For a complete list of publications, search Pubmed 
  1. Guthrie, L.M., Soma, S., Yuan, S., Silva, A., Zulkifli, M., Snavely, T.C., Greene, H.F., Nunez, E., Lynch, B., De Ville, C., Shanbhag, V., Lopez, F.R., Acharya, A., Petris, M.J., Kim, B.E., Gohil, V.M., Sacchettini, J.C. (2020) Elesclomol alleviates Menkes pathology and mortality by escorting Cu to cuproenzymes in mice. Science. 368(6491):620-625.
  2. Iadarola, D.M., Ball, W.B., Trivedi, P.P., Fu, G., Nan, B., Gohil, V.M. (2020) Vps39 is required for ethanolamine-stimulated elevation in mitochondrial phosphatidylethanolamine. Biochim Biophys Acta Mol Cell Biol Lipids. 1865(6):158655.
  3. Soma, S., Morgada, M.N., Naik, M.T., Boulet, A., Roesler, A.A., Dziuba,N., Ghosh, A., Yu, Q., Lindahl, P.A., Ames, J.B., Leary, S.C., Vila, A.J., Gohil, V.M. (2019) COA6 Is Structurally Tuned to Function as a Thiol-Disulfide Oxidoreductase in Copper Delivery to Mitochondrial Cytochrome c Oxidase.  Cell Reports.  29(12):4114-4126.e5.
  4. Ghosh S., Iadarola D.M., Ball W.B., Gohil V.M. (2019) Mitochondrial Dysfunctions in Barth Syndrome. IUBMB Life. 71: 791-801. 
  5. Soma, S., Latimer, A.J., Chun, H., Vicary, A.C., Timbalia, S.A., Boulet, A., Rahn, J.J., Chan, S.S.L., Leary, S.C., Kim, B.-E., Gitlin, J.D., Gohil, V.M. (2018) Elesclomol restores mitochondrial function in genetic models of copper deficiency. Proc. Natl. Acad. Sci. U.S.A. 115: 8161-6.
  6. Ball, W.B., Baker, C.D., Neff, J.K., Apfel, G.L., Lagerborg, K.A., Zun, G., Petrovic, U., Jain, M., Gohil, V.M. (2018) Ethanolamine ameliorates mitochondrial dysfunction in cardiolipin-deficient yeast cells. J. Biol. Chem. 293: 10870-83.
  7. Ball, W.B., Neff, J.K., Gohil, V.M. (2017) The role of nonbilayer phospholipids in mitochondrial structure and function. FEBS Lett. 592: 1273-290.
  8. Baker, C.D., Ball, W.B., Pryce, E.N., Gohil, V.M. (2016) Specific requirements of non-bilayer phospholipids in mitochondrial respiratory chain function and formation. Mol. Biol. Cell. 27: 2161-171. 
  9. Tomar, D., Dong, Z., Shanmughapriya, S., Koch, D.A., Thomas, T., Hoffman, N.E., Timbalia, S.A., Goldman, S.J., Breves, S.L., Corbally, D.P., Nemani, N., Fairweather, J.P., Cutri, A.R., Zhang, X., Song, J., Jaña, F., Huang, J., Barrero, C., Rabinowitz, J., Luongo, T., Schumacher, S.M., Rockman, M.E., Dietrich, A., Merali, S., Caplan, J., Stathopulos, P., Ahima, R.S., Cheung, J.Y., Houser, S.R., Koch, W.J., Patel, V., Gohil, V.M., Elrod, J.W., Sudarsan, R., Madesh, M. (2016) MCUR1 Is a scaffold factor for the MCU complex function and promotes mitochondrial bioenergetics. Cell Reports. 15: 1673–685. 
  10. Ghosh, A., Pratt, A.T., Soma, S., Theriault, S.G., Griffin, A.T., Trivedi, P.P., Gohil, V.M. (2015) Mitochondrial disease genes COA6, COX6B and SCO2 have overlapping roles in COX2 biogenesis. Hum. Mol. Genet. 25: 660-71.
  11. Kishi, S., Campanholle, G., Gohil, V.M., Perocchi, G., Brooks, C.R., Morizane, R., Sabbisetti, V., Ichimura, T., Mootha, V.K., Bonventre, J.V. (2015) Meclizine preconditioning protects the kidney against ichemia-reperfusion injury. EBioMedicine. 9: 1090-101.
  12. Ghosh, A., Trivedi, P.P., Timbalia, S.A., Griffin, A.T., Rahn, J.J., Chan, S.S.L., Gohil, V.M. (2014) Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency. Hum. Mol. Genet. 23: 3596-606.
  13. Jhurry, N.D., Chakrabarti, M., McCormick, S.P., Gohil, V.M., Lindahl, P.A. (2013) Mössbauer study and modeling of iron import and trafficking in human Jurkat cells. Biochemistry 52: 7926-942.
  14. Gohil, V.M., Zhu, L., Baker, C.D., Cracan, V., Yaseen, A., Jain, M., Clish, C.B., Brookes, P.S., Bakovic, M., Mootha, V.K. (2013) Meclizine inhibits mitochondrial respiration through direct targeting of cytosolic phosphoethanolamine metabolism. J. Biol. Chem. 288: 5387-395.
  15. Patil, V.A., Fox, J.L., Gohil, V.M., Winge, D.R., & Greenberg, M.L. (2013) Loss of cardiolipin leads to perturbation of mitochondrial and cellular iron homeostasis. J. Biol. Chem. 288: 1696-705.
  16. Gohil, V.M., Offner, N., Walker, J.A., Sheth, S.A., Fossale, E., Gusella, J.F., MacDonald, M.E., Neri, C., Mootha, V.K. (2011) Meclizine is neuroprotective in models of Huntington’s disease. Hum. Mol. Genet. 20: 294-300.
  17. Perocchi, F., Gohil, V.M., Girgis, H.S., Bao, X.R., McCombs, J.E., Palmer, A.E., Mootha, V.K. (2010) MICU1 encodes a mitochondrial EF hand protein required for Ca(2+) uptake. Nature 467: 291-6.
  18. Gohil, V.M., Nilsson, R., Belcher-Timme, C.A., Luo, B., Root, D.E., Mootha, V.K. (2010) Mitochondrial and nuclear genomic responses to loss of LRPPRC expression. J. Biol. Chem 285: 13742-7.
  19. Gohil, V.M., Sheth, S.A., Nilsson, R., Wojtovich, A.P., Lee, J.H., Perocchi, F., Chen, W., Clish, C.B., Ayata, C., Brookes, P.S., Mootha, V.K. (2010) Nutrient-sensitized screening for drugs that shift energy metabolism from mitochondrial respiration to glycolysis. Nat. Biotechnol. 28: 249-55.
Elesclomol alleviates Menkes pathology and mortality by escorting Cu to cuproenzymes in mice.