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Browsing publications by Professor Zofia Chrzanowska-Lightowlers.

Newcastle AuthorsTitleYearFull text
Matt Zorkau
Dr Christin Albus
Dr Rolando Berlinguer Palmini
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
et al.
High-resolution imaging reveals compartmentalisation of mitochondrial protein synthesis in cultured human cells2021
Dr Francesco Bruni
Yasmin Proctor-Kent
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Messenger RNA delivery to mitoribosomes: hints from a bacterial toxin2021
Dr Christin Albus
Dr Rolando Berlinguer Palmini
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Matthew Zorkau
et al.
Mitochondrial Translation Occurs preferentially in the Peri-Nuclear Mitochondrial Network of Cultured Human Cells2021
Matt Zorkau
Yasmin Proctor-Kent
Dr Rolando Berlinguer Palmini
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
et al.
Visualizing Mitochondrial Ribosomal RNA and Mitochondrial Protein Synthesis in Human Cell Lines2021
Dr Francesco Bruni
Dr Langping He
Professor Robert Taylor
Professor Zofia Chrzanowska-Lightowlers
Biallelic Mutations in MTPAP Associated with a Lethal Encephalophy2020
Professor Zofia Chrzanowska-Lightowlers
Breaking a single hydrogen bond in the mitochondrial tRNAPhe-PheRS complex leads to phenotypic pleiotropy of human disease2020
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Dr Oliver Russell
Mitochondrial transplantation—a possible therapeutic for mitochondrial dysfunction?: Mitochondrial transfer is a potential cure for many diseases but proof of efficacy and safety is still lacking2020
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Redecorating the Mitochondrial Inner Membrane: A Treatment for mtDNA Disorders2020
Dr Shreya Ayyub
Dr Fei Gao
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Rescuing stalled mammalian mitoribosomes - what can we learn from bacteria?2020
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
How much does a disrupted mitochondrial network influence neuronal dysfunction?2019
Dr Rawaa Al-Faresi
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Mammalian mitochondrial translation - revealing consequences of divergent evolution2019
Dr Kyle Thompson
Dr Monika Olahova
Dr Filippo Scialo
Dr Nichola Lax
Dr Fiona Robertson
et al.
OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect2018
Dr Francesco Bruni
Professor Bobby McFarland
Professor Zofia Chrzanowska-Lightowlers
Dr Langping He
Professor Robert Taylor
et al.
Clinical, biochemical and genetic features associated with VARS2-related mitochondrial disease2018
Christie Waddington
Ewen Sommerville
Sila Hopton
Dr Angela Pyle
Professor Zofia Chrzanowska-Lightowlers
et al.
Defective mitochondrial protease LonP1 can cause classical mitochondrial disease2018
Dr Fei Gao
Maria Wesolowska
Dr Conor Lawless
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
Using mitoribosomal profiling to investigate human mitochondrial translation [version 2; referees: 2 approved]2018
Dr Fei Gao
Professor Zofia Chrzanowska-Lightowlers
Autophagy impairment with lysosomal and mitochondrial dysfunction is an important characteristic of oxidative stress-induced senescence2017
Dr Monika Olahova
Dr Kyle Thompson
Dr Charlotte Alston
Professor Patrick Chinnery
Professor Zofia Chrzanowska-Lightowlers
et al.
Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies2017
Dr Francesco Bruni
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Human mitochondrial nucleases2017
Professor Zofia Chrzanowska-Lightowlers
Dr Joanna Rorbach
Human mitochondrial ribosomes can switch structural tRNAs – but when and why?2017
Professor Zofia Chrzanowska-Lightowlers
Kinetic and structural changes in H smtPheRS, induced by pathogenic mutations in human FARS22017
Dr Monika Olahova
Dr Kyle Thompson
Dr Steven Hardy
Maria-Eleni Anagnostou
Dr Kathryn White
et al.
