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.
4. Enhanced striatal dopamine transmission and motor performance with LRRK2 overexpression in mice is eliminated by familial Parkinson's disease mutation G2019S. Li X; Patel JC; Wang J; Avshalumov MV; Nicholson C; Buxbaum JD; Elder GA; Rice ME; Yue Z J Neurosci; 2010 Feb; 30(5):1788-97. PubMed ID: 20130188 [TBL] [Abstract][Full Text] [Related]
5. Pathogenic LRRK2 mutations, through increased kinase activity, produce enlarged lysosomes with reduced degradative capacity and increase ATP13A2 expression. Henry AG; Aghamohammadzadeh S; Samaroo H; Chen Y; Mou K; Needle E; Hirst WD Hum Mol Genet; 2015 Nov; 24(21):6013-28. PubMed ID: 26251043 [TBL] [Abstract][Full Text] [Related]
6. Selective expression of Parkinson's disease-related Leucine-rich repeat kinase 2 G2019S missense mutation in midbrain dopaminergic neurons impairs dopamine release and dopaminergic gene expression. Liu G; Sgobio C; Gu X; Sun L; Lin X; Yu J; Parisiadou L; Xie C; Sastry N; Ding J; Lohr KM; Miller GW; Mateo Y; Lovinger DM; Cai H Hum Mol Genet; 2015 Sep; 24(18):5299-312. PubMed ID: 26123485 [TBL] [Abstract][Full Text] [Related]
7. Preclinical modeling of chronic inhibition of the Parkinson's disease associated kinase LRRK2 reveals altered function of the endolysosomal system in vivo. Kluss JH; Mazza MC; Li Y; Manzoni C; Lewis PA; Cookson MR; Mamais A Mol Neurodegener; 2021 Mar; 16(1):17. PubMed ID: 33741046 [TBL] [Abstract][Full Text] [Related]
8. Adenoviral-mediated expression of G2019S LRRK2 induces striatal pathology in a kinase-dependent manner in a rat model of Parkinson's disease. Tsika E; Nguyen AP; Dusonchet J; Colin P; Schneider BL; Moore DJ Neurobiol Dis; 2015 May; 77():49-61. PubMed ID: 25731749 [TBL] [Abstract][Full Text] [Related]
9. (G2019S) LRRK2 activates MKK4-JNK pathway and causes degeneration of SN dopaminergic neurons in a transgenic mouse model of PD. Chen CY; Weng YH; Chien KY; Lin KJ; Yeh TH; Cheng YP; Lu CS; Wang HL Cell Death Differ; 2012 Oct; 19(10):1623-33. PubMed ID: 22539006 [TBL] [Abstract][Full Text] [Related]
10. Dysregulated Wnt and NFAT signaling in a Parkinson's disease LRRK2 G2019S knock-in model. Wetzel A; Lei SH; Liu T; Hughes MP; Peng Y; McKay T; Waddington SN; Grannò S; Rahim AA; Harvey K Sci Rep; 2024 May; 14(1):12393. PubMed ID: 38811759 [TBL] [Abstract][Full Text] [Related]
13. Genetic and pharmacological evidence that G2019S LRRK2 confers a hyperkinetic phenotype, resistant to motor decline associated with aging. Longo F; Russo I; Shimshek DR; Greggio E; Morari M Neurobiol Dis; 2014 Nov; 71():62-73. PubMed ID: 25107341 [TBL] [Abstract][Full Text] [Related]
14. Phosphorylation-dependent 14-3-3 binding to LRRK2 is impaired by common mutations of familial Parkinson's disease. Li X; Wang QJ; Pan N; Lee S; Zhao Y; Chait BT; Yue Z PLoS One; 2011 Mar; 6(3):e17153. PubMed ID: 21390248 [TBL] [Abstract][Full Text] [Related]
16. A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia. Illarioshkin SN; Shadrina MI; Slominsky PA; Bespalova EV; Zagorovskaya TB; Bagyeva GKh; Markova ED; Limborska SA; Ivanova-Smolenskaya IA Eur J Neurol; 2007 Apr; 14(4):413-7. PubMed ID: 17388990 [TBL] [Abstract][Full Text] [Related]
17. The G2385R variant of leucine-rich repeat kinase 2 associated with Parkinson's disease is a partial loss-of-function mutation. Rudenko IN; Kaganovich A; Hauser DN; Beylina A; Chia R; Ding J; Maric D; Jaffe H; Cookson MR Biochem J; 2012 Aug; 446(1):99-111. PubMed ID: 22612223 [TBL] [Abstract][Full Text] [Related]
18. Biochemical and molecular features of LRRK2 and its pathophysiological roles in Parkinson's disease. Seol W BMB Rep; 2010 Apr; 43(4):233-44. PubMed ID: 20423607 [TBL] [Abstract][Full Text] [Related]
19. Development of inducible leucine-rich repeat kinase 2 (LRRK2) cell lines for therapeutics development in Parkinson's disease. Huang L; Shimoji M; Wang J; Shah S; Kamila S; Biehl ER; Lim S; Chang A; Maguire-Zeiss KA; Su X; Federoff HJ Neurotherapeutics; 2013 Oct; 10(4):840-51. PubMed ID: 23963789 [TBL] [Abstract][Full Text] [Related]