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Reduction in flippase activity contributes to surface presentation of phosphatidylserine in human senescent erythrocytes

Journal of cellular and molecular medicine, 2020-12, Vol.24 (23), p.13991-14000

2020

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ATP11C T418N, a gene mutation causing congenital hemolytic anemia, reduces flippase activity due to improper membrane trafficking

Biochemical and biophysical research communications, 2019-08, Vol.516 (3), p.705-712

2019

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

Biochemistry (Easton), 2016-06, Vol.55 (25), p.3504-3513

2016

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Novel multivalent S100A8 inhibitory peptides attenuate tumor progression and metastasis by inhibiting the TLR4-dependent pathway

Cancer gene therapy, 2023-07, Vol.30 (7), p.973-984

2023

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Monoallelic CRMP1 gene variants cause neurodevelopmental disorder

eLife, 2022-12, Vol.11

2022

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Maintenance and regulation of asymmetric phospholipid distribution in human erythrocyte membranes: implications for erythrocyte functions

Current opinion in hematology, 2017-05, Vol.24 (3), p.167-172

2017

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The covalent modification of spectrin in red cell membranes by the lipid peroxidation product 4-hydroxy-2-nonenal

Biochemical and biophysical research communications, 2010-01, Vol.391 (3), p.1543-1547

2010

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Membrane Peroxidation and Methemoglobin Formation Are Both Necessary for Band 3 Clustering: Mechanistic Insights into Human Erythrocyte Senescence

Biochemistry (Easton), 2013-08, Vol.52 (34), p.5760-5769

2013

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Storage-Related Changes in Autologous Whole Blood and Irradiated Allogeneic Red Blood Cells and Their Ex Vivo Effects on Deformability, Indices, and Density of Circulating Erythrocytes in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass

Journal of cardiothoracic and vascular anesthesia, 2022-03, Vol.36 (3), p.855-861

2022

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3627 PHOSPHATIDYLSERINE EXPOSURE AND SHORTENED LIFE SPAN OF ERYTHROCYTES IN RENAL ANEMIA

Nephrology, dialysis, transplantation, 2023-06, Vol.38 (Supplement_1)

2023

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Parallel Reductions in Stomatin and Na,K-ATPase through the Exosomal Pathway during Reticulocyte Maturation in Dogs: Stomatin as a Genotypic and Phenotypic Marker of High K+ and Low K+ Red Cells

Journal of Veterinary Medical Science, 2010, Vol.72(7), pp.893-901

2010

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Changes in Erythrocyte Morphology at Initiation of Cardiopulmonary Bypass Without Blood Transfusion Were Not Associated With Less Deformability During Cardiac Surgery

Journal of cardiothoracic and vascular anesthesia, 2019-11, Vol.33 (11), p.2960-2967

2019

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Membrane skeleton hyperstability due to a novel alternatively spliced 4.1R can account for ellipsoidal camelid red cells with decreased deformability

The Journal of biological chemistry, 2023-02, Vol.299 (2), p.102877-102877, Article 102877

2023

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

Haematologica (Roma), 2016-05, Vol.101 (5), p.559

2016

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Cholesterol-binding protein TSPO2 coordinates maturation and proliferation of terminally differentiating erythroblasts

The Journal of biological chemistry, 2020-06, Vol.295 (23), p.8048-8063

2020

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Structural implications of the EL(K/Q)(L/C)LD(A/G)DD sequence in the C-terminal cytoplasmic tail for proper targeting of anion exchanger 1 to the plasma membrane

The Japanese Journal of Veterinary Research, 2009-11, Vol.57 (3), p.135-146

2009

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Band 3 phosphorylation induces irreversible alterations of stored red blood cells

American journal of hematology, 2018-05, Vol.93 (5), p.E110-E112

2018

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Extrusion of Na, K-ATPase and transferrin receptor with lipid raft-associated proteins in different populations of exosomes during reticulocyte maturation in dogs

The Japanese journal of veterinary research, 2010-05, Vol.58 (1), p.17-27

2010

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Modification of Spectrin in Red Cell Membranes by the Lipid Peroxidation Product 4-Hydroxy-2-nonenal Associated with the Changes in Red Cell Membrane Properties