Pathogenic variants in HTRA2 cause an early-onset mitochondrial syndrome associated with 3-methylglutaconic aciduria2017
Professor Rita Horvath
Dr Hue Hornig - Do
Professor Zofia Chrzanowska-Lightowlers
Store-Operated Ca2+ Entry Controls Induction of Lipolysis and the Transcriptional Reprogramming to Lipid Metabolism2017
Dr Agata Rozanska
Dr Joanna Rorbach
Dr Fei Gao
Professor Rick Lewis
Professor Zofia Chrzanowska-Lightowlers
et al.
The human RNA-binding protein RBFA promotes the maturation of the mitochondrial ribosome2017
Dr Agata Rozanska
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
The pseudouridine synthase RPUSD4 is an essential component of mitochondrial RNA granules2017
Dr Fei Gao
Maria Wesolowska
Dr Conor Lawless
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
Using mitoribosomal profiling to investigate human mitochondrial translation2017
Dr Joanna Rorbach
Dr Fei Gao
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Human mitochondrial ribosomes can switch their structural RNA composition2016
Dr Agata Rozanska
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
SLIRP stabilizes LRPPRC via an RRM-PPR protein interface2016
Nicole Mai
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
The process of mammalian mitochondrial protein synthesis2016
Dr Monika Olahova
Dr Steven Hardy
Dr John Yarham
William Wilson
Dr Charlotte Alston
et al.
LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population2015
Dr Monika Olahova
Dr Charlotte Alston
Jess Houghton
Dr Langping He
Dr Andrew Morris
et al.
A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency2015
Maria Wesolowska
Professor Grainne Gorman
Dr Charlotte Alston
Aleksandra Pajak
Dr Angela Pyle
et al.
Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease2015
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Response to "Ribosome Rescue and Translation Termination at Non-standard Stop Codons by ICT1 in Mammalian Mitochondria"2015
Dr Joanna Elson
Dr Paul Smith
Dr Laura Greaves
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease2015
William Wilson
Dr Hue Hornig - Do
Dr Francesco Bruni
Professor Rick Lewis
Dr Loraine Hewitt
et al.
A human mitochondrial poly(A) polymerase mutation reveals the complexities of post-transcriptional mitochondrial gene expression2014
Dr Hue Hornig - Do
Dr Arianna Montanari
Dr Agata Rozanska
Dr Helen Tuppen
Abdulraheem Almalki
et al.
Human mitochondrial leucyl tRNA synthetase can suppress non cognate pathogenic mt-tRNA mutations2014
Professor Robert Lightowlers
Dr Agata Rozanska
Professor Zofia Chrzanowska-Lightowlers
Mitochondrial protein synthesis: Figuring the fundamentals, complexities and complications, of mammalian mitochondrial translation2014
Abdulraheem Almalki
Dr Charlotte Alston
Dr Mojgan Reza
Professor Robert Lightowlers
Professor Bobby McFarland
et al.
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency2014
Maria Wesolowska
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Overcoming stalled translation in human mitochondria2014
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Salvaging hope: Is increasing NAD+ a key to treating mitochondrial myopathy?2014
Dr Mateusz Wydro
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
GRSF1 Regulates RNA Processing in Mitochondrial RNA Granules2013
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Human pentatricopeptide proteins: Only a few and what do they do?2013
Ricarda Richter
Professor Zofia Chrzanowska-Lightowlers
Interactions between peptidyl tRNA hydrolase homologs and the ribosomal release factor Mrf1 in S. pombe mitochondria2013
Dr Agata Rozanska
Professor Zofia Chrzanowska-Lightowlers
Mutations in mitochondrial ribosomal protein MRPL12 leads to growth retardation, neurological deterioration and mitochondrial translation deficiency2013
Dr Francesco Bruni
Dr Pasqua Gramegna
Dr Jorge Oliveira
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
REXO2 is an oligoribonuclease active in human mitochondria2013
Dr Paul Smith
Dr Joanna Elson
Dr Laura Greaves
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
The role of the mitochondrial ribosome in human disease: Searching for mutations in 12S mitochondrial rRNA with high disruptive potential2013
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Exploring our origins-the importance of OriL in mtDNA maintenance and replication2012
Dr Christine Challen
Dr John Anderson
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Professor John Lunec
et al.
