Rutger O. Vogel

发表

Different Effects of Exogenous Cues in a Visual Detection and Discrimination Task: Delayed Attention Withdrawal and/or Speeded Motor Inhibition?

Rob H. J. van der Lubbe, Albert Postma, Rutger O. Vogel, 2005, Journal of Cognitive Neuroscience.

Subunits of Mitochondrial Complex I Exist as Part of Matrix- and Membrane-associated Subcomplexes in Living Cells*

Rutger O. Vogel, R. Roepman, J. Fransen, 2008, Journal of Biological Chemistry.

Transcriptome analysis of complex I-deficient patients reveals distinct expression programs for subunits and assembly factors of the oxidative phosphorylation system

Martijn A. Huynen, Rutger O. Vogel, Radek Szklarczyk, 2015, BMC Genomics.

Analysis of 953 Human Proteins from a Mitochondrial HEK293 Fraction by Complexome Profiling

Jolein Gloerich, Hans J. C. T. Wessels, Rutger O. Vogel, 2013, PloS one.

LC‐MS/MS as an alternative for SDS‐PAGE in blue native analysis of protein complexes

Rutger O. Vogel, Hans J C T Wessels, R. Rodenburg, 2009, Proteomics.

Investigation of the complex I assembly chaperones B17.2L and NDUFAF1 in a cohort of CI deficient patients.

Rutger O. Vogel, R. Rodenburg, J. Smeitink, 2007, Molecular genetics and metabolism.

Inhibition of the ER stress IRE1α inflammatory pathway protects against cell death in mitochondrial complex I mutant cells

Rutger O. Vogel, P. Puigserver, S. Gygi, 2018, Cell Death & Disease.

Human mitochondrial complex I assembly is mediated by NDUFAF1

Rutger O. Vogel, M. Zeviani, J. Smeitink, 2005, The FEBS journal.

Assembly factors as a new class of disease genes for mitochondrial complex I deficiency: cause, pathology and treatment options.

Rutger O. Vogel, J. Smeitink, L. Nijtmans, 2012, Brain : a journal of neurology.

Human mitochondrial complex I assembly: a dynamic and versatile process.

Rutger O. Vogel, J. Smeitink, L. Nijtmans, 2007, Biochimica et biophysica acta.

The assembly of Mitochondrial Complex I: A product of nuclear-mitochondrial synergy

Rutger O. Vogel, 2007 .

Mutations in NDUFAF3 (C3ORF60), encoding an NDUFAF4 (C6ORF66)-interacting complex I assembly protein, cause fatal neonatal mitochondrial disease.

Rutger O. Vogel, M. Huynen, H. Venselaar, 2009, American journal of human genetics.

Complex I assembly: a puzzling problem

Rutger O. Vogel, J. Smeitink, L. P. Van den Heuvel, 2004, Current opinion in neurology.

Human mitochondrial complex I assembles through the combination of evolutionary conserved modules: a framework to interpret complex I deficiencies.

Rutger O. Vogel, J. Smeitink, R. Huijbens, 2004, Human molecular genetics.

Clk2 and B56β mediate insulin-regulated assembly of the PP2A phosphatase holoenzyme complex on Akt.

Rutger O. Vogel, P. Puigserver, J. T. Rodgers, 2011, Molecular cell.

Bromodomain Inhibitors Correct Bioenergetic Deficiency Caused by Mitochondrial Disease Complex I Mutations.

Rutger O. Vogel, P. Puigserver, S. Gygi, 2016, Molecular cell.

Defective Mitochondrial Morphology and Bioenergetic Function in Mice Lacking the Transcription Factor Yin Yang 1 in Skeletal Muscle

Rutger O. Vogel, P. Puigserver, F. Vazquez, 2012, Molecular and Cellular Biology.

Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly.

Rutger O. Vogel, J. Smeitink, L. P. Van den Heuvel, 2007, Genes & development.

Acyl-CoA dehydrogenase 9 is required for the biogenesis of oxidative phosphorylation complex I.

Rutger O. Vogel, M. Huynen, R. Rodenburg, 2010, Cell metabolism.

Glia are critical for the neuropathology of complex I deficiency in Drosophila.

Rutger O. Vogel, M. Feany, Vijay R Hegde, 2014, Human molecular genetics.

Identification of Mitochondrial Complex I Assembly Intermediates by Tracing Tagged NDUFS3 Demonstrates the Entry Point of Mitochondrial Subunits*

Rutger O. Vogel, J. Smeitink, L. P. Van den Heuvel, 2007, Journal of Biological Chemistry.