ENU mutagenesis, a way forward to understand gene function.
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Steve D. M. Brown | Sara Wells | Abraham Acevedo-Arozena | S. Wells | R. Cox | A. Acevedo-Arozena | P. Potter | Paul Potter | Steve D M Brown | Roger D Cox | Michelle Kelly | M. Kelly | Steve D. M. Brown
[1] M. Lyon,et al. Mutation rates at a new set of specific loci in the mouse. , 1966, Genetical research.
[2] T. Hudson,et al. A genome-wide association study identifies novel risk loci for type 2 diabetes , 2007, Nature.
[3] Gerhard K. H. Przemeck,et al. A Genetic Screen for Modifiers of the Delta1-Dependent Notch Signaling Function in the Mouse , 2007, Genetics.
[4] Steve D. M. Brown,et al. A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse. , 2006, Human molecular genetics.
[5] Klaus Schughart,et al. Genome-wide, large-scale production of mutant mice by ENU mutagenesis , 2000, Nature Genetics.
[6] R. Cox,et al. A new mouse model of type 2 diabetes, produced by N-ethyl-nitrosourea mutagenesis, is the result of a missense mutation in the glucokinase gene. , 2004, Diabetes.
[7] F. Ashcroft,et al. Nicotinamide nucleotide transhydrogenase: a key role in insulin secretion. , 2006, Cell metabolism.
[8] Hiroshi Masuya,et al. A series of maturity onset diabetes of the young, type 2 (MODY2) mouse models generated by a large-scale ENU mutagenesis program. , 2004, Human molecular genetics.
[9] W. Frankel,et al. Severe epilepsy resulting from genetic interaction between Scn2a and Kcnq2. , 2006, Human molecular genetics.
[10] Judy H. Cho,et al. A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene , 2006, Science.
[11] K. Anderson,et al. Rab23 is an essential negative regulator of the mouse Sonic hedgehog signalling pathway , 2001, Nature.
[12] S. Neubauer,et al. Identification of cardiac malformations in mice lacking Ptdsr using a novel high-throughput magnetic resonance imaging technique , 2004, BMC Developmental Biology.
[13] T. Clark,et al. Estimating the number of coding mutations in genotypic and phenotypic driven N-ethyl-N-nitrosourea (ENU) screens: revisited , 2006, Mammalian Genome.
[14] C. G. Wright,et al. Characterization of a new allele of Ames waltzer generated by ENU mutagenesis , 2005, Hearing Research.
[15] P M Nolan,et al. Screening for novel ENU‐induced rhythm, entrainment and activity mutants , 2004, Genes, brain, and behavior.
[16] Kieran Clarke,et al. µMRI–HREM pipeline for high‐throughput, high‐resolution phenotyping of murine embryos , 2007, Journal of anatomy.
[17] U. Heinzmann,et al. A missense mutation in the WD40 domain of murine Lyst is linked to severe progressive Purkinje cell degeneration , 2006, Acta Neuropathologica.
[18] R. Cox,et al. ENU mutagenesis in the mouse: application to human genetic disease. , 2002, Briefings in functional genomics & proteomics.
[19] B. Libby,et al. Mouse mutants from chemically mutagenized embryonic stem cells , 2000, Nature Genetics.
[20] J. Bielas,et al. Proliferation is necessary for both repair and mutation in transgenic mouse cells. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[21] M. Justice,et al. The mutagenic action of N-ethyl-N-nitrosourea in the mouse , 2000, Mammalian Genome.
[22] P. Hunsicker,et al. Comparison of the genetic effects of equimolar doses of ENU and MNU: while the chemicals differ dramatically in their mutagenicity in stem-cell spermatogonia, both elicit very high mutation rates in differentiating spermatogonia. , 2007, Mutation research.
[23] P. Selby,et al. A strategy for fine-structure functional analysis of a 6- to 11-centimorgan region of mouse chromosome 7 by high-efficiency mutagenesis. , 1990, Proceedings of the National Academy of Sciences of the United States of America.
[24] Steve D. M. Brown,et al. Rodent models of genetic disease. , 2003, Current opinion in genetics & development.
[25] H. Fuchs,et al. Screening for dysmorphological abnormalities—a powerful tool to isolate new mouse mutants , 2000, Mammalian Genome.
