Narla Mohandas
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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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(Suggest an Edit or Addition)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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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