Shankar K. Sankarappa

Author

The Ohio State University

Also Known As

S. K. SANKARAPPA, S. K. Sankarappa, S. Sankarappa, S.K. Sankarappa, Shankar K. Sankarappa, Shankar Sankarappa

Publications

976

Citations

H-Index

Concepts

All Affiliations

The Ohio State University

About

Shankar K. Sankarappa is an author at The Ohio State University specializing in biochemistry, pharmacology, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	6	6	867
2	Medicine	4	4	836
3	Natural Sciences	4	4	740
4	Engineering	2	2	29
5	Health Sciences	1	1	61

Shankar K. Sankarappa

Publications

917

Citations

H-Index

Page 1

	Year	Citations
The metabolism of 7,10,13,16,19-docosapentaenoic acid to 4,7,10,13,16,19-docosahexaenoic acid in rat liver is independent of a 4-desaturase. Anne Voss, Meri Reinhart, Shankar K. Sankarappa, Journal of Biological Chemistry 4,7,10,13,16,19-Docosahexaenoic AcidBiosynthesisHepatotoxicity7,10,13,16,19-Docosapentaenoic AcidAlcohol Dehydrogenases	1991	661
Studies to determine if rat liver contains chain-length-specific acyl-CoA 6-desaturases M. Geiger, B. Selma Mohammed, Shankar K. Sankarappa, Biochimica et Biophysica Acta (BBA) - Lipids and Lipid Metabolism HepatologyBiochemistryMedicineLiver PhysiologyPathology	1993	66
Reevaluation of the Pathway for the Metabolism of 7,10,13,16-Docosatetraenoic Acid to 4,7,10,13,16-Docosapentaenoic Acid in Rat-Liver B.S. Mohammed, Shankar K. Sankarappa, Michelle Geiger, Archives of Biochemistry and Biophysics BiosynthesisAldehyde DehydrogenaseBiochemistry4,7,10,13,16-Docosapentaenoic AcidLiver Physiology	1995	61
Selective inhibitors of platelet lipoxygenase: 4,7,10,13-icosatetraynoic acid and 5,8,11,14-henicosatetraynoic acid Teresa Emily Wilhelm, Shankar K. Sankarappa, Mike VanRollins, Prostaglandins ThrombopoiesisThrombosisMedicinal ChemistryBiochemistryBlood Platelet	1981	48
Synthesis of ethyl 6-substituted-chroman- and -chromone-2-carboxylates. Comparative structure-activity study employing the 6-phenyl and phenoxy analogs in the triton hyperlipidemic rat model Donald T. Witiak, William P. Heilman, Shankar K. Sankarappa, Journal of Medicinal Chemistry	1975	36
Delta four acetylenic acids — selective inhibitors of the formation of slow reacting substance Barbara A. Jakschik, Denise M. Disantis, Shankar K. Sankarappa, Biochemical and Biophysical Research Communications Medicinal ChemistrySlow Reacting SubstanceBiochemistryNatural SciencesDelta Four	1981	16
1-Acetyl-6-oxo-8a-methyl-3,4,6,7,8,8a-hexahydronaphthalene<sup>1</sup> Melvin S. Newman, S. Ramachandran, Shankar K. Sankarappa, The Journal of Organic Chemistry Chemical MeasurementEngineeringChemical AnalysisBiochemistryDonut Icon	1961	15
Acid-Catalyzed Rearrangements of Some Bicyclic δ-Hydroxy-α,β-enones S. Swaminathan, R. Natarajan, S. Ramachandran, The Journal of Organic Chemistry EngineeringDonut IconAltmetric Attention ScoreOrganic ChemistrySocial Media Presence	1966	14

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