ethylnitrosourea has been researched along with Atrophy in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (50.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Adams, DJ; Beltran, S; Breuss, M; Dürnberger, G; Edwards, A; Flint, J; Gstrein, T; Gut, I; Gut, M; Hansen, AH; Hochstoeger, T; Honzik, T; Keane, TM; Keays, DA; Kmoch, S; Landler, L; Leca, I; Mechtler, K; Pilat-Carotta, S; Přistoupilová, A; Repic, M; Rosoklija, G; Sherr, E; Stránecký, V; Traunbauer, AK; Tripathy, R; Zuber, J | 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 |
2 other study(ies) available for ethylnitrosourea and Atrophy
| Article | Year |
|---|---|
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans.
Topics: Alkylating Agents; Animals; Animals, Newborn; Atrophy; Autophagy; Brain; Cell Movement; Disease Models, Animal; Embryo, Mammalian; Ethylnitrosourea; Female; Gene Expression Regulation, Developmental; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurodevelopmental Disorders; Neurons; Signal Transduction; Vacuolar Proton-Translocating ATPases | 2018 |
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 |