Author

K. Jang

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· 2

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:drug response / drug discovery· 1 Organism:human· 1 Organism:mouse· 1 Assay:organoid / primary culture· 1

Frequent Co-Authors

A. R. Nookala· 1 shared D. Choi· 1 shared D. McKenzie· 1 shared D. V. Manatakis· 1 shared G. Hamilton· 1 shared G. Luo· 1 shared H. Park· 1 shared J. Eom· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperCell Biology

A. R. Nookala

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2 papers

Recent·Most cited

Assessment of Human Renal Transporter Based Drug-Drug Interactions Using Proximal Tubule Kidney-Chip

A. R. Nookala, J. Ronxhi, J. Sliz, S. Jeanty, D. V. Manatakis, S. Jadalannagari, G. Hamilton, H. Park, Y. He, M. Lavarias, G. Luo, K. Jang, D. McKenzie

This study develops a human Proximal Tubule Kidney-Chip to assess renal transporter-based drug-drug interactions and demonstrates its ability to predict clinical outcomes and clearance values.

bioRxiv · May 12, 2022 · PreprintCell Biology

Ex vivo therapeutic base and prime editing using chemically derived hepatic progenitors in a mouse model of tyrosinemia type 1

Y. Kim, J. Yu, S.-A. Hong, J. Eom, K. Jang, S.-N. Lee, J.-S. Woo, J. Jeong, S. Bae, D. Choi

This study corrects a disease-causing mutation in a mouse model of tyrosinemia type 1 using ex vivo base and prime editing with chemically derived hepatic progenitors, improving survival rates.

bioRxiv · Sep 14, 2020 · PreprintCell Biology