CLUH granules coordinate translation of mitochondrial proteins with mTORC1 signaling and mitophagy von Pla‐Martín, David, Schatton, Désirée, Wiederstein, Janica L, Marx, Marie‐Charlotte, Khiati, Salim, Krüger, Marcus, Rugarli, Elena I

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Mitochondrial membrane proteins and VPS35 orchestrate selective removal of mtDNA von Sen, Ayesha, Kallabis, Sebastian, Gaedke, Felix, Jüngst, Christian, Boix, Julia, Nüchel, Julian, Maliphol, Kanjanamas, Hofmann, Julia, Schauss, Astrid C., Krüger, Marcus, Wiesner, Rudolf J., Pla-Martín, David

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Combined fibre atrophy and decreased muscle regeneration capacity driven by mitochondrial DNA alterations underlie the development of sarcopenia von Kimoloi, Sammy, Sen, Ayesha, Guenther, Stefan, Braun, Thomas, Brügmann, Tobias, Sasse, Philipp, Wiesner, Rudolf J., Pla‐Martín, David, Baris, Olivier R.

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Selective Neuron Vulnerability in Common and Rare Diseases—Mitochondria in the Focus von Paß, Thomas, Wiesner, Rudolf J., Pla-Martín, David

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Endosomal-dependent mitophagy coordinates mitochondrial nucleoid and mtDNA elimination von Sen, Ayesha, Boix, Julia, Pla-Martín, David

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Junctophilin-1 is a modifier gene of GDAP1-related Charcot-Marie-Tooth disease von Pla-Martín, David, Calpena, Eduardo, Lupo, Vincenzo, Márquez, Celedonio, Rivas, Eloy, Sivera, Rafael, Sevilla, Teresa, Palau, Francesc, Espinós, Carmen

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Silencing of the Charcot–Marie–Tooth disease-associated gene GDAP1 induces abnormal mitochondrial distribution and affects Ca2+ homeostasis by reducing store-operated Ca2+ entry... von Pla-Martín, David, Rueda, Carlos B., Estela, Anna, Sánchez-Piris, Maribel, González-Sánchez, Paloma, Traba, Javier, de la Fuente, Sergio, Scorrano, Luca, Renau-Piqueras, Jaime, Alvarez, Javier, Satrústegui, Jorgina, Palau, Francesc

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CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca2+ entry-stimulated respiration von González-Sánchez, Paloma, Pla-Martín, David, Martínez-Valero, Paula, Rueda, Carlos B., Calpena, Eduardo, del Arco, Araceli, Palau, Francesc, Satrústegui, Jorgina

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Extraocular Muscle Reveals Selective Vulnerability of Type IIB Fibers to Respiratory Chain Defects Induced by Mitochondrial DNA Alterations von Oexner, Rafael R, Pla-Martín, David, Paß, Thomas, Wiesen, Martin H J, Zentis, Peter, Schauss, Astrid, Baris, Olivier R, Kimoloi, Sammy, Wiesner, Rudolf J

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Charcot-Marie-Tooth-related Gene GDAP1 Complements Cell Cycle Delay at G2/M Phase in Saccharomyces cerevisiae fis1 Gene-defective Cells von Estela, Anna, Pla-Martín, David, Sánchez-Piris, Maribel, Sesaki, Hiromi, Palau, Francesc

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Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolism von Bolinches-Amorós, Arantxa, Mollá, Belén, Pla-Martín, David, Palau, Francesc, González-Cabo, Pilar

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CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins von Gao, Jie, Schatton, Désirée, Martinelli, Paola, Hansen, Henriette, Pla-Martin, David, Barth, Esther, Becker, Christian, Altmueller, Janine, Frommolt, Peter, Sardiello, Marco, Rugarli, Elena I

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Reshaping membranes to build mitochondrial DNA von Pla-Martin, David, Wiesner, Rudolf J

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CLUH regulates mitochondrial metabolism by controlling translation and decay of target mRNAs von Schatton, Désirée, Pla-Martin, David, Marx, Marie-Charlotte, Hansen, Henriette, Mourier, Arnaud, Nemazanyy, Ivan, Pessia, Alberto, Zentis, Peter, Corona, Teresa, Kondylis, Vangelis, Barth, Esther, Schauss, Astrid C, Velagapudi, Vidya, Rugarli, Elena I

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Inner membrane turns inside out to exit mitochondrial organelles von Pla-Martín, David, Reichert, Andreas S.

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Lack of GDAP1 induces neuronal calcium and mitochondrial defects in a knockout mouse model of charcot-marie-tooth neuropathy von Barneo-Muñoz, Manuela, Juárez, Paula, Civera-Tregón, Azahara, Yndriago, Laura, Pla-Martin, David, Zenker, Jennifer, Cuevas-Martín, Carmen, Estela, Anna, Sánchez-Aragó, María, Forteza-Vila, Jerónimo, Cuezva, José M, Chrast, Roman, Palau, Francesc

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Localization of Mitochondrial Nucleoids by Transmission Electron Microscopy Using the Transgenic Expression of the Mitochondrial Helicase Twinkle and APEX2 von Pla-Martín, David, Babatz, Felix, Schauss, Astrid C.

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Author Response: K320E-Twinkle skm Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls von Kimoloi, Sammy, Pla-Martín, David, Oexner, Rafael R., Baris, Olivier R., Wiesner, Rudolf J.

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CMT-linked loss-of-function mutations in GDAP1 impair store-operated Ca 2+ entry-stimulated respiration von González-Sánchez, Paloma, Pla-Martín, David, Martínez-Valero, Paula, Rueda, Carlos B, Calpena, Eduardo, Del Arco, Araceli, Palau, Francesc, Satrústegui, Jorgina

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Author Response: K320E-Twinkleskm Mice Are Genetically Heterogeneous for Secondary mtDNA Deletions Impairing Comparison With Controls von Kimoloi, Sammy, Pla-Martín, David, Oexner, Rafael R, Baris, Olivier R, Wiesner, Rudolf J

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