Narla Mohandas

Q: What Schools Are Affiliated With Narla Mohandas

Narla Mohandas is affiliated with the following schools: University of California, Berkeley, University of Oxford, La Trobe University, McMaster University, Icahn School of Medicine at Mount Sinai, University of Verona, University of Vienna, Monash University, University of Kent, Yale University, University of Minnesota, University of British Columbia, Vanderbilt University, Tokyo Women's Medical University, Massachusetts Institute of Technology, Stanford University, Purdue University, University of Cambridge, Harvard University

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Narla Mohandas

Computer Science

#3468

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#3640

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Machine Learning

#414

World Rank

#420

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Artificial Intelligence

#610

World Rank

#621

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Database

#838

World Rank

#879

Historical Rank

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Computer Science

Narla Mohandas's Degrees

Masters Computer Science Stanford University
Bachelors Computer Science University of California, Berkeley

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Narla Mohandas's Published Works

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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Red cell membrane: past, present, and future. (2008) (869)
The gene encoding ribosomal protein S19 is mutated in Diamond-Blackfan anaemia (1999) (813)
The FERM domain: a unique module involved in the linkage of cytoplasmic proteins to the membrane. (1998) (542)
Mechanical properties of the red cell membrane in relation to molecular structure and genetic defects. (1994) (536)
A molecular mechanism of artemisinin resistance in Plasmodium falciparum malaria (2015) (491)
Primary role for adherent leukocytes in sickle cell vascular occlusion: A new paradigm (2002) (444)
Erythroblastic islands: niches for erythropoiesis. (2008) (432)
Transgenic knockout mice with exclusively human sickle hemoglobin and sickle cell disease. (1997) (422)
Resolving the distinct stages in erythroid differentiation based on dynamic changes in membrane protein expression during erythropoiesis (2009) (415)
Red blood cell deformability, membrane material properties and shape: regulation by transmembrane, skeletal and cytosolic proteins and lipids. (1993) (376)
Analysis of factors regulating erythrocyte deformability. (1980) (354)
Osmotic gradient ektacytometry: comprehensive characterization of red cell volume and surface maintenance. (1983) (351)
Disorders of red cell membrane (2008) (341)
Molecular maps of red cell deformation: hidden elasticity and in situ connectivity. (1994) (340)
Contribution of parasite proteins to altered mechanical properties of malaria-infected red blood cells. (2002) (337)
A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane. (2003) (337)
The dendritic cell receptor Clec9A binds damaged cells via exposed actin filaments. (2012) (284)
Isolation and functional characterization of human erythroblasts at distinct stages: implications for understanding of normal and disordered erythropoiesis in vivo. (2013) (275)
Global transcriptome analyses of human and murine terminal erythroid differentiation. (2014) (272)
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders. (2013) (269)
Anion Exchanger 1 (Band 3) Is Required to Prevent Erythrocyte Membrane Surface Loss but Not to Form the Membrane Skeleton (1996) (267)
Effect of hydrogen peroxide exposure on normal human erythrocyte deformability, morphology, surface characteristics, and spectrin-hemoglobin cross-linking. (1985) (266)
Identification of a functional role for lipid asymmetry in biological membranes: Phosphatidylserine-skeletal protein interactions modulate membrane stability (2002) (257)
Erythrocyte membrane deformability and stability: two distinct membrane properties that are independently regulated by skeletal protein associations (1986) (256)
Vacuolar uptake of host components, and a role for cholesterol and sphingomyelin in malarial infection (2000) (236)
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression. (1999) (232)
Protein 4.1R-dependent multiprotein complex: New insights into the structural organization of the red blood cell membrane (2008) (227)
Hepcidin as a therapeutic tool to limit iron overload and improve anemia in β-thalassemic mice. (2010) (224)
The malaria-infected red blood cell: Structural and functional changes (2001) (216)
The influence of membrane skeleton on red cell deformability, membrane material properties, and shape. (1983) (215)
Glucose and glutamine metabolism regulate human hematopoietic stem cell lineage specification. (2014) (211)
Malaria, erythrocytic infection, and anemia. (2009) (210)
The Role of Cholesterol and Glycosylphosphatidylinositol-anchored Proteins of Erythrocyte Rafts in Regulating Raft Protein Content and Malarial Infection* (2001) (197)
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stability. (1981) (195)
Thrombospondin mediates adherence of CD36+ sickle reticulocytes to endothelial cells. (1992) (194)
Diamond-Blackfan anemia. (2001) (193)
Modulation of Erythrocyte Membrane Mechanical Function by Protein 4.1 Phosphorylation* (2005) (191)
Static and dynamic rigidities of normal and sickle erythrocytes. Major influence of cell hemoglobin concentration. (1984) (189)
Accurate and independent measurement of volume and hemoglobin concentration of individual red cells by laser light scattering. (1986) (188)
A Maurer's cleft–associated protein is essential for expression of the major malaria virulence antigen on the surface of infected red blood cells (2006) (187)
Racial Difference in Human Platelet PAR4 Reactivity Reflects Expression of PCTP and miR-376c (2013) (185)
Quantitative analysis of murine terminal erythroid differentiation in vivo: novel method to study normal and disordered erythropoiesis. (2013) (184)
The sensing of poorly deformable red blood cells by the human spleen can be mimicked in vitro. (2011) (183)
Hereditary spherocytosis (2008) (179)
Molecular cloning of protein 4.1, a major structural element of the human erythrocyte membrane skeleton. (1986) (176)
Lamins regulate cell trafficking and lineage maturation of adult human hematopoietic cells (2013) (167)
Erythrocyte G Protein-Coupled Receptor Signaling in Malarial Infection (2003) (166)
Red blood cell glycophorins. (1992) (165)
Red blood cell blood group antigens: structure and function. (2004) (165)
Identification of New Prognosis Factors from the Clinical and Epidemiologic Analysis of a Registry of 229 Diamond-Blackfan Anemia Patients (1999) (165)
Oxidation-induced changes in microrheologic properties of the red blood cell membrane. (1990) (159)
Deformability of oxygenated irreversibly sickled cells. (1980) (158)
Membrane remodeling during reticulocyte maturation. (2010) (156)
Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease. (2013) (154)
Comprehensive Proteomic Analysis of Human Erythropoiesis (2016) (154)
Cellular and membrane properties of alpha and beta thalassemic erythrocytes are different: implication for differences in clinical manifestations. (1989) (153)
Erythrocyte detergent-resistant membrane proteins: their characterization and selective uptake during malarial infection. (2004) (153)
Mapping the Binding Domains Involved in the Interaction between the Plasmodium falciparum Knob-associated Histidine-rich Protein (KAHRP) and the Cytoadherence Ligand P. falciparumErythrocyte Membrane Protein 1 (PfEMP1)* (1999) (152)
Adherence of sickle erythrocytes to vascular endothelial cells: requirement for both cell membrane changes and plasma factors. (1984) (150)
A dynamic intron retention program enriched in RNA processing genes regulates gene expression during terminal erythropoiesis (2015) (148)
Modulation of Erythrocyte Membrane Mechanical Function by β-Spectrin Phosphorylation and Dephosphorylation (*) (1995) (148)
Molecular basis for membrane rigidity of hereditary ovalocytosis. A novel mechanism involving the cytoplasmic domain of band 3. (1992) (146)
Malaria and the red blood cell membrane. (2004) (145)
The ring-infected erythrocyte surface antigen (RESA) of Plasmodium falciparum stabilizes spectrin tetramers and suppresses further invasion. (2007) (144)
Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis. (2001) (142)
A Novel Neuron-Enriched Homolog of the Erythrocyte Membrane Cytoskeletal Protein 4.1 (1999) (141)
Tissue- and development-specific alternative RNA splicing regulates expression of multiple isoforms of erythroid membrane protein 4.1. (1991) (141)
Characterization of Human RhCG and Mouse Rhcg as Novel Nonerythroid Rh Glycoprotein Homologues Predominantly Expressed in Kidney and Testis* (2000) (140)
Fluctuations of the red blood cell membrane: relation to mechanical properties and lack of ATP dependence. (2008) (139)
Adducin forms a bridge between the erythrocyte membrane and its cytoskeleton and regulates membrane cohesion. (2009) (139)