[26] J. O’Neill,et al. DNA damage, DNA repair, cell proliferation, and DNA replication: how do gene mutations result? , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[27] H. Himmelbauer,et al. Mouse splice mutant generation from ENU-treated ES cells--a gene-driven approach. , 2005, Genomics.
[28] Steve D. M. Brown,et al. Novel ENU-induced eye mutations in the mouse: models for human eye disease. , 2002, Human molecular genetics.
[29] John G. Sled,et al. Behavioral Phenotypes of Disc1 Missense Mutations in Mice , 2007, Neuron.
[30] Steve D. M. Brown,et al. The Deaf Mouse Mutant Jeff (Jf) is a Single Gene Model of Otitis Media , 2003, Journal of the Association for Research in Otolaryngology.
[31] C. Goodnow,et al. Illuminating autoimmune regulators through controlled variation of the mouse genome sequence. , 2004, Immunity.
[32] Werner Müller,et al. Introducing the German Mouse Clinic: open access platform for standardized phenotyping , 2005, Nature Methods.
[33] Steve D. M. Brown,et al. Dissecting the genetic complexity of human 6p deletion syndromes by using a region-specific, phenotype-driven mouse screen. , 2005, Proceedings of the National Academy of Sciences of the United States of America.
[34] H. Masuya,et al. Molecular characterization of ENU mouse mutagenesis and archives. , 2005, Biochemical and biophysical research communications.
[35] M. Justice,et al. Efficient generation and mapping of recessive developmental mutations using ENU mutagenesis , 2002, Nature Genetics.
[36] Kathryn E. Hentges,et al. Checks and balancers: balancer chromosomes to facilitate genome annotation. , 2004, Trends in genetics : TIG.
[37] M. Jarvelin,et al. A Common Variant in the FTO Gene Is Associated with Body Mass Index and Predisposes to Childhood and Adult Obesity , 2007, Science.
[38] L. Greensmith,et al. A mutation in dynein rescues axonal transport defects and extends the life span of ALS mice , 2005, The Journal of cell biology.
[39] B. Beutler,et al. Unraveling innate immunity using large scale N-ethyl-N-nitrosourea mutagenesis. , 2005, Tissue antigens.
[40] S. Wells,et al. Spectrum of ENU‐induced mutations in phenotype‐driven and gene‐driven screens in the mouse , 2007, Environmental and molecular mutagenesis.
[41] Judy H Cho,et al. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis , 2007, Nature Genetics.
[42] Steve D. M. Brown,et al. The European dimension for the mouse genome mutagenesis program , 2004 .
[43] M. Mayhaus,et al. Efficient and fast targeted production of murine models based on ENU mutagenesis , 2005, Mammalian Genome.
[44] K. Steel,et al. Multiple mutations in mouse Chd7 provide models for CHARGE syndrome. , 2005, Human molecular genetics.
[45] T. Skopek,et al. Toxicity, mutagenicity, and mutational spectra of N-ethyl-N-nitrosourea in human cell lines with different DNA repair phenotypes. , 1991, Cancer research.
[46] E. Rinchik. Chemical mutagenesis and fine-structure functional analysis of the mouse genome. , 1991, Trends in genetics : TIG.
[47] B. Beutler,et al. Analysis of the MCMV resistome by ENU mutagenesis , 2006, Mammalian Genome.
[48] M. Pagano,et al. The After-Hours Mutant Reveals a Role for Fbxl3 in Determining Mammalian Circadian Period , 2007, Science.
[49] Bin Liu,et al. Functional genetic analysis of mouse chromosome 11 , 2003, Nature.
[50] W. Frankel,et al. Mutation Rate and Predicted Phenotypic Target Sizes in Ethylnitrosourea-Treated Mice , 2004, Genetics.
[51] Steve D. M. Brown,et al. Dynein mutations impair autophagic clearance of aggregate-prone proteins , 2005, Nature Genetics.
[52] Steve D. M. Brown,et al. A gene-driven approach to the identification of ENU mutants in the mouse , 2002, Nature Genetics.
[53] Kevin Eggan,et al. Non–cell autonomous effect of glia on motor neurons in an embryonic stem cell–based ALS model , 2007, Nature Neuroscience.
