Literature DB >> 12891685

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

Stephen Hague1, 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.   

Abstract

Mutations in DJ-1 have been linked to an autosomal recessive form of early-onset parkinsonism. To identify mutations causing Parkinson's disease (PD), we sequenced exons 1 through 7 of DJ-1 in 107 early-onset (age at diagnosis up to 50 years) PD subjects. One subject had a frameshift mutation in the first coding exon and an exon 7 splice mutation both predicted to result in a loss of functional protein. This subject was diagnosed with probable PD at age 24 years with asymmetric onset and an excellent response to levodopa therapy. Our observations suggest that sequence alterations in DJ-1 are a rare cause of early-onset PD.

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Year:  2003        PMID: 12891685     DOI: 10.1002/ana.10663

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  63 in total

1.  Engineered disulfide bonds restore chaperone-like function of DJ-1 mutants linked to familial Parkinson's disease.

Authors:  Todd Logan; Lindsay Clark; Soumya S Ray
Journal:  Biochemistry       Date:  2010-07-13       Impact factor: 3.162

Review 2.  Neurodegenerative disorders: Parkinson's disease and Huntington's disease.

Authors:  S M Hague; S Klaffke; O Bandmann
Journal:  J Neurol Neurosurg Psychiatry       Date:  2005-08       Impact factor: 10.154

3.  Structural effects of Parkinson's disease linked DJ-1 mutations.

Authors:  Gaetano Malgieri; David Eliezer
Journal:  Protein Sci       Date:  2008-05       Impact factor: 6.725

Review 4.  Progress in the pathogenesis and genetics of Parkinson's disease.

Authors:  Yoshikuni Mizuno; Nobutaka Hattori; Shin-Ichiro Kubo; Shigeto Sato; Kenya Nishioka; Taku Hatano; Hiroyuki Tomiyama; Manabu Funayama; Yutaka Machida; Hideki Mochizuki
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2008-06-27       Impact factor: 6.237

5.  Quantitative proteomic analysis of single pancreatic islets.

Authors:  Leonie F Waanders; Karolina Chwalek; Mara Monetti; Chanchal Kumar; Eckhard Lammert; Matthias Mann
Journal:  Proc Natl Acad Sci U S A       Date:  2009-10-21       Impact factor: 11.205

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

Authors:  Ji-feng Guo; Xue-wei Zhang; Li-luo Nie; Hai-nan Zhang; Bin Liao; Jing Li; Lei Wang; Xin-xiang Yan; Bei-sha Tang
Journal:  J Neurol       Date:  2010-02-10       Impact factor: 4.849

Review 7.  DJ-1, PINK1, and their effects on mitochondrial pathways.

Authors:  Mark R Cookson
Journal:  Mov Disord       Date:  2010       Impact factor: 10.338

8.  DJ-1 gene deletion reveals that DJ-1 is an atypical peroxiredoxin-like peroxidase.

Authors:  Eva Andres-Mateos; Celine Perier; Li Zhang; Beatrice Blanchard-Fillion; Todd M Greco; Bobby Thomas; Han Seok Ko; Masayuki Sasaki; Harry Ischiropoulos; Serge Przedborski; Ted M Dawson; Valina L Dawson
Journal:  Proc Natl Acad Sci U S A       Date:  2007-08-31       Impact factor: 11.205

9.  DJ-1 deficient mice demonstrate similar vulnerability to pathogenic Ala53Thr human alpha-syn toxicity.

Authors:  Chenere P Ramsey; Elpida Tsika; Harry Ischiropoulos; Benoit I Giasson
Journal:  Hum Mol Genet       Date:  2010-01-20       Impact factor: 6.150

10.  Dissembled DJ-1 high molecular weight complex in cortex mitochondria from Parkinson's disease patients.

Authors:  Hikmet Nural; Ping He; Thomas Beach; Lucia Sue; Weiming Xia; Yong Shen
Journal:  Mol Neurodegener       Date:  2009-06-04       Impact factor: 14.195

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