Page last updated: 2024-08-21

ethylnitrosourea and Chronic Illness

ethylnitrosourea has been researched along with Chronic Illness in 2 studies

Research

Studies (2)

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

Authors	Studies
Ball, G; Bhutta, MF; Brown, SDM; Burton, MJ; Crompton, M; Dean, CH; Gale, R; Hardisty-Hughes, RE; Mallon, AM; Parker, A; Purnell, T; Simon, MM; Tateossian, H; Tyrer, HE; Wells, S; Williams, D	1
Aponte, JL; Carpenter, DA; Culiat, CT; Dhar, MS; Hauser, LJ; Johnson, DK; Rinchik, EM; Sega, GA; Withrow, CM	1

Other Studies

2 other study(ies) available for ethylnitrosourea and Chronic Illness

Article	Year
A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways. PLoS genetics, 2017, Volume: 13, Issue:8 Topics: Alleles; Animals; Chromosome Mapping; Chronic Disease; Disease Models, Animal; Ear, Middle; Ethylnitrosourea; Female; Genotyping Techniques; Heterozygote; Homozygote; Humans; Imidazoline Receptors; Inflammation; Integrin alpha6; Intracellular Signaling Peptides and Proteins; Lim Kinases; Male; Mice; Mice, Knockout; Mutation, Missense; Neuropeptides; NF-kappa B; Otitis Media; p21-Activated Kinases; Penetrance; rac1 GTP-Binding Protein; Sequence Analysis, DNA; Up-Regulation; Vascular Endothelial Growth Factor A	2017
Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1. Proceedings of the National Academy of Sciences of the United States of America, 2001, Jan-16, Volume: 98, Issue:2 Topics: Acute Disease; Alleles; Amino Acid Substitution; Animals; Animals, Newborn; Base Sequence; Biomarkers; Chronic Disease; Crosses, Genetic; DNA, Complementary; Enzyme Induction; Ethylnitrosourea; Exons; Female; Frameshift Mutation; Genes; Genes, Lethal; Heptanoates; Humans; Hydrolases; Kidney; Liver; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Models, Animal; Molecular Sequence Data; Mutagenesis; Mutation, Missense; Point Mutation; RNA Splicing; RNA, Messenger; Tyrosinemias	2001

Article

Year

A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways.

PLoS genetics, 2017, Volume: 13, Issue:8

Topics: Alleles; Animals; Chromosome Mapping; Chronic Disease; Disease Models, Animal; Ear, Middle; Ethylnitrosourea; Female; Genotyping Techniques; Heterozygote; Homozygote; Humans; Imidazoline Receptors; Inflammation; Integrin alpha6; Intracellular Signaling Peptides and Proteins; Lim Kinases; Male; Mice; Mice, Knockout; Mutation, Missense; Neuropeptides; NF-kappa B; Otitis Media; p21-Activated Kinases; Penetrance; rac1 GTP-Binding Protein; Sequence Analysis, DNA; Up-Regulation; Vascular Endothelial Growth Factor A

2017

Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1.

Proceedings of the National Academy of Sciences of the United States of America, 2001, Jan-16, Volume: 98, Issue:2

Topics: Acute Disease; Alleles; Amino Acid Substitution; Animals; Animals, Newborn; Base Sequence; Biomarkers; Chronic Disease; Crosses, Genetic; DNA, Complementary; Enzyme Induction; Ethylnitrosourea; Exons; Female; Frameshift Mutation; Genes; Genes, Lethal; Heptanoates; Humans; Hydrolases; Kidney; Liver; Male; Mice; Mice, Inbred BALB C; Mice, Inbred C3H; Mice, Inbred C57BL; Mice, Mutant Strains; Models, Animal; Molecular Sequence Data; Mutagenesis; Mutation, Missense; Point Mutation; RNA Splicing; RNA, Messenger; Tyrosinemias

2001