(Q40242619)

18 September 2017

title

Fast fluorometric method for measuring pendrin (SLC26A4) Cl-/I- transport activity (English)

1 reference

18 September 2017

16

Markus Paulmichl

0 references

Silvia Dossena

1

object named as

Silvia Dossena

0 references

Paolo Beck-Peccoz

14

object named as

Paolo Beck-Peccoz

0 references

author name string

Silvia Dossena

1

1 reference

18 September 2017

Simona Rodighiero

2

1 reference

18 September 2017

Valeria Vezzoli

3

1 reference

18 September 2017

Claudia Bazzini

4

1 reference

18 September 2017

Chiara Sironi

5

1 reference

18 September 2017

Giuliano Meyer

6

1 reference

18 September 2017

Johannes Fürst

7

1 reference

18 September 2017

Markus Ritter

8

1 reference

18 September 2017

Maria L Garavaglia

9

1 reference

18 September 2017

Laura Fugazzola

10

1 reference

18 September 2017

Luca Persani

11

1 reference

18 September 2017

Patrick Zorowka

12

1 reference

18 September 2017

Carlo Storelli

13

1 reference

18 September 2017

Guido Bottá

15

1 reference

18 September 2017

Markus Paulmichl

16

1 reference

18 September 2017

publication date

15 August 2006

1 reference

Cellular Physiology and Biochemistry

18 September 2017

published in

1 reference

18 September 2017

volume

18

1 reference

18 September 2017

issue

1-3

1 reference

18 September 2017

page(s)

67-74

1 reference

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

18 September 2017

cites work

1 reference

Functional characterization of pendrin in a polarized cell system. Evidence for pendrin-mediated apical iodide efflux

21 January 2018

1 reference

The Pendred syndrome gene encodes a chloride-iodide transport protein

21 January 2018

1 reference

The SLC26 gene family of multifunctional anion exchangers

21 January 2018

1 reference

Expression pattern of the mouse ortholog of the Pendred's syndrome gene (Pds) suggests a key role for pendrin in the inner ear

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

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

Effects of thyroglobulin and pendrin on iodide flux through the thyrocyte

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

Radiological malformations of the ear in Pendred syndrome.

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000095164

1 reference

18 September 2017

1 reference