174 related articles for article (PubMed ID: 21335413)
1. Variable expression of the Fragile X Mental Retardation 1 (FMR1) gene in patients with premature ovarian failure syndrome is not dependent on number of (CGG)n triplets in exon 1.
Schuettler J; Peng Z; Zimmer J; Sinn P; von Hagens C; Strowitzki T; Vogt PH
Hum Reprod; 2011 May; 26(5):1241-51. PubMed ID: 21335413
[TBL] [Abstract][Full Text] [Related]
2. Analysis of the molecular parameters that could predict the risk of manifesting premature ovarian failure in female premutation carriers of fragile X syndrome.
Tejada MI; García-Alegría E; Bilbao A; Martínez-Bouzas C; Beristain E; Poch M; Ramos-Arroyo MA; López B; Fernandez Carvajal I; Ribate MP; Ramos F
Menopause; 2008; 15(5):945-9. PubMed ID: 18427356
[TBL] [Abstract][Full Text] [Related]
3. FMR1 and the continuum of primary ovarian insufficiency.
Sullivan SD; Welt C; Sherman S
Semin Reprod Med; 2011 Jul; 29(4):299-307. PubMed ID: 21969264
[TBL] [Abstract][Full Text] [Related]
4. A woman with spontaneous premature ovarian failure gives birth to a child with fragile X syndrome.
Corrigan EC; Raygada MJ; Vanderhoof VH; Nelson LM
Fertil Steril; 2005 Nov; 84(5):1508. PubMed ID: 16275254
[TBL] [Abstract][Full Text] [Related]
5. FMR1 expression in human granulosa cells increases with exon 1 CGG repeat length depending on ovarian reserve.
Rehnitz J; Alcoba DD; Brum IS; Dietrich JE; Youness B; Hinderhofer K; Messmer B; Freis A; Strowitzki T; Germeyer A
Reprod Biol Endocrinol; 2018 Jul; 16(1):65. PubMed ID: 29981579
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Reproductive health of adolescent girls who carry the FMR1 premutation: expected phenotype based on current knowledge of fragile x-associated primary ovarian insufficiency.
De Caro JJ; Dominguez C; Sherman SL
Ann N Y Acad Sci; 2008; 1135():99-111. PubMed ID: 18574214
[TBL] [Abstract][Full Text] [Related]
8. Premature ovarian failure with FMR1 premutation, X chromosome mosaicism and blood lymphocyte microchimerism.
Gersak K; Franic D; Veble A; Pajnic IZ; Teran N; Writzl K
Climacteric; 2011 Apr; 14(2):289-93. PubMed ID: 20575655
[TBL] [Abstract][Full Text] [Related]
9. Granulosa cell and oocyte mitochondrial abnormalities in a mouse model of fragile X primary ovarian insufficiency.
Conca Dioguardi C; Uslu B; Haynes M; Kurus M; Gul M; Miao DQ; De Santis L; Ferrari M; Bellone S; Santin A; Giulivi C; Hoffman G; Usdin K; Johnson J
Mol Hum Reprod; 2016 Jun; 22(6):384-96. PubMed ID: 26965313
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. FMR1 premutation: not only important in premature ovarian failure but also in diminished ovarian reserve.
Eslami A; Farahmand K; Totonchi M; Madani T; Asadpour U; Zari Moradi S; Gourabi H; Mohseni-Meybodi A
Hum Fertil (Camb); 2017 Jun; 20(2):120-125. PubMed ID: 27876427
[TBL] [Abstract][Full Text] [Related]
12. Influence of intermediate and uninterrupted FMR1 CGG expansions in premature ovarian failure manifestation.
Bodega B; Bione S; Dalprà L; Toniolo D; Ornaghi F; Vegetti W; Ginelli E; Marozzi A
Hum Reprod; 2006 Apr; 21(4):952-7. PubMed ID: 16361284
[TBL] [Abstract][Full Text] [Related]
13. A molecular and cytogenetic investigation of FMR1 gene premutations in Polish patients with primary ovarian insufficiency.
Rajkiewicz M; Szlendak-Sauer K; Sulek A; Gawlik-Zawislak S; Krysa W; Radowicki S; Zaremba J
Eur J Obstet Gynecol Reprod Biol; 2011 Apr; 155(2):176-9. PubMed ID: 21276648
[TBL] [Abstract][Full Text] [Related]
14. Differential increases of specific FMR1 mRNA isoforms in premutation carriers.
Pretto DI; Eid JS; Yrigollen CM; Tang HT; Loomis EW; Raske C; Durbin-Johnson B; Hagerman PJ; Tassone F
J Med Genet; 2015 Jan; 52(1):42-52. PubMed ID: 25358671
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Fragile X premutation RNA is sufficient to cause primary ovarian insufficiency in mice.
Lu C; Lin L; Tan H; Wu H; Sherman SL; Gao F; Jin P; Chen D
Hum Mol Genet; 2012 Dec; 21(23):5039-47. PubMed ID: 22914733
[TBL] [Abstract][Full Text] [Related]
17. Correlation of triple repeats on the FMR1 (fragile X) gene to ovarian reserve: a new infertility test?
Gleicher N; Weghofer A; Oktay K; Barad DH
Acta Obstet Gynecol Scand; 2009; 88(9):1024-30. PubMed ID: 19642041
[TBL] [Abstract][Full Text] [Related]
18. Premutations of FMR1 CGG repeats are not related to idiopathic premature ovarian failure in Iranian patients: A case control study.
Asadi R; Omrani MD; Ghaedi H; Mirfakhraie R; Azargashb E; Habibi M; Pouresmaeili F
Gene; 2018 Nov; 676():189-194. PubMed ID: 30030199
[TBL] [Abstract][Full Text] [Related]
19. Evidence for a fragile X messenger ribonucleoprotein 1 (FMR1) mRNA gain-of-function toxicity mechanism contributing to the pathogenesis of fragile X-associated premature ovarian insufficiency.
Rosario R; Stewart HL; Choudhury NR; Michlewski G; Charlet-Berguerand N; Anderson RA
FASEB J; 2022 Nov; 36(11):e22612. PubMed ID: 36250920
[TBL] [Abstract][Full Text] [Related]
20. Very early premature ovarian failure in two sisters compound heterozygous for the FMR1 premutation.
Van Esch H; Buekenhout L; Race V; Matthijs G
Eur J Med Genet; 2009; 52(1):37-40. PubMed ID: 19041959
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
