(Q24338303)

calcium-activated potassium channel activity

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

author

Raphael Rapetti-Mauss

Raphael Rapetti-Mauss

1

0 references

Hélène Guizouarn

Hélène Guizouarn

19

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David Salgado

David Salgado

9

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Jean-Pierre Desvignes

Jean-Pierre Desvignes

10

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Olivier Soriani

Olivier Soriani

14

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Christophe Beroud

Christophe Béroud

11

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author name string

Caroline Lacoste

2

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Véronique Picard

3

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Corinne Guitton

4

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Elise Lombard

5

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Marie Loosveld

6

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Vanessa Nivaggioni

7

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Nathalie Dasilva

8

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Patrick Viout

12

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Monique Bernard

13

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Henri Vinti

15

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Valérie Lacroze

16

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Madeleine Feneant-Thibault

17

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Isabelle Thuret

18

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Catherine Badens

Missense mutations in the ABCB6 transporter cause dominant familial pseudohyperkalemia.

20

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language of work or name

English

0 references

publication date

10 September 2015

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published in

Blood

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volume

126

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issue

11

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page(s)

1273-80

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cites work

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Importance of several cysteine residues for the chloride conductance of trout anion exchanger 1 (tAE1).

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

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Refinement of the hereditary xerocytosis locus on chromosome 16q in a large Canadian kindred.

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Vanadate-induced Ca(2+) and Co(2+) uptake in human red blood cells

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Hereditary spherocytosis, elliptocytosis, and other red cell membrane disorders

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

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Structure of the gating domain of a Ca2+-activated K+ channel complexed with Ca2+/calmodulin

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Dehydrated hereditary stomatocytosis linked to gain-of-function mutations in mechanically activated PIEZO1 ion channels

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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

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

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hSK4, a member of a novel subfamily of calcium-activated potassium channels

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Calmodulin mediates calcium-dependent activation of the intermediate conductance KCa channel, IKCa1

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

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Contribution of the KCa3.1 channel-calmodulin interactions to the regulation of the KCa3.1 gating process

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Endothelial small-conductance and intermediate-conductance KCa channels: an update on their pharmacology and usefulness as cardiovascular targets

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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

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Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis

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

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Local membrane deformations activate Ca2+-dependent K+ and anionic currents in intact human red blood cells

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