BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 20067892)

  • 1. The transcription factor FOXL2 in ovarian function and dysfunction.
    De Baere E; Fellous M; Veitia RA
    Folia Histochem Cytobiol; 2009; 47(5):S43-9. PubMed ID: 20067892
    [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. 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 impairment in human disease.
    Verdin H; De Baere E
    Horm Res Paediatr; 2012; 77(1):2-11. PubMed ID: 22248822
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Clinical characterization and identification of five novel FOXL2 pathogenic variants in a cohort of 12 Mexican subjects with the syndrome of blepharophimosis-ptosis-epicanthus inversus.
    Chacón-Camacho OF; Salgado-Medina A; Alcaraz-Lares N; López-Moreno D; Barragán-Arévalo T; Nava-Castañeda A; Rodríguez-Uribe G; Lieberman E; Rodríguez-Cabrera L; González-Del Angel A; Borbolla AM; Fernández-Hernández L; Graue-Hernández EO; Zenteno JC
    Gene; 2019 Jul; 706():62-68. PubMed ID: 31048069
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency.
    Yang XW; He WB; Gong F; Li W; Li XR; Zhong CG; Lu GX; Lin G; Du J; Tan YQ
    Mol Genet Genomic Med; 2018 Mar; 6(2):261-267. PubMed ID: 29378385
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new heterozygous mutation of the FOXL2 gene is associated with a large ovarian cyst and ovarian dysfunction in an adolescent girl with blepharophimosis/ptosis/epicanthus inversus syndrome.
    Raile K; Stobbe H; Tröbs RB; Kiess W; Pfäffle R
    Eur J Endocrinol; 2005 Sep; 153(3):353-8. PubMed ID: 16131596
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II.
    Haghighi A; Verdin H; Haghighi-Kakhki H; Piri N; Gohari NS; De Baere E
    Mol Vis; 2012; 18():211-8. PubMed ID: 22312189
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Identification of a novel FOXL2 mutation in a single family with both types of blepharophimosis‑-ptosis-epicanthus inversus syndrome.
    Yang L; Li T; Xing Y
    Mol Med Rep; 2017 Oct; 16(4):5529-5532. PubMed ID: 28849110
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Characterization of endocrine features and genotype-phenotypes correlations in blepharophimosis-ptosis-epicanthus inversus syndrome type 1.
    Nuovo S; Passeri M; Di Benedetto E; Calanchini M; Meldolesi I; Di Giacomo MC; Petruzzi D; Piemontese MR; Zelante L; Sangiuolo F; Novelli G; Fabbri A; Brancati F
    J Endocrinol Invest; 2016 Feb; 39(2):227-33. PubMed ID: 26100530
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. Differential apoptotic and proliferative activities of wild-type FOXL2 and blepharophimosis-ptosis-epicanthus inversus syndrome (BPES)-associated mutant FOXL2 proteins.
    Kim JH; Bae J
    J Reprod Dev; 2014 Mar; 60(1):14-20. PubMed ID: 24240106
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Novel FOXL2 mutations in two Chinese families with blepharophimosis-ptosis-epicanthus inversus syndrome.
    Xue M; Zheng J; Zhou Q; Hejtmancik JF; Wang Y; Li S
    BMC Med Genet; 2015 Sep; 16():73. PubMed ID: 26323275
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Premature ovarian insufficiency as a variable feature of blepharophimosis, ptosis, and epicanthus inversus syndrome associated with c.223C > T p.(Leu75Phe) FOXL2 mutation: a case report.
    Grzechocińska B; Warzecha D; Wypchło M; Ploski R; Wielgoś M
    BMC Med Genet; 2019 Jul; 20(1):132. PubMed ID: 31366388
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.