Mitochondrial ATP synthase: architecture, function and pathology

por Jonckheere, An I., Smeitink, Jan A. M., Rodenburg, Richard J. T.
Publicado 2011

Intra‐patient variability of heteroplasmy levels in urinary epithelial cells in carriers of the m.3243A>G mutation

por de Laat, Paul, Rodenburg, Richard J., Smeitink, Jan A. M., Janssen, Mirian C. H.
Publicado 2018

Feeding difficulties, a key feature of the Drosophila NDUFS4 mitochondrial disease model

por Foriel, Sarah, Beyrath, Julien, Eidhof, Ilse, Rodenburg, Richard J., Schenck, Annette, Smeitink, Jan A. M.
Publicado 2018

Dissecting Drug-Induced Cytotoxicity and Metabolic Dysfunction in Conditionally Immortalized Human Proximal Tubule Cells

por Hoogstraten, Charlotte A., Smeitink, Jan A. M., Russel, Frans G. M., Schirris, Tom J. J.
Publicado 2022

Photo-Induction and Automated Quantification of Reversible Mitochondrial Permeability Transition Pore Opening in Primary Mouse Myotubes

por Blanchet, Lionel, Grefte, Sander, Smeitink, Jan A. M., Willems, Peter H. G. M., Koopman, Werner J. H.
Publicado 2014

Live-Imaging Readouts and Cell Models for Phenotypic Profiling of Mitochondrial Function

por Iannetti, Eligio F., Prigione, Alessandro, Smeitink, Jan A. M., Koopman, Werner J. H., Beyrath, Julien, Renkema, Herma
Publicado 2019

Five non-mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes phenotype adult patients with m.3243A>G mutation after kidney transplantation: follow-up a...

por de Laat, Paul, van Engelen, Nienke, Wetzels, Jack F, Smeitink, Jan A M, Janssen, Mirian C H
Publicado 2019

Reconstructing the evolution of the mitochondrial ribosomal proteome

por Smits, Paulien, Smeitink, Jan A. M., van den Heuvel, Lambert P., Huynen, Martijn A., Ettema, Thijs J. G.
Publicado 2007

Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD(+)

por Iannetti, Eligio F., Smeitink, Jan A. M., Willems, Peter H. G. M., Beyrath, Julien, Koopman, Werner J. H.
Publicado 2018

The antioxidant Trolox restores mitochondrial membrane potential and Ca(2+)-stimulated ATP production in human complex I deficiency

por Distelmaier, Felix, Visch, Henk-Jan, Smeitink, Jan A. M., Mayatepek, Ertan, Koopman, Werner J. H., Willems, Peter H. G. M.
Publicado 2009

Modeling mitochondrial dysfunctions in the brain: from mice to men

por Breuer, Megan E., Willems, Peter H. G. M., Russel, Frans G. M., Koopman, Werner J. H., Smeitink, Jan A. M.
Publicado 2011

Three families with ‘de novo’ m.3243A > G mutation

por de Laat, Paul, Janssen, Mirian C.H., Alston, Charlotte L., Taylor, Robert W., Rodenburg, Richard J.T., Smeitink, Jan A.M.
Publicado 2016

A Drosophila Mitochondrial Complex I Deficiency Phenotype Array

por Foriel, Sarah, Renkema, G. Herma, Lasarzewski, Yvonne, Berkhout, Job, Rodenburg, Richard J., Smeitink, Jan A. M., Beyrath, Julien, Schenck, Annette
Publicado 2019

Correction to: The antioxidant Trolox restores mitochondrial membrane potential and Ca(2+)-stimulated ATP production in human complex I deficiency

por Distelmaier, Felix, Visch, Henk-Jan, Smeitink, Jan A. M., Mayatepek, Ertan, Koopman, Werner J. H., Willems, Peter H. G. M.
Publicado 2021

Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant

por Klein, Inge‐Lot, Verhaak, Christianne M., Smeitink, Jan A. M., de Laat, Paul, Janssen, Mirian C. H., Custers, José A. E.
Publicado 2022

Mitochondrial ADP/ATP exchange inhibition: a novel off-target mechanism underlying ibipinabant-induced myotoxicity

por Schirris, Tom J. J., Ritschel, Tina, Herma Renkema, G., Willems, Peter H. G. M., Smeitink, Jan A. M., Russel, Frans G. M.
Publicado 2015

Erratum to: Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A>G mutation

por de Laat, Paul, Koene, Saskia, vd Heuvel, Lambert P. W. J., Rodenburg, Richard J. T., Janssen, Mirian C. H., Smeitink, Jan A. M.
Publicado 2012

Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation

por de Laat, Paul, Koene, Saskia, van den Heuvel, Lambert P. W. J., Rodenburg, Richard J. T., Janssen, Mirian C. H., Smeitink, Jan A. M.
Publicado 2012

KH176 Safeguards Mitochondrial Diseased Cells from Redox Stress-Induced Cell Death by Interacting with the Thioredoxin System/Peroxiredoxin Enzyme Machinery

por Beyrath, Julien, Pellegrini, Mina, Renkema, Herma, Houben, Lisanne, Pecheritsyna, Svetlana, van Zandvoort, Peter, van den Broek, Petra, Bekel, Akkiz, Eftekhari, Pierre, Smeitink, Jan A. M.
Publicado 2018

The Redox Modulating Sonlicromanol Active Metabolite KH176m and the Antioxidant MPG Protect Against Short-Duration Cardiac Ischemia-Reperfusion Injury

por Xiao, Yang, Yim, Karen, Zhang, Hong, Bakker, Diane, Nederlof, Rianne, Smeitink, Jan A. M., Renkema, Herma, Hollmann, Markus W., Weber, Nina C., Zuurbier, Coert J.
Publicado 2021