Author

A. Hinds

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Cell Biology· 3

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Research Focus:differential expression· 3 Organism:human· 3 Approach:experimental assay· 2 Assay:scRNA-seq· 2 Assay:bulk RNA-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

C. Villacorta-Martin· 3 shared D. N. Kotton· 3 shared E. Bullitt· 2 shared F. Wang· 2 shared J. Huang· 2 shared J. Lindstrom-Vautrin· 2 shared A. A. Wilson· 1 shared A. Babu· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 34 mutual co-author links

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3 shared papersCell Biology

C. Villacorta-Martin

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Generation of human alveolar epithelial type I cells from pluripotent stem cells

C. L. Burgess, J. Huang, P. Bawa, K.-D. Alysandratos, K. Minakin, M. P. Morley, A. Babu, C. Villacorta-Martin, A. Hinds, B. R. Thapa, F. Wang, A. M. Matschulat, E. E. Morrisey, X. Varelas, D. N. Kotton

This study generates human alveolar epithelial type I cells from iPSCs by activating YAP signaling, revealing Hippo-LATS-YAP's role in their differentiation.

bioRxiv · Jan 19, 2023Cell Biology

Modeling of Alpha-1 Antitrypsin Deficiency with Syngeneic Human iPSC-Hepatocytes Reveals Metabolic Dysregulation and Cellular Heterogeneity in PiMZ and PiZZ Hepatocytes

J. Kaserman, R. B. Werder, F. Wang, T. Matte, M. I. Higgins, M. Dodge, J. Lindstrom-Vautrin, A. Hinds, E. Bullitt, I. Caballero, X. Shi, R. E. Gerszten, N. Brunetti-Pierri, M. Liesa, C. Villacorta-Martin, , A. A. Wilson

This study uses CRISPR-Cas9 to create syngeneic iPSC-derived hepatocytes with ZAAT heterozygosity, revealing metabolic dysregulation and cellular heterogeneity in MZ and ZZ cells.

bioRxiv · Feb 1, 2022 · PreprintCell Biology

Human airway lineages derived from pluripotent stem cells reveal the epithelial responses to SARS-CoV-2 infection

R. Wang, A. Hume, M. L. Beermann, C. Simone-Roach, J. Lindstrom-Vautrin, J. Le Suer, J. Huang, J. Olejnik, C. Villacorta-Martin, E. Bullitt, A. Hinds, M. Ghaedi, R. Werder, K. Abo, A. Wilson, , F. J. Hawkins

This study uses iPSC-derived airway cells to model SARS-CoV-2 infection, showing multiciliated cells as primary targets and demonstrating antiviral responses to remdesivir and camostat methylate.

bioRxiv · Jul 6, 2021Cell Biology