(Q37430770)

English

Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression

scientific article published on 19 August 2009

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scholarly article

1 reference

Europe PubMed Central

20 August 2017

Developmental delays consistent with cochlear hypothyroidism contribute to failure to develop hearing in mice lacking Slc26a4/pendrin expression (English)

1 reference

Europe PubMed Central

20 August 2017

Philine Wangemann

1

object named as

Philine Wangemann

1 reference

Europe PubMed Central

20 August 2017

author name string

Hyoung-Mi Kim

2

1 reference

Europe PubMed Central

20 August 2017

Sara Billings

3

1 reference

Europe PubMed Central

20 August 2017

Kazuhiro Nakaya

4

1 reference

Europe PubMed Central

20 August 2017

Xiangming Li

5

1 reference

Europe PubMed Central

20 August 2017

Ruchira Singh

6

1 reference

Europe PubMed Central

20 August 2017

David S Sharlin

7

1 reference

Europe PubMed Central

20 August 2017

Douglas Forrest

8

1 reference

Europe PubMed Central

20 August 2017

Daniel C Marcus

9

1 reference

Europe PubMed Central

20 August 2017

Peying Fong

10

1 reference

Europe PubMed Central

20 August 2017

publication date

19 August 2009

1 reference

Europe PubMed Central

20 August 2017

American Journal of Physiology - Renal Physiology

1 reference

Europe PubMed Central

20 August 2017

297

1 reference

Europe PubMed Central

20 August 2017

5

1 reference

Europe PubMed Central

20 August 2017

F1435-47

1 reference

Europe PubMed Central

20 August 2017

Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

A protective role for type 3 deiodinase, a thyroid hormone-inactivating enzyme, in cochlear development and auditory function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Diverse transport modes by the solute carrier 26 family of anion transporters

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Pendred syndrome and iodide transport in the thyroid

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Deiodinase-mediated thyroid hormone inactivation minimizes thyroid hormone signaling in the early development of fetal skeleton

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Integration of signaling pathways regulating chondrocyte differentiation during endochondral bone formation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Congenital hypothyroidism, dwarfism, and hearing impairment caused by a missense mutation in the mouse dual oxidase 2 gene, Duox2

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Loss of cochlear HCO3- secretion causes deafness via endolymphatic acidification and inhibition of Ca2+ reabsorption in a Pendred syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Thyroid hormone and the growth plate

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

The loss of the chloride channel, ClC-5, delays apical iodide efflux and induces a euthyroid goiter in the mouse thyroid gland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Molecular insight into the effects of hypothyroidism on the developing cerebellum.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Microarray-based comparison of three amplification methods for nanogram amounts of total RNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Hearing loss and retarded cochlear development in mice lacking type 2 iodothyronine deiodinase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

The molecular actions of thyroid hormone in bone

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Assumption-free analysis of quantitative real-time polymerase chain reaction (PCR) data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Pendrin is an iodide-specific apical porter responsible for iodide efflux from thyroid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Pendrin: an apical Cl-/OH-/HCO3- exchanger in the kidney cortex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Expression of pendrin and the Pendred syndrome (PDS) gene in human thyroid tissues

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Gap junction systems in the mammalian cochlea

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Type 2 iodothyronine deiodinase expression in the cochlea before the onset of hearing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Human pendrin expressed in Xenopus laevis oocytes mediates chloride/formate exchange

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Distortion product otoacoustic emissions and outer hair cell defects in the hyt/hyt mutant mouse

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Inwardly rectifying K+ channel Kir7.1 is highly expressed in thyroid follicular cells, intestinal epithelial cells and choroid plexus epithelial cells: implication for a functional coupling with Na+,K+-ATPase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

The Pendred syndrome gene encodes a chloride-iodide transport protein

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Non-syndromic hearing loss associated with enlarged vestibular aqueduct is caused by PDS mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Postnatal leptin surge and regulation of circadian rhythm of leptin by feeding. Implications for energy homeostasis and neuroendocrine function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

Thyroid hormone receptor beta is essential for development of auditory function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

An Experimental Approach to the Understanding and Treatment of Hereditary Syndromes with Congenital Deafness and Hypothyroidism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

23 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

14 September 2017

Binding and internalization of thyroglobulin: selectivity, pH dependence, and lack of tissue specificity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

28 September 2017

Tectorial membrane changes in hypothyroid rats during postnatal development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

28 September 2017

Hearing loss in athyroid pax8 knockout mice and effects of thyroxine substitution

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

26 June 2018

Hypothyroidism prevents developmental neuronal loss during auditory organ development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

26 June 2018

Effects of hypothyroidism on the structural development of the organ of Corti in the rat.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

26 June 2018

Epithelial-mesenchymal tissue interactions guiding otic capsule formation: the role of the otocyst

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

26 June 2018

Electrophysiological correlates of fluid transport in cultured porcine thyroid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

26 June 2018

Bidirectional ion transport in thyroid: secretion of anions by monolayer cultures that absorb sodium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

26 June 2018

Cardiac-specific overexpression of the human short CLC-3 chloride channel isoform in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Effect of cytosolic pH on epithelial Na+ channel in normal and cystic fibrosis sweat ducts

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Postnatal development of the organ of Corti in dominant-negative Gjb2 transgenic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

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.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Reduced ENaC protein abundance contributes to the lower blood pressure observed in pendrin-null mice.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Thyroid hormone receptor alpha1 is a critical regulator for the expression of ion channels during final differentiation of outer hair cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Olivocochlear efferent innervation of the organ of corti in hypothyroid rats.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Thyroid hormone-deficient period prior to the onset of hearing is associated with reduced levels of beta-tectorin protein in the tectorial membrane: implication for hearing loss

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Neuronal expression of synaptotagmin-related gene 1 is regulated by thyroid hormone during cerebellar development.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Targeted disruption of mouse Pds provides insight about the inner-ear defects encountered in Pendred syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Thyroid hormone deficiency before the onset of hearing causes irreversible damage to peripheral and central auditory systems.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

Progressive hearing loss, hypoplasia of the cochlea and widened vestibular aqueducts are very common features in Pendred's syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2781347

2 September 2018

DEAF-MUTISM AND GOITRE

1 reference

https://api.crossref.org/works/10.1152%2FAJPRENAL.00011.2009

21 January 2018

Expression of CFTR in human and bovine thyroid epithelium

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Anionic iodotyrosine residues are required for iodothyronine synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two common and three novel PDS mutations in Thai patients with Pendred syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cochlear synaptogenesis in the hypothyroid rat

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chloride channels in the apical membrane of thyroid epithelial cells are regulated by cyclic AMP

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channel heterogeneity in the apical membrane of porcine thyroid epithelial cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dityrosine bridge formation and thyroid hormone synthesis are tightly linked and are both dependent on N-glycans

1 reference

https://pubmed.ncbi.nlm.nih.gov/19692489

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1152/AJPRENAL.00011.2009

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

1 reference

Europe PubMed Central

20 August 2017

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0 references

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