HuGE Literature Finder
Records 1-15
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Genetic risk factors in Finnish patients with Parkinson's disease.
Parkinsonism & related disorders 2017 Sep . Ylönen Susanna, Siitonen Ari, Nalls Michael A, Ylikotila Pauli, Autere Jaana, Eerola-Rautio Johanna, Gibbs Raphael, Hiltunen Mikko, Tienari Pentti J, Soininen Hilkka, Singleton Andrew B, Majamaa Ka |
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Mitochondrial transcription factor A (TFAM) rs1937 and AP endonuclease 1 (APE1) rs1130409 alleles are associated with reduced cognitive performance.
Neuroscience letters 2017 Feb . Lillenes Meryl S, Støen Mari, Günther Clara-Cecilie, Selnes Per, Stenset Vidar T V, Espeseth Thomas, Reinvang Ivar, Fladby Tormod, Tønjum To |
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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease.
Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
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Evidence for polymerase gamma, POLG1 variation in reduced mitochondrial DNA copy number in Parkinson's disease.
Parkinsonism & related disorders 2015 Mar 21 (3): 282-6. Gui Ya-Xing, Xu Zhong-Ping, Lv Wen, Zhao Jin-Jia, Hu Xing-Y |
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Rare POLG1 CAG variants do not influence Parkinson's disease or polymerase gamma function.
Mitochondrion 2014 Mar 15 65-8. Bentley Steven R, Shan Jianguo, Todorovic Michael, Wood Stephen A, Mellick George |
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Genetic diagnosis of Charcot-Marie-Tooth disease in a population by next-generation sequencing.
BioMed research international 2014 2014 210401. Høyer Helle, Braathen Geir J, Busk Øyvind L, Holla Øystein L, Svendsen Marit, Hilmarsen Hilde T, Strand Linda, Skjelbred Camilla F, Russell Michael |
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Variations of mitochondrial DNA polymerase ? in patients with Parkinson's disease.
Journal of neurology 2013 Dec 260 (12): 3144-9. Ylönen S, Ylikotila P, Siitonen A, Finnilä S, Autere J, Majamaa |
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Association of Mitochondrial DNA Polymerase ? Gene POLG1 Polymorphisms with Parkinsonism in Chinese Populations.
PloS one 2012 7 (12): 12. Gui YX, Xu ZP, Lv W, Liu HM, Zhao JJ, Hu XY |
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Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population.
Mitochondrion 2012 Nov 12 (6): 640-3. Balafkan Novin, Tzoulis Charalampos, Müller Bernd, Haugarvoll Kristoffer, Tysnes Ole-Bjørn, Larsen Jan Petter, Bindoff Laurence |
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POLG1 polyglutamine tract variants associated with Parkinson's disease.
Neuroscience letters 2010 Jun 477 (1): 1-5. Eerola Johanna, Luoma Petri T, Peuralinna Terhi, Scholz Sonja, Paisan-Ruiz Coro, Suomalainen Anu, Singleton Andrew B, Tienari Pentti |
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Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patients.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2008 Dec 29 (6): 489-93. Heidari Mohammad Mehdi, Houshmand Massoud, Hosseinkhani Saman, Nafissi Shahriar, Scheiber-Mojdehkar Barbara, Khatami Meh |
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Mitochondrial DNA polymerase gamma variants in idiopathic sporadic Parkinson disease.
Neurology 2007 Sep 69 (11): 1152-9. Luoma P T, Eerola J, Ahola S, Hakonen A H, Hellström O, Kivistö K T, Tienari P J, Suomalainen |
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Common mitochondrial DNA and POLG1 mutations are rare in the Chinese patients with adult-onset ataxia on Taiwan.
Journal of the neurological sciences 2007 Mar 254 (1-2): 65-8. Lee Yi-Chung, Lu Yi-Chun, Chang Ming-Hon, Soong Bing-W |
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POLG1 in idiopathic Parkinson disease.
Neurology 2006 Nov 67 (9): 1698-700. Tiangyou W, Hudson G, Ghezzi D, Ferrari G, Zeviani M, Burn D J, Chinnery P |
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Analysis of the trinucleotide CAG repeat from the DNA polymerase gamma gene (POLG) in patients with Parkinson's disease.
Neuroscience letters 2005 Mar 376 (1): 56-9. Taanman Jan-Willem, Schapira Anthony H |
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- Page last updated:Apr 06, 2020
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