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 *

137 related articles for article (PubMed ID: 34727551)

  • 1. The Genetics and Biology of FOXL2.
    Tucker EJ
    Sex Dev; 2022; 16(2-3):184-193. PubMed ID: 34727551
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. Functional study on new FOXL2 mutations found in Chinese patients with blepharophimosis, ptosis, epicanthus inversus syndrome.
    Zhou L; Wang J; Wang T
    BMC Med Genet; 2018 Jul; 19(1):121. PubMed ID: 30029625
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Genetic and Clinical Features of
    Méjécase C; Nigam C; Moosajee M; Bladen JC
    Genes (Basel); 2021 Mar; 12(3):. PubMed ID: 33806295
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Shifting the landscape: Dominant C-terminal rare missense FOXL2 variants in non-syndromic primary ovarian failure etiology.
    Jordan P; Verebi C; Hervé B; Perol S; Chakhtoura Z; Courtillot C; Bachelot A; Karila D; Renard C; Grouthier V; de la Croix SM; Bernard V; Fouveaut C; de la Perrière AB; Jonard-Catteau S; Touraine P; Plu-Bureau G; Dupont JM; Christin-Maitre S; Bienvenu T
    Clin Genet; 2024 Jul; 106(1):102-108. PubMed ID: 38558253
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Blepharophimosis-ptosis-epicanthus inversus syndrome plus: deletion 3q22.3q23 in a patient with characteristic facial features and with genital anomalies, spastic diplegia, and speech delay.
    Zahanova S; Meaney B; Łabieniec B; Verdin H; De Baere E; Nowaczyk MJM
    Clin Dysmorphol; 2012 Jan; 21(1):48-52. PubMed ID: 21934608
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. FOXL2 mutations in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
    Wang J; Liu J; Zhang Q
    Mol Vis; 2007 Jan; 13():108-13. PubMed ID: 17277738
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Blepharophimosis, ptosis, and epicanthus inversus syndrome: clinical and molecular analysis of a case.
    Mari F; Giachino D; Russo L; Pilia G; Ariani F; Scala E; Chiappe F; Sampieri K; Caporossi A; Renieri A; Lasorella G
    J AAPOS; 2006 Jun; 10(3):279-80. PubMed ID: 16814186
    [TBL] [Abstract][Full Text] [Related]  

  • 17.
    Mubeen A; Parra-Herran C
    J Clin Pathol; 2023 Dec; 76(12):798-801. PubMed ID: 37798106
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Clinical and genetic studies of 17 Han Chinese pedigrees and 31 sporadic patients with blepharophimosis-ptosis-epicanthus inversus syndrome.
    Wang Y; Wu Q; Cao W; Huang L; Liu W; Li C; Li N
    Mol Vis; 2022; 28():352-358. PubMed ID: 36338666
    [TBL] [Abstract][Full Text] [Related]  

  • 20. FOXL2: a central transcription factor of the ovary.
    Georges A; Auguste A; Bessière L; Vanet A; Todeschini AL; Veitia RA
    J Mol Endocrinol; 2014 Feb; 52(1):R17-33. PubMed ID: 24049064
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.