PINK1-linked parkinsonism is associated with Lewy body pathology

LRRK2 and neurodegeneration

(2009) Gabriel Santpere et al.   ACTA NEUROPATHOLOGICA

Protein Misfolding and Aggregation in Parkinson's Disease

(2009) Jeanne M.M. Tan et al.   ANTIOXIDANTS & REDOX SIGNALING

Mitochondrial autophagy as a compensatory response to PINK1 deficiency

(2009) Salvatore J. Cherra III et al.   Autophagy

Loss of PINK1 Function Promotes Mitophagy through Effects on Oxidative Stress and Mitochondrial Fission

(2009) Ruben K. Dagda et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Parkin, PINK1, and DJ-1 form a ubiquitin E3 ligase complex promoting unfolded protein degradation

(2009) Hui Xiong et al.   JOURNAL OF CLINICAL INVESTIGATION

Mutant Pink1 induces mitochondrial dysfunction in a neuronal cell model of Parkinson’s disease by disturbing calcium flux

(2009) Roberta Marongiu et al.   JOURNAL OF NEUROCHEMISTRY

Formation and development of Lewy pathology: a critical update

(2009) Kurt A. Jellinger   JOURNAL OF NEUROLOGY

Familial Parkinsonism and early onset Parkinson's disease in a Brazilian movement disorders clinic: Phenotypic characterization and frequency ofSNCA,PRKN,PINK1, andLRRK2mutations

(2009) Sarah Teixeira Camargos et al.   MOVEMENT DISORDERS

A new complex homozygous large rearrangement of the PINK1 gene in a Sudanese family with early onset Parkinson’s disease

(2009) Cécile Cazeneuve et al.   NEUROGENETICS

PINK1 Defect Causes Mitochondrial Dysfunction, Proteasomal Deficit and α-Synuclein Aggregation in Cell Culture Models of Parkinson's Disease

(2009) Wencheng Liu et al.   PLoS One

Parkinson Phenotype in Aged PINK1-Deficient Mice Is Accompanied by Progressive Mitochondrial Dysfunction in Absence of Neurodegeneration

(2009) Suzana Gispert et al.   PLoS One

PINK1-dependent recruitment of Parkin to mitochondria in mitophagy

(2009) C. Vives-Bauza et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Pink1 suppresses α-synuclein-induced phenotypes in a Drosophila model of Parkinson’s disease

(2008) Amy M. Todd et al.   GENOME

PINK1heterozygous rare variants: prevalence, significance and phenotypic spectrum

(2008) Roberta Marongiu et al.   HUMAN MUTATION

PINK1 mutations and parkinsonism

(2008) L. Ishihara-Paul et al.   NEUROLOGY

Identification of the novel D297fsX318 PINK1 mutation and phenotype variation in a family with early-onset Parkinson's disease

(2008) Giovanni Savettieri et al.   PARKINSONISM & RELATED DISORDERS