ethylnitrosourea has been researched along with Eye Abnormalities in 7 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (14.29) | 18.2507 |
| 2000's | 4 (57.14) | 29.6817 |
| 2010's | 2 (28.57) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bouriez-Jones, T; Bull, KR; Chaudhry, S; Cornall, RJ; Crockford, TL; Goodnow, CC; Hough, TA; Mason, T; Rimmer, AJ; Roberts, IS; Silver, KL | 1 |
| Budde, B; Esposito, I; Fuchs, H; Graw, J; Hrabé de Angelis, M; Löster, J; Michel-Soewarto, D; Nürnberg, P; Puk, O; Söker, T; Wolf, E | 1 |
| Ahmad, N; Calzada-Wack, J; Dalke, C; de Angelis, MH; Graw, J; Klaften, M; Puk, O; Wagner, S | 1 |
| Denny, P; Gregory-Evans, CY; Gregory-Evans, K; McKeone, R; Vieira, H | 1 |
| Adamson, SL; Anderson, N; Aubin, JE; Bai, D; Bruneau, BG; Ciliberti, N; Fleming, C; Flenniken, AM; Gittens, JE; Gong, XQ; Grynpas, M; Henderson, JE; Henkelman, RM; Kelsey, LB; Kidder, GM; Laird, DW; Lounsbury, C; McKerlie, C; Moreno, L; Nieman, BJ; Osborne, LR; Peterson, K; Qu, D; Roscoe, W; Rossant, J; Shao, Q; Sled, JG; Stanford, WL; Tong, D; Veitch, GI; Voronina, I; Vukobradovic, I; Wood, GA; Zhu, Y; Zirngibl, RA | 1 |
| Brockerhoff, SE; Dowling, JE; Driever, W; Hurley, JB; Janssen-Bienhold, U; Neuhauss, SC | 1 |
| Alexander, WS; Baird, PN; Chiu, D; Foote, SJ; Guymer, RH; Hilton, DJ; Vincent, AL | 1 |
7 other study(ies) available for ethylnitrosourea and Eye Abnormalities
| Article | Year |
|---|---|
Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome.
Topics: Abnormalities, Multiple; Animals; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Eye Abnormalities; Genetic Association Studies; Genetic Predisposition to Disease; High-Throughput Nucleotide Sequencing; Kidney Tubules; Laminin; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Mutant Strains; Mutation; Myasthenic Syndromes, Congenital; Nephrotic Syndrome; Pedigree; Phenotype; Proteinuria; Pupil Disorders | 2014 |
A new Fgf10 mutation in the mouse leads to atrophy of the harderian gland and slit-eye phenotype in heterozygotes: a novel model for dry-eye disease?
Topics: Amino Acid Sequence; Animals; Atrophy; Base Sequence; Chromosomes, Mammalian; Disease Models, Animal; Dry Eye Syndromes; Ethylnitrosourea; Eye Abnormalities; Female; Fibroblast Growth Factor 10; Genome-Wide Association Study; Harderian Gland; Heterozygote; In Situ Hybridization; Lens, Crystalline; Male; Mice; Mice, Inbred C3H; Mice, Inbred C57BL; Molecular Sequence Data; Mutation; Phenotype; Polymerase Chain Reaction; Retina | 2009 |
Reduced corneal thickness and enlarged anterior chamber in a novel ColVIIIa2G257D mutant mouse.
Topics: Alkylating Agents; Animals; Anterior Chamber; Collagen Type VIII; Cornea; Disease Models, Animal; Ethylnitrosourea; Eye Abnormalities; Female; Genetic Linkage; Immunoenzyme Techniques; In Situ Hybridization; Interferometry; Light; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Mutant Strains; Microsatellite Repeats; Mutagenesis, Site-Directed; Ophthalmoscopy; Point Mutation; Polymerase Chain Reaction; Polymorphism, Single Nucleotide; Visual Acuity | 2009 |
Foxf2: a novel locus for anterior segment dysgenesis adjacent to the Foxc1 gene.
Topics: Aging; Amino Acid Sequence; Animals; Base Sequence; Biological Specimen Banks; Cornea; DNA; Embryo, Mammalian; Ethylnitrosourea; Eye Abnormalities; Forkhead Transcription Factors; Genetic Loci; Homozygote; Iris; Mice; Molecular Sequence Data; Mutation; Phenotype; Phylogeny | 2011 |
A Gja1 missense mutation in a mouse model of oculodentodigital dysplasia.
Topics: Abnormalities, Multiple; Animals; Biomechanical Phenomena; Bone and Bones; Bone Density; Connexin 43; Craniofacial Abnormalities; Dental Enamel Hypoplasia; Disease Models, Animal; Ethylnitrosourea; Eye Abnormalities; Gap Junctions; Heart Defects, Congenital; Humans; Mice; Penetrance; Point Mutation; Stem Cells; Syndactyly | 2005 |
A behavioral screen for isolating zebrafish mutants with visual system defects.
Topics: Animals; Behavior, Animal; Crosses, Genetic; Electroretinography; Ethylnitrosourea; Eye; Eye Abnormalities; Genes, Recessive; Larva; Light; Mutagenesis; Mutation; Nystagmus, Optokinetic; Optic Nerve; Retina; Selection, Genetic; Zebrafish | 1995 |
Generating mouse models of retinal disease using ENU mutagenesis.
Topics: Animals; Breeding; Ethylnitrosourea; Eye Abnormalities; Female; Germ-Line Mutation; Male; Mice; Mice, Inbred C57BL; Models, Animal; Mutagens; Phenotype; Point Mutation; Retinal Diseases; Testis | 2002 |