Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
Export 5 results:
Author Title [ Type
] Year Filters: Keyword is Fetal Hemoglobin [Clear All Filters]
(2013). Functional analysis of a novel KLF1 gene promoter variation associated with hereditary persistence of fetal hemoglobin..
Ann Hematol. 92(1), 53-8.
(2019). Genomic variants in members of the Krüppel-like factor gene family are associated with disease severity and hydroxyurea treatment efficacy in β-hemoglobinopathies patients..
Pharmacogenomics. 20(11), 791-801.
(2010). Haploinsufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin..
Nat Genet. 42(9), 801-5.
(2012). KLF10 gene expression is associated with high fetal hemoglobin levels and with response to hydroxyurea treatment in β-hemoglobinopathy patients..
Pharmacogenomics. 13(13), 1487-500.
