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Spectrin interacts with EVL (Enabled/vasodilator-stimulated phosphoprotein-like protein), a protein involved in actin polymerizationEmerin caps the pointed end of actin filaments: evidence for an actin cortical network at the nuclear inner membraneSuppression of hepcidin expression and iron overload mediate Salmonella susceptibility in ankyrin 1 ENU-induced mutantAn emerin "proteome": purification of distinct emerin-containing complexes from HeLa cells suggests molecular basis for diverse roles including gene regulation, mRNA splicing, signaling, mechanosensing, and nuclear architecture.Automated structure refinement for a protein heterodimer complex using limited EPR spectroscopic data and a rigid-body docking algorithm: a three-dimensional model for an ankyrin-CDB3 complexHaemolytic disease of the newbornAnkyrins and human disease: what the electrophysiologist should know.Weighing in on molecular anchors: the role of ankyrin polypeptides in human arrhythmia.Contribution of a common single-nucleotide polymorphism to the genetic predisposition for erythropoietic protoporphyria.Determination of structural models of the complex between the cytoplasmic domain of erythrocyte band 3 and ankyrin-R repeats 13-24Identification of a novel p.Q1772X ANK1 mutation in a Korean family with hereditary spherocytosis.Hereditary haemolytic anaemias: unexpected sequelae of mutations in the genes for erythroid membrane skeletal proteins.Coinheritance of hereditary spherocytosis and reversibility of cirrhosis in a young female patient with hereditary hemochromatosisDiagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometerIron refractory iron deficiency anemiaTranscriptional divergence and conservation of human and mouse erythropoiesis.Expression analysis of epb41l4a during Xenopus laevis embryogenesis.Physical and Chemical Processes and the Morphofunctional Characteristics of Human Erythrocytes in Hyperglycaemia.K-Cl cotransport in red blood cells from patients with KCC3 isoform mutants.Analysis of the SLC4A1 gene in three Mexican patients with hereditary spherocytosis: Report of a novel mutationMarked changes in red cell membrane proteins in hereditary spherocytosis: a proteomics approach.A neonate with Coombs-negative hemolytic jaundice with spherocytes but normal erythrocyte indices: a rare case of autosomal-recessive hereditary spherocytosis due to alpha-spectrin deficiency.Targeted next-generation sequencing identifies a novel nonsense mutation in SPTB for hereditary spherocytosis: A case report of a Korean family.Protein deficiency balance as a predictor of clinical outcome in hereditary spherocytosis.Multiple congenital anomalies-intellectual disability (MCA-ID) and neuroblastoma in a patient harboring a de novo 14q23.1q23.3 deletion
P2860
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P2860
description
2002 nî lūn-bûn
@nan
2002 թուականին հրատարակուած գիտական յօդուած
@hyw
2002 թվականին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Molecular basis of red cell membrane disorders
@ast
Molecular basis of red cell membrane disorders
@en
Molecular basis of red cell membrane disorders
@nl
type
label
Molecular basis of red cell membrane disorders
@ast
Molecular basis of red cell membrane disorders
@en
Molecular basis of red cell membrane disorders
@nl
prefLabel
Molecular basis of red cell membrane disorders
@ast
Molecular basis of red cell membrane disorders
@en
Molecular basis of red cell membrane disorders
@nl
P356
P1433
P1476
Molecular basis of red cell membrane disorders
@en
P2093
Jean Delaunay
P356
10.1159/000065657
P407
P577
2002-01-01T00:00:00Z