Knockout Mouse Project
Names
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Knockout Mouse Project
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
KOMP
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Names
More detailed information about this field from each metasource.
Knockout Mouse Project
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
KOMP
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Names
More detailed information about this field from each metasource.
Knockout Mouse Project
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
KOMP
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Knockout mutant mice strains. The KOMP repository is a resource of mouse embryonic stem (ES) cells containing a null mutation in every gene in the mouse genome. The KOMP collection of mice, ES Cells, and vectors are now distributed through the Mutant Mouse Resource and Research Center at UC Davis.
Description
More detailed information about this field from each metasource.
Knockout mutant mice strains. The KOMP repository is a resource of mouse embryonic stem (ES) cells containing a null mutation in every gene in the mouse genome. The KOMP collection of mice, ES Cells, and vectors are now distributed through the Mutant Mouse Resource and Research Center at UC Davis.
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Webpage:
https://www.komp.org/index.phpWebpage
More detailed information about this field from each metasource.
https://www.komp.org/index.php
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Publications:
Publications
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The knockout mouse project
PMID: 15340423
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Publications
More detailed information about this field from each metasource.
The knockout mouse project
PMID: 15340423
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
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The knockout mouse project
PubMed citations: 241.
241 articles citing: The knockout mouse project
PIWI-Interacting RNA (piRNA) and Epigenetic Editing in Environmental Health Sciences. PMID:35917009
Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model. PMID:35675330
GIMAP6 regulates autophagy, immune competence, and inflammation in mice and humans. PMID:35551368
Partial and complete loss of myosin binding protein H-like cause cardiac conduction defects. PMID:35533732
From Reductionism Toward Integration: Understanding How Social Behavior Emerges From Integrated Circuits. PMID:35431824
SGII: Systematic Identification of Essential lncRNAs in Mouse and Human Genome With lncRNA-Protein-Protein Heterogeneous Interaction Network. PMID:35386279
Why rare disease needs precision medicine-and precision medicine needs rare disease. PMID:35243424
The mouse resource at National Resource Center for Mutant Mice. PMID:35138443
SIDT1 plays a key role in type I IFN responses to nucleic acids in plasmacytoid dendritic cells and mediates the pathogenesis of an imiquimod-induced psoriasis model. PMID:35065421
Progress towards completing the mutant mouse null resource. PMID:34698892
Tip60 might be a candidate for the acetylation of hepatic carbonic anhydrase I and III in mice. PMID:34651296
Path to improving the life cycle and quality of genome-scale models of metabolism. PMID:34555324
Strategies to Uplift Novel Mendelian Gene Discovery for Improved Clinical Outcomes. PMID:34220947
Using "-omics" Data to Inform Genome-wide Association Studies (GWASs) in the Osteoporosis Field. PMID:34125409
Loss of growth hormone signaling in the mouse germline or in adulthood reduces islet mass and alters islet function with notable sex differences. PMID:33938235
Differential effects by sex with Kmt5b loss. PMID:33871180
A resource of targeted mutant mouse lines for 5,061 genes. PMID:33833456
Efficient collection of a large number of mutations by mutagenesis of DNA damage response defective animals. PMID:33828169
MaveRegistry: a collaboration platform for multiplexed assays of variant effect. PMID:33774657
Hypoglossal Nerve Abnormalities as Biomarkers for Central Nervous System Defects in Mouse Lines Producing Embryonically Lethal Offspring. PMID:33584208
Male-derived copulatory plugs enhance implantation success in female Mus musculus. PMID:33355341
A most formidable arsenal: genetic technologies for building a better mouse. PMID:33004485
A Single Test to Study Social Behavior and Repetitive Self-grooming in Mice. PMID:32699808
Genes adapt to outsmart gene-targeting strategies in mutant mouse strains by skipping exons to reinitiate transcription and translation. PMID:32646486
