These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
123 related articles for article (PubMed ID: 35912088)
1. Mitochondrial DNA variation in Parkinson's disease: Analysis of "out-of-place" population variants as a risk factor. Müller-Nedebock AC; Pfaff AL; Pienaar IS; Kõks S; van der Westhuizen FH; Elson JL; Bardien S Front Aging Neurosci; 2022; 14():921412. PubMed ID: 35912088 [TBL] [Abstract][Full Text] [Related]
2. Increased blood-derived mitochondrial DNA copy number in African ancestry individuals with Parkinson's disease. Müller-Nedebock AC; Meldau S; Lombard C; Abrahams S; van der Westhuizen FH; Bardien S Parkinsonism Relat Disord; 2022 Aug; 101():1-5. PubMed ID: 35728366 [TBL] [Abstract][Full Text] [Related]
3. Mitochondrial DNA variants, haplogroups and risk of Parkinson's disease: A systematic review and meta-analysis. Sena-Dos-Santos C; Moura DD; Epifane-de-Assunção MC; Ribeiro-Dos-Santos Â; Santos-Lobato BL Parkinsonism Relat Disord; 2024 Aug; 125():107044. PubMed ID: 38917640 [TBL] [Abstract][Full Text] [Related]
4. Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease. Simon DK; Pankratz N; Kissell DK; Pauciulo MW; Halter CA; Rudolph A; Pfeiffer RF; Nichols WC; Foroud T; BMC Med Genet; 2010 Apr; 11():53. PubMed ID: 20356410 [TBL] [Abstract][Full Text] [Related]
5. Nuclear Genes Associated with Mitochondrial DNA Processes as Contributors to Parkinson's Disease Risk. Müller-Nedebock AC; van der Westhuizen FH; Kõks S; Bardien S Mov Disord; 2021 Apr; 36(4):815-831. PubMed ID: 33513296 [TBL] [Abstract][Full Text] [Related]
6. Two-stage association study and meta-analysis of mitochondrial DNA variants in Parkinson disease. Hudson G; Nalls M; Evans JR; Breen DP; Winder-Rhodes S; Morrison KE; Morris HR; Williams-Gray CH; Barker RA; Singleton AB; Hardy J; Wood NE; Burn DJ; Chinnery PF Neurology; 2013 May; 80(22):2042-8. PubMed ID: 23645593 [TBL] [Abstract][Full Text] [Related]
7. Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease. Gaare JJ; Nido GS; Sztromwasser P; Knappskog PM; Dahl O; Lund-Johansen M; Maple-Grødem J; Alves G; Tysnes OB; Johansson S; Haugarvoll K; Tzoulis C Mov Disord; 2018 Oct; 33(10):1591-1600. PubMed ID: 30256453 [TBL] [Abstract][Full Text] [Related]
8. Mitochondrial Dysfunction in Parkinson's Disease: Focus on Mitochondrial DNA. Buneeva O; Fedchenko V; Kopylov A; Medvedev A Biomedicines; 2020 Dec; 8(12):. PubMed ID: 33321831 [TBL] [Abstract][Full Text] [Related]
9. A mitochondrial etiology of neurodegenerative diseases: evidence from Parkinson's disease. Khusnutdinova E; Gilyazova I; Ruiz-Pesini E; Derbeneva O; Khusainova R; Khidiyatova I; Magzhanov R; Wallace DC Ann N Y Acad Sci; 2008 Dec; 1147():1-20. PubMed ID: 19076426 [TBL] [Abstract][Full Text] [Related]
10. Accumulation of mitochondrial 7S DNA in idiopathic and LRRK2 associated Parkinson's disease. Podlesniy P; Puigròs M; Serra N; Fernández-Santiago R; Ezquerra M; Tolosa E; Trullas R EBioMedicine; 2019 Oct; 48():554-567. PubMed ID: 31631040 [TBL] [Abstract][Full Text] [Related]
11. No evidence of association between common European mitochondrial DNA variants in Alzheimer, Parkinson, and migraine in the Spanish population. Fachal L; Mosquera-Miguel A; Pastor P; Ortega-Cubero S; Lorenzo E; Oterino-Durán A; Toriello M; Quintáns B; Camiña-Tato M; Sesar A; Vega A; Sobrido MJ; Salas A Am J Med Genet B Neuropsychiatr Genet; 2015 Jan; 168B(1):54-65. PubMed ID: 25349034 [TBL] [Abstract][Full Text] [Related]
12. A genome on shaky ground: exploring the impact of mitochondrial DNA integrity on Parkinson's disease by highlighting the use of cybrid models. Lang M; Grünewald A; Pramstaller PP; Hicks AA; Pichler I Cell Mol Life Sci; 2022 May; 79(5):283. PubMed ID: 35513611 [TBL] [Abstract][Full Text] [Related]
13. Relationship between mitochondrial DNA A10398G polymorphism and Parkinson's disease: a meta-analysis. Hua F; Zhang X; Hou B; Xue L; Xie A Oncotarget; 2017 Sep; 8(44):78023-78030. PubMed ID: 29100444 [TBL] [Abstract][Full Text] [Related]
14. mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the Irish. Ross OA; McCormack R; Maxwell LD; Duguid RA; Quinn DJ; Barnett YA; Rea IM; El-Agnaf OM; Gibson JM; Wallace A; Middleton D; Curran MD Exp Gerontol; 2003 Apr; 38(4):397-405. PubMed ID: 12670626 [TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 25585994 [TBL] [Abstract][Full Text] [Related]
16. Altered Transcriptional Profile of Mitochondrial DNA-Encoded OXPHOS Subunits, Mitochondria Quality Control Genes, and Intracellular ATP Levels in Blood Samples of Patients with Parkinson's Disease. Gezen-Ak D; Alaylıoğlu M; Genç G; Şengül B; Keskin E; Sordu P; Güleç ZEK; Apaydın H; Bayram-Gürel Ç; Ulutin T; Yılmazer S; Ertan S; Dursun E J Alzheimers Dis; 2020; 74(1):287-307. PubMed ID: 32007957 [TBL] [Abstract][Full Text] [Related]
17. Evidence for Compartmentalized Axonal Mitochondrial Biogenesis: Mitochondrial DNA Replication Increases in Distal Axons As an Early Response to Parkinson's Disease-Relevant Stress. Van Laar VS; Arnold B; Howlett EH; Calderon MJ; St Croix CM; Greenamyre JT; Sanders LH; Berman SB J Neurosci; 2018 Aug; 38(34):7505-7515. PubMed ID: 30030401 [TBL] [Abstract][Full Text] [Related]
18. Mitochondrial DNA polymorphisms as risk factors for Parkinson's disease and Parkinson's disease dementia. Autere J; Moilanen JS; Finnilä S; Soininen H; Mannermaa A; Hartikainen P; Hallikainen M; Majamaa K Hum Genet; 2004 Jun; 115(1):29-35. PubMed ID: 15108120 [TBL] [Abstract][Full Text] [Related]
19. Mitochondrial superclusters influence age of onset of Parkinson's disease in a gender specific manner in the Cypriot population: A case-control study. Georgiou A; Demetriou CA; Heraclides A; Christou YP; Leonidou E; Loukaides P; Yiasoumi E; Panagiotou D; Manoli P; Thomson P; Loizidou MA; Hadjisavvas A; Zamba-Papanicolaou E PLoS One; 2017; 12(9):e0183444. PubMed ID: 28877188 [TBL] [Abstract][Full Text] [Related]