Timothy J. Maher

Massachusetts College of Pharmacy and Health Sciences 
Pharmacology, Toxicology, Neuroscience Biology
"Timothy Maher"
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Takeda AJ, Maher TJ, Zhang Y, et al. (2019) Human PI3Kγ deficiency and its microbiota-dependent mouse model reveal immunodeficiency and tissue immunopathology. Nature Communications. 10: 4364
Ye Q, Trivedi M, Zhang Y, et al. (2018) Brain iron loading impairs DNA methylation and alters GABAergic function in mice. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. fj201801116RR
Gugnani KS, Vu N, Rondón-Ortiz AN, et al. (2017) Neuroprotective activity of macamides on manganese-induced mitochondrial disruption in U-87 MG glioblastoma cells. Toxicology and Applied Pharmacology
Rondón-Ortiz AN, Lino Cardenas CL, Martínez-Málaga J, et al. (2017) High Concentrations of Rosiglitazone Reduce mRNA and Protein Levels of LRP1 in HepG2 Cells. Frontiers in Pharmacology. 8: 772
Batran RZ, Dawood DH, El-Seginy SA, et al. (2017) Coumarinyl pyranopyrimidines as new neuropeptide S receptor antagonists; design, synthesis, homology and molecular docking. Bioorganic Chemistry. 75: 274-290
Batran RZ, Dawood DH, El-Seginy SA, et al. (2017) New Coumarin Derivatives as Anti-Breast and Anti-Cervical Cancer Agents Targeting VEGFR-2 and p38α MAPK. Archiv Der Pharmazie
Towiwat P, Phattanarudee S, Maher TJ, et al. (2015) Modulation of inducible nitric oxide synthase (iNOS) expression and cardiovascular responses during static exercise following iNOS antagonism within the ventrolateral medulla. Molecular and Cellular Biochemistry. 398: 185-94
Nofal ZM, Soliman EA, Abd El-Karim SS, et al. (2014) Synthesis of some new benzimidazole-thiazole derivatives as anticancer agents Journal of Heterocyclic Chemistry. 51: 1797-1806
Wu H, Kelley CJ, Pino-Figueroa A, et al. (2013) Macamides and their synthetic analogs: evaluation of in vitro FAAH inhibition. Bioorganic & Medicinal Chemistry. 21: 5188-97
Almukadi H, Wu H, Böhlke M, et al. (2013) The macamide N-3-methoxybenzyl-linoleamide is a time-dependent fatty acid amide hydrolase (FAAH) inhibitor. Molecular Neurobiology. 48: 333-9
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