Red cell membrane disorders

An Unrecognized Function of Cholesterol: Regulating the Mechanism Controlling Membrane Phospholipid Asymmetry

(2016) Nobuto Arashiki et al.   BIOCHEMISTRY

Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer

(2016) Lydie Da Costa et al.   BLOOD CELLS MOLECULES AND DISEASES

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia

(2016) N. Arashiki et al.   HAEMATOLOGICA

ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia

(2016) N. Arashiki et al.   HAEMATOLOGICA

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

(2015) E. Glogowska et al.   BLOOD

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

(2013) Lydie Da Costa et al.   BLOOD REVIEWS

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

(2012) R. Zarychanski et al.   BLOOD

Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen

(2012) I. Safeukui et al.   BLOOD

Red cell membrane: past, present, and future

(2008) N. Mohandas et al.   BLOOD

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein

(2008) L. J. Bruce et al.   BLOOD

Hereditary spherocytosis

(2008) Silverio Perrotta et al.   LANCET