Author

Gemma L. Pearson

University of MichiganORCID 0000-0003-4253-1830Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Assay:proteomics· 1

Frequent Co-Authors

Jie ZhuiD· 2 shared Scott A. SoleimanpouriD· 2 shared Vaibhav SidaralaiD· 2 shared Aaron RenbergiD· 1 shared Anne C. LietzkeiD· 1 shared Ava M. Stendahl· 1 shared Belle A. Henry-Kanarek· 1 shared Biaoxin Chai· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersDevelopmental Biology

Jie ZhuORCID

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2 papers

Recent·Most cited

Developmental BiologybioRxivPreprintJul 26, 2024

Limitations in PPAR-dependent mitochondrial programming restrain the differentiation of human stem cell-derived β cells

Anne C. Lietzke, Emily M. Walker, Elizabeth J. Bealer…·Scott A. Soleimanpour

This study identifies PPAR-dependent mitochondrial programming as a limiting factor in the differentiation of human stem cell-derived β cells and shows that PPAR agonists can enhance β cell formation and function.

4 citations

humanbulk RNA-seq

𝕏 PostBluesky

Molecular BiologybioRxivPreprintSep 3, 2021

The human disease gene CLEC16A encodes an intrinsically disordered protein region required for mitochondrial quality control

Morgan A. Gingerich, Xueying Liu, Biaoxin Chai…·Scott A. Soleimanpour

This study identifies an intrinsically disordered protein region in CLEC16A critical for mitochondrial quality control and diabetes prevention.

1 citation

humanproteomics

𝕏 PostBluesky