Recombinant human MDM2 oncoprotein shows sequence composition selectivity for binding to both RNA and DNA2012
Dr Veronika Boczonadi
Dr Paul Smith
Kamil Sitarz
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
et al.
Studying the molecular basis of the reversibility in infantile reversible cytochrome c oxidase deficiency2012
Dr Francesco Bruni
Dr Pasqua Gramegna
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
The mystery of mitochondrial RNases2012
Dr Angela Pyle
Vivienne Neeve
Dr Helen Tuppen
Professor Hanns Lochmuller
Professor Bobby McFarland
et al.
Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency2011
Professor Zofia Chrzanowska-Lightowlers
Alexksandra Pajak
Professor Robert Lightowlers
Termination of Protein Synthesis in Mammalian Mitochondria2011
Ricarda Richter
Dr Joanna Rorbach
Aleksandra Pajak
Dr Paul Smith
Professor Robert Lightowlers
et al.
A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome2010
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Defective Mitochondrial mRNA Maturation Is Associated with Spastic Ataxia2010
Dr Vanessa Hogan
Dr Langping He
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Taylor
Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy2010
Sven Dennerlein
Dr Agata Rozanska
Dr Mateusz Wydro
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
et al.
Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit.2010
Dr Richard Temperley
Dr Mateusz Wydro
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Human mitochondrial mRNAs - like members of all families, similar but different2010
Dr Richard Temperley
Ricarda Richter
Sven Dennerlein
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
Hungry Codons Promote Frameshifting in Human Mitochondrial Ribosomes2010
Professor Rita Horvath
Dr Helen Tuppen
Dr Gavin Hudson
Dr Angela Pyle
Dr Paul Smith
et al.
Infantile reversible COX deficiency myopathy caused by the m.14674T > C mutation in mt-tRNA(Glu) in a German family2010
Sven Dennerlein
Dr Paul Smith
Dr Agata Rozanska
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
Knowing when to stop - human mitochondrial translation termination2010
Professor Zofia Chrzanowska-Lightowlers
Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect2010
Dr Mateusz Wydro
Agnieszka Bobrowicz
Dr Richard Temperley
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
Targeting of the cytosolic poly(A) binding protein PABPC1 to mitochondria causes mitochondrial translation inhibition2010
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Terminating human mitochondrial protein synthesis : a shift in our thinking2010
Dr Helen Tuppen
Dr Vanessa Hogan
Dr Langping He
Dr Mazhor Aldosary
Dr Gabriele Saretzki
et al.
The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families2010
Sven Dennerlein
Dr Agata Rozanska
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Translation termination in human mitochondrial ribosomes2010
Professor Zofia Chrzanowska-Lightowlers
Professor John Hesketh
Fine mapping of interactions between eEF1 alpha protein and 3 ' UTR of metallothionein-1 mRNA2009
Dr Petter Sanaker
Professor Zofia Chrzanowska-Lightowlers
Dr Vanessa Hogan
Professor Robert Taylor
G.P.11.01: RNA processing differences explain tissue specificity in exercise intolerance myopathy due to ISCU intronic mutation2009
Professor Rita Horvath
Dr Helen Tuppen
Dr Gavin Hudson
Dr Angela Pyle
Dr Paul Smith
et al.
Molecular basis of infantile reversible cytochrome c oxidase deficiency myopathy2009
Dr Pierre Boesch
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Mitochondrial DNA and Diseases2008
Dr Joanna Rorbach
Dr Helen Tuppen
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Taylor
Emeritus Professor Doug Turnbull
et al.
Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation2008
Agnieszka Bobrowicz
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Polyadenylation and degradation of mRNA in mammalian mitochondria: A missing link?2008
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
PPR (pentatricopeptide repeat) proteins in mammals: important aids to mitochondrial gene expression.2008
Dr Joanna Rorbach
Dr Mateusz Wydro
Marcin Pekalski
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
et al.
