Joseph P. Marino, Ph.D.

Affiliations: 
Chemistry and Biochemistry University of Notre Dame, Notre Dame, IN, United States 
Area:
Synthetic Chemistry
Website:
http://chemistry.nd.edu/faculty/detail/jmarino/#bio
Google:
"Joseph P. Marino"
Bio:

http://chemistry.library.nd.edu/resources/genealogy/chemistry/documents/MarinoJP.pdf
http://um2017.org/faculty-history/faculty/joseph-p-marino
http://chemistry.nd.edu/people/joseph-p-marino/

Cross-listing: Chemistry Tree

Parents

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Roy Arne Olofson grad student 1968 Harvard (Chemistry Tree)
 (Oxysulfonium cations)
Robert B. Woodward post-doc 1967-1969 Harvard (Chemistry Tree)

Children

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Robert S. Paley grad student 1986 University of Michigan (Chemistry Tree)
Fábio Cohen Tucci grad student 1992-1993 Notre Dame (Chemistry Tree)
Paulo Henrique Menezes da Silva grad student 1996-1997 University of Michigan (Chemistry Tree)
Luis Henrique Sanfelice Rahmeier grad student 1996-1997 Michigan - Ann Arbor (Chemistry Tree)
Russell J. Linderman grad student 2002 University of Michigan (Chemistry Tree)
Ganfeng Cao grad student 2005 University of Michigan (Chemistry Tree)
José Tércio Barbosa Ferreira research scientist 1991-1991 Universidade Federal de Sao Carlos (Chemistry Tree)

Collaborators

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João V. Comasseto collaborator 1985-2006 Notre Dame (Chemistry Tree)
BETA: Related publications

Publications

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Seo K, Rainer PP, Shalkey Hahn V, et al. (2014) Combined TRPC3 and TRPC6 blockade by selective small-molecule or genetic deletion inhibits pathological cardiac hypertrophy. Proceedings of the National Academy of Sciences of the United States of America. 111: 1551-6
Seo K, Rainer PP, Hahn VS, et al. (2014) Combined TRPC3 and TRPC6 blockade by selective small-molecule or genetic deletion inhibits pathological cardiac hypertrophy (Proceedings of the National Academy of Sciences of the United States of America (2014) 111, 4, (1551-1556) doi:10.1073/pnas.1308963111) Proceedings of the National Academy of Sciences of the United States of America. 111: 6115
Washburn DG, Holt DA, Dodson J, et al. (2013) The discovery of potent blockers of the canonical transient receptor channels, TRPC3 and TRPC6, based on an anilino-thiazole pharmacophore. Bioorganic & Medicinal Chemistry Letters. 23: 4979-84
Thalji RK, McAtee JJ, Belyanskaya S, et al. (2013) Discovery of 1-(1,3,5-triazin-2-yl)piperidine-4-carboxamides as inhibitors of soluble epoxide hydrolase. Bioorganic & Medicinal Chemistry Letters. 23: 3584-8
Silveira GP, Marino JP. (2013) Enantioselective synthesis of dihydro-1H-benzindoles. The Journal of Organic Chemistry. 78: 3379-83
Podolin PL, Bolognese BJ, Foley JF, et al. (2013) In vitro and in vivo characterization of a novel soluble epoxide hydrolase inhibitor. Prostaglandins & Other Lipid Mediators. 104: 25-31
Morgan LA, Olzinski AR, Upson JJ, et al. (2013) Soluble epoxide hydrolase inhibition does not prevent cardiac remodeling and dysfunction after aortic constriction in rats and mice. Journal of Cardiovascular Pharmacology. 61: 291-301
Kompa AR, Wang BH, Xu G, et al. (2013) Soluble epoxide hydrolase inhibition exerts beneficial anti-remodeling actions post-myocardial infarction. International Journal of Cardiology. 167: 210-9
Marino JP, Kieler KA, Kim MW. (2011) An enantioselective synthesis of (-)-4-hydroxy-6-methoxy-3a,8a- dihydrofuro[2,3-b]benzofuran: An advanced intermediate in the synthesis of (-)-aflatoxin B1 and G1 Tetrahedron. 67: 837-841
Thalji RK, Aiyar N, Davenport EA, et al. (2010) Benzofuran-substituted urea derivatives as novel P2Y(1) receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 20: 4104-7
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