arginine has been researched along with Crigler Najjar Syndrome in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Emi, Y; Ohnishi, A | 1 |
| Bamba, T; Doida, Y; Fujiyama, Y; Sato, H; Yamamoto, K | 1 |
| Capel, L; Francoual, J; Gottrand, F; Khrouf, N; Labrune, P; Le Bihan, B; Lindenbaum, A; Mokrani, C; Myara, A; Rivierre, A | 1 |
3 other study(ies) available for arginine and Crigler Najjar Syndrome
| Article | Year |
|---|---|
Rapid proteasomal degradation of translocation-deficient UDP-glucuronosyltransferase 1A1 proteins in patients with Crigler-Najjar type II.
Topics: Animals; Arginine; Cell Membrane; COS Cells; Crigler-Najjar Syndrome; Cysteine Endopeptidases; Endoplasmic Reticulum; Female; Glucuronosyltransferase; Glycoside Hydrolases; Humans; Leucine; Middle Aged; Multienzyme Complexes; Mutation; Plasmids; Precipitin Tests; Protease Inhibitors; Proteasome Endopeptidase Complex; Protein Sorting Signals; Protein Transport; Time Factors; Transfection; Trypsin | 2003 |
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II.
Topics: Animals; Arginine; Aspartic Acid; Blotting, Western; COS Cells; Crigler-Najjar Syndrome; Enzyme Activation; Gilbert Disease; Glucuronosyltransferase; Glycine; Homozygote; Humans; Mutation, Missense; Phenotype; Transfection; Tyrosine | 1998 |
Crigler-Najjar syndrome type I in Tunisia may be associated with a founder effect related to the Q357R mutation within the UGT1 gene.
Topics: Amino Acid Substitution; Arginine; Crigler-Najjar Syndrome; Founder Effect; Glutamine; Humans; Monosaccharide Transport Proteins; Mutation; Tunisia | 2002 |