Zobrazeno 1 - 10
of 455
pro vyhledávání: '"LHCGR"'
Autor:
Rohit Barnabas, Swati Jadhav, Anurag Ranjan Lila, Sirisha Kusuma Boddu, Saba Samad Memon, Sneha Arya, Samiksha Chandrashekhar Hegishte, Manjiri Karlekar, Virendra A Patil, Vijaya Sarathi, Nalini S Shah, Tushar Bandgar
Publikováno v:
Endocrine Connections, Vol 13, Iss 11, Pp 1-11 (2024)
Background: The data on Leydig cell hypoplasia (LCH) resulting from biallelic Luteinizing hormone/chorionic gonadotropin receptor (LHCGR) inactivating variants is limited to case series. Methods: We aim to describe our patients and perform systematic
Externí odkaz:
https://doaj.org/article/0c84a8f16afb46e9a6732b9c23a31184
Autor:
Jayesh Amin, Naga Sandhya Alle, Ami Patel, Bansi Prajapathi, Paresh Makwana, Jaya Prakash, Kota Murali Krishna
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 22, Iss 7, Pp 539-552 (2024)
Abstract Background: Follicle-stimulating hormone receptor (FSHR) and luteinizing hormone/choriogonadotropin receptor (LHCGR) are integral to ovarian function, facilitating follicle development and maturation through their respective hormonal interac
Externí odkaz:
https://doaj.org/article/3904372f12074d62a63bb722ccf608e3
Publikováno v:
Journal of Basic and Applied Zoology, Vol 85, Iss 1, Pp 1-14 (2024)
Abstract Background PCOS is a serious endocrine-metabolic condition characterized by hyperandrogenemia, anovulation, or oligo-ovulation, and links to obesity, insulin resistance, and an elevated risk of type 2 diabetes mellitus. The pathophysiology o
Externí odkaz:
https://doaj.org/article/f13e89c1bd644afda294ec35be5e02b9
Akademický článek
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Publikováno v:
Annals of Pediatric Endocrinology & Metabolism, Vol 29, Iss 1, Pp 60-66 (2024)
Familial male-limited precocious puberty (FMPP) is a rare form of gonadotropin-independent precocious puberty that is caused by an activating mutation of the LHCGR gene. Herein, we report a case of FMPP with a mutation of the LHCGR gene in a Korean b
Externí odkaz:
https://doaj.org/article/ea4bdcbba66943119a49084e047d440d
Autor:
N. A. Oohayyed, M. M. Mohammed, A. M. Al-Rahim, R. N. Al Chalabi, S. A. Shaban, A. A. J. Suleiman
Publikováno v:
Акушерство, гинекология и репродукция, Vol 17, Iss 5, Pp 607-624 (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
Externí odkaz:
https://doaj.org/article/07684dbf423b4cfea9f8d1e083928457
Autor:
Silke Wemmert, Martina Pyrski, Lukas Pillong, Maximilian Linxweiler, Frank Zufall, Trese Leinders-Zufall, Bernhard Schick
Publikováno v:
Cells, Vol 13, Iss 14, p 1217 (2024)
Juvenile angiofibroma (JA) is a rare, sex-specific, and highly vascularized nasal tumor that almost exclusively affects male adolescents, but its etiology has been controversial. The G protein-coupled hormone receptor LHCGR [luteinizing hormone (LH)/
Externí odkaz:
https://doaj.org/article/4e5fbf4754444d30a97f395f6cc0417f
Publikováno v:
Journal of Ovarian Research, Vol 16, Iss 1, Pp 1-11 (2023)
Abstract Background The concentration of human chorionic gonadotropin (hCG)/ luteinizing hormone (LH) after triggering is generally accepted as a predictor of the normal ovarian response to the trigger, but few studies have explored the distribution
Externí odkaz:
https://doaj.org/article/7ab9d295147142f88c5487a12bd7018a
Autor:
Yktiyar Sarybayev, Yessengali Ussenbekov, Orynbassar Turebekov, Bekbolat Bekbolat, Ibragim Tutkyshbay
Publikováno v:
Open Veterinary Journal, Vol 13, Iss 3, Pp 352-357 (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 g
Externí odkaz:
https://doaj.org/article/fded58b99fb64dd18c42f750dc9503b9
Publikováno v:
BMC Endocrine Disorders, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Polycystic ovary syndrome (PCOS) is an endocrine-metabolic disorder that affects women at their child bearing age. The exact etiology is uncertain, however the involvement of multiple genes and environmental interactions has been
Externí odkaz:
https://doaj.org/article/ab011c3482f647e1a743805f9d5de359