-
1
-
-
80054845638
-
KLF1 gene mutations cause borderline HbA2
-
Perseu L, Satta S, Moi P, et al. KLF1 gene mutations cause borderline HbA2. Blood. 2011;118(16):4454-4458.
-
(2011)
Blood
, vol.118
, Issue.16
, pp. 4454-4458
-
-
Perseu, L.1
Satta, S.2
Moi, P.3
-
2
-
-
79955732301
-
Erythroid phenotypes associated with KLF1 mutations
-
Borg J, Patrinos GP, Felice AE, Philipsen S. Erythroid phenotypes associated with KLF1 mutations. Haematologica. 2011;96(5):635-638.
-
(2011)
Haematologica
, vol.96
, Issue.5
, pp. 635-638
-
-
Borg, J.1
Patrinos, G.P.2
Felice, A.E.3
Philipsen, S.4
-
3
-
-
80052153840
-
The multifunctional role of EKLF/KLF1 during erythropoiesis
-
Siatecka M, Bieker JJ. The multifunctional role of EKLF/KLF1 during erythropoiesis. Blood. 2011;118(8): 2044-2054.
-
(2011)
Blood
, vol.118
, Issue.8
, pp. 2044-2054
-
-
Siatecka, M.1
Bieker, J.J.2
-
4
-
-
52649088204
-
Mutations in EKLF/KLF1 form the molecular basis of the rare blood group in(Lu) phenotype
-
Singleton BK, Burton NM, Green C, Brady RL, Anstee DJ. Mutations in EKLF/KLF1 form the molecular basis of the rare blood group In(Lu) phenotype. Blood. 2008;112(5): 2081-2088.
-
(2008)
Blood
, vol.112
, Issue.5
, pp. 2081-2088
-
-
Singleton, B.K.1
Burton, N.M.2
Green, C.3
Brady, R.L.4
Anstee, D.J.5
-
5
-
-
78249264453
-
A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia
-
Arnaud L, Saison C, Helias V, et al. A dominant mutation in the gene encoding the erythroid transcription factor KLF1 causes a congenital dyserythropoietic anemia. Am J Hum Genet. 2010;87(5):721-727.
-
(2010)
Am J Hum Genet
, vol.87
, Issue.5
, pp. 721-727
-
-
Arnaud, L.1
Saison, C.2
Helias, V.3
-
6
-
-
77956622584
-
Haploin-sufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin
-
Borg J, Papadopoulos P, Georgitsi M, et al. Haploin-sufficiency for the erythroid transcription factor KLF1 causes hereditary persistence of fetal hemoglobin. Nat Genet. 2010; 42(9):801-805.
-
(2010)
Nat Genet
, vol.42
, Issue.9
, pp. 801-805
-
-
Borg, J.1
Papadopoulos, P.2
Georgitsi, M.3
-
7
-
-
77950930726
-
Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6
-
Xu J, Sankaran VG, Ni M, et al. Transcriptional silencing of {gamma}-globin by BCL11A involves long-range interactions and cooperation with SOX6. Genes Dev. 2010;24(8):783-798.
-
(2010)
Genes Dev
, vol.24
, Issue.8
, pp. 783-798
-
-
Xu, J.1
Sankaran, V.G.2
Ni, M.3
-
8
-
-
77956630402
-
KLF1 regulates BCL11A expression and gamma- To beta-globin gene switching
-
Zhou D, Liu K, Sun CW, Pawlik KM, Townes TM. KLF1 regulates BCL11A expression and gamma- to beta-globin gene switching. Nat Genet. 2010;42(9):742-744.
-
(2010)
Nat Genet
, vol.42
, Issue.9
, pp. 742-744
-
-
Zhou, D.1
Liu, K.2
Sun, C.W.3
Pawlik, K.M.4
Townes, T.M.5
-
9
-
-
79955738088
-
Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin
-
Satta S, Perseu L, Moi P, et al. Compound heterozygosity for KLF1 mutations associated with remarkable increase of fetal hemoglobin and red cell protoporphyrin. Haematologica. 2011;96(5):767-770.
-
(2011)
Haematologica
, vol.96
, Issue.5
, pp. 767-770
-
-
Satta, S.1
Perseu, L.2
Moi, P.3
-
10
-
-
80052919973
-
Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes
-
published online ahead of print July 21
-
Singleton BK, Lau W, Fairweather VS, et al. Mutations in the second zinc finger of human EKLF reduce promoter affinity but give rise to benign and disease phenotypes [published online ahead of print July 21, 2011]. Blood.
-
(2011)
Blood
-
-
Singleton, B.K.1
Lau, W.2
Fairweather, V.S.3
|