software sas jmp statistical discovery v14 pro (SAS institute)
90
Structured Review
SAS institute
software sas jmp statistical discovery v14 pro
Software Sas Jmp Statistical Discovery V14 Pro, supplied by SAS institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software+sas+jmp+statistical+discovery+v14+pro/software+sas+jmp+statistical+discovery+v14+pro/pm35595151-110-20-22
Average 90 stars, based on 1 article reviews
Software Sas Jmp Statistical Discovery V14 Pro, supplied by SAS institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/software+sas+jmp+statistical+discovery+v14+pro/software+sas+jmp+statistical+discovery+v14+pro/pm35595151-110-20-22
Average 90 stars, based on 1 article reviews
software sas jmp statistical discovery v14 pro - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
Expressing:Article Title: Intracellular distribution of vinclozolin and its metabolites differently affects 5α-dihydrotestosterone (DHT)-induced PSA secretion in LNCaP cells. Article Snippet: Endocrine disruption mechanisms in prostate are an overlooked issue.. The anti-androgenic properties of the fungicide vinclozolin (VIN) and its active metabolites 2-[[(3,5dichlorophenyl)-carbamoyl]oxy]− 2-methyl-3butenoic acid (M1) and 3’5’-dichloro-2-hydroxy-2methylbut-3-enanilide (M2) were assessed on human prostate-derived cells (LNCaP); the effects were investigated also upon co-treatment with 5α-dihydrotestosterone (DHT), the physiological androgen receptor (AR)-agonist, and compared to the anti-androgenic drugs, 2-hydroxy-flutamide (2OH-FTA) and bicalutamide (BIC).. Assessed endpoints were the cellular uptake and subcellular localization of VIN, M1 and M2, DHT-induced PSA gene expression and secretion. Software:Article Title: Intracellular distribution of vinclozolin and its metabolites differently affects 5α-dihydrotestosterone (DHT)-induced PSA secretion in LNCaP cells. Article Snippet: Endocrine disruption mechanisms in prostate are an overlooked issue.. The anti-androgenic properties of the fungicide vinclozolin (VIN) and its active metabolites 2-[[(3,5dichlorophenyl)-carbamoyl]oxy]− 2-methyl-3butenoic acid (M1) and 3’5’-dichloro-2-hydroxy-2methylbut-3-enanilide (M2) were assessed on human prostate-derived cells (LNCaP); the effects were investigated also upon co-treatment with 5α-dihydrotestosterone (DHT), the physiological androgen receptor (AR)-agonist, and compared to the anti-androgenic drugs, 2-hydroxy-flutamide (2OH-FTA) and bicalutamide (BIC).. Assessed endpoints were the cellular uptake and subcellular localization of VIN, M1 and M2, DHT-induced PSA gene expression and secretion. |