mTOR hyperactivity mediates lysosomal dysfunction in Gaucher's disease iPSC-neuronal cells von Brown, Robert A, Voit, Antanina, Srikanth, Manasa P, Thayer, Julia A, Kingsbury, Tami J, Jacobson, Marlene A, Lipinski, Marta M, Feldman, Ricardo A, Awad, Ola

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Disparate bone anabolic cues activate bone formation by regulating the rapid lysosomal degradation of sclerostin protein von Gould, Nicole R., Williams, Katrina M., Joca, Humberto C., Torre, Olivia M., Lyons, James S., Leser, Jenna M., Srikanth, Manasa P., Hughes, Marcus, Khairallah, Ramzi J., Feldman, Ricardo A., Ward, Christopher W., Stains, Joseph P.

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Altered Differentiation Potential of Gaucher’s Disease iPSC Neuronal Progenitors due to Wnt/β-Catenin Downregulation von Awad, Ola, Panicker, Leelamma M., Deranieh, Rania M., Srikanth, Manasa P., Brown, Robert A., Voit, Antanina, Peesay, Tejasvi, Park, Tea Soon, Zambidis, Elias T., Feldman, Ricardo A.

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Altered Differentiation Potential of Gaucherâs Disease iPSC Neuronal Progenitors due to Wnt/β-Catenin Downregulation von Ola Awad, Leelamma M. Panicker, Rania M. Deranieh, Manasa P. Srikanth, Robert A. Brown, Antanina Voit, Tejasvi Peesay, Tea Soon Park, Elias T. Zambidis, Ricardo A. Feldman

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Characterization of succinate dehydrogenase flavoprotein from Staphylococcus aureus ATCC 12600 von V, Swarupa, S, Yeswanth, UV, Prasad, D, Vasu, K, Venkatesh, L, Srikanth, P, Anitha, C, Manasa, P, Santhosh Kumar, G, Sowjenya, Y, Nandakumar, A, Chaudhary, PVGK, Sarma

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