The human mitochondrial ribosome recycling factor is essential for cell viability2008
Dr Joanna Rorbach
Dr Hamid Reza Soleimanpour Lichaei
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
How do mammalian mitochondria synthesize proteins?2007
Dr Hamid Reza Soleimanpour Lichaei
Dr Joao Passos
Dr Mateusz Wydro
Dr Joanna Rorbach
Dr Richard Temperley
et al.
mtRF1a Is a Human Mitochondrial Translation Release Factor Decoding the Major Termination Codons UAA and UAG2007
Dr Ian Mickleburgh
Dr Herve Chabanon
David Nury
Brian Burtle
Professor Zofia Chrzanowska-Lightowlers
et al.
Elongation factor 1α binds to the region of the metallothionein-1 mRNA implicated in perinuclear localization - Importance of an internal stem-loop2006
Dr Debbie Pye
Dimitra-Smaragda Kyriakouli
Geoffrey Taylor
Dr Matthias Elstner
Professor Zofia Chrzanowska-Lightowlers
et al.
Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants2006
Dr Kate Rennie
Dr Matthias Elstner
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Doug Turnbull
Professor Robert Taylor
et al.
Sporadic intragenic inversion of the mitochondrial DNA MTND1 gene causing fatal infantile lactic acidosis2006
Professor Zofia Chrzanowska-Lightowlers
Professor John Hesketh
Annexin A2 binds to the localization signal in the 3′ untranslated region of c-myc mRNA2005
Dr Richard Temperley
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Serum-deprivation stimulates cap-binding by PARN at the expense of eIF4E, consistent with the observed decrease in mRNA stability2005
Professor Bobby McFarland
Dr Debbie Pye
Dr Michael Glanville
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Doug Turnbull
et al.
A homoplasmic mtDNA mutation promotes rapid decay of deacylated mt-tRNAVal2004
Professor Robert Taylor
Dr Margaret Johnson
Professor Zofia Chrzanowska-Lightowlers
Dr Andrew Morris
Emeritus Professor Doug Turnbull
et al.
A novel point mutation in the mitochondrial tRNA(Trp) gene produces a neurogastrointestinal syndrome2004
Professor Zofia Chrzanowska-Lightowlers
Dr Richard Temperley
Dr Paul Smith
Professor Robert Lightowlers
Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codons2004
Professor Zofia Chrzanowska-Lightowlers
Dr Richard Temperley
Professor Robert Lightowlers
Human mitochondria possess a translation-dependent deadenylation decay pathway2004
Dr Ian Mickleburgh
Brian Burtle
David Nury
Dr Herve Chabanon
Professor Zofia Chrzanowska-Lightowlers
et al.
Isolation and identification of a protein binding to the localization element of Metallothionein-1 mRNA2004
Dr Richard Temperley
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Messenger RNA stability in mitochondria: Different means to an end2004
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Nuclear DNA-encoded tRNAs targeted into mitochondria can rescue a mitochondrial DNA mutation associated with the MERRF syndrome in cultured human cells2004
Dr Margaret Jackson
Dr Margaret Johnson
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Taylor
Professor Robert Lightowlers
et al.
Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene2004
Professor Zofia Chrzanowska-Lightowlers
Dr Morteza Pourfarzam
Professor Robert Taylor
Emeritus Professor Doug Turnbull
A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency2003
Dr Pamela Kearns
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Andy Hall
Expression of GSTM isoforms in childhood acute lymphoblastoid leukaemia2003
Dr Richard Temperley
Dr Kasia Tonska
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Investigation of a pathogenic mtDNA microdeletion reveals a translation-dependent deadenylation decay pathway in human mitochondria2003
Dr Pamela Kearns
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Andy Hall
Mu class glutathione S-transferase mRNA isoform expression in acute lymphoblastic leukaemia2003
Fiona Menzies
Dr Mark Cookson
Professor Robert Taylor
Emeritus Professor Doug Turnbull
Professor Zofia Chrzanowska-Lightowlers
et al.
