ethylnitrosourea has been researched along with Abnormalities, Multiple in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (50.00) | 29.6817 |
| 2010's | 4 (50.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hernández-García, A; Justice, MJ; Kim, BJ; Lee, B; Oghalai, JS; Pereira, FA; Scott, DA; Seymour, ML; Shchelochkov, OA; Stockton, DW; Yu, Z; Zaveri, HP | 1 |
| Bouriez-Jones, T; Bull, KR; Chaudhry, S; Cornall, RJ; Crockford, TL; Goodnow, CC; Hough, TA; Mason, T; Rimmer, AJ; Roberts, IS; Silver, KL | 1 |
| Cheng, CY; Fann, MJ; Hong, CJ; Kao, LS; Liou, YJ; Nian, FS; Tai, CY; Tsai, JW; Tsai, SJ; Wu, JC; Wu, PC | 1 |
| Abe, K; Imai, K; Ishikawa, K; Lisse, T; Lisse, TS; Mashimo, T; Sakurai, Y; Serikawa, T; Takamatsu, N; Tanimoto, S; Tsurumi, T | 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 |
| Chatterjee, B; Leatherbury, L; Lo, CW; Lucas, J; Pappas, MA; Rosenthal, J; Shen, Y; Siegfried, B; Svenson, K; Wessels, A; Yu, Q | 1 |
| Barbaric, I; Brown, SD; Cheeseman, M; Dear, TN; Hough, T; Hunter, AJ; Marusic, A; Perry, MJ; Rodrigues Da Costa, A; Salopek, D; Wells, S | 1 |
| Bergstrom, RA; Browning, VL; John, SW; Libby, B; Munroe, RJ; Schimenti, JC; Schimenti, KJ; Smith, R; Zheng, QY | 1 |
8 other study(ies) available for ethylnitrosourea and Abnormalities, Multiple
| Article | Year |
|---|---|
An allelic series of mice reveals a role for RERE in the development of multiple organs affected in chromosome 1p36 deletions.
Topics: Abnormalities, Multiple; Alleles; Animals; Body Weight; Cardiovascular Diseases; Chromosome Deletion; Chromosome Disorders; Chromosomes; Chromosomes, Human, Pair 1; Embryonic Development; Ethylnitrosourea; Hearing Loss; Hippocampus; Male; Mice; Mice, Inbred C57BL; Nerve Tissue Proteins; Neurons; Phenotype; Repressor Proteins | 2013 |
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 |
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 |
Novel ENU-Induced Mutation in Tbx6 Causes Dominant Spondylocostal Dysostosis-Like Vertebral Malformations in the Rat.
Topics: Abnormalities, Multiple; Animals; Base Sequence; Chromosome Mapping; Disease Models, Animal; DNA Mutational Analysis; Ethylnitrosourea; Female; Gene Expression Regulation; Gene Order; Genes, Dominant; Genetic Loci; Genotype; Hernia, Diaphragmatic; Male; Mutation; Phenotype; Rats; Sequence Alignment; Spine | 2015 |
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 |
Cardiovascular phenotyping of fetal mice by noninvasive high-frequency ultrasound facilitates recovery of ENU-induced mutations causing congenital cardiac and extracardiac defects.
Topics: Abnormalities, Multiple; Animals; Cardiovascular Physiological Phenomena; Ethylnitrosourea; Female; Fetus; Heart Defects, Congenital; Mice; Mutation; Pregnancy; Ultrasonography, Prenatal | 2005 |
An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Animals; Bone Density; Bone Diseases, Metabolic; Conserved Sequence; Craniofacial Abnormalities; DNA-Binding Proteins; Ethylnitrosourea; Female; Genes, Lethal; Kyphosis; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Mutant Strains; Molecular Sequence Data; Mutagenesis; Mutation, Missense; Phenotype; Point Mutation; Repressor Proteins; Sequence Alignment; Sequence Homology, Amino Acid | 2008 |
Mouse mutants from chemically mutagenized embryonic stem cells.
Topics: Abnormalities, Drug-Induced; Abnormalities, Multiple; Animals; Bone and Bones; Chimera; Ethyl Methanesulfonate; Ethylnitrosourea; Female; Genes, Lethal; Hypoxanthine Phosphoribosyltransferase; Limb Deformities, Congenital; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Mutagenesis; Mutagens; Point Mutation; Retina; RNA Splicing; Stem Cells; Testis | 2000 |