Inhibiting SLC26A4 reverses cardiac hypertrophy in H9C2 cells and in rats by Liqun Tang, Xiaoqin Yu, Yangyang Zheng, Ning Zhou

Subjects: “…SLC26A4…”
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Interleukin-4 Induces CpG Site-Specific Demethylation of the Pendrin Promoter in Primary Human Bronchial Epithelial Cells by Giada Scantamburlo, Simone Vanoni, Silvia Dossena, Selma M. Soyal, Emanuele Bernardinelli, Davide Antonio Civello, Wolfgang Patsch, Markus Paulmichl, Charity Nofziger

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A case of Landau-Kleffner syndrome with SLC26A4-related hearing impairment by Pan Gong, Xianru Jiao, Zhixian Yang

Subjects: “…SLC26A4…”
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Validating the splicing effect of rare variants in the SLC26A4 gene using minigene assay by Yixin Zhao, Yan Long, Tao Shi, Xin Ma, Chengyu Lian, Hanjun Wang, Hongen Xu, Lisheng Yu, Xiaotao Zhao

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Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort by Simone da Costa e Silva Carvalho, Carlos Henrique Paiva Grangeiro, Clarissa Gondim Picanço-Albuquerque, Thaís Oliveira dos Anjos, Greice Andreotti De Molfetta, Wilson Araujo Silva, Victor Evangelista de Faria Ferraz

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The Human Pendrin Promoter Contains two N4 GAS Motifs with Different Functional Relevance by Simone Vanoni, Charity Nofziger, Silvia Dossena, Selma M. Soyal, Wolfgang Patsch, Paolo Plevani, Albert Duschl, Markus Paulmichl

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Case report: A case of SLC26A4 mutations causing pendred syndrome and non-cystic fibrosis bronchiectasis by Kang Zhu, Yingkang Jin

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Two Compound Heterozygous Were Identified in Gene in Two Chinese Families With Enlarged Vestibular Aqueduct by Yongbo Yu, Yang Yang, Jie Lu, Yaqiong Jin, Yeran Yang, Enyu Hong, Jin Shi, Feng Chen, Shujing Han, Ping Chu, Yongli Guo, Xin Ni

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Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next‐generation sequencing of the SLC26A4 gene by Yongan Tian, Hongen Xu, Danhua Liu, Juanli Zhang, Zengguang Yang, Sen Zhang, Huanfei Liu, Ruijun Li, Yingtao Tian, Beiping Zeng, Tong Li, Qianyu Lin, Haili Wang, Xiaohua Li, Wei Lu, Ying Shi, Yan Zhang, Hui Zhang, Chang Jiang, Ying Xu, Bei Chen, Jun Liu, Wenxue Tang

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Mutation screening of the SLC26A4 gene in a cohort of 192 Chinese patients with congenital hypothyroidism by Chunyun Fu, Haiyang Zheng, Shujie Zhang, Yun Chen, Jiasun Su, Jin Wang, Bobo Xie, Xuyun Hu, Xin Fan, Jingsi Luo, Chuan Li, Rongyu Chen, Yiping Shen, Shaoke Chen

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Editorial: Autoinflammation of the inner ear by Hiroshi Nakanishi, Takayuki Okano, Taku Ito, Byung Yoon Choi, Michael Hoa

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SLC26A4 correlates with homologous recombination deficiency and patient prognosis in prostate cancer by Cong Luo, Zhi Liu, Yu Gan, Xiaomei Gao, Xiongbing Zu, Ye Zhang, Wenrui Ye, Yi Cai

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Functional interplay between CFTR and pendrin: physiological and pathophysiological relevance by Grazia Tamma, Silvia Dossena

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Molecular architecture underlying fluid absorption by the developing inner ear by Keiji Honda, Sung Huhn Kim, Michael C Kelly, Joseph C Burns, Laura Constance, Xiangming Li, Fei Zhou, Michael Hoa, Matthew W Kelley, Philine Wangemann, Robert J Morell, Andrew J Griffith

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Comparative analysis of allele frequencies of 15 deafness gene variants between hearing-loss and normal populations in Henan, China by Yuan Tian, Aimin Chang, Jing Zhao, Xiaofeng Tian, Zhixing Zhao, Ying Shi

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Synopsis of the 48th Annual Meeting of the Lake Cumberland Biological Transport Group and the Second Biannual Meeting of the Pendrin Consortium by Silvia Dossena, Charity Nofziger, Rossana Morabito, Norma C. Adragna, Markus Paulmichl

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A novel intronic variant causing aberrant splicing identified in two deaf Chinese siblings with enlarged vestibular aqueducts by Suyang Wang, Yi‐Ming Zhu, ChenYang Xu, Wenjuan Ding, Hui Jia, Panpan Bian, Baicheng Xu, Yufen Guo, Xiaowen Liu

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Mutation Screening and Functional Study of SLC26A4 in Chinese Patients with Congenital Hypothyroidism by Chang-Run Zhang, Yuan-Ping Shi, Cao-Xu Zhang, Feng Sun, Wen-Jiao Zhu, Rui-Jia Zhang, Ya Fang, Qian-Yue Zhang, Chen-Yan Yan, Ying-Xia Ying, Shuang-Xia Zhao, Huai-Dong Song

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Mutation analysis of the SLC26A4, FOXI1 and KCNJ10 genes in individuals with congenital hearing loss by Lynn M. Pique, Marie-Luise Brennan, Colin J. Davidson, Frederick Schaefer, John Greinwald Jr, Iris Schrijver

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Investigating the Effects of Exposure to Continuous White Noise on SLC26A4 Gene Expression Levels in Male Rat Cochlea by Maryam Mirzaei Hotkani, Kolsoum Inanloorahatloo, Mohammad Reza MonazzamEsmaeilpoor3, Amir Abbasi Garmaroudi, Monireh Khadem

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