Results 101 to 110 of about 11,587 (188)

LHCGR Gene [PDF]

, 2020
openaire   +1 more source

LHCGR gene variants are associated with ovarian response and miscarriage risk following fresh and frozen embryo transfer

The aim of the present study was to analyze the possibility of using variants rs12470652 and rs2293275 of the LHCGR gene to predict ovarian response or pregnancy outcome in assisted reproductive technologies, including the influence of cryopreservation ...
Lomteva, S. V., Sidelnikova, I. M., Sagamonova, K. V., Lyangasova, O. V., Shkurat, T. P.   +4 more
core   +1 more source

LHCGR Missense Mutation [PDF]

, 2020
openaire   +1 more source

LHCGR wt Allele [PDF]

, 2020
openaire   +1 more source

LHCGR Gene Mutation [PDF]

, 2020
openaire   +1 more source

Genotyping FSHR and LHCGR genes enhances prediction accuracy of unexpected poor ovarian response in normo-prognosis women undergoing IVF

Egyptian Journal of Medical Human Genetics
Purpose The aim of the research was to study the association of FSHR rs6166 and LHCGR rs2293275 genetic variants, and their gene-gene interactions, with poor ovarian response in women with normal prognosis based on the POSEIDON criteria, to enable ...
Olga V. Lyangasova, Karina Y. Sagamonova, Tatiana P. Shkurat   +2 more
doaj   +1 more source

Luteinizing hormone/choriogonadotropin receptor (LHCGR; LHR) [PDF]

Science-Business eXchange, 2009
openaire   +1 more source

Phenotype-Specific Association of <i>LHCGR</i> rs13405728 Polymorphism with Anovulatory Infertility in Malay Women with Polycystic Ovary Syndrome: A Case-Control Study. [PDF]

Int J Fertil Steril
Elbadie M, Abdul Hamid H, Ahmad Z, Ling KH.   +3 more
europepmc   +1 more source

The extragonadal biology of gonadotropin hormones: should we rename these? [PDF]

Endocr Connect
Kim SM, Korkmaz F, Kang S, Sen F, Sims SL, Gimenez-Roig J, Cheliadinova U, Vasilyeva D, Barak O, Hutchison S, Macdonald A, Latif R, Goosens K, Frolinger T, Pallapati A, Rojekar S, Ryu V, Lizneva D, Yuen T, Zaidi M.   +19 more
europepmc   +1 more source

Two adult 46,XY sisters with female-like phenotype due to a novel homozygous <i>LHCGR</i> splice-site variant. [PDF]

JCEM Case Rep
Meirelles MG, Scalco RC, Marques JM, Lima Junior J, Bueno CF, Mendonca BB.   +5 more
europepmc   +1 more source