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Items: 1 to 20 of 118

1.

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 12;87(5):721-7. doi: 10.1016/j.ajhg.2010.10.010. Epub 2010 Nov 4.

2.

Congenital dyserythropoietic anemias.

Iolascon A, Russo R, Delaunay J.

Curr Opin Hematol. 2011 May;18(3):146-51. doi: 10.1097/MOH.0b013e32834521b0. Review.

PMID:
21378561
3.

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.

4.

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. doi: 10.1080/03630269.2016.1267017.

PMID:
28361594
5.

Congenital dyserythropoietic anemias: molecular insights and diagnostic approach.

Iolascon A, Heimpel H, Wahlin A, Tamary H.

Blood. 2013 Sep 26;122(13):2162-6. doi: 10.1182/blood-2013-05-468223. Epub 2013 Aug 12. Review.

6.

Krüppel-like transcription factors KLF1 and KLF2 have unique and coordinate roles in regulating embryonic erythroid precursor maturation.

Vinjamur DS, Wade KJ, Mohamad SF, Haar JL, Sawyer ST, Lloyd JA.

Haematologica. 2014 Oct;99(10):1565-73. doi: 10.3324/haematol.2014.104943. Epub 2014 Aug 22.

7.

Kruppel-like factor 1 (KLF1), KLF2, and Myc control a regulatory network essential for embryonic erythropoiesis.

Pang CJ, Lemsaddek W, Alhashem YN, Bondzi C, Redmond LC, Ah-Son N, Dumur CI, Archer KJ, Haar JL, Lloyd JA, Trudel M.

Mol Cell Biol. 2012 Jul;32(13):2628-44. doi: 10.1128/MCB.00104-12. Epub 2012 May 7.

8.

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 9;125(15):2405-17. doi: 10.1182/blood-2014-08-590968. Epub 2015 Feb 27.

9.

Congenital dyserythropoietic anemia in China: a case report from two families and a review.

Ru Y, Liu G, Bai J, Dong S, Nie N, Zhang H, Zhao S, Zheng Y, Zhu X, Nie G, Zhang F, Eyden B.

Ann Hematol. 2014 May;93(5):773-7. doi: 10.1007/s00277-013-1933-8. Epub 2013 Nov 7. Review.

PMID:
24196372
10.

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. doi: 10.1038/ejhg.2014.291. Epub 2015 Jan 14.

11.

[Diagnosis and genetics of congenital dyserythropoietic anemias (CDA)].

Rössler J, Havers W.

Klin Padiatr. 2000 Jul-Aug;212(4):153-8. Review. German.

PMID:
10994542
12.

A global role for KLF1 in erythropoiesis revealed by ChIP-seq in primary erythroid cells.

Tallack MR, Whitington T, Yuen WS, Wainwright EN, Keys JR, Gardiner BB, Nourbakhsh E, Cloonan N, Grimmond SM, Bailey TL, Perkins AC.

Genome Res. 2010 Aug;20(8):1052-63. doi: 10.1101/gr.106575.110. Epub 2010 May 27. Erratum in: Genome Res. 2010 Dec;20(12):1748.

13.

Novel roles for KLF1 in erythropoiesis revealed by mRNA-seq.

Tallack MR, Magor GW, Dartigues B, Sun L, Huang S, Fittock JM, Fry SV, Glazov EA, Bailey TL, Perkins AC.

Genome Res. 2012 Dec;22(12):2385-98. doi: 10.1101/gr.135707.111. Epub 2012 Jul 26.

14.

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
15.
16.

Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.

Fujino H, Doisaki S, Park YD, Hama A, Muramatsu H, Kojima S, Sumimoto S.

Int J Hematol. 2013 May;97(5):650-3. doi: 10.1007/s12185-013-1338-4. Epub 2013 Apr 19.

PMID:
23605369
17.

Transcription factors KLF1 and KLF2 positively regulate embryonic and fetal beta-globin genes through direct promoter binding.

Alhashem YN, Vinjamur DS, Basu M, Klingmüller U, Gaensler KM, Lloyd JA.

J Biol Chem. 2011 Jul 15;286(28):24819-27. doi: 10.1074/jbc.M111.247536. Epub 2011 May 24.

18.
19.

The congenital dyserythropoietic anemias.

Renella R, Wood WG.

Hematol Oncol Clin North Am. 2009 Apr;23(2):283-306. doi: 10.1016/j.hoc.2009.01.010. Review.

PMID:
19327584
20.

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 Jr, Lloyd JA.

PLoS One. 2016 Feb 3;11(2):e0146802. doi: 10.1371/journal.pone.0146802. eCollection 2016.

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