Defects in trafficking bridge Parkinson's disease pathology and genetics (Q39004335)

8 September 2017

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title

Defects in trafficking bridge Parkinson's disease pathology and genetics (English)

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8 September 2017

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1 reference

Asa Abeliovich

1

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PubMed ID

27830778

8 September 2017

Aaron D Gitler

series ordinal

2

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PubMed ID

27830778

8 September 2017

language of work or name

English

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publication date

9 November 2016

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8 September 2017

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8 September 2017

539

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8 September 2017

7628

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8 September 2017

207-216

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https://scigraph.springernature.com/pub.10.1038/nature20414

8 September 2017

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1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

100 years of Lewy pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson's disease and parkinsonism: neuropathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Alpha-synuclein in Lewy bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Pathoanatomy of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Genetics and genomics of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

alpha-Synuclein locus triplication causes Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Alpha-synuclein locus duplication as a cause of familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mechanisms of Parkinson's disease linked to pathological alpha-synuclein: new targets for drug discovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Alternative α-synuclein transcript usage as a convergent mechanism in Parkinson's disease pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Alpha-synuclein blocks ER-Golgi traffic and Rab1 rescues neuron loss in Parkinson's models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Yeast cells provide insight into alpha-synuclein biology and pathobiology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Identification and rescue of α-synuclein toxicity in Parkinson patient-derived neurons

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

Gaucher disease glucocerebrosidase and α-synuclein form a bidirectional pathogenic loop in synucleinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

α-Synuclein-induced lysosomal dysfunction occurs through disruptions in protein trafficking in human midbrain synucleinopathy models

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Formation of α-synuclein Lewy neurite-like aggregates in axons impedes the transport of distinct endosomes

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

Structural disorder of monomeric α-synuclein persists in mammalian cells.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

α-Synuclein assembles into higher-order multimers upon membrane binding to promote SNARE complex formation

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

α-Synuclein occurs physiologically as a helically folded tetramer that resists aggregation

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson-causing α-synuclein missense mutations shift native tetramers to monomers as a mechanism for disease initiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Pathological α-synuclein transmission initiates Parkinson-like neurodegeneration in nontransgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Exogenous α-synuclein fibrils induce Lewy body pathology leading to synaptic dysfunction and neuron death

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Isogenic human iPSC Parkinson's model shows nitrosative stress-induced dysfunction in MEF2-PGC1α transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Endogenous Parkin Preserves Dopaminergic Substantia Nigral Neurons following Mitochondrial DNA Mutagenic Stress

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

21 January 2018

Mechanisms of mitophagy

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

A53T human α-synuclein overexpression in transgenic mice induces pervasive mitochondria macroautophagy defects preceding dopamine neuron degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The roles of PINK1, parkin, and mitochondrial fidelity in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The polarisome is required for segregation and retrograde transport of protein aggregates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Autophagic failure promotes the exocytosis and intercellular transfer of α-synuclein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson's disease-linked human PARK9/ATP13A2 maintains zinc homeostasis and promotes α-Synuclein externalization via exosomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

ATP13A2/PARK9 regulates secretion of exosomes and α-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Toll-like receptor 4 is required for α-synuclein dependent activation of microglia and astroglia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Exogenous α-synuclein induces toll-like receptor 4 dependent inflammatory responses in astrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Neuron-released oligomeric α-synuclein is an endogenous agonist of TLR2 for paracrine activation of microglia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

α-Synuclein, a chemoattractant, directs microglial migration via H2O2-dependent Lyn phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mice lacking alpha-synuclein display functional deficits in the nigrostriatal dopamine system

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

Alpha-synuclein cooperates with CSPalpha in preventing neurodegeneration

21 January 2018

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https://api.crossref.org/works/10.1038%2FNATURE20414

Alpha-synuclein promotes SNARE-complex assembly in vivo and in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

A combinatorial code for the interaction of alpha-synuclein with membranes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Direct membrane association drives mitochondrial fission by the Parkinson disease-associated protein alpha-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The familial Parkinsonism gene LRRK2 regulates neurite process morphology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Novel ethyl methanesulfonate (EMS)-induced null alleles of the Drosophila homolog of LRRK2 reveal a crucial role in endolysosomal functions and autophagy in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Ribosomal protein s15 phosphorylation mediates LRRK2 neurodegeneration in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

LRRK2 transport is regulated by its novel interacting partner Rab32

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Phosphoproteomics reveals that Parkinson's disease kinase LRRK2 regulates a subset of Rab GTPases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Loss of leucine-rich repeat kinase 2 causes impairment of protein degradation pathways, accumulation of alpha-synuclein, and apoptotic cell death in aged mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Effect of selective LRRK2 kinase inhibition on nonhuman primate lung.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Gaucher disease and parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Carrier screening for Gaucher disease: lessons for low-penetrance, treatable diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinsonism among Gaucher disease carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

LIMP-2 expression is critical for β-glucocerebrosidase activity and α-synuclein clearance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Alpha-synuclein is part of a diverse and highly conserved interaction network that includes PARK9 and manganese toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

α-Synuclein-independent histopathological and motor deficits in mice lacking the endolysosomal Parkinsonism protein Atp13a2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Deficiency of ATP13A2 leads to lysosomal dysfunction, α-synuclein accumulation, and neurotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The Parkinson's disease-associated genes ATP13A2 and SYT11 regulate autophagy via a common pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Altered splicing of ATP6AP2 causes X-linked parkinsonism with spasticity (XPDS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Molecular mechanism and physiological functions of clathrin-mediated endocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

