Author

Sydney M. Escobar

Amgen (United States)ORCID 0009-0004-2957-9244Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Research Focus:host-pathogen & immune response· 1 Approach:statistical model· 1

Frequent Co-Authors

Benjamin J. CryeriD· 1 shared Brian J. ThomasiD· 1 shared Chi-Ming LiiD· 1 shared Daniel LuiD· 1 shared Donald H. BurkeiD· 1 shared Edwin Lamas· 1 shared Heather A. ArnettiD· 1 shared Hong ZhouiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperCancer Biology

Benjamin J. CryerORCID

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2 papers

Recent·Most cited

DUSP11 is an intracellular innate immune checkpoint in lung adenocarcinoma

Brian J. Thomas, Xue Bai, Benjamin J. Cryer, Sydney M. Escobar, Lee‐Ann H. Allen, Mark A. Daniëls, Margaret J. Lange, Donald H. Burke

This study identifies DUSP11 as an intracellular innate immune checkpoint in LUAD, showing its role in tumor survival and growth, and suggests it as a potential therapeutic target.

Cancer Immunology Research · Sep 4, 2025Peer-reviewedCancer Biology

Limited differential expression of miRNAs and other small RNAs in LPS-stimulated human monocytes

Daniel Lu, Tracy Yamawaki, Hong Zhou, Wen-Yu Chou, Mark Chhoa, Edwin Lamas, Sydney M. Escobar, Heather A. Arnett, Huanying Ge, Todd Juan, Songli Wang, Chi-Ming Li

The paper profiles small RNA expression in LPS-stimulated human monocytes and identifies a limited set of miRNAs upregulated during inflammation.

PLoS ONE · Mar 25, 2019Peer-reviewedGenomics