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Blood Reviews|May 30, 2006
The molecular basis of hereditary red cell membrane disordersJean DelaunayThe Hematology Journal : the Official Journal of the European Haematology Association|July 23, 2003
Red cell membrane and erythropoiesis genetic defectsJean DelaunaySeminars in Hematology|April 9, 2004
The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cationsJean DelaunayHaematologica|May 2, 2009
Close to unraveling the secrets of congenital dyserythropoietic anemia types I and IIAchille Iolascon, Jean DelaunayCurrent Opinion in Hematology|March 8, 2011
Congenital dyserythropoietic anemiasAchille Iolascon, Roberta Russo, Jean DelaunayBlood Cells, Molecules & Diseases|September 25, 2010
Nonsense-mediated mRNA decay (NMD) blockage promotes nonsense mRNA stabilization in protein 4.1R deficient cells carrying the 4.1R Coimbra variant of hereditary elliptocytosisMadeleine Morinière, François Delhommeau, Alain Calender, et al.Pediatric Blood & Cancer|April 14, 2011
Wiskott-Aldrich syndrome presenting with early onset recurrent acute hemorrhagic edema and hyperostosisShanmuganathan Chandrakasan, Surjit Singh, Sunil Dogra, et al.Blood|January 28, 2006
Two new human DMT1 gene mutations in a patient with microcytic anemia, low ferritinemia, and liver iron overloadCarole Beaumont, Jean Delaunay, Gilles Hetet, et al.The Journal of Biological Chemistry|October 23, 2003
Caspase 3-mediated proteolysis of the N-terminal cytoplasmic domain of the human erythroid anion exchanger 1 (band 3)Debabrata Mandal, Veronique Baudin-Creuza, Asima Bhattacharyya, et al.Pageof 6