cysteine has been researched along with Adrenal Hyperplasia, Congenital in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 2 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Baj, F; DiNardo, G; Gilardi, G; Pandey, AV; Parween, S; Zhang, C | 1 |
| Chugh, V; Dutt Sharma, S; Garg, M; Mangla, A; Mitharwal, P | 1 |
| Li, J; Li, JX; Wang, YP; Zhang, DY; Zhao, YJ | 1 |
| Cingöz, S; Döneray, H; Ozkan, B; Sakizli, M | 1 |
4 other study(ies) available for cysteine and Adrenal Hyperplasia, Congenital
| Article | Year |
|---|---|
Differential effects of variations in human P450 oxidoreductase on the aromatase activity of CYP19A1 polymorphisms R264C and R264H.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Substitution; Androstenedione; Arginine; Aromatase; Cysteine; Cytochrome P-450 CYP1A1; Cytochrome P-450 Enzyme System; Enzyme Activation; Histidine; Humans; Models, Molecular; Mutation, Missense; Polymorphism, Single Nucleotide; Protein Conformation; Structure-Activity Relationship | 2020 |
Non-classical lipoid adrenal hyperplasia presenting as hypoglycemic seizures.
Topics: Adrenal Hyperplasia, Congenital; Adrenal Insufficiency; Amino Acid Substitution; Arginine; Child, Preschool; Cysteine; Diagnosis, Differential; Disorder of Sex Development, 46,XY; Female; Homozygote; Humans; Hypoglycemia; India; Mutation, Missense; Phosphoproteins; Seizures | 2020 |
Three novel CYP17A1 gene mutations (A82D, R125X, and C442R) found in combined 17α-hydroxylase/17,20-lyase deficiency.
Topics: Adrenal Hyperplasia, Congenital; Adult; Alanine; Amino Acid Substitution; Arginine; Aspartic Acid; Base Sequence; Cells, Cultured; Cysteine; Female; Humans; Mutation, Missense; Steroid 17-alpha-Hydroxylase; Young Adult | 2011 |
Familial pericentric inversion chromosome 3 and R448C mutation of CYP11B1 gene in Turkish kindred with 11beta-hydroxylase deficiency.
Topics: Adrenal Hyperplasia, Congenital; Amino Acid Substitution; Arginine; Child; Child, Preschool; Chromosome Inversion; Chromosomes, Human, Pair 3; Cysteine; DNA Mutational Analysis; Humans; Male; Mutation, Missense; Pedigree; Steroid 11-beta-Hydroxylase; Turkey | 2007 |