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Journal Abstract Search

330 related items for PubMed ID: 17846414

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  • 2. Variations of the CAG trinucleotide repeat in DNA polymerase γ (POLG1) is associated with Parkinson's disease in Sweden.
    Anvret A, Westerlund M, Sydow O, Willows T, Lind C, Galter D, Belin AC.
    Neurosci Lett; 2010 Nov 19; 485(2):117-20. PubMed ID: 20826197
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  • 3. Analysis of the trinucleotide CAG repeat from the DNA polymerase gamma gene (POLG) in patients with Parkinson's disease.
    Taanman JW, Schapira AH.
    Neurosci Lett; 2005 Mar 07; 376(1):56-9. PubMed ID: 15694274
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  • 5. CARD15 variants in patients with sporadic Parkinson's disease.
    Bialecka M, Kurzawski M, Klodowska-Duda G, Opala G, Juzwiak S, Kurzawski G, Tan EK, Drozdzik M.
    Neurosci Res; 2007 Mar 07; 57(3):473-6. PubMed ID: 17174426
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  • 7. Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism.
    Hudson G, Schaefer AM, Taylor RW, Tiangyou W, Gibson A, Venables G, Griffiths P, Burn DJ, Turnbull DM, Chinnery PF.
    Arch Neurol; 2007 Apr 07; 64(4):553-7. PubMed ID: 17420318
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  • 12. POLG1 in idiopathic Parkinson disease.
    Tiangyou W, Hudson G, Ghezzi D, Ferrari G, Zeviani M, Burn DJ, Chinnery PF.
    Neurology; 2006 Nov 14; 67(9):1698-700. PubMed ID: 16943369
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  • 14. Two novel POLG mutations causing hepatic mitochondrial DNA depletion with recurrent hypoketotic hypoglycaemia and fatal liver dysfunction.
    Bortot B, Barbi E, Biffi S, Lunazzi G, Bussani R, Burlina A, Norbedo S, Ventura A, Carrozzi M, Severini GM.
    Dig Liver Dis; 2009 Jul 14; 41(7):494-9. PubMed ID: 19195941
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  • 16. Optimization of the Y831C mutation detection in human DNA polymerase gamma by allelic discrimination assay.
    Stopińska K, Grzybowski T, Malyarchuk BA, Derenko MV, Miścicka-Sliwka D.
    Acta Biochim Pol; 2006 Jul 14; 53(3):591-5. PubMed ID: 16929381
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  • 17. POLG1 polyglutamine tract variants associated with Parkinson's disease.
    Eerola J, Luoma PT, Peuralinna T, Scholz S, Paisan-Ruiz C, Suomalainen A, Singleton AB, Tienari PJ.
    Neurosci Lett; 2010 Jun 14; 477(1):1-5. PubMed ID: 20399836
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  • 18. Alzheimer pathology associated with POLG1 mutation, multiple mtDNA deletions, and APOE4/4: premature ageing or just coincidence?
    Melberg A, Nennesmo I, Moslemi AR, Kollberg G, Luoma P, Suomalainen A, Holme E, Oldfors A.
    Acta Neuropathol; 2005 Sep 14; 110(3):315-6. PubMed ID: 15981013
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  • 20. Depletion of mitochondrial DNA in leukocytes of patients with poly-Q diseases.
    Liu CS, Cheng WL, Kuo SJ, Li JY, Soong BW, Wei YH.
    J Neurol Sci; 2008 Jan 15; 264(1-2):18-21. PubMed ID: 17720200
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