Literature DB >> 23582660

Genetic analysis of the fused in sarcoma gene in Chinese Han patients with essential tremor.

Wen Zheng1, Xiong Deng, Hui Liang, Zhi Song, Kai Gao, Yan Yang, Hao Deng.   

Abstract

We conducted genetic analysis of the fused in sarcoma gene (FUS) in Chinese Han patients with essential tremor (ET) in a case-control association study. One hundred eighty unrelated patients with ET were screened for mutations in the coding region and exon-intron boundaries of FUS. Reverse transcriptase polymerase chain reaction analysis was performed to evaluate if the c.1176G>A variant results in change of splice site. Two hundred seventy-three normal control subjects were also analyzed when DNA variants were identified in ET cohort. A novel missense mutation, c.1176G>A (p.M392I), in FUS was identified in a 62-year-old patient. Four known variants (c.52C>A, p.P18T; c.147C>A, p.G49G; c.291T>C, p.Y97Y; c.684C>T, p.G228G) were observed in the case-control study without statistically significant differences in genotype and allele distributions. Mutation(s) in FUS might be associated with a small subset of ET cases in the Chinese population.
Copyright © 2013 Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23582660     DOI: 10.1016/j.neurobiolaging.2013.03.001

Source DB:  PubMed          Journal:  Neurobiol Aging        ISSN: 0197-4580            Impact factor:   4.673


  14 in total

1.  Systematic Genetic Analysis of the SMPD1 Gene in Chinese Patients with Parkinson's Disease.

Authors:  Sheng Deng; Xiong Deng; Zhi Song; Xiaofei Xiu; Yi Guo; Jingjing Xiao; Hao Deng
Journal:  Mol Neurobiol       Date:  2015-09-16       Impact factor: 5.590

2.  Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.

Authors:  Hyun Hor; Ludmila Francescatto; Luca Bartesaghi; Sara Ortega-Cubero; Maria Kousi; Oswaldo Lorenzo-Betancor; Felix J Jiménez-Jiménez; Alexandre Gironell; Jordi Clarimón; Oliver Drechsel; José A G Agúndez; Daniela Kenzelmann Broz; Ruth Chiquet-Ehrismann; Alberto Lleó; Francisco Coria; Elena García-Martin; Hortensia Alonso-Navarro; Maria J Martí; Jaume Kulisevsky; Charlotte N Hor; Stephan Ossowski; Roman Chrast; Nicholas Katsanis; Pau Pastor; Xavier Estivill
Journal:  Hum Mol Genet       Date:  2015-07-17       Impact factor: 6.150

Review 3.  The role of FUS gene variants in neurodegenerative diseases.

Authors:  Hao Deng; Kai Gao; Joseph Jankovic
Journal:  Nat Rev Neurol       Date:  2014-05-20       Impact factor: 42.937

4.  Identification of FUS p.R377W in essential tremor.

Authors:  A Rajput; A H Rajput; M L Rajput; M Encarnacion; C Q Bernales; J P Ross; M J Farrer; C Vilariño-Güell
Journal:  Eur J Neurol       Date:  2013-07-03       Impact factor: 6.089

Review 5.  Role of FET proteins in neurodegenerative disorders.

Authors:  Francesca Svetoni; Paola Frisone; Maria Paola Paronetto
Journal:  RNA Biol       Date:  2016-07-14       Impact factor: 4.652

6.  Assessment of Three New Loci from Genome-wide Association Study in Essential Tremor in Chinese population.

Authors:  Yuan Zhang; Yuwen Zhao; Xiaoting Zhou; Kai Li; Minhan Yi; Jifeng Guo; Xinxiang Yan; Beisha Tang; Qiying Sun
Journal:  Sci Rep       Date:  2017-08-11       Impact factor: 4.379

7.  Identification of a novel CACNA1A mutation in a Chinese family with autosomal recessive progressive myoclonic epilepsy.

Authors:  Yudan Lv; Zan Wang; Chang Liu; Li Cui
Journal:  Neuropsychiatr Dis Treat       Date:  2017-10-19       Impact factor: 2.570

8.  Compound heterozygous POMT1 mutations in a Chinese family with autosomal recessive muscular dystrophy-dystroglycanopathy C1.

Authors:  Pengzhi Hu; Song Wu; Lamei Yuan; Qiongfen Lin; Wen Zheng; Hong Xia; Hongbo Xu; Liping Guan; Hao Deng
Journal:  J Cell Mol Med       Date:  2017-02-03       Impact factor: 5.310

Review 9.  Genomic Markers for Essential Tremor.

Authors:  Félix Javier Jiménez-Jiménez; Hortensia Alonso-Navarro; Elena García-Martín; Ignacio Álvarez; Pau Pastor; José A G Agúndez
Journal:  Pharmaceuticals (Basel)       Date:  2021-05-27

10.  Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss.

Authors:  Hong Xia; Xiangjun Huang; Yi Guo; Pengzhi Hu; Guangxiang He; Xiong Deng; Hongbo Xu; Zhijian Yang; Hao Deng
Journal:  PLoS One       Date:  2015-08-26       Impact factor: 3.240

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