| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1019613304 |
| P356 | DOI | 10.1038/78140 |
| P698 | PubMed publication ID | 10932191 |
| P2093 | author name string | P. M. Nolan | |
| A. Erven | |||
| X. Liu | |||
| K. P. Steel | |||
| S. D. Brown | |||
| P. Mburu | |||
| A. Isaacs | |||
| A. Kiernan | |||
| C. Nickols | |||
| C. Thaung | |||
| C. Thornton | |||
| C. Wells | |||
| D. Brooker | |||
| D. Rogers | |||
| E. M. Fisher | |||
| E. Whitehill | |||
| I. C. Gray | |||
| J. A. Stevenson | |||
| J. Hagan | |||
| J. Hunter | |||
| J. L. Guenet | |||
| J. Martin | |||
| J. Peters | |||
| K. Davies | |||
| K. Pickford | |||
| L. Vizor | |||
| M. Browne | |||
| M. Hewitt | |||
| M. Nasse | |||
| M. Strivens | |||
| N. Spurr | |||
| P. Glenister | |||
| P. Roby | |||
| R. Arkell | |||
| R. Hardisty | |||
| R. Sadri | |||
| R. Selley | |||
| R. Washbourne | |||
| S. Greenaway | |||
| S. McCormack | |||
| S. Rastan | |||
| S. Voegeling | |||
| T. Hough | |||
| Z. Tymowska-Lalanne | |||
| P2860 | cites work | Large numbers of mice established by in vitro fertilization with cryopreserved spermatozoa: implications and applications for genetic resource banks, mutagenesis screens, and mouse backcrosses | Q30780214 |
| Mouse mutagenesis-systematic studies of mammalian gene function | Q32022434 | ||
| Mouse ENU mutagenesis | Q33724129 | ||
| Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment | Q34441265 | ||
| Random mutagenesis screen for dominant behavioral mutations in mice | Q38553450 | ||
| Combining mutagenesis and genomics in the mouse--closing the phenotype gap. | Q40921551 | ||
| Startle habituation and sensorimotor gating in schizophrenia and related animal models | Q41443315 | ||
| Genome-wide, large-scale production of mutant mice by ENU mutagenesis. | Q43520565 | ||
| Effect of cryoprotectants on the survival of follicles in frozen mouse ovaries. | Q52194634 | ||
| Comprehensive observational assessment: Ia. A systematic, quantitative procedure for assessing the behavioral and physiologic state of the mouse | Q72110918 | ||
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | phenotype | Q104053 |
| Chromodomain helicase DNA binding protein 7 | Q15311456 | ||
| Cadherin, EGF LAG seven-pass G-type receptor 1 | Q21494076 | ||
| F-box protein 11 | Q21495687 | ||
| Zinc finger protein ZIC 2 | Q21984265 | ||
| P304 | page(s) | 440–443 | |
| P577 | publication date | 2000-08-01 | |
| P1433 | published in | Nature Genetics | Q976454 |
| P1476 | title | A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse | |
| P478 | volume | 25 |
| Q52095673 | A Novel Ataxic Mutant Mouse Line Having Sensory Neuropathy Shows Heavy Iron Deposition in Kidney. |
| Q50486350 | A compendium of mouse knockouts with inner ear defects. |
| Q30532357 | A dictionary of behavioral motifs reveals clusters of genes affecting Caenorhabditis elegans locomotion. |
| Q30542925 | A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse. |
| Q24798758 | A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development |
| Q35140803 | A forward-genetic approach for analysis of the immune system |
| Q30841444 | A gene-driven ENU-based approach to generating an allelic series in any gene |
| Q31039073 | A gene-driven approach to the identification of ENU mutants in the mouse |
| Q35729853 | A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse |
| Q30743647 | A genomewide screening of N-ethyl-N-nitrosourea-mutagenized mice for musculoskeletal phenotypes☆ |
| Q43199676 | A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment |
| Q28594074 | A monogenic dominant mutation in Rom1 generated by N-ethyl-N-nitrosourea mutagenesis causes retinal degeneration in mice |
| Q57667437 | A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to aCol2a1mutation |
| Q28483790 | A mouse model of early-onset renal failure due to a xanthine dehydrogenase nonsense mutation |
| Q74191885 | A mutant mouse menagerie |
| Q34468672 | A mutant mouse with a highly specific contextual fear-conditioning deficit found in an N-ethyl-N-nitrosourea (ENU) mutagenesis screen |
| Q48256073 | A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse. |
