Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness
Published 2014 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Atrophic thyroid follicles and inner ear defects reminiscent of cochlear hypothyroidism in Slc26a4-related deafness
Authors
Keywords
Thyroid Hormone, Hair Cell, Thyroid Gland, Congenital Hypothyroidism, Sensory Epithelium
Journal
MAMMALIAN GENOME
Volume 25, Issue 7-8, Pages 304-316
Publisher
Springer Nature
Online
2014-04-23
DOI
10.1007/s00335-014-9515-1
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Integration of Human and Mouse Genetics Reveals Pendrin Function in Hearing and Deafness
- (2011) Amiel A. Dror et al. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
- Analysis of Cellular Localization and Function of Carboxy-Terminal Mutants of Pendrin
- (2011) Aigerim Bizhanova et al. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
- Controversies Concerning the Role of Pendrin as an Apical Iodide Transporter in Thyroid Follicular Cells
- (2011) Aigerim Bizhanova et al. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY
- TSH Regulates Pendrin Membrane Abundance and Enhances Iodide Efflux in Thyroid Cells
- (2011) Liuska Pesce et al. ENDOCRINOLOGY
- Genetic Background of Prop1 df Mutants Provides Remarkable Protection Against Hypothyroidism-Induced Hearing Impairment
- (2011) Qing Fang et al. JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY
- Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin
- (2011) Hyoung-Mi Kim et al. PLoS One
- Establishment of a Knock-In Mouse Model with the SLC26A4 c.919-2A>G Mutation and Characterization of Its Pathology
- (2011) Ying-Chang Lu et al. PLoS One
- NEUROLOGICAL SIGNS IN CONGENITAL IODINE-DEFICIENCY DISORDER (ENDEMIC CRETINISM)
- (2010) G. Robert DeLong et al. DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY
- 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
- 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
- Prediction of disease-related mutations affecting protein localization
- (2009) Kirsti Laurila et al. BMC GENOMICS
- A Novel SLC26A4 (PDS) Deafness Mutation Retained in the Endoplasmic Reticulum
- (2008) Zippora N. Brownstein et al. ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY
- The tectorial membrane: one slice of a complex cochlear sandwich
- (2008) Guy P Richardson et al. Current Opinion in Otolaryngology & Head and Neck Surgery
- The Solute Carrier 26 Family of Proteins in Epithelial Ion Transport
- (2008) Michael R. Dorwart et al. PHYSIOLOGY
- 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
Discover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversationPublish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn More