-
Integration of Human and Mouse Genetics Reveals Pendrin Function in Hearing and Deafness
Amiel A. Dror, Zippora Brownstein, and Karen B. Avraham
Cellular Physiology and Biochemistry
(2011)
28 :535
-
Developmental expression of solute carrier family 26A member 4 (SLC26A4/pendrin) during amelogenesis in developing rodent
teeth
Antonius L. J. J. Bronckers, Jing Guo, Behrouz Zandieh-Doulabi, Theodore J. Bervoets, Donacian M. Lyaruu, Xiangming Li, Philine
Wangemann, and Pamela DenBesten
European Journal of Oral Sciences
(2011)
119 :185
-
STAT6 Links IL-4/IL-13 Stimulation With Pendrin Expression in Asthma and Chronic Obstructive Pulmonary Disease
C Nofziger, V Vezzoli, S Dossena, T Schönherr, J Studnicka, J Nofziger, S Vanoni, S Stephan, M E Silva, G Meyer, and M Paulmichl
Clinical Pharmacology & Therapeutics
(2011)
90 :399
-
Familial Syndromes Associated with Thyroid Cancer in the Era of Personalized Medicine
Melanie L. Richards
Thyroid
(2010)
20 :707
-
<i>SLC26A4</i> Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct
Taku Ito, Byung Yoon Choi, Kelly A. King, Christopher K. Zalewski, Julie Muskett, Parna Chattaraj, Thomas Shawker, James C.
Reynolds, John A. Butman, Carmen C. Brewer, Philine Wangemann, Seth L. Alper, and Andrew J. Griffith
Cellular Physiology and Biochemistry
(2011)
28 :545
-
Transcriptional Regulation of the Pendrin Gene
Julia Rozenfeld, Edna Efrati, Lior Adler, Osnat Tal, Stephen L. Carrithers, Seth L. Alper, and Israel Zelikovic
Cellular Physiology and Biochemistry
(2011)
28 :385
-
Identification of Allelic Variants of Pendrin (SLC26A4) with Loss and Gain of Function
Silvia Dossena, Aigerim Bizhanova, Charity Nofziger, Emanuele Bernardinelli, Josef Ramsauer, Peter Kopp, and Markus Paulmichl
Cellular Physiology and Biochemistry
(2011)
28 :467
-
Pendrin: the Thyrocyte Apical Membrane Iodide Transporter?
Laure Twyffels, Claude Massart, Philippe E. Golstein, Eric Raspe, Jacqueline Van Sande, Jacques E. Dumont, Renaud Beauwens,
and Véronique Kruys
Cellular Physiology and Biochemistry
(2011)
28 :491
-
Thyroid Cancer of Follicular Cell Origin in Inherited Tumor Syndromes
Vânia Nosé
Advances in Anatomic Pathology
(2010)
17 :428
-
Screening ofSLC26A4gene in autoimmune thyroid diseases
R. Kallel, M. Niasme-Grare, S. Belguith-Maalej, M. Mnif, M. Abid, H. Ayadi, S. Masmoudi, L. Jonard, and H. Hadj Kacem
International Journal of Immunogenetics
(2012)
:n/a
-
Controversies Concerning the Role of Pendrin as an Apical Iodide Transporter in Thyroid Follicular Cells
Aigerim Bizhanova and Peter Kopp
Cellular Physiology and Biochemistry
(2011)
28 :485
-
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with
Pendred syndrome
Mariem Ben Said, Houria Dhouib, Zeineb BenZina, AbdelMoneem Ghorbel, Felipe Moreno, Saber Masmoudi, Hammadi Ayadi, and Mounira
Hmani-Aifa
International Journal of Pediatric Otorhinolaryngology
(2012)
76 :832
-
Impact of Bicarbonate, Ammonium Chloride, and Acetazolamide on Hepatic and Renal SLC26A4 Expression
Ioana Alesutan, Arezoo Daryadel, Nilufar Mohebbi, Lisann Pelzl, Christina Leibrock, Jakob Voelkl, Soline Bourgeois, Silvia
Dossena, Charity Nofziger, Markus Paulmichl, Carsten A. Wagner, and Florian Lang
Cellular Physiology and Biochemistry
(2011)
28 :553
-
Role of iodine in thyroid physiology
Angela Leung, Elizabeth N Pearce, and Lewis E Braverman
Expert Review of Endocrinology & Metabolism
(2010)
5 :593
-
A novel synonymous mutation causing complete skipping of exon 16 in the SLC26A4 gene in a Korean family with hearing loss
Yoonjung Kim, Hui Ram Kim, Juwon Kim, Joong-Wook Shin, Hong-Joon Park, Jae Young Choi, Un-Kyung Kim, and Kyung-A Lee
Biochemical and Biophysical Research Communications
(2013)
430 :1147
-
Genetic causes of nonsyndromic hearing loss in Iran in comparison with other populations
Nejat Mahdieh, Bahareh Rabbani, Susan Wiley, Mohammad Taghi Akbari, and Sirous Zeinali
Journal of Human Genetics
(2010)
55 :639
-
Hearing Impairment: A Panoply of Genes and Functions
Amiel A. Dror and Karen B. Avraham
Neuron
(2010)
68 :293
-
Roles of 17-AAG-induced molecular chaperones and Rma1 E3 ubiquitin ligase in folding and degradation of Pendrin
Kanghyun Lee, Tae-Joon Hong, and Ji-Sook Hahn
FEBS Letters
(2012)
586 :2535
-
SLC26A4 gene copy number variations in Chinese patients with non-syndromic enlarged vestibular aqueduct
Jiandong Zhao, Yongyi Yuan, Jing Chen, Shasha Huang, Guojian Wang, Dongyi Han, and Pu Dai
Journal of Translational Medicine
(2012)
10 :82
-
Analysis of Cellular Localization and Function of Carboxy-Terminal Mutants of Pendrin
Aigerim Bizhanova, Teng-Leong Chew, Satya Khuon, and Peter Kopp
Cellular Physiology and Biochemistry
(2011)
28 :423
-
DOCA Sensitive Pendrin Expression in Kidney, Heart, Lung and Thyroid Tissues
Lisann Pelzl, Tatsiana Pakladok, Ganesh Pathare, Hajar Fakhri, Diana Michael, Carsten A. Wagner, Markus Paulmichl, and Florian
Lang
Cellular Physiology and Biochemistry
(2012)
30 :1491
-
Functional Characterization of Pendrin Mutations Found in the Israeli and Palestinian Populations
Silvia Dossena, Charity Nofziger, Zippora Brownstein, Moien Kanaan, Karen B. Avraham, and Markus Paulmichl
Cellular Physiology and Biochemistry
(2011)
28 :477
-
Molecular and Functional Characterization of Human Pendrin and its Allelic Variants
Silvia Dossena, Charity Nofziger, Grazia Tamma, Emanuele Bernardinelli, Simone Vanoni, Christoph Nowak, Elisabeth Grabmayer,
Sonja Kössler, Susanne Stephan, Wolfgang Patsch, and Markus Paulmichl
Cellular Physiology and Biochemistry
(2011)
28 :451
-
Salicylate restores transport function and anion exchanger activity of missense pendrin mutations
Kenji Ishihara, Shuhei Okuyama, Shun Kumano, Koji Iida, Hiroshi Hamana, Michio Murakoshi, Toshimitsu Kobayashi, Shinichi Usami,
Katsuhisa Ikeda, Yoichi Haga, Kohei Tsumoto, Hiroyuki Nakamura, Noriyasu Hirasawa, and Hiroshi Wada
Hearing Research
(2010)
270 :110
