lysine has been researched along with Hirschsprung Disease in 1 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Chen, B; Ouyang, HL; Wang, WH; Xue, ZF; Yan, LN; Yang, B; Yin, YH | 1 |
1 other study(ies) available for lysine and Hirschsprung Disease
Article | Year |
---|---|
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.
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 |