(Q38880050)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

review article

1 reference

title

Advances in understanding the pathogenesis of the red cell volume disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

author name string

Catherine Badens

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

language of work or name

English

0 references

publication date

29 June 2016

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

British Journal of Haematology

16 March 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

volume

174

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

page(s)

674-685

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

16 March 2020

cites work

1 reference

Multiple clinical forms of dehydrated hereditary stomatocytosis arise from mutations in PIEZO1.

21 January 2018

1 reference

Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).

21 January 2018

1 reference

Crystal structure of the anion exchanger domain of human erythrocyte band 3

21 January 2018

1 reference

Improvements in haemolysis and indicators of erythrocyte survival do not correlate with acute vaso-occlusive crises in patients with sickle cell disease: a phase III randomized, placebo-controlled, double-blind study of the Gardos channel blocker se

21 January 2018

1 reference

Human PIEZO1: removing inactivation

21 January 2018

1 reference

Xerocytosis is caused by mutations that alter the kinetics of the mechanosensitive channel PIEZO1

21 January 2018

1 reference

Piezo proteins: regulators of mechanosensation and other cellular processes

21 January 2018

1 reference

The challenge of understanding ammonium homeostasis and the role of the Rh glycoproteins

21 January 2018

1 reference

Band 3 missense mutations and stomatocytosis: insight into the molecular mechanism responsible for monovalent cation leak

21 January 2018

1 reference

Dual transport properties of anion exchanger 1: the same transmembrane segment is involved in anion exchange and in a cation leak

21 January 2018

1 reference

Structural model of the anion exchanger 1 (SLC4A1) and identification of transmembrane segments forming the transport site.

21 January 2018

1 reference

An infant with pseudohyperkalemia, hemolysis, and seizures: cation-leaky GLUT1-deficiency syndrome due to a SLC2A1 mutation.

21 January 2018

1 reference

Familial pseudohyperkalemia in blood donors: a novel mutation with implications for transfusion practice

21 January 2018

1 reference

Expression of the human erythroid Rh glycoprotein (RhAG) enhances both NH3 and NH4+ transport in HeLa cells

21 January 2018

1 reference

Cryohydrocytosis: increased activity of cation carriers in red cells from a patient with a band 3 mutation

21 January 2018

1 reference

The expanding phenotype of GLUT1-deficiency syndrome

21 January 2018

1 reference

Hereditary stomatocytosis and cation-leaky red cells--recent developments.

21 January 2018

1 reference

Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1

21 January 2018

1 reference

The monovalent cation leak in overhydrated stomatocytic red blood cells results from amino acid substitutions in the Rh-associated glycoprotein

21 January 2018

1 reference

Piezo1 links mechanical forces to red blood cell volume

21 January 2018

1 reference

RH blood group system and molecular basis of Rh-deficiency

21 January 2018

1 reference

Pharmacological gating modulation of small- and intermediate-conductance Ca(2+)-activated K(+) channels (KCa2.x and KCa3.1)

21 January 2018

1 reference

Temperature effects on cation transport in hereditary stomatocytosis and allied disorders

21 January 2018

1 reference

Piezo proteins are pore-forming subunits of mechanically activated channels

21 January 2018

1 reference

Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

21 January 2018

1 reference

The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations

21 January 2018

1 reference

Review. Leaky Cl--HCO3- exchangers: cation fluxes via modified AE1.

21 January 2018

1 reference

RhAG protein of the Rhesus complex is a CO2 channel in the human red cell membrane

21 January 2018

1 reference

Piezo1 plays a role in erythrocyte volume homeostasis.

21 January 2018

1 reference

Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome

21 January 2018

1 reference

Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis

21 January 2018

1 reference

The "stomatin" gene and protein in overhydrated hereditary stomatocytosis.

21 January 2018

1 reference

Disorders of red cell volume regulation

21 January 2018

1 reference

Architecture of the mammalian mechanosensitive Piezo1 channel

21 January 2018

1 reference

Human RhAG ammonia channel is impaired by the Phe65Ser mutation in overhydrated stomatocytic red cells

21 January 2018

1 reference

Congenital hemolytic anemia associated with dehydrated erythrocytes and increased potassium loss

21 January 2018

1 reference

Disorders of erythrocyte volume homeostasis

21 January 2018

1 reference

Mutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis

21 January 2018

1 reference

Ionic Selectivity and Permeation Properties of Human PIEZO1 Channels

21 January 2018

1 reference

Four pedigrees of the cation-leaky hereditary stomatocytosis class presenting with pseudohyperkalaemia. Novel profile of temperature dependence of Na+-K+ leak in a xerocytic form.

