ethylnitrosourea has been researched along with Heart Defects, Congenital in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 3 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Anderton, S; Chen, G; Devine, W; Francis, R; Kim, AJ; Kim, Y; Leatherbury, L; Liu, X; Lo, CW; Morgan, J; Pratt, HC; Ramirez, R; Reinholdt, L; Subramanian, R; Tobita, K; Wong, L | 1 |
Beier, DR; Bjork, BC; Hentges, KE; Justice, MJ; Kamp, A; Moran, J; Moskowitz, IP; Peterson, MA; Rajapaksha, TW; Seidman, CE; Seidman, JG; Svenson, KL | 1 |
Damrau, C; Dean, CH; Ermakov, A; Formstone, C; Henderson, DJ; Lalanne, Z; Lu, X; Murdoch, JN; Norris, DP; Patterson, VL; Paudyal, A; Wells, S | 1 |
Chatterjee, B; Kirby, ML; Leatherbury, L; Lo, CW; Lucas, JF; Rosenthal, J; Shen, Y; Siegfried, BH; Spurney, CF; Svenson, K; Wessels, A; Wu, YJ; Yu, Q | 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 |
6 other study(ies) available for ethylnitrosourea and Heart Defects, Congenital
Article | Year |
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Interrogating congenital heart defects with noninvasive fetal echocardiography in a mouse forward genetic screen.
Topics: Animals; Disease Models, Animal; Echocardiography, Doppler; Echocardiography, Doppler, Color; Ethylnitrosourea; Female; Fetal Heart; Genetic Predisposition to Disease; Genetic Testing; Heart Defects, Congenital; Heredity; High-Throughput Screening Assays; Male; Mice; Mice, Inbred C57BL; Microscopy, Acoustic; Mutation; Pedigree; Phenotype; Ultrasonography, Prenatal | 2014 |
Genome-wide identification of mouse congenital heart disease loci.
Topics: Animals; Animals, Newborn; Chromosome Mapping; Crosses, Genetic; Disease Models, Animal; Ethylnitrosourea; Female; Genetic Predisposition to Disease; Genetic Testing; Genome-Wide Association Study; Heart Defects, Congenital; Humans; Male; Mice; Mice, Inbred C57BL; Mice, Mutant Strains; Myocardium | 2010 |
The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear.
Topics: Animals; Cell Polarity; Disease Models, Animal; Ear, Inner; Ethylnitrosourea; Heart Defects, Congenital; Humans; Lung; Mice; Mutagenesis, Insertional; Nerve Tissue Proteins; Neural Crest; Neural Tube Defects; Receptor Protein-Tyrosine Kinases; Receptors, G-Protein-Coupled; Signal Transduction | 2010 |
ENU induced mutations causing congenital cardiovascular anomalies.
Topics: Amino Acid Sequence; Animals; Chromosomes, Mammalian; Connexin 43; DiGeorge Syndrome; Ethylnitrosourea; Female; Fetus; Heart Defects, Congenital; Limb Deformities, Congenital; Mice; Molecular Sequence Data; Mutation; T-Box Domain Proteins; Truncus Arteriosus, Persistent; Ultrasonography | 2004 |
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 |