Controversies Concerning the Role of Pendrin as an Apical Iodide Transporter in Thyroid Follicular Cells

Analysis of Cellular Localization and Function of Carboxy-Terminal Mutants of Pendrin

(2011) Aigerim Bizhanova et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Identification of Allelic Variants of Pendrin (SLC26A4) with Loss and Gain of Function

(2011) Silvia Dossena et al.   CELLULAR PHYSIOLOGY AND BIOCHEMISTRY

Calcium Oxalate Stone Formation in the Inner Ear as a Result of anSlc26a4Mutation

(2010) Amiel A. Dror et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

A Coherent Organization of Differentiation Proteins Is Required to Maintain an Appropriate Thyroid Function in the Pendred Thyroid

(2010) Maximin Senou et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM

Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion

(2010) Caterina Di Cosmo et al.   JOURNAL OF CLINICAL INVESTIGATION

Genetics and phenomics of hypothyroidism and goiter due to TPO mutations

(2010) Carrie Ris-Stalpers et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Genetics and phenomics of Pendred syndrome

(2010) Aigerim Bizhanova et al.   MOLECULAR AND CELLULAR ENDOCRINOLOGY

Failure of Fluid Absorption in the Endolymphatic Sac Initiates Cochlear Enlargement that Leads to Deafness in Mice Lacking Pendrin Expression

(2010) Hyoung-Mi Kim et al.   PLoS One

Hypo-FunctionalSLC26A4variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: Genotype-phenotype correlation or coincidental polymorphisms?

(2009) Byung Yoon Choi et al.   HUMAN MUTATION

Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome

(2009) Silvia Dossena et al.   JOURNAL OF MOLECULAR ENDOCRINOLOGY

PKC-ε-dependent cytosol-to-membrane translocation of pendrin in rat thyroid PC Cl3 cells

(2008) A. Muscella et al.   JOURNAL OF CELLULAR PHYSIOLOGY

The Slc26a4 transporter functions as an electroneutral Cl−/I−/HCO3−exchanger: role of Slc26a4 and Slc26a6 in I−and HCO3−secretion and in regulation of CFTR in the parotid duct

(2008) Nikolay Shcheynikov et al.   JOURNAL OF PHYSIOLOGY-LONDON

Mutations in the Iodotyrosine Deiodinase Gene and Hypothyroidism

(2008) José C. Moreno et al.   NEW ENGLAND JOURNAL OF MEDICINE

Functional assessment of allelic variants in the SLC26A4 gene involved in Pendred syndrome and nonsyndromic EVA

(2008) A. Pera et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA