Mark T. Quinn

Affiliations: 
Veterinary Molecular Biology Montana State University, Bozeman, MT 
Area:
Molecular Biology, Immunology
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"Mark Quinn"
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Publications

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Crocetti L, Giovannoni MP, Cantini N, et al. (2020) Novel Sulfonamide Analogs of Sivelestat as Potent Human Neutrophil Elastase Inhibitors. Frontiers in Chemistry. 8: 795
Kirpotina LN, Schepetkin IA, Hammaker D, et al. (2020) Therapeutic Effects of Tryptanthrin and Tryptanthrin-6-Oxime in Models of Rheumatoid Arthritis. Frontiers in Pharmacology. 11: 1145
Crocetti L, Vergelli C, Guerrini G, et al. (2020) Novel formyl peptide receptors (FPRs) agonists with pyridinone and pyrimidindione scaffolds that are potentially useful for the treatment of rheumatoid arthritis. Bioorganic Chemistry. 100: 103880
Kibler E, Lavrinenko A, Kolesnik I, et al. (2020) Electrosprayed poly(lactic-co-glycolic acid) particles as a promising drug delivery system for the novel JNK inhibitor IQ-1. European Polymer Journal. 127
Siemsen DW, Kirpotina LN, Malachowa N, et al. (2020) Isolation of Neutrophils from Nonhuman Species. Methods in Molecular Biology (Clifton, N.J.). 2087: 43-59
Stankevich KS, Schepetkin IA, Goreninskii SI, et al. (2019) Poly(ε-caprolactone) Scaffolds Doped with c-Jun N-terminal Kinase Inhibitors Modulate Phagocyte Activation. Acs Biomaterials Science & Engineering. 5: 5990-5999
Giovannoni MP, Crocetti L, Cantini N, et al. (2019) New 3-unsubstituted isoxazolones as potent human neutrophil elastase inhibitors: Synthesis and molecular dynamic simulation. Drug Development Research
Giovannoni MP, Cantini N, Crocetti L, et al. (2019) Further modifications of 1H-pyrrolo[2,3-b]pyridine derivatives as inhibitors of human neutrophil elastase. Drug Development Research
Schepetkin IA, Khlebnikov AI, Potapov AS, et al. (2018) Synthesis, biological evaluation, and molecular modeling of 11H-indeno[1,2-b]quinoxalin-11-one derivatives and tryptanthrin-6-oxime as c-Jun N-terminal kinase inhibitors. European Journal of Medicinal Chemistry. 161: 179-191
Schepetkin IA, Kirpotina LN, Mitchell PT, et al. (2017) The natural sesquiterpene lactones arglabin, grosheimin, agracin, parthenolide, and estafiatin inhibit T cell receptor (TCR) activation. Phytochemistry. 146: 36-46
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