| Q41513620 | A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways |
| Q92533624 | A new mouse model of GLUT1 deficiency syndrome exhibits abnormal sleep-wake patterns and alterations of glucose kinetics in the brain |
| Q34549521 | A novel Akt3 mutation associated with enhanced kinase activity and seizure susceptibility in mice |
| Q46796125 | A phenotype-driven ENU mutagenesis screen for the identification of dominant mutations involved in alcohol consumption. |
| Q60955662 | A radiation hybrid transcript map of the mouse genome |
| Q33260768 | A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud. |
| Q39693546 | A three-dimensional MRI atlas of the mouse brain with estimates of the average and variability |
| Q24798797 | A7DB: a relational database for mutational, physiological and pharmacological data related to the alpha7 nicotinic acetylcholine receptor |
| Q24812780 | ARTS: a web-based tool for the set-up of high-throughput genome-wide mapping panels for the SNP genotyping of mouse mutants |
| Q35870519 | Abnormal pigmentation in hypomelanosis of Ito and pigmentary mosaicism: the role of pigmentary genes |
| Q42501734 | Abnormal sebaceous gland differentiation in 10 kittens ('sebaceous gland dysplasia') associated with generalized hypotrichosis and scaling |
| Q35364326 | Activin B antagonizes RhoA signaling to stimulate mesenchymal morphology and invasiveness of clear cell renal cell carcinomas |
| Q36309428 | Activin B regulates islet composition and islet mass but not whole body glucose homeostasis or insulin sensitivity |
| Q46827741 | Activin signals via SMAD2/3 between germ and somatic cells in the human fetal ovary and regulates kit ligand expression |
| Q38079493 | Activin, neutrophils, and inflammation: just coincidence? |
| Q36190270 | Activins and their related proteins in colon carcinogenesis: insights from early and advanced azoxymethane rat models of colon cancer |
| Q24307781 | Activins, inhibins, and follistatins: from endocrinology to signaling. A paradigm for the new millennium |
| Q57147628 | An -Ethyl--Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion |
| Q24651733 | An ENU-induced mutation in mouse glycyl-tRNA synthetase (GARS) causes peripheral sensory and motor phenotypes creating a model of Charcot-Marie-Tooth type 2D peripheral neuropathy |
| Q28588584 | An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda |
| Q34031998 | An ENU-induced mutation of Nrg1 causes dilated pupils and a reduction in muscarinic receptors in the sphincter pupillae |
| Q34618250 | An N-ethyl-N-nitrosourea mutagenesis screen for epigenetic mutations in the mouse |
| Q52608849 | An intronic mutation in Chd7 creates a cryptic splice site, causing aberrant splicing in a mouse model of CHARGE syndrome. |
| Q51812502 | An siRNA-based screen in C2C12 myoblasts identifies novel genes involved in myogenic differentiation. |
| Q30485081 | Analysis of the mouse mutant Cloth-ears shows a role for the voltage-gated sodium channel Scn8a in peripheral neural hearing loss |
| Q29615723 | Animal models of human disease: zebrafish swim into view |
| Q37032354 | Applicability, usability, and limitations of murine embryonic imaging with optical coherence tomography and optical projection tomography |
| Q36533740 | Approaches to lipid metabolism gene identification and characterization in the postgenomic era. |
| Q35830418 | Artemis sheds new light on V(D)J recombination |
| Q34635853 | Assessing antidepressant activity in rodents: recent developments and future needs |
| Q45240677 | Assessment of a systematic expression profiling approach in ENU-induced mouse mutant lines |
| Q34065954 | Auditory and vestibular mouse mutants: models for human deafness |
| Q34576536 | Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5 |
| Q30500276 | Behavioral and other phenotypes in a cytoplasmic Dynein light intermediate chain 1 mutant mouse |
| Q35586667 | Behavioural screening in mutagenised mice—in search for novel animal models of psychiatric disorders |
| Q52119252 | Building-blocks of embryogenesis. |
