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The reduced fertilisation and pregnancy rate was associated with a lower LH receptor density and a lack of essential down-regulation of the FSH (zeige BRD2 ELISA Kits) and LH receptor.
This work demonstrates that the expression of FSHR (zeige FSHR ELISA Kits) and LHCGR can be induced in hGL5 cells but that the FSHR (zeige FSHR ELISA Kits)-dependent cAMP/PKA pathway is constitutively silenced, possibly to protect cells from FSHR (zeige FSHR ELISA Kits)-cAMP-PKA-induced apoptosis.
Inactivating mutations of the LHCGR gene may be a common cause of 46,XY primary amenorrhea.
data demonstrate that the majority of LHR mutations lead to intracellular retention and highlight the potential for novel pharmacological chaperone therapeutics that can "rescue" expression/function of retained mutant GPCRs.
expression and activation of LHCGR and ARF6 (zeige ARF6 ELISA Kits) are up-regulated in GC from PCOS women but the mechanism of agonist-induced LHCGR internalization is unaltered
We showed that GNRHR and LHCGR were highly expressed in some wildtype aldosterone-producing adenoma samples, and that they positively correlated with GnRH-stimulated aldosterone production.
Mutation in the LHCGR gene is associated with Testotoxicosis.
The luteinizing hormone/human chorionic gonadotrophin receptor (LHCGR) variant N312S and the follicle-stimulating hormone receptor (FSHR (zeige FSHR ELISA Kits)) variant N680S can be utilized for the prediction of pregnancy chances in women undergoing IVF (zeige SCN5A ELISA Kits).
Data indicate two patients with peripheral precocious puberty and an activating mutation in the luteinizing hormone (LH))/choriogonadotropin receptor (LHCGR) gene.
LHbeta (zeige LHB ELISA Kits) G1052A and LHCGR G935A genes polymorphisms are associated with increased risk of polycystic ovary syndrome in Egyptian women especially in obese cases.
Study tested for the first time a role of ZFP36L2 (zeige ZFP36L2 ELISA Kits) in the decay of LHR mRNA, when transcription was inhibited; results of our cell-based assay support the conclusion that LHR mRNA expression is controlled post-transcriptionally by ZFP36L2 (zeige ZFP36L2 ELISA Kits).
FSHR (zeige FSHR ELISA Kits) and LHR proteins are significantly upregulated in CCs (zeige CCS ELISA Kits) surrounding oocytes arrested at the 2-cell stage, reflecting their developmental incompetence.
Triptorelin and cetrorelix induce immune responses and affect uterine development and expressions of genes and proteins of ESR1 (zeige ESR1 ELISA Kits), LHR, and FSHR (zeige FSHR ELISA Kits)
Data suggest that persistent cAMP signals from internalized luteinizing hormone receptor (LH receptors) contribute to transmitting LH effects inside follicle cells and ultimately to the oocyte.
Demonstrate the presence of LH receptors. Activation resulted in a dose-dependent increase in glucose-induced release of insulin (zeige INS ELISA Kits).
LHCGR signaling in regulating the Ahr (zeige AHR ELISA Kits) message involves protein kinase A pathway and is attributable to decreased transcription rate.
Data from mutant mouse strain (gain-of-function mutation in LHR, D578G; most common mutation found in familial male-limited precocious puberty) confirm that LHR is critical for male steroidogenesis, gametogenesis, and Leydig cell development.
LH/hCG (zeige CGA ELISA Kits) tightly up-regulates MKP-3 (zeige DUSP6 ELISA Kits) which in turn, dephosphorylates ERK1/2 (zeige MAPK1/3 ELISA Kits) and drives p21 expression.
Data suggest that Lhcgr in endometrium and luteinizing hormone in blastocyst are involved in embryo/blastocyst implantation; expression of Lhcgr is up-regulated in endometrial epithelium in estrus cycle at time of implantation readiness (estrus).
Through the LHR, LH/hCG (zeige CGA ELISA Kits) tightly regulates MKP-2 (zeige DUSP4 ELISA Kits) expression, which modulates the induction of CYP11A1 (zeige CYP11A1 ELISA Kits) by 8Br-cAMP.
The outcomes of the present study support a dynamic multi-facetted regulation of LHR during pre-translation.
expression of LHR mRNA in bovine granulosa cells is established after follicle deviation, and the lower abundance of LRBP (zeige MVK ELISA Kits) mRNA after the expected time of deviation may contribute to greater expression of LHR in the bovine dominant follicle
These results suggested an acute regulation of INSL3 (zeige INSL3 ELISA Kits) by luteinizing hormone (LH) because INSL3 (zeige INSL3 ELISA Kits) concentrations increased immediately after endogenous and exogenous LH stimulation.
INVESTIGATION OF STAT5A (zeige STAT5A ELISA Kits), FSHR (zeige FSHR ELISA Kits) AND LHR GENE POLYMORPHISMS IN TURKISH INDIGENOUS CATTLE BREEDS
These findings strongly support the concept that IGF-1 (zeige IGF1 ELISA Kits) upregulates LHR expression in granulosa cells and that IGF-1 (zeige IGF1 ELISA Kits) is required for determining which follicle becomes dominant and acquires ovulatory capacity.
LHCGR mRNA expression in granulosa cells was significantly higher in large antral follicles than in cysts, and not detected in granulosa cells of small and medium antral follicles.
The luteinizing hormone receptor [LHR] splicing pattern is complex in bovine Leydig cells, and expression of full-length LHR and isoforms A and B changes when induced with LH.
The LHCGR gene is a potential marker for superovulation response and can be used to predict the most appropriate dose of FSH (zeige BRD2 ELISA Kits) for superovulation in Chinese Holstein cows.
Dominant follicles experience a reduction in FSH (zeige BRD2 ELISA Kits) dependence (diminished expression of FSHR (zeige FSHR ELISA Kits)), but acquire increased LH dependence (enhanced expression of LHCGR) as they grow during the low FSH (zeige BRD2 ELISA Kits) milieu of follicular waves.
Three single nucleotide polymorphisms in LHCGR were significantly associated with variations in cattle fertility and production traits.
Data show that double mutation of follicle-stimulating hormone receptor (fshr (zeige FSHR ELISA Kits)) and luteinizing hormone receptor (lhcgr) resulted in infertile males
Data show for the first time in a vertebrate species that Leydig cells as well as Sertoli cells express the mRNAs for both fshr (zeige FSHR ELISA Kits) and lhcgr.
In porcine ovaries, MAb found 6 distinct LHR bands migrating at approximately 92, 80, 68, 59, 52 & 48 kDa. There is a possible role for LHR in the development of abnormal pregnancy, pelvic floor disorders & Alzheimer's disease.
This gene encodes the receptor for both luteinizing hormone and choriogonadotropin. This receptor belongs to the G-protein coupled receptor 1 family, and its activity is mediated by G proteins which activate adenylate cyclase. Mutations in this gene result in disorders of male secondary sexual character development, including familial male precocious puberty, also known as testotoxicosis, hypogonadotropic hypogonadism, Leydig cell adenoma with precocious puberty, and male pseudohermaphtoditism with Leydig cell hypoplasia.
, lutropin-choriogonadotropic hormone receptor
, lutropin/choriogonadotropin receptor
, luteinizing hormone receptor
, LH receptor
, luteinizing hormone receptor 2 protein
, luteinizing hormone receptor precursor variant 1
, luteinizing hormone receptor precursor variant 2
, lutropin-choriogonadotropin receptor
, luteinizing hormone/choriogonadotropin receptor
, lutropin-choriogonadotropic hormone receptor-like