Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Hearing Loss and UCN[original query] |
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| Mutational analysis of the mitochondrial 12S rRNA and tRNASer(UCN) genes in Tunisian patients with nonsyndromic hearing loss. Biochemical and biophysical research communications 2006 Feb 340 (4): 1251-8. Mkaouar-Rebai Emna, Tlili Abdelaziz, Masmoudi Saber, Louhichi Nacim, Charfeddine Ilhem, Ben Amor Mohamed, Lahmar Imed, Driss Nabil, Drira Mohamed, Ayadi Hammadi, Fakhfakh Fai |
| Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients. Mitochondrion 2008 Dec 8 (5-6): 377-82. Konings Annelies, Van Camp Guy, Goethals Alain, Van Eyken Els, Vandevelde Ann, Ben Azza Jamila, Peeters Nils, Wuyts Wim, Smeets Hubert, Van Laer L |
| Molecular analysis of mitochondrial gene mutations in Korean patients with nonsyndromic hearing loss. International journal of molecular medicine 2008 Aug 22 (2): 175-80. Bae Jae Woong, Lee Kyu Yup, Choi Soo Young, Lee Sang Heun, Park Hong-Joon, Kim Un-Kyu |
| Splice variant IVS2-2A>G in the SLC26A5 (Prestin) gene in five Estonian families with hearing loss. International journal of pediatric otorhinolaryngology 2009 Jan 73 (1): 103-7. Teek Rita, Oitmaa Eneli, Kruustük Katrin, Zordania Riina, Joost Kairit, Raukas Elve, Tõnisson Neeme, Gardner Phyllis, Schrijver Iris, Kull Mart, Ounap Katr |
| Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China. Journal of translational medicine 2009 7 (1): 79. Yuan Yongyi, You Yiwen, Huang Deliang, Cui Jinghong, Wang Yong, Wang Qiang, Yu Fei, Kang Dongyang, Yuan Huijun, Han Dongyi, Dai |
| [Analysis of mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in patients with nonsyndromic sensorineural hearing loss from various regions of Russia]. Genetika 2009 Jul 45 (7): 982-91. Dzhemileva L U, Posukh O L, Tazetdinov A M, Barashkov N A, Zhuravski? S G, Ponidelko S N, Markova T G, Tadinova V N, Fedorova S A, Maksimova N R, Khusnutdinova E |
| [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia]. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2009 Apr 44 (4): 292-6. Yuan Yong-yi, Dai Pu, Zhu Xiu-hui, Kang Dong-yang, Zhang Xin, Huang De-lia |
| Screening of the general Polish population for deafness-associated mutations in mitochondrial 12S rRNA and tRNA Ser(UCN) genes. Genetic testing and molecular biomarkers 2009 Apr 13 (2): 167-72. Rydzanicz Ma?gorzata, Wróbel Maciej, Cywi?ska Karolina, Froehlich Dominika, Gawecki Wojciech, Szyfter Witold, Szyfter Krzyszt |
| Detection of deafness-causing mutations in the Greek mitochondrial genome. Disease markers 2011 30 (6): 283-9. Kokotas Haris, Grigoriadou Maria, Korres George S, Ferekidou Elisabeth, Kandiloros Dimitrios, Korres Stavros, Petersen Michael |
| The contribution of the mitochondrial COI/tRNA(Ser(UCN)) gene mutations to non-syndromic and aminoglycoside-induced hearing loss in Polish patients. Molecular genetics and metabolism 0 104 (1-2): 153-9. Rydzanicz Ma?gorzata, Cywi?ska Karolina, Wróbel Maciej, Pollak Agnieszka, Gaw?cki Wojciech, Wojsyk-Banaszak Irena, Lechowicz Urszula, Mueller-Malesi?ska Ma?gorzata, O?dak Monika, P?oski Rafa?, Skar?y?ski Henryk, Szyfter Krzysztof, Szyfter Wito |
| mtDNA mutations, hearing loss and aminoglycoside treatment in Mexicans. Brazilian journal of otorhinolaryngology 0 77 (5): 573-6. Meza G, Torres-Ruíz N M, Tirado-Gutiérrez C, Aguilera |
| Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation. BMC medical genetics 2011 12 (1): 135. Mutai Hideki, Kouike Hiroko, Teruya Eiko, Takahashi-Kodomari Ikuko, Kakishima Hiroki, Taiji Hidenobu, Usami Shin-ichi, Okuyama Torayuki, Matsunaga Tats |
| Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss. Molecular biology reports 2013 Mar 40 (3): 2689-95. Dowlati Mohammad Ali, Derakhshandeh-Peykar Pupak, Houshmand Massoud, Farhadi Mohammad, Shojaei Azadeh, Fallah Masoomeh, Mohammadi Esmaiil, Tajdini Ardavan, Arastoo Shima, Tavakkoly-Bazzaz Jav |
| Hearing impairment in Estonia: an algorithm to investigate genetic causes in pediatric patients. Advances in medical sciences 2013 58 (2): 419-28. Teek R, Kruustük K, Žordania R, Joost K, Kahre T, Tõnisson N, Nelis M, Zilina O, Tranebjaerg L, Reimand T, Ounap |
| Mutation in PCDH15 may modify the phenotypic expression of the 7511T>C mutation in MT-TS1 in a Chinese Han family with maternally inherited nonsyndromic hearing loss. International journal of pediatric otorhinolaryngology 2015 Oct 79 (10): 1654-7. Chen Dong-Ye, Zhu Wei-Dong, Chai Yong-Chuan, Chen Ying, Sun Lianhua, Yang Tao, Wu H |
| Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss. Mitochondrion 2015 Jul 23 17-24. Tang Xiaowen, Zheng Jing, Ying Zhengbiao, Cai Zhaoyang, Gao Yinglong, He Zheyun, Yu Han, Yao Juan, Yang Yaling, Wang Hui, Chen Ye, Guan Min-X |
| Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals. Annals of human genetics 2016 Sep 80 (5): 257-73. Subathra Mahalingam, Ramesh Arabandi, Selvakumari Mathiyalagan, Karthikeyen N P, Srisailapathy C R Srikuma |
| Application of next?generation sequencing to identify mitochondrial mutations: Study on m.7511T>C in patients with hearing loss. Molecular medicine reports 2018 Jan 17 (1): 1782-1790. Lechowicz Urszula, Pollak Agnieszka, Fr?czak Agnieszka, Rydzanicz Ma?gorzata, Stawi?ski Piotr, Lorens Artur, Skar?y?ski Piotr H, Skar?y?ski Henryk, P?oski Rafa?, O?dak Moni |
| Low penetrance of hearing loss in two Chinese families carrying the mitochondrial tRNASer(UCN) mutations. Molecular medicine reports 2020 5 22 (1): 77-86. Peng Wei, Zhong Yi, Zhao Xueyan, Yuan J |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 30, 2023
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