| 1 | Aging, cellular senescence and Parkinson's disease | 2.2 | 36 | Citations (PDF) |
| 2 | Pathological α-synuclein elicits granulovacuolar degeneration independent of tau | 8.3 | 3 | Citations (PDF) |
| 3 | VPS35 and retromer dysfunction in Parkinson's disease | 2.6 | 21 | Citations (PDF) |
| 4 | Adult-onset deletion of ATP13A2 in mice induces progressive nigrostriatal pathway dopaminergic degeneration and lysosomal abnormalities | 4.5 | 18 | Citations (PDF) |
| 5 | Heterozygous loss of and α-synucleinopathy (En1/SYN): A dual-hit preclinical mouse model of Parkinson's disease, analyzed with artificial intelligence | 3.6 | 3 | Citations (PDF) |
| 6 | Neuropathology in an α-synuclein preformed fibril mouse model occurs independent of the Parkinson's disease-linked lysosomal ATP13A2 protein | 3.6 | 11 | Citations (PDF) |
| 7 | VPS35 and α-Synuclein fail to interact to modulate neurodegeneration in rodent models of Parkinson’s disease | 9.8 | 10 | Citations (PDF) |
| 8 | Hippocampal subfield vulnerability to α-synuclein pathology precedes neurodegeneration and cognitive dysfunction | 4.5 | 30 | Citations (PDF) |
| 9 | Formation of templated inclusions in a forebrain α-synuclein mouse model is independent of LRRK2 | 3.6 | 4 | Citations (PDF) |
| 10 | Understanding the contributions of VPS35 and the retromer in neurodegenerative disease | 3.6 | 51 | Citations (PDF) |
| 11 | Log in to my account | 2.2 | 15 | Citations (PDF) |
| 12 | Neuronal VPS35 deletion induces spinal cord motor neuron degeneration and early post-natal lethality. | 2.0 | 24 | Citations (PDF) |
| 13 | Multiple genetic pathways regulating lifespan extension are neuroprotective in a G2019S LRRK2 nematode model of Parkinson's disease | 3.6 | 16 | Citations (PDF) |
| 14 | Log in to my account | 2.2 | 96 | Citations (PDF) |
| 15 | People also looked at | 2.0 | 26 | Citations (PDF) |
| 16 | Dopaminergic neurodegeneration induced by Parkinson's disease-linked G2019S LRRK2 is dependent on kinase and GTPase activity | 5.3 | 62 | Citations (PDF) |
| 17 | Time course and magnitude of alpha-synuclein inclusion formation and nigrostriatal degeneration in the rat model of synucleinopathy triggered by intrastriatal α-synuclein preformed fibrils | 3.6 | 107 | Citations (PDF) |
| 18 | Parkinson’s disease-linked D620N VPS35 knockin mice manifest tau neuropathology and dopaminergic neurodegeneration | 5.3 | 111 | Citations (PDF) |
| 19 | Pathogenic alpha-synuclein aggregates preferentially bind to mitochondria and affect cellular respiration | 3.4 | 203 | Citations (PDF) |
| 20 | G2019S LRRK2 enhances the neuronal transmission of tau in the mouse brain. | 2.1 | 49 | Citations (PDF) |
| 21 | Deciphering the role of VPS35 in Parkinson's disease | 2.0 | 4 | Citations (PDF) |
| 22 | Parkin mediates the ubiquitination of VPS35 and modulates retromer-dependent endosomal sorting | 2.1 | 67 | Citations (PDF) |
| 23 | Parkin functionally interacts with PGC-1α to preserve mitochondria and protect dopaminergic neurons | 2.1 | 60 | Citations (PDF) |
| 24 | Mechanisms of LRRK2-dependent neurodegeneration: role of enzymatic activity and protein aggregation | 2.7 | 64 | Citations (PDF) |
| 25 | Log in to my account | 2.2 | 158 | Citations (PDF) |
| 26 | Ubiqutination via K27 and K29 chains signals aggregation and neuronal protection of LRRK2 by WSB1 | 11.0 | 76 | Citations (PDF) |
| 27 | Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) | 12.0 | 5,058 | Citations (PDF) |