Lineage and species-specific long noncoding RNAs during erythro-megakaryocytic development. (2014) (135)
Concurrent sickle cell anemia and alpha-thalassemia. Effect on pathological properties of sickle erythrocytes. (1984) (135)
Molecular and Functional Characterization of Protein 4.1B, a Novel Member of the Protein 4.1 Family with High Level, Focal Expression in Brain* (2000) (130)
Targeted gene deletion demonstrates that the cell adhesion molecule ICAM-4 is critical for erythroblastic island formation. (2005) (130)
Sickle erythrocyte adherence to vascular endothelium. Morphologic correlates and the requirement for divalent cations and collagen-binding plasma proteins. (1985) (129)
Protein 4.1R-deficient mice are viable but have erythroid membrane skeleton abnormalities. (1999) (129)
Isolation and transcriptome analyses of human erythroid progenitors: BFU-E and CFU-E. (2014) (128)
Regulation of CD44-Protein 4.1 Interaction by Ca2+and Calmodulin (1997) (127)
The effect of malonyldialdehyde, a product of lipid peroxidation, on the deformability, dehydration and 51Cr‐survival of erythrocytes (1983) (127)
The contribution of endothelial cell P-selectin to the microvascular flow of mouse sickle erythrocytes in vivo. (2004) (126)
Red cell abnormalities in hereditary spherocytosis: relevance to diagnosis and understanding of the variable expression of clinical severity. (1996) (125)
KLF1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of β-thalassemia. (2014) (124)
Functional Analysis of Aquaporin-1 Deficient Red Cells (1996) (123)
Protein 4.1R core domain structure and insights into regulation of cytoskeletal organization (2000) (121)
Targeted disruption of the beta adducin gene (Add2) causes red blood cell spherocytosis in mice. (1999) (121)
Erythrocyte membrane rigidity induced by glycophorin A-ligand interaction. Evidence for a ligand-induced association between glycophorin A and skeletal proteins. (1985) (119)
Structural and Functional Studies of Interaction between Plasmodium falciparum Knob-associated Histidine-rich Protein (KAHRP) and Erythrocyte Spectrin* (2005) (119)
Short survival of phosphatidylserine-exposing red blood cells in murine sickle cell anemia. (2001) (119)
Membrane assembly and remodeling during reticulocyte maturation. (1989) (117)
Lutheran blood group glycoprotein and its newly characterized mouse homologue specifically bind alpha5 chain-containing human laminin with high affinity. (2001) (116)
Quantitative assessment of sensing and sequestration of spherocytic erythrocytes by the human spleen. (2012) (113)
Multiple protein 4.1 isoforms produced by alternative splicing in human erythroid cells. (1988) (113)
A Congenital Haemolytic Anaemia with Thermal Sensitivity of the Erythrocyte Membrane (1975) (113)
Phosphatidylserine binding sites in erythroid spectrin: location and implications for membrane stability. (2004) (112)
Significant Biochemical, Biophysical and Metabolic Diversity in Circulating Human Cord Blood Reticulocytes (2013) (110)
Malaria and human red blood cells (2012) (110)
Shear-Response of the Spectrin Dimer-Tetramer Equilibrium in the Red Blood Cell Membrane* (2002) (110)
Diamond-Blackfan anemia (2000) (109)
Lipid translocation across the human erythrocyte membrane. Regulatory factors. (1982) (108)
Restoration of normal membrane stability to unstable protein 4.1-deficient erythrocyte membranes by incorporation of purified protein 4.1. (1986) (108)
Mechanochemistry of protein 4.1's spectrin-actin-binding domain: ternary complex interactions, membrane binding, network integration, structural strengthening (1995) (108)
Thromboerythrocytes. In vitro studies of a potential autologous, semi-artificial alternative to platelet transfusions. (1992) (108)
Structural Protein 4.1 in the Nucleus of Human Cells: Dynamic Rearrangements during Cell Division (1997) (107)
Sickle Red Cell Microrheology and Sickle Blood Rheology (2004) (107)
Rac GTPases regulate the morphology and deformability of the erythrocyte cytoskeleton. (2006) (107)
Cloning and characterization of 4.1G (EPB41L2), a new member of the skeletal protein 4.1 (EPB41) gene family. (1998) (106)
The 13-kD FK506 Binding Protein, FKBP13, Interacts with a Novel Homologue of the Erythrocyte Membrane Cytoskeletal Protein 4.1 (1998) (105)
Contribution of the band 3-ankyrin interaction to erythrocyte membrane mechanical stability. (1991) (104)
Erythrocyte remodeling by malaria parasites (2007) (101)
Relationship of post‐transfusion viability to deformability of stored red cells (1983) (101)
Regulation of Protein 4.1R, p55, and Glycophorin C Ternary Complex in Human Erythrocyte Membrane* (2000) (100)
Evaluation of biochemical changes during in vivo erythrocyte senescence in the dog. (1999) (99)
Mechanochemistry of the alternatively spliced spectrin-actin binding domain in membrane skeletal protein 4.1. (1993) (99)
Stabilization of erythrocyte membranes by polyamines. (1983) (98)
Functional characterization of spectrin-actin-binding domains in 4.1 family of proteins. (2002) (97)
Glycophorin C content of human erythrocyte membrane is regulated by protein 4.1. (1990) (96)
Mechanism of protein sorting during erythroblast enucleation: role of cytoskeletal connectivity. (2004) (95)
Identification of the Membrane Attachment Sites for Protein 4.1 in the Human Erythrocyte (*) (1995) (95)
Native ultrastructure of the red cell cytoskeleton by cryo-electron tomography. (2011) (94)
Decreased membrane mechanical stability and in vivo loss of surface area reflect spectrin deficiencies in hereditary spherocytosis. (1988) (94)
Association between morphologic distortion of sickle cells and deoxygenation-induced cation permeability increase. (1986) (93)
A transgenic mouse model demonstrates a dominant negative effect of a point mutation in the RPS19 gene associated with Diamond-Blackfan anemia. (2010) (92)
Natural history of hereditary spherocytosis during the first year of life. (2000) (92)
Differentiation-associated switches in protein 4.1 expression. Synthesis of multiple structural isoforms during normal human erythropoiesis. (1993) (92)
Erythrocyte membrane vesiculation: model for the molecular mechanism of protein sorting. (1997) (92)
Resveratrol accelerates erythroid maturation by activation of FoxO3 and ameliorates anemia in beta-thalassemic mice (2014) (90)
The unusual pathobiology of hemoglobin constant spring red blood cells. (1997) (90)
Red cell indices in classification and treatment of anemias: from M.M. Wintrobes's original 1934 classification to the third millennium (2013) (88)
Clarification of role of ATP in red-cell morphology and function (1977) (88)
Modulation of Band 3-Ankyrin Interaction by Protein 4.1 (1996) (87)
Elastic thickness compressibilty of the red cell membrane. (2001) (87)
Mature parasite-infected erythrocyte surface antigen (MESA) of Plasmodium falciparum binds to the 30-kDa domain of protein 4.1 in malaria-infected red blood cells. (2003) (87)
Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis (2019) (87)
Functional alteration of red blood cells by a megadalton protein of Plasmodium falciparum. (2009) (86)
Characterization of glycolytic enzyme interactions with murine erythrocyte membranes in wild-type and membrane protein knockout mice. (2008) (86)
Modulation of erythrocyte membrane material properties by Ca2+ and calmodulin. Implications for their role in regulation of skeletal protein interactions. (1988) (86)
Glycophorin A dimerization and band 3 interaction during erythroid membrane biogenesis: in vivo studies in human glycophorin A transgenic mice. (2001) (86)
Molecular and functional changes in spectrin from patients with hereditary pyropoikilocytosis. (1983) (85)
Mild spherocytosis and altered red cell ion transport in protein 4. 2-null mice. (1999) (85)
Separate mechanisms of deformability loss in ATP-depleted and Ca-loaded erythrocytes. (1981) (85)
Generation of normal human red cell volume, hemoglobin content, and membrane area distributions by "birth" or regulation? (1995) (85)
Effects of oxygen inhalation on endogenous erythropoietin kinetics, erythropoiesis, and properties of blood cells in sickle-cell anemia. (1984) (85)
Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer. (2016) (85)
Red cell membrane stiffness in iron deficiency. (1983) (85)
Function and dysfunction. (2018) (85)
Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease. (2001) (84)
Protein and lipid trafficking induced in erythrocytes infected by malaria parasites (2002) (84)
Rigid membranes of Malayan ovalocytes: a likely genetic barrier against malaria (1984) (83)
The N-terminal 11 amino acids of human erythrocyte band 3 are critical for aldolase binding and protein phosphorylation: implications for band 3 function. (2005) (82)
Stomatocytosis is absent in "stomatin"-deficient murine red blood cells. (1999) (82)
A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders. (1982) (82)
Membrane peroxidation and methemoglobin formation are both necessary for band 3 clustering: mechanistic insights into human erythrocyte senescence. (2013) (82)
