Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
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Neuroacanthocytosis: Observations, Theories and Perspectives on the Origin and Significance of AcanthocytesAbnormalities of the erythrocyte membraneEpistasis and the sensitivity of phenotypic screens for beta thalassaemiaNew insights on hereditary erythrocyte membrane defectsBiomechanical properties of red blood cells in health and disease towards microfluidics.Profiling individual human red blood cells using common-path diffraction optical tomographyDiagnostic approaches for inherited hemolytic anemia in the genetic eraCirculating primitive erythroblasts establish a functional, protein 4.1R-dependent cytoskeletal network prior to enucleating.The pathophysiology of extracellular hemoglobin associated with enhanced oxidative reactions.Cell rigidity and shape override CD47's "self"-signaling in phagocytosis by hyperactivating myosin-II.Red Blood Cell Homeostasis: Pharmacological Interventions to Explore Biochemical, Morphological and Mechanical Properties.Advances in understanding erythropoiesis: evolving perspectivesAutomated Fourier space region-recognition filtering for off-axis digital holographic microscopy.Exome sequencing results in successful diagnosis and treatment of a severe congenital anemia.Red blood cell vesiculation in hereditary hemolytic anemia.Focusing and alignment of erythrocytes in a viscoelastic medium.Involvement of membrane skeletal molecules in the Schmidt-Lanterman incisure in Schwann cells.Flow cytometry in hematological nonmalignant disorders.Advances in understanding the pathogenesis of the red cell volume disorders.The Proteome of the Red Blood Cell: An Auspicious Source of New Insights into Membrane-Centered Regulation of HomeostasisHematological disorders and pulmonary hypertension.Dystrophin and Spectrin, Two Highly Dissimilar Sisters of the Same Family.Red cell membrane disorders.Hereditary Elliptocytosis with Pyropoikilocytosis.The knockout of urea transporter-B improves the hemorheological properties of erythrocyte.Interspecies diversity of erythrocyte mechanical stability at various combinations in magnitude and duration of shear stress, and osmolality.A biomimetic microfluidic chip to study the circulation and mechanical retention of red blood cells in the spleen.Genotype-phenotype correlations in hereditary elliptocytosis and hereditary pyropoikilocytosis.Chemical Transport Knockout for Oxidized Vitamin C, Dehydroascorbic Acid, Reveals Its Functions in vivo.Biochemical analysis of ascites fluid as an aid to etiological diagnosis: a series of 100 cases of nonimmune fetal ascites.Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families.Complement Depletion Improves Human Red Blood Cell Reconstitution in Immunodeficient Mice.Association of Single-Nucleotide Polymorphism in ANK1 with Late-Onset Alzheimer's Disease in Han Chinese.The involvement of erythrocyte metabolism in organismal homeostasis in health and disease.Stabilization of F-actin by tropomyosin isoforms regulates the morphology and mechanical behavior of red blood cells.Image-based model of the spectrin cytoskeleton for red blood cell simulation.Flow cytometric analysis of patients with hereditary spherocytosis - an Indian scenario.Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.Alu element insertion in PKLR gene as a novel cause of pyruvate kinase deficiency in Middle Eastern patients.Increased mean corpuscular haemoglobin concentration: artefact or pathological condition?
P2860
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P2860
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
description
article científic
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article scientifique
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articol științific
@ro
articolo scientifico
@it
artigo científico
@gl
artigo científico
@pt
artigo científico
@pt-br
artikel ilmiah
@id
artikull shkencor
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artículo científico
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name
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
@en
type
label
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
@en
prefLabel
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
@en
P2093
P1433
P1476
Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders.
@en
P2093
Julie Galimand
Lydie Da Costa
Odile Fenneteau
P304
P356
10.1016/J.BLRE.2013.04.003
P577
2013-05-09T00:00:00Z