📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

TREM2 Alzheimer's variant R47H causes similar transcriptional dysregulation to knockout, yet only subtle functional phenotypes in human iPSC-derived macrophages. (2020)

First Author: Hall-Roberts H

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1186/s13195-020-00709-z

PubMed Identifier: 33198789

Publication URI: http://europepmc.org/abstract/MED/33198789

Type: Journal Article/Review

Volume: 12

Parent Publication: Alzheimer's research & therapy

Issue: 1