Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

4,396 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1.
Leary SC, Sasarman F, Nishimura T, Shoubridge EA. Leary SC, et al. Among authors: nishimura t. Hum Mol Genet. 2009 Jun 15;18(12):2230-40. doi: 10.1093/hmg/ddp158. Epub 2009 Mar 31. Hum Mol Genet. 2009. PMID: 19336478
COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux.
Leary SC, Cobine PA, Nishimura T, Verdijk RM, de Krijger R, de Coo R, Tarnopolsky MA, Winge DR, Shoubridge EA. Leary SC, et al. Among authors: nishimura t. Mol Biol Cell. 2013 Mar;24(6):683-91. doi: 10.1091/mbc.E12-09-0705. Epub 2013 Jan 23. Mol Biol Cell. 2013. PMID: 23345593 Free PMC article.
An N-terminal formyl methionine on COX 1 is required for the assembly of cytochrome c oxidase.
Hinttala R, Sasarman F, Nishimura T, Antonicka H, Brunel-Guitton C, Schwartzentruber J, Fahiminiya S, Majewski J, Faubert D, Ostergaard E, Smeitink JA, Shoubridge EA. Hinttala R, et al. Among authors: nishimura t. Hum Mol Genet. 2015 Jul 15;24(14):4103-13. doi: 10.1093/hmg/ddv149. Epub 2015 Apr 24. Hum Mol Genet. 2015. PMID: 25911677 Free PMC article.
Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome.
Sasarman F, Nishimura T, Antonicka H, Weraarpachai W, Shoubridge EA; LSFC Consortium. Sasarman F, et al. Among authors: nishimura t. Hum Mol Genet. 2015 Jan 15;24(2):480-91. doi: 10.1093/hmg/ddu468. Epub 2014 Sep 11. Hum Mol Genet. 2015. PMID: 25214534 Free PMC article.
The mitochondrial RNA-binding protein GRSF1 localizes to RNA granules and is required for posttranscriptional mitochondrial gene expression.
Antonicka H, Sasarman F, Nishimura T, Paupe V, Shoubridge EA. Antonicka H, et al. Among authors: nishimura t. Cell Metab. 2013 Mar 5;17(3):386-98. doi: 10.1016/j.cmet.2013.02.006. Cell Metab. 2013. PMID: 23473033
The conserved interaction of C7orf30 with MRPL14 promotes biogenesis of the mitochondrial large ribosomal subunit and mitochondrial translation.
Fung S, Nishimura T, Sasarman F, Shoubridge EA. Fung S, et al. Among authors: nishimura t. Mol Biol Cell. 2013 Feb;24(3):184-93. doi: 10.1091/mbc.E12-09-0651. Epub 2012 Nov 21. Mol Biol Cell. 2013. PMID: 23171548 Free PMC article.
An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect.
Janer A, Antonicka H, Lalonde E, Nishimura T, Sasarman F, Brown GK, Brown RM, Majewski J, Shoubridge EA. Janer A, et al. Among authors: nishimura t. Am J Hum Genet. 2012 Oct 5;91(4):737-43. doi: 10.1016/j.ajhg.2012.08.020. Epub 2012 Sep 27. Am J Hum Genet. 2012. PMID: 23022098 Free PMC article.
A novel mutation in YARS2 causes myopathy with lactic acidosis and sideroblastic anemia.
Sasarman F, Nishimura T, Thiffault I, Shoubridge EA. Sasarman F, et al. Among authors: nishimura t. Hum Mutat. 2012 Aug;33(8):1201-6. doi: 10.1002/humu.22098. Epub 2012 May 7. Hum Mutat. 2012. PMID: 22504945
Mutations in C12orf62, a factor that couples COX I synthesis with cytochrome c oxidase assembly, cause fatal neonatal lactic acidosis.
Weraarpachai W, Sasarman F, Nishimura T, Antonicka H, Auré K, Rötig A, Lombès A, Shoubridge EA. Weraarpachai W, et al. Among authors: nishimura t. Am J Hum Genet. 2012 Jan 13;90(1):142-51. doi: 10.1016/j.ajhg.2011.11.027. Am J Hum Genet. 2012. PMID: 22243966 Free PMC article.
Chemogenomic profiling predicts antifungal synergies.
Jansen G, Lee AY, Epp E, Fredette A, Surprenant J, Harcus D, Scott M, Tan E, Nishimura T, Whiteway M, Hallett M, Thomas DY. Jansen G, et al. Among authors: nishimura t. Mol Syst Biol. 2009;5:338. doi: 10.1038/msb.2009.95. Epub 2009 Dec 22. Mol Syst Biol. 2009. PMID: 20029371 Free PMC article.
4,396 results
Jump to page
Feedback