The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations.
about
Red cell membrane: past, present, and futureNew insights on hereditary erythrocyte membrane defectsLoss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65SCation-leak stomatocytosis in standard schnauzers does not cosegregate with coding mutations in the RhAG, SLC4A1, or GLUT1 genes associated with human diseaseInterpretation of osmotic gradient ektacytometry (osmoscan) data: a comparative study for methodological standards.The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytesDual transport properties of anion exchanger 1: the same transmembrane segment is involved in anion exchange and in a cation leakDehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channelsDisorders of red cell membrane.Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis.Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak.Alterations of red blood cell metabolome in overhydrated hereditary stomatocytosis.'Gardos Channelopathy': a variant of hereditary Stomatocytosis with complex molecular regulationDiagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometerUnusual thermal disassembly of the SPFH domain oligomer from Pyrococcus horikoshii.Determinants of erythrocyte hydration.Hereditary red cell membrane disorders and laboratory diagnostic testing.Review of the Association between Splenectomy and Chronic Thromboembolic Pulmonary Hypertension.Advances in understanding the pathogenesis of the red cell volume disorders.Red cell membrane disorders.Biochemical and cellular changes in leukocyte-depleted red blood cells stored for transfusionCryohydrocytosis: increased activity of cation carriers in red cells from a patient with a band 3 mutation.Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families.The hereditary stomatocytosesFamilial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice.Osmotic gradient ektacytometry: A valuable screening test for hereditary spherocytosis and other red blood cell membrane disorders.Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).Large Deformation Properties of Red Blood Cell Membrane Based on a Higher Order Gradient Quasi-continuum Model.ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.Hereditary xerocytosis, a misleading anemia.Common PIEZO1 Allele in African Populations Causes RBC Dehydration and Attenuates Plasmodium Infection.
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P2860
The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
The hereditary stomatocytoses: ...... ability to monovalent cations.
@ast
The hereditary stomatocytoses: ...... ability to monovalent cations.
@en
type
label
The hereditary stomatocytoses: ...... ability to monovalent cations.
@ast
The hereditary stomatocytoses: ...... ability to monovalent cations.
@en
prefLabel
The hereditary stomatocytoses: ...... ability to monovalent cations.
@ast
The hereditary stomatocytoses: ...... ability to monovalent cations.
@en
P1476
The hereditary stomatocytoses: ...... ability to monovalent cations.
@en
P2093
Jean Delaunay
P304
P356
10.1053/J.SEMINHEMATOL.2004.02.005
P577
2004-04-01T00:00:00Z