199 related articles for article (PubMed ID: 21368765)
1. PLA2G6 variant in Parkinson's disease.
Tomiyama H; Yoshino H; Ogaki K; Li L; Yamashita C; Li Y; Funayama M; Sasaki R; Kokubo Y; Kuzuhara S; Hattori N
J Hum Genet; 2011 May; 56(5):401-3. PubMed ID: 21368765
[TBL] [Abstract][Full Text] [Related]
2. The PLA2G6 gene in early-onset Parkinson's disease.
Kauther KM; Höft C; Rissling I; Oertel WH; Möller JC
Mov Disord; 2011 Nov; 26(13):2415-7. PubMed ID: 21812034
[TBL] [Abstract][Full Text] [Related]
3. PLA2G6 variants associated with the number of affected alleles in Parkinson's disease in Japan.
Daida K; Nishioka K; Li Y; Yoshino H; Shimada T; Dougu N; Nakatsuji Y; Ohara S; Hashimoto T; Okiyama R; Yokochi F; Suzuki C; Tomiyama M; Kimura K; Ueda N; Tanaka F; Yamada H; Fujioka S; Tsuboi Y; Uozumi T; Takei T; Matsuzaki S; Shibasaki M; Kashihara K; Kurisaki R; Yamashita T; Fujita N; Hirata Y; Ii Y; Wada C; Eura N; Sugie K; Higuchi Y; Kojima F; Imai H; Noda K; Shimo Y; Funayama M; Hattori N
Neurobiol Aging; 2021 Jan; 97():147.e1-147.e9. PubMed ID: 32771225
[TBL] [Abstract][Full Text] [Related]
4. PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.
Lu CS; Lai SC; Wu RM; Weng YH; Huang CL; Chen RS; Chang HC; Wu-Chou YH; Yeh TH
Am J Med Genet B Neuropsychiatr Genet; 2012 Mar; 159B(2):183-91. PubMed ID: 22213678
[TBL] [Abstract][Full Text] [Related]
5. Phenotypic spectrum of patients with PLA2G6 mutation and PARK14-linked parkinsonism.
Yoshino H; Tomiyama H; Tachibana N; Ogaki K; Li Y; Funayama M; Hashimoto T; Takashima S; Hattori N
Neurology; 2010 Oct; 75(15):1356-61. PubMed ID: 20938027
[TBL] [Abstract][Full Text] [Related]
6. Association of rare heterozygous PLA2G6 variants with the risk of Parkinson's disease.
Liu H; Wang Y; Pan H; Xu K; Jiang L; Zhao Y; Xu Q; Sun Q; Tan J; Yan X; Li J; Tang B; Guo J
Neurobiol Aging; 2021 May; 101():297.e5-297.e8. PubMed ID: 33279242
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Four novel rare mutations of PLA2G6 in Chinese population with Parkinson's disease.
Gui YX; Xu ZP; Wen-Lv ; Liu HM; Zhao JJ; Hu XY
Parkinsonism Relat Disord; 2013 Jan; 19(1):21-6. PubMed ID: 23182313
[TBL] [Abstract][Full Text] [Related]
9. 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; 57(3):473-6. PubMed ID: 17174426
[TBL] [Abstract][Full Text] [Related]
10. PLA2G6 accumulates in Lewy bodies in PARK14 and idiopathic Parkinson's disease.
Miki Y; Tanji K; Mori F; Kakita A; Takahashi H; Wakabayashi K
Neurosci Lett; 2017 Apr; 645():40-45. PubMed ID: 28213071
[TBL] [Abstract][Full Text] [Related]
11. Genotype-phenotype correlations of adult-onset PLA2G6-associated Neurodegeneration: case series and literature review.
Chu YT; Lin HY; Chen PL; Lin CH
BMC Neurol; 2020 Mar; 20(1):101. PubMed ID: 32183746
[TBL] [Abstract][Full Text] [Related]
12. Translated mutation in the Nurr1 gene as a cause for Parkinson's disease.
Grimes DA; Han F; Panisset M; Racacho L; Xiao F; Zou R; Westaff K; Bulman DE
Mov Disord; 2006 Jul; 21(7):906-9. PubMed ID: 16532445
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Association between PLA2G6 gene polymorphisms and Parkinson's disease in the Chinese Han population.
Lv Z; Guo J; Sun Q; Li K; Yu R; Tian J; Yan X; Tang B
Parkinsonism Relat Disord; 2012 Jun; 18(5):641-4. PubMed ID: 22459563
[TBL] [Abstract][Full Text] [Related]
15. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease.
Nichols WC; Uniacke SK; Pankratz N; Reed T; Simon DK; Halter C; Rudolph A; Shults CW; Conneally PM; Foroud T;
Mov Disord; 2004 Jun; 19(6):649-55. PubMed ID: 15197702
[TBL] [Abstract][Full Text] [Related]
16. Mutation screening of PLA2G6 in Japanese patients with early onset dystonia-parkinsonism.
Yamashita C; Funayama M; Li Y; Yoshino H; Yamada H; Seino Y; Tomiyama H; Hattori N
J Neural Transm (Vienna); 2017 Apr; 124(4):431-435. PubMed ID: 27942883
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. SNP rs7684318 of the alpha-synuclein gene is associated with Parkinson's disease in the Han Chinese population.
Yu L; Xu P; He X; Hu F; Lin Z; Zhu M; Liu Z; He L; Xu Y
Brain Res; 2010 Jul; 1346():262-5. PubMed ID: 20513365
[TBL] [Abstract][Full Text] [Related]
19. Genetic analysis of ATP13A2, PLA2G6 and FBXO7 in a cohort of Chinese patients with early-onset Parkinson's disease.
Shen T; Pu J; Lai HY; Xu L; Si X; Yan Y; Jiang Y; Zhang B
Sci Rep; 2018 Sep; 8(1):14028. PubMed ID: 30232368
[TBL] [Abstract][Full Text] [Related]
20. Variant cytochrome P450 CYP2D6 allelic frequencies in Parkinson's disease.
Kurth MC; Kurth JH
Am J Med Genet; 1993 Oct; 48(3):166-8. PubMed ID: 8291573
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]