Mitochondrial parts, pathways, and pathogenesis by Calvo, Sarah E

Get full text

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.

Get full text

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

Get full text

Comparative RNA editing in autistic and neurotypical cerebella by Eran, A., Li, J. B., Vatalaro, K., McCarthy, J., Rahimov, F., Collins, C., Markianos, K., Margulies, David M., Calvo, Sarah E., Kohane, Isaac, Kunkel, Louis M., Brown, Emery N.

Get full text
Get full text

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

Get full text
Get full text