Krüppel-like factor 1: hematologic phenotypes associated withKLF1gene mutations
Author:
Affiliation:
1. Hamilton Regional Laboratory Medicine Program; Hamilton Health Sciences; Hamilton Ontario L8N 3Z5 Canada
2. Department of Pathology and Molecular Medicine; McMaster University; Hamilton Ontario L8N 3Z5 Canada
Publisher
Wiley
Subject
Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine
Reference25 articles.
1. The multifunctional role of EKLF/KLF1 during erythropoiesis;Siatecka;Blood,2011
2. Mutations in EKLF/KLF1form the molecular basis of the rare blood group In(Lu) phenotype;Singleton;Blood,2008
3. Erythroid phenotypes associated with KLF1 mutations;Borg;Haematologica,2011
4. Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin;Borg;Nat Genet,2010
5. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin;Satta;Haematologica,2011
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1. Generation, characterization, and use of EKLF(Klf1)/CRE knock-in mice for cell-restricted analyses;Frontiers in Hematology;2024-01-19
2. Association of DDX5/p68 protein with the upstream erythroid enhancer element (EHS1) of the gene encoding the KLF1 transcription factor;Journal of Biological Chemistry;2023-12
3. VPS37C facilitates erythroid differentiation by promoting EKLF stability;Biochemical and Biophysical Research Communications;2023-09
4. Molecular and haematological characterisation of haemolytic anaemia associated with biallelic KLF1 mutations: a case series;Journal of Clinical Pathology;2023-07-28
5. Identification of a genomic DNA sequence that quantitatively modulates KLF1 transcription factor expression in differentiating human hematopoietic cells;Scientific Reports;2023-05-10
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