Zobrazeno 1 - 10
of 261
pro vyhledávání: '"Quinagolide"'
Autor:
Álida Alves dos Santos, Lucas Faria de Castro, Caroline Lourenço de Lima, Lucilia Domingues Casulari da Motta, Luiz Augusto Casulari Roxo da Motta, Angélica Amorim Amato
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-20 (2024)
Abstract This systematic review of clinical studies investigated whether circulating PRL levels differed between subjects with systemic lupus erythematosus (SLE) and healthy controls, the correlation between circulating PRL and SLE activity, and the
Externí odkaz:
https://doaj.org/article/427d4618a32e4b41a864eddf0161a4c5
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2024)
Externí odkaz:
https://doaj.org/article/18f0e5d2b461445088f8d9a1c6011d54
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
PurposeThree dopamine agonists [bromocriptine, cabergoline, and quinagolide (CV)] have been used for hyperprolactinemia treatment for decades. Several studies have reviewed the efficacy and safety of bromocriptine and cabergoline. However, no systema
Externí odkaz:
https://doaj.org/article/613d080dba2d4709ad87859c582967db
Akademický článek
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Publikováno v:
Animal, Vol 13, Iss , Pp s35-s41 (2019)
Accumulating evidence supports that the hormone prolactin (PRL) is galactopoietic in dairy ruminants. Accordingly, the inhibition of PRL secretion by the dopamine agonists quinagolide and cabergoline causes a sharp decline in milk production and coul
Externí odkaz:
https://doaj.org/article/f976fa0172fb472b9060c30b6c09ef1a
Publikováno v:
The Journal of Organic Chemistry. 86:9344-9352
The diastereoselective formal synthesis of (-)-quinagolide, a D2 receptor agonist, has been achieved. The synthesis started from l-pyroglutamic acid and relied on utilization of (a) a stereospecific catalytic hydrogenation and diastereoselective Horn
Autor:
Corinne Iampietro, Alessia Brossa, Stefano Canosa, Stefania Tritta, Glenn E. Croston, Torsten Michael Reinheimer, Filippo Bonelli, Andrea Roberto Carosso, Gianluca Gennarelli, Stefano Cosma, Chiara Benedetto, Alberto Revelli, Benedetta Bussolati
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 1775, p 1775 (2022)
International Journal of Molecular Sciences; Volume 23; Issue 3; Pages: 1775
International Journal of Molecular Sciences; Volume 23; Issue 3; Pages: 1775
Endometrial mesenchymal stromal cells (E-MSCs) extensively contribute to the establishment and progression of endometrial ectopic lesions through formation of the stromal vascular tissue, and support to its growth and vascularization. As E-MSCs lack
Akademický článek
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Publikováno v:
ACS Omega, Vol 4, Iss 5, Pp 8231-8238 (2019)
A potent dopamine (D2) receptor agonist (±)-quinagolide, which is used for the treatment of hyperprolactinemia, was synthesized using the ring closing metathesis (RCM) approach from meta-hydroxyben...
Publikováno v:
Neuroendocrinology. 109:34-41
The discovery of dopamine inhibitory effects on prolactin secretion has led to an era of successful dopaminergic therapy for prolactinomas. Herein we provide an overview of the evolution of dopamine agonists and their use in patients with PRL-secreti