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Items: 1 to 20 of 90

1.

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. doi: 10.1016/j.neulet.2010.08.082. Epub 2010 Sep 6.

PMID:
20826197
2.

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. doi: 10.1016/j.neulet.2010.04.021. Epub 2010 Apr 24.

3.

Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease.

Luoma PT, Eerola J, Ahola S, Hakonen AH, Hellström O, Kivistö KT, Tienari PJ, Suomalainen A.

Neurology. 2007 Sep 11;69(11):1152-9.

PMID:
17846414
4.

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 7;376(1):56-9. Epub 2004 Dec 8.

PMID:
15694274
5.

Association of mitochondrial DNA polymerase γ gene POLG1 polymorphisms with parkinsonism in Chinese populations.

Gui YX, Xu ZP, Lv W, Liu HM, Zhao JJ, Hu XY.

PLoS One. 2012;7(12):e50086. doi: 10.1371/journal.pone.0050086. Epub 2012 Dec 10.

6.

Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population.

Balafkan N, Tzoulis C, Müller B, Haugarvoll K, Tysnes OB, Larsen JP, Bindoff LA.

Mitochondrion. 2012 Nov;12(6):640-3. doi: 10.1016/j.mito.2012.08.004. Epub 2012 Aug 29.

PMID:
22963882
7.

Variations of mitochondrial DNA polymerase γ in patients with Parkinson's disease.

Ylönen S, Ylikotila P, Siitonen A, Finnilä S, Autere J, Majamaa K.

J Neurol. 2013 Dec;260(12):3144-9.

PMID:
24122062
8.

Rare POLG1 CAG variants do not influence Parkinson's disease or polymerase gamma function.

Bentley SR, Shan J, Todorovic M, Wood SA, Mellick GD.

Mitochondrion. 2014 Mar;15:65-8. doi: 10.1016/j.mito.2014.01.004. Epub 2014 Jan 31.

PMID:
24491464
9.

The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase gamma gene is not associated with oligozoospermia.

Brusco A, Michielotto C, Gatta V, Foresta C, Matullo G, Zeviani M, Ferrari G, Dragone E, Calabrese G, Rossato M, Stuppia L, Migone N.

J Endocrinol Invest. 2006 Jan;29(1):1-4.

PMID:
16553026
10.

Analysis of the trinucleotide CAG repeat from the human mitochondrial DNA polymerase gene in healthy and diseased individuals.

Rovio A, Tiranti V, Bednarz AL, Suomalainen A, Spelbrink JN, Lecrenier N, Melberg A, Zeviani M, Poulton J, Foury F, Jacobs HT.

Eur J Hum Genet. 1999 Feb-Mar;7(2):140-6.

11.

[Different instability of microsatellite CAG repeat in two groups of haplotypes of the human mitochondrial gamma-DNA-polymerase gene].

Maliarchuk BA, Perkova MA, Derenko MV.

Mol Biol (Mosk). 2009 Jul-Aug;43(4):623-7. Russian.

PMID:
19807024
12.

Evidence for polymerase gamma, POLG1 variation in reduced mitochondrial DNA copy number in Parkinson's disease.

Gui YX, Xu ZP, Lv W, Zhao JJ, Hu XY.

Parkinsonism Relat Disord. 2015 Mar;21(3):282-6. doi: 10.1016/j.parkreldis.2014.12.030. Epub 2015 Jan 6.

PMID:
25585994
13.

CAG repeat variants in the POLG1 gene encoding mtDNA polymerase-gamma and risk of breast cancer in African-American women.

Azrak S, Ayyasamy V, Zirpoli G, Ambrosone C, Bandera EV, Bovbjerg DH, Jandorf L, Ciupak G, Davis W, Pawlish KS, Liang P, Singh K.

PLoS One. 2012;7(1):e29548. doi: 10.1371/journal.pone.0029548. Epub 2012 Jan 20.

14.

CAG repeat variation in the mtDNA polymerase gamma is not associated with oligoasthenozoospermia.

Rani DS, Carlus SJ, Poongothai J, Jyothi A, Pavani K, Gupta NJ, Reddy AG, Rajan MM, Rao K, Chakravarty B, Singh L, Thangaraj K.

Int J Androl. 2009 Dec;32(6):647-55. doi: 10.1111/j.1365-2605.2008.00919.x. Epub 2008 Sep 16.

PMID:
18798765
15.

Association study of two genetic variants in mitochondrial transcription factor A (TFAM) in Alzheimer's and Parkinson's disease.

Belin AC, Björk BF, Westerlund M, Galter D, Sydow O, Lind C, Pernold K, Rosvall L, Håkansson A, Winblad B, Nissbrandt H, Graff C, Olson L.

Neurosci Lett. 2007 Jun 15;420(3):257-62. Epub 2007 May 10.

PMID:
17537576
16.

Analysis of ERDA1, CTG18.1, and uncloned CAG/CTG repeat sequences in familial Parkinson's disease with anticipation.

Schraen-Maschke S, Brique S, Chartier-Harlin MC, Brique E, Destée A, Sablonnière B.

Am J Med Genet. 1999 Dec 15;88(6):738-41.

PMID:
10581499
17.

Mitochondrial DNA polymorphisms and risk of Parkinson's disease in Spanish population.

Huerta C, Castro MG, Coto E, Blázquez M, Ribacoba R, Guisasola LM, Salvador C, Martínez C, Lahoz CH, Alvarez V.

J Neurol Sci. 2005 Sep 15;236(1-2):49-54.

PMID:
15975594
18.

CAG repeat length variation in the polymerase gamma (POLG) gene: effect on semen quality.

Westerveld GH, Kaaij-Visser L, Tanck M, van der Veen F, Repping S.

Mol Hum Reprod. 2008 Apr;14(4):245-9. doi: 10.1093/molehr/gan012. Epub 2008 Mar 3.

PMID:
18316366
19.

Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.

Mellick GD, Buchanan DD, McCann SJ, James KM, Johnson AG, Davis DR, Liyou N, Chan D, Le Couteur DG.

Mov Disord. 1999 Mar;14(2):219-24.

PMID:
10091612
20.

Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan.

Lee YC, Lu YC, Chang MH, Soong BW.

J Neurol Sci. 2007 Mar 15;254(1-2):65-8. Epub 2007 Feb 14.

PMID:
17300808

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