These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

196 related articles for article (PubMed ID: 12149404)

  • 1. Identification of novel mutations in FOXL2 associated with premature ovarian failure.
    Harris SE; Chand AL; Winship IM; Gersak K; Aittomäki K; Shelling AN
    Mol Hum Reprod; 2002 Aug; 8(8):729-33. PubMed ID: 12149404
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype--phenotype correlation.
    De Baere E; Dixon MJ; Small KW; Jabs EW; Leroy BP; Devriendt K; Gillerot Y; Mortier G; Meire F; Van Maldergem L; Courtens W; Hjalgrim H; Huang S; Liebaers I; Van Regemorter N; Touraine P; Praphanphoj V; Verloes A; Udar N; Yellore V; Chalukya M; Yelchits S; De Paepe A; Kuttenn F; Fellous M; Veitia R; Messiaen L
    Hum Mol Genet; 2001 Jul; 10(15):1591-600. PubMed ID: 11468277
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Screening for FOXL2 gene mutations in women with premature ovarian failure: an Indian experience.
    Chatterjee S; Modi D; Maitra A; Kadam S; Patel Z; Gokrall J; Meherji P
    Reprod Biomed Online; 2007 Nov; 15(5):554-60. PubMed ID: 18028747
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report.
    Gersak K; Harris SE; Smale WJ; Shelling AN
    Hum Reprod; 2004 Dec; 19(12):2767-70. PubMed ID: 15459170
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure.
    Bodega B; Porta C; Crosignani PG; Ginelli E; Marozzi A
    Mol Hum Reprod; 2004 Aug; 10(8):555-7. PubMed ID: 15181179
    [TBL] [Abstract][Full Text] [Related]  

  • 6. An investigation into FOXE1 polyalanine tract length in premature ovarian failure.
    Watkins WJ; Harris SE; Craven MJ; Vincent AL; Winship IM; Gersak K; Shelling AN
    Mol Hum Reprod; 2006 Mar; 12(3):145-9. PubMed ID: 16481406
    [TBL] [Abstract][Full Text] [Related]  

  • 7. FOXL2 mutation screening in a large panel of POF patients and XX males.
    De Baere E; Lemercier B; Christin-Maitre S; Durval D; Messiaen L; Fellous M; Veitia R
    J Med Genet; 2002 Aug; 39(8):e43. PubMed ID: 12161610
    [No Abstract]   [Full Text] [Related]  

  • 8. Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure.
    Watkins WJ; Umbers AJ; Woad KJ; Harris SE; Winship IM; Gersak K; Shelling AN
    Fertil Steril; 2006 Nov; 86(5):1518-21. PubMed ID: 16979636
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Inhibin: a candidate gene for premature ovarian failure.
    Shelling AN; Burton KA; Chand AL; van Ee CC; France JT; Farquhar CM; Milsom SR; Love DR; Gersak K; Aittomäki K; Winship IM
    Hum Reprod; 2000 Dec; 15(12):2644-9. PubMed ID: 11098038
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Genes and translocations involved in POF.
    Schlessinger D; Herrera L; Crisponi L; Mumm S; Percesepe A; Pellegrini M; Pilia G; Forabosco A
    Am J Med Genet; 2002 Aug; 111(3):328-33. PubMed ID: 12210333
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The human FOXL2 mutation database.
    Beysen D; Vandesompele J; Messiaen L; De Paepe A; De Baere E
    Hum Mutat; 2004 Sep; 24(3):189-93. PubMed ID: 15300845
    [TBL] [Abstract][Full Text] [Related]  

  • 12. FOXL2 and BPES: mutational hotspots, phenotypic variability, and revision of the genotype-phenotype correlation.
    De Baere E; Beysen D; Oley C; Lorenz B; Cocquet J; De Sutter P; Devriendt K; Dixon M; Fellous M; Fryns JP; Garza A; Jonsrud C; Koivisto PA; Krause A; Leroy BP; Meire F; Plomp A; Van Maldergem L; De Paepe A; Veitia R; Messiaen L
    Am J Hum Genet; 2003 Feb; 72(2):478-87. PubMed ID: 12529855
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Association of FOXE1 gene polymorphism with idiopathic premature ovarian failure].
    Qin C; Yao J; Yuan Z; Ren X; Xie J; Wu W
    Zhonghua Fu Chan Ke Za Zhi; 2015 Feb; 50(2):116-9. PubMed ID: 25877608
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Functional Analysis of a Novel FOXL2 Indel Mutation in Chinese Families with Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type I.
    Chai P; Li F; Fan J; Jia R; Zhang H; Fan X
    Int J Biol Sci; 2017; 13(8):1019-1028. PubMed ID: 28924383
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutant Forkhead L2 (FOXL2) proteins associated with premature ovarian failure (POF) dimerize with wild-type FOXL2, leading to altered regulation of genes associated with granulosa cell differentiation.
    Kuo FT; Bentsi-Barnes IK; Barlow GM; Pisarska MD
    Endocrinology; 2011 Oct; 152(10):3917-29. PubMed ID: 21862621
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Investigating the association between inhibin alpha gene promoter polymorphisms and premature ovarian failure.
    Woad KJ; Pearson SM; Harris SE; Gersak K; Shelling AN
    Fertil Steril; 2009 Jan; 91(1):62-6. PubMed ID: 18249384
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure.
    Qin Y; Jiao X; Dalgleish R; Vujovic S; Li J; Simpson JL; Al-Azzawi F; Chen ZJ
    Fertil Steril; 2014 Apr; 101(4):1104-1109.e6. PubMed ID: 24524832
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Foxl2 disruption causes mouse ovarian failure by pervasive blockage of follicle development.
    Uda M; Ottolenghi C; Crisponi L; Garcia JE; Deiana M; Kimber W; Forabosco A; Cao A; Schlessinger D; Pilia G
    Hum Mol Genet; 2004 Jun; 13(11):1171-81. PubMed ID: 15056605
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure.
    Ni F; Wen Q; Wang B; Zhou S; Wang J; Mu Y; Ma X; Cao Y
    Gynecol Endocrinol; 2010 Apr; 26(4):246-9. PubMed ID: 20222838
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel polyalanine expansion in FOXL2: the first evidence for a recessive form of the blepharophimosis syndrome (BPES) associated with ovarian dysfunction.
    Nallathambi J; Moumné L; De Baere E; Beysen D; Usha K; Sundaresan P; Veitia RA
    Hum Genet; 2007 Mar; 121(1):107-12. PubMed ID: 17089161
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.