For a complete list of publications, search Pubmed.

  1. 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. (doi: 10.1073/pnas.1806296115).
  2. 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. (doi: 10.1074/jbc.RA118.004014).
  3. 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.
  4. 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. 
  5. 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. 
  6. 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.
  7. 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
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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