The Mitochondrial RNA-Binding Protein GRSF1 Localizes to RNA Granules and Is Required for Posttranscriptional Mitochondrial Gene Expression
Antonicka, Hana, Sasarman, Florin, Nishimura, Tamiko, Paupe, Vincent, Shoubridge, Eric A.
Published in Cell metabolism (05.03.2013)
Published in Cell metabolism (05.03.2013)
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Journal Article
MITRAC Links Mitochondrial Protein Translocation to Respiratory-Chain Assembly and Translational Regulation
Mick, David U., Dennerlein, Sven, Wiese, Heike, Reinhold, Robert, Pacheu-Grau, David, Lorenzi, Isotta, Sasarman, Florin, Weraarpachai, Woranontee, Shoubridge, Eric A., Warscheid, Bettina, Rehling, Peter
Published in Cell (21.12.2012)
Published in Cell (21.12.2012)
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Journal Article
Mutation in TACO1 , encoding a translational activator of COX I, results in cytochrome c oxidase deficiency and late-onset Leigh syndrome
Chevrette, Mario, Antonicka, Hana, Weraarpachai, Woranontee, Sasarman, Florin, Shoubridge, Eric A, Schrank, Bertold, Kaufman, Brett A, Kolesar, Jill E, Lochmüller, Hanns, Horvath, Rita, Seeger, Jürgen
Published in Nature genetics (01.07.2009)
Published in Nature genetics (01.07.2009)
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Journal Article
Mitochondrial Diseases and Cardiomyopathies
Brunel-Guitton, Catherine, MD, Levtova, Alina, MD, Sasarman, Florin, PhD
Published in Canadian journal of cardiology (01.11.2015)
Published in Canadian journal of cardiology (01.11.2015)
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Journal Article
Radioactive labeling of mitochondrial translation products in cultured cells
Sasarman, Florin, Shoubridge, Eric A
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2012)
Published in Methods in molecular biology (Clifton, N.J.) (01.01.2012)
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Journal Article
Mutations in the mitochondrial methionyl-tRNA synthetase cause a neurodegenerative phenotype in flies and a recessive ataxia (ARSAL) in humans
Bayat, Vafa, Thiffault, Isabelle, Jaiswal, Manish, Tétreault, Martine, Donti, Taraka, Sasarman, Florin, Bernard, Geneviève, Demers-Lamarche, Julie, Dicaire, Marie-Josée, Mathieu, Jean, Vanasse, Michel, Bouchard, Jean-Pierre, Rioux, Marie-France, Lourenco, Charles M, Li, Zhihong, Haueter, Claire, Shoubridge, Eric A, Graham, Brett H, Brais, Bernard, Bellen, Hugo J
Published in PLoS biology (01.03.2012)
Published in PLoS biology (01.03.2012)
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Journal Article
Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency
Coenen, Marieke J.H, Antonicka, Hana, Ugalde, Cristina, Sasarman, Florin, Rossi, Rainer, Heister, J.G.A.M. Angelien, Newbold, Robert F, Trijbels, Frans J.M.F, van den Heuvel, Lambert P, Shoubridge, Eric A, Smeitink, Jan A.M
Published in The New England journal of medicine (11.11.2004)
Published in The New England journal of medicine (11.11.2004)
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Journal Article
The P174L Mutation in Human Sco1 Severely Compromises Cox17-dependent Metallation but Does Not Impair Copper Binding
Cobine, Paul A., Pierrel, Fabien, Leary, Scot C., Sasarman, Florin, Horng, Yih-Chern, Shoubridge, Eric A., Winge, Dennis R.
Published in The Journal of biological chemistry (05.05.2006)
Published in The Journal of biological chemistry (05.05.2006)
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Journal Article
LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondria
Sasarman, Florin, Brunel-Guitton, Catherine, Antonicka, Hana, Wai, Timothy, Shoubridge, Eric A
Published in Molecular biology of the cell (15.04.2010)
Published in Molecular biology of the cell (15.04.2010)
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Journal Article
The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translation
Fung, Stephen, Nishimura, Tamiko, Sasarman, Florin, Shoubridge, Eric A
Published in Molecular biology of the cell (01.02.2013)
Published in Molecular biology of the cell (01.02.2013)
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Journal Article
A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia
Sasarman, Florin, Nishimura, Tamiko, Thiffault, Isabelle, Shoubridge, Eric A.
