Author

C. Kwon

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

Biology Disciplines

Click to filter author papers

Cell Biology· 3 Biochemistry· 1 Cancer Biology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 4 Approach:experimental assay· 3 Organism:mouse· 3 Approach:deep learning· 2 Research Focus:differential expression· 2 Assay:proteomics· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2

Frequent Co-Authors

S. Kannan· 3 shared K. E. Mahoney· 2 shared M. Miyamoto· 2 shared P. Andersen· 2 shared S. A. Malaker· 2 shared T. M. Lucas· 2 shared A. D. Steigmeyer· 1 shared A. Kervadec· 1 shared

Activity by Year

2019-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersCell Biology

S. Kannan

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

False positive glycopeptide identification via in-FAIMS fragmentation

V. Rangel-Angarita, K. E. Mahoney, C. Kwon, R. Sarker, T. M. Lucas, S. A. Malaker

This study identifies a phenomenon called 'in FAIMS fragmentation' that increases spectral matches in glycopeptide analysis, highlighting potential benefits and limitations of FAIMS for O-glycoproteomics.

bioRxiv · May 28, 2023 · PreprintBiochemistry

Glycoproteomic landscape and structural dynamics of TIM family immune checkpoints enabled by mucinase SmE

J. Chongsaritsinsuk, A. D. Steigmeyer, K. E. Mahoney, M. A. Rosenfeld, T. M. Lucas, D. Ince, F. L. Kearns, A. S. Battison, M. A. Hollenhorst, J. Shon, K. H. Tiemeyer, V. Attah, C. Kwon, C. R. Bertozzi, M. J. Ferracane, , S. A. Malaker

The paper uses a mucinase to analyze glycoproteomic features of TIM family proteins and shows how glycosylation affects their structure through molecular dynamics simulations.

bioRxiv · Feb 1, 2023Cancer Biology

Conserved Transcription Factors Control Chromatin Accessibility and Gene Expression to Maintain Cell Fate Stability and Restrict Reprogramming of Differentiated Cells

M. A. Missinato, S. A. Murphy, M. Lynott, A. Kervadec, M. S. Yu, Y.-L. Chang, S. Kannan, M. Loreti, C. Lee, P. Amatya, H. Tanaka, C.-T. Huang, P. L. Puri, C. Kwon, P. D. Adams, , A. R. Colas

This study identifies four conserved transcription factors that oppose cell fate reprogramming by controlling chromatin accessibility and gene expression, and shows their potential as therapeutic targets for regenerative medicine.

bioRxiv · Jun 28, 2021 · PreprintCell Biology

Trajectory reconstruction identifies dysregulation of perinatal maturation programs in pluripotent stem cell-derived cardiomyocytes

S. Kannan, M. Miyamoto, B. L. Lin, C. Kwon

This study compares in vivo and in vitro cardiomyocyte maturation using single-cell RNA-seq, identifying dysregulated transcription factors in pluripotent stem cell-derived cardiomyocytes.

bioRxiv · Jan 31, 2021Cell Biology

Large particle fluorescence-activated cell sorting enables high quality single cell RNA-sequencing and functional analysis of adult cardiomyocytes

S. Kannan, M. Miyamoto, B. Lin, R. Zhu, S. Murphy, D. Kass, P. Andersen, C. Kwon

This study demonstrates that large-particle fluorescence-activated cell sorting (LP-FACS) improves the isolation of viable adult cardiomyocytes, enabling high-quality single-cell RNA sequencing and functional analysis.

bioRxiv · May 30, 2019Cell Biology