| 28 | Adenoviral-mediated expression of G2019S LRRK2 induces striatal pathology in a kinase-dependent manner in a rat model of Parkinson's disease | 3.6 | 48 | Citations (PDF) |
| 29 | α-Synuclein-induced dopaminergic neurodegeneration in a rat model of Parkinson's disease occurs independent of ATP13A2 (PARK9) | 3.6 | 41 | Citations (PDF) |
| 30 | Functional interaction of Parkinson's disease-associated LRRK2 with members of the dynamin GTPase superfamily. | 2.1 | 129 | Citations (PDF) |
| 31 | Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration. | 2.1 | 150 | Citations (PDF) |
| 32 | A Parkinson's disease gene regulatory network identifies the signaling protein RGS2 as a modulator of LRRK2 activity and neuronal toxicity. | 2.1 | 52 | Citations (PDF) |
| 33 | Conditional expression of Parkinson's disease-related R1441C LRRK2 in midbrain dopaminergic neurons of mice causes nuclear abnormalities without neurodegeneration | 3.6 | 75 | Citations (PDF) |
| 34 | LRRK2 secretion in exosomes is regulated by 14-3-3. | 2.1 | 165 | Citations (PDF) |
| 35 | GTPase activity regulates kinase activity and cellular phenotypes of Parkinson's disease-associated LRRK2. | 2.1 | 153 | Citations (PDF) |
| 36 | Divergent α-synuclein solubility and aggregation properties in G2019S LRRK2 Parkinson's disease brains with Lewy Body pathology compared to idiopathic cases | 3.6 | 51 | Citations (PDF) |
| 37 | Contribution of GTPase activity to LRRK2-associated Parkinson disease | 0.6 | 53 | Citations (PDF) |
| 38 | GTPase Activity and Neuronal Toxicity of Parkinson's Disease–Associated LRRK2 Is Regulated by ArfGAP1 | 2.2 | 134 | Citations (PDF) |
| 39 | PARK9-associated ATP13A2 localizes to intracellular acidic vesicles and regulates cation homeostasis and neuronal integrity | 2.1 | 161 | Citations (PDF) |
| 40 | Neurodegenerative phenotypes in an A53T α-synuclein transgenic mouse model are independent of LRRK2 | 2.1 | 100 | Citations (PDF) |
| 41 | Mitochondrial Dysfunction in Genetic Animal Models of Parkinson's Disease | 4.2 | 87 | Citations (PDF) |
| 42 | α-Synuclein in Central Nervous System and from Erythrocytes, Mammalian Cells, and Escherichia coli Exists Predominantly as Disordered Monomer* | 1.3 | 538 | Citations (PDF) |
| 43 | Mechanisms of LRRK2-Mediated Neurodegeneration | 4.1 | 70 | Citations (PDF) |
| 44 | Common Pathogenic Effects of Missense Mutations in the P-Type ATPase ATP13A2 (PARK9) Associated with Early-Onset Parkinsonism | 1.5 | 72 | Citations (PDF) |
| 45 | Phosphorylation of 4E-BP1 in the Mammalian Brain Is Not Altered by LRRK2 Expression or Pathogenic Mutations | 1.5 | 42 | Citations (PDF) |
| 46 | Dopaminergic Neuronal Loss, Reduced Neurite Complexity and Autophagic Abnormalities in Transgenic Mice Expressing G2019S Mutant LRRK2 | 1.5 | 380 | Citations (PDF) |
| 47 | Localization of MAP1-LC3 in vulnerable neurons and Lewy bodies in brains of patients with dementia with Lewy bodies. | 1.5 | 61 | Citations (PDF) |
| 48 | Parkin promotes the ubiquitination and degradation of the mitochondrial fusion factor mitofusin 1. | 2.7 | 220 | Citations (PDF) |
| 49 | Reevaluation of Phosphorylation Sites in the Parkinson Disease-associated Leucine-rich Repeat Kinase 2* | 1.3 | 56 | Citations (PDF) |
| 50 | PINK1-dependent recruitment of Parkin to mitochondria in mitophagy | 5.3 | 1,603 | Citations (PDF) |
| 51 | GTPase Activity Plays a Key Role in the Pathobiology of LRRK2 | 2.2 | 197 | Citations (PDF) |
| 52 | CHIP regulates leucine-rich repeat kinase-2 ubiquitination, degradation, and toxicity | 5.3 | 210 | Citations (PDF) |
