Literature DB >> 20146068

Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism.

Ji-feng Guo1, Xue-wei Zhang, Li-luo Nie, Hai-nan Zhang, Bin Liao, Jing Li, Lei Wang, Xin-xiang Yan, Bei-sha Tang.   

Abstract

Early onset parkinsonism (EOP) has been associated with mutations in the Parkin, PINK1, and DJ-1 genes. We studied the prevalence of mutations in all three genes in 127 unrelated Chinese patients with apparently sporadic EOP using direct sequencing analysis and real-time quantitative PCR analysis assay. There are 16 patients (12.6%) with mutations of Parkin gene, four patients (3.1%) with mutations of PINK1 gene, and three patients (2.4%) with mutation of DJ-1 gene. In conclusion, Parkin gene mutation is the most common pathogenic factor in Chinese patients with sporadic EOP. Mutations of DJ-1 and PINK1 gene are also found in Chinese patients with sporadic EOP.

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Year:  2010        PMID: 20146068     DOI: 10.1007/s00415-010-5485-8

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  21 in total

1.  Parkin mutations are frequent in patients with isolated early-onset parkinsonism.

Authors:  Magali Periquet; Morwena Latouche; Ebba Lohmann; Nina Rawal; Giuseppe De Michele; Sylvain Ricard; Hélio Teive; Valérie Fraix; Marie Vidailhet; David Nicholl; Paolo Barone; Nick W Wood; Salmo Raskin; Jean-François Deleuze; Yves Agid; Alexandra Dürr; Alexis Brice
Journal:  Brain       Date:  2003-06       Impact factor: 13.501

2.  Mutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.

Authors:  Ji-Feng Guo; Bin Xiao; Bing Liao; Xue-Wei Zhang; Li-Luo Nie; Yu-Hu Zhang; Lu Shen; Hong Jiang; Kun Xia; Qian Pan; Xin-Xiang Yan; Bei-Sha Tang
Journal:  Mov Disord       Date:  2008-10-30       Impact factor: 10.338

3.  Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Authors:  T Kitada; S Asakawa; N Hattori; H Matsumine; Y Yamamura; S Minoshima; M Yokochi; Y Mizuno; N Shimizu
Journal:  Nature       Date:  1998-04-09       Impact factor: 49.962

4.  Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.

Authors:  Ruey-Meei Wu; Rebecca Bounds; Sarah Lincoln; Mary Hulihan; Chin-Hsien Lin; Wuh-Liang Hwu; Judy Chen; Katrina Gwinn-Hardy; Matt Farrer
Journal:  Arch Neurol       Date:  2005-01

5.  Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.

Authors:  Vincenzo Bonifati; Patrizia Rizzu; Marijke J van Baren; Onno Schaap; Guido J Breedveld; Elmar Krieger; Marieke C J Dekker; Ferdinando Squitieri; Pablo Ibanez; Marijke Joosse; Jeroen W van Dongen; Nicola Vanacore; John C van Swieten; Alexis Brice; Giuseppe Meco; Cornelia M van Duijn; Ben A Oostra; Peter Heutink
Journal:  Science       Date:  2002-11-21       Impact factor: 47.728

6.  Novel PINK1 mutations in early-onset parkinsonism.

Authors:  Yasuko Hatano; Yuanzhe Li; Kenichi Sato; Shuichi Asakawa; Yasuhiro Yamamura; Hiroyuki Tomiyama; Hiroyo Yoshino; Masato Asahina; Susumu Kobayashi; Sharon Hassin-Baer; Chin-Song Lu; Arlene R Ng; Raymond L Rosales; Nobuyoshi Shimizu; Tatsushi Toda; Yoshikuni Mizuno; Nobutaka Hattori
Journal:  Ann Neurol       Date:  2004-09       Impact factor: 10.422

7.  Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation.

Authors:  Stephen Hague; Ekaterina Rogaeva; Dena Hernandez; Cindy Gulick; Amanda Singleton; Melissa Hanson; Janel Johnson; Roberto Weiser; Marisol Gallardo; Bernard Ravina; Katrina Gwinn-Hardy; Anthony Crawley; Peter H St George-Hyslop; Anthony E Lang; Peter Heutink; Vincenzo Bonifati; John Hardy; Andrew Singleton
Journal:  Ann Neurol       Date:  2003-08       Impact factor: 10.422

8.  Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism.

