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Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of func...

Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of func...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10175346

Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation

About this item

Full title

Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

Journal title

Acta neuropathologica, 2023-06, Vol.145 (6), p.749-772

Language

English

Formats

Publication information

Publisher

Berlin/Heidelberg: Springer Berlin Heidelberg

More information

Scope and Contents

Contents

TREM2 is an innate immune receptor expressed by microglia in the adult brain. Genetic variation in the
TREM2
gene has been implicated in risk for Alzheimer’s disease and frontotemporal dementia, while homozygous
TREM2
mutations cause a rare leukodystrophy, Nasu-Hakola disease (NHD). Despite extensive investigation, the role of TREM2 in...

Alternative Titles

Full title

Defects in lysosomal function and lipid metabolism in human microglia harboring a TREM2 loss of function mutation

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10175346

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10175346

Other Identifiers

ISSN

0001-6322,1432-0533

E-ISSN

1432-0533

DOI

10.1007/s00401-023-02568-y

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