For a complete list of publications, search Pubmed.

  1. Ghosh S., Iadarola D.M., Ball W.B., Gohil V.M. (2019) Mitochondrial Dysfunctions in Barth Syndrome. IUBMB Life. (doi: 10.1002/iub.2018). 
  2. 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.
  3. 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.
  4. 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.
  5. 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. 
  6. 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. 
  7. 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.
  8. 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.
  9. 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.
  10. 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.
  11. 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.
  12. 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.
  13. 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.
  14. 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.
  15. 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.
  16. 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.