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2015
A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh Syndrome.Thompson Legault, J., Strittmatter L., Tardif J., Sharma R., Tremblay-Vaillancourt V., Aubut C., Boucher G., Clish CB, Cyr D., Daneault C., Waters PJ, LSFC Consortium, Vachon L., Morin C., Laprise C., Rioux JD, Mootha VK, and Des Rosiers C. Cell reports, 2015/11/03, Volume 13, Issue 5, p.981-9, (2015) Read More / View Supplemental Materials
Abstract
2014
Metabolic enzyme expression highlights a key role for MTHFD2 and the mitochondrial folate pathway in cancer.Nilsson, R., Jain M., Madhusudhan N., Sheppard NG, Strittmatter L., Kampf C., Huang J., Asplund A., and Mootha VK Nature communications, 2014/01/23, Volume 5, p.3128, (2014) Read More / View Supplemental Materials
Abstract
2013
MICU2, a Paralog of MICU1, Resides within the Mitochondrial Uniporter Complex to Regulate Calcium Handling.Plovanich, M., Bogorad RL, Sancak Y., Kamer KJ, Strittmatter L., Li AA, Girgis HS, Kuchimanchi S., De Groot J., Speciner L., Taneja N., Oshea J., Koteliansky V., and Mootha VK PloS one, 2013/01/01, Volume 8, Issue 2, p.e55785, (2013) Read More / View Supplemental Materials
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2012
Metabolic consequences of mitochondrial coenzyme A deficiency in patients with PANK2 mutations.Leoni, V., Strittmatter L., Zorzi G., Zibordi F., Dusi S., Garavaglia B., Venco P., Caccia C., Souza AL, Deik A., Clish CB, Rimoldi M., Ciusani E., Bertini E., Nardocci N., Mootha VK, and Tiranti V. Molecular genetics and metabolism, 2012/03/01, Volume 105, Issue 3, p.463-71, (2012) Read More / View Supplemental Materials
Abstract
2011
Integrative genomics identifies MCU as an essential component of the mitochondrial calcium uniporter.Baughman, JM, Perocchi F., Girgis HS, Plovanich M., Belcher-Timme CA, Sancak Y., Bao XR, Strittmatter L., Goldberger O., Bogorad RL, Koteliansky V., and Mootha VK Nature, 2011/06/19, Volume 476, Issue 7360, p.341-5, (2011) Read More / View Supplemental Materials
Abstract
  • Showing 1-5 of 5 Results