Compounds > ethylnitrosourea
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ethylnitrosourea and Abnormalities, Congenital

ethylnitrosourea has been researched along with Abnormalities, Congenital in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19901 (16.67)18.7374
1990's0 (0.00)18.2507
2000's4 (66.67)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Abud, HE; Arkell, RM; Bagheri-Fam, S; Bertram, JF; Caruana, G; Cole, TJ; Dobbie, MS; Farlie, PG; Gordon, CT; Harley, VR; Hart, AH; Miller, KA; Smyth, IM; Wallace, MJ; Whittle, B1
Chen, Y; Magnuson, T; Schneider, E; Vivian, JL; Yee, D1
Anderson, KV1
Balling, R; Fella, C; Heffner, S; Hrabé de Angelis, M; Marschall, S; Pargent, W; Rathkolb, B; Soewarto, D; Teubner, A; Wolf, E1
Balling, R; Fuchs, H; Hrabé de Angelis, M; Schughart, K; Wolf, E1
Nagao, T1

Reviews

1 review(s) available for ethylnitrosourea and Abnormalities, Congenital

ArticleYear
Finding the genes that direct mammalian development : ENU mutagenesis in the mouse.
    Trends in genetics : TIG, 2000, Volume: 16, Issue:3

    Topics: Animals; Chromosome Mapping; Congenital Abnormalities; Embryonic and Fetal Development; Ethylnitrosourea; Gene Expression Regulation, Developmental; Genes; Genetic Testing; Humans; Mammals; Mice; Mice, Mutant Strains; Mutagenesis; Species Specificity

2000

Other Studies

5 other study(ies) available for ethylnitrosourea and Abnormalities, Congenital

ArticleYear
Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.
    PloS one, 2013, Volume: 8, Issue:3

    Topics: Alleles; Animals; Congenital Abnormalities; Disease Models, Animal; DNA Ligase ATP; DNA Ligases; Ethylnitrosourea; Exome; Extracellular Matrix Proteins; Female; Genome-Wide Association Study; Genotype; Germ-Line Mutation; High-Throughput Nucleotide Sequencing; Homozygote; Left-Right Determination Factors; Male; Mice; Mice, Inbred C57BL; Mutagenesis; Mutagens; Phenotype; Polymorphism, Single Nucleotide

2013
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.
    Proceedings of the National Academy of Sciences of the United States of America, 2002, Nov-26, Volume: 99, Issue:24

    Topics: Alleles; Amino Acid Substitution; Animals; Blastocyst; Chimera; Codon; Congenital Abnormalities; Crosses, Genetic; DNA-Binding Proteins; Ethylnitrosourea; Fetal Death; Fetal Heart; Genes; Genes, Dominant; Genes, Lethal; Genetic Testing; Genotype; Mice; Mice, Inbred C57BL; Mutagenesis; Mutation; Pericardium; Point Mutation; Protein Structure, Tertiary; RNA Splicing; Sequence Deletion; Smad2 Protein; Smad4 Protein; Stem Cells; Trans-Activators

2002
The large-scale Munich ENU-mouse-mutagenesis screen.
    Mammalian genome : official journal of the International Mammalian Genome Society, 2000, Volume: 11, Issue:7

    Topics: Animals; Chromosome Mapping; Congenital Abnormalities; Databases, Factual; Disease Models, Animal; Ethylnitrosourea; Genetic Diseases, Inborn; Genetic Testing; Human Genome Project; Internet; Mice; Mice, Mutant Strains; Mutagenesis; Mutagens

2000
Screening for dysmorphological abnormalities--a powerful tool to isolate new mouse mutants.
    Mammalian genome : official journal of the International Mammalian Genome Society, 2000, Volume: 11, Issue:7

    Topics: Animals; Congenital Abnormalities; Crosses, Genetic; Disease Models, Animal; Ethylnitrosourea; Female; Genetic Testing; Internet; Male; Mice; Mice, Inbred Strains; Mutagenesis; Mutagens; Mutation; Phenotype

2000
Congenital defects in the offspring of male mice treated with ethylnitrosourea.
    Mutation research, 1988, Volume: 202, Issue:1

    Topics: Animals; Congenital Abnormalities; Ethylnitrosourea; Female; Fetal Death; Male; Mice; Mice, Inbred ICR; Pregnancy; Spermatogonia; Spermatozoa

1988