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PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent...

PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_cce63f55680a422093d5b6e2ee7601ed

PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent stem cells

About this item

Full title

PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent stem cells

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2025-03, Vol.15 (1), p.10375-13, Article 10375

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Autosomal dominant polycystic kidney disease (ADPKD) is the most common renal genetic disease, with most patients carrying mutations in
PKD1
. The main feature is the formation of bilateral renal cysts, leading to end stage renal failure in a significant proportion of those affected. Despite recent advances made in understanding ADPKD, there...

Alternative Titles

Full title

PKD1 mutation perturbs morphogenesis in tubular epithelial organoids derived from human pluripotent stem cells

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_cce63f55680a422093d5b6e2ee7601ed

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_cce63f55680a422093d5b6e2ee7601ed

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/s41598-025-94855-9

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