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    Article

    Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin

    Sjaak Philipsen and colleagues report that haploinsufficiency for KLF1 causes hereditary persistence of fetal hemoglobin in a large Maltese family. They further show that KLF1 is a key activator of BCL11A, whi...

    Joseph Borg, Petros Papadopoulos, Marianthi Georgitsi, Laura Gutiérrez in Nature Genetics (2010)

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    Open Access

    Robust hematopoietic specification requires the ubiquitous Sp1 and Sp3 transcription factors

    Both tissue-specific and ubiquitously expressed transcription factors, such as Sp-family members, are required for correct development. However, the molecular details of how ubiquitous factors are involved in ...

    Jane Gilmour, Leigh O’Connor, Christopher P. Middleton in Epigenetics & Chromatin (2019)