The Japanese Journal of Veterinary Research, 2010, Vol.58 (2), p.144-144

Nobuto Arashiki

2010

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Identification of genes for two major sialoglycoproteins, glycophorin A and glycophorin C in canine red cell membranes

The Japanese Journal of Veterinary Research, 2008-02, Vol.55 (4), p.103-114

2008

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ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia

Blood, 2015-12, Vol.126 (23), p.2131-2131

2015

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Expression of alpha-hemoglobin stabilizing protein and cellular prion protein in a subclone of murine erythroleukemia cell line MEL

The Japanese journal of veterinary research, 2008-08, Vol.56 (2), p.75-84

2008

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Senescence mechanism of human erythrocytes

Rinshō ketsueki, 2014-06, Vol.55 (6), p.643

2014

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Mechanism of the promoter activation and the role of erythroid Kruppel-like factor in bovine γ- to β-globin gene switching

The Japanese Journal of Veterinary Research, 2005, Vol.53 (1/2), p.96-96

Nobuto Arashiki

2005

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Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle

Journal of cell science, 2006-09, Vol.119 (Pt 17), p.3602-3612

2006

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Reduction in flippase activity contributes to surface presentation of phosphatidylserine in human senescent erythrocytes

ATP11C T418N, a gene mutation causing congenital hemolytic anemia, reduces flippase activity due to improper membrane trafficking

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

Novel multivalent S100A8 inhibitory peptides attenuate tumor progression and metastasis by inhibiting the TLR4-dependent pathway

Monoallelic CRMP1 gene variants cause neurodevelopmental disorder

Maintenance and regulation of asymmetric phospholipid distribution in human erythrocyte membranes: implications for erythrocyte functions

The covalent modification of spectrin in red cell membranes by the lipid peroxidation product 4-hydroxy-2-nonenal

Membrane Peroxidation and Methemoglobin Formation Are Both Necessary for Band 3 Clustering: Mechanistic Insights into Human Erythrocyte Senescence

Storage-Related Changes in Autologous Whole Blood and Irradiated Allogeneic Red Blood Cells and Their Ex Vivo Effects on Deformability, Indices, and Density of Circulating Erythrocytes in Patients Undergoing Cardiac Surgery With Cardiopulmonary Bypass

3627 PHOSPHATIDYLSERINE EXPOSURE AND SHORTENED LIFE SPAN OF ERYTHROCYTES IN RENAL ANEMIA

Parallel Reductions in Stomatin and Na,K-ATPase through the Exosomal Pathway during Reticulocyte Maturation in Dogs: Stomatin as a Genotypic and Phenotypic Marker of High K+ and Low K+ Red Cells

Changes in Erythrocyte Morphology at Initiation of Cardiopulmonary Bypass Without Blood Transfusion Were Not Associated With Less Deformability During Cardiac Surgery

Membrane skeleton hyperstability due to a novel alternatively spliced 4.1R can account for ellipsoidal camelid red cells with decreased deformability

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

Cholesterol-binding protein TSPO2 coordinates maturation and proliferation of terminally differentiating erythroblasts

Structural implications of the EL(K/Q)(L/C)LD(A/G)DD sequence in the C-terminal cytoplasmic tail for proper targeting of anion exchanger 1 to the plasma membrane

Band 3 phosphorylation induces irreversible alterations of stored red blood cells

Extrusion of Na, K-ATPase and transferrin receptor with lipid raft-associated proteins in different populations of exosomes during reticulocyte maturation in dogs

Modification of Spectrin in Red Cell Membranes by the Lipid Peroxidation Product 4-Hydroxy-2-nonenal Associated with the Changes in Red Cell Membrane Properties

Identification of genes for two major sialoglycoproteins, glycophorin A and glycophorin C in canine red cell membranes

ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia

Expression of alpha-hemoglobin stabilizing protein and cellular prion protein in a subclone of murine erythroleukemia cell line MEL

Senescence mechanism of human erythrocytes

Mechanism of the promoter activation and the role of erythroid Kruppel-like factor in bovine γ- to β-globin gene switching

Ubiquitylation-independent ER-associated degradation of an AE1 mutant associated with dominant hereditary spherocytosis in cattle

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