Literature DB >> 24126164

DNAJ mutations are rare in Chinese Parkinson's disease patients and controls.

Jia Nee Foo1, Herty Liany1, Louis C Tan2, Wing-Lok Au2, Kumar-M Prakash2, Jianjun Liu1, Eng-King Tan3.   

Abstract

Mutations in DNAJC13, DNAJC6 and DNAJC5 have been implicated in Parkinson's disease (PD). To determine if rare coding variants in these genes play a role in PD risk in the Chinese population, we sequenced all coding exons of the three genes in 99 early-onset PD cases and 99 controls, and genotyped 8 missense variants in another 711 PD cases and 539 controls. Besides two common missense variants that did not show association with PD, the remaining missense variants were extremely rare (<0.5%), found in healthy population controls and did not show enrichment in PD cases. Our results suggest that missense mutations in DNAJC13, DNAJC5 and DNAJC6 do not play a major role in PD in the Chinese population.
Copyright © 2014 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Association; Chinese population; DNAJ family; Mutation; Parkinson's disease

Mesh:

Substances:

Year:  2013        PMID: 24126164     DOI: 10.1016/j.neurobiolaging.2013.09.018

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


  8 in total

1.  TMEM230 in Parkinson's disease.

Authors:  Laura Ibanez; Umber Dube; John Budde; Kathleen Black; Alexandra Medvedeva; Albert A Davis; Joel S Perlmutter; Bruno A Benitez; Carlos Cruchaga
Journal:  Neurobiol Aging       Date:  2017-03-16       Impact factor: 4.673

2.  Genetic Analysis of HSP40/DNAJ Family Genes in Parkinson's Disease: a Large Case-Control Study.

Authors:  Kailin Zhang; Hongxu Pan; Yuwen Zhao; Yige Wang; Qian Zeng; Xun Zhou; Runcheng He; Xiaoxia Zhou; Yaqin Xiang; Zhou Zhou; Yu Li; Qian Xu; Qiying Sun; Jieqiong Tan; Xinxiang Yan; Jinchen Li; Jifeng Guo; Beisha Tang; Zhenhua Liu
Journal:  Mol Neurobiol       Date:  2022-06-17       Impact factor: 5.682

3.  Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease.

Authors:  Prabhjyot Saini; Uladzislau Rudakou; Eric Yu; Jennifer A Ruskey; Farnaz Asayesh; Sandra B Laurent; Dan Spiegelman; Stanley Fahn; Cheryl Waters; Oury Monchi; Yves Dauvilliers; Nicolas Dupré; Lior Greenbaum; Sharon Hassin-Baer; Alberto J Espay; Guy A Rouleau; Roy N Alcalay; Edward A Fon; Ronald B Postuma; Ziv Gan-Or
Journal:  Neurobiol Aging       Date:  2020-10-31       Impact factor: 4.673

Review 4.  DNAJC proteins and pathways to parkinsonism.

Authors:  Dorien A Roosen; Cornelis Blauwendraat; Mark R Cookson; Patrick A Lewis
Journal:  FEBS J       Date:  2019-06-20       Impact factor: 5.622

Review 5.  New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.

Authors:  Andreas Puschmann
Journal:  Curr Neurol Neurosci Rep       Date:  2017-09       Impact factor: 5.081

6.  Lack of evidence for association of UQCRC1 with Parkinson's disease in Europeans.

Authors:  Konstantin Senkevich; Sara Bandres-Ciga; Ziv Gan-Or; Lynne Krohn
Journal:  Neurobiol Aging       Date:  2020-11-02       Impact factor: 4.673

7.  Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.

Authors:  Lamei Yuan; Zhi Song; Xiong Deng; Wen Zheng; Yi Guo; Zhijian Yang; Hao Deng
Journal:  Sci Rep       Date:  2016-09-22       Impact factor: 4.379

8.  Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease.

Authors:  Ran Zheng; Chong-Yao Jin; Ying Chen; Yang Ruan; Ting Gao; Zhi-Hao Lin; Jia-Xian Dong; Ya-Ping Yan; Jun Tian; Jia-Li Pu; Bao-Rong Zhang
Journal:  Mol Genet Genomic Med       Date:  2020-08-14       Impact factor: 2.183

  8 in total

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