A dynamic alternative splicing program regulates gene expression during terminal erythropoiesis (2014) (82)
Red cell membrane disorders (2017) (82)
The hydration state of human red blood cells and their susceptibility to invasion by Plasmodium falciparum. (2005) (81)
A dynamic intron retention program in the mammalian megakaryocyte and erythrocyte lineages. (2015) (80)
Kinematics of red cell aspiration by fluorescence-imaged microdeformation. (1996) (79)
Red cell membrane and cation deficiency in Rh null syndrome. (1984) (79)
The relationship between in vivo generated hemoglobin skeletal protein complex and increased red cell membrane rigidity. (1988) (78)
Remodeling of the malaria parasite and host human red cell by vesicle amplification that induces artemisinin resistance. (2018) (77)
Identification of a functional role for human erythrocyte sialoglycoproteins beta and gamma. (1987) (77)
Erythrocyte G Protein as a Novel Target for Malarial Chemotherapy (2006) (76)
Comparison of mechanisms of anemia in mice with sickle cell disease and beta-thalassemia: peripheral destruction, ineffective erythropoiesis, and phospholipid scramblase-mediated phosphatidylserine exposure. (2002) (76)
The spectrin-based membrane skeleton stabilizes mouse megakaryocyte membrane systems and is essential for proplatelet and platelet formation. (2011) (76)
Hypoxia-induced acute lung injury in murine models of sickle cell disease. (2004) (76)
Identification of a third Protein 4.1 tumor suppressor, Protein 4.1R, in meningioma pathogenesis (2003) (75)
Nucleolar localization of RPS19 protein in normal cells and mislocalization due to mutations in the nucleolar localization signals in 2 Diamond-Blackfan anemia patients: potential insights into pathophysiology. (2003) (75)
Molecular basis of hereditary elliptocytosis due to protein 4.1 deficiency. (1986) (75)
Deformability of isolated red blood cell membranes. (1982) (75)
Characterization of multiple isoforms of protein 4.1R expressed during erythroid terminal differentiation. (1998) (74)
Ribosomal protein S19 expression during erythroid differentiation. (2003) (72)
Deformability of stored red blood cells. Relationship to degree of packing (1982) (72)
Primary hematopoietic cells from DBA patients with mutations in RPL11 and RPS19 genes exhibit distinct erythroid phenotype in vitro (2012) (72)
Cooperative action between band 3 and glycophorin A in human erythrocytes: immobilization of band 3 induced by antibodies to glycophorin A. (1994) (71)
Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia. (2001) (71)
Reticulocyte motility and form: studies on maturation and classification. (1977) (71)
Variability in erythrocyte deformability among various mammals. (1979) (70)
Lethal α–thalassaemia created by gene targeting in mice and its genetic rescue (1995) (69)
Globin-chain specificity of oxidation-induced changes in red blood cell membrane properties. (1992) (69)
Signal transduction by glycophorin A: role of extracellular and cytoplasmic domains in a modulatable process (1988) (69)
Conformational Stabilities of the Structural Repeats of Erythroid Spectrin and Their Functional Implications* (2006) (69)
Pomalidomide reverses γ-globin silencing through the transcriptional reprogramming of adult hematopoietic progenitors. (2016) (69)
Recurrent fatal hydrops fetalis associated with a nucleotide substitution in the erythrocyte beta-spectrin gene. (1995) (69)
Lipid rafts and malaria parasite infection of erythrocytes (Review) (2006) (67)
Ca(2+)-dependent and Ca(2+)-independent calmodulin binding sites in erythrocyte protein 4.1. Implications for regulation of protein 4.1 interactions with transmembrane proteins. (2000) (67)
Membrane association of peroxiredoxin-2 in red cells is mediated by the N-terminal cytoplasmic domain of band 3. (2013) (67)
Targeted deletion of alpha-adducin results in absent beta- and gamma-adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice. (2007) (65)
Erythrocyte membrane changes of chorea-acanthocytosis are the result of altered Lyn kinase activity. (2011) (65)
Identification and Functional Characterization of Protein 4.1R and Actin-Binding Sites in Erythrocyte β Spectrin: Regulation of the Interactions by Phosphatidylinositol-4,5-bisphosphate† (2005) (65)
Membrane assembly and remodeling during reticulocyte maturation (1989) (64)
Phosphatidylinositol-4,5-biphosphate (PIP2) differentially regulates the interaction of human erythrocyte protein 4.1 (4.1R) with membrane proteins. (2006) (63)
The role of membrane protein sulfhydryl groups in hydrogen peroxide-mediated membrane damage in human erythrocytes. (1988) (63)
An update on the pathogenesis and diagnosis of Diamond–Blackfan anemia (2018) (63)
The water channel aquaporin-1 partitions into exosomes during reticulocyte maturation: implication for the regulation of cell volume. (2009) (62)
Structural protein 4.1 is located in mammalian centrosomes. (1997) (61)
Membrane-associated sickle hemoglobin: a major determinant of sickle erythrocyte rigidity. (1987) (61)
Altered phosphorylation of cytoskeleton proteins in sickle red blood cells: the role of protein kinase C, Rac GTPases, and reactive oxygen species. (2010) (61)
Plasmodium falciparum Erythrocyte Membrane Protein 3 (PfEMP3) Destabilizes Erythrocyte Membrane Skeleton* (2007) (61)
Four paralogous protein 4.1 genes map to distinct chromosomes in mouse and human. (1998) (61)
A technique to detect reduced mechanical stability of red cell membranes: relevance to elliptocytic disorders (1982) (61)
Identification of critical amino-acid residues on the erythroid intercellular adhesion molecule-4 (ICAM-4) mediating adhesion to alpha V integrins. (2004) (60)
Plasmodium falciparum histidine-rich protein 1 associates with the band 3 binding domain of ankyrin in the infected red cell membrane. (2000) (60)
Transport mechanisms in Plasmodium-infected erythrocytes: lipid rafts and a tubovesicular network. (2001) (59)
Defining the Minimal Domain of the Plasmodium falciparum Protein MESA Involved in the Interaction with the Red Cell Membrane Skeletal Protein 4.1* (1997) (59)
Detachment of agglutinin-bonded red blood cells. II. Mechanical energies to separate large contact areas. (1991) (59)
Association of red cell spherocytosis with deletion of the short arm of chromosome 8. (1987) (58)
New insights into functions of erythroid proteins in nonerythroid cells. (2000) (58)
Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation. (2010) (58)
Three-dimensional model of bone marrow. (1978) (57)
Recombinant erythropoietin therapy as an alternative to blood transfusions in infants with hereditary spherocytosis. (2000) (57)
Bilayer balance and regulation of red cell shape changes. (1978) (56)
Absolute proteome quantification of highly purified populations of circulating reticulocytes and mature erythrocytes. (2018) (56)
Mapping the domains of the cytoadherence ligand Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) that bind to the knob-associated histidine-rich protein (KAHRP). (2002) (56)
Distinct distribution of specific members of protein 4.1 gene family in the mouse nephron. (2003) (56)
Defining of the Minimal Domain of Protein 4.1 Involved in Spectrin-Actin Binding (*) (1995) (56)
Peptides based on alphaV-binding domains of erythrocyte ICAM-4 inhibit sickle red cell-endothelial interactions and vaso-occlusion in the microcirculation. (2006) (54)
Hypoxia-induced in vivo sickling of transgenic mouse red cells. (1991) (54)
Neurobehavioral deficits in mice lacking the erythrocyte membrane cytoskeletal protein 4.1 (1998) (53)
Three-dimensional model of bone marrow (1978) (53)
Cell Shape-dependent Regulation of Protein 4.1 Alternative Pre-mRNA Splicing in Mammary Epithelial Cells* (1997) (53)
Tropomyosin modulates erythrocyte membrane stability. (2007) (52)
Cytoplasmic remodeling of erythrocyte raft lipids during infection by the human malaria parasite Plasmodium falciparum. (2007) (52)
Oxidative red blood cell membrane injury in the pathophysiology of severe mouse beta-thalassemia. (1992) (52)
Surface Area Loss and Increased Sphericity Account for the Splenic Entrapment of Subpopulations of Plasmodium falciparum Ring-Infected Erythrocytes (2013) (52)
Control of human hemoglobin switching by LIN28B-mediated regulation of BCL11A translation (2018) (51)
Intracellular structures of normal and aberrant Plasmodium falciparum malaria parasites imaged by soft x-ray microscopy. (1997) (51)
Protein 4.1R links E-cadherin/beta-catenin complex to the cytoskeleton through its direct interaction with beta-catenin and modulates adherens junction integrity. (2009) (51)
Nuclear substructure reorganization during late-stage erythropoiesis is selective and does not involve caspase cleavage of major nuclear substructural proteins. (2005) (51)
Inaccuracies associated with the automated measurement of mean cell hemoglobin concentration in dehydrated cells. (1980) (50)
Cytoskeletal Protein 4.1R Affects Repolarization and Regulates Calcium Handling in the Heart (2008) (50)
