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Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson’s disease in midbr...

Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson’s disease in midbr...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fc1ba7fa6d614cbe962ce2b5a05c4fa6

Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson’s disease in midbrain dopaminergic neurons

About this item

Full title

Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson’s disease in midbrain dopaminergic neurons

Publisher

London: Nature Publishing Group UK

Journal title

NPJ Parkinson's Disease, 2022-11, Vol.8 (1), p.162-162, Article 162

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Mutations in the
SNCA
gene cause autosomal dominant Parkinson’s disease (PD), with loss of dopaminergic neurons in the substantia nigra, and aggregation of α-synuclein. The sequence of molecular events that proceed from an
SNCA
mutation during development, to end-stage pathology is unknown. Utilising human-induced pluripotent stem cells...

Alternative Titles

Full title

Protein aggregation and calcium dysregulation are hallmarks of familial Parkinson’s disease in midbrain dopaminergic neurons

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_fc1ba7fa6d614cbe962ce2b5a05c4fa6

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_fc1ba7fa6d614cbe962ce2b5a05c4fa6

Other Identifiers

ISSN

2373-8057

E-ISSN

2373-8057

DOI

10.1038/s41531-022-00423-7

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