Intracellular vesicle trafficking plays an essential role in mitochondrial quality control

por Gerards, Mike, Cannino, Giuseppe, González de Cózar, Jose M., Jacobs, Howard T.
Publicado 2018

RNase H1 promotes replication fork progression through oppositely transcribed regions of Drosophila mitochondrial DNA

por González de Cózar, Jose M., Gerards, Mike, Teeri, Eveliina, George, Jack, Dufour, Eric, Jacobs, Howard T., Jõers, Priit
Publicado 2019

Screen for mitochondrial DNA copy number maintenance genes reveals essential role for ATP synthase

por Fukuoh, Atsushi, Cannino, Giuseppe, Gerards, Mike, Buckley, Suzanne, Kazancioglu, Selena, Scialo, Filippo, Lihavainen, Eero, Ribeiro, Andre, Dufour, Eric, Jacobs, Howard T
Publicado 2014

Tfam Knockdown Results in Reduction of mtDNA Copy Number, OXPHOS Deficiency and Abnormalities in Zebrafish Embryos

por Otten, Auke B. C., Kamps, Rick, Lindsey, Patrick, Gerards, Mike, Pendeville-Samain, Hélène, Muller, Marc, van Tienen, Florence H. J., Smeets, Hubert J. M.
Publicado 2020

Manipulating mtDNA in vivo reprograms metabolism via novel response mechanisms

por Bahhir, Diana, Yalgin, Cagri, Ots, Liina, Järvinen, Sampsa, George, Jack, Naudí, Alba, Krama, Tatjana, Krams, Indrikis, Tamm, Mairi, Andjelković, Ana, Dufour, Eric, González de Cózar, Jose M., Gerards, Mike, Parhiala, Mikael, Pamplona, Reinald, Jacobs, Howard T., Jõers, Priit
Publicado 2019

Selection and Characterization of Palmitic Acid Responsive Patients with an OXPHOS Complex I Defect

por Theunissen, Tom E. J., Gerards, Mike, Hellebrekers, Debby M. E. I., van Tienen, Florence H., Kamps, Rick, Sallevelt, Suzanne C. E. H., Hartog, Elvira N. M. M.-D., Scholte, Hans R., Verdijk, Robert M., Schoonderwoerd, Kees, de Coo, Irenaeus F. M., Szklarczyk, Radek, Smeets, Hubert J. M.
Publicado 2017

Specific MRI Abnormalities Reveal Severe Perrault Syndrome due to CLPP Defects

por Theunissen, Tom E. J., Szklarczyk, Radek, Gerards, Mike, Hellebrekers, Debby M. E. I., Mulder-Den Hartog, Elvira N. M., Vanoevelen, Jo, Kamps, Rick, de Koning, Bart, Rutledge, S. Lane, Schmitt-Mechelke, Thomas, van Berkel, Carola G. M., van der Knaap, Marjo S., de Coo, Irenaeus F. M., Smeets, Hubert J. M.
Publicado 2016

Whole Exome Sequencing Is the Preferred Strategy to Identify the Genetic Defect in Patients With a Probable or Possible Mitochondrial Cause

por Theunissen, Tom E. J., Nguyen, Minh, Kamps, Rick, Hendrickx, Alexandra T., Sallevelt, Suzanne C. E. H., Gottschalk, Ralph W. H., Calis, Chantal M., Stassen, Alphons P. M., de Koning, Bart, Mulder-Den Hartog, Elvira N. M., Schoonderwoerd, Kees, Fuchs, Sabine A., Hilhorst-Hofstee, Yvonne, de Visser, Marianne, Vanoevelen, Jo, Szklarczyk, Radek, Gerards, Mike, de Coo, Irenaeus F. M., Hellebrekers, Debby M. E. I., Smeets, Hubert J. M.
Publicado 2018