79 related articles for article (PubMed ID: 21683950)
1. Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome.
Yariz KO; Walsh T; Uzak A; Spiliopoulos M; Duman D; Onalan G; King MC; Tekin M
Fertil Steril; 2011 Aug; 96(2):e125-30. PubMed ID: 21683950
[TBL] [Abstract][Full Text] [Related]
2. Exome sequencing in genuine empty follicle syndrome: Novel candidate genes.
Lledó B; Piqueras JJ; Lozano FM; Hortal M; Morales R; Ortiz JA; Guerrero J; Benabeu A; Bernabeu R
Eur J Obstet Gynecol Reprod Biol; 2024 Jun; 297():221-226. PubMed ID: 38691974
[TBL] [Abstract][Full Text] [Related]
3. Genetic evidence of 'genuine' empty follicle syndrome: a novel effective mutation in the LHCGR gene and review of the literature.
Yuan P; He Z; Zheng L; Wang W; Li Y; Zhao H; Zhang VW; Zhang Q; Yang D
Hum Reprod; 2017 Apr; 32(4):944-953. PubMed ID: 28175319
[TBL] [Abstract][Full Text] [Related]
4. A Recurrent Missense Mutation in ZP3 Causes Empty Follicle Syndrome and Female Infertility.
Chen T; Bian Y; Liu X; Zhao S; Wu K; Yan L; Li M; Yang Z; Liu H; Zhao H; Chen ZJ
Am J Hum Genet; 2017 Sep; 101(3):459-465. PubMed ID: 28886344
[TBL] [Abstract][Full Text] [Related]
5. ZP1 mutations are associated with empty follicle syndrome: evidence for the existence of an intact oocyte and a zona pellucida in follicles up to the early antral stage. A case report.
Dai C; Chen Y; Hu L; Du J; Gong F; Dai J; Zhang S; Wang M; Chen J; Guo J; Zheng W; Lu C; Wu Y; Lu G; Lin G
Hum Reprod; 2019 Nov; 34(11):2201-2207. PubMed ID: 31734689
[TBL] [Abstract][Full Text] [Related]
6. Mitochondrial Dynamics as Potential Modulators of Hormonal Therapy Effectiveness in Males.
Errico A; Vinco S; Ambrosini G; Dalla Pozza E; Marroncelli N; Zampieri N; Dando I
Biology (Basel); 2023 Apr; 12(4):. PubMed ID: 37106748
[TBL] [Abstract][Full Text] [Related]
7. Hinge region mediates signal transmission of luteinizing hormone and chorionic gonadotropin receptor.
He X; Duan J; Ji Y; Zhao L; Jiang H; Jiang Y; Eric Xu H; Cheng X
Comput Struct Biotechnol J; 2022; 20():6503-6511. PubMed ID: 36467583
[TBL] [Abstract][Full Text] [Related]
8. A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females.
Loeuillet C; Dhellemmes M; Cazin C; Kherraf ZE; Fourati Ben Mustapha S; Zouari R; Thierry-Mieg N; Arnoult C; Ray PF
Clin Genet; 2022 Jul; 102(1):22-29. PubMed ID: 35460069
[TBL] [Abstract][Full Text] [Related]
9. Targeted Next-Generation Sequencing Indicates a Frequent Oligogenic Involvement in Primary Ovarian Insufficiency Onset.
Rossetti R; Moleri S; Guizzardi F; Gentilini D; Libera L; Marozzi A; Moretti C; Brancati F; Bonomi M; Persani L
Front Endocrinol (Lausanne); 2021; 12():664645. PubMed ID: 34803902
[TBL] [Abstract][Full Text] [Related]
10. Severe Ovarian Hyperstimulation Syndrome in a Case of Nonmutated Recurrent Genuine Empty Follicle Syndrome.
Mannur S; Jabeen T; Khader MA; Namoju R; Rao LSS
J Hum Reprod Sci; 2021; 14(3):321-324. PubMed ID: 34759625
[TBL] [Abstract][Full Text] [Related]
11. A novel homozygous nonsense mutation in zona pellucida 1 (ZP1) causes human female empty follicle syndrome.
Wang J; Yang X; Sun X; Ma L; Yin Y; He G; Zhang Y; Zhou J; Cai L; Liu J; Ma X
J Assist Reprod Genet; 2021 Jun; 38(6):1459-1468. PubMed ID: 33665726
[TBL] [Abstract][Full Text] [Related]
12. Glycoprotein G-protein Coupled Receptors in Disease: Luteinizing Hormone Receptors and Follicle Stimulating Hormone Receptors.
Althumairy D; Zhang X; Baez N; Barisas G; Roess DA; Bousfield GR; Crans DC
Diseases; 2020 Sep; 8(3):. PubMed ID: 32942611
[TBL] [Abstract][Full Text] [Related]
13. Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome.
Zhang Z; Wu L; Diao F; Chen B; Fu J; Mao X; Yan Z; Li B; Mu J; Zhou Z; Wang W; Zhao L; Dong J; Zeng Y; Du J; Kuang Y; Sun X; He L; Sang Q; Wang L
J Assist Reprod Genet; 2020 Nov; 37(11):2861-2868. PubMed ID: 32860205
[TBL] [Abstract][Full Text] [Related]
14. Novel mutations in ZP1 and ZP2 cause primary infertility due to empty follicle syndrome and abnormal zona pellucida.
Luo G; Zhu L; Liu Z; Yang X; Xi Q; Li Z; Duan J; Jin L; Zhang X
J Assist Reprod Genet; 2020 Nov; 37(11):2853-2860. PubMed ID: 32829425
[TBL] [Abstract][Full Text] [Related]
15. Novel biallelic loss-of-function variants in ZP1 identified in an infertile female with empty follicle syndrome.
Liu M; Shen Y; Zhang X; Wang X; Li D; Wang Y
J Assist Reprod Genet; 2020 Sep; 37(9):2151-2157. PubMed ID: 32556881
[TBL] [Abstract][Full Text] [Related]
16. Multiple association analysis of loci and candidate genes that regulate body size at three growth stages in Simmental beef cattle.
An B; Xu L; Xia J; Wang X; Miao J; Chang T; Song M; Ni J; Xu L; Zhang L; Li J; Gao H
BMC Genet; 2020 Mar; 21(1):32. PubMed ID: 32171250
[TBL] [Abstract][Full Text] [Related]
17. Recurrent empty follicle syndrome with different stimulation protocols - A case report.
Kaluarachchi A; Seneviratne HR; Batcha TM; Wijeratne S; Jayawardena GRMUGP
J Family Med Prim Care; 2019 Jul; 8(7):2536-2537. PubMed ID: 31463291
[TBL] [Abstract][Full Text] [Related]
18. Novel Concepts for Inducing Final Oocyte Maturation in In Vitro Fertilization Treatment.
Abbara A; Clarke SA; Dhillo WS
Endocr Rev; 2018 Oct; 39(5):593-628. PubMed ID: 29982525
[TBL] [Abstract][Full Text] [Related]
19. A case of empty follicle syndrome who conceived after aspiration of an endometrial cyst.
Tanaka R; Murase M; Aizawa Y; Segino M; Ishidera Y; Kitagawa M; Katayama K; Takashima K; Yumura Y; Yoshida H; Sakakibara H; Hirahara F
Reprod Med Biol; 2013 Jul; 12(3):111-115. PubMed ID: 29699138
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]