Page last updated: 2024-08-17

lysine and ethylnitrosourea

lysine 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	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
Grosse, J; Nehls, MC; Peters, T; Popp, A; Russ, A; Schlueter, V; Sedlmeier, R; Thaete, C; Wolf, S	1
Chen, B; Ouyang, HL; Wang, WH; Xue, ZF; Yan, LN; Yang, B; Yin, YH	1

Other Studies

2 other study(ies) available for lysine and ethylnitrosourea

Article	Year
A mouse model for cystinuria type I. Human molecular genetics, 2003, Sep-01, Volume: 12, Issue:17 Topics: Amino Acid Sequence; Amino Acid Transport Systems, Basic; Amino Acids; Animals; Arginine; Carrier Proteins; Chromosome Mapping; Cystine; Cystinuria; Disease Models, Animal; Ethylnitrosourea; Female; Genotype; Lysine; Male; Membrane Glycoproteins; Mice; Mice, Inbred C3H; Mice, Knockout; Molecular Sequence Data; Mutagenesis; Mutation; Ornithine; Phenotype; Sequence Homology, Amino Acid; Urinary Bladder Calculi; Urinary Calculi	2003
Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line. Experimental animals, 2016, Jul-29, Volume: 65, Issue:3 Topics: Animals; Chromosomes, Human, Pair 14; Disease Models, Animal; Ethylnitrosourea; Female; Ganglia; Genetic Association Studies; Hirschsprung Disease; Humans; Intestinal Obstruction; Lysine; Male; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Mutant Strains; Mutation, Missense; Protein Domains; Receptor, Endothelin B; Receptors, G-Protein-Coupled	2016

Article

Year

A mouse model for cystinuria type I.

Human molecular genetics, 2003, Sep-01, Volume: 12, Issue:17

Topics: Amino Acid Sequence; Amino Acid Transport Systems, Basic; Amino Acids; Animals; Arginine; Carrier Proteins; Chromosome Mapping; Cystine; Cystinuria; Disease Models, Animal; Ethylnitrosourea; Female; Genotype; Lysine; Male; Membrane Glycoproteins; Mice; Mice, Inbred C3H; Mice, Knockout; Molecular Sequence Data; Mutagenesis; Mutation; Ornithine; Phenotype; Sequence Homology, Amino Acid; Urinary Bladder Calculi; Urinary Calculi

2003

Hirschsprung disease is associated with an L286P mutation in the fifth transmembrane domain of the endothelin-B receptor in the N-ethyl-N-nitrosourea-induced mutant line.

Experimental animals, 2016, Jul-29, Volume: 65, Issue:3

Topics: Animals; Chromosomes, Human, Pair 14; Disease Models, Animal; Ethylnitrosourea; Female; Ganglia; Genetic Association Studies; Hirschsprung Disease; Humans; Intestinal Obstruction; Lysine; Male; Mice, Inbred C57BL; Mice, Inbred DBA; Mice, Mutant Strains; Mutation, Missense; Protein Domains; Receptor, Endothelin B; Receptors, G-Protein-Coupled

2016