| Q38084235 | Cancer of mice and men: old twists and new tails |
| Q34186639 | Capitalizing on large-scale mouse mutagenesis screens |
| Q37006621 | Centralized mouse repositories |
| Q34989563 | Characterization of Sleeping Beauty transposition and its application to genetic screening in mice |
| Q44268455 | Characterization of trimethylpsoralen as a mutagen for mouse embryonic stem cells |
| Q31881396 | Chemical genetics: ligand-based discovery of gene function |
| Q37232958 | Chimera analysis of the Clock mutation in mice shows that complex cellular integration determines circadian behavior |
| Q28206335 | Chromosomal microdeletions: dissecting del22q11 syndrome |
| Q36462154 | Cloned mice and embryonic stem cell establishment from adult somatic cells. |
| Q37494507 | Cognitive assessment of mice strains heterozygous for cell-adhesion genes reveals strain-specific alterations in timing |
| Q33285195 | Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease |
| Q37115953 | Comparative genomics for detecting human disease genes |
| Q53962268 | Comparative transcriptome and histological analyses provide insights into the prenatal skin pigmentation in goat (Capra hircus). |
| Q35092551 | Congenic mice: cutting tools for complex immune disorders |
| Q24644570 | Constitutional downregulation of SEMA5A expression in autism |
| Q50593343 | Cooperative effect of ribosomal protein s19 and Pim-1 kinase on murine c-Myc expression and myeloid/erythroid cellularity. |
| Q50304324 | Creation of miniature pig model of human Waardenburg syndrome type 2A by ENU mutagenesis |
| Q63977492 | Current Awareness on Comparative and Functional Genomics |
| Q26785773 | Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing |
| Q37298023 | Cytoplasmic dynein heavy chain: the servant of many masters |
| Q38960929 | Decoding sORF translation - from small proteins to gene regulation |
| Q46112482 | Defining brain wiring patterns and mechanisms through gene trapping in mice. |
| Q47259668 | Design and Evaluation of a Robotic Device for Automated Tail Vein Cannulations in Rodent Models |
| Q37023265 | Diabetes models by screen for hyperglycemia in phenotype-driven ENU mouse mutagenesis projects |
| Q42544712 | Diffusion microscopic MRI of the mouse embryo: Protocol and practical implementation in the splotch mouse model |
| Q24652124 | Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal development |
| Q36265438 | Discovery genetics: serendipity in basic research |
| Q27002466 | Dissecting immunity by germline mutagenesis |
| Q37060493 | Dissecting innate immunity by germline mutagenesis |
| Q28513404 | Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen |
| Q30440634 | Dominant β-catenin mutations cause intellectual disability with recognizable syndromic features |
| Q55041356 | EMPReSS: standardized phenotype screens for functional annotation of the mouse genome. |
| Q33964080 | ENU Mutagenesis in the Mouse |
| Q30474524 | ENU induced single mutation locus on chr 16 leads to high-frequency hearing loss in mice |
| Q28594698 | ENU mutagenesis identifies mice with mitochondrial branched-chain aminotransferase deficiency resembling human maple syrup urine disease |
| Q43937639 | ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis |
| Q35636403 | ENU mutagenesis screen to establish motor phenotypes in wild-type mice and modifiers of a pre-existing motor phenotype in tau mutant mice |
| Q33732572 | ENU-Based Gene-Driven Mutagenesis in the Mouse: A Next-Generation Gene-Targeting System |
| Q33543443 | ENU-induced mutant mice for a next-generation gene-targeting system |
| Q34457048 | ENU-induced phenovariance in mice: inferences from 587 mutations |
| Q36016473 | EVI1 acts as an inducible negative-feedback regulator of NF-κB by inhibiting p65 acetylation |
| Q36684795 | Early doors (Edo) mutant mouse reveals the importance of period 2 (PER2) PAS domain structure for circadian pacemaking. |
| Q37621089 | Early motor deficits in mouse disease models are reliably uncovered using an automated home-cage wheel-running system: a cross-laboratory validation. |
| Q33510181 | Effect of IVF and laser zona dissection on DNA methylation pattern of mouse zygotes |
