Human Genome Epidemiology Literature Finder
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Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey. European journal of pediatrics 2003 Mar 162 (3): 154-8. Tekin M, Duman T, Bo?oçlu G, Incesulu A, Comak E, Fitoz S, Yilmaz E, Ilhan I, Akar |
Prevalence of the A1555G (12S rRNA) and tRNASer(UCN) mitochondrial mutations in hearing-impaired Brazilian patients. Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2006 Feb 39 (2): 219-26. Abreu-Silva R S, Lezirovitz K, Braga M C C, Spinelli M, Pirana S, Della-Rosa V A, Otto P A, Mingroni-Netto R |
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 |
Investigation of the A1555G mutation in mitochondrial DNA (MT-RNR1) in groups of Brazilian individuals with nonsyndromic deafness and normal-hearing. Indian journal of human genetics 2013 Jan 19 (1): 54-7. Salomão Karina Bezerra, Ayo Christiane Maria, Della-Rosa Valter Augus |
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 |
Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial. BMC medical genomics 2014 7 (1): 73. Liu Yuqi, Zhu Qinglei, Zhu Chao, Wang Xueping, Yang Jie, Yin Tong, Gao Jinliao, Li Zongbin, Ma Qinghua, Guan Minxin, Li Yang, Chen Yund |
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 |
Mitochondrial tRNA mutations in Chinese hypertensive individuals. Mitochondrion 2016 Feb . Liu Yuqi, Li Yang, Wang Xin, Ma Qinha, Zhu Chao, Li Zongbin, Yin Tong, Yang Jie, Chen Yundai, Guan Minx |
Cardiac CRFR1 Expression Is Elevated in Human Heart Failure and Modulated by Genetic Variation and Alternative Splicing. Endocrinology 2016 Oct en20161448. Pilbrow Anna P, Lewis Kathy A, Perrin Marilyn H, Sweet Wendy E, Moravec Christine S, Tang W H Wilson, Huising Mark O, Troughton Richard W, Cameron Vicky |
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 |
Prognostic value of immune-related genes in clear cell renal cell carcinoma. Aging 2019 12 11 (23): 11474-11489. Wan Bangbei, Liu Bo, Huang Yuan, Yu Gang, Lv C |
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 |
Fast diagnostic test for familial Mediterranean fever based on a kinase inhibitor. Annals of the rheumatic diseases 2020 10 80 (1): 128-132. Magnotti Flora, Malsot Tiphaine, Georgin-Lavialle Sophie, Abbas Fatima, Martin Amandine, Belot Alexandre, Fauter Maxime, Rabilloud Muriel, Gerfaud-Valentin Mathieu, Sève Pascal, Duquesne Agnes, Hot Arnaud, Durupt Stephane, Savey Léa, Giurgea Irina, Grateau Gilles, Henry Thomas, Jamilloux Yv |
Evaluation of D-loop hypervariable region I variations, haplogroups and copy number of mitochondrial DNA in Bangladeshi population with type 2 diabetes. Heliyon 2021 Jul 7 (7): e07573. Saha Sajoy Kanti, Saba Abdullah Al, Hasib Md, Rimon Razoan Al, Hasan Imrul, Alam Md Sohrab, Mahmud Ishtiaq, Nabi A H M Nur |
Immune-related risk prognostic model for clear cell renal cell carcinoma: Implications for immunotherapy. Medicine 2023 9 102 (34): e34786. Ronghui Chen, Jun Wu, Shan Liu, Yefeng Sun, Guozhi Liu, Lin Zhang, Qing Yu, Juan Xu, Lingxin Me |
An immune-related biomarker index for predicting the effectiveness of immunotherapy and prognosis in hepatocellular carcinoma. Journal of cancer research and clinical oncology 2023 6 . Xiang'an Wu, Bao Jin, Xiao Liu, Yilei Mao, Xueshuai Wan, Shunda |
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- Page last updated:Apr 29, 2024
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