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Browsing by Author Fisher, C.A.
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Showing results 17 to 23 of 23
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Issue Date
Title
Author(s)
2018
Phenotypic and molecular characterization of a serum-free miniature erythroid differentiation system suitable for high-throughput screening and single-cell assays
Mettananda, S.
;
Clark, K.
;
Fisher, C.A.
;
Sloane-Stanley, J.A.
;
Gibbons, R.J.
;
Higgs, D.R.
2015
Rare hemoglobin variants: Hb G-Szuhu (HBB: c.243C>G), Hb G-Coushatta (HBB: c.68A>C) and Hb Mizuho (HBB:c.206T>C) in Sri Lankan families
Perera, P.S.
;
Silva, I.
;
Hapugoda, M.
;
Wickramarathne, M.N.
;
Wijesiriwardena, I.
;
Efremov, D.G.
;
Fisher, C.A.
;
Weatherall, D.J.
;
Premawardhena, A.
2004
Response of jaundice to phenobarbitone in thalassaemic patients co-inheriting Gilbert syndrome
Premawardhena, A.P.
;
Arambepola, M.
;
Fisher, C.A.
;
Oliveiri, N.F.
;
Weatherall, D.J.
2017
Selective silencing of α-globin by the histone demethylase inhibitor IOX1: A potentially new pathway for treatment of β-thalassemia
Mettananda, S.
;
Fisher, C.A.
;
Sloane-Stanley, J.A.
;
Taylor, S.
;
Oppermann, U.
;
Gibbons, R.J.
;
Higgs, D.R.
2000
Thalassaemia in Sri Lanka: implications for the future health burden of asian populations
de Silva, S.
;
Fisher, C.A.
;
Premawardhena, A.P.
;
Lamabadusuriya, S.P.
;
Peto, T.E.
;
Perera, G.
;
Old, J.M.
;
Clegg, J.B.
;
Olivieri, N.F.
;
Weatherall, D.J.
;
Sri Lanka Thalassaemia Study Group
2004
Thalassemia in Sri Lanka: a progress report
Premawardhena, A.P.
;
de Silva, S.
;
Arambepola, M.
;
Olivieri, N.
;
Merson, L.
;
Muraco, J.
;
Allen, A.
;
Fisher, C.A.
;
Peto, T.
;
Vichinsky, E.
;
Weatherall, D.J.
2003
The worldwide prevalence of the UGT-1A1 promoter polymorphism as a contributor for phenotypic variability in thalassaemia
Premawardhena, A.P.
;
Lilt, Y.T.
;
Fisher, C.A.
;
Clegg, J.B.
;
Weatherall, D.J.