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Type I Interferon Signaling Drives Microglial Dysfunction and Senescence in Human iPSC Models of Dow...

Type I Interferon Signaling Drives Microglial Dysfunction and Senescence in Human iPSC Models of Dow...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2613014729

Type I Interferon Signaling Drives Microglial Dysfunction and Senescence in Human iPSC Models of Down Syndrome and Alzheimers Disease

About this item

Full title

Type I Interferon Signaling Drives Microglial Dysfunction and Senescence in Human iPSC Models of Down Syndrome and Alzheimers Disease

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

Journal title

bioRxiv, 2021-12

Language

English

Formats

Publication information

Publisher

Cold Spring Harbor: Cold Spring Harbor Laboratory Press

More information

Scope and Contents

Contents

Microglia are critical for brain development and play a central role in Alzheimers disease (AD) etiology. Down syndrome (DS), also known as trisomy 21, is the most common genetic origin of intellectual disability and the most common risk factor for AD. Surprisingly, little information is available on the impact of trisomy of human chromosome 21 (Hs...

Alternative Titles

Full title

Type I Interferon Signaling Drives Microglial Dysfunction and Senescence in Human iPSC Models of Down Syndrome and Alzheimers Disease

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_proquest_journals_2613014729

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2613014729

Other Identifiers

DOI

10.1101/2021.12.22.473858