proline and pregnenolone

proline has been researched along with pregnenolone in 2 studies

Research

Studies (2)

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

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

Other Studies

2 other study(ies) available for proline and pregnenolone

Article	Year
Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency. The Journal of biological chemistry, 1991, Aug-25, Volume: 266, Issue:24 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. The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:9 Topics: Adrenal Hyperplasia, Congenital; DNA Mutational Analysis; Female; Humans; Infant; Leucine; Microsatellite Repeats; Mutation, Missense; Pedigree; Phosphoproteins; Pregnenolone; Proline; Switzerland	2005

Article

Year

Missense mutation serine106----proline causes 17 alpha-hydroxylase deficiency.

The Journal of biological chemistry, 1991, Aug-25, Volume: 266, Issue:24

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.

The Journal of clinical endocrinology and metabolism, 2005, Volume: 90, Issue:9

Topics: Adrenal Hyperplasia, Congenital; DNA Mutational Analysis; Female; Humans; Infant; Leucine; Microsatellite Repeats; Mutation, Missense; Pedigree; Phosphoproteins; Pregnenolone; Proline; Switzerland

2005