Translational Geroscience: From invertebrate models to companion animal and human interventions. PMID:32368707
Establishment of a conditional Nomo1 mouse model by CRISPR/Cas9 technology. PMID:31833031
Identifying gene function and module connections by the integration of multispecies expression compendia. PMID:31754022
High-mobility group nucleosomal binding domain 2 protects against microcephaly by maintaining global chromatin accessibility during corticogenesis. PMID:31699896
Genetic backgrounds have unique seizure response profiles and behavioral outcomes following convulsant administration. PMID:31698263
A Genocentric Approach to Discovery of Mendelian Disorders. PMID:31668702
Neurexophilin4 is a selectively expressed α-neurexin ligand that modulates specific cerebellar synapses and motor functions. PMID:31524598
Reproducibility of CRISPR-Cas9 methods for generation of conditional mouse alleles: a multi-center evaluation. PMID:31446895
The transcriptome landscape associated with Disrupted-in-Schizophrenia-1 locus impairment in early development and adulthood. PMID:31204062
The NCATS BioPlanet - An Integrated Platform for Exploring the Universe of Cellular Signaling Pathways for Toxicology, Systems Biology, and Chemical Genomics. PMID:31133849
Computational 3D histological phenotyping of whole zebrafish by X-ray histotomography. PMID:31063133
Robust mouse tracking in complex environments using neural networks. PMID:30937403
Ontology-based validation and identification of regulatory phenotypes. PMID:30423068
Chimeric Mouse Generation by ES Cell Blastocyst Microinjection and Uterine Transfer. PMID:30353510
Understanding Tendons: Lessons from Transgenic Mouse Models. PMID:29978741
Trans-inner Cell Mass Injection of Embryonic Stem Cells Leads to Higher Chimerism Rates. PMID:29912196
Immunity against the Obligate Intracellular Bacterial Pathogen Rickettsia australis Requires a Functional Complement System. PMID:29581196
Aminode: Identification of Evolutionary Constraints in the Human Proteome. PMID:29358731
Deleting the mouse Hsd17b1 gene results in a hypomorphic Naglu allele and a phenotype mimicking a lysosomal storage disease. PMID:29180785
Emerging and evolving concepts in gene essentiality. PMID:29033457
Highly Variable Genomic Landscape of Endogenous Retroviruses in the C57BL/6J Inbred Strain, Depending on Individual Mouse, Gender, Organ Type, and Organ Location. PMID:28951865
Differences in bone structure and unloading-induced bone loss between C57BL/6N and C57BL/6J mice. PMID:28913652
Mouse models of human ocular disease for translational research. PMID:28859131
Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse. PMID:28838066
Phenotyping cardiac and structural birth defects in fetal and newborn mice. PMID:28544620
Integrative Physiology: At the Crossroads of Nutrition, Microbiota, Animal Physiology, and Human Health. PMID:28273475
CRISPR/Cas9-mediated genome editing in wild-derived mice: generation of tamed wild-derived strains by mutation of the a (nonagouti) gene. PMID:28195201
A simple DNA recombination screening method by RT-PCR as an alternative to Southern blot. PMID:28105543
Efficient gene targeting in mouse zygotes mediated by CRISPR/Cas9-protein. PMID:27905063
An improved Red/ET recombineering system and mouse ES cells culture conditions for the generation of targeted mutant mice. PMID:27890869
Mouse-based genetic modeling and analysis of Down syndrome. PMID:27789459
Redefining 'stress resistance genes', and why it matters. PMID:27702993
Whole-Organism Cellular Pathology: A Systems Approach to Phenomics. PMID:27503355
Copulatory plugs inhibit the reproductive success of rival males. PMID:27488082
PiggyBac transposon-based polyadenylation-signal trap for genome-wide mutagenesis in mice. PMID:27292714
Update of neurotrophic factors in neurobiology of addiction and future directions. PMID:27189755
Gene Targeting Using Homologous Recombination in Embryonic Stem Cells: The Future for Behavior Genetics? PMID:27148349
The genetics of bone mass and susceptibility to bone diseases. PMID:27052486
Genomic landscapes of endogenous retroviruses unveil intricate genetics of conventional and genetically-engineered laboratory mouse strains. PMID:26779669
Endothelial Cell Surface Expressed Chemotaxis and Apoptosis Regulator (ECSCR) Regulates Lipolysis in White Adipocytes via the PTEN/AKT Signaling Pathway. PMID:26692198
The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation. PMID:26664249
Assessment of Full-Eye Response to Osmotic Stress in Mouse Model In Vivo Using Optical Coherence Tomography. PMID:26491552
Linking RNA biology to lncRNAs. PMID:26430155
