proline has been researched along with pregnenolone in 2 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (50.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Harikrishna, JA; Jones, KL; Lin, D; Miller, WL; Moore, CC | 1 |
Achermann, JC; Flück, CE; Leheup, B; Mallet, D; Maret, A; Morel, Y; Mullis, PE; Portrat-Doyen, S; Theintz, GE | 1 |
2 other study(ies) available for proline and pregnenolone
Article | Year |
---|---|
Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.
Topics: Adolescent; Adrenal Hyperplasia, Congenital; Alleles; Base Sequence; Blotting, Northern; Blotting, Southern; Chromatography, Thin Layer; DNA; Electrophoresis, Polyacrylamide Gel; Female; Homozygote; Humans; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Polymerase Chain Reaction; Pregnenolone; Progesterone; Proline; RNA; Serine; Steroid 17-alpha-Hydroxylase | 1991 |
A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of Swiss ancestry with congenital lipoid adrenal hyperplasia.
Topics: Adrenal Hyperplasia, Congenital; DNA Mutational Analysis; Female; Humans; Infant; Leucine; Microsatellite Repeats; Mutation, Missense; Pedigree; Phosphoproteins; Pregnenolone; Proline; Switzerland | 2005 |