| Q28509225 | Effects of G-protein mutations on skin color |
| Q42212782 | Effects of chronic hepatitis C genotype 1 and 4 on serum activins and follistatin in treatment naïve patients and their correlations with interleukin-6, tumour necrosis factor-α, viral load and liver damage. |
| Q33220908 | Efficient and fast targeted production of murine models based on ENU mutagenesis |
| Q33930324 | Efficient chromosomal transposition of a Tc1/mariner- like transposon Sleeping Beauty in mice. |
| Q25255702 | Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice |
| Q38469448 | Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis |
| Q92881931 | Efficient genome-wide first-generation phenotypic screening system in mice using the piggyBac transposon |
| Q40763346 | Enhancement of Sleeping Beauty transposition by CpG methylation: possible role of heterochromatin formation |
| Q46976638 | Estimating the number of coding mutations in genotypic- and phenotypic-driven N-ethyl-N-nitrosourea (ENU) screens |
| Q30490127 | Evaluation of animal models of neurobehavioral disorders |
| Q24305929 | Expression of activin subunits and receptors in the developing human ovary: activin A promotes germ cell survival and proliferation before primordial follicle formation |
| Q24791942 | Focusing on the genetics of hearing: you ain't heard nothin' yet. |
| Q92609296 | Forward genetic approach for behavioral neuroscience using animal models |
| Q37980649 | Forward genetic approaches to understanding complex behaviors. |
| Q46683464 | From ENU mutagenesis to population genetics |
| Q36005259 | From guts to brains: using zebrafish genetics to understand the innards of organogenesis |
| Q38578808 | From mice to men: lessons from mutant ataxic mice |
| Q34462487 | Full-speed mammalian genetics: in vivo target validation in the drug discovery process |
| Q46905044 | Functional analysis of secreted and transmembrane proteins critical to mouse development. |
| Q30597227 | Functional and genetic analysis of choroid plexus development in zebrafish |
| Q33894561 | Functional annotation of mammalian genomic DNA sequence by chemical mutagenesis: a fine-structure genetic mutation map of a 1- to 2-cM segment of mouse chromosome 7 corresponding to human chromosome 11p14-p15. |
| Q38345938 | Functional annotation of mouse mutations in embryonic stem cells by use of expression profiling |
| Q35167516 | Functional genomics and proteomics: charting a multidimensional map of the yeast cell |
| Q34609125 | Functional genomics approaches to understanding brain disorders |
| Q35155809 | Functional genomics of sleep. |
| Q34303207 | Functional genomics of the murine immune system |
| Q35882819 | Functional genomics tools for the analysis of zebrafish pigment |
| Q55014626 | G-protein-coupled receptor signaling and neural tube closure defects. |
| Q34375846 | Gene targeting reveals a role for the glutamate receptors mGluR5 and GluR2 in learning and memory |
| Q89175920 | Generation and Identification of Mutations Resulting in Chronic and Age-Related Phenotypes in Mice |
| Q57198013 | Generation of ENU-Induced Mouse Mutants with Hypocholesterolemia: Novel Tools for Dissecting Plasma Lipoprotein Homeostasis |
| Q50537421 | Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in hematological parameters. |
| Q46158738 | Generation of N-ethyl-N-nitrosourea-induced mouse mutants with deviations in plasma enzyme activities as novel organ-specific disease models |
| Q43729214 | Generation of precise point mutation mice by footprintless genome modification. |
| Q80448597 | Generation of rat mutants using a coat color-tagged Sleeping Beauty transposon system |
| Q36825572 | Genetic architecture of quantitative traits in mice, flies, and humans |
| Q38610506 | Genetic influences on the human oral microbiome |
| Q35813847 | Genetic insights into the morphogenesis of inner ear hair cells. |
| Q34435156 | Genetics and genomics in neuropsychopharmacology: the impact on drug discovery and development |
| Q35145888 | Genetics and genomics of behavioral and psychiatric disorders |