[54] D. P. King,et al. Mutagenesis and mapping of a mouse gene, Clock, essential for circadian behavior. , 1994, Science.
[55] Minoru Tanaka,et al. Positional Cloning of the Mouse Circadian Clock Gene , 1997, Cell.
[56] B. Beutler,et al. Jinx, an MCMV susceptibility phenotype caused by disruption of Unc13d: a mouse model of type 3 familial hemophagocytic lymphohistiocytosis , 2007, The Journal of Experimental Medicine.
[57] Simon C. Potter,et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants , 2007, Nature Genetics.
[58] T. Schöneberg,et al. N-ethyl-N-nitrosourea-based generation of mouse models for mutant G protein-coupled receptors. , 2006, Physiological genomics.
[59] L. Tarantino,et al. A Forward Genetics Screen in Mice Identifies Recessive Deafness Traits and Reveals That Pejvakin Is Essential for Outer Hair Cell Function , 2007, The Journal of Neuroscience.
[60] M. Traka,et al. Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit , 2006, Mammalian Genome.
[61] M. Kas,et al. Dissecting complex behaviours in the post-genomic era , 2004, Trends in Neurosciences.
[62] Yasushi Hiraoka,et al. Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport , 2003, Science.
[63] Steve D. M. Brown,et al. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse , 2000, Nature Genetics.
[64] Steve D. M. Brown,et al. Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy , 2000 .
[65] N. Claij,et al. DNA mismatch repair deficiency stimulates N-ethyl-N-nitrosourea-induced mutagenesis and lymphomagenesis. , 2003, Cancer research.
[66] V. Chapman,et al. Effects of ENU dosage on mouse strains , 2000, Mammalian Genome.
[67] H. Masuya,et al. A novel dominant-negative mutation in Gdf5 generated by ENU mutagenesis impairs joint formation and causes osteoarthritis in mice. , 2007, Human molecular genetics.
[68] M. Justice,et al. Optimal N‐Ethyl‐N‐nitrosourea (ENU) doses for inbred mouse strains , 2000, Genesis.
[69] D. Reed,et al. Forty mouse strain survey of body composition , 2007, Physiology & Behavior.
[70] P. Visscher,et al. Marker-assisted introgression in backcross breeding programs. , 1996, Genetics.
[71] Jason P. DeBruyne,et al. A Clock Shock: Mouse CLOCK Is Not Required for Circadian Oscillator Function , 2006, Neuron.
[72] W L Russell,et al. Dose-repetition increases the mutagenic effectiveness of N-ethyl-N-nitrosourea in mouse spermatogonia. , 1985, Proceedings of the National Academy of Sciences of the United States of America.
[73] Richard J. Mural,et al. Genome-wide single-nucleotide polymorphism analysis defines haplotype patterns in mouse , 2003, Proceedings of the National Academy of Sciences of the United States of America.
[74] C. Goodnow,et al. Connecting mammalian genome with phenome by ENU mouse mutagenesis: gene combinations specifying the immune system. , 2005, Annual review of genetics.
[75] Terry Magnuson,et al. An allelic series of mutations in Smad2 and Smad4 identified in a genotype-based screen of N-ethyl-N- nitrosourea-mutagenized mouse embryonic stem cells , 2002, Proceedings of the National Academy of Sciences of the United States of America.
[76] John M. Hancock,et al. Understanding Mammalian Genetic Systems: The Challenge of Phenotyping in the Mouse , 2006, PLoS genetics.
[77] M. J. Justice,et al. Mouse ENU mutagenesis. , 1999, Human molecular genetics.
[78] R. Copley,et al. A RING-type ubiquitin ligase family member required to repress follicular helper T cells and autoimmunity , 2005, Nature.
[79] Steve D. M. Brown,et al. A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse , 2003, The Journal of Neuroscience.
[80] M. Bucan,et al. Mutations in Rab3a alter circadian period and homeostatic response to sleep loss in the mouse , 2002, Nature Genetics.
[81] Steve D. M. Brown,et al. A gene-driven ENU-based approach to generating an allelic series in any gene , 2004, Mammalian Genome.
[82] H. Fuchs,et al. Autoimmunity and inflammation due to a gain-of-function mutation in phospholipase C gamma 2 that specifically increases external Ca2+ entry. , 2005, Immunity.
