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Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of...

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_74724d48da6d4ad88e09abfe678d8216

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

About this item

Full title

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

Publisher

London: Nature Publishing Group UK

Journal title

Nature communications, 2020-02, Vol.11 (1), p.1031-15, Article 1031

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Clathrin-mediated endocytosis (CME) is critical for internalisation of molecules across cell membranes. The FCH domain only 1 (FCHO1) protein is key molecule involved in the early stages of CME formation. The consequences of mutations in
FCHO1
in humans were unknown. We identify ten unrelated patients with variable T and B cell lymphopenia, w...

Alternative Titles

Full title

Human FCHO1 deficiency reveals role for clathrin-mediated endocytosis in development and function of T cells

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_74724d48da6d4ad88e09abfe678d8216

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_74724d48da6d4ad88e09abfe678d8216

Other Identifiers

ISSN

2041-1723

E-ISSN

2041-1723

DOI

10.1038/s41467-020-14809-9

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