A mutation in VPS35, encoding a subunit of the retromer complex, causes late-onset Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

VPS35 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Sorting nexin 6, a novel SNX, interacts with the transforming growth factor-beta family of receptor serine-threonine kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Analysis of the Retromer complex-WASH complex interaction illuminates new avenues to explore in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mutation in VPS35 associated with Parkinson's disease impairs WASH complex association and inhibits autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson's disease genes VPS35 and EIF4G1 interact genetically and converge on α-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Parkinson's disease-linked mutations in VPS35 induce dopaminergic neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Role of the mammalian retromer in sorting of the cation-independent mannose 6-phosphate receptor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Functional architecture of the retromer cargo-recognition complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Retromer binding to FAM21 and the WASH complex is perturbed by the Parkinson disease-linked VPS35(D620N) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

VPS35 dysfunction impairs lysosomal degradation of α-synuclein and exacerbates neurotoxicity in a Drosophila model of Parkinson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

VPS35 in Dopamine Neurons Is Required for Endosome-to-Golgi Retrieval of Lamp2a, a Receptor of Chaperone-Mediated Autophagy That Is Critical for α-Synuclein Degradation and Prevention of Pathogenesis of Parkinson's Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

DNAJC13 mutations in Parkinson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mutation in the SYNJ1 gene associated with autosomal recessive, early-onset Parkinsonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The Sac1 domain of SYNJ1 identified mutated in a family with early-onset progressive Parkinsonism with generalized seizures

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Increased expression of alpha-synuclein reduces neurotransmitter release by inhibiting synaptic vesicle reclustering after endocytosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

LRRK2 functions in synaptic vesicle endocytosis through a kinase-dependent mechanism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Retromer-dependent neurotransmitter receptor trafficking to synapses is altered by the Parkinson's disease VPS35 mutation p.D620N.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Identification of TMEM230 mutations in familial Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Genome-wide association study reveals genetic risk underlying Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Colocalization of Tau and Alpha-Synuclein Epitopes in Lewy Bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Prion-like disorders: blurring the divide between transmissibility and infectivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Self-propagation of pathogenic protein aggregates in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Brain homogenates from human tauopathies induce tau inclusions in mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Glucocerebrosidase depletion enhances cell-to-cell transmission of α-synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

A critical appraisal of the pathogenic protein spread hypothesis of neurodegeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Innate immune recognition

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The immunology of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

MHCII is required for α-synuclein-induced activation of microglia, CD4 T cell proliferation, and dopaminergic neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Synuclein activates microglia in a model of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Antagonizing Neuronal Toll-like Receptor 2 Prevents Synucleinopathy by Activating Autophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Clearance and deposition of extracellular alpha-synuclein aggregates in microglia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Aggregated alpha-synuclein activates microglia: a process leading to disease progression in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Kinetic stabilization of the alpha-synuclein protofibril by a dopamine-alpha-synuclein adduct

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Interplay between cytosolic dopamine, calcium, and alpha-synuclein causes selective death of substantia nigra neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Autophagosomes initiate distally and mature during transport toward the cell soma in primary neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Mitophagy of damaged mitochondria occurs locally in distal neuronal axons and requires PINK1 and Parkin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

'Rejuvenation' protects neurons in mouse models of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The role of autophagy in neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Retromer in Alzheimer disease, Parkinson disease and other neurological disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Autophagy and human disease: emerging themes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Autophagosome dynamics in neurodegeneration at a glance

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

TFEB-mediated autophagy rescues midbrain dopamine neurons from α-synuclein toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

A GCase chaperone improves motor function in a mouse model of synucleinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Leucine-rich Repeat Kinase 2 (LRRK2) Pharmacological Inhibition Abates α-Synuclein Gene-induced Neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Pharmacological chaperones stabilize retromer to limit APP processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Α-synuclein immunotherapy blocks uptake and templated propagation of misfolded α-synuclein and neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The molecular machinery of neurotransmitter release (Nobel lecture).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Prions and Protein Assemblies that Convey Biological Information in Health and Disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Rab GTPases as coordinators of vesicle traffic

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

The biogenesis of lysosomes and lysosome-related organelles

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Optineurin is an autophagy receptor for damaged mitochondria in parkin-mediated mitophagy that is disrupted by an ALS-linked mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

alpha-synuclein gene haplotypes are associated with Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Prime Time for -Synuclein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNATURE20414

Proteolysis: from the lysosome to ubiquitin and the proteasome

21 January 2018

1 reference

12 December 2020

The role of innate and adaptive immunity in Parkinson's disease

1 reference

12 December 2020

iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis.

1 reference

12 December 2020

Dopamine-modified alpha-synuclein blocks chaperone-mediated autophagy

1 reference

12 December 2020

Dopamine (3-hydroxytyramine) in the central nervous system and its relation to the Parkinson syndrome in man

1 reference

12 December 2020

The role of autophagy in Parkinson's disease.

1 reference

12 December 2020

Identifiers

DOI

10.1038/NATURE20414

1 reference

8 September 2017

1 reference

PubMed ID

27830778