Stomatin and sensory neuron mechanotransduction. (2007) (50)
Phosphorylation-dependent perturbations of the 4.1R-associated multiprotein complex of the erythrocyte membrane. (2011) (50)
The role of membrane skeletal-associated alpha-globin in the pathophysiology of beta-thalassemia. (1990) (50)
Unraveling Macrophage Heterogeneity in Erythroblastic Islands (2017) (50)
Distinct roles for TET family proteins in regulating human erythropoiesis. (2017) (49)
In vivo blood flow abnormalities in the transgenic knockout sickle cell mouse. (1999) (49)
Erythroblastic islands, terminal erythroid differentiation and reticulocyte maturation (2011) (49)
Mammalian alpha I-spectrin is a neofunctionalized polypeptide adapted to small highly deformable erythrocytes. (2006) (49)
Analysis of Integral Membrane Protein Contributions to the Deformability and Stability of the Human Erythrocyte Membrane* (2001) (48)
Cell Membrane and Volume Changes during Red Cell Development and Aging a (1989) (48)
ATP11C is a major flippase in human erythrocytes and its defect causes congenital hemolytic anemia (2016) (48)
Cellular adhesive phenomena in apicomplexan parasites of red blood cells. (2005) (47)
Hydration of sickle cells using the sodium ionophore Monensin. A model for therapy. (1982) (47)
Blood group antigens in health and disease (2005) (47)
The adhesive sickle erythrocyte: cause and consequence of abnormal interactions with endothelium, monocytes/macrophages and model membranes. (1985) (46)
Novel secreted isoform of adhesion molecule ICAM-4: potential regulator of membrane-associated ICAM-4 interactions. (2003) (46)
Identification of a Novel Role for Dematin in Regulating Red Cell Membrane Function by Modulating Spectrin-Actin Interaction* (2012) (45)
Assignment of functional roles to parasite proteins in malaria‐infected red blood cells by competitive flow‐based adhesion assay (2002) (45)
Malaria Induces Anemia through CD8+ T Cell-Dependent Parasite Clearance and Erythrocyte Removal in the Spleen (2015) (45)
Decreasing TfR1 expression reverses anemia and hepcidin suppression in β-thalassemic mice. (2017) (45)
Identification and characterization of a newly recognized population of high-Na+, low-K+, low-density sickle and normal red cells. (2000) (44)
The 4.1B cytoskeletal protein regulates the domain organization and sheath thickness of myelinated axons (2013) (44)
Diamond-Blackfan Anemia. (2020) (43)
Mutation of a highly conserved residue of betaI spectrin associated with fatal and near-fatal neonatal hemolytic anemia. (1997) (43)
Membrane dynamics of the water transport protein aquaporin-1 in intact human red cells. (1999) (43)
Interaction of Plasmodium falciparum knob-associated histidine-rich protein (KAHRP) with erythrocyte ankyrin R is required for its attachment to the erythrocyte membrane. (2014) (43)
Altered Chromatin Occupancy of Master Regulators Underlies Evolutionary Divergence in the Transcriptional Landscape of Erythroid Differentiation (2014) (42)
Structural and Functional Characterization of Protein 4.1R-Phosphatidylserine Interaction (2001) (41)
Automated quantitation of cell density distribution and hyperdense cell fraction in RBC disorders. (1989) (41)
The erythroblastic island as an emerging paradigm in the anemia of inflammation (2015) (41)
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. (1993) (41)
Interaction of the exported malaria protein Pf332 with the red blood cell membrane skeleton. (2010) (41)
Macrothrombocytopenia with abnormal demarcation membranes in megakaryocytes and neutropenia with a complete lack of sialyl-Lewis-X antigen in leukocytes--a new syndrome? (2001) (40)
Human and murine erythropoiesis (2015) (40)
Cytoskeletal protein 4.1R negatively regulates T-cell activation by inhibiting the phosphorylation of LAT. (2009) (40)
Deciphering the nuclear import pathway for the cytoskeletal red cell protein 4.1R. (1999) (40)
Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis (1993) (39)
Ektacytometric analysis of factors regulating red cell deformability. (1980) (39)
TET2 deficiency leads to stem cell factor-dependent clonal expansion of dysfunctional erythroid progenitors. (2018) (39)
Interactions of Plasmodium falciparum erythrocyte membrane protein 3 with the red blood cell membrane skeleton. (2007) (39)
Effects of abnormal cation transport on deformability of desiccytes. (1978) (39)
High frequency of alternative first exons in erythroid genes suggests a critical role in regulating gene function. (2006) (39)
Inhibition of malarial parasite invasion by monoclonal antibodies against glycophorin A correlates with reduction in red cell membrane deformability. (1989) (38)
Control of erythrocyte membrane-skeletal cohesion by the spectrin-membrane linkage. (2010) (38)
Laser Diffraction Patterns of Sickle Cells in Fluid Shear Fields (1978) (38)
Two Distinct Domains of Protein 4.1 Critical for Assembly of Functional Nuclei in Vitro * (2002) (38)
Phospholipid binding by proteins of the spectrin family: a comparative study. (2005) (38)
Rigid membranes of Malayan ovalocytes: a likely genetic barrier against malaria. (1984) (37)
Cysteine shotgun–mass spectrometry (CS-MS) reveals dynamic sequence of protein structure changes within mutant and stressed cells (2011) (37)
Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cells. (2006) (37)
An Unrecognized Function of Cholesterol: Regulating the Mechanism Controlling Membrane Phospholipid Asymmetry. (2016) (37)
Developmental differences between neonatal and adult human erythropoiesis (2018) (36)
Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis. (1990) (36)
Role of the Plasmodium falciparum mature-parasite-infected erythrocyte surface antigen (MESA/PfEMP-2) in malarial infection of erythrocytes. (1995) (36)
A Golgi-associated protein 4.1B variant is required for assimilation of proteins in the membrane (2009) (36)
Membrane assembly during erythropoiesis (2011) (36)
Hereditary elliptocytosis due to both qualitative and quantitative defects in membrane skeletal protein 4.1. (1991) (36)
Intrasplicing coordinates alternative first exons with alternative splicing in the protein 4.1R gene (2008) (35)
The Aging Process of Human Neonatal Erythrocytes (1986) (35)
The Laminin 511/521-binding site on the Lutheran blood group glycoprotein is located at the flexible junction of Ig domains 2 and 3. (2007) (35)
Unique alpha-spectrin mutant in a kindred with common hereditary elliptocytosis. (1987) (35)
Evidence for a protective role of the Gardos channel against hemolysis in murine spherocytosis. (2005) (35)
In vivo studies support the role of trafficking and cytoskeletal-binding motifs in the interaction of MESA with the membrane skeleton of Plasmodium falciparum-infected red blood cells. (2008) (35)
Lethal alpha-thalassaemia created by gene targeting in mice and its genetic rescue. (1995) (35)
Adhesive activity of Lu glycoproteins is regulated by interaction with spectrin. (2008) (35)
Protein 4.1R regulates cell adhesion, spreading, migration and motility of mouse keratinocytes by modulating surface expression of β1 integrin (2011) (34)
Decreased in vivo survival of hydrogen peroxide-damaged baboon red blood cells. (1990) (34)
Detection of detergent-resistant membranes in asexual blood-stage parasites of Plasmodium falciparum. (2003) (33)
Modulation of erythrocyte membrane mechanical stability by 2,3-diphosphoglycerate in the neonatal poikilocytosis/elliptocytosis syndrome. (1987) (33)
Reversible deformation-dependent erythrocyte cation leak. Extreme sensitivity conferred by minimal peroxidation. (1991) (32)
Dissecting the transcriptional phenotype of ribosomal protein deficiency: implications for Diamond-Blackfan Anemia (2014) (32)
Differential domain evolution and complex RNA processing in a family of paralogous EPB41 (protein 4.1) genes facilitate expression of diverse tissue-specific isoforms. (2004) (32)
Lack of Protein 4.1G Causes Altered Expression and Localization of the Cell Adhesion Molecule Nectin-Like 4 in Testis and Can Cause Male Infertility (2011) (32)
Molecular characterization of erythrocyte glycophorin C variants. (1991) (32)
Removal of erythrocyte membrane iron in vivo ameliorates the pathobiology of murine thalassemia. (1997) (32)
Measuring Deformability and Red Cell Heterogeneity in Blood by Ektacytometry. (2018) (32)
Murine recessive hereditary spherocytosis, sph/sph, is caused by a mutation in the erythroid alpha-spectrin gene. (2000) (32)
Thermal stabilities of brain spectrin and the constituent repeats of subunits. (2006) (32)
Peroxiredoxin-2: A Novel Regulator of Iron Homeostasis in Ineffective Erythropoiesis. (2018) (31)
A Unique Epigenomic Landscape Defines Human Erythropoiesis (2019) (31)
The structural organization of skeletal proteins influences lipid translocation across erythrocyte membrane. (1985) (31)
Influence of Red Cell Water Content on the Morphology of Sickling (1980) (31)
Integral protein linkage and the bilayer-skeletal separation energy in red blood cells. (2008) (31)
A simple laboratory alternative to irreversibly sickled cell (ISC) counts (1982) (31)
