Page last updated: 2024-08-21

ethylnitrosourea and Tyrosinemias

ethylnitrosourea has been researched along with Tyrosinemias in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	1 (50.00)	18.2507
2000's	1 (50.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Al-Dhalimy, M; Finegold, M; Grompe, M; Manning, K	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 Tyrosinemias

Article	Year
In vivo suppressor mutations correct a murine model of hereditary tyrosinemia type I. Proceedings of the National Academy of Sciences of the United States of America, 1999, Oct-12, Volume: 96, Issue:21 Topics: Acetoacetates; Alanine Transaminase; Animals; Cloning, Molecular; Crosses, Genetic; Disease Models, Animal; Ethylnitrosourea; Gene Conversion; Gene Deletion; Genotype; Heterozygote; Liver; Loss of Heterozygosity; Mice; Mice, Knockout; Models, Genetic; Mutagenesis; Precancerous Conditions; Reverse Transcriptase Polymerase Chain Reaction; Suppression, Genetic; Tyrosine; Tyrosinemias	1999
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

In vivo suppressor mutations correct a murine model of hereditary tyrosinemia type I.

Proceedings of the National Academy of Sciences of the United States of America, 1999, Oct-12, Volume: 96, Issue:21

Topics: Acetoacetates; Alanine Transaminase; Animals; Cloning, Molecular; Crosses, Genetic; Disease Models, Animal; Ethylnitrosourea; Gene Conversion; Gene Deletion; Genotype; Heterozygote; Liver; Loss of Heterozygosity; Mice; Mice, Knockout; Models, Genetic; Mutagenesis; Precancerous Conditions; Reverse Transcriptase Polymerase Chain Reaction; Suppression, Genetic; Tyrosine; Tyrosinemias

1999

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