Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis (Q34270548)

1 August 2017

title

Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis (English)

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1 August 2017

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Vincent P Schulz

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1 August 2017

Brett L Houston

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Ryan Zarychanski

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Yelena Maksimova

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1 August 2017

Donald S Houston

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1 August 2017

Brian Smith

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1 August 2017

Jesse Rinehart

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1 August 2017

Patrick G Gallagher

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1 August 2017

language of work or name

English

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publication date

23 April 2012

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1 August 2017

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inferred from page(s)

published in

Blood

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1 August 2017

volume

120

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1 August 2017

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1 August 2017

page(s)

1908-1915

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Piezo proteins are pore-forming subunits of mechanically activated channels

1 August 2017

cites work

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The mechanosensitive ion channel Piezo1 is inhibited by the peptide GsMTx4

6 July 2018

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Piezo1 and Piezo2 Are Essential Components of Distinct Mechanically Activated Cation Channels

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).

6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

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6 July 2018

1 reference

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6 July 2018

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28 October 2018

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28 October 2018

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Evidence for a mechanosensitive calcium influx into red cells

28 October 2018

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A new variant of hereditary hemolytic anemia with stomatocytosis and erythrocyte cation abnormality

28 October 2018

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12 December 2020

Abnormal spectrin in hereditary elliptocytosis

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12 December 2020

Physiological shear stresses enhance the Ca2+ permeability of human erythrocytes

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12 December 2020

Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24

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12 December 2020

Differences in Ca2+ pumping activity between sub-populations of human red cells

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12 December 2020

Distribution of plasma membrane Ca2+ pump activity in normal human red blood cells

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12 December 2020

10.1182/BLOOD-2012-04-422253

Identifiers

DOI

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1 August 2017

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1 August 2017

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