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. I. Biochemical identification of rearrangements in the spectrin/actin binding domain and functional characterizations. (1990) (31)
Identification and functional characterization of protein 4.1R and actin-binding sites in erythrocyte beta spectrin: regulation of the interactions by phosphatidylinositol-4,5-bisphosphate. (2005) (31)
ATP-dependent Mechanism Protects Spectrin against Glycation in Human Erythrocytes* (2010) (30)
Rheological and adherence properties of sickle cells. Potential contribution to hematologic manifestations of the disease. (1989) (30)
Sensing of red blood cells with decreased membrane deformability by the human spleen. (2018) (30)
Effects of heat and metabolic depletion on erythrocyte deformability, spectrin extractability and phosphorylation. (1978) (30)
Marked difference in membrane-protein-binding properties of the two isoforms of protein 4.1R expressed at early and late stages of erythroid differentiation. (2009) (30)
Regulation of globin-heme balance in Diamond-Blackfan anemia by HSP70/GATA1. (2019) (29)
Human reticulocyte maturation and its relevance to erythropoietic stress. (1979) (29)
Interactions between Plasmodium falciparum skeleton-binding protein 1 and the membrane skeleton of malaria-infected red blood cells. (2015) (29)
Alternative 5' exons and differential splicing regulate expression of protein 4.1R isoforms with distinct N-termini. (2003) (29)
Splenic sequestration associated with sickle cell trait and hereditary spherocytosis (1992) (29)
SF3B1 deficiency impairs human erythropoiesis via activation of p53 pathway: implications for understanding of ineffective erythropoiesis in MDS (2018) (28)
p53 activation during ribosome biogenesis regulates normal erythroid differentiation. (2020) (28)
The Interplay Between Peroxiredoxin-2 and Nuclear Factor-Erythroid 2 Is Important in Limiting Oxidative Mediated Dysfunction in β-Thalassemic Erythropoiesis. (2015) (28)
Role of the Plasmodium falciparum mature-parasite-infected erythrocyte surface antigen (MESA/PfEMP-2) in malarial infection of erythrocytes (1995) (28)
The role of membrane-associated enzymes in regulation of erythrocyte shape and deformability. (1981) (28)
Pathophysiology of a Sickle Cell Trait Mouse Model: Human αβS Transgenes with One Mouse β-Globin Allele (2001) (28)
Efficient in Vivo Manipulation of Alternative Pre-mRNA Splicing Events Using Antisense Morpholinos in Mice* (2010) (28)
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins of rearrangements. (1990) (28)
Inherited hemolytic anemia: a possessive beginner's guide. (2018) (27)
A Bacterial Phosphatase-Like Enzyme of the Malaria Parasite Plasmodium falciparum Possesses Tyrosine Phosphatase Activity and Is Implicated in the Regulation of Band 3 Dynamics during Parasite Invasion (2013) (27)
Effect of complete protein 4.1R deficiency on ion transport properties of murine erythrocytes. (2006) (27)
Long-term follow-up of subtotal splenectomy for hereditary spherocytosis: a single-center study. (2016) (27)
Red blood cell abnormalities in hereditary elliptocytosis and their relevance to variable clinical expression. (1997) (26)
Molecular basis for red cell membrane viscoelastic properties. (1992) (26)
Fyn kinase is a novel modulator of erythropoietin signaling and stress erythropoiesis (2018) (26)
The severe phenotype of Diamond-Blackfan anemia is modulated by heat shock protein 70. (2017) (26)
Role of ATP Depletion on Red Cell Shape and Deformability (1978) (26)
Comprehensive proteomic analysis of murine terminal erythroid differentiation. (2020) (26)
Control of red cell deformability and shape. (1978) (25)
A simple laboratory alternative to irreversibly sickled cell (ISC) counts. (1982) (25)
Monozygotic twins with sickle cell anemia and discordant clinical courses: clinical and laboratory studies. (1991) (25)
The erythroid niche: molecular processes occurring within erythroblastic islands. (2010) (25)
New insights into function of red cell membrane proteins and their interaction with spectrin-based membrane skeleton. (2006) (24)
Mutations in the murine erythroid alpha-spectrin gene alter spectrin mRNA and protein levels and spectrin incorporation into the red blood cell membrane skeleton. (2003) (24)
Two Protein 4.1 Domains Essential for Mitotic Spindle and Aster Microtubule Dynamics and Organization in Vitro* (2004) (24)
Impaired Intestinal Calcium Absorption in Protein 4.1R-deficient Mice Due to Altered Expression of Plasma Membrane Calcium ATPase 1b (PMCA1b)* (2013) (24)
Differential use of protein 4.1 translation initiation sites during erythropoiesis: implications for a mutation-induced stage-specific deficiency of protein 4.1 during erythroid development. (1996) (24)
Phosphatidylserine binding sites in red cell spectrin. (2004) (24)
Deubiquitylase USP7 regulates human terminal erythroid differentiation by stabilizing GATA1 (2019) (24)
Putative regulators for the continuum of erythroid differentiation revealed by single-cell transcriptome of human BM and UCB cells (2020) (24)
Abnormal red cell features associated with hereditary neurodegenerative disorders: the neuroacanthocytosis syndromes (2014) (23)
Diamond-Blackfan anemia, ribosome and erythropoiesis. (2010) (23)
New insights into potential functions for the protein 4.1 superfamily of proteins in kidney epithelium. (2005) (23)
Defective spectrin integrity and neonatal thrombosis in the first mouse model for severe hereditary elliptocytosis. (2001) (22)
Steroid-resistance in Diamond Blackfan anemia associates with p57Kip2 dysregulation in erythroid progenitors. (2020) (22)
An IDH1-vitamin C crosstalk drives human erythroid development by inhibiting pro-oxidant mitochondrial metabolism. (2020) (22)
Regulation of red cell membrane deformability and stability by skeletal protein network. (1990) (22)
Red Cell Membranes (1988) (21)
Molecular analysis of glycophorin C deficiency in human erythrocytes. (1993) (21)
Characterization, regulation, and targeting of erythroid progenitors in normal and disordered human erythropoiesis (2017) (21)
Hydration of red cells in α and β thalassemias differs : a useful approach to distinguish between these red cell phenotypes (1994) (21)
Plasmodium falciparum: influence of malarial and host erythrocyte skeletal protein interactions on phosphorylation in infected erythrocytes. (1998) (20)
Study of the effects of proteasome inhibitors on ribosomal protein S19 (RPS19) mutants, identified in patients with Diamond-Blackfan anemia (2008) (20)
Selective erythroid replacement in murine beta-thalassemia using fetal hematopoietic stem cells. (1993) (20)
Putative tumor suppressor protein 4.1B is differentially expressed in kidney and brain via alternative promoters and 5' alternative splicing. (2004) (19)
Comprehensive characterization of expression patterns of protein 4.1 family members in mouse adrenal gland: implications for functions (2010) (19)
Interplay between cofactors and transcription factors in hematopoiesis and hematological malignancies (2021) (19)
Identification of the hereditary pyropoikilocytosis carrier state (1984) (18)
Mature erythrocyte membrane homeostasis is compromised by loss of the GATA1-FOG1 interaction. (2012) (18)
Deep Intron Elements Mediate Nested Splicing Events at Consecutive AG Dinucleotides To Regulate Alternative 3′ Splice Site Choice in Vertebrate 4.1 Genes (2012) (18)
The molecular species composition of phosphatidylcholine affects cellular properties in normal and sickle erythrocytes. (1987) (18)
Hereditary plasma lecithin-cholesterol acyl transferase deficiency: a heterozygous variant with erythrocyte membrane abnormalities. (1982) (18)
miR-326 regulates HbF synthesis by targeting EKLF in human erythroid cells. (2018) (17)
Evolutionarily conserved alternative pre-mRNA splicing regulates structure and function of the spectrin-actin binding domain of erythroid protein 4.1. (1995) (17)
Severely impaired terminal erythroid differentiation as an independent prognostic marker in myelodysplastic syndromes. (2018) (17)
Targeted deletion of the γ‐adducin gene (Add3) in mice reveals differences in α‐adducin interactions in erythroid and nonerythroid cells (2009) (17)
Measurements of red cell deformability and hydration reflect HbF and HbA2 in blood from patients with sickle cell anemia. (2017) (17)
Echinocytic sensitivity and deformability of human newborn red cells. (1982) (17)
Abnormal erythroid maturation leads to microcytic anemia in the TSAP6/Steap3 null mouse model (2015) (17)
Dusty protein kinases: primary structure, gene evolution, tissue specific expression and unique features of the catalytic domain. (2006) (16)
Influence of red cell water content on the morphology of sickling. (1980) (16)
Unexpected role for p19INK4d in posttranscriptional regulation of GATA1 and modulation of human terminal erythropoiesis. (2017) (16)
Inactivation of Rb and E2f8 Synergizes To Trigger Stressed DNA Replication during Erythroid Terminal Differentiation (2014) (16)
