Upstream open reading frames cause widespread reduction of protein expression and are polymorphic among humans by Calvo, Sarah E., Pagliarini, David J., Mootha, Vamsi K.

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Purifying Selection against Pathogenic Mitochondrial DNA in Human T Cells by Walker, Melissa A, Lareau, Caleb A, Ludwig, Leif S, Karaa, Amel, Sankaran, Vijay G, Regev, Aviv, Mootha, Vamsi K

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Proteomic Mapping of Mitochondria in Living Cells via Spatially Restricted Enzymatic Tagging by Martell, Jeffrey Daniel, Ting, Alice Y., Rhee, Hyun-Woo, Zou, Peng, Udeshi, Namrata D., Mootha, Vamsi K., Carr, Steven A.

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A plasma signature of human mitochondrial disease revealed through metabolic profiling of spent media from cultured muscle cells by Shaham, Oded, Slate, Nancy G., Goldberger, Olga A., Xu, Qiuwei, Ramanathan, Arvind, Souza, Amanda, Clish, Clary, Sims, Katherine, Mootha, Vamsi K.

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Directed evolution of APEX2 for electron microscopy and proximity labeling by Kamer, Kimberli J, Deerinck, Thomas J, Ellisman, Mark H, Mootha, Vamsi K, Lam, Stephanie Shih-Min, Martell, Jeffrey Daniel, Ting, Alice Y

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Engineered ascorbate peroxidase as a genetically encoded reporter for electron microscopy by Deerinck, Thomas J., Sancak, Yasemin, Poulos, Thomas L., Mootha, Vamsi K., Sosinsky, Gina E., Ellisman, Mark H., Martell, Jeffrey Daniel, Ting, Alice Y.

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Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial disease by Lieber Daniel S, Vafai Scott B, Horton Laura C, Slate Nancy G, Liu Shangtao, Borowsky Mark L, Calvo Sarah E, Schmahmann Jeremy D, Mootha Vamsi K

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MICU2, a Paralog of MICU1, Resides within the Mitochondrial Uniporter Complex to Regulate Calcium Handling by Plovanich, Molly, Bogorad, Roman, Sancak, Yasemin, Kamer, Kimberli J., Strittmatter, Laura, Li, Andrew A., Girgis, Hany S., Kuchimanchi, Satya, Groot, Jack De, Speciner, Lauren, Taneja, Nathan, OShea, Jonathan, Kotelianski, Victor E., Mootha, Vamsi K.

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Mitochondrial dysfunction remodels one-carbon metabolism in human cells by Bao, Xiaoyan Robert, Ong, Shao-En, Goldberger, Olga, Peng, Jun, Sharma, Rohit, Thompson, Dawn A, Vafai, Scott B, Cox, Andrew G, Marutani, Eizo, Ichinose, Fumito, Goessling, Wolfram, Carr, Steven A, Clish, Clary B, Mootha, Vamsi K, Regev, Aviv

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Mutations in MTFMT Underlie a Human Disorder of Formylation Causing Impaired Mitochondrial Translation by Tucker, Elena J., Hershman, Steven G., Belcher-Timme, Casey A., Patel, Jinal, Goldberger, Olga A., Christodoulou, John, Silberstein, Jonathon M., McKenzie, Matthew, Ryan, Michael T., Compton, Alison G., Jaffe, Jacob D., Carr, Steven A., Calvo, Sarah E., RajBhandary, Uttam L., Thorburn, David R., Mootha, Vamsi K., Koehrer, Caroline

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How many human proteoforms are there? by Aebersold, Ruedi, Agar, Jeffrey N, Amster, I Jonathan, Baker, Mark S, Bertozzi, Carolyn R, Boja, Emily S, Costello, Catherine E, Cravatt, Benjamin F, Fenselau, Catherine, Garcia, Benjamin A, Ge, Ying, Gunawardena, Jeremy, Hendrickson, Ronald C, Hergenrother, Paul J, Huber, Christian G, Ivanov, Alexander R, Jensen, Ole N, Jewett, Michael C, Kelleher, Neil L, Krogan, Nevan J, Larsen, Martin R, Loo, Joseph A, Ogorzalek Loo, Rachel R, Lundberg, Emma, MacCoss, Michael J, Mallick, Parag, Mootha, Vamsi K, Mrksich, Milan, Muir, Tom W, Patrie, Steven M, Pesavento, James J, Pitteri, Sharon J, Rodriguez, Henry, Saghatelian, Alan, Sandoval, Wendy, Schlüter, Hartmut, Sechi, Salvatore, Slavoff, Sarah A, Smith, Lloyd M, Snyder, Michael P, Thomas, Paul M, Uhlén, Mathias, Van Eyk, Jennifer E, Vidal, Marc, Walt, David R, White, Forest M, Williams, Evan R, Wohlschlager, Therese, Wysocki, Vicki H, Yates, Nathan A, Young, Nicolas L, Zhang, Bing, Kiessling, Laura L

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