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Journal ArticleDOI

The expression of α-, β-, and γ-synucleins in olfactory mucosa from patients with and without neurodegenerative diseases

TLDR
It is shown here for the first time that α-, β-, and γ-synucleins are differentially expressed in cells of the OE and respiratory epithelium and that α- Synuclein is the most abundant synuclein in the olfactory mucosa, where it is prominently expressed in ORNs.
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This article is published in Experimental Neurology.The article was published on 1999-12-01. It has received 127 citations till now. The article focuses on the topics: Olfactory epithelium & Olfactory mucosa.

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Intracerebral inoculation of pathological α-synuclein initiates a rapidly progressive neurodegenerative α-synucleinopathy in mice.

TL;DR: Synthetic a-Synuclein fibrils injected into the brain spread far beyond the injection site and are sufficient to accelerate Parkinson’s disease–like pathology in mice.
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Parkinson's disease: a dual-hit hypothesis.

TL;DR: It is concluded that the most parsimonious explanation for the initial events of sporadic Parkinson's disease is pathogenic access to the brain through the stomach and nose – hence the term ‘dual‐hit’.
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Olfactory dysfunction in Parkinson disease

TL;DR: Neuroanatomical findings suggest that deficits in cholinergic, noradrenergic and serotonergic function may contribute to the olfactory loss in Parkinson disease.
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Synucleinopathies: Clinical and Pathological Implications

TL;DR: The synucleinopathies are a diverse group of neurodegenerative disorders that share a common pathologic lesion composed of aggregates of insoluble alpha-synuclein protein in selectively vulnerable populations of neurons and glia, and clarification of this enigmatic symmetry will have a profound impact on understanding the mechanisms underlying all these disorders.
References
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Mutation in the α-synuclein gene identified in families with Parkinson's disease

TL;DR: A mutation was identified in the α-synuclein gene, which codes for a presynaptic protein thought to be involved in neuronal plasticity, in the Italian kindred and in three unrelated families of Greek origin with autosomal dominant inheritance for the PD phenotype.
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Handbook of Sensory Physiology

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Alpha-synuclein in Lewy bodies.

TL;DR: Strong staining of Lewy bodies from idiopathic Parkinson's disease with antibodies for α-synuclein, a presynaptic protein of unknown function which is mutated in some familial cases of the disease, indicates that the LewY bodies from these two diseases may have identical compositions.
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α-Synuclein in filamentous inclusions of Lewy bodies from Parkinson’s disease and dementia with Lewy bodies

TL;DR: It is shown thatLewy bodies and Lewy neurites from Parkinson’s disease and dementia with Lewy bodies are stained strongly by antibodies directed against amino- terminal and carboxyl-terminal sequences of α-synuclein, showing the presence of full- length or close to full-length α- synuclein.
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