Sustained treatment of sickle cell mice with haptoglobin increases HO‐1 and H‐ferritin expression and decreases iron deposition in the kidney without improvement in kidney function (2016) (16)
Pathophysiology of a sickle cell trait mouse model: human alpha(beta)(S) transgenes with one mouse beta-globin allele. (2001) (15)
Case series supporting heme detoxification via therapeutic plasma exchange in acute multiorgan failure syndrome resistant to red blood cell exchange in sickle cell disease (2018) (15)
Hereditary poikilocytic anemia associated with the co-inheritance of two alpha spectrin abnormalities. (1988) (15)
Deletion of a Malaria Invasion Gene Reduces Death and Anemia, in Model Hosts (2011) (15)
Morphological and functional platelet abnormalities in Berkeley sickle cell mice. (2008) (15)
Normal membrane function of abnormal β‐related erythrocyte sialoglycoproteins (1987) (15)
A 130-kDa Protein 4.1B Regulates Cell Adhesion, Spreading, and Migration of Mouse Embryo Fibroblasts by Influencing Actin Cytoskeleton Organization* (2013) (15)
The human Kell blood group binds the erythroid 4.1R protein: new insights into the 4.1R‐dependent red cell membrane complex (2015) (14)
Red cell rheology (1978) (14)
Characterization of circulating erythroid progenitor cells in human newborn blood. (1981) (14)
Malaria Parasite Proteins and Their Role in Alteration of the Structure and Function of Red Blood Cells. (2016) (14)
Carbon Monoxide Religation Kinetics to Hemoglobin S Polymers following Ligand Photolysis (*) (1995) (14)
Red Cell Structure, Shapes and Deformability (1975) (14)
First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond–Blackfan anemia (2013) (13)
Prognostic factors of disease severity in infants with sickle cell anemia: A comprehensive longitudinal cohort study (2018) (13)
Red cell membrane and malaria. (2010) (12)
Introduction and expression of the human Bs-globin gene in transgenic mice. (1988) (12)
Evolutionarily conserved coupling of transcription and alternative splicing in the EPB41 (protein 4.1R) and EPB41L3 (protein 4.1B) genes. (2005) (12)
Regulation of erythrocyte ghost membrane mechanical stability by chlorpromazine. (2001) (12)
Fetal hemoglobin rescues ineffective erythropoiesis in sickle cell disease (2020) (12)
Banking on red blood cells (2005) (12)
Bad Blood: A trigger for TRALI (2010) (11)
Procoagulant activity in patients with sickle cell trait (2012) (11)
Interaction of amphipathic drugs with erythrocytes from various species. (1982) (11)
Targeted deletion of (cid:1) -adducin results in absent (cid:2) - and (cid:3) -adducin, compensated hemolytic anemia, and lethal hydrocephalus in mice (2008) (11)
Similarities and differences in the structure and function of 4.1G and 4.1R135, two protein 4.1 paralogues expressed in erythroid cells. (2010) (11)
What do mouse gene knockouts tell us about the structure and function of the red cell membrane? (1999) (11)
Deformability and spectrin properties in three types of elongated red cells (1980) (11)
Circulating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating (2017) (11)
The equilibrative nucleoside transporter 1 (ENT1) is critical for nucleotide homeostasis and optimal erythropoiesis. (2021) (11)
Lipid Translocation across the Human Erythrocyte Membrane (2001) (11)
The interplay between peroxiredoxin-2 and Nrf2 is important in limiting oxidative mediated dysfunction in b-thalassemic erythropoiesis (2015) (11)
Nanosecond absorption study of kinetics associated with carbon monoxide rebinding to hemoglobin S and hemoglobin C following ligand photolysis. (1994) (10)
Tissue Factor Deficiency Decreases Sickle Cell-Induced Vascular Stasis in a Hematopoietic Stem Cell Transplant Model of Murine Sickle Cell Disease. (2004) (10)
Comprehensive phenotyping of erythropoiesis in human bone marrow: Evaluation of normal and ineffective erythropoiesis (2021) (10)
Confounding in ex vivo models of Diamond-Blackfan anemia. (2017) (10)
Southeast Asian ovalocytosis in White persons. (1999) (10)
First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond–Blackfan anemia. (2013) (10)
No evidence for cell activation or brain vaso-occlusion with plerixafor mobilization in sickle cell mice. (2016) (10)
Erythropoietic stress, macrocytosis, and hemoglobin switching in HbAA sheep. (1980) (9)
XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemia. (2019) (9)
Rheological properties of antibody‐coated red cells (1984) (9)
Modulation of Erythrocyte Membrane Material Properties by Ca 2 + and Calmodulin (2013) (9)
Dynamic changes in murine erythropoiesis from birth to adulthood: implications for the study of murine models of anemia. (2020) (9)
Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia (2016) (9)
Lentiviral globin gene therapy with reduced-intensity conditioning in adults with β-thalassemia: a phase 1 trial (2022) (9)
Genetic variants in the noncoding region of RPS19 gene in Diamond‐Blackfan anemia: Potential implications for phenotypic heterogeneity (2010) (9)
Hydration of red cells in alpha and beta thalassemias differs. A useful approach to distinguish between these red cell phenotypes. (1994) (9)
A study of the mechanisms of slow religation to sickle cell hemoglobin polymers following laser photolysis. (1996) (8)
Epigenetic inactivation of ERF reactivates γ-globin expression in β-thalassemia. (2021) (8)
Cell-cell interactions and erythropoiesis. (1991) (8)
Erythrocytic vacuolar rafts induced by malaria parasites (2001) (8)
Protein 4.1G Regulates Cell Adhesion, Spreading, and Migration of Mouse Embryonic Fibroblasts through the β1 Integrin Pathway* (2015) (8)
Antibody-Induced Spherocytic Anemia II. Splenic Passage and Sequestration of Red Cells (1978) (8)
Human STEAP3 mutations with no phenotypic red cell changes. (2016) (8)
Erythroid Krüppel-like factor mutations are relatively more common in a thalassemia endemic region and ameliorate the clinical and hematological severity of β-thalassemia (2014) (7)
The role of membrane skeletal-associated alpha-globin in the pathophysiology of beta-thalassemia (1990) (7)
Cholesterol-binding protein TSPO2 coordinates maturation and proliferation of terminally differentiating erythroblasts (2020) (7)
low-density sickle and normal red cells (2000) (7)
NIH Workshop 2018: Towards Minimally Invasive or Noninvasive Approaches to Assess Tissue Oxygenation Pre- and Post-transfusion. (2020) (7)
Congenital Erythropoietic Porphyria: Characterization of Murine Models of the Severe Common (C73R/C73R) and Later-Onset Genotypes (2011) (7)
Characterization of cellular determinants and plasma factors responsible for increased adherence of sickle cells to vascular endothelium. (1987) (7)
Effect of human beta (s)-globin chains on cellular properties of red cells from beta-thalassemic mice. (1988) (6)
Merozoite surface proteins 4 and 5 of Plasmodium knowlesi have differing cellular localisation and association with lipid rafts. (2004) (6)
Cytoskeletal Protein 4.1R Is a Positive Regulator of the FcεRI Signaling and Chemotaxis in Mast Cells (2020) (6)
Hereditary Disorders of the Red Cell Membrane and Disorders of Red Cell Metabolism (2015) (6)
Comprehensive characterization of protein 4.1 expression in epithelium of large intestine (2014) (6)
Fetal hematopoietic stem cell transplantation into β-thalassemic mice (1993) (6)
Crystallization and preliminary X-ray crystallographic analysis of the 30 kDa membrane-binding domain of protein 4.1 from human erythrocytes. (2000) (6)
Fetal hematopoietic stem cell transplantation into beta-thalassemic mice. (1993) (5)
Antibody-Induced Spherocytic Anemia I. Changes in Red Cell Deformability (1978) (5)
XPO1 (Exportin-1) Is a Major Regulator of Human Erythroid Differentiation. Potential Clinical Applications to Decrease Ineffective Erythropoiesis of Beta-Thalassemia (2015) (5)
XPO1 regulates erythroid differentiation and is a new target for the treatment of β-thalassemia (2019) (5)
To shrink or not to shrink. (2013) (5)
Erythrocyte deformability changes in autoimmune hemolytic anemia during development of NZB mice and their (NZB/NZW)F1 hybrid. (1985) (5)
Canine elliptocytosis due to a mutant beta-spectrin. (2009) (5)
Factors that limit whole cell deformability in erythrocytes after calcium loading and ATP depletion. (1981) (5)
Piebaldism in diamond–blackfan anaemia: a new phenotype? (2002) (5)
Inter-subunit interactions in erythroid and non-erythroid spectrins. (2011) (5)
Protein 4.1N is required for the formation of the lateral membrane domain in human bronchial epithelial cells. (2018) (5)
malaria-infected red blood cells Plasmodium falciparum binds to the 30-kDa domain of protein 4.1 in Mature parasite-infected erythrocyte surface antigen (MESA) of (2013) (4)
Role of tissue-specific promoter DNA methylation in regulating the human EKLF gene. (2018) (4)
Enhancing diversity in the hematology biomedical research workforce: A mentoring program to improve the odds of career success for early stage investigators (2017) (4)
RED CELLS , IRON , AND ERYTHROPOIESIS KLF 1 mutations are relatively more common in a thalassemia endemic region and ameliorate the severity of b-thalassemia (2014) (4)
