Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: FOXI1[original query] |
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Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome. Audiology & neuro-otology 2010 15 (1): 57-66. Wu Chen-Chi, Lu Ying-Chang, Chen Pei-Jer, Yeh Po-Lin, Su Yi-Nin, Hwu Wuh-Liang, Hsu Chuan-J |
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 |
Heredity and cardiometabolic risk: naturally occurring polymorphisms in the human neuropeptide Y(2) receptor promoter disrupt multiple transcriptional response motifs. Journal of hypertension 2012 Nov . Wei Z, Zhang K, Wen G, Balasubramanian K, Shih PA, Rao F, Friese RS, Miramontes-Gonzalez JP, Schmid-Schoenbein GW, Kim HS, Mahata SK, O'Connor DT |
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 |
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 |
Next-generation sequencing-based mutation analysis of genes associated with enlarged vestibular aqueduct in Chinese families. European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery 2020 5 277 (12): 3331-3339. Liu Yalan, Wen Jie, Sang Shushan, Mei Lingyun, He Chufeng, Jiang Lu, Huang Sida, Feng Yo |
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism. Journal of endocrinological investigation 2022 9 46 (2): 393-404. Gentilini D, Muzza M, de Filippis T, Vigone M C, Weber G, Calzari L, Cassio A, Di Frenna M, Bartolucci M, Grassi E S, Carbone E, Olivieri A, Persani |
Epigenomic charting and functional annotation of risk loci in renal cell carcinoma. Nature communications 2023 1 14 (1): 346. Nassar Amin H, Abou Alaiwi Sarah, Baca Sylvan C, Adib Elio, Corona Rosario I, Seo Ji-Heui, Fonseca Marcos A S, Spisak Sandor, El Zarif Talal, Tisza Viktoria, Braun David A, Du Heng, He Monica, Flaifel Abdallah, Alchoueiry Michel, Denize Thomas, Matar Sayed G, Acosta Andres, Shukla Sachet, Hou Yue, Steinharter John, Bouchard Gabrielle, Berchuck Jacob E, O'Connor Edward, Bell Connor, Nuzzo Pier Vitale, Mary Lee Gwo-Shu, Signoretti Sabina, Hirsch Michelle S, Pomerantz Mark, Henske Elizabeth, Gusev Alexander, Lawrenson Kate, Choueiri Toni K, Kwiatkowski David J, Freedman Matthew |
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- Page last updated:Mar 25, 2024
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