BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

173 related articles for article (PubMed ID: 27165002)

  • 1. The sub-nucleolar localization of PHF6 defines its role in rDNA transcription and early processing events.
    Todd MA; Huh MS; Picketts DJ
    Eur J Hum Genet; 2016 Oct; 24(10):1453-9. PubMed ID: 27165002
    [TBL] [Abstract][Full Text] [Related]  

  • 2. PHF6 functions as a tumor suppressor by recruiting methyltransferase SUV39H1 to nucleolar region and offers a novel therapeutic target for PHF6-muntant leukemia.
    Tsai HI; Wu Y; Huang R; Su D; Wu Y; Liu X; Wang L; Xu Z; Pang Y; Sun C; He C; Shu F; Zhu H; Wang D; Cheng F; Huang L; Chen H
    Acta Pharm Sin B; 2022 Apr; 12(4):1913-1927. PubMed ID: 35847518
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PHF6 interacts with the nucleosome remodeling and deacetylation (NuRD) complex.
    Todd MA; Picketts DJ
    J Proteome Res; 2012 Aug; 11(8):4326-37. PubMed ID: 22720776
    [TBL] [Abstract][Full Text] [Related]  

  • 4. PHF6 regulates cell cycle progression by suppressing ribosomal RNA synthesis.
    Wang J; Leung JW; Gong Z; Feng L; Shi X; Chen J
    J Biol Chem; 2013 Feb; 288(5):3174-83. PubMed ID: 23229552
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Structural and functional insights into the human Börjeson-Forssman-Lehmann syndrome-associated protein PHF6.
    Liu Z; Li F; Ruan K; Zhang J; Mei Y; Wu J; Shi Y
    J Biol Chem; 2014 Apr; 289(14):10069-83. PubMed ID: 24554700
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 1H, 13C and 15N resonance assignments and secondary structure of the human PHF6-ePHD1 domain.
    Bao Y; Liu Z; Zhang J; Wu J; Shi Y
    Biomol NMR Assign; 2016 Apr; 10(1):1-4. PubMed ID: 26286319
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Pathogenesis of Börjeson-Forssman-Lehmann syndrome: Insights from PHF6 function.
    Jahani-Asl A; Cheng C; Zhang C; Bonni A
    Neurobiol Dis; 2016 Dec; 96():227-235. PubMed ID: 27633282
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Protein and gene expression analysis of Phf6, the gene mutated in the Börjeson-Forssman-Lehmann Syndrome of intellectual disability and obesity.
    Voss AK; Gamble R; Collin C; Shoubridge C; Corbett M; Gécz J; Thomas T
    Gene Expr Patterns; 2007 Oct; 7(8):858-71. PubMed ID: 17698420
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in PHF6 are associated with Börjeson-Forssman-Lehmann syndrome.
    Lower KM; Turner G; Kerr BA; Mathews KD; Shaw MA; Gedeon AK; Schelley S; Hoyme HE; White SM; Delatycki MB; Lampe AK; Clayton-Smith J; Stewart H; van Ravenswaay CM; de Vries BB; Cox B; Grompe M; Ross S; Thomas P; Mulley JC; Gécz J
    Nat Genet; 2002 Dec; 32(4):661-5. PubMed ID: 12415272
    [TBL] [Abstract][Full Text] [Related]  

  • 10. T-cell acute lymphoblastic leukemia in association with Börjeson-Forssman-Lehmann syndrome due to a mutation in PHF6.
    Chao MM; Todd MA; Kontny U; Neas K; Sullivan MJ; Hunter AG; Picketts DJ; Kratz CP
    Pediatr Blood Cancer; 2010 Oct; 55(4):722-4. PubMed ID: 20806366
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The Role of PHF6 in Hematopoiesis and Hematologic Malignancies.
    Eisa YA; Guo Y; Yang FC
    Stem Cell Rev Rep; 2023 Jan; 19(1):67-75. PubMed ID: 36008597
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Structural basis of plant homeodomain finger 6 (PHF6) recognition by the retinoblastoma binding protein 4 (RBBP4) component of the nucleosome remodeling and deacetylase (NuRD) complex.
    Liu Z; Li F; Zhang B; Li S; Wu J; Shi Y
    J Biol Chem; 2015 Mar; 290(10):6630-8. PubMed ID: 25601084
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PHF6 Degrees of Separation: The Multifaceted Roles of a Chromatin Adaptor Protein.
    Todd MA; Ivanochko D; Picketts DJ
    Genes (Basel); 2015 Jun; 6(2):325-52. PubMed ID: 26103525
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.
    Zweier C; Rittinger O; Bader I; Berland S; Cole T; Degenhardt F; Di Donato N; Graul-Neumann L; Hoyer J; Lynch SA; Vlasak I; Wieczorek D
    Am J Med Genet C Semin Med Genet; 2014 Sep; 166C(3):290-301. PubMed ID: 25099957
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Börjeson-Forssman-Lehmann Syndrome due to a novel plant homeodomain zinc finger mutation in the PHF6 gene.
    Mangelsdorf M; Chevrier E; Mustonen A; Picketts DJ
    J Child Neurol; 2009 May; 24(5):610-4. PubMed ID: 19264739
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation screening in Borjeson-Forssman-Lehmann syndrome: identification of a novel de novo PHF6 mutation in a female patient.
    Crawford J; Lower KM; Hennekam RC; Van Esch H; Mégarbané A; Lynch SA; Turner G; Gécz J
    J Med Genet; 2006 Mar; 43(3):238-43. PubMed ID: 15994862
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The depletion of PHF6 decreases the drug sensitivity of T-cell acute lymphoblastic leukemia to prednisolone.
    Xiang J; Wang G; Xia T; Chen Z
    Biomed Pharmacother; 2019 Jan; 109():2210-2217. PubMed ID: 30551478
    [TBL] [Abstract][Full Text] [Related]  

  • 18. MXD1 localizes in the nucleolus, binds UBF and impairs rRNA synthesis.
    Lafita-Navarro MC; Blanco R; Mata-Garrido J; Liaño-Pons J; Tapia O; García-Gutiérrez L; García-Alegría E; Berciano MT; Lafarga M; León J
    Oncotarget; 2016 Oct; 7(43):69536-69548. PubMed ID: 27588501
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype.
    Zweier C; Kraus C; Brueton L; Cole T; Degenhardt F; Engels H; Gillessen-Kaesbach G; Graul-Neumann L; Horn D; Hoyer J; Just W; Rauch A; Reis A; Wollnik B; Zeschnigk M; Lüdecke HJ; Wieczorek D
    J Med Genet; 2013 Dec; 50(12):838-47. PubMed ID: 24092917
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Distinct phenotype of PHF6 deletions in females.
    Di Donato N; Isidor B; Lopez Cazaux S; Le Caignec C; Klink B; Kraus C; Schrock E; Hackmann K
    Eur J Med Genet; 2014 Feb; 57(2-3):85-9. PubMed ID: 24380767
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.