| Q35963838 | Genetics of dark skin in mice |
| Q36314245 | Genetics of graviperception in animals. |
| Q34158811 | Genetics of sensory mechanotransduction |
| Q44573145 | Genetics: a balancing act. |
| Q37763941 | Genome-wide ENU mutagenesis for the discovery of novel male fertility regulators |
| Q34376881 | Genome-wide ENU mutagenesis to reveal immune regulators |
| Q36769182 | Genome-wide association studies of pit-and-fissure- and smooth-surface caries in permanent dentition |
| Q43520565 | Genome-wide, large-scale production of mutant mice by ENU mutagenesis. |
| Q45187730 | Genomewide two-generation screens for recessive mutations by ES cell mutagenesis |
| Q53502363 | Genomics. Beyond the book of life. |
| Q74098267 | Genomics: saviour or millstone? |
| Q33881293 | Genotype, phenotype, and karyotype correlation in the XO mouse model of Turner Syndrome |
| Q42231754 | Germline transgenesis in rodents by pronuclear microinjection of Sleeping Beauty transposons. |
| Q28202486 | High-throughput engineering of the mouse genome coupled with high-resolution expression analysis |
| Q52601624 | High-throughput mouse phenomics for characterizing mammalian gene function. |
| Q34156586 | High-throughput mouse phenotyping |
| Q48537271 | Histomorphological Phenotyping of the Adult Mouse Brain |
| Q35538187 | Human and animal models of V(D)J recombination deficiency |
| Q45041079 | Hypercholesterolemia in ENU-induced mouse mutants |
| Q28589778 | Identification of a novel point mutation of mouse proto-oncogene c-kit through N-ethyl-N-nitrosourea mutagenesis |
| Q24808964 | Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique |
| Q46717321 | Identification of mutations from phenotype-driven ENU mutagenesis in mouse chromosome 7. |
| Q44624383 | Identification of two novel mutations in the murine Nsdhl sterol dehydrogenase gene and development of a functional complementation assay in yeast |
| Q35937612 | Identifying early vascular genes through gene trapping in mouse embryonic stem cells |
| Q50904385 | Impact of IVC housing on emotionality and fear learning in male C3HeB/FeJ and C57BL/6J mice. |
| Q35994005 | Implementing large-scale ENU mutagenesis screens in North America |
| Q34292427 | In search of a depressed mouse: utility of models for studying depression-related behavior in genetically modified mice |
| Q37598783 | Inducible gene trapping with drug-selectable markers and Cre/loxP to identify developmentally regulated genes |
| Q28259871 | Insertional mutagenesis in mice: new perspectives and tools |
| Q24803197 | Intraocular pressure in genetically distinct mice: an update and strain survey |
| Q30488888 | Joint mouse-human phenome-wide association to test gene function and disease risk |
| Q38035234 | Large-scale mouse knockouts and phenotypes |
| Q36414964 | Large-scale mutagenesis and phenotypic screens for the nervous system and behavior in mice. |
| Q34257296 | Linking yeast Gcn5p catalytic function and gene regulation using a quantitative, graded dominant mutant approach |
| Q35008497 | Long-term experiment to study the development, interaction, and influencing factors of DEXA parameters |
| Q30434519 | Loss of inhibin alpha uncouples oocyte-granulosa cell dynamics and disrupts postnatal folliculogenesis |
| Q37550614 | Loss-of-function genetic tools for animal models: cross-species and cross-platform differences |
| Q29619081 | Mammalian circadian biology: elucidating genome-wide levels of temporal organization |
| Q35119688 | Manipulation of the mouse genome: a multiple impact resource for drug discovery and development |
| Q92110199 | Mice with a Brd4 Mutation Represent a New Model of Nephrocalcinosis |
| Q92709644 | Mice with an autosomal dominant Charcot-Marie-Tooth type 2O disease mutation in both dynein alleles display severe moto-sensory phenotypes |
| Q27024434 | Modelling age-related metabolic disorders in the mouse |
| Q33903868 | Modifier screens in the mouse: time to move forward with reverse genetics |
| Q34613926 | Molecular characterization of Pax6(2Neu) through Pax6(10Neu): an extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus. |
