Polymorphism in the human DJ-1 gene is not associated with sporadic dementia with Lewy bodies or Parkinson's disease

Neuroscience Letters

Volumn 352, Issue 2, 2003, Pages 151-153

  Morris, Christopher M ^a   O'Brien, Kirsty K ^a   Gibson, Alison M ^a   Hardy, John A ^b   Singleton, Andrew B ^b  

^a NEWCASTLE GENERAL HOSPITAL   (United Kingdom)

^b NATIONAL INSTITUTES OF HEALTH   (United States)

Author keywords

Apolipoprotein E; DJ 1; Lewy body; Parkinson's disease

Indexed keywords

APOLIPOPROTEIN E4; BRAIN PROTEIN;

ADULT; AGED; ALLELISM; ARTICLE; CONTROLLED STUDY; DEMENTIA; DISEASE COURSE; DJ 1 GENE; DNA POLYMORPHISM; GENE; GENE DELETION; GENE LINKAGE DISEQUILIBRIUM; GENOTYPE; HUMAN; HUMAN TISSUE; INTRON; LEWY BODY; PARKINSON DISEASE; PRIORITY JOURNAL; RISK FACTOR;

EID: 0242558789     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2003.08.037     Document Type: Article

References (14)

1. Bonifati V., Rizzu P., Van Baren M.J., Schaap O., Breedveld G.J., Krieger E., Dekker M.C., Squitieri F., Ibanez P., Joosse M., Van Dongen J.W., Vanacore N., Van Swieten J.C., Brice A., Meco G., Van Duijn C.M., Oostra B.A., Heutink P. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science. 299:2003;256-259.
2. Cookson M.R. Pathways to Parkinsonism. Neuron. 37:2003;7-10.
3. Farrer M.J., Maraganore D.M., Lockhart P., Singleton A.B., Lesnick T.G., de Andrade M., West A., de Silva R., Hardy J.A., Hernandez D. α-synuclein gene haplotypes are associated with Parkinson's disease. Hum. Mol. Gene. 10:2001;1847-1851.
4. Hixon J.E., Vernier D.T. Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI. J. Lipid Res. 31:1990;545-548.
5. Hughes A.J., Ben-Shlomo Y., Daniel S.E., Lees A.J. What features improve the accuracy of clinical diagnosis in Parkinson's disease: a clinicopathologic study. Neurology. 42:1992;1142-1146.
6. Ince P.G., Perry E.K., Morris C.M. Dementia with Lewy bodies. A distinct non-Alzheimer dementia syndrome? Brain Pathol. 8:1998;299-324.
7. Kitada T., Asakawa S., Hattori N., Matsumine H., Yamamura Y., Minoshima S., Yokochi M., Mizuno Y., Shimizu N. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature. 392:1998;605-608.
8. Leroy E., Boyer R., Auburger G., Leube B., Ulm G., Mezey E., Harta G., Brownstein M.J., Jonnalagada S., Chernova T., Dehejia A., Lavedan C., Gasser T., Steinbach P.J., Wilkinson K.D., Polymeropoulos M.H. The ubiquitin pathway in Parkinson's disease. Nature. 395:1998;451-452.
9. McKeith I.G., Galasko D., Kosaka K., Perry E.K., Dickson D.W., Hansen L.A., Salmon D.P., Lowe J., Mirra S.S., Byrne E.J., Lennox G., Quinn N.P., Edwardson J.A., Ince P.G., Bergerson C., Burns A., Miller B.L., Lovestone S., Collerton D., Jansen E.N., Ballard C., de Vos R.A., Wilcock G.K., Jellinger K.A., Perry R.H. Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop. Neurology. 47:1996;1113-1124.
10. Polymeropoulos M.H., Lavendan C., Leroy E., Ide S.E., Dehejia A., Dutra A., Pike B., Root H., Rubenstein J., Boyer R., Stenroos E.S., Chandrasekharappa S., Athanassiadou A., Papapetropoulos T., Johnson W.G., Lazzarinin A.M., Duvoisin R.C., Di Iorio G., Golbe L.I., Nussbaum R.L. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science. 276:1997;2045-2047.
11. Sveinsbjorndottir S., Hicks A.A., Jonsson T., Petursson H., Guomundsson G., Frigge M.L., Kong A., Gulcher J.R., Stefansson K. Familial aggregation of Parkinson's disease in Iceland. N. Engl. J. Med. 343:2000;1765-1770.
12. Tao X., Tong L. Crystal structure of human DJ-1, a protein associated with early-onset Parkinson's disease. J. Biol. Chem. 278:2003;31372-31379.
13. Wenham P.R., Price W.H., Blundell G. Apolipoprotein E genotyping by one-stage PCR. Lancet. 337:1991;1158-1159.
14. West A.B., Maraganore D., Crook J., Lesnick T., Lockhart P.J., Wilkes K.M., Kapatos G., Hardy J.A., Farrer M.J. Functional association of the parkin gene promoter with idiopathic Parkinson's disease. Hum. Mol. Genet. 11:2002;2787-2792.