Published in Biophys J on October 01, 1996
Simulations of the erythrocyte cytoskeleton at large deformation. II. Micropipette aspiration. Biophys J (1998) 2.79
Power-law rheology of isolated nuclei with deformation mapping of nuclear substructures. Biophys J (2005) 2.19
Elasticity of the red cell membrane and its relation to hemolytic disorders: an optical tweezers study. Biophys J (1999) 1.69
Deformation-enhanced fluctuations in the red cell skeleton with theoretical relations to elasticity, connectivity, and spectrin unfolding. Biophys J (2001) 1.64
Mechanical properties of the cell nucleus and the effect of emerin deficiency. Biophys J (2006) 1.40
Molecular mechanisms of cellular mechanosensing. Nat Mater (2013) 1.34
Micropipet-based pico force transducer: in depth analysis and experimental verification. Biophys J (1998) 1.27
Twenty odd years of stretch-sensitive channels. Pflugers Arch (2006) 1.26
Topographical pattern dynamics in passive adhesion of cell membranes. Biophys J (2004) 1.21
Statistical thermodynamics of membrane bending-mediated protein-protein attractions. Biophys J (2001) 1.14
Native ultrastructure of the red cell cytoskeleton by cryo-electron tomography. Biophys J (2011) 1.11
Erythrocyte membrane vesiculation: model for the molecular mechanism of protein sorting. Proc Natl Acad Sci U S A (1997) 1.07
Temperature transitions of protein properties in human red blood cells. Biophys J (1998) 1.01
Direct measures of large, anisotropic strains in deformation of the erythrocyte cytoskeleton. Biophys J (1999) 0.99
Membrane dynamics of the water transport protein aquaporin-1 in intact human red cells. Biophys J (1999) 0.97
Diffusion in a fluid membrane with a flexible cortical cytoskeleton. Biophys J (2009) 0.97
Actin protofilament orientation at the erythrocyte membrane. Biophys J (1999) 0.96
Integral protein linkage and the bilayer-skeletal separation energy in red blood cells. Biophys J (2008) 0.92
Multiscale simulation of erythrocyte membranes. Phys Rev E Stat Nonlin Soft Matter Phys (2010) 0.88
Actin protofilament orientation in deformation of the erythrocyte membrane skeleton. Biophys J (2000) 0.88
A novel strain energy relationship for red blood cell membrane skeleton based on spectrin stiffness and its application to micropipette deformation. Biomech Model Mechanobiol (2015) 0.77
Mechanical diagnosis of human erythrocytes by ultra-high speed manipulation unraveled critical time window for global cytoskeletal remodeling. Sci Rep (2017) 0.75
The rapid intermixing of cell surface antigens after formation of mouse-human heterokaryons. J Cell Sci (1970) 9.02
Uniaxial loading of the red-cell membrane. J Biomech (1972) 4.70
Theory of the sphering of red blood cells. Biophys J (1968) 3.79
Molecular maps of red cell deformation: hidden elasticity and in situ connectivity. Science (1994) 3.66
Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects. Annu Rev Biophys Biomol Struct (1994) 3.65
Lateral mobility of band 3 in the human erythrocyte membrane studied by fluorescence photobleaching recovery: evidence for control by cytoskeletal interactions. Proc Natl Acad Sci U S A (1980) 3.62
Visualization of the protein associations in the erythrocyte membrane skeleton. Proc Natl Acad Sci U S A (1985) 3.26
The use of a charge-coupled device for quantitative optical microscopy of biological structures. Science (1987) 2.64
Molecular crowding on the cell surface. Science (1988) 2.47
Lateral diffusion of membrane-spanning and glycosylphosphatidylinositol-linked proteins: toward establishing rules governing the lateral mobility of membrane proteins. J Cell Biol (1991) 2.28
A solid-liquid composite model of the red cell membrane. J Membr Biol (1977) 2.09
Restriction of the lateral motion of band 3 in the erythrocyte membrane by the cytoskeletal network: dependence on spectrin association state. Biochemistry (1986) 2.05
Regulation of band 3 mobilities in erythrocyte ghost membranes by protein association and cytoskeletal meshwork. Biochemistry (1988) 1.89
Structure and deformation properties of red blood cells: concepts and quantitative methods. Methods Enzymol (1989) 1.89
Drosophilia spectrin. I. Characterization of the purified protein. J Cell Biol (1987) 1.72
Fractionation of dextran and Ficoll by chromatography on Sephadex G-200. Biochim Biophys Acta (1967) 1.70
