Modeling sex differences in Alzheimer’s Disease using isogenic hiPSC lines with different sex chromosome complements and APOE alleles

The new hiPSC lines are being differentiated to AD-relevant cell types, including neurons, microglia, and cortical organoids, for transcriptomic and functional analyses to elucidate how APOE alleles and genetic sex interact to modulate risk in LOAD pathology.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.093548
Primary Topic
Gene expression and cancer classification
Type
article
Field-Weighted Citation Impact
0.00
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article

Modeling sex differences in Alzheimer’s Disease using isogenic hiPSC lines with different sex chromosome complements and APOE alleles

Xinxian Deng, Theo K. Bammler, Julie Mathieu, Swati Mishra et al.
Alzheimer s & Dementia
Gene expression and cancer classification
article

Modeling sex differences in Alzheimer’s Disease using isogenic hiPSC lines with different sex chromosome complements and APOE alleles

Xinxian Deng, Theo K. Bammler, Julie Mathieu, Swati Mishra, Anne Skakkebæk, Jessica E. Young, Claus Højbjerg Gravholt, Daniel L. Van Dyke, Suman Jayadev, Christine M. Distèche, G. N. Filippova, Michelle Casad, James W. MacDonald, Joel B. Berletch, Camille Groneck, Kathleen K.S. Hui
article en

Abstract

The new hiPSC lines are being differentiated to AD-relevant cell types, including neurons, microglia, and cortical organoids, for transcriptomic and functional analyses to elucidate how APOE alleles and genetic sex interact to modulate risk in LOAD pathology.

Alzheimer s & DementiaVol. 20(S1)
California Institute for Regenerative Medicine (US), University of Washington (US), Aarhus University (DK), Mayo Clinic in Arizona (US)
Good health and well-being
Openalex Percentile: Top 78%
Gene expression and cancer classification
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Modeling sex differences in Alzheimer’s Disease using isogenic hiPSC lines with different sex chromosome complements and APOE alleles — Xinxian Deng, Theo K. Bammler, et al. · Alzheimer s & Dementia (2024) | TGRS Research Map | TGRS