Author

John C. Biber

University at Buffalo, State University of New YorkORCID 0009-0004-6483-1628Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genomics· 2

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:mouse· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Bat‐Ider TumenbayariD· 2 shared Khanh PhamiD· 2 shared Yongho BaeiD· 2 shared Joseph A. Brazzo· 1 shared Peng YaoiD· 1 shared Rhonda DrewesiD· 1 shared Vincent M. TutinoiD· 1 shared

Activity by Year

2024-2024 · peak 2/yr

Co-Author Collaboration Network

7 top collaborators · 18 mutual co-author links

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2 shared papersGenomics

Bat‐Ider TumenbayarORCID

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2 papers

Recent·Most cited

GenomicsCytoskeletonPeer-reviewedDec 9, 2024

FAK and p130Cas modulate stiffness-mediated early transcription and cellular metabolism

Bat‐Ider Tumenbayar, Khanh Pham, John C. Biber…·Yongho Bae

This study shows that FAK and p130Cas modulate early transcription and metabolism in response to substrate stiffness using RNA sequencing in mouse cells.

5 citations

mousebulk RNA-seq

𝕏 PostBluesky

GenomicsIEEE Transactions on Molecular Biological and Multi-Scale CommunicationsPeer-reviewedNov 18, 2024

Transcriptomic and multi-scale network analyses reveal key drivers of cardiovascular disease

Bat‐Ider Tumenbayar, Khanh Pham, John C. Biber…·Yongho Bae

The paper analyzes gene expression and protein networks in vascular injury models to show similarities with cardiovascular disease mechanisms.

1 citation

mousebulk RNA-seq

𝕏 PostBluesky