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Items: 13

1.

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. doi: 10.1038/ng.630. Epub 2010 Aug 1.

2.

Three fingers on the switch: Krüppel-like factor 1 regulation of γ-globin to β-globin gene switching.

Tallack MR, Perkins AC.

Curr Opin Hematol. 2013 May;20(3):193-200. doi: 10.1097/MOH.0b013e32835f59ba. Review.

PMID:
23474875
3.

Molecular basis of hereditary persistence of fetal hemoglobin.

Forget BG.

Ann N Y Acad Sci. 1998 Jun 30;850:38-44. Review.

PMID:
9668525
4.

DNA sequences regulating human globin gene transcription in nondeletional hereditary persistence of fetal hemoglobin.

Ottolenghi S, Mantovani R, Nicolis S, Ronchi A, Giglioni B.

Hemoglobin. 1989;13(6):523-41. Review.

PMID:
2481658
5.

KLF1 directly coordinates almost all aspects of terminal erythroid differentiation.

Tallack MR, Perkins AC.

IUBMB Life. 2010 Dec;62(12):886-90. doi: 10.1002/iub.404. Review.

6.

Reawakening fetal hemoglobin: prospects for new therapies for the β-globin disorders.

Bauer DE, Kamran SC, Orkin SH.

Blood. 2012 Oct 11;120(15):2945-53. doi: 10.1182/blood-2012-06-292078. Epub 2012 Aug 17. Review.

7.

Update on fetal hemoglobin gene regulation in hemoglobinopathies.

Bauer DE, Orkin SH.

Curr Opin Pediatr. 2011 Feb;23(1):1-8. doi: 10.1097/MOP.0b013e3283420fd0. Review.

8.

Probing the onset and regulation of erythroid cell-specific gene expression.

Bieker JJ.

Mt Sinai J Med. 2005 Sep;72(5):333-8. Review.

PMID:
16184297
9.

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. doi: 10.1016/j.bcmd.2013.02.006. Epub 2013 Mar 20. Review.

10.

The multifunctional role of EKLF/KLF1 during erythropoiesis.

Siatecka M, Bieker JJ.

Blood. 2011 Aug 25;118(8):2044-54. doi: 10.1182/blood-2011-03-331371. Epub 2011 May 25. Review.

11.

Control of fetal hemoglobin: new insights emerging from genomics and clinical implications.

Thein SL, Menzel S, Lathrop M, Garner C.

Hum Mol Genet. 2009 Oct 15;18(R2):R216-23. doi: 10.1093/hmg/ddp401. Review.

12.

Blood group phenotypes resulting from mutations in erythroid transcription factors.

Singleton BK, Frayne J, Anstee DJ.

Curr Opin Hematol. 2012 Nov;19(6):486-93. doi: 10.1097/MOH.0b013e328358f92e. Review.

PMID:
22954727
13.

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. doi: 10.1111/ijlh.12356. Review.

PMID:
25976964
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