| Q36586217 | Molecular mechanisms of midfacial developmental defects |
| Q38371715 | Mouse Genome Informatics (MGI) Resource: Genetic, Genomic, and Biological Knowledgebase for the Laboratory Mouse |
| Q34258471 | Mouse genomics: making sense of the sequence |
| Q24631734 | Mouse large-scale phenotyping initiatives: overview of the European Mouse Disease Clinic (EUMODIC) and of the Wellcome Trust Sanger Institute Mouse Genetics Project |
| Q36569492 | Mouse models as a tool to unravel the genetic basis for human otitis media |
| Q27491017 | Mouse models for human otitis media |
| Q35172443 | Mouse models for neurological disease |
| Q34140872 | Mouse models of blood pressure regulation and hypertension |
| Q45243964 | Mouse mutagenesis identifies novel roles for left-right patterning genes in pulmonary, craniofacial, ocular, and limb development |
| Q55034919 | Mouse mutagenesis on target. |
| Q42941345 | Mouse mutagenesis with the chemical supermutagen ENU. |
| Q34426092 | Mouse-based phenogenomics for modelling human disease. |
| Q31125643 | Mutagenesis strategies for identifying novel loci associated with disease phenotypes |
| Q27346517 | Mutant glycyl-tRNA synthetase (Gars) ameliorates SOD1(G93A) motor neuron degeneration phenotype but has little affect on Loa dynein heavy chain mutant mice |
| Q34459252 | Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: annotated tables |
| Q28586559 | Mutation at the Evi1 locus in Junbo mice causes susceptibility to otitis media |
| Q89966234 | Mutation in Fbxo11 Leads to Altered Immune Cell Content in Jeff Mouse Model of Otitis Media |
| Q28184694 | Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse |
| Q28512322 | Mutation of l7Rn3 shows that Odz4 is required for mouse gastrulation |
| Q27329518 | Mutation of the diamond-blackfan anemia gene Rps7 in mouse results in morphological and neuroanatomical phenotypes |
| Q28534250 | Mutations in Mll2, an H3K4 methyltransferase, result in insulin resistance and impaired glucose tolerance in mice |
| Q34600929 | Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans |
| Q28302883 | Mutations in the Gabrb1 gene promote alcohol consumption through increased tonic inhibition |
| Q28546036 | N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse models |
| Q37231400 | N-ethyl-N-nitrosourea mutagenesis produced a small number of mice with altered plasma electrolyte levels |
| Q33940306 | N-ethyl-N-nitrosourea mutagenesis: boarding the mouse mutant express |
| Q33244414 | N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors |
| Q30463349 | New insights into behaviour using mouse ENU mutagenesis |
| Q28589837 | New semidominant mutations that affect mouse development |
| Q33765741 | Next-generation mammalian genetics toward organism-level systems biology |
| Q34547272 | Novel approaches for identifying genes regulating lymphocyte development and function |
| Q27333508 | Novel gene function revealed by mouse mutagenesis screens for models of age-related disease. |
| Q39769149 | Novel method for high-throughput phenotyping of sleep in mice. |
| Q46797404 | Novel mouse model for Gardner syndrome generated by a large-scale N-ethyl-N-nitrosourea mutagenesis program |
| Q30600757 | Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis |
| Q37798972 | Now and future of mouse mutagenesis for human disease models |
| Q34133340 | Nuts and bolts of psychiatric genetics: building on the Human Genome Project |
| Q30355710 | Optical coherence tomography for embryonic imaging: a review. |
| Q30453755 | Otitis media in the Tgif knockout mouse implicates TGFβ signalling in chronic middle ear inflammatory disease |
| Q33302384 | PBmice: an integrated database system of piggyBac (PB) insertional mutations and their characterizations in mice |
| Q34937350 | Pathbase: a database of mutant mouse pathology |
| Q36974098 | Pausing for thought: disrupting the early transcription elongation checkpoint leads to developmental defects and tumourigenesis. |
| Q34042381 | Perspectives for vascular genomics |
| Q36039949 | Phenotype-first screening for the identification of novel drug targets |