Comprehensive comparative homeobox gene annotation in human and mouse. PMID:26412852
[Application Progress of CRISPR/Cas9 System for Gene Editing in Tumor Research]. PMID:26383982
Beyond knockouts: the International Knockout Mouse Consortium delivers modular and evolving tools for investigating mammalian genes. PMID:26340938
Applications of comparative evolution to human disease genetics. PMID:26338499
Network Modules of the Cross-Species Genotype-Phenotype Map Reflect the Clinical Severity of Human Diseases. PMID:26301634
High-throughput screening of mouse gene knockouts identifies established and novel skeletal phenotypes. PMID:26273529
Passenger Mutations Confound Interpretation of All Genetically Modified Congenic Mice. PMID:26163370
Publisher’s Note:Abstraction for data integration:Fusing mammalian molecular, cellular and phenotype big datasets for better knowledge extraction. PMID:26101093
Gene Perturbation Atlas (GPA): a single-gene perturbation repository for characterizing functional mechanisms of coding and non-coding genes. PMID:26039571
Spatiotemporal expression and transcriptional perturbations by long noncoding RNAs in the mouse brain. PMID:26034286
Advantages of using the CRISPR/Cas9 system of genome editing to investigate male reproductive mechanisms using mouse models. PMID:25994645
A novel transcriptional factor Nkapl is a germ cell-specific suppressor of Notch signaling and is indispensable for spermatogenesis. PMID:25875095
Common Polymorphisms in the Age of Research Domain Criteria (RDoC): Integration and Translation. PMID:25680673
Association of novelty-related behaviors and intravenous cocaine self-administration in Diversity Outbred mice. PMID:25238945
Generation of Ugt1-deficient murine liver cell lines using TALEN technology. PMID:25118822
Integrating EMR-linked and in vivo functional genetic data to identify new genotype-phenotype associations. PMID:24949630
Automated pipeline for anatomical phenotyping of mouse embryos using micro-CT. PMID:24850858
Colorectal polyp model established by transplacental BMP4 RNAi. PMID:24806485
Fighting in the home cage: Agonistic encounters and effects on neurobiological markers within the social decision-making network of house mice (Mus musculus). PMID:24602985
Rationally optimized cryopreservation of multiple mouse embryonic stem cell lines: II--Mathematical prediction and experimental validation of optimal cryopreservation protocols. PMID:24560712
Automatic structural parcellation of mouse brain MRI using multi-atlas label fusion. PMID:24475148
Rationally optimized cryopreservation of multiple mouse embryonic stem cell lines: I--Comparative fundamental cryobiology of multiple mouse embryonic stem cell lines and the implications for embryonic stem cell cryopreservation protocols. PMID:24384367
Transgenic mouse technology in skin biology: generation of complete or tissue-specific knockout mice. PMID:24352082
Newer gene editing technologies toward HIV gene therapy. PMID:24284874
Pheno-Pub: a total support system for the publication of mouse phenotypic data on the web. PMID:24220852
Mouse models in bone marrow transplantation and adoptive cellular therapy. PMID:24216170
The roles of FMRP-regulated genes in autism spectrum disorder: single- and multiple-hit genetic etiologies. PMID:24207117
Genetically engineered humanized mouse models for preclinical antibody studies. PMID:24150980
MADM-ML, a mouse genetic mosaic system with increased clonal efficiency. PMID:24143253
AMP deaminase 3 deficiency enhanced 5'-AMP induction of hypometabolism. PMID:24066180
Phenotypic characterization of the KK/HlJ inbred mouse strain. PMID:24009271
The perfect host: a mouse host embryo facilitating more efficient germ line transmission of genetically modified embryonic stem cells. PMID:23844102
Pancreas-specific Cre driver lines and considerations for their prudent use. PMID:23823474
What have we learned from murine models of otitis media? PMID:23775349
Microcomputed tomography provides high accuracy congenital heart disease diagnosis in neonatal and fetal mice. PMID:23759365
Improving the measurement of semantic similarity between gene ontology terms and gene products: insights from an edge- and IC-based hybrid method. PMID:23741529
High-efficiency and heritable gene targeting in mouse by transcription activator-like effector nucleases. PMID:23630316
Going forward with genetics: recent technological advances and forward genetics in mice. PMID:23608223
Suppressed pro-inflammatory response of microglia in CX3CR1 knockout mice. PMID:23499256
