192 related articles for article (PubMed ID: 34535703)
1. Novel variants in Krueppel like factor 1 that cause persistence of fetal hemoglobin in In(Lu) individuals.
Eernstman J; Veldhuisen B; Ligthart P; von Lindern M; van der Schoot CE; van den Akker E
Sci Rep; 2021 Sep; 11(1):18557. PubMed ID: 34535703
[TBL] [Abstract][Full Text] [Related]
2. Molecular analysis of the rare in(Lu) blood type: toward decoding the phenotypic outcome of haploinsufficiency for the transcription factor KLF1.
Helias V; Saison C; Peyrard T; Vera E; Prehu C; Cartron JP; Arnaud L
Hum Mutat; 2013 Jan; 34(1):221-8. PubMed ID: 23125034
[TBL] [Abstract][Full Text] [Related]
3. Genetic Variants Within the Erythroid Transcription Factor, KLF1, and Reduction of the Expression of Lutheran and Other Blood Group Antigens: Review of the In(Lu) Phenotype.
Fraser NS; Knauth CM; Moussa A; Dean MM; Hyland CA; Perkins AC; Flower RL; Schoeman EM
Transfus Med Rev; 2019 Apr; 33(2):111-117. PubMed ID: 31023581
[TBL] [Abstract][Full Text] [Related]
4. Investigation of the variable In(Lu) phenotype caused by KLF1 variants.
Fraser NS; Knauth CM; Schoeman EM; Moussa A; Perkins AC; Walsh T; Millard GM; Dean MM; Hyland CA; Flower RL
Transfusion; 2018 Oct; 58(10):2414-2420. PubMed ID: 30222867
[TBL] [Abstract][Full Text] [Related]
5. Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype.
Kawai M; Obara K; Onodera T; Enomoto T; Ogasawara K; Tsuneyama H; Uchikawa M; Inaba S
Transfusion; 2017 Apr; 57(4):1072-1077. PubMed ID: 28194794
[TBL] [Abstract][Full Text] [Related]
6. KLF1 drives the expression of fetal hemoglobin in British HPFH.
Wienert B; Martyn GE; Kurita R; Nakamura Y; Quinlan KGR; Crossley M
Blood; 2017 Aug; 130(6):803-807. PubMed ID: 28659276
[TBL] [Abstract][Full Text] [Related]
7. Identification of new KLF1 and LU alleles during the resolution of Lutheran typing discrepancies.
Garcia-Sanchez F; Pardi C; Kupatawintu P; Thornton N; Rodriguez MA; Lucea I; Sood C; Ochoa-Garay G
Transfusion; 2016 Jun; 56(6):1413-8. PubMed ID: 27043150
[TBL] [Abstract][Full Text] [Related]
8. Impact of transcription factors KLF1 and GATA1 on red blood cell antigen expression: a review.
Lopez GH; Sarri ME; Flower RL; Hyland CA
Immunohematology; 2024 Apr; 40(1):1-9. PubMed ID: 38739025
[TBL] [Abstract][Full Text] [Related]
9. Delayed fetal hemoglobin switching in subjects with KLF1 gene mutation.
Satta S; Perseu L; Maccioni L; Giagu N; Galanello R
Blood Cells Mol Dis; 2012 Jan; 48(1):22-4. PubMed ID: 22093801
[TBL] [Abstract][Full Text] [Related]
10. Mild dyserythropoiesis and β-like globin gene expression imbalance due to the loss of histone chaperone ASF1B.
Papadopoulos P; Kafasi A; De Cuyper IM; Barroca V; Lewandowski D; Kadri Z; Veldthuis M; Berghuis J; Gillemans N; Benavente Cuesta CM; Grosveld FG; van Zwieten R; Philipsen S; Vernet M; Gutiérrez L; Patrinos GP
Hum Genomics; 2020 Oct; 14(1):39. PubMed ID: 33066815
[TBL] [Abstract][Full Text] [Related]
11. Epigenomic analysis of KLF1 haploinsufficiency in primary human erythroblasts.
Heshusius S; Grech L; Gillemans N; Brouwer RWW; den Dekker XT; van IJcken WFJ; Nota B; Felice AE; van Dijk TB; von Lindern M; Borg J; van den Akker E; Philipsen S
Sci Rep; 2022 Jan; 12(1):336. PubMed ID: 35013432
[TBL] [Abstract][Full Text] [Related]
12. Targeted next-generation sequencing and long-read HiFi sequencing provide novel insights into clinically significant KLF1 variants.
Ye L; Wang C; Li A; Li M; Pi Y; Yang J; Zhu Z; Lu D
BMC Genomics; 2024 Mar; 25(1):230. PubMed ID: 38429690
[TBL] [Abstract][Full Text] [Related]
13. Alterations on high HbF levels may be associated with KLF1 gene mutations.
Aydin M; Rencuzogullari E; Bayram S; Sevgiler Y; Genc A
Cell Mol Biol (Noisy-le-grand); 2017 Aug; 63(8):51-57. PubMed ID: 28886314
[TBL] [Abstract][Full Text] [Related]
14. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin.
Borg J; Papadopoulos P; Georgitsi M; Gutiérrez L; Grech G; Fanis P; Phylactides M; Verkerk AJ; van der Spek PJ; Scerri CA; Cassar W; Galdies R; van Ijcken W; Ozgür Z; Gillemans N; Hou J; Bugeja M; Grosveld FG; von Lindern M; Felice AE; Patrinos GP; Philipsen S
Nat Genet; 2010 Sep; 42(9):801-5. PubMed ID: 20676099
[TBL] [Abstract][Full Text] [Related]
15. Krüppel-Like Transcription Factor KLF1 Is Required for Optimal γ- and β-Globin Expression in Human Fetal Erythroblasts.
Vinjamur DS; Alhashem YN; Mohamad SF; Amin P; Williams DC; Lloyd JA
PLoS One; 2016; 11(2):e0146802. PubMed ID: 26840243
[TBL] [Abstract][Full Text] [Related]
16. Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin.
Radmilovic M; Zukic B; Petrovic MS; Bartsakoulia M; Stankovic B; Kotur N; Dokmanovic L; Georgitsi M; Patrinos GP; Pavlovic S
Ann Hematol; 2013 Jan; 92(1):53-8. PubMed ID: 23161389
[TBL] [Abstract][Full Text] [Related]
17. Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Hariharan P; Colah R; Ghosh K; Nadkarni A
Genomics; 2019 Dec; 111(6):1771-1776. PubMed ID: 30529538
[TBL] [Abstract][Full Text] [Related]
18. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype.
Singleton BK; Burton NM; Green C; Brady RL; Anstee DJ
Blood; 2008 Sep; 112(5):2081-8. PubMed ID: 18487511
[TBL] [Abstract][Full Text] [Related]
19. Simvastatin and t-butylhydroquinone suppress KLF1 and BCL11A gene expression and additively increase fetal hemoglobin in primary human erythroid cells.
Macari ER; Schaeffer EK; West RJ; Lowrey CH
Blood; 2013 Jan; 121(5):830-9. PubMed ID: 23223429
[TBL] [Abstract][Full Text] [Related]
20. Induction of adult levels of β-globin in human erythroid cells that intrinsically express embryonic or fetal globin by transduction with KLF1 and BCL11A-XL.
Trakarnsanga K; Wilson MC; Lau W; Singleton BK; Parsons SF; Sakuntanaga P; Kurita R; Nakamura Y; Anstee DJ; Frayne J
Haematologica; 2014 Nov; 99(11):1677-85. PubMed ID: 25107887
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