| 53 | Conditional transgenic mice expressing C-terminally truncated human α-synuclein (αSyn119) exhibit reduced striatal dopamine without loss of nigrostriatal pathway dopaminergic neurons | 9.8 | 92 | Citations (PDF) |
| 54 | Abnormal localization of leucine-rich repeat kinase 2 to the endosomal-lysosomal compartment in lewy body disease. | 1.5 | 79 | Citations (PDF) |
| 55 | Value of genetic models in understanding the cause and mechanisms of Parkinson’s disease | 4.1 | 46 | Citations (PDF) |
| 56 | Parkin mediates the degradation-independent ubiquitination of Hsp70. | 2.7 | 104 | Citations (PDF) |
| 57 | The Chaperone Activity of Heat Shock Protein 90 Is Critical for Maintaining the Stability of Leucine-Rich Repeat Kinase 2 | 2.3 | 192 | Citations (PDF) |
| 58 | Parkinson's disease-associated mutations in LRRK2 link enhanced GTP-binding and kinase activities to neuronal toxicity | 2.1 | 588 | Citations (PDF) |
| 59 | Expression and localization of Parkinson's disease-associated leucine-rich repeat kinase 2 in the mouse brain. | 2.7 | 111 | Citations (PDF) |
| 60 | Dynamic and redundant regulation of LRRK2 and LRRK1 expression | 1.5 | 147 | Citations (PDF) |
| 61 | Localization of Parkinson’s disease-associated LRRK2 in normal and pathological human brain | 1.9 | 145 | Citations (PDF) |
| 62 | Detrimental deletions: mitochondria, aging and Parkinson's disease | 1.7 | 36 | Citations (PDF) |
| 63 | Localization of LRRK2 to membranous and vesicular structures in mammalian brain | 4.7 | 508 | Citations (PDF) |
| 64 | Lessons from Drosophila Models of DJ-1 Deficiency | 1.0 | 29 | Citations (PDF) |
| 65 | Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress. | 2.1 | 238 | Citations (PDF) |
| 66 | Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degeneration | 5.3 | 408 | Citations (PDF) |
| 67 | Mitochondrial localization of the Parkinson's disease related protein DJ-1: implications for pathogenesis. | 2.1 | 399 | Citations (PDF) |
| 68 | MOLECULAR PATHOPHYSIOLOGY OF PARKINSON'S DISEASE | 7.2 | 1,200 | Citations (PDF) |
| 69 | Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity | 5.3 | 1,224 | Citations (PDF) |
| 70 | Role for the ubiquitin-proteasome system in Parkinson’s disease and other neurodegenerative brain amyloidoses | 2.2 | 52 | Citations (PDF) |
| 71 | A missense mutation (L166P) in DJ-1, linked to familial Parkinson's disease, confers reduced protein stability and impairs homo-oligomerization. | 2.7 | 207 | Citations (PDF) |
| 72 | GPR105, a novel G-coupled UDP-glucose receptor expressed on brain glia and peripheral immune cells, is regulated by immunologic challenge: possible role in neuroimmune function | 2.5 | 98 | Citations (PDF) |
| 73 | Expression pattern of human P2Y receptor subtypes: a quantitative reverse transcription–polymerase chain reaction study | 3.3 | 129 | Citations (PDF) |
| 74 | Human R1441C LRRK2 regulates the synaptic vesicle proteome and phosphoproteome in a Drosophila model of Parkinson's disease. | 2.1 | 76 | Citations (PDF) |
| 75 | LRRK2 regulates ArfGAP1 membrane localization, activity and neuronal integrity via phosphorylation within its lipid-sensing ALPS2 motif. | 2.4 | 0 | Citations (PDF) |
| 76 | Interaction of G2019S LRRK2 and metabolic syndrome in a two-hit mouse model of Parkinson's disease: LRRK2-driven systemic depletion of pyrimidine nucleosides. | 4.5 | 1 | Citations (PDF) |
| 77 | Parkinson's disease-linked D620N mutation selectively alters the brain-specific protein interactome of VPS35. | 3.6 | 0 | Citations (PDF) |