Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons

α-Synuclein aggregation contributes to Parkinson’s disease and related disorders. Here the authors investigate patterns of α-synuclein aggregation in human dopaminergic neurons in response to fibrils derived from individuals with Parkinson’s disease or multiple system atrophy.

Guardado en:
Detalles Bibliográficos
Autores principales: Benedict Tanudjojo, Samiha S. Shaikh, Alexis Fenyi, Luc Bousset, Devika Agarwal, Jade Marsh, Christos Zois, Sabrina Heman-Ackah, Roman Fischer, David Sims, Ronald Melki, George K. Tofaris
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
Q
Acceso en línea:https://doaj.org/article/ba1ca4aa1df444ff85f3d901ea6d3c50
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:ba1ca4aa1df444ff85f3d901ea6d3c50
record_format dspace
spelling oai:doaj.org-article:ba1ca4aa1df444ff85f3d901ea6d3c502021-12-02T16:06:03ZPhenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons10.1038/s41467-021-23682-z2041-1723https://doaj.org/article/ba1ca4aa1df444ff85f3d901ea6d3c502021-06-01T00:00:00Zhttps://doi.org/10.1038/s41467-021-23682-zhttps://doaj.org/toc/2041-1723α-Synuclein aggregation contributes to Parkinson’s disease and related disorders. Here the authors investigate patterns of α-synuclein aggregation in human dopaminergic neurons in response to fibrils derived from individuals with Parkinson’s disease or multiple system atrophy.Benedict TanudjojoSamiha S. ShaikhAlexis FenyiLuc BoussetDevika AgarwalJade MarshChristos ZoisSabrina Heman-AckahRoman FischerDavid SimsRonald MelkiGeorge K. TofarisNature PortfolioarticleScienceQENNature Communications, Vol 12, Iss 1, Pp 1-16 (2021)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Benedict Tanudjojo
Samiha S. Shaikh
Alexis Fenyi
Luc Bousset
Devika Agarwal
Jade Marsh
Christos Zois
Sabrina Heman-Ackah
Roman Fischer
David Sims
Ronald Melki
George K. Tofaris
Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons
description α-Synuclein aggregation contributes to Parkinson’s disease and related disorders. Here the authors investigate patterns of α-synuclein aggregation in human dopaminergic neurons in response to fibrils derived from individuals with Parkinson’s disease or multiple system atrophy.
format article
author Benedict Tanudjojo
Samiha S. Shaikh
Alexis Fenyi
Luc Bousset
Devika Agarwal
Jade Marsh
Christos Zois
Sabrina Heman-Ackah
Roman Fischer
David Sims
Ronald Melki
George K. Tofaris
author_facet Benedict Tanudjojo
Samiha S. Shaikh
Alexis Fenyi
Luc Bousset
Devika Agarwal
Jade Marsh
Christos Zois
Sabrina Heman-Ackah
Roman Fischer
David Sims
Ronald Melki
George K. Tofaris
author_sort Benedict Tanudjojo
title Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons
title_short Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons
title_full Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons
title_fullStr Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons
title_full_unstemmed Phenotypic manifestation of α-synuclein strains derived from Parkinson’s disease and multiple system atrophy in human dopaminergic neurons
title_sort phenotypic manifestation of α-synuclein strains derived from parkinson’s disease and multiple system atrophy in human dopaminergic neurons
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/ba1ca4aa1df444ff85f3d901ea6d3c50
work_keys_str_mv AT benedicttanudjojo phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT samihasshaikh phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT alexisfenyi phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT lucbousset phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT devikaagarwal phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT jademarsh phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT christoszois phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT sabrinahemanackah phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT romanfischer phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT davidsims phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT ronaldmelki phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
AT georgektofaris phenotypicmanifestationofasynucleinstrainsderivedfromparkinsonsdiseaseandmultiplesystematrophyinhumandopaminergicneurons
_version_ 1718385172230963200