Results 1 to 10 of about 11,587 (188)

LHCGR phamacodynamic effects during follicular maturation [PDF]

open access: yesFrontiers in Endocrinology
Luteinizing hormone (LH) and human chorionic gonadotropin (hCG) are glycoprotein hormones that regulate human reproduction. Although they bind the same G protein-coupled membrane receptor (LHCGR) and have high percentage of structural identity, recent ...
Carmela Perri   +4 more
doaj   +5 more sources

Downregulation of LHCGR Attenuates COX-2 Expression and Induces Luteinized Unruptured Follicle Syndrome in Endometriosis

open access: yesFrontiers in Endocrinology, 2022
An association between endometriosis and luteinized unruptured follicle syndrome (LUFs) has long been identified. Although inactivating mutation of luteinizing hormone/choriogonadotropin receptor (LHGCR) results in LUFs, whether LHCGR contributes to ...
Zhidan Hong, Yuming Cao
exaly   +5 more sources

A case of micropenis caused by compound heterozygote mutations in luteinizing hormone/choriogonadotropin receptor (LHCGR) [PDF]

open access: yesJichu yixue yu linchuang, 2022
Objective To investigate the pathogenic gene mutations and clinical characteristics in a patient with compound heterozygote gene mutations in luteinizing hormone/choriogonadotropin receptor (LHCGR) gene.
YANG Yu-fan, ZHAO Ya-ling, WANG Xi, NIE Min, WU Xue-yan, MAO Jiang-feng
doaj   +2 more sources

The G-protein coupled estrogen receptor (GPER/GPR30) is a gonadotropin receptor dependent positive prognosticator in ovarian carcinoma patients. [PDF]

open access: yesPLoS ONE, 2013
Follicle stimulating hormone receptor (FSHR) and luteinizing hormone receptor (LHCGR) were demonstrated to impact upon survival of patients suffering from epithelial ovarian cancer (EOC).
Sabine Heublein   +6 more
doaj   +2 more sources

Genetic variants (Lhcgr W495X/+) and environmental toxicants (DEHP) synergistically induce DSD by interfering with steroidogenic gene expression [PDF]

open access: yesBiology of Sex Differences
Background Emerging evidence suggests that genetic variants and environmental toxicants may synergistically contribute to DSD. To test this hypothesis, we employed Lhcgr W495X/+ (luteinizing hormone/chorionic gonadotropin receptor) male mice subjected to
Xie Qigen   +5 more
doaj   +2 more sources

Identification of key miRNAs as regulatory biomarkers of gonadotropins leading to infertility in males

open access: yesАкушерство, гинекология и репродукция, 2023
Introduction. Infertility is a highly fatal reproductive system disorder that affects the ability of a couple to reproduce. Over the past decades, a drastic uplift has been recorded in infertility cases among males ranging from 20 to 70 % indicating ...
N. A. Oohayyed   +5 more
doaj   +1 more source

Genotyping of cows by LHCGR, FSHR loci and determination of the level of ovulation depending on the expression of the studied genes

open access: yesOpen Veterinary Journal, 2023
Background: Genotyping offers a promising avenue for identifying the healthy reproductive system in cows. The healthy reproductive system in cows is determined by measuring the level of ovulation and by identifying the type polymorphism of specific ...
Yktiyar Sarybayev   +4 more
doaj   +1 more source

Evidence for gating roles of protein kinase A and protein kinase C in estradiol-induced luteinizing hormone receptor (lhcgr) expression in zebrafish ovarian follicle cells. [PDF]

open access: yesPLoS ONE, 2013
Estradiol (E2) stimulates luteinizing hormone receptor (lhcgr) expression in zebrafish follicle cells via nuclear estrogen receptors (nERs) that are likely expressed on the membrane, and lhcgr responds to E2 in a biphasic manner during 24-h treatment ...
Ka-Cheuk Liu, Wei Ge
doaj   +1 more source

Pilot study on evaluation and determination of the prevalence of Polycystic Ovarian Syndrome (PCOS) associated gene markers in the South Indian population

open access: yesIndian Journal of Endocrinology and Metabolism, 2021
Background: Polycystic ovarian syndrome (PCOS) is typically characterized by a spectrum of manifestations that include menstrual irregularities, anovulation, cysts, hyperandrogenic features like hirsutism, acne, alopecia, and various metabolic ...
Balaji Ramanathan   +2 more
doaj   +1 more source

Mutations in a novel, cryptic exon of the luteinizing hormone/chorionic gonadotropin receptor gene cause male pseudohermaphroditism. [PDF]

open access: yesPLoS Medicine, 2008
Male pseudohermaphroditism, or Leydig cell hypoplasia (LCH), is an autosomal recessive disorder in individuals with a 46,XY karyotype, characterized by a predominantly female phenotype, a blind-ending vagina, absence of breast development, primary ...
Nina Kossack   +4 more
doaj   +1 more source

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