151 related articles for article (PubMed ID: 21944929)
1. Number of CGG repeats in the FMR1 gene of Japanese patients with primary ovarian insufficiency.
Ishizuka B; Okamoto N; Hamada N; Sugishita Y; Saito J; Takahashi N; Ogata T; Itoh MT
Fertil Steril; 2011 Nov; 96(5):1170-4. PubMed ID: 21944929
[TBL] [Abstract][Full Text] [Related]
2. The significance of fragile X mental retardation gene 1 CGG repeat sizes in the normal and intermediate range in women with primary ovarian insufficiency.
Voorhuis M; Onland-Moret NC; Janse F; Ploos van Amstel HK; Goverde AJ; Lambalk CB; Laven JS; van der Schouw YT; Broekmans FJ; Fauser BC;
Hum Reprod; 2014 Jul; 29(7):1585-93. PubMed ID: 24812319
[TBL] [Abstract][Full Text] [Related]
3. The significance of FMR1 CGG repeats in Chinese women with premature ovarian insufficiency and diminished ovarian reserve.
Tang R; Yu Q
Reprod Biol Endocrinol; 2020 Aug; 18(1):82. PubMed ID: 32787884
[TBL] [Abstract][Full Text] [Related]
4. The 'normal' range of FMR1 triple CGG repeats may be associated with primary ovarian insufficiency in China.
Lu CL; Li R; Chen XN; Xu YY; Yan LY; Yan J; Zhang YY; Jin HY; Zhang WX; Qiao J; Zhen XM
Reprod Biomed Online; 2017 Feb; 34(2):175-180. PubMed ID: 27916452
[TBL] [Abstract][Full Text] [Related]
5. FMR1 premutation is an uncommon explanation for premature ovarian failure in Han Chinese.
Guo T; Qin Y; Jiao X; Li G; Simpson JL; Chen ZJ
PLoS One; 2014; 9(7):e103316. PubMed ID: 25050920
[TBL] [Abstract][Full Text] [Related]
6. Diminished ovarian reserve is not observed in infertility patients with high normal CGG repeats on the fragile X mental retardation 1 (FMR1) gene.
Schufreider A; McQueen DB; Lee SM; Allon R; Uhler ML; Davie J; Feinberg EC
Hum Reprod; 2015 Nov; 30(11):2686-92. PubMed ID: 26345686
[TBL] [Abstract][Full Text] [Related]
7. Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure.
Ye Y; Lan X; Cong J; Li N; Wu Y; Zhang M; Liu J; Cui Y; Wu BL; An Y; Wu J
Reprod Biomed Online; 2014 Sep; 29(3):382-7. PubMed ID: 24912415
[TBL] [Abstract][Full Text] [Related]
8. Stratification of the risk of ovarian dysfunction by studying the complexity of intermediate and premutation alleles of the FMR1 gene.
Quilichini J; Perol S; Cuisset L; Grotto S; Fouveaut C; Barbot JC; Verebi C; Jordan P; Héron D; Molina-Gomes D; Pipiras E; Grynberg M; Catteau-Jonard S; Touraine P; Christin-Maître S; Plu-Bureau G; El Khattabi L; Bienvenu T
Am J Med Genet A; 2024 Apr; 194(4):e63479. PubMed ID: 37987117
[TBL] [Abstract][Full Text] [Related]
9. Elevated prevalence of 35-44 FMR1 trinucleotide repeats in women with diminished ovarian reserve.
Pastore LM; Young SL; Baker VL; Karns LB; Williams CD; Silverman LM
Reprod Sci; 2012 Nov; 19(11):1226-31. PubMed ID: 22581803
[TBL] [Abstract][Full Text] [Related]
10. A pilot study of premature ovarian senescence: I. Correlation of triple CGG repeats on the FMR1 gene to ovarian reserve parameters FSH and anti-Müllerian hormone.
Gleicher N; Weghofer A; Barad DH
Fertil Steril; 2009 May; 91(5):1700-6. PubMed ID: 18384775
[TBL] [Abstract][Full Text] [Related]
11. Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations.
Beke A; Piko H; Haltrich I; Karcagi V; Rigo J; Molnar MJ; Fekete G
BMC Med Genet; 2018 Jul; 19(1):113. PubMed ID: 29986653
[TBL] [Abstract][Full Text] [Related]
12. Distribution of the FMR1 gene in females by race/ethnicity: women with diminished ovarian reserve versus women with normal fertility (SWAN study).
Pastore LM; Young SL; Manichaikul A; Baker VL; Wang XQ; Finkelstein JS
Fertil Steril; 2017 Jan; 107(1):205-211.e1. PubMed ID: 27816231
[TBL] [Abstract][Full Text] [Related]
13. Study of FMR1 gene association with ovarian dysfunction in a sample from the Basque Country.
Barasoain M; Barrenetxea G; Huerta I; Télez M; Carrillo A; Pérez C; Criado B; Arrieta I
Gene; 2013 May; 521(1):145-9. PubMed ID: 23537988
[TBL] [Abstract][Full Text] [Related]
14. Association between mutations in the FMR1 gene and ovarian dysfunction in Brazilian patients.
Ramos C; Ocampos M; Barbato IT; Niehues VMS; Bicalho MDG; Nisihara R
JBRA Assist Reprod; 2022 Apr; 26(2):237-240. PubMed ID: 34542254
[TBL] [Abstract][Full Text] [Related]
15. Association between the
Huang J; Zhang W; Liu Y; Liu Y; Wang J; Jiang H
Artif Cells Nanomed Biotechnol; 2019 Dec; 47(1):3116-3122. PubMed ID: 31352801
[No Abstract] [Full Text] [Related]
16. Molecular Characterization of FMR1 Gene by TP-PCR in Women of Reproductive Age and Women with Premature Ovarian Insufficiency.
Dean DD; Agarwal S; Kapoor D; Singh K; Vati C
Mol Diagn Ther; 2018 Feb; 22(1):91-100. PubMed ID: 29188551
[TBL] [Abstract][Full Text] [Related]
17. Use of human-derived stem cells to create a novel, in vitro model designed to explore FMR1 CGG repeat instability amongst female premutation carriers.
Gustin SLF; Wang G; Baker VM; Latham G; Sebastiano V
J Assist Reprod Genet; 2018 Aug; 35(8):1443-1455. PubMed ID: 29926373
[TBL] [Abstract][Full Text] [Related]
18. The ovarian response in fragile X patients and premutation carriers undergoing IVF-PGD: reappraisal.
Avraham S; Almog B; Reches A; Zakar L; Malcov M; Sokolov A; Alpern S; Azem F
Hum Reprod; 2017 Jul; 32(7):1508-1511. PubMed ID: 28472405
[TBL] [Abstract][Full Text] [Related]
19. Increased frequency of occult fragile X-associated primary ovarian insufficiency in infertile women with evidence of impaired ovarian function.
Karimov CB; Moragianni VA; Cronister A; Srouji S; Petrozza J; Racowsky C; Ginsburg E; Thornton KL; Welt CK
Hum Reprod; 2011 Aug; 26(8):2077-83. PubMed ID: 21646280
[TBL] [Abstract][Full Text] [Related]
20. Does the presence of AGG interruptions within the CGG repeat tract have a protective effect on the fertility phenotype of female FMR1 premutation carriers?
Friedman-Gohas M; Kirshenbaum M; Michaeli A; Domniz N; Elizur S; Raanani H; Orvieto R; Cohen Y
J Assist Reprod Genet; 2020 Apr; 37(4):849-854. PubMed ID: 32096109
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
