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CryoET reveals organelle phenotypes in huntington disease patient iPSC-derived and mouse primary neu...

CryoET reveals organelle phenotypes in huntington disease patient iPSC-derived and mouse primary neu...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_27dd4928dbf643889186e8bd55e8a97e

CryoET reveals organelle phenotypes in huntington disease patient iPSC-derived and mouse primary neurons

About this item

Full title

CryoET reveals organelle phenotypes in huntington disease patient iPSC-derived and mouse primary neurons

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2023-02, Vol.14 (1), p.692-692, Article 692

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Huntington’s disease (HD) is caused by an expanded CAG repeat in the huntingtin gene, yielding a Huntingtin protein with an expanded polyglutamine tract. While experiments with patient-derived induced pluripotent stem cells (iPSCs) can help understand disease, defining pathological biomarkers remains challenging. Here, we used cryogenic electron to...

Alternative Titles

Full title

CryoET reveals organelle phenotypes in huntington disease patient iPSC-derived and mouse primary neurons

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_27dd4928dbf643889186e8bd55e8a97e

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_27dd4928dbf643889186e8bd55e8a97e

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-023-36096-w

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