204 related articles for article (PubMed ID: 30691934)
1. Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome.
He WB; Du J; Yang XW; Li W; Tang WL; Dai C; Chen YZ; Zhang YX; Lu GX; Lin G; Gong F; Tan YQ
Reprod Biomed Online; 2019 Mar; 38(3):397-406. PubMed ID: 30691934
[TBL] [Abstract][Full Text] [Related]
2. A novel homozygous mutation in the FSHR gene is causative for primary ovarian insufficiency.
Liu H; Xu X; Han T; Yan L; Cheng L; Qin Y; Liu W; Zhao S; Chen ZJ
Fertil Steril; 2017 Dec; 108(6):1050-1055.e2. PubMed ID: 29157895
[TBL] [Abstract][Full Text] [Related]
3. A novel follicle-stimulating hormone receptor mutation causing primary ovarian failure: a fertility application of whole exome sequencing.
Bramble MS; Goldstein EH; Lipson A; Ngun T; Eskin A; Gosschalk JE; Roach L; Vashist N; Barseghyan H; Lee E; Arboleda VA; Vaiman D; Yuksel Z; Fellous M; Vilain E
Hum Reprod; 2016 Apr; 31(4):905-14. PubMed ID: 26911863
[TBL] [Abstract][Full Text] [Related]
4. Novel FSHR mutations in Han Chinese women with sporadic premature ovarian insufficiency.
Liu H; Guo T; Gong Z; Yu Y; Zhang Y; Zhao S; Qin Y
Mol Cell Endocrinol; 2019 Jul; 492():110446. PubMed ID: 31077743
[TBL] [Abstract][Full Text] [Related]
5. Identification and characterization of novel compound heterozygous variants in
Chen X; Chen L; Wang Y; Shu C; Zhou Y; Wu R; Jin B; Yang L; Sun J; Qi M; Shu J
Front Endocrinol (Lausanne); 2022; 13():1013894. PubMed ID: 36704038
[TBL] [Abstract][Full Text] [Related]
6. Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure.
Katari S; Wood-Trageser MA; Jiang H; Kalynchuk E; Muzumdar R; Yatsenko SA; Rajkovic A
J Clin Endocrinol Metab; 2015 Jun; 100(6):2154-7. PubMed ID: 25875778
[TBL] [Abstract][Full Text] [Related]
7. Novel FSHR variants causing female resistant ovary syndrome.
Khor S; Lyu Q; Kuang Y; Lu X
Mol Genet Genomic Med; 2020 Feb; 8(2):e1082. PubMed ID: 31830376
[TBL] [Abstract][Full Text] [Related]
8. A Novel Mutation in the FSH Receptor (I423T) Affecting Receptor Activation and Leading to Primary Ovarian Failure.
Zariñán T; Mayorga J; Jardón-Valadez E; Gutiérrez-Sagal R; Maravillas-Montero JL; Mejía-Domínguez NR; Martínez-Luis I; Yacini-Torres OG; Cravioto MD; Reiter E; Ulloa-Aguirre A
J Clin Endocrinol Metab; 2021 Jan; 106(2):e534-e550. PubMed ID: 33119067
[TBL] [Abstract][Full Text] [Related]
9. A Novel mutation in the FSH receptor inhibiting signal transduction and causing primary ovarian failure.
Doherty E; Pakarinen P; Tiitinen A; Kiilavuori A; Huhtaniemi I; Forrest S; Aittomäki K
J Clin Endocrinol Metab; 2002 Mar; 87(3):1151-5. PubMed ID: 11889179
[TBL] [Abstract][Full Text] [Related]
10. [Study of two Chinese families affected with resistant ovarian syndrome resulted from novel mutations of FSHR gene].
Li W; He W; Zhou L; Hu X; Li S; Gong F; Tan Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Apr; 34(2):196-199. PubMed ID: 28397217
[TBL] [Abstract][Full Text] [Related]
11. Successful in vitro maturation of oocytes in a woman with gonadotropin-resistant ovary syndrome associated with a novel combination of FSH receptor gene variants: a case report.
Flageole C; Toufaily C; Bernard DJ; Ates S; Blais V; Chénier S; Benkhalifa M; Miron P
J Assist Reprod Genet; 2019 Mar; 36(3):425-432. PubMed ID: 30610662
[TBL] [Abstract][Full Text] [Related]
12. New natural inactivating mutations of the follicle-stimulating hormone receptor: correlations between receptor function and phenotype.
Touraine P; Beau I; Gougeon A; Meduri G; Desroches A; Pichard C; Detoeuf M; Paniel B; Prieur M; Zorn JR; Milgrom E; Kuttenn F; Misrahi M
Mol Endocrinol; 1999 Nov; 13(11):1844-54. PubMed ID: 10551778
[TBL] [Abstract][Full Text] [Related]
13. FSH receptor gene variants are rarely associated with premature ovarian failure.
Woad KJ; Prendergast D; Winship IM; Shelling AN
Reprod Biomed Online; 2013 Apr; 26(4):396-9. PubMed ID: 23419799
[TBL] [Abstract][Full Text] [Related]
14. Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis.
Sassi A; Désir J; Janssens V; Marangoni M; Daneels D; Gheldof A; Bonduelle M; Van Dooren S; Costagliola S; Delbaere A
F S Rep; 2020 Dec; 1(3):193-201. PubMed ID: 34223243
[TBL] [Abstract][Full Text] [Related]
15. AMH mutations with reduced in vitro bioactivity are related to premature ovarian insufficiency.
Alvaro Mercadal B; Imbert R; Demeestere I; Gervy C; De Leener A; Englert Y; Costagliola S; Delbaere A
Hum Reprod; 2015 May; 30(5):1196-202. PubMed ID: 25750103
[TBL] [Abstract][Full Text] [Related]
16. Effects of FSHR polymorphisms on premature ovarian insufficiency in human beings: a meta-analysis.
Huang W; Cao Y; Shi L
Reprod Biol Endocrinol; 2019 Oct; 17(1):80. PubMed ID: 31629411
[TBL] [Abstract][Full Text] [Related]
17. Are FSHR polymorphisms risk factors to premature ovarian insufficiency?
Cordts EB; Santos MC; Bianco B; Barbosa CP; Christofolini DM
Gynecol Endocrinol; 2015; 31(8):663-6. PubMed ID: 26291798
[TBL] [Abstract][Full Text] [Related]
18. Mutations in MSH5 in primary ovarian insufficiency.
Guo T; Zhao S; Zhao S; Chen M; Li G; Jiao X; Wang Z; Zhao Y; Qin Y; Gao F; Chen ZJ
Hum Mol Genet; 2017 Apr; 26(8):1452-1457. PubMed ID: 28175301
[TBL] [Abstract][Full Text] [Related]
19. Functional characterization of two naturally occurring mutations (Val514Ala and Ala575Val) in follicle-stimulating hormone receptor.
Desai SS; Achrekar SK; Sahasrabuddhe KA; Meharji PK; Desai SK; Mangoli VS; Mahale SD
J Clin Endocrinol Metab; 2015 Apr; 100(4):E638-45. PubMed ID: 25581598
[TBL] [Abstract][Full Text] [Related]
20. Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing.
Wang B; Li L; Zhu Y; Zhang W; Wang X; Chen B; Li T; Pan H; Wang J; Kee K; Cao Y
Hum Reprod; 2017 Oct; 32(10):2138-2146. PubMed ID: 28938739
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
