نتایج جستجو برای: buserelin

تعداد نتایج: 226  

Journal: :Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2007
Sigrid Nyberg Torbjörn Bäckström Elisabeth Zingmark Robert H Purdy Inger Sundström Poromaa

BACKGROUND Neurosteroids such as allopregnanolone and pregnanolone are suggested to be of importance for the pathophysiology of premenstrual dysphoric disorder. The aim of this study was to investigate whether the luteal-phase serum concentrations of these neurosteroids are associated with improvement of premenstrual symptoms in 12 women with severe premenstrual syndrome after treatment with lo...

Journal: :British medical journal 1985
J Waxman A Man W F Hendry H N Whitfield G M Besser R C Tiptaft A M Paris R T Oliver

Left ventricular thrombi seen by ventriculography are a significant risk factor for stroke in open-heart surgery. Nature of deposits in a tubular membrane oxygenator after prolonged extracorporeal circulation: a scanning electromicroscopy study. the microcirculation of the cerebral cortex of dogs subjected to pulsatile and non-pulsatile flow during extracorporeal circulation. In: A propos du de...

Journal: :Molecular endocrinology 1998
X Lin J A Janovick S Brothers M Blömenrohr J Bogerd P M Conn

Mammalian GnRH receptor (GnRHR) is unique among G protein-coupled seven-transmembrane segment receptors due to the absence of an intracellular C-terminal tail frequently important for internalization and/or desensitization of other G protein-coupled receptors. The recent cloning of nonmammalian (i.e. catfish, goldfish, frog, and chicken) GnRHRs shows that these contain an intracellular C termin...

Journal: :Theriogenology 2011
J S Vicente R Lavara F Marco-Jiménez M P Viudes-de-Castro

The study evaluated a seminal effect on the ability to induce ovulation of a synthetic GnRH analogue, buserelin acetate, administered by vaginal mucosa in rabbit does. In a first experiment, 751 receptive nulliparous and multiparous non-lactating does were randomly assigned to groups of different seminal doses (6, 12, 24, 50, and 100 million total sperm in 0.5 mL). All seminal doses contained 5...

2017
Marie-Laure Calvez Nathalie Benz Florentin Huguet Aude Saint-Pierre Elise Rouillé Christelle Coraux Claude Férec Mathieu Kerbiriou Pascal Trouvé

Cystic fibrosis (CF) is the most common autosomal recessive disease in Caucasians caused by mutations in the gene encoding the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) chloride (Cl-) channel regulated by protein kinases, phosphatases, divalent cations and by protein-protein interactions. Among protein-protein interactions, we previously showed that Annexin A5 (AnxA5) binds to ...

Journal: :European journal of endocrinology 1998
Y Katsuki Y Takano Y Futamura Y Shibutani D Aoki Y Udagawa S Nozawa

OBJECTIVE Dienogest, a synthetic steroid with progestational activity, is used as a component of oral contraceptives and is currently being evaluated clinically for the treatment of endometriosis. The present study was conducted to confirm the effects of dienogest on experimental endometriosis in rats and to elucidate its mechanism of action. DESIGN Experimental endometriosis induced by autot...

Journal: :Indian journal of physiology and pharmacology 1994
B Coksevim M Tayyar

The spontaneous contractions of the rabbit uterine horns and the human myometrial strips were stimulated by oxytocin and buserelin acetate in isolated preparations. Spironolactone application to these models produced inhibitory effects on the contractions. It is concluded that spironolactone has inhibitory effect on the rabbit uterine horn and the human myometrial strip contractions.

2015
Céline Pirard Ernest Loumaye Pascale Laurent Christine Wyns

Background. The aim of this pilot study was to evaluate intranasal buserelin for luteal phase support and compare its efficacy with standard vaginal progesterone in IVF/ICSI antagonist cycles. Methods. This is a prospective, randomized, open, parallel group study. Forty patients underwent ovarian hyperstimulation with human menopausal gonadotropin under pituitary inhibition with gonadotropin-re...

Journal: :Biosensors & bioelectronics 2016
I Nederpelt R D Vergroesen A P IJzerman L H Heitman

The gonadotropin-releasing hormone (GnRH) receptor is a drug target for certain hormone-dependent diseases such as prostate cancer. In this study, we examined the activation profiles of the endogenous ligand, GnRH and a well-known marketed analog, buserelin using a label-free assay in pituitary αT3-1 cells with endogenous GnRH receptor expression. This whole cell impedance-based technology allo...

Journal: :The Journal of endocrinology 2010
Massimo Zerani Francesco Parillo Gabriele Brecchia Gabriella Guelfi Cecilia Dall'Aglio Lorena Lilli Margherita Maranesi Anna Gobbetti Cristiano Boiti

The expression of type I GNRH receptor (GNRHR-I) and the direct role of GNRH-I on corpora lutea (CL) function were studied in the pseudopregnant rabbit model. Immunohistochemistry evidenced GNRHR-I and GNRH-I in luteal cells at early (day 4 pseudopregnancy)-, mid (day 9)-, and late (day 13)-luteal stages. Real-time RT-PCR and western blotting revealed GNRHR-I mRNA and protein at the three lutea...

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