نتایج جستجو برای: gnrh antagonist

تعداد نتایج: 64289  

Journal: :Human Reproduction 2023

Abstract Study question Can progestins be used to prevent spontaneous LH surge during ovarian stimulation (OS) without affecting the euploid blastocyst rate (EBR) per metaphase-II (MII) oocytes? Summary answer Progestin Primed Ovarian Stimulation (PPOS) (conducted with norethisterone acetate) and conventional-OS GnRH-antagonist show similar EBR MII-oocytes What is known already PPOS a novel OS ...

2015
Chow

Volume 1 | Issue 1 Abstract A monoclonal antibody (Mab) designated as GHR106 was generated against the extracellular domain (N1-29 synthetic peptide) of human gonadotropin releasing hormone (GnRH) receptor. It is a first-in-class GnRH analog and can serve as a drug candidate for potential applications in the treatment of human cancers and/or fertility regulations. Both Mabs in murine (mGHR106) ...

2006
Efstratios Kolibianakis

The recent introduction of GnRH antagonists in assisted reproductive technologies (ART) has simplified ovarian stimulation (1). This is mainly due to the immediate mode of antagonist action, which allows their administration during the follicular phase, when the inhibition of premature LH surge is required. In this way, the prolonged period of downregulation, necessary in the long agonist proto...

Journal: :Endocrinology 2006
Guillaume Galmiche Nicolas Richard Sophie Corvaisier Marie-Laure Kottler

The role of estrogens is dual: they suppress basal expression of gonadotropins and enhance GnRH responsiveness at the time of the LH surge. Estrogens are synthesized by cytochrome P450 aromatase (P450arom), encoded by the cyp19 gene. We focused on the cyp19 gene in rat and showed that it is expressed in gonadotropes through promoters PII and PI.f, using RT-PCR and dual fluorescence labeling wit...

Journal: :Human reproduction 1998
D de Jong N S Macklon B M Mannaerts H J Coelingh Bennink B C Fauser

This case report describes the first attempt to treat imminent ovarian hyperstimulation syndrome (OHSS) by using a gonadotrophin-releasing hormone (GnRH) antagonist. A 33 year old, normo-ovulatory woman undergoing in-vitro fertilization received daily subcutaneous injections of 150 IU of recombinant follicle-stimulating hormone (recFSH) from cycle day 2, together with GnRH antagonist (ganirelix...

Journal: :Journal of neuroendocrinology 1996
W G Rossmanith D L Marks R A Steiner D K Clifton

Galanin mRNA levels in GnRH neurons increase in association with a steroid-induced LH surge in female rats. Both the steroid-induced LH surge and the concomitant increase of galanin mRNA in GnRH neurons are blocked by non-specific inhibition of central nervous system activity imposed by pentobarbital and specific central alpha-adrenergic receptor blockade. Based on these observations, we hypoth...

Nikpour F, Soleimani Rad J

Background: Male factors, mainly spermatogenesis disorder, are responsible for 20-30% of infertility occurred in different societies. One of the known causes of spermatogenesis disorder is chemotherapy in patients with cancer. The side effect of chemotherapic agents may last from 10 years up to the end of the life. Since dividing cells are mainly affected by anticancer drugs, the aim of the pre...

Aghahosseini M Aleyaseen A Kashani L,

Background: Deep suppression of LH in GnRH antagonist cycles may have detrimental effect on reproductive out come. It was hypnotized that adding LH activity via the administration of low dose HCG in late follicular phase shortened the duration of stimulation, decreased consumption of gonadotropin and increased estrogen levels. This study was designed to evaluate the effect of adding low dose HC...

Mohammadi Roushandeh A Mohammadnejad D,

Background: Infertility problem affects 20-30% of young couples. One of the known causes of spermatogenesis disorder is chemotherapy in patients with cancer which its side effect may last up to the end of the life. The aim of the present study is to investigate the effect of GnRH on viability of ovarian follicles defect produced by anticancer drug. Materials and Methods: In the present study ad...

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