Peroxiredoxin-2: A Novel Factor Involved in Iron Homeostasis (2015) (4)
Reduced transglutaminase-catalyzed cross-linking of exogenous amines to membrane proteins in sickle erythrocytes. (1985) (4)
Functional role for glycophorin C and its interaction with the human red cell membrane skeletal component, protein 4.1. (1989) (4)
Ca2+-dependent and Ca2+-independent Calmodulin Binding Sites in Erythrocyte Protein 4.1 (2000) (4)
Jekyll and Hyde: the role of heme oxygenase-1 in erythroid biology (2015) (3)
A micro-bead device to explore Plasmodium falciparum-infected, spherocytic or aged red blood cells prone to mechanical retention by spleen endothelial slits (2010) (3)
Erythroblastic islands foster granulopoiesis in parallel to terminal erythropoiesis. (2022) (3)
"Baby" red cells to the rescue. (2011) (3)
Malaria, erythrocytic infection, and anemia Malaria, erythrocytic infection, and anemia Malaria, erythrocytic infection, and anemia Malaria, erythrocytic infection, and anemia Malaria, erythrocytic infection, and anemia (2009) (3)
Identification of the hereditary pyropoikilocytosis carrier state. (1984) (3)
RED CELLS , IRON , AND ERYTHROPOIESIS Unexpected role for p 19 INK 4 d in posttranscriptional regulation of GATA 1 and modulation of human terminal erythropoiesis (2016) (3)
Deciphering the nuclear import pathway for the cytoskeletal protein 4.1R (1999) (3)
Molecular Analysis of Insertion / Deletion Mutations in Protein 4 . 1 in Elliptocytosis I 1 (3)
[Quantitative study of changes of the shape of erythrocytes produced by cationic and anionic derivatives of phenothiazine]. (1974) (3)
invasion by Plasmodium falciparum The hydration state of human red blood cells and their susceptibility to (2013) (3)
Red blood cells and malaria (2009) (2)
Heterogeneous phenotype of Hereditary Xerocytosis in association with PIEZO1 variants. (2020) (2)
Dynamic Palmitoylation of Red Cell Membrane Proteins Governs Susceptibility to Invasion by the Malaria Parasite, Plasmodium falciparum. (2022) (2)
Protein 4.1R links E-cadherin/β-catenin complex to the cytoskeleton through its direct interaction with β-catenin and modulates adherens junction integrity (2015) (2)
Erythrocyte membrane proteins and their diseases: introduction (2004) (2)
Malaria and human red blood cells (2012) (2)
Selective effects of protein 4.1N deficiency on neuroendocrine and reproductive systems (2020) (2)
More than one way to shrink. (2015) (2)
Staying hydrated is important also for erythroblasts (2020) (2)
Polyamines do not inhibit erythrocyte ATPase activities. (1983) (2)
A Dynamic Spectrin-Dimer Self Association Regulates of Red cell MembraneMechanical Stability. (2001) (2)
Developments in red cell rheology at the Institut de Pathologie Cellulaire. (1986) (2)
Adducin Forms a Bridge between the Spectrin-Actin Junctional Complex and Band 3. (2005) (2)
The erythrocyte "cytoskeleton" and its apparent role in cellular functions. (1981) (2)
A new method for studying the deformability of isolated erythrocyte membranes. (1981) (2)
Homozygous hereditary elliptocytosis: implications for the function of membrane protein band 4.1. (1982) (2)
Isolation and Functional Characterization of Human Erythroid Progenitors: BFU-E and CFU-E (2011) (2)
The iron fist: malaria and hepcidin. (2014) (2)
X-ray microscopic visualization of specific labeling of adhesive molecule CD36 and cytoadherence by Plasmodium falciparum infected erythrocytes. (1998) (2)
Initial assessment of the beneficial effect of partial splenectomy in hereditary spherocytosis. (1993) (1)
A fork in the road. (2019) (1)
Iconographies supplémentaires de l'article : Red cell membrane and malaria (2010) (1)
Ineffective Erythropoiesis Is the Major Cause of Microcytic Anemia in the TSAP6/Steap3 Null Mouse Model (2014) (1)
Murine Spherocytosis: Evidence for a Functional Interaction between Protein 4.1 and Na/H Exchange and for a “Protective” Role of the Gardos Channel Against Hemolysis. (2004) (1)
Evidence for a second diamond-blackfan anemia gene on human chromosome 8p23-22, and for at least one other dba gene (2000) (1)
Normal membrane function of abnormal beta-related erythrocyte sialoglycoproteins. (1987) (1)
Lack of the human choline transporter‐like protein SLC44A2 causes hearing impairment and a rare red blood phenotype (2023) (1)
'Erythritol', a safe natural sweetener exhibits multi-stage anti-malarial activity by permeating into Plasmodium falciparum through aquaglyceroporin channel. (2022) (1)
Erratum to First de novo mutation in RPS19 gene as the cause of hydrops fetalis in Diamond–Blackfan anemia (2013) (1)
Anemia lurking in introns. (2019) (1)
Of mice and men: the voracious spleen (2006) (1)
Glucocorticoids Induce the Expansion of an Immature Human CFU-E Population (2019) (1)
Assessment of Plasmodium falciparum Artemisinin Resistance Independent of kelch13 Polymorphisms and with Escalating Malaria in Bangladesh (2022) (1)
Correction: Selective Erythroid Replacement in Murine |beta-Thalassemia Using Fetal Hematopoietic Stem Cells (1994) (1)
A cell by any other name (2005) (1)
Regulatory factors of erythrocyte membrane stability (1994) (1)
αI-spectrin represents evolutionary optimization of spectrin for red blood cell deformability (2021) (1)
An open-and-shut case? (2013) (1)
Inhibition of Human Erythropoiesis during Inflammation Is Mediated By High Mobility Group Box Protein 1 (HMGB1) through Decreased Commitment of Hematopoietic Stem Cells to the Erythroid Lineage and By Increased Apoptosis of Terminally Differentiating Erythroblasts (2016) (1)
Vesicular formation regulated by ERK/MAPK pathway mediates human erythroblast enucleation (2021) (1)
Exit strategy: one that works. (2012) (1)
Supplemental Information Comprehensive Proteomic Analysis of Human Erythropoiesis (2016) (1)
Single dose, long-term treatment of beta-thalassemia in mice following intramuscular administration of the erythropoietin gene (1997) (1)
New Insights into the Function of N-Terminal 11 Amino Acids of Band 3 from Structural and Functional Study of a Naturally Occuring Band 3 Variant. (2004) (1)
Down-Regulation of TfR1 Increases Erythroid Precursor Enucleation and Hepatocyte Hepcidin Expression in ß-Thalassemic Mice (2015) (1)
Unravelling Macrophage Heterogeneity in Erythroblastic Islands Between Species (2016) (0)
Dynamic Changes Of DNA Methylation and a Functional Role For TET2 DNA Dioxygenase In Human Erythroid Differentiation (2013) (0)
Nuclear actin is essential for assembly and maintenance of nuclear structure (2003) (0)
Ektacytometry and the Measurement of Cell Physical Properties. Commentary of papers (1981) (0)
144 VASCULAR P-SELECTIN MODULATION OF MICROVASCULAR FLOW IN A MOUSE MODEL OF SICKLE CELL DISEASE. (2004) (0)
Lentiviral globin gene therapy with reduced-intensity conditioning in adults with β-thalassemia: a phase 1 trial (2022) (0)
cytoskeletal connectivity Mechanism of protein sorting during erythroblast enucleation: role of (2010) (0)
The sticking point (2005) (0)
of altered Lyn kinase activity Erythrocyte membrane changes of chorea-acanthocytosis are the result (2013) (0)
PIEBALDISM I N DIAMOND-BLACKFAN A NAEMIA: A NEW PHENOTYPE? (2002) (0)
Erythropoiesis Diamond-Blackfan anemia , ribosome and erythropoiesis L ’ anémie (2010) (0)
Editorial introductions. (2019) (0)
ATP11C Encodes a Major Flippase in Human Erythrocyte and Its Genetic Defect Causes Congenital Non-Spherocytic Hemolytic Anemia (2015) (0)
P1405: ARGININE-DEPENDENT REGULATION OF THE EUKARYOTIC TRANSLATION INITIATION FACTOR (EIF)5A CONTROLS HUMAN HEMATOPOIETIC PROGENITOR FATE TO THE ERYTHROID LINEAGE (2022) (0)
Splicing Mechanisms That Generate Distinct Isoforms of Protein 4.1R During Terminal Erythroid Differentiation. (2009) (0)
Dynamic Changes in Membrane Protein Expression During Murine and Human Erythropoiesis: Resolving the Distinct Stages in Terminal Erythroid Differentiation. (2009) (0)
Nuclear substructure reorganization during terminal erythroid differentiation (2004) (0)
erythrocyte cytoskeleton Rac GTPases regulate the morphology and deformability of the (2013) (0)
Protein 4.1 interactions with chromatin-associated proteins (2004) (0)
Abundance of Alternative Splicing Events and Differentiation Stage-Specific Changes in Splicing Suggest A Major Role in Regulation of Gene Expression During Late Erythropoiesis (2012) (0)
Narla invasion stabilizes spectrin tetramers and suppresses further falciparum Plasmodium The ring-infected erythrocyte surface antigen ( RESA ) (2007) (0)
The Human Ankyrin Insulator Supports Production of Therapeutic Levels of Adult Hemoglobin Following β-Globin Gene Transfer in Hematopoietic Cells Derived From Thalassemic and Sickle Cell Patients (2011) (0)
Additional file 4: Table S3. of SF3B1 deficiency impairs human erythropoiesis via activation of p53 pathway: implications for understanding of ineffective erythropoiesis in MDS (2018) (0)
NewOpticalTechnique forMeasuring Erythrocyte Deformability withthe Ektacytometer (1980) (0)
"Capping": necessary for graduation. (2010) (0)
Characterization of the Gene Coding for Human Erythrocyte Protein 4.1 (2020) (0)
