How much does a disrupted mitochondrial network influence neuronal dysfunction? by Zofia MA Chrzanowska‐Lightowlers, Robert N Lightowlers

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Salvaging hope: Is increasing NAD+ a key to treating mitochondrial myopathy? by Robert N Lightowlers, Zofia MA Chrzanowska‐Lightowlers

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Cl-out is a novel cooperative optogenetic tool for extruding chloride from neurons by Hannah Alfonsa, Jeremy H. Lakey, Robert N. Lightowlers, Andrew J. Trevelyan

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REXO2 is an oligoribonuclease active in human mitochondria. by Francesco Bruni, Pasqua Gramegna, Jorge M A Oliveira, Robert N Lightowlers, Zofia M A Chrzanowska-Lightowlers

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M2I-1 disrupts the in vivo interaction between CDC20 and MAD2 and increases the sensitivities of cancer cell lines to anti-mitotic drugs via MCL-1s by Jianquan Li, Nanmao Dang, Nuria Martinez-Lopez, Paul A. Jowsey, Dong Huang, Robert N. Lightowlers, Fei Gao, Jun-Yong Huang

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Using mitoribosomal profiling to investigate human mitochondrial translation [version 2; referees: 2 approved] by Fei Gao, Maria Wesolowska, Reuven Agami, Koos Rooijers, Fabricio Loayza-Puch, Conor Lawless, Robert N. Lightowlers, Zofia M. A. Chrzanowska-Lightowlers

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Using mitoribosomal profiling to investigate human mitochondrial translation [version 1; referees: 2 approved] by Fei Gao, Maria Wesolowska, Reuven Agami, Koos Rooijers, Fabricio Loayza-Puch, Conor Lawless, Robert N. Lightowlers, Zofia M. A. Chrzanowska-Lightowlers

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Mitochondrial Translation Occurs Preferentially in the Peri-Nuclear Mitochondrial Network of Cultured Human Cells by Christin A. Albus, Rolando Berlinguer-Palmini, Caroline Hewison, Fiona McFarlane, Elisabeta-Ana Savu, Robert N. Lightowlers, Zofia M. Chrzanowska-Lightowlers, Matthew Zorkau

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Analysis of 953 human proteins from a mitochondrial HEK293 fraction by complexome profiling. by Hans J C T Wessels, Rutger O Vogel, Robert N Lightowlers, Johannes N Spelbrink, Richard J Rodenburg, Lambert P van den Heuvel, Alain J van Gool, Jolein Gloerich, Jan A M Smeitink, Leo G Nijtmans

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OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect by Kyle Thompson, Nicole Mai, Monika Oláhová, Filippo Scialó, Luke E Formosa, David A Stroud, Madeleine Garrett, Nichola Z Lax, Fiona M Robertson, Cristina Jou, Andres Nascimento, Carlos Ortez, Cecilia Jimenez‐Mallebrera, Steven A Hardy, Langping He, Garry K Brown, Paula Marttinen, Robert McFarland, Alberto Sanz, Brendan J Battersby, Penelope E Bonnen, Michael T Ryan, Zofia MA Chrzanowska‐Lightowlers, Robert N Lightowlers, Robert W Taylor

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