Associated Papers
Krüppel-Like Factor 1: A Pivotal Gene Regulator in Erythropoiesis.
Caria CA et al.
Cells, 2022
Compound Heterozygosity for KLF1 Mutations Causing Hemolytic Anemia in Children: A Case Report and Literature Review.
Xu L et al.
Frontiers in Genetics, 2021
Mutations of the KLF1 gene detected in Japanese with the In(Lu) phenotype.
Kawai M et al.
Transfusion, 2017
Can mutations in the gene encoding transcription factor EKLF (Erythroid Krüppel-Like Factor) protect us against infectious and parasitic diseases?
Mikołajczyk K et al.
Postepy Higieny I Medycyny Doswiadczalnej (online), 2016
Krüppeling erythropoiesis: an unexpected broad spectrum of human red blood cell disorders due to KLF1 variants.
Perkins A et al.
Blood, 2016
Krüppel-like factor 1: hematologic phenotypes associated with KLF1 gene mutations.
Waye JS et al.
International Journal of Laboratory Hematology, 2015
A new Krüppel-like factor 1 mutation (c.947G > A or p.C316Y) in humans causes β-thalassemia minor.
Nitta T et al.
Hemoglobin, 2015
Blood group phenotypes resulting from mutations in erythroid transcription factors.
Singleton BK et al.
Current Opinion in Hematology, 2012
Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes.
Singleton BK et al.
Blood, 2011
Erythroid phenotypes associated with KLF1 mutations.
Borg J et al.
Haematologica, 2011
Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype.
Singleton BK et al.
Blood, 2008
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