Author

G. Post

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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Cancer Biology· 2 Immunology· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:non-human primate· 2 Approach:statistical model· 2 Assay:whole-exome sequencing· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:clustering· 1

Frequent Co-Authors

A. Miller· 1 shared A. Ruhe· 1 shared A. Sekulic· 1 shared B. Davis· 1 shared B. Lewis· 1 shared C. Khanna· 1 shared C. Legendre· 1 shared C. Lopes· 1 shared

Activity by Year

2017-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCancer Biology

A. Miller

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3 papers

Recent·Most cited

Shared hotspot mutations in spontaneously arising cancers position dog as an unparalleled comparative model for precision therapeutics

L. Rodrigues, J. Watson, Y. Feng, B. Lewis, G. Harvey, G. Post, K. Megquier, L. Lambert, A. Miller, C. Lopes, S. Zhao

This study identifies shared hotspot mutations in canine and human cancers, highlighting dogs as a valuable model for precision cancer therapeutics.

bioRxiv · Oct 22, 2021 · PreprintCancer Biology

Rad52 mediates class-switch DNA recombination to IgD

Y. Xu, H. Zhou, G. Post, H. Zan, P. Casali

This paper identifies Rad52's role in facilitating class-switch DNA recombination to IgD through microhomology-mediated alternative end joining, involving Zfp318 modulation and phosphorylation.

bioRxiv · Jun 28, 2021Immunology

Somatic inactivating PTPRJ mutations and dysregulated pathways identified in canine melanoma by integrated comparative genomic analysis

W. P. D. Hendricks, V. Zismann, K. Sivaprakasam, C. Legendre, K. Poorman, W. Tembe, J. Kiefer, W. Liang, V. DeLuca, M. Stark, A. Ruhe, R. Froman, N. Duesbury, M. Washington, J. Aldrich, , J. Trent

This study identifies somatic PTPRJ mutations and dysregulated pathways in canine melanoma through genomic analysis, revealing similarities with human melanoma subtypes and potential therapeutic targets.

bioRxiv · Sep 30, 2017Cancer Biology