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Paul M Smith

Showing results (31-40 of 41) with videos related to

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Frontiers in Physiology|June 26, 2023
Structural analysis of mitochondrial rRNA gene variants identified in patients with deafnessAntón Vila-Sanjurjo, Natalia Mallo, Joanna L Elson, et al.
Biochimica Et Biophysica Acta|October 3, 2003
Bridging PNAs can bind preferentially to a deleted mitochondrial DNA template but replication by mitochondrial DNA polymerase gamma in vitro is not impairedAlistair McGregor, Paul M Smith, Günther F Ross, et al.
European Journal of Biochemistry|June 26, 2003
Specific targeting of a DNA-alkylating reagent to mitochondria. Synthesis and characterization of [4-((11aS)-7-methoxy-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-on-8-oxy)butyl]-triphenylphosphonium iodideAndrew M James, Frances H Blaikie, Robin A J Smith, et al.
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Journal of Sports Sciences|January 16, 2013
Effects of playing surface on physiological responses and performance variables in a controlled football simulationMichael G Hughes, Laurence Birdsey, Rob Meyers, et al.
Mitochondrion|September 9, 2015
The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human diseaseJoanna L Elson, Paul M Smith, Laura C Greaves, et al.
The EMBO Journal|February 27, 2010
A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosomeRicarda Richter, Joanna Rorbach, Aleksandra Pajak, et al.
Journal of Inherited Metabolic Disease|December 15, 2010
Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutationsUlrike Schara, Jürgen-Christoph von Kleist-Retzow, Elke Lainka, et al.
Human Molecular Genetics|October 5, 2013
The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potentialPaul M Smith, Joanna L Elson, Laura C Greaves, et al.
Brain : a Journal of Neurology|December 21, 2010
Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiencyJohn P Kemp, Paul M Smith, Angela Pyle, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Frontiers in Physiology|June 26, 2023
Structural analysis of mitochondrial rRNA gene variants identified in patients with deafnessAntón Vila-Sanjurjo, Natalia Mallo, Joanna L Elson, et al.
Biochimica Et Biophysica Acta|October 3, 2003
Bridging PNAs can bind preferentially to a deleted mitochondrial DNA template but replication by mitochondrial DNA polymerase gamma in vitro is not impairedAlistair McGregor, Paul M Smith, Günther F Ross, et al.
European Journal of Biochemistry|June 26, 2003
Specific targeting of a DNA-alkylating reagent to mitochondria. Synthesis and characterization of [4-((11aS)-7-methoxy-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-on-8-oxy)butyl]-triphenylphosphonium iodideAndrew M James, Frances H Blaikie, Robin A J Smith, et al.
Human Molecular Genetics|July 2, 2013
Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiencyVeronika Boczonadi, Paul M Smith, Angela Pyle, et al.
Journal of Sports Sciences|January 16, 2013
Effects of playing surface on physiological responses and performance variables in a controlled football simulationMichael G Hughes, Laurence Birdsey, Rob Meyers, et al.
Mitochondrion|September 9, 2015
The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human diseaseJoanna L Elson, Paul M Smith, Laura C Greaves, et al.
The EMBO Journal|February 27, 2010
A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosomeRicarda Richter, Joanna Rorbach, Aleksandra Pajak, et al.
Journal of Inherited Metabolic Disease|December 15, 2010
Acute liver failure with subsequent cirrhosis as the primary manifestation of TRMU mutationsUlrike Schara, Jürgen-Christoph von Kleist-Retzow, Elke Lainka, et al.
Human Molecular Genetics|October 5, 2013
The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potentialPaul M Smith, Joanna L Elson, Laura C Greaves, et al.
Brain : a Journal of Neurology|December 21, 2010
Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiencyJohn P Kemp, Paul M Smith, Angela Pyle, et al.
Pageof 5