Efficient methods for targeted mutagenesis in zebrafish using zinc-finger nucleases: data from targeting of nine genes using CompoZr or CoDA ZFNs. PMID:23451191
A novel selection marker for efficient DNA cloning and recombineering in E. coli. PMID:23437314
Genetic disruption of the copulatory plug in mice leads to severely reduced fertility. PMID:23341775
Murine infection models for vaccine development: the malaria example. PMID:23249712
Deconstructing Mus gemischus: advances in understanding ancestry, structure, and variation in the genome of the laboratory mouse. PMID:23223940
Using genetically engineered animal models in the postgenomic era to understand gene function in alcoholism. PMID:23134044
A fast and sensitive alternative for β-galactosidase detection in mouse embryos. PMID:23132248
The mammalian gene function resource: the International Knockout Mouse Consortium. PMID:22968824
The Mammalian Phenotype Ontology as a unifying standard for experimental and high-throughput phenotyping data. PMID:22961259
Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project. PMID:22961258
Centralized mouse repositories. PMID:22945696
Permissive and restricted virus infection of murine embryonic stem cells. PMID:22815272
Conditional gene manipulation: Cre-ating a new biological era. PMID:22761243
Rapid and cost-effective gene targeting in rat embryonic stem cells by TALENs. PMID:22749015
Experimental and husbandry procedures as potential modifiers of the results of phenotyping tests. PMID:22713295
Regulated Expression of Chromobox Homolog 5 Revealed in Tumors of Apc(Min) (/+) ROSA11 Gene Trap Mice. PMID:22670227
Dynamic gene expression in the human cerebral cortex distinguishes children from adults. PMID:22666384
A resource for the conditional ablation of microRNAs in the mouse. PMID:22570807
Dual function of the UNC-45b chaperone with myosin and GATA4 in cardiac development. PMID:22553207
Elephant transcriptome provides insights into the evolution of eutherian placentation. PMID:22546564
Conditional gene expression in the mouse inner ear using Cre-loxP. PMID:22526732
Emerging functional and mechanistic paradigms of mammalian long non-coding RNAs. PMID:22492512
Mixture of differentially tagged Tol2 transposons accelerates conditional disruption of a broad spectrum of genes in mouse embryonic stem cells. PMID:22447447
Mouse genetic and phenotypic resources for human genetics. PMID:22422677
Disruption of IFT complex A causes cystic kidneys without mitotic spindle misorientation. PMID:22282595
The blessings and curses of C57BL/6 substrains in mouse genetic studies. PMID:22211972
A knockout mouse resource for the biomedical research community. PMID:22211970
GeneWeaver: a web-based system for integrative functional genomics. PMID:22080549
Optical Coherence Tomography for live imaging of mammalian development. PMID:21962442
Evaluation of social and physical enrichment in modulation of behavioural phenotype in C57BL/6J female mice. PMID:21931844
BioMart as an integration solution for the International Knockout Mouse Consortium. PMID:21930503
Mouse models for Down syndrome-associated developmental cognitive disabilities. PMID:21865664
A resource of vectors and ES cells for targeted deletion of microRNAs in mice. PMID:21822254
The future of model organisms in human disease research. PMID:21765459
Identification of fat4 and tsc22d1 as novel candidate genes for spontaneous pulmonary adenomas. PMID:21764761
Cyto- and chemoarchitecture of the hypothalamic paraventricular nucleus in the C57BL/6J male mouse: a study of immunostaining and multiple fluorescent tract tracing. PMID:21674499
Charting a course for genomic medicine from base pairs to bedside. PMID:21307933
Bi-allelic gene targeting in mouse embryonic stem cells. PMID:21288739
Sensitized phenotypic screening identifies gene dosage sensitive region on chromosome 11 that predisposes to disease in mice. PMID:21204268
Mouse mutants and phenotypes: accessing information for the study of mammalian gene function. PMID:21185380
New genetic resources for mammalian developmental biologists. PMID:21173845
Genome-wide interrogation of Mammalian stem cell fate determinants by nested chromosome deletions. PMID:21170304
Laboratory mouse models for the human genome-wide associations. PMID:21072174
Mouse models in male fertility research. PMID:21057516
The UCSC Genome Browser database: update 2011. PMID:20959295
Molecular networks in drug discovery. PMID:20932236
The IKMC web portal: a central point of entry to data and resources from the International Knockout Mouse Consortium. PMID:20929875
High-sensitivity O-glycomic analysis of mice deficient in core 2 {beta}1,6-N-acetylglucosaminyltransferases. PMID:20855471
