BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 31126231)

  • 1. Corrupted DNA-binding specificity and ectopic transcription underpin dominant neomorphic mutations in KLF/SP transcription factors.
    Ilsley MD; Huang S; Magor GW; Landsberg MJ; Gillinder KR; Perkins AC
    BMC Genomics; 2019 May; 20(1):417. PubMed ID: 31126231
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A
    Kulczynska K; Bieker JJ; Siatecka M
    Mol Cell Biol; 2020 Feb; 40(5):. PubMed ID: 31818881
    [TBL] [Abstract][Full Text] [Related]  

  • 3. KLF1 mutation E325K induces cell cycle arrest in erythroid cells differentiated from congenital dyserythropoietic anemia patient-specific induced pluripotent stem cells.
    Kohara H; Utsugisawa T; Sakamoto C; Hirose L; Ogawa Y; Ogura H; Sugawara A; Liao J; Aoki T; Iwasaki T; Asai T; Doisaki S; Okuno Y; Muramatsu H; Abe T; Kurita R; Miyamoto S; Sakuma T; Shiba M; Yamamoto T; Ohga S; Yoshida K; Ogawa S; Ito E; Kojima S; Kanno H; Tani K
    Exp Hematol; 2019 May; 73():25-37.e8. PubMed ID: 30876823
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Severe anemia caused by dominant mutations in Krüppel-like factor 1 (KLF1).
    Kulczynska-Figurny K; Bieker JJ; Siatecka M
    Mutat Res Rev Mutat Res; 2020; 786():108336. PubMed ID: 33339573
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Case of Congenital Dyserythropoeitic Anemia Type IV Caused by E325K Mutation in Erythroid Transcription Factor KLF1.
    Ortolano R; Forouhar M; Warwick A; Harper D
    J Pediatr Hematol Oncol; 2018 Aug; 40(6):e389-e391. PubMed ID: 29200155
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic disarray follows mutant KLF1-E325K expression in a congenital dyserythropoietic anemia patient.
    Varricchio L; Planutis A; Manwani D; Jaffray J; Mitchell WB; Migliaccio AR; Bieker JJ
    Haematologica; 2019 Dec; 104(12):2372-2380. PubMed ID: 30872368
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Promiscuous DNA-binding of a mutant zinc finger protein corrupts the transcriptome and diminishes cell viability.
    Gillinder KR; Ilsley MD; Nébor D; Sachidanandam R; Lajoie M; Magor GW; Tallack MR; Bailey T; Landsberg MJ; Mackay JP; Parker MW; Miles LA; Graber JH; Peters LL; Bieker JJ; Perkins AC
    Nucleic Acids Res; 2017 Feb; 45(3):1130-1143. PubMed ID: 28180284
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Erythroid transcription factor EKLF/KLF1 mutation causing congenital dyserythropoietic anemia type IV in a patient of Taiwanese origin: review of all reported cases and development of a clinical diagnostic paradigm.
    Jaffray JA; Mitchell WB; Gnanapragasam MN; Seshan SV; Guo X; Westhoff CM; Bieker JJ; Manwani D
    Blood Cells Mol Dis; 2013 Aug; 51(2):71-5. PubMed ID: 23522491
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia.
    Arnaud L; Saison C; Helias V; Lucien N; Steschenko D; Giarratana MC; Prehu C; Foliguet B; Montout L; de Brevern AG; Francina A; Ripoche P; Fenneteau O; Da Costa L; Peyrard T; Coghlan G; Illum N; Birgens H; Tamary H; Iolascon A; Delaunay J; Tchernia G; Cartron JP
    Am J Hum Genet; 2010 Nov; 87(5):721-7. PubMed ID: 21055716
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hemoglobin switching in mice carrying the
    Korporaal A; Gillemans N; Heshusius S; Cantú I; van den Akker E; van Dijk TB; von Lindern M; Philipsen S
    Haematologica; 2021 Feb; 106(2):464-473. PubMed ID: 32467144
    [TBL] [Abstract][Full Text] [Related]  

  • 11. An Unusual Hydrops Fetalis Associated with Compound Heterozygosity for Krüppel-like Factor 1 mutations.
    Lee HH; Mak AS; Kou KO; Poon CF; Wong WS; Chiu KH; Au PK; Chan KY; Kan AS; Tang MH; Leung KY
    Hemoglobin; 2016 Nov; 40(6):431-434. PubMed ID: 28361594
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Direct competition between DNA binding factors highlights the role of Krüppel-like Factor 1 in the erythroid/megakaryocyte switch.
    Norton LJ; Hallal S; Stout ES; Funnell APW; Pearson RCM; Crossley M; Quinlan KGR
    Sci Rep; 2017 Jun; 7(1):3137. PubMed ID: 28600522
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutations in KLF1 encoding the In(Lu) phenotype reflect a diversity of clinical presentations.
    Keller J; Vege S; Horn T; Keller MA; Leger RM; Aeschlimann J; Lomas-Francis C; Westhoff CM
    Transfusion; 2018 Jan; 58(1):196-199. PubMed ID: 29047116
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mutant KLF1 in Adult Anemic Nan Mice Leads to Profound Transcriptome Changes and Disordered Erythropoiesis.
    Nébor D; Graber JH; Ciciotte SL; Robledo RF; Papoin J; Hartman E; Gillinder KR; Perkins AC; Bieker JJ; Blanc L; Peters LL
    Sci Rep; 2018 Aug; 8(1):12793. PubMed ID: 30143664
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Krüppel-like factor 1: hematologic phenotypes associated with KLF1 gene mutations.
    Waye JS; Eng B
    Int J Lab Hematol; 2015 May; 37 Suppl 1():78-84. PubMed ID: 25976964
    [TBL] [Abstract][Full Text] [Related]  

  • 16. KLF1-null neonates display hydrops fetalis and a deranged erythroid transcriptome.
    Magor GW; Tallack MR; Gillinder KR; Bell CC; McCallum N; Williams B; Perkins AC
    Blood; 2015 Apr; 125(15):2405-17. PubMed ID: 25724378
    [TBL] [Abstract][Full Text] [Related]  

  • 17. KLF1 E325K-associated Congenital Dyserythropoietic Anemia Type IV: Insights Into the Variable Clinical Severity.
    Ravindranath Y; Johnson RM; Goyette G; Buck S; Gadgeel M; Gallagher PG
    J Pediatr Hematol Oncol; 2018 Aug; 40(6):e405-e409. PubMed ID: 29300242
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Compound heterozygosity for KLF1 mutations is associated with microcytic hypochromic anemia and increased fetal hemoglobin.
    Huang J; Zhang X; Liu D; Wei X; Shang X; Xiong F; Yu L; Yin X; Xu X
    Eur J Hum Genet; 2015 Oct; 23(10):1341-8. PubMed ID: 25585695
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Modelling the erythroblastic island niche of dyserythropoietic anaemia type IV patients using induced pluripotent stem cells.
    May A; Ventura T; Fidanza A; Volmer H; Taylor H; Romanò N; D'Souza SL; Bieker JJ; Forrester LM
    Front Cell Dev Biol; 2023; 11():1148013. PubMed ID: 37113767
    [No Abstract]   [Full Text] [Related]  

  • 20. EKLF/Klf1 regulates erythroid transcription by its pioneering activity and selective control of RNA Pol II pause-release.
    Mukherjee K; Bieker JJ
    Cell Rep; 2022 Dec; 41(12):111830. PubMed ID: 36543143
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.