Page last updated: 2024-08-17

cycloheximide and Adrenal Cortex Diseases

cycloheximide has been researched along with Adrenal Cortex Diseases in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	1 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bertagna, X; Bertherat, J; Boikos, S; Carney, JA; Cephise-Velayoudom, FL; Chanson, P; Conte-Devolx, B; Gentil, A; Groussin, L; Horvath, A; Jullian, E; Lefebvre, H; Lucas, M; Malchoff, CD; Rene-Corail, F; Stratakis, CA; Tissier, F; Vantyghem, MC	1

Other Studies

1 other study(ies) available for cycloheximide and Adrenal Cortex Diseases

Article	Year
A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds. The Journal of clinical endocrinology and metabolism, 2006, Volume: 91, Issue:5 Topics: Adolescent; Adrenal Cortex Diseases; Adult; Cells, Cultured; Cushing Syndrome; Cyclic AMP-Dependent Protein Kinase RIalpha Subunit; Cyclic AMP-Dependent Protein Kinases; Cycloheximide; DNA; Female; Founder Effect; Genotype; Haplotypes; Humans; Introns; Male; Mutation; Pedigree; Penetrance; Phenotype; Protein Synthesis Inhibitors; RNA, Messenger	2006

Article

Year

A PRKAR1A mutation associated with primary pigmented nodular adrenocortical disease in 12 kindreds.

The Journal of clinical endocrinology and metabolism, 2006, Volume: 91, Issue:5

Topics: Adolescent; Adrenal Cortex Diseases; Adult; Cells, Cultured; Cushing Syndrome; Cyclic AMP-Dependent Protein Kinase RIalpha Subunit; Cyclic AMP-Dependent Protein Kinases; Cycloheximide; DNA; Female; Founder Effect; Genotype; Haplotypes; Humans; Introns; Male; Mutation; Pedigree; Penetrance; Phenotype; Protein Synthesis Inhibitors; RNA, Messenger

2006