Lateral mobility of phospholipid and cholesterol in the human erythrocyte membrane: effects of protein-lipid interactions. Biochemistry (1984) 1.54
Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1. J Clin Invest (1986) 1.47
Three-dimensional map of the dimeric membrane domain of the human erythrocyte anion exchanger, Band 3. EMBO J (1994) 1.45
The human erythrocyte membrane skeleton may be an ionic gel. I. Membrane mechanochemical properties. Eur Biophys J (1986) 1.42
Mechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengthening. J Cell Biol (1995) 1.40
Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3. J Clin Invest (1992) 1.31
Force relaxation and permanent deformation of erythrocyte membrane. Biophys J (1983) 1.29
Spectrin and related molecules. CRC Crit Rev Biochem (1988) 1.27
Band 3-glycophorin A association in erythrocyte membrane demonstrated by combining protein diffusion measurements with antibody-induced cross-linking. Biochemistry (1980) 1.27
Effects of abnormal cytoskeletal structure on erythrocyte membrane mechanical properties. Cell Motil (1983) 1.22
Restricted diffusion of integral membrane proteins and polyphosphoinositides leads to their depletion in microvesicles released from human erythrocytes. Biochem J (1990) 1.04
High lateral mobility of endogenous and transfected alkaline phosphatase: a phosphatidylinositol-anchored membrane protein. J Cell Biol (1987) 1.02
Alterations of the apparent area expansivity modulus of red blood cell membrane by electric fields. Biophys J (1990) 1.02
Structural and functional characterization of band 3 from Southeast Asian ovalocytes. J Biol Chem (1992) 0.99
Effect of anti-spectrin antibody and ATP on deformability of resealed erythrocyte membranes. Proc Natl Acad Sci U S A (1978) 0.97
Analysis of lateral diffusion from a spherical cell surface to a tubular projection. Biophys J (1992) 0.96
Defective regulation of complement by the sickle erythrocyte: evidence for a defect in control of membrane attack complex formation. Blood (1994) 0.85
Existence of a flat phase in red cell membrane skeletons. Science (1993) 0.83
RBC membrane instability for large pipette deformation. A theoretical approach. Biorheology (1988) 0.82
Measurement of the elastic modulus for red cell membrane using a fluid mechanical technique. Biophys J (1973) 6.41
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia. Nat Genet (1999) 6.23
Uniaxial loading of the red-cell membrane. J Biomech (1972) 4.70
Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease. Science (1997) 4.25
Molecular maps of red cell deformation: hidden elasticity and in situ connectivity. Science (1994) 3.66
The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane. Trends Biochem Sci (1998) 3.24
Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton. Proc Natl Acad Sci U S A (1986) 3.22
Analysis of factors regulating erythrocyte deformability. J Clin Invest (1980) 2.29
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability. J Clin Invest (1981) 2.27
A congenital haemolytic anaemia with thermal sensitivity of the erythrocyte membrane. Br J Haematol (1975) 2.15
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression. Blood (1999) 2.07
The malaria-infected red blood cell: structural and functional changes. Adv Parasitol (2001) 1.91
Anion exchanger 1 (band 3) is required to prevent erythrocyte membrane surface loss but not to form the membrane skeleton. Cell (1996) 1.85
Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations. J Cell Biol (1986) 1.70
Computational and biological analysis of 680 kb of DNA sequence from the human 5q31 cytokine gene cluster region. Genome Res (1997) 1.69
Surface adhesion, deformation and detachment at low shear of red cells and white cells. Trans Am Soc Artif Intern Organs (1972) 1.68
Membrane assembly and remodeling during reticulocyte maturation. Blood (1989) 1.68
Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance. Blood (1983) 1.64
Targeted disruption of the beta adducin gene (Add2) causes red blood cell spherocytosis in mice. Proc Natl Acad Sci U S A (1999) 1.57
The influence of membrane skeleton on red cell deformability, membrane material properties, and shape. Semin Hematol (1983) 1.54
Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities. J Clin Invest (1999) 1.53