Authors:  Paul J Lockhart; Rebecca Bounds; Mary Hulihan; Jennifer Kachergus; Sarah Lincoln; Chin-Hsien Lin; Ruey-Meei Wu; Matthew J Farrer
Journal:  Mov Disord       Date:  2004-09       Impact factor: 10.338

9.  Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.

Authors:  V Bonifati; C F Rohé; G J Breedveld; E Fabrizio; M De Mari; C Tassorelli; A Tavella; R Marconi; D J Nicholl; H F Chien; E Fincati; G Abbruzzese; P Marini; A De Gaetano; M W Horstink; J A Maat-Kievit; C Sampaio; A Antonini; F Stocchi; P Montagna; V Toni; M Guidi; A Dalla Libera; M Tinazzi; F De Pandis; G Fabbrini; S Goldwurm; A de Klein; E Barbosa; L Lopiano; E Martignoni; P Lamberti; N Vanacore; G Meco; B A Oostra
Journal:  Neurology       Date:  2005-07-12       Impact factor: 9.910

10.  PINK1 mutations are associated with sporadic early-onset parkinsonism.

Authors:  Enza Maria Valente; Sergio Salvi; Tamara Ialongo; Roberta Marongiu; Antonio Emanuele Elia; Viviana Caputo; Luigi Romito; Alberto Albanese; Bruno Dallapiccola; Anna Rita Bentivoglio
Journal:  Ann Neurol       Date:  2004-09       Impact factor: 10.422

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Journal:  Mol Biol Rep       Date:  2022-09-12       Impact factor: 2.742

2.  Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array.

Authors:  Imelda S Barber; Anne Braae; Naomi Clement; Tulsi Patel; Tamar Guetta-Baranes; Keeley Brookes; Christopher Medway; Sally Chappell; Rita Guerreiro; Jose Bras; Dena Hernandez; Andrew Singleton; John Hardy; David M Mann; Kevin Morgan
Journal:  Neurobiol Aging       Date:  2016-09-23       Impact factor: 4.673

3.  Analysis of Dosage Mutation in PARK2 among Korean Patients with Early-Onset or Familial Parkinson's Disease.

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Review 4.  Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach.

Authors:  Valentina La Cognata; Giovanna Morello; Velia D'Agata; Sebastiano Cavallaro
Journal:  Hum Genet       Date:  2016-11-28       Impact factor: 4.132

5.  A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's disease.

Authors:  Valentina La Cognata; Giovanna Morello; Giulia Gentile; Velia D'Agata; Chiara Criscuolo; Francesca Cavalcanti; Sebastiano Cavallaro
Journal:  Neurogenetics       Date:  2016-09-17       Impact factor: 2.660

6.  Novel compound heterozygous mutations in the PARK2 gene identified in a Chinese pedigree with early-onset Parkinson's disease.

Authors:  Yingying Shi; Hideshi Kawakami; Weizhou Zang; Gang Li; Jiewen Zhang; Changshui Xu
Journal:  Brain Behav       Date:  2017-12-19       Impact factor: 2.708

7.  Mutations in PRKN and SNCA Genes Important for the Progress of Parkinson's Disease.

Authors:  Anna Oczkowska; Wojciech Kozubski; Margarita Lianeri; Jolanta Dorszewska
Journal:  Curr Genomics       Date:  2013-12       Impact factor: 2.236

8.  Genetic insights into sporadic Parkinson's disease pathogenesis.

Authors:  Chou Chai; Kah-Leong Lim
Journal:  Curr Genomics       Date:  2013-12       Impact factor: 2.236

9.  T313M polymorphism of the PINK1 gene in Parkinson's disease.

Authors:  Qin Luo; Xinling Yang; Yani Yao; Hongjuan Li; Yuling Wang
Journal:  Exp Ther Med       Date:  2014-05-08       Impact factor: 2.447

10.  Analysis of PRKN Variants and Clinical Features in Polish Patients with Parkinson's Disease.

Authors:  Anna Oczkowska; Jolanta Florczak-Wyspianska; Agnieszka Permoda-Osip; Michal Owecki; Margarita Lianeri; Wojciech Kozubski; Jolanta Dorszewska
Journal:  Curr Genomics       Date:  2015-08       Impact factor: 2.236

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