[83] S. Rastan,et al. Novel Mouse Model of Autosomal Semidominant Adult Hypophosphatasia Has a Splice Site Mutation in the Tissue Nonspecific Alkaline Phosphatase Gene Akp2 , 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.
[84] T. Skopek,et al. Mutational spectrum at the Hprt locus in splenic T cells of B6C3F1 mice exposed to N-ethyl-N-nitrosourea. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[85] D. Hilton,et al. The art and design of genetic screens: mouse , 2005, Nature Reviews Genetics.
[86] M. Justice,et al. A new ENU-induced allele of mouse quaking causes severe CNS dysmyelination , 2005, Mammalian Genome.
[87] Steve D. M. Brown,et al. Novel phenotypes identified by plasma biochemical screening in the mouse , 2002, Mammalian Genome.
[88] J. Favor. The mutagenic activity of ethylnitrosourea at low doses in spermatogonia of the mouse as assessed by the specific-locus test. , 1998, Mutation research.
[89] Steve D. M. Brown,et al. Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media , 2006, PLoS genetics.
[90] T. Magnuson,et al. Genotype-based screen for ENU-induced mutations in mouse embryonic stem cells , 2000, Nature Genetics.
[91] Steve D. M. Brown,et al. Association of the FBXO11 gene with chronic otitis media with effusion and recurrent otitis media: the Minnesota COME/ROM Family Study. , 2006, Archives of otolaryngology--head & neck surgery.
[92] E. Fisher,et al. Behavioral and functional analysis of mouse phenotype: SHIRPA, a proposed protocol for comprehensive phenotype assessment , 1997, Mammalian Genome.
[93] J. Roder,et al. Forward genetic screen of mouse reveals dominant missense mutation in the P/Q‐type voltage‐dependent calcium channel, CACNA1A , 2007, Genes, brain, and behavior.
[94] R. A. Bailey,et al. Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes , 2007, Nature Genetics.
[95] Y. Gondo,et al. Mutational pattern and frequency of induced nucleotide changes in mouse ENU mutagenesis , 2007, BMC Molecular Biology.
[96] Steve D. M. Brown,et al. Mutations in α-Tubulin Cause Abnormal Neuronal Migration in Mice and Lissencephaly in Humans , 2007, Cell.
[97] M. MacDonald,et al. Huntington's disease: seeing the pathogenic process through a genetic lens. , 2006, Trends in biochemical sciences.
[98] C. Goodnow,et al. Genome-wide ENU mutagenesis to reveal immune regulators. , 2001, Immunity.
[99] D. Carpenter,et al. Effect of dose fractionation on the ethylnitrosourea induction of specific-locus mutations in mouse spermatogonia. , 1982, Proceedings of the National Academy of Sciences of the United States of America.
[100] Joseph H. Nadeau,et al. Implementing Large-Scale ENU Mutagenesis Screens in North America , 2004, Genetica.
[101] P. Hunsicker,et al. Specific-locus test shows ethylnitrosourea to be the most potent mutagen in the mouse. , 1979, Proceedings of the National Academy of Sciences of the United States of America.
[102] W. Alexander,et al. Suppressor screen in Mpl-/- mice: c-Myb mutation causes supraphysiological production of platelets in the absence of thrombopoietin signaling. , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[103] S. Cross,et al. Genotype-phenotype correlation of mouse pde6b mutations. , 2005, Investigative ophthalmology & visual science.
[104] R. Balling. ENU mutagenesis: analyzing gene function in mice. , 2001, Annual review of genomics and human genetics.
[105] P Chambon,et al. EMPReSS: standardized phenotype screens for functional annotation of the mouse genome , 2005, Nature Genetics.
[106] R. E. Olszewski,et al. Efficient gene-driven germ-line point mutagenesis of C57BL/6J mice , 2005, BMC Genomics.
[107] T. Shibuya,et al. The induction of recessive mutations in mouse primordial germ cells with N-ethyl-N-nitrosourea. , 1993, Mutation research.
[108] W. Frankel,et al. Three ENU-induced neurological mutations in the pore loopof sodium channel Scn8a (Nav1.6) and a genetically linkedretinal mutation, rd13 , 2004, Mammalian Genome.
[109] D. Rubinsztein. Lessons from animal models of Huntington's disease. , 2002, Trends in genetics : TIG.