Characterization of human RhCG and mouse Rhcg as novel nonerythroid Rh glycoprotein homologues predominantly expressed in kidney and testis. J Biol Chem (2000) 1.52
The adhesive sickle erythrocyte: cause and consequence of abnormal interactions with endothelium, monocytes/macrophages and model membranes. Clin Haematol (1985) 1.51
Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1. J Biol Chem (1991) 1.50
Multiple protein 4.1 isoforms produced by alternative splicing in human erythroid cells. Proc Natl Acad Sci U S A (1988) 1.49
A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders. Blood (1982) 1.49
Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. Blood (2001) 1.48
Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1. J Clin Invest (1986) 1.47
Detachment of agglutinin-bonded red blood cells. II. Mechanical energies to separate large contact areas. Biophys J (1991) 1.46
Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser light scattering. Blood (1986) 1.46
Vacuolar uptake of host components, and a role for cholesterol and sphingomyelin in malarial infection. EMBO J (2000) 1.45
Molecular and functional characterization of protein 4.1B, a novel member of the protein 4.1 family with high level, focal expression in brain. J Biol Chem (2000) 1.45
Modulation of erythrocyte membrane mechanical function by beta-spectrin phosphorylation and dephosphorylation. J Biol Chem (1995) 1.42
Mechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengthening. J Cell Biol (1995) 1.40
Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis. J Clin Invest (1983) 1.39
Erythrocyte membrane rigidity induced by glycophorin A-ligand interaction. Evidence for a ligand-induced association between glycophorin A and skeletal proteins. J Clin Invest (1985) 1.38
Effect of hydrogen peroxide exposure on normal human erythrocyte deformability, morphology, surface characteristics, and spectrin-hemoglobin cross-linking. J Clin Invest (1985) 1.38
Static and dynamic rigidities of normal and sickle erythrocytes. Major influence of cell hemoglobin concentration. J Clin Invest (1984) 1.37
The role of cholesterol and glycosylphosphatidylinositol-anchored proteins of erythrocyte rafts in regulating raft protein content and malarial infection. J Biol Chem (2001) 1.37
Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic mice. Blood (2001) 1.36
Deformability of oxygenated irreversibly sickled cells. J Clin Invest (1980) 1.36
Protein 4.1R core domain structure and insights into regulation of cytoskeletal organization. Nat Struct Biol (2000) 1.34
Adherence of sickle erythrocytes to vascular endothelial cells: requirement for both cell membrane changes and plasma factors. Blood (1984) 1.31
Lethal alpha-thalassaemia created by gene targeting in mice and its genetic rescue. Nat Genet (1995) 1.27
Functional analysis of aquaporin-1 deficient red cells. The Colton-null phenotype. J Biol Chem (1996) 1.26
Red blood cell glycophorins. Blood (1992) 1.26
Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells. Blood (1992) 1.24
A novel neuron-enriched homolog of the erythrocyte membrane cytoskeletal protein 4.1. J Neurosci (1999) 1.24
Cooperative action between band 3 and glycophorin A in human erythrocytes: immobilization of band 3 induced by antibodies to glycophorin A. Biophys J (1994) 1.23
Contribution of the band 3-ankyrin interaction to erythrocyte membrane mechanical stability. Blood (1991) 1.21
Cloning and characterization of 4.1G (EPB41L2), a new member of the skeletal protein 4.1 (EPB41) gene family. Genomics (1998) 1.20
Adhesion of red cells to foreign surfaces in the presence of flow. J Biomed Mater Res (1974) 1.19
Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency. N Engl J Med (1986) 1.19
Mechanochemistry of the alternatively spliced spectrin-actin binding domain in membrane skeletal protein 4.1. J Biol Chem (1993) 1.19
Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice. J Clin Invest (1999) 1.19
Sickle erythrocyte adherence to vascular endothelium. Morphologic correlates and the requirement for divalent cations and collagen-binding plasma proteins. J Clin Invest (1985) 1.18
Short survival of phosphatidylserine-exposing red blood cells in murine sickle cell anemia. Blood (2001) 1.17
Structural protein 4.1 in the nucleus of human cells: dynamic rearrangements during cell division. J Cell Biol (1997) 1.17