Mitochondrial dysfunction in a cell culture model of familial amyotrophic lateral sclerosis2002
Professor Zofia Chrzanowska-Lightowlers
rugose (rg), a drosophila a kinase anchor protein, is required for retinal pattern formation and interacts genetically with multiple signaling pathways2002
Dr Alexei von Delwig
Dr Jeong-Jin Lee
Professor Zofia Chrzanowska-Lightowlers
Professor John Robinson
TGF-β1 and IFN-γ cross-regulate antigen presentation to CD4 T cells by macrophages2002
Dr Richard Temperley
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Absence of expression from RNA internalised into electroporated mammalian mitochondria2001
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Fending off decay: A combinatorial approach in intact cells for identifying mRNA stability elements2001
Professor Robert Lightowlers
Simon Selwood
Professor Zofia Chrzanowska-Lightowlers
Genetic disease: Non-Mendelian2001
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Import of yeast tRNA derivatives into human mitochondria in vivo.2001
Simon Selwood
Anthony McGregor
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Inhibition of mitochondrial protein synthesis promotes autonomous regulation of mtDNA expression and generation of a new mitochondrial RNA species2001
Suad Awad
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Clarke Slater
Sodium channel mRNAs at the neuromuscular junction: Distinct patterns of accumulation and effects of muscle activity2001
Simon Selwood
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Does the mitochondrial transcription-termination complex play an essential role in controlling differential transcription of mitochondrial DNA?2000
Kim Clark
Professor Robert Taylor
Dr Margaret Johnson
Professor Patrick Chinnery
Professor Zofia Chrzanowska-Lightowlers
et al.
An mtDNA mutation in the initiation codon of the cytochrome C oxidase subunit II gene results in lower levels of the protein and a mitochondrial encephalomyopathy1999
Professor Robert Taylor
Dr Margaret Johnson
Professor Patrick Chinnery
Professor Zofia Chrzanowska-Lightowlers
Professor Michael Hanna
et al.
An mtDNA Mutation in the Initiation Codon of the Cytochrome C Oxidase Subunit II Gene Results in Lower Levels of the Protein and a Mitochondrial Encephalomyopathy1999
Professor Zofia Chrzanowska-Lightowlers
Dr Richard Temperley
Professor Robert Lightowlers
Conversion of a reporter gene for mitochondrial gene expression using iterative mega-prime PCR1999
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Glutamate dehydrogenase: an organelle specific mRNA-binding protein1997
Dr Margaret Johnson
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Intracellular mitochondrial triplasmy in a patient with two heteroplasmic base changes1997
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Targeting proteins to mitochondria: Is there a role for mRNA localization?1996
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Emeritus Professor Doug Turnbull
Gene Therapy for Mitochondrial DNA Defects - is it possible?1995
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
The mRNA-binding protein COLBP is glutamate dehydrogenase1995
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
Inhibition of Mitochondrial Protein Synthesis Promotes Increased Stability of Nuclear-Encoded Respiratory Gene Transcripts.1994
Professor Zofia Chrzanowska-Lightowlers
Professor Robert Lightowlers
The tissue-specific RNA-binding protein COLBP is differentially regulated during myogenesis1994
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Doug Turnbull
Professor Robert Lightowlers
A microtitre plate assay for cytochrome c oxidase in permeabilized whole cells.1993
Professor Zofia Chrzanowska-Lightowlers
Emeritus Professor Doug Turnbull
Professor Robert Lightowlers
An antisense oligodeoxynucleotide approach to investigate the function of the nuclear-encoded subunits of human cytochrome c oxidase1993
Professor Robert Lightowlers
Professor Zofia Chrzanowska-Lightowlers
Subunit function in eukaryote cytochrome c oxidase: A mutation in the nuclear-coded subunit IV allows assembly but alters the function and stability of yeast cytochrome c oxidase1991