| Q37373139 | Phenotypic comparison of common mouse strains developing high-fat diet-induced hepatosteatosis |
| Q37433902 | Phylooncogenomics: Examining the cancer genome in the context of vertebrate evolution. |
| Q33894475 | Pilot study of large-scale production of mutant pigs by ENU mutagenesis |
| Q50645688 | Postnatal regulation of germ cells by activin: the establishment of the initial follicle pool. |
| Q34934319 | Preclinical models: status of basic research in depression |
| Q44002082 | Presence of visual head tracking differentiates normal sighted from retinal degenerate mice |
| Q24289028 | Progress in genetic studies of pain and analgesia |
| Q48515873 | Progress in using mouse inbred strains, consomics, and mutants to identify genes related to stress, anxiety, and alcohol phenotypes |
| Q33715878 | Propagation of an infertile hermaphrodite mouse lacking germ cells by using nuclear transfer and embryonic stem cell technology |
| Q30671070 | Protein--protein interaction maps: a lead towards cellular functions |
| Q31165060 | Quantification of brain maturation and growth patterns in C57BL/6J mice via computational neuroanatomy of diffusion tensor images |
| Q37087936 | Quiet as a mouse: dissecting the molecular and genetic basis of hearing |
| Q36732466 | RNA-seq-based mapping and candidate identification of mutations from forward genetic screens |
| Q47074000 | Radiographic analysis of zebrafish skeletal defects |
| Q35053230 | Random mutagenesis in the mouse as a tool in drug discovery |
| Q37174167 | Random mutagenesis of the mouse genome: a strategy for discovering gene function and the molecular basis of disease |
| Q37271710 | Regulation of TGF-beta signalling by Fbxo11, the gene mutated in the Jeff otitis media mouse mutant |
| Q30487860 | Reliability, robustness, and reproducibility in mouse behavioral phenotyping: a cross-laboratory study |
| Q40022642 | Removing the cloak of invisibility: phenotyping the mouse |
| Q35145877 | Rodent models of genetic disease |
| Q28513813 | Role of the transcription factor sox4 in insulin secretion and impaired glucose tolerance |
| Q33951133 | SHIRPA, a protocol for behavioral assessment: validation for longitudinal study of neurological dysfunction in mice. |
| Q57197907 | Screen for alterations of iron related parameters in N-ethyl-N-nitrosourea-treated mice identified mutant lines with increased plasma ferritin levels |
| Q28505175 | Screening for increased plasma urea levels in a large-scale ENU mouse mutagenesis project reveals kidney disease models |
| Q44974504 | Screening for novel ENU-induced rhythm, entrainment and activity mutants. |
| Q38615493 | Sensitized mutagenesis screen in Factor V Leiden mice identifies thrombosis suppressor loci. |
| Q34446134 | Sensitized polygenic trait analysis |
| Q88345284 | Sequential ALK Inhibitors Can Select for Lorlatinib-Resistant Compound ALK Mutations in ALK-Positive Lung Cancer |
| Q34414535 | Sex specific retinoic acid signaling is required for the initiation of urogenital sinus bud development. |
| Q28585371 | Signaling through the TGF beta-activin receptors ALK4/5/7 regulates testis formation and male germ cell development |
| Q35650387 | Sleep, circadian rhythms, and interval timing: evolutionary strategies to time information |
| Q33784240 | Spatiotemporal maturation patterns of murine brain quantified by diffusion tensor MRI and deformation-based morphometry |
| Q48081611 | Spectrum of ENU-induced mutations in phenotype-driven and gene-driven screens in the mouse. |
| Q36150477 | Spontaneous inflammatory pain model from a mouse line with N-ethyl-N-nitrosourea mutagenesis. |
| Q89621682 | Studies on N-Ethyl-N-nitrosourea Mutagenesis in BALB/c Mice |
| Q33695715 | Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling |
| Q59052723 | Surviving a knockout blow |
| Q35172304 | TGFβ superfamily signaling regulators are differentially expressed in the developing and adult mouse testis |
| Q34426086 | Taking a functional genomics approach in molecular medicine |
| Q30050478 | Talking about a Revolution |
| Q34267418 | Target discovery |
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