ethylnitrosourea has been researched along with Microphthalmia in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 2 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Cheng, CY; Fann, MJ; Hong, CJ; Kao, LS; Liou, YJ; Nian, FS; Tai, CY; Tsai, JW; Tsai, SJ; Wu, JC; Wu, PC | 1 |
| Ahmad, N; de Angelis, MH; Graw, J; Puk, O; Wagner, S | 1 |
| Favor, J; Fuchs, H; Graw, J; Haubst, N; Hrabé de Angelis, M; Löster, J; Meyer, B; Münster, D; Nürnberg, P; Pretsch, W; Puk, O; Selby, P; Soewarto, D; Wolf, E | 1 |
| Fisher, G; Loutit, JF; Marshall, MJ; Nisbet, NW; Perry, VH; West, JD | 1 |
4 other study(ies) available for ethylnitrosourea and Microphthalmia
| Article | Year |
|---|---|
ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18.
Topics: Abnormalities, Multiple; Age Factors; Animals; Axons; Cataract; Cornea; Disease Models, Animal; Endoplasmic Reticulum; Ethylnitrosourea; Eye; Hypogonadism; Intellectual Disability; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Microcephaly; Microphthalmos; Mutagenesis; Nerve Degeneration; Optic Atrophy; Optic Nerve Diseases; Psychomotor Performance; rab GTP-Binding Proteins; Sequence Deletion; Testis; Touch Perception | 2015 |
Microphakia and congenital cataract formation in a novel Lim2(C51R) mutant mouse.
Topics: Animals; Base Sequence; Cataract; Disease Models, Animal; Ethylnitrosourea; Eye; Eye Proteins; Female; Founder Effect; Genetic Linkage; Heterozygote; Homozygote; Lens, Crystalline; Male; Membrane Glycoproteins; Mice; Mice, Inbred C57BL; Microphthalmos; Molecular Sequence Data; Mutation; Polymorphism, Single Nucleotide | 2011 |
Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters.
Topics: Alleles; Amino Acid Sequence; Animals; Base Sequence; Ethylnitrosourea; Eye Proteins; Female; Fluorescent Antibody Technique, Indirect; Genes, Reporter; Homeobox Protein SIX3; Homeodomain Proteins; In Situ Hybridization; Male; Mice; Mice, Inbred C3H; Microphthalmos; Molecular Sequence Data; Mutagenesis; Mutation; Nerve Tissue Proteins; Paired Box Transcription Factors; PAX6 Transcription Factor; Phenotype; Promoter Regions, Genetic; Repressor Proteins; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger | 2005 |
A new allele of microphthalmia induced in the mouse: microphthalmia--defective iris (midi).
Topics: Alleles; Animals; Bone Resorption; Crosses, Genetic; Ethylnitrosourea; Female; Iris; Male; Mice; Mice, Mutant Strains; Microphthalmos; Mutation | 1985 |