Page last updated: 2024-08-17

histidine and Cushing Syndrome

histidine has been researched along with Cushing Syndrome 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
Bertherat, J; Boikos, S; Giatzakis, C; Greene, E; Horvath, A; Libè, R; Nesterova, M; Osorio, P; Patronas, Y; Remmers, E; Robinson-White, A; Stratakis, CA; Tsang, K	1

Other Studies

1 other study(ies) available for histidine and Cushing Syndrome

Article	Year
A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex. European journal of human genetics : EJHG, 2008, Volume: 16, Issue:10 Topics: 3',5'-Cyclic-AMP Phosphodiesterases; Adolescent; Adrenal Cortex; Adrenal Cortex Diseases; Adrenal Cortex Neoplasms; Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Animals; Base Sequence; Child; Child, Preschool; Conserved Sequence; Cushing Syndrome; Female; Histidine; Humans; Infant; Isoenzymes; Male; Mice; Molecular Sequence Data; Mutation; Pedigree; Proline	2008

Article

Year

A cAMP-specific phosphodiesterase (PDE8B) that is mutated in adrenal hyperplasia is expressed widely in human and mouse tissues: a novel PDE8B isoform in human adrenal cortex.

European journal of human genetics : EJHG, 2008, Volume: 16, Issue:10

Topics: 3',5'-Cyclic-AMP Phosphodiesterases; Adolescent; Adrenal Cortex; Adrenal Cortex Diseases; Adrenal Cortex Neoplasms; Adrenal Hyperplasia, Congenital; Amino Acid Sequence; Animals; Base Sequence; Child; Child, Preschool; Conserved Sequence; Cushing Syndrome; Female; Histidine; Humans; Infant; Isoenzymes; Male; Mice; Molecular Sequence Data; Mutation; Pedigree; Proline

2008