(Q50463919)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16791000%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

title

Functional characterization of wild-type and a mutated form of SLC26A4 identified in a patient with Pendred syndrome (English)

1 reference

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25 December 2019

1 reference

13

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25 December 2019

Valeria Vezzoli

2

1 reference

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25 December 2019

Markus Ritter

11

1 reference

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25 December 2019

16

Paolo Beck-Peccoz

1 reference

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25 December 2019

author name string

Silvia Dossena

1

1 reference

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25 December 2019

Nadia Cerutti

3

1 reference

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25 December 2019

Claudia Bazzini

4

1 reference

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25 December 2019

Marisa Tosco

5

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25 December 2019

Chiara Sironi

6

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25 December 2019

Simona Rodighiero

7

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25 December 2019

Giuliano Meyer

8

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25 December 2019

Umberto Fascio

9

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25 December 2019

Johannes Fürst

10

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25 December 2019

Laura Fugazzola

12

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25 December 2019

Patrick Zorowka

14

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25 December 2019

Carlo Storelli

15

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25 December 2019

Guido Bottà

17

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25 December 2019

Markus Paulmichl

18

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25 December 2019

publication date

20 June 2006

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Cellular Physiology and Biochemistry

25 December 2019

published in

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25 December 2019

volume

17

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25 December 2019

issue

5-6

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25 December 2019

page(s)

245-256

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Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

25 December 2019

cites work

1 reference

The SLC26 gene family of multifunctional anion exchangers

21 January 2018

1 reference

Pendrin, the protein encoded by the Pendred syndrome gene (PDS), is an apical porter of iodide in the thyroid and is regulated by thyroglobulin in FRTL-5 cells

21 January 2018

1 reference

Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.

21 January 2018

1 reference

Differential diagnosis between Pendred and pseudo-Pendred syndromes: clinical, radiologic, and molecular studies

21 January 2018

1 reference

Deoxycorticosterone upregulates PDS (Slc26a4) in mouse kidney: role of pendrin in mineralocorticoid-induced hypertension

21 January 2018

1 reference

Immunocytochemical localization of pendrin in intercalated cell subtypes in rat and mouse kidney

21 January 2018

1 reference

Pendrin, encoded by the Pendred syndrome gene, resides in the apical region of renal intercalated cells and mediates bicarbonate secretion

21 January 2018

1 reference

The Pendred syndrome gene encodes a chloride-iodide transport protein

21 January 2018

1 reference

Cl- channel blockers NPPB and niflumic acid blunt Ca(2+)-induced erythrocyte 'apoptosis'.

21 January 2018

1 reference

Localization and functional studies of pendrin in the mouse inner ear provide insight about the etiology of deafness in pendred syndrome

21 January 2018

1 reference

Regulation of the apical Cl-/HCO-3 exchanger pendrin in rat cortical collecting duct in metabolic acidosis

21 January 2018

1 reference

Acid incubation reverses the polarity of intercalated cell transporters, an effect mediated by hensin

21 January 2018

1 reference

A molecular mechanism for aberrant CFTR-dependent HCO(3)(-) transport in cystic fibrosis

21 January 2018

1 reference

Mechanism of iodide/chloride exchange by pendrin

21 January 2018

1 reference

Regulation of the expression of the Cl-/anion exchanger pendrin in mouse kidney by acid-base status

21 January 2018

1 reference

Regulated expression of pendrin in rat kidney in response to chronic NH4Cl or NaHCO3 loading.

21 January 2018

1 reference

NaCl restriction upregulates renal Slc26a4 through subcellular redistribution: role in Cl- conservation

21 January 2018

1 reference

Prolactin regulation of the pendrin-iodide transporter in the mammary gland

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000094137

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16791000%20AND%20SRC:MED&resulttype=core&format=json

25 December 2019

1 reference