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Red cell membrane disorders

International journal of laboratory hematology, 2017-05, Vol.39 (S1), p.47-52

2017

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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.559-565

2016

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Metabolomic signatures of ideal cardiovascular health in black adults

Scientific reports, 2024-01, Vol.14 (1), p.1794-1794, Article 1794

2024

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Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice

Haematologica (Roma), 2014-02, Vol.99 (2), p.267-275

2014

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DNA methylation in childhood dental caries and hypomineralization

Journal of dentistry, 2022-02, Vol.117, p.103913-103913, Article 103913

2022

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Primary Role for Adherent Leukocytes in Sickle Cell Vascular Occlusion: A New Paradigm

Proceedings of the National Academy of Sciences - PNAS, 2002-03, Vol.99 (5), p.3047-3051

2002

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Novel aspects of Kindlin‐3 function in humans based on a new case of leukocyte adhesion deficiency III

Journal of thrombosis and haemostasis, 2012-07, Vol.10 (7), p.1397-1408

2012

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Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro

Cell death & disease, 2012-07, Vol.3 (7), p.e356-e356

2012

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Hereditary spherocytosis

The Lancet (British edition), 2008-10, Vol.372 (9647), p.1411-1426

2008

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The malaria-infected red blood cell: Structural and functional changes

Advances in Parasitology, 2001, Vol.50, p.1-86

2001

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Characterization of Human RhCG and Mouse Rhcg as Novel Nonerythroid Rh Glycoprotein Homologues Predominantly Expressed in Kidney and Testis

The Journal of biological chemistry, 2000-08, Vol.275 (33), p.25641-25651

2000

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Regulation of Protein 4.1R, p55, and Glycophorin C Ternary Complex in Human Erythrocyte Membrane

The Journal of biological chemistry, 2000-08, Vol.275 (32), p.24540-24546

2000

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Red cell membrane and malaria

Transfusion clinique et biologique (Paris), 2010-09, Vol.17 (3), p.197-199

2010

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Molecular Maps of Red Cell Deformation: Hidden Elasticity and in Situ Connectivity

Science (American Association for the Advancement of Science), 1994-11, Vol.266 (5187), p.1032-1035

1994

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Diamond-Blackfan anemia, ribosome and erythropoiesis

Transfusion clinique et biologique (Paris), 2010-09, Vol.17 (3), p.112-119

2010

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Red blood cell deformability, membrane material properties and shape: regulation by transmembrane, skeletal and cytosolic proteins and lipids

Seminars in hematology, 1993-07, Vol.30 (3), p.171-192

1993

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Modulation of Erythrocyte Membrane Mechanical Function by Protein 4.1 Phosphorylation

The Journal of biological chemistry, 2005-03, Vol.280 (9), p.7581-7587

2005

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Natural history of hereditary spherocytosis during the first year of life

Blood, 2000-01, Vol.95 (2), p.393-397

2000

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Kinematics of red cell aspiration by fluorescence-imaged microdeformation

Biophysical journal, 1996-10, Vol.71 (4), p.1680-1694

1996

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Cloning and Characterization of 4.1G (EPB41L2), a New Member of the Skeletal Protein 4.1 (EPB41) Gene Family

Genomics (San Diego, Calif.), 1998-04, Vol.49 (2), p.298-306

1998

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New insights into function of red cell membrane proteins and their interaction with spectrin-based membrane skeleton

Transfusion clinique et biologique (Paris), 2006-03, Vol.13 (1), p.29-30

2006

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Characterization of multiple isoforms of protein 4.1R expressed during erythroid terminal differentiation

Blood, 1998-12, Vol.92 (11), p.4404-4414

1998

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Identification of a Functional Role for Lipid Asymmetry in Biological Membranes: Phosphatidylserine-Skeletal Protein Interactions Modulate Membrane Stability

Proceedings of the National Academy of Sciences - PNAS, 2002-02, Vol.99 (4), p.1943-1948

2002

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Mechanochemistry of the alternatively spliced spectrin-actin binding domain in membrane skeletal protein 4.1

The Journal of biological chemistry, 1993-04, Vol.268 (10), p.7186-7195

1993

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Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1

The Journal of biological chemistry, 1991-05, Vol.266 (13), p.8273-8280

1991

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Red cell membrane disorders

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

Metabolomic signatures of ideal cardiovascular health in black adults

Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice

DNA methylation in childhood dental caries and hypomineralization

Primary Role for Adherent Leukocytes in Sickle Cell Vascular Occlusion: A New Paradigm

Novel aspects of Kindlin‐3 function in humans based on a new case of leukocyte adhesion deficiency III

Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro

Hereditary spherocytosis

The malaria-infected red blood cell: Structural and functional changes

Characterization of Human RhCG and Mouse Rhcg as Novel Nonerythroid Rh Glycoprotein Homologues Predominantly Expressed in Kidney and Testis

Regulation of Protein 4.1R, p55, and Glycophorin C Ternary Complex in Human Erythrocyte Membrane

Red cell membrane and malaria

Molecular Maps of Red Cell Deformation: Hidden Elasticity and in Situ Connectivity

Diamond-Blackfan anemia, ribosome and erythropoiesis

Red blood cell deformability, membrane material properties and shape: regulation by transmembrane, skeletal and cytosolic proteins and lipids

Modulation of Erythrocyte Membrane Mechanical Function by Protein 4.1 Phosphorylation

Natural history of hereditary spherocytosis during the first year of life

Kinematics of red cell aspiration by fluorescence-imaged microdeformation

Cloning and Characterization of 4.1G (EPB41L2), a New Member of the Skeletal Protein 4.1 (EPB41) Gene Family

New insights into function of red cell membrane proteins and their interaction with spectrin-based membrane skeleton

Characterization of multiple isoforms of protein 4.1R expressed during erythroid terminal differentiation

Identification of a Functional Role for Lipid Asymmetry in Biological Membranes: Phosphatidylserine-Skeletal Protein Interactions Modulate Membrane Stability

Mechanochemistry of the alternatively spliced spectrin-actin binding domain in membrane skeletal protein 4.1

Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1

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