Functional phenotyping of the maternal albumin turnover in the mouse placenta by dynamic contrast-enhanced MRI. PMID:20686857
ROSA26Flpo deleter mice promote efficient inversion of conditional gene traps in vivo. PMID:20665730
MamPhEA: a web tool for mammalian phenotype enrichment analysis. PMID:20605928
Efficient generation of germ line transmitting chimeras from C57BL/6N ES cells by aggregation with outbred host embryos. PMID:20582321
A mouse knockout library for secreted and transmembrane proteins. PMID:20562862
Deficiencies in the region syntenic to human 21q22.3 cause cognitive deficits in mice. PMID:20512340
Multi-scale characterization of the PEPCK-C mouse through 3D cryo-imaging. PMID:20467563
Contrasting genetic paths to morphological and physiological evolution. PMID:20368429
Genetically modified mice-successes and failures of a widely used technology. PMID:20140450
Granulin epithelin precursor: a bone morphogenic protein 2-inducible growth factor that activates Erk1/2 signaling and JunB transcription factor in chondrogenesis. PMID:20124436
Identification and validation of novel spinophilin-associated proteins in rodent striatum using an enhanced ex vivo shotgun proteomics approach. PMID:20124353
The mammalian phenotype ontology: enabling robust annotation and comparative analysis. PMID:20052305
High-throughput behavioral phenotyping in the expanded panel of BXD recombinant inbred strains. PMID:19958391
The UCSC Genome Browser database: update 2010. PMID:19906737
Transgenic mouse technology: principles and methods. PMID:19763515
Where's the mouse info? PMID:19605899
Male infertility caused by spermiogenic defects: lessons from gene knockouts. PMID:19481682
Towards better mouse models: enhanced genotypes, systemic phenotyping and envirotype modelling. PMID:19434078
Genetic architecture of quantitative traits in mice, flies, and humans. PMID:19411597
Reconstructing generalized logical networks of transcriptional regulation in mouse brain from temporal gene expression data. PMID:19300527
Cancer gene discovery in mouse and man. PMID:19285540
Mouse models for human otitis media. PMID:19272362
Elevated plus maze for mice. PMID:19229173
PRIME importance of pathology expertise. PMID:19131991
Removing the cloak of invisibility: phenotyping the mouse. PMID:19048073
Large-scale gene trapping in C57BL/6N mouse embryonic stem cells. PMID:18799693
Search for informative polymorphisms in candidate genes: clock genes and circadian behaviour in blue tits. PMID:18792794
Genetically engineered mouse models for skin research: taking the next step. PMID:18511240
Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study. PMID:18505770
Null mutations in human and mouse orthologs frequently result in different phenotypes. PMID:18458337
Genetic background determines metabolic phenotypes in the mouse. PMID:18392653
Optimization of volumetric computed tomography for skeletal analysis of model genetic organisms. PMID:18286615
An improved cryopreservation method for a mouse embryonic stem cell line. PMID:18191827
Reduced body weight is a common effect of gene knockout in mice. PMID:18182103
Mutagenesis in rodents using the L1 retrotransposon. PMID:18047693
'One medicine---one pathology': are veterinary and human pathology prepared? PMID:18040269
Virtues and limitations of the preimplantation mouse embryo as a model system. PMID:18023855
The UniTrap resource: tools for the biologist enabling optimized use of gene trap clones. PMID:17942430
PBmice: an integrated database system of piggyBac (PB) insertional mutations and their characterizations in mice. PMID:17932058
Genetic variation in C57BL/6 ES cell lines and genetic instability in the Bruce4 C57BL/6 ES cell line. PMID:17828574
Large-scale, saturating insertional mutagenesis of the mouse genome. PMID:17720809
Genomewide discovery and classification of candidate ovarian fertility genes in the mouse. PMID:17660561
Efficient genome-wide mutagenesis of zebrafish genes by retroviral insertions. PMID:17640903
Modeling insertional mutagenesis using gene length and expression in murine embryonic stem cells. PMID:17637833
Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease. PMID:17514509
BAC to immunology--bacterial artificial chromosome-mediated transgenesis for targeting of immune cells. PMID:17437533
A recombineering based approach for high-throughput conditional knockout targeting vector construction. PMID:17426124
Adopting the good reFLEXes when generating conditional alterations in the mouse genome. PMID:17415672
Induced mitotic recombination of p53 in vivo. PMID:17360553
