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Ronald J. Moore

Researcher at Pacific Northwest National Laboratory

Publications -  185
Citations -  16228

Ronald J. Moore is an academic researcher from Pacific Northwest National Laboratory. The author has contributed to research in topics: Proteome & Proteomics. The author has an hindex of 57, co-authored 171 publications receiving 13299 citations. Previous affiliations of Ronald J. Moore include G. D. Searle & Company & University of California, Los Angeles.

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Journal Article

Antiangiogenic and Antitumor Activities of Cyclooxygenase-2 Inhibitors

TL;DR: Evidence that cyclooxygenase (COX)-2-derived prostaglandins contribute to tumor growth by inducing newly formed blood vessels (neoangiogenesis) that sustain tumor cell viability and growth and a novel application of this anti-inflammatory drug in the treatment of human cancer is provided.
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Toward a Human Blood Serum Proteome Analysis By Multidimensional Separation Coupled With Mass Spectrometry

TL;DR: This study has performed the most extensive analysis of serum proteins to date and laid the foundation for future refinements in the identification of novel protein biomarkers of disease.
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Integrated Proteogenomic Characterization of Human High-Grade Serous Ovarian Cancer

TL;DR: A view of how the somatic genome drives the cancer proteome and associations between protein and post-translational modification levels and clinical outcomes in HGSC is provided.
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Reversed‐phase chromatography with multiple fraction concatenation strategy for proteome profiling of human MCF10A cells

TL;DR: The results demonstrate that the concatenated high pH reversed‐phased strategy is an attractive alternative to strong cation exchange for two‐dimensional shotgun proteomic analysis of trypsin‐digested human MCF10A cell sample.
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Proteogenomic Analysis of Human Colon Cancer Reveals New Therapeutic Opportunities.

Suhas Vasaikar, +82 more
- 02 May 2019 - 
TL;DR: Comparative proteomic and phosphoproteomic analysis of paired tumor and normal adjacent tissues produced a catalog of colon cancer-associated proteins and phosphosites, including known and putative new biomarkers, drug targets, and cancer/testis antigens, which suggested glycolysis as a potential target to overcome the resistance of MSI-H tumors to immune checkpoint blockade.