66 related articles for article (PubMed ID: 14767722)
1. A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.
Mellick GD; Silburn PA; Prince JA; Brookes AJ
J Neural Transm (Vienna); 2004 Feb; 111(2):191-9. PubMed ID: 14767722
[TBL] [Abstract][Full Text] [Related]
2. High frequency of mitochondrial complex I mutations in Parkinson's disease and aging.
Smigrodzki R; Parks J; Parker WD
Neurobiol Aging; 2004; 25(10):1273-81. PubMed ID: 15465623
[TBL] [Abstract][Full Text] [Related]
3. 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; 236(1-2):49-54. PubMed ID: 15975594
[TBL] [Abstract][Full Text] [Related]
4. Alzheimer's disease and Parkinson's disease genome-wide association study top hits and risk of Parkinson's disease in Korean population.
Chung SJ; Jung Y; Hong M; Kim MJ; You S; Kim YJ; Kim J; Song K
Neurobiol Aging; 2013 Nov; 34(11):2695.e1-7. PubMed ID: 23820587
[TBL] [Abstract][Full Text] [Related]
5. Mitochondrial polymporphisms in Parkinson's Disease.
Otaegui D; Paisán C; Sáenz A; Martí I; Ribate M; Martí-Massó JF; Pérez-Tur J; López de Munain A
Neurosci Lett; 2004 Nov; 370(2-3):171-4. PubMed ID: 15488317
[TBL] [Abstract][Full Text] [Related]
6. Toward identification of susceptibility genes for sporadic Parkinson's disease.
Toda T; Momose Y; Murata M; Tamiya G; Yamamoto M; Hattori N; Inoko H
J Neurol; 2003 Oct; 250 Suppl 3():III40-3. PubMed ID: 14579123
[TBL] [Abstract][Full Text] [Related]
7. Identification of a risk haplotype of the alpha-synuclein gene in Japanese with sporadic Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Mov Disord; 2006 Dec; 21(12):2157-64. PubMed ID: 17078049
[TBL] [Abstract][Full Text] [Related]
8. Association of a polymorphism in the ABCB1 gene with Parkinson's disease.
Westerlund M; Belin AC; Anvret A; Håkansson A; Nissbrandt H; Lind C; Sydow O; Olson L; Galter D
Parkinsonism Relat Disord; 2009 Jul; 15(6):422-4. PubMed ID: 19196542
[TBL] [Abstract][Full Text] [Related]
9. Complex I polymorphisms, bigenomic heterogeneity, and family history in Virginians with Parkinson's disease.
Swerdlow RH; Weaver B; Grawey A; Wenger C; Freed E; Worrall BB
J Neurol Sci; 2006 Sep; 247(2):224-30. PubMed ID: 16784756
[TBL] [Abstract][Full Text] [Related]
10. Association between the estrogen receptor beta gene and age of onset of Parkinson's disease.
Westberg L; Håkansson A; Melke J; Shahabi HN; Nilsson S; Buervenich S; Carmine A; Ahlberg J; Grundell MB; Schulhof B; Klingborg K; Holmberg B; Sydow O; Olson L; Johnels EB; Eriksson E; Nissbrandt H
Psychoneuroendocrinology; 2004 Sep; 29(8):993-8. PubMed ID: 15219649
[TBL] [Abstract][Full Text] [Related]
11. Parkinson's disease and mitochondrial gene variations: a review.
Andalib S; Vafaee MS; Gjedde A
J Neurol Sci; 2014 Nov; 346(1-2):11-9. PubMed ID: 25151610
[TBL] [Abstract][Full Text] [Related]
12. Association of a variation in the promoter region of the brain-derived neurotrophic factor gene with familial Parkinson's disease.
Parsian A; Sinha R; Racette B; Zhao JH; Perlmutter JS
Parkinsonism Relat Disord; 2004 Jun; 10(4):213-9. PubMed ID: 15120095
[TBL] [Abstract][Full Text] [Related]
13. SNCA polymorphisms, smoking, and sporadic Parkinson's disease in Japanese.
Miyake Y; Tanaka K; Fukushima W; Kiyohara C; Sasaki S; Tsuboi Y; Yamada T; Oeda T; Shimada H; Kawamura N; Sakae N; Fukuyama H; Hirota Y; Nagai M;
Parkinsonism Relat Disord; 2012 Jun; 18(5):557-61. PubMed ID: 22425546
[TBL] [Abstract][Full Text] [Related]
14. LINGO-2 polymorphism and the risk of Parkinson's disease in Taiwan.
Su FC; Chen CM; Chen YC; Wu YR
Parkinsonism Relat Disord; 2012 Jun; 18(5):609-11. PubMed ID: 22123311
[TBL] [Abstract][Full Text] [Related]
15. A common A340T variant in PINK1 gene associated with late-onset Parkinson's disease in Chinese.
Wang F; Feng X; Ma J; Zou H; Chan P
Neurosci Lett; 2006 Dec; 410(2):121-5. PubMed ID: 17084972
[TBL] [Abstract][Full Text] [Related]
16. Female genetic distribution bias in mitochondrial genome observed in Parkinson's Disease patients in northern China.
Chu Q; Luo X; Zhan X; Ren Y; Pang H
Sci Rep; 2015 Nov; 5():17170. PubMed ID: 26602989
[TBL] [Abstract][Full Text] [Related]
17. Analysis of mutations and the association between polymorphisms in the cerebral dopamine neurotrophic factor (CDNF) gene and Parkinson disease.
Choi JM; Hong JH; Chae MJ; Ngyuen PH; Kang HS; Ma HI; Kim YJ
Neurosci Lett; 2011 Apr; 493(3):97-101. PubMed ID: 21320571
[TBL] [Abstract][Full Text] [Related]
18. Role of polymorphisms in dopamine synthesis and metabolism genes and association of DBH haplotypes with Parkinson's disease among North Indians.
Punia S; Das M; Behari M; Mishra BK; Sahani AK; Govindappa ST; Jayaram S; Muthane UB; K TB; Juyal RC
Pharmacogenet Genomics; 2010 Jul; 20(7):435-41. PubMed ID: 20498626
[TBL] [Abstract][Full Text] [Related]
19. Evidence of an association between the scavenger receptor class B member 2 gene and Parkinson's disease.
Michelakakis H; Xiromerisiou G; Dardiotis E; Bozi M; Vassilatis D; Kountra PM; Patramani G; Moraitou M; Papadimitriou D; Stamboulis E; Stefanis L; Zintzaras E; Hadjigeorgiou GM
Mov Disord; 2012 Mar; 27(3):400-5. PubMed ID: 22223122
[TBL] [Abstract][Full Text] [Related]
20. Correlation of tau gene polymorphism with age at onset of Parkinson's disease.
Kobayashi H; Ujike H; Hasegawa J; Yamamoto M; Kanzaki A; Sora I
Neurosci Lett; 2006 Sep; 405(3):202-6. PubMed ID: 16876320
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]