Modeling sporadic loss of heterozygosity in mice by using mosaic analysis with double markers (MADM). PMID:17360552
Developmental and adult phenotyping directly from mutant embryonic stem cells. PMID:17360545
Interpretation of knockout experiments: the congenic footprint. PMID:17331107
Assessing human germ-cell mutagenesis in the Postgenome Era: a celebration of the legacy of William Lawson (Bill) Russell. PMID:17295306
Power matters in closing the phenotyping gap. PMID:17216184
Using mouse genomics to understand idiopathic interstitial fibrosis. PMID:17202297
Mutagenesis of diploid mammalian genes by gene entrapment. PMID:17062627
Transgenic mice carrying the H258N mutation in the gene encoding the beta-subunit of phosphodiesterase-6 (PDE6B) provide a model for human congenital stationary night blindness. PMID:17044014
Recording long-term potentiation of synaptic transmission by three-dimensional multi-electrode arrays. PMID:16942609
Understanding mammalian genetic systems: the challenge of phenotyping in the mouse. PMID:16933996
Mouse models as a tool to unravel the genetic basis for human otitis media. PMID:16917982
Modeling chromosomes in mouse to explore the function of genes, genomic disorders, and chromosomal organization. PMID:16839184
Tslc1 (nectin-like molecule-2) is essential for spermatozoa motility and male fertility. PMID:16837733
Schizophrenia-relevant behavioral testing in rodent models: a uniquely human disorder? PMID:16797265
Virtual histology of transgenic mouse embryos for high-throughput phenotyping. PMID:16683035
Production of knockout mice by random or targeted mutagenesis in spermatogonial stem cells. PMID:16679411
Learning from small fry: the zebrafish as a genetic model organism for aquaculture fish species. PMID:16670967
Finding the molecular basis of complex genetic variation in humans and mice. PMID:16524828
Large-scale mutagenesis and phenotypic screens for the nervous system and behavior in mice. PMID:16519954
Integration of double-fluorescence expression vectors into zebrafish genome for the selection of site-directed knockout/knockin. PMID:16501876
Conditional and inducible gene recombineering in the mouse inner ear. PMID:16488403
High-throughput trapping of secretory pathway genes in mouse embryonic stem cells. PMID:16478711
Pol II-expressed shRNA knocks down Sod2 gene expression and causes phenotypes of the gene knockout in mice. PMID:16450009
The International Gene Trap Consortium Website: a portal to all publicly available gene trap cell lines in mouse. PMID:16381950
Rapid and quantitative detection of homologous and non-homologous recombination events using three oligonucleotide MLPA. PMID:16340005
Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice. PMID:16300676
TAK1, but not TAB1 or TAB2, plays an essential role in multiple signaling pathways in vivo. PMID:16260493
Two ways to trap a gene in mice. PMID:16150712
Conditional knockdown of Fgfr2 in mice using Cre-LoxP induced RNA interference. PMID:15987787
Adding precision tools to the plant biologists' toolbox with chemical genomics. PMID:15955916
Disruption of the mouse inositol 1,3,4,5,6-pentakisphosphate 2-kinase gene, associated lethality, and tissue distribution of 2-kinase expression. PMID:15939868
Genomewide production of multipurpose alleles for the functional analysis of the mouse genome. PMID:15870191
The problem with academic medicine: engineering our way into and out of the mess. PMID:15839728
Suppression of nonsense-mediated mRNA decay permits unbiased gene trapping in mouse embryonic stem cells. PMID:15687378
The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information. PMID:15642099
Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique. PMID:15615595
All systems GO for understanding mouse gene function. PMID:15610553
The European dimension for the mouse genome mutagenesis program. PMID:15340424
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gene
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
gene knockout
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
genetic strain
metasource: Fairsharing.org
version: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
Tags
More detailed information about this field from each metasource.
gene
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
gene knockout
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
genetic strain
metasource: Fairsharing.orgversion: FAIRsharing.org: KOMP; Knockout Mouse Project; DOI: https://doi.org/10.25504/FAIRsharing.an4drj; Last edited: April 26, 2021, 3:34 p.m.; Last accessed: Jan 03 2022 7:07 p.m.
gene gene knockout genetic strain
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