Rigid membranes of Malayan ovalocytes: a likely genetic barrier against malaria. Blood (1984) 1.17
Reticulocyte motility and form: studies on maturation and classification. Blood (1977) 1.16
Modulation of band 3-ankyrin interaction by protein 4.1. Functional implications in regulation of erythrocyte membrane mechanical properties. J Biol Chem (1996) 1.16
Lipid translocation across the human erythrocyte membrane. Regulatory factors. J Biol Chem (1982) 1.15
Differentiation-associated switches in protein 4.1 expression. Synthesis of multiple structural isoforms during normal human erythropoiesis. J Clin Invest (1993) 1.15
An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells. J Clin Invest (1993) 1.15
Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes. J Clin Invest (1984) 1.14
Generation of normal human red cell volume, hemoglobin content, and membrane area distributions by "birth" or regulation? Blood (1995) 1.14
Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro. Cell Death Dis (2012) 1.12
Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease. Blood (2001) 1.12
Diamond-Blackfan anemia. Curr Opin Pediatr (2001) 1.11
Regulation of CD44-protein 4.1 interaction by Ca2+ and calmodulin. Implications for modulation of CD44-ankyrin interaction. J Biol Chem (1997) 1.11
Elastic thickness compressibilty of the red cell membrane. Biophys J (2001) 1.10
Structural protein 4.1 is located in mammalian centrosomes. Proc Natl Acad Sci U S A (1997) 1.09
Association between morphologic distortion of sickle cells and deoxygenation-induced cation permeability increase. Blood (1986) 1.08
Regulation of protein 4.1R, p55, and glycophorin C ternary complex in human erythrocyte membrane. J Biol Chem (2000) 1.08
Erythrocyte membrane vesiculation: model for the molecular mechanism of protein sorting. Proc Natl Acad Sci U S A (1997) 1.07
Variability in erythrocyte deformability among various mammals. Am J Physiol (1979) 1.07
Hypoxia-induced in vivo sickling of transgenic mouse red cells. J Clin Invest (1991) 1.07
Role of the Plasmodium falciparum mature-parasite-infected erythrocyte surface antigen (MESA/PfEMP-2) in malarial infection of erythrocytes. Blood (1995) 1.06
The 13-kD FK506 binding protein, FKBP13, interacts with a novel homologue of the erythrocyte membrane cytoskeletal protein 4.1. J Cell Biol (1998) 1.06
Clarification of role of ATP in red-cell morphology and function. Nature (1977) 1.06
Red cell membrane stiffness in iron deficiency. Blood (1983) 1.05
Red blood cell deformability and hemolytic anemias. Semin Hematol (1979) 1.05
Identification of a functional role for human erythrocyte sialoglycoproteins beta and gamma. Blood (1987) 1.05
Oxidation-induced changes in microrheologic properties of the red blood cell membrane. Blood (1990) 1.05
Red cell membrane and cation deficiency in Rh null syndrome. Blood (1984) 1.04
Glycophorin C content of human erythrocyte membrane is regulated by protein 4.1. Blood (1990) 1.04
Relationship of post-transfusion viability to deformability of stored red cells. Br J Haematol (1983) 1.04
New insights into functions of erythroid proteins in nonerythroid cells. Curr Opin Hematol (2000) 1.04
Identification of the membrane attachment sites for protein 4.1 in the human erythrocyte. J Biol Chem (1995) 1.04
Influence of red cell water content on the morphology of sickling. Blood (1980) 1.03
Signal transduction by glycophorin A: role of extracellular and cytoplasmic domains in a modulatable process. J Cell Biol (1988) 1.03
Plasmodium falciparum histidine-rich protein 1 associates with the band 3 binding domain of ankyrin in the infected red cell membrane. Biochim Biophys Acta (2000) 1.02
Cellular and membrane properties of alpha and beta thalassemic erythrocytes are different: implication for differences in clinical manifestations. Blood (1989) 1.02
Automated ektacytometry: a new method of measuring red cell deformability and red cell indices. Blood Cells (1980) 1.02
Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia. Blood (2001) 1.02
Natural history of hereditary spherocytosis during the first year of life. Blood (2000) 1.01
Human reticulocyte maturation and its relevance to erythropoietic stress. J Lab Clin Med (1979) 1.00
Oxidative red blood cell membrane injury in the pathophysiology of severe mouse beta-thalassemia. Blood (1992) 1.00