Author

B. S. Mallon

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· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 3 Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:drug response / drug discovery· 1 Assay:electronic health records· 1 Research Focus:metabolism & bioenergetics· 1

Frequent Co-Authors

D. Maric· 2 shared K. G. Chen· 2 shared K. Park· 2 shared P. G. Robey· 2 shared A. R. Nickolls· 1 shared C. G. Bonnemann· 1 shared F. Yang· 1 shared K. J. Johnson· 1 shared

Activity by Year

2019-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 22 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

2 shared papersBiochemistry

D. Maric

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Metabolic Quadrivalency in RSeT Human Embryonic Stem Cells

K. G. Chen, K. Park, D. Maric, K. R. Johnson, P. G. Robey, B. S. Mallon

This study identifies a unique metabolic state in RSeT human embryonic stem cells characterized by quadrivalency, linking it to growth independence from oxygen and resistance to naive reprogramming.

bioRxiv · Feb 21, 2024 · PreprintBiochemistry

Resistance to Naive and Formative Pluripotency Conversion in RSeT Human Embryonic Stem Cells

K. G. Chen, K. J. Johnson, K. Park, D. Maric, F. Yang, W. F. Liu, Y. C. Fann, B. S. Mallon, P. G. Robey

This study characterizes a new pluripotent state in RSeT hESCs, showing resistance to naive and formative conversion and distinct transcriptomic and signaling features.

bioRxiv · Feb 16, 2024 · PreprintCell Biology

Human embryoid bodies model basal lamina assembly and muscular dystrophy

A. R. Nickolls, M. M. Lee, K. Zukosky, B. S. Mallon, C. G. Bonnemann

This study uses human induced pluripotent stem cells to generate embryoid bodies that model basal lamina formation and dystroglycanopathy-related ECM defects in muscular dystrophies.

bioRxiv · Sep 10, 2019 · PreprintCell Biology