21 January 2018

1 reference

Properties of the CA2+-activated K+ conductance of human red cells as revealed by the patch-clamp technique.

21 January 2018

1 reference

Evidence for up-regulation of the endogenous Na-K-2Cl co-transporter by molecular interactions with the anion exchanger tAE1 expressed in Xenopus oocyte.

21 January 2018

1 reference

Point mutations involved in red cell stomatocytosis convert the electroneutral anion exchanger 1 to a nonselective cation conductance.

21 January 2018

1 reference

South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.

21 January 2018

1 reference

ABCB6 is dispensable for erythropoiesis and specifies the new blood group system Langereis

21 January 2018

1 reference

Cysteine-scanning mutagenesis of transmembrane segment 7 of the GLUT1 glucose transporter

21 January 2018

1 reference

A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis

21 January 2018

1 reference

An extreme consequence of splenectomy in dehydrated hereditary stomatocytosis: gradual thrombo-embolic pulmonary hypertension and lung-heart transplantation.

21 January 2018

1 reference

Duplication of 10 nucleotides in the erythroid band 3 (AE1) gene in a kindred with hereditary spherocytosis and band 3 protein deficiency (band 3PRAGUE).

21 January 2018

1 reference

Role of transferrin receptor and the ABC transporters ABCB6 and ABCB7 for resistance and differentiation of tumor cells towards artesunate

21 January 2018

1 reference

The role of Drosophila Piezo in mechanical nociception

21 January 2018

1 reference

ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders.

21 January 2018

1 reference

Impaired PIEZO1 function in patients with a novel autosomal recessive congenital lymphatic dysplasia

21 January 2018

1 reference

The Gárdos channel: a review of the Ca2+-activated K+ channel in human erythrocytes

21 January 2018

1 reference

New insights into function of red cell membrane proteins and their interaction with spectrin-based membrane skeleton

21 January 2018

1 reference

Red cell membrane: past, present, and future

21 January 2018

1 reference

Erythrocyte Glut1 triggers dehydroascorbic acid uptake in mammals unable to synthesize vitamin C

21 January 2018

1 reference

Transmembrane segment 12 of the Glut1 glucose transporter is an outer helix and is not directly involved in the transport mechanism.

21 January 2018

1 reference

Functional interaction between Rh proteins and the spectrin-based skeleton in erythroid and epithelial cells

21 January 2018

1 reference

Molecular Dynamics Simulations of the Human Glucose Transporter GLUT1

21 January 2018

1 reference

21 January 2018

Hereditary spherocytosis

1 reference

Piezo1, a mechanically activated ion channel, is required for vascular development in mice.

21 January 2018

1 reference

A mutation in the Gardos channel is associated with hereditary xerocytosis

21 January 2018

1 reference

Human Rhesus-associated glycoprotein mediates facilitated transport of NH(3) into red blood cells

21 January 2018

1 reference

The K+ channel KCa3.1 as a novel target for idiopathic pulmonary fibrosis

21 January 2018

1 reference

Stomatin interacts with GLUT1/SLC2A1, band 3/SLC4A1, and aquaporin-1 in human erythrocyte membrane domains.

21 January 2018

1 reference

Defective anion transport activity of the abnormal band 3 in hereditary ovalocytic red blood cells

21 January 2018

1 reference

A transport metabolon. Functional interaction of carbonic anhydrase II and chloride/bicarbonate exchangers

21 January 2018

1 reference

Hemolytic disease due to membrane ion channel disorders

21 January 2018

1 reference

The GPA-dependent, spherostomatocytosis mutant AE1 E758K induces GPA-independent, endogenous cation transport in amphibian oocytes

21 January 2018

1 reference

Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis

21 January 2018

1 reference

Loss-of-function and gain-of-function phenotypes of stomatocytosis mutant RhAG F65S

21 January 2018

1 reference

Ion channels in human red blood cell membrane: actors or relics?

21 January 2018

1 reference

K(Ca)3.1 channel-blockade attenuates airway pathophysiology in a sheep model of chronic asthma

21 January 2018

1 reference

Slips, leaks and channels in glutamate transporters

21 January 2018

1 reference

Glycophorin A: Band 3 aid.

21 January 2018

1 reference

Therapeutic potential of KCa3.1 blockers: recent advances and promising trends

21 January 2018

1 reference

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

21 January 2018

1 reference

A band 3-based macrocomplex of integral and peripheral proteins in the RBC membrane

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/BJH.14197

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27353637%20AND%20SRC:MED&resulttype=core&format=json

16 March 2020

1 reference