Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation
about
Murine bone marrow Lin⁻Sca⁻1⁺CD45⁻ very small embryonic-like (VSEL) cells are heterogeneous population lacking Oct-4A expressionMice expressing RHAG and RHD human blood group genesLoss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65SComparative proteomics reveals deficiency of SLC9A1 (sodium/hydrogen exchanger NHE1) in β-adducin null red cells.Brain, blood, and iron: perspectives on the roles of erythrocytes and iron in neurodegeneration.Protein distribution during human erythroblast enucleation in vitroNormal and disordered reticulocyte maturation.The sorting of blood group active proteins during enucleation'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulationThe human Kell blood group binds the erythroid 4.1R protein: new insights into the 4.1R-dependent red cell membrane complex.The erythroid niche: molecular processes occurring within erythroblastic islands.Severe Ankyrin-R deficiency results in impaired surface retention and lysosomal degradation of RhAG in human erythroblasts.A 130-kDa protein 4.1B regulates cell adhesion, spreading, and migration of mouse embryo fibroblasts by influencing actin cytoskeleton organization.Erythroblast enucleation.A genetic features and gene interaction study for identifying the genes that cause hereditary spherocytosis.Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis.From the Cradle to the Grave: The Role of Macrophages in Erythropoiesis and Erythrophagocytosis.Diffusion of glycophorin A in human erythrocytes.Refinement of the genetics of the host response to Salmonella infection in MOLF/Ei: regulation of type 1 IFN and TRP3 pathways by Ity2.Critical band 3 multiprotein complex interactions establish early during human erythropoiesis.Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families.Scanning Electron Microscopy Reveals Two Distinct Classes of Erythroblastic Island Isolated from Adult Mammalian Bone Marrow.Flow Cytometric Analysis of Erythroblast Enucleation.Band 3 nullVIENNA , a novel homozygous SLC4A1 p.Ser477X variant causing severe hemolytic anemia, dyserythropoiesis and complete distal renal tubular acidosis.Automated reticulocyte parameters for hereditary spherocytosis screening.
P2860
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P2860
Hereditary spherocytosis and hereditary elliptocytosis: aberrant protein sorting during erythroblast enucleation
description
2010 nî lūn-bûn
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2010 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մարտին հրատարակված գիտական հոդված
@hy
2010年の論文
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2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@ast
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@en
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@nl
type
label
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@ast
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@en
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@nl
prefLabel
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@ast
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@en
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@nl
P2093
P2860
P50
P1433
P1476
Hereditary spherocytosis and h ...... uring erythroblast enucleation
@en
P2093
Jonathan Villalobos
Marcela Salomao
P2860
P304
P356
10.1182/BLOOD-2010-02-264127
P407
P577
2010-03-25T00:00:00Z