Hemoglobin content of individual erythroblasts in hematopoietic dysplasia: marked heterogeneity at late stages of maturation. (1984) (0)
Answer to Commentaries (1981) (0)
The Erythroid Intron Retention Program Encompasses Developmentally Stable and Dynamic Networks and Regulates Diverse Gene Classes (2015) (0)
Cell Reports Resource Comprehensive Proteomic Analysis of Human Erythropoiesis (2017) (0)
Three Months of Human Haptoglobin Treatment Decreases Iron Deposition in the Kidneys of Townes Sickle Mice (2015) (0)
Short title: Endothelial P-selectin slows mouse sickle cell flow in vivo (2013) (0)
Mechanisms that link promoter choice with downstream alternative splicing in the protein 4.1R gene (2007) (0)
Inhibiting Binding of Sickle Red Cell ICAM-4 to Endothelial Cell αVβ3 Integrin Decreases Red Cell Adhesion and Vaso-Occlusion. (2004) (0)
Sickle cell disease: a step closer to the dream. (1996) (0)
Induced changes at the membrane of the parasite-infected red blood cell (1998) (0)
S4.1. Characterization of cellular and membrane properties of red cells by ektacytometry (1995) (0)
Long-Term Follow up of the Beneficial Effects and of Issues in Subtotal Splenectomy for Hereditary Spherocytosis (2015) (0)
Racial Differences In Thrombin-Induced Human Platelet PAR4 Reactivity (2013) (0)
Sickle Erythrocytes Have Increased Adducin Phosphorylation and Increased ROS Production Mediated by Signaling Pathways Involving Protein Kinase C and Rac GTPases. (2009) (0)
Pomalidomide and Dexamethasone Regulate Human Erythroid Progenitor Signaling through Two Distinct Pathways (2016) (0)
Protein 4.1 : the family is getting larger (2000) (0)
Expression and function of red cell protein 4.1 and its homologues in erythroid and non-erythroid cells (1998) (0)
Two Distinct Mechanisms Are Responsible for Regulation of Ribosomal Protein S19 Expression Level in Diamond-Blackfan Anemia by NF-κB Pathway. (2007) (0)
Kindlin-3 deficiency leads to impaired erythropoiesis and erythrocyte cytoskeleton. (2023) (0)
Effect of Human #5-Globin Chains on Cellular Properties of Red Cells from #l-Thalassemic Mice (1988) (0)
high affinity 5 chain-containing human laminin with α homologue specifically bind Lutheran blood group glycoprotein and its newly characterized mouse (2013) (0)
‘Erythritol’, a safe natural sweetener exhibits multi-stage anti-malarial activity by blocking Plasmodium falciparum membrane transporter ‘aquaporin’ (2022) (0)
Evolutionarily Conserved Coupling of Transcription and Alternative Splicing in the Protein 4.1R and 4.1B Genes Regulates N-Terminal Protein Structure. (2005) (0)
Distinct Roles of TET Proteins in the Regulation of Normal and Disordered Human Erythropoiesis (2015) (0)
Arginine metabolism regulates human erythroid differentiation through hypusination of eIF5A. (2023) (0)
p19INK4d Modulates Human Terminal Erythroid Differentiation By Post-Transcriptionally Regulating GATA1 Expression (2016) (0)
RBC membrane based macrocomplex of integral and peripheral proteins in the (2013) (0)
Commentary of papers (1981) (0)
Tropomyosin modulates erythrocyte membrane stability. Commentary (2007) (0)
Arginine-dependent hypusination of the eukaryotic translation initiation factor (eIF)5A drives erythroid lineage differentiation (2022) (0)
The erythroblastic island as an emerging paradigm in the anemia of inflammation (2015) (0)
membranes in wild type and membrane protein knockout mice Characterization of glycolytic enzyme interactions with murine erythrocyte (2013) (0)
RED CELLS, IRON, AND ERYTHROPOIESIS Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease (2013) (0)
Screen “play” for drug discovery (2022) (0)
RED BLOOD CELL (RBC) MEMBRANE DEFORMABILITY AND WHOLE BLOOD VISCOSITY IN INFANTS OF DIABETIC MOTHERS (IDM) (1984) (0)
Pomalidomide Modulates Transcription Networks Regulating Human Erythropoiesis and Globin Switching: Implications for Treatment of Hemoglobinopathies (2014) (0)
An Erythroid-Specific Intron Retention Program Regulates Expression of Selected Genes during Terminal Erythropoiesis (2014) (0)
Discussion of Papers (1978) (0)
Expression of Concern: A Golgi-associated protein 4.1B variant is required for assimilation of proteins in the membrane (doi:10.1242/jcs.039644) (2019) (0)
integrins V α intercellular adhesion molecule-4 (ICAM-4) mediating adhesion to Identification of critical amino-acid residues on the erythroid (2013) (0)
HSP70, the Key to Account for Erythroid Tropism of Diamond-Blackfan Anemia? (2015) (0)
Comprehensive characterization of protein 4.1 expression in epithelium of large intestine (2014) (0)
glycoprotein is located at the flexible junction of Ig domains 2 and 3 The Laminin 511/521binding site on the Lutheran blood group (2009) (0)
Membrane skeleton hyperstability due to a novel alternatively spliced 4.1R can account for ellipsoidal camelid red cells with decreased deformability (2023) (0)
Selective erythroid replacement in murine ,-thalassemia using fetal hematopoietic stem cells ( erythropoiesis / transplantation / hemoglobinopathies ) (2005) (0)
Protein-protein interactions that influence the abnormal rheological properties of malaria-infected red blood cells (1999) (0)
critical for erythroblastic island formation Targeted gene deletion demonstrates that cell adhesion molecule ICAM-4 is (2013) (0)
normal and disordered erythropoiesis in vivo (2017) (0)
Simultaneous adjunctive treatment of malaria and its co-evolved genetic disorder sickle cell anaemia (2022) (0)
novel method to study normal and disordered erythropoiesis Quantitative analysis of murine terminal erythroid differentiation in vivo (2013) (0)
Elevated Reactive Oxygen Species Production In Sickle Erythrocytes Is Modulated by a Pathway Involving Endothelin-1, TGFβ1, PKC, and Rac GTPases (2010) (0)
Plenary paper Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia (2001) (0)
can be mimicked in vitro The sensing of poorly deformable red blood cells by the human spleen (2014) (0)
Editorial introductions. (2021) (0)
Distinct Differences in in Vitro Erythroid Proliferation and Differentiation, p53 and Apoptosis Pathways in Diamond-Blackfan Anemia in Conjunction with Depletion of RPS19, RPL5 and RPL11 mRNA. (2009) (0)
No Evidence for Cell Activation or Vaso-Occlusion with Plerixafor Treatment of Sickle Cell Mice (2015) (0)
Lack of the human choline transporter-like protein CTL2 causes hearing impairment and a rare red blood cell phenotype (2022) (0)
Fyn is Involved in Erythropoietin Signaling Pathway and Interfaces Oxidation to Regulate Erythropoiesis (2018) (0)
The novel GATA1-interacting protein HES6 is an essential transcriptional cofactor for human erythropoiesis. (2023) (0)
membrane systems and is essential for proplatelet and platelet formation The spectrin-based membrane skeleton stabilizes mouse megakaryocyte (2011) (0)
X-ray microscopy of human malaria (1997) (0)
Molecular basis for the abnormal rheological properties of malaria-infected red blood cells (1999) (0)
In Vivo Analysis of Erythroid Protein 4.1 Pre-mRNA Splicing Mechanisms: Use of Antisense Morpholinos to Assay Function of Deep Intron Regulatory Elements (2010) (0)
Is the erythropoietin receptor the key to the identification of the central macrophage in erythroblastic islands? (2020) (0)
Stomatocytosis is absent in 'stomatin'-deficient mouse red cells (2001) (0)
Measurement of erythrocyte membrane bilayer separation forces using fluorescence imaged magnetic tweezers (1999) (0)
The Human Kell Blood Group Binds the Erythroid 4.1R Protein: New Insights into the 4.1R-Dependent Red Cell Membrane Complex (2015) (0)
Using the Sodium lonophore Monensin A MODEL FOR THERAPY (1982) (0)
Phenotypic and Genetic Discordance in Monozygotic Twins with Sickle Anemia and ð-Thalassemia. (2009) (0)
To the editor: Age-sex–specific ranges of platelet count and all-cause mortality: prospective findings from the MOLI-SANI study (2016) (0)
Correction: A Golgi-associated protein 4.1B variant is required for assimilation of proteins in the membrane (doi:10.1242/jcs.039644) (2019) (0)
Mechanisms That Link Promoter Choice with Downstream Alternative Splicing in the Erythroid Protein 4.1R Gene. (2006) (0)
Modulating Spectrin-Actin Interaction Functionin Regulating Red Cell Membrane Identification of a Novel Role for Dematin Membrane Biology : (2012) (0)
Pomalidomide Transcriptionally Reprograms Adult Erythroid Progenitors Independently of Ikaros Proteasomal Degradation (2015) (0)
S12.2. Red cell membrane mechanical properties: Insights from genetic lesions (1995) (0)
Physical Separation and Characterization of Reticulocytes and Other Cell Fractions from Rat Bone Marrow, and the 1g Mini-Staflo (1979) (0)
malaria-infected red blood cells Contribution of parasite proteins to altered mechanical properties of (2013) (0)
in murine spherocytosis Evidence for a protective role of the Gardos channel against hemolysis (2013) (0)
Workshop on signal transduction in hematopoietic cells (1995) (0)
The road not taken? (2016) (0)
Circulating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating (2017) (0)

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