Hana Antonicka

Hana Antonicka

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Hana Antonicka

Hana Antonicka

Publications by authors named "Hana Antonicka"

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Stomatin-like protein 2 deficiency results in impaired mitochondrial translation.

PLoS One 2017 27;12(6):e0179967. Epub 2017 Jun 27.

Microbiome and Disease Tolerance Centre, Department of Microbiology and Immunology, McGill University, Montreal, Quebec, Canada.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0179967PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5487072PMC
September 2017

A pseudouridine synthase module is essential for mitochondrial protein synthesis and cell viability.

EMBO Rep 2017 01 14;18(1):28-38. Epub 2016 Dec 14.

Department of Human Genetics, Montreal Neurological Institute, McGill University, Montreal, QC, Canada

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http://dx.doi.org/10.15252/embr.201643391DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210091PMC
January 2017

A Mutation in the Flavin Adenine Dinucleotide-Dependent Oxidoreductase FOXRED1 Results in Cell-Type-Specific Assembly Defects in Oxidative Phosphorylation Complexes I and II.

Mol Cell Biol 2016 08 29;36(16):2132-40. Epub 2016 Jul 29.

Montreal Neurological Institute and Department of Human Genetics, McGill University, Montreal, Quebec, Canada

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http://dx.doi.org/10.1128/MCB.00066-16DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4968213PMC
August 2016

Mitochondrial RNA Granules Are Centers for Posttranscriptional RNA Processing and Ribosome Biogenesis.

Cell Rep 2015 Feb 13;10(6):920-932. Epub 2015 Feb 13.

Montreal Neurological Institute and Department of Human Genetics, McGill University, Montreal, QC H3A 2B4, Canada. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2015.01.030DOI Listing
February 2015

Tissue-specific responses to the LRPPRC founder mutation in French Canadian Leigh Syndrome.

Hum Mol Genet 2015 Jan 11;24(2):480-91. Epub 2014 Sep 11.

Montreal Neurological Institute and Department of Human Genetics, McGill University, Montreal, QC H3A 2B4, Canada

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http://dx.doi.org/10.1093/hmg/ddu468DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4275074PMC
January 2015

Novel mutations in SCO1 as a cause of fatal infantile encephalopathy and lactic acidosis.

Hum Mutat 2013 Oct 12;34(10):1366-70. Epub 2013 Aug 12.

Department of Biochemistry, University of Saskatchewan, Saskatoon, Canada.

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http://dx.doi.org/10.1002/humu.22385DOI Listing
October 2013

The mitochondrial RNA-binding protein GRSF1 localizes to RNA granules and is required for posttranscriptional mitochondrial gene expression.

Cell Metab 2013 Mar;17(3):386-98

Montreal Neurological Institute and Department of Human Genetics, McGill University, Montreal, QC H3A 2B4, Canada.

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http://dx.doi.org/10.1016/j.cmet.2013.02.006DOI Listing
March 2013

LRPPRC and SLIRP interact in a ribonucleoprotein complex that regulates posttranscriptional gene expression in mitochondria.

Mol Biol Cell 2010 Apr 3;21(8):1315-23. Epub 2010 Mar 3.

Department of Human Genetics, Montreal Neurological Institute, McGill University, Montreal, QC, H3A 2B4, Canada.

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http://www.molbiolcell.org/doi/10.1091/mbc.e10-01-0047
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http://dx.doi.org/10.1091/mbc.e10-01-0047DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854090PMC
April 2010

The A3243G tRNALeu(UUR) MELAS mutation causes amino acid misincorporation and a combined respiratory chain assembly defect partially suppressed by overexpression of EFTu and EFG2.

Hum Mol Genet 2008 Dec 27;17(23):3697-707. Epub 2008 Aug 27.

Montreal Neurological Institute, Montreal, QC, Canada.

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http://dx.doi.org/10.1093/hmg/ddn265DOI Listing
December 2008

A sequence predicted to form a stem-loop is proposed to be required for formation of an RNA-protein complex involving the 3'UTR of beta-subunit F0F1-ATPase mRNA.

Biochim Biophys Acta 2008 Jul-Aug;1777(7-8):747-57. Epub 2008 Jun 4.

The Wenner-Gren Institute, The Arrhenius Laboratories F3, Stockholm University, SE-106 91 Stockholm, Sweden.

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http://dx.doi.org/10.1016/j.bbabio.2008.05.446DOI Listing
August 2008

The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1.

Hum Mol Genet 2006 Jun 21;15(11):1835-46. Epub 2006 Apr 21.

Montreal Neurological Institute, McGill University, 3801 University Street, Montreal, Quebec, Canada.

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http://dx.doi.org/10.1093/hmg/ddl106DOI Listing
June 2006

Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency.

N Engl J Med 2004 Nov;351(20):2080-6

Nijmegen Center for Mitochondrial Disorders, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1056/NEJMoa041878DOI Listing
November 2004

Mutations in COX10 result in a defect in mitochondrial heme A biosynthesis and account for multiple, early-onset clinical phenotypes associated with isolated COX deficiency.

Hum Mol Genet 2003 Oct 19;12(20):2693-702. Epub 2003 Aug 19.

Montreal Neurological Institute, Department of Human Genetics, McGill University, Montreal, H3A 2B4, Canada.

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http://dx.doi.org/10.1093/hmg/ddg284DOI Listing
October 2003

Identification and characterization of a common set of complex I assembly intermediates in mitochondria from patients with complex I deficiency.

J Biol Chem 2003 Oct 26;278(44):43081-8. Epub 2003 Aug 26.

Montreal Neurological Institute and Department of Human Genetics, McGill University, Montreal, Quebec, Canada H3A 2B4.

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http://dx.doi.org/10.1074/jbc.M304998200DOI Listing
October 2003