applications. Used to map bisulfite treated sequencing reads to genome of interest and perform methylation calls in single step. | Map bisulfite treated sequence reads, determine cytosine methylation states, genome, sequence reads, perform methylation calls, bio.tools |
is listed by: OMICtools is listed by: Debian is listed by: bio.tools has parent organization: Babraham Institute |
PMID:21493656 DOI:10.1093/bioinformatics/btr167 |
Free, Available for download, Freely available | biotools:bismark, OMICS_00575 | https://github.com/FelixKrueger/Bismark, https://bio.tools/bismark | https://sources.debian.org/src/bismark/ | SCR_005604 | SciCrunch Registry | 2026-10-24 12:45:29 | 1200 | |||||
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Onto-Translate Resource Report Resource Website 1+ mentions |
Onto-Translate (RRID:SCR_005725) | Onto-Translate | analysis service resource, data analysis service, data or information resource, database, production service resource, service resource | In the annotation world, the same piece of information can be stored and viewed differently across different databases. For instance, more than one Affymetrix probe ID can refer to the same GenBank sequence (accession number) and more than one nucleotide sequence from GenBank can be grouped in a single UniGene cluster. The result of Onto-Express depends on whether the input list contains Affymetrix probe IDs, GenBank accession numbers or UniGene cluster IDs. The user has to be aware of relations between the different forms of the data in order to interpret correctly the results. Even if the user is aware of the relationships and knows how to convert them, most existing tools allow conversions of individual genes. Onto-Translate is a tool that allows the user to perform easily such translations. Affymetrix probe IDs, etc., translate GO terms into other identifiers like GenBank accession number, Uniprot IDs. User account required. Platform: Online tool | annotation, gene, analysis, database or data warehouse, other analysis, affymetrix probe id, affymetrix, probe id, translate go terms into other identifiers like genbank accession number, genbank accession number, uniprot id, gene ontology, translate |
is listed by: Gene Ontology Tools is related to: Gene Ontology has parent organization: Wayne State University; Michigan; USA |
PMID:15215428 | Free for academic use | nlx_149182 | SCR_005725 | SciCrunch Registry | 2026-10-24 12:45:31 | 3 | |||||||
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jMHC Resource Report Resource Website 10+ mentions |
jMHC (RRID:SCR_005605) | jMHC | software resource | Software for analyzing and visualization of the results of deep amplicon sequencing. | matlab |
is listed by: OMICtools has parent organization: Google Code |
PMID:21676201 | GNU General Public License, v3, Acknowledgement requested | OMICS_00300 | SCR_005605 | SciCrunch Registry | jmhc - software for analyzing and visualization of the results of deep amplicon sequencing | 2026-10-24 12:45:29 | 10 | ||||||
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ToppGene Suite Resource Report Resource Website 1000+ mentions |
ToppGene Suite (RRID:SCR_005726) | analysis service resource, data analysis service, data or information resource, database, portal, production service resource, resource, service resource | ToppGene Suite is a one-stop portal for gene list enrichment analysis and candidate gene prioritization based on functional annotations and protein interactions network. ToppGene Suite is a one-stop portal for (i) gene list functional enrichment, (ii) candidate gene prioritization using either functional annotations or network analysis and (iii) identification and prioritization of novel disease candidate genes in the interactome. Functional annotation-based disease candidate gene prioritization uses a fuzzy-based similarity measure to compute the similarity between any two genes based on semantic annotations. The similarity scores from individual features are combined into an overall score using statistical meta-analysis. | gene portal, enrichment analysis, functional annotation, gene prioritization, protein interaction, bio.tools, FASEB list |
is listed by: Gene Ontology Tools is listed by: NIDDK Information Network (dkNET) is listed by: GUDMAP Ontology is listed by: Debian is listed by: bio.tools is related to: Gene Ontology is related to: ToppCluster |
State of Ohio Computational Medicine Center ODD TECH 04-042; NIDDK 1U01DK70219; NIDDK P30DK078392 |
PMID:19465376 | Free for academic use | nlx_149183, biotools:toppgene_suite | https://bio.tools/toppgene_suite | SCR_005726 | SciCrunch Registry | ToppGene | 2026-10-24 12:45:31 | 1131 | |||||
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Brain Basics Resource Report Resource Website |
Brain Basics (RRID:SCR_005606) | Brain Basics | data or information resource, narrative resource, training material, video resource | Brain Basics provides information on how the brain works, how mental illnesses are disorders of the brain, and ongoing research that helps us better understand and treat disorders. Mental disorders are common. You may have a friend, colleague, or relative with a mental disorder, or perhaps you have experienced one yourself at some point. Such disorders include depression, anxiety disorders, bipolar disorder, attention deficit hyperactivity disorder (ADHD), and many others. Some people who develop a mental illness may recover completely; others may have repeated episodes of illness with relatively stable periods in between. Still others live with symptoms of mental illness every day. They can be moderate, or serious and cause severe disability. Through research, we know that mental disorders are brain disorders. Evidence shows that they can be related to changes in the anatomy, physiology, and chemistry of the nervous system. When the brain cannot effectively coordinate the billions of cells in the body, the results can affect many aspects of life. Scientists are continually learning more about how the brain grows and works in healthy people, and how normal brain development and function can go awry, leading to mental illnesses. Brain Basics will introduce you to some of this science, such as: * How the brain develops * How genes and the environment affect the brain * The basic structure of the brain * How different parts of the brain communicate and work with each other * How changes in the brain can lead to mental disorders, such as depression. | brain, depression, anxiety disorder, bipolar disorder, attention deficit-hyperactivity disorder, depressive disorder, mental disease, gene, environment | has parent organization: NIMH Educational Resources | NIMH | nlx_146226 | SCR_005606 | SciCrunch Registry | NIMH Brain Basics | 2026-10-24 12:45:29 | 0 |
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Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
