tyrosine and ethylnitrosourea

tyrosine has been researched along with ethylnitrosourea 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	0 (0.00)	29.6817
2010's	1 (50.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Al-Dhalimy, M; Finegold, M; Grompe, M; Manning, K	1
Gekakis, N; Lloyd, DJ; Wheeler, MC	1

Other Studies

2 other study(ies) available for tyrosine and ethylnitrosourea

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
A point mutation in Sec61alpha1 leads to diabetes and hepatosteatosis in mice. Diabetes, 2010, Volume: 59, Issue:2 Topics: Amino Acid Substitution; Animals; Diabetes Mellitus; DNA Primers; Ethylnitrosourea; Fatty Liver; Heterozygote; Histidine; Homozygote; Humans; Immunohistochemistry; Islets of Langerhans; Liver; Membrane Proteins; Mice; Mice, Inbred C57BL; Mutagenesis; Pancreas; Phenotype; Point Mutation; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; SEC Translocation Channels; Tyrosine	2010

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

A point mutation in Sec61alpha1 leads to diabetes and hepatosteatosis in mice.

Diabetes, 2010, Volume: 59, Issue:2

Topics: Amino Acid Substitution; Animals; Diabetes Mellitus; DNA Primers; Ethylnitrosourea; Fatty Liver; Heterozygote; Histidine; Homozygote; Humans; Immunohistochemistry; Islets of Langerhans; Liver; Membrane Proteins; Mice; Mice, Inbred C57BL; Mutagenesis; Pancreas; Phenotype; Point Mutation; Reverse Transcriptase Polymerase Chain Reaction; Risk Factors; SEC Translocation Channels; Tyrosine

2010