Log in to save to my catalogue

Generating a novel and reliable human iPSC‐derived midbrain organoid model of sporadic progressive s...

Generating a novel and reliable human iPSC‐derived midbrain organoid model of sporadic progressive s...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11709690

Generating a novel and reliable human iPSC‐derived midbrain organoid model of sporadic progressive supranuclear palsy

About this item

Full title

Generating a novel and reliable human iPSC‐derived midbrain organoid model of sporadic progressive supranuclear palsy

Publisher

Hoboken: John Wiley and Sons Inc

Journal title

Alzheimer's & dementia, 2024-12, Vol.20 (S1), p.n/a

Language

English

Formats

Publication information

Publisher

Hoboken: John Wiley and Sons Inc

Subjects

More information

Scope and Contents

Contents

Background
The accumulation of abnormal tau protein in neurons and glia in the human brain is the defining feature of neurodegenerative diseases known as tauopathies. Progressive supranuclear palsy (PSP), the most common primary tauopathy, is typified by selective vulnerability of dopaminergic neurons and glia in the midbrain leading to an atypi...

Alternative Titles

Full title

Generating a novel and reliable human iPSC‐derived midbrain organoid model of sporadic progressive supranuclear palsy

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11709690

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11709690

Other Identifiers

ISSN

1552-5260

E-ISSN

1552-5279

DOI

10.1002/alz.093263

How to access this item