Published in Human mutation (01.08.2012)
Published in Human mutation (01.08.2012)
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Journal Article
Biosynthesis of glycosaminoglycans: associated disorders and biochemical tests
Sasarman, Florin, Maftei, Catalina, Campeau, Philippe M., Brunel-Guitton, Catherine, Mitchell, Grant A., Allard, Pierre
Published in Journal of Inherited Metabolic Disease (01.03.2016)
Published in Journal of Inherited Metabolic Disease (01.03.2016)
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Book Review
Mutations in C12orf62, a Factor that Couples COX I Synthesis with Cytochrome c Oxidase Assembly, Cause Fatal Neonatal Lactic Acidosis
Weraarpachai, Woranontee, Sasarman, Florin, Nishimura, Tamiko, Antonicka, Hana, Auré, Karine, Rötig, Agnès, Lombès, Anne, Shoubridge, Eric A.
Published in American journal of human genetics (13.01.2012)
Published in American journal of human genetics (13.01.2012)
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Journal Article
The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1
Antonicka, Hana, Sasarman, Florin, Kennaway, Nancy G., Shoubridge, Eric A.
Published in Human molecular genetics (01.06.2006)
Published in Human molecular genetics (01.06.2006)
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Journal Article
A Metabolic Signature of Mitochondrial Dysfunction Revealed through a Monogenic Form of Leigh Syndrome
Thompson Legault, Julie, Strittmatter, Laura, Tardif, Jessica, Sharma, Rohit, Tremblay-Vaillancourt, Vanessa, Aubut, Chantale, Boucher, Gabrielle, Clish, Clary B., Cyr, Denis, Daneault, Caroline, Waters, Paula J., Aliskashani, Azadeh, Allen, Bruce G., Aubut, Chantale, Beauchamp, Claudine, Bemeur, Chantal, Burelle, Yan, Charron, Guy, Coderre, Lise, Des Rosiers, Christine, Deschênes, Sonia, Labarthe, François, Landry, Jeannine, Laprise, Catherine, Lavallée, Geneviève, Lavoie, Pierre, Maranda, Bruno, Morin, Charles, Mukaneza, Yvette, Nishimura, Tamiko, Rioux, John D., Rivard, Marie-Ève, Sasarman, Florin, Shoubridge, Eric A., Tardif, Jessica, Thompson Legault, Julie, Tremblay, Nancy, Tremblay-Vaillancourt, Vanessa, Vachon, Luc, Villeneuve, Josée, Vachon, Luc, Morin, Charles, Laprise, Catherine, Rioux, John D., Mootha, Vamsi K., Des Rosiers, Christine
Published in Cell reports (Cambridge) (03.11.2015)
Published in Cell reports (Cambridge) (03.11.2015)
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Journal Article
An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect
JANER, Alexandre, ANTONICKA, Hana, LALONDE, Emilie, NISHIMURA, Tamiko, SASARMAN, Florin, BROWN, Garry K, BROWN, Ruth M, MAJEWSKI, Jacek, SHOUBRIDGE, Eric A
Published in American journal of human genetics (05.10.2012)
Published in American journal of human genetics (05.10.2012)
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Journal Article
Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect
Antonicka, Hana, Østergaard, Elsebet, Sasarman, Florin, Weraarpachai, Woranontee, Wibrand, Flemming, Pedersen, Anne Marie B., Rodenburg, Richard J., van der Knaap, Marjo S., Smeitink, Jan A.M., Chrzanowska-Lightowlers, Zofia M., Shoubridge, Eric A.
Published in American journal of human genetics (09.07.2010)
Published in American journal of human genetics (09.07.2010)
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