arginine has been researched along with Klein Syndrome in 2 studies
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 | Studies |
---|---|
Lai, CC; Lai, IL; Lin, PL; Wu, TF; Yang, WM; Yao, YL | 1 |
Beier, DR; Cockroft, JL; Goldowitz, D; Matera, I; Moran, JL; Pavan, WJ | 1 |
2 other study(ies) available for arginine and Klein Syndrome
Article | Year |
---|---|
Loading of PAX3 to Mitotic Chromosomes Is Mediated by Arginine Methylation and Associated with Waardenburg Syndrome.
Topics: Animals; Arginine; Chromosomes, Human; HEK293 Cells; Humans; Larva; Methylation; Mitosis; Paired Box Transcription Factors; PAX3 Transcription Factor; Protein-Arginine N-Methyltransferases; Waardenburg Syndrome; Zebrafish | 2015 |
A mouse model of Waardenburg syndrome type IV resulting from an ENU-induced mutation in endothelin 3.
Topics: Animals; Arginine; Chromosome Mapping; Disease Models, Animal; Endothelin-3; Ethylnitrosourea; Gene Expression Regulation; Genetic Linkage; Histidine; Humans; Mice; Mutation; Pigmentation; Point Mutation; Waardenburg Syndrome | 2007 |