Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Hearing and KCNJ10[original query] |
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Analysis of gene polymorphisms associated with K ion circulation in the inner ear of patients susceptible and resistant to noise-induced hearing loss. Annals of human genetics 2009 Jul 73 (Pt 4): 411-21. Pawelczyk Malgorzata, Van Laer Lut, Fransen Erik, Rajkowska Elzbieta, Konings Annelies, Carlsson Per-Inge, Borg Erik, Van Camp Guy, Sliwinska-Kowalska Mario |
Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct. International journal of pediatric otorhinolaryngology 2010 Sep 74 (9): 1049-53. Jonard Laurence, Niasme-Grare Magali, Bonnet Crystel, Feldmann Delphine, Rouillon Isabelle, Loundon Natalie, Calais Catherine, Catros Hélène, David Albert, Dollfus Hélène, Drouin-Garraud Valérie, Duriez Françoise, Eliot Marie Madeleine, Fellmann Florence, Francannet Christine, Gilbert-Dussardier Brigitte, Gohler Catherine, Goizet Cyril, Journel Hubert, Mom Thierry, Thuillier-Obstoy Marie-Françoise, Couderc Remy, Garabédian Eréa Noël, Denoyelle Françoise, Marlin Sandri |
Identification of SLC26A4 mutations in patients with hearing loss and enlarged vestibular aqueduct using high-resolution melting curve analysis. Genetic testing and molecular biomarkers 2011 May 15 (5): 365-8. Mercer Stephen, Mutton Patricia, Dahl Hans-Henrik |
Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2012 Jun 146 (6): 972-8. Chen Kaitian, Wang Xianren, Sun Liang, Jiang Hongy |
Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China. American journal of medical genetics. Part A 2013 Sep 161A (9): 2226-33. Chai Yongchuan, Huang Zhiwu, Tao Zheng, Li Xiaohua, Li Lei, Li Yun, Wu Hao, Yang T |
Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts. BMC medical genetics 2013 14 85. Landa Priya, Differ Ann-Marie, Rajput Kaukab, Jenkins Lucy, Bitner-Glindzicz Mar |
KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects. PloS one 2014 9 (11): e108134. Zhao Jiandong, Yuan Yongyi, Huang Shasha, Huang Bangqing, Cheng Jing, Kang Dongyang, Wang Guojian, Han Dongyi, Dai |
Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct. The Journal of molecular diagnostics : JMD 2018 10 21 (1): 138-148. Lin Yin-Hung, Wu Chen-Chi, Lin Yi-Hsin, Lu Ying-Chang, Chen Chih-Shan, Liu Tien-Chen, Chen Pei-Lung, Hsu Chuan-J |
Analysis of mutations in the FOXI1 and KCNJ10 genes in infants with a single-allele SLC26A4 mutation. Bioscience trends 2019 6 13 (3): 261-266. Zhao Xuelei, Cheng Xiaohua, Huang Lihui, Wang Xianlei, Wen Cheng, Wang Xueyao, Zhao Lipi |
Association Analysis of Candidate Gene Polymorphisms and Audiometric Measures of Noise-Induced Hearing Loss in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2020 3 41 (5): e538-e547. Bhatt Ishan Sunilkumar, Dias Raquel, Washnik Nilesh, Wang Jin, Guthrie O'neil, Skelton Michael, Lane Jeffery, Wilder Jas |
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China. Frontiers in genetics 2021 12 637096. Cai Luhang, Liu Ya, Xu Yaping, Yang Hang, Lv Lihui, Li Yang, Chen Qiongqiong, Lin Xiaojiang, Yang Yihui, Hu Guangwei, Zheng Guofeng, Zhou Jing, Qian Qiyong, Xu Mei-Ai, Fang Jin, Ding Jianjun, Chen Wei, Gao Jio |
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