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 *

262 related articles for article (PubMed ID: 18726931)

  • 1. FOXL2 mutations and genomic rearrangements in BPES.
    Beysen D; De Paepe A; De Baere E
    Hum Mutat; 2009 Feb; 30(2):158-69. PubMed ID: 18726931
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A new FOXL2 gene mutation in a woman with premature ovarian failure and sporadic blepharophimosis-ptosis-epicanthus inversus syndrome.
    Corrêa FJ; Tavares AB; Pereira RW; Abrão MS
    Fertil Steril; 2010 Feb; 93(3):1006.e3-6. PubMed ID: 19969293
    [TBL] [Abstract][Full Text] [Related]  

  • 4. FOXL2 mutations lead to different ovarian phenotypes in BPES patients: Case Report.
    Méduri G; Bachelot A; Duflos C; Bständig B; Poirot C; Genestie C; Veitia R; De Baere E; Touraine P
    Hum Reprod; 2010 Jan; 25(1):235-43. PubMed ID: 19819892
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation analysis of the FOXL2 gene in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
    Tang S; Wang X; Lin L; Sun Y; Wang Y; Yu H
    Mutagenesis; 2006 Jan; 21(1):35-9. PubMed ID: 16394030
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of 34 novel and 56 known FOXL2 mutations in patients with Blepharophimosis syndrome.
    Beysen D; De Jaegere S; Amor D; Bouchard P; Christin-Maitre S; Fellous M; Touraine P; Grix AW; Hennekam R; Meire F; Oyen N; Wilson LC; Barel D; Clayton-Smith J; de Ravel T; Decock C; Delbeke P; Ensenauer R; Ebinger F; Gillessen-Kaesbach G; Hendriks Y; Kimonis V; Laframboise R; Laissue P; Leppig K; Leroy BP; Miller DT; Mowat D; Neumann L; Plomp A; Van Regemorter N; Wieczorek D; Veitia RA; De Paepe A; De Baere E
    Hum Mutat; 2008 Nov; 29(11):E205-19. PubMed ID: 18642388
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems.
    Dipietromaria A; Benayoun BA; Todeschini AL; Rivals I; Bazin C; Veitia RA
    Hum Mol Genet; 2009 Sep; 18(17):3324-33. PubMed ID: 19515849
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Premature ovarian failure and forkhead transcription factor FOXL2: blepharophimosis-ptosis-epicanthus inversus syndrome and ovarian dysfunction.
    De Baere E; Copelli S; Caburet S; Laissue P; Beysen D; Christin-Maitre S; Bouchard P; Veitia R; Fellous M
    Pediatr Endocrinol Rev; 2005 Jun; 2(4):653-60. PubMed ID: 16208278
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.
    Beysen D; Moumné L; Veitia R; Peters H; Leroy BP; De Paepe A; De Baere E
    Hum Mol Genet; 2008 Jul; 17(13):2030-8. PubMed ID: 18372316
    [TBL] [Abstract][Full Text] [Related]  

  • 10. FOXL2 copy number changes in the molecular pathogenesis of BPES: unique cohort of 17 deletions.
    D'haene B; Nevado J; Pugeat M; Pierquin G; Lowry RB; Reardon W; Delicado A; García-Miñaur S; Palomares M; Courtens W; Stefanova M; Wallace S; Watkins W; Shelling AN; Wieczorek D; Veitia RA; De Paepe A; Lapunzina P; De Baere E
    Hum Mutat; 2010 May; 31(5):E1332-47. PubMed ID: 20232352
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. The mutations and potential targets of the forkhead transcription factor FOXL2.
    Moumné L; Batista F; Benayoun BA; Nallathambi J; Fellous M; Sundaresan P; Veitia RA
    Mol Cell Endocrinol; 2008 Jan; 282(1-2):2-11. PubMed ID: 18155828
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Functional study on a novel missense mutation of the transcription factor FOXL2 causes blepharophimosis-ptosis-epicanthus inversus syndrome (BPES).
    Fan JY; Han B; Qiao J; Liu BL; Ji YR; Ge SF; Song HD; Fan XQ
    Mutagenesis; 2011 Mar; 26(2):283-9. PubMed ID: 21068205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Foxl2 function in ovarian development.
    Uhlenhaut NH; Treier M
    Mol Genet Metab; 2006 Jul; 88(3):225-34. PubMed ID: 16647286
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blepharophimosis-ptosis-epicanthus inversus syndrome in a girl with chromosome translocation t(2;3)(q33;q23).
    Tzschach A; Kelbova C; Weidensee S; Peters H; Ropers HH; Ullmann R; Erdogan F; Jurkatis J; Menzel C; Kalscheuer V; Demuth S
    Ophthalmic Genet; 2008 Mar; 29(1):37-40. PubMed ID: 18363172
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic analysis of a five generation Indian family with BPES: a novel missense mutation (p.Y215C).
    Kumar A; Babu M; Raghunath A; Venkatesh CP
    Mol Vis; 2004 Jul; 10():445-9. PubMed ID: 15257268
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Functional evidence implicating FOXL2 in non-syndromic premature ovarian failure and in the regulation of the transcription factor OSR2.
    Laissue P; Lakhal B; Benayoun BA; Dipietromaria A; Braham R; Elghezal H; Philibert P; Saâd A; Sultan C; Fellous M; Veitia RA
    J Med Genet; 2009 Jul; 46(7):455-7. PubMed ID: 19429596
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Blepharophimosis and bilateral Duane syndrome associated with a FOXL2 mutation.
    Vincent AL; Watkins WJ; Sloan BH; Shelling AN
    Clin Genet; 2005 Dec; 68(6):520-3. PubMed ID: 16283882
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 14.