Profiling peripheral nerve macrophages reveals two macrophage subsets with distinct localization, transcriptome and response to injury von Ydens, Elke, Amann, Lukas, Asselbergh, Bob, Scott, Charlotte L., Martens, Liesbet, Sichien, Dorine, Mossad, Omar, Blank, Thomas, De Prijck, Sofie, Low, Donovan, Masuda, Takahiro, Saeys, Yvan, Timmerman, Vincent, Stumm, Ralf, Ginhoux, Florent, Prinz, Marco, Janssens, Sophie, Guilliams, Martin

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Mitochondria-associated membranes as hubs for neurodegeneration von Krols, Michiel, van Isterdael, Gert, Asselbergh, Bob, Kremer, Anna, Lippens, Saskia, Timmerman, Vincent, Janssens, Sophie

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Global Switches and Fine-Tuning--ABA Modulates Plant Pathogen Defense von Asselbergh, B, Vleesschauwer, D. de, Hofte, M

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Neutrophil extracellular trap cell death requires both autophagy and superoxide generation von Remijsen, Quinten, Berghe, Tom Vanden, Wirawan, Ellen, Asselbergh, Bob, Parthoens, Eef, De Rycke, Riet, Noppen, Sam, Delforge, Michel, Willems, Jean, Vandenabeele, Peter

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Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies von Haidar, Mansour, Asselbergh, Bob, Adriaenssens, Elias, De Winter, Vicky, Timmermans, Jean-Pierre, Auer-Grumbach, Michaela, Juneja, Manisha, Timmerman, Vincent

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BAG3 Pro209 mutants associated with myopathy and neuropathy relocate chaperones of the CASA-complex to aggresomes von Adriaenssens, Elias, Tedesco, Barbara, Mediani, Laura, Asselbergh, Bob, Crippa, Valeria, Antoniani, Francesco, Carra, Serena, Poletti, Angelo, Timmerman, Vincent

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Acute injury in the peripheral nervous system triggers an alternative macrophage response von Ydens, Elke, Cauwels, Anje, Asselbergh, Bob, Goethals, Sofie, Peeraer, Lieve, Lornet, Guillaume, Almeida-Souza, Leonardo, Van Ginderachter, Jo A, Timmerman, Vincent, Janssens, Sophie

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A knock-in/knock-out mouse model of HSPB8-associated distal hereditary motor neuropathy and myopathy reveals toxic gain-of-function of mutant Hspb8 von Bouhy, Delphine, Juneja, Manisha, Katona, Istvan, Holmgren, Anne, Asselbergh, Bob, De Winter, Vicky, Hochepied, Tino, Goossens, Steven, Haigh, Jody J., Libert, Claude, Ceuterick-de Groote, Chantal, Irobi, Joy, Weis, Joachim, Timmerman, Vincent

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Sensory neuropathy-causing mutations in ATL3 affect ER-mitochondria contact sites and impair axonal mitochondrial distribution von Krols, Michiel, Asselbergh, Bob, De Rycke, Riet, De Winter, Vicky, Seyer, Alexandre, Müller, Franz-Josef, Kurth, Ingo, Bultynck, Geert, Timmerman, Vincent, Janssens, Sophie

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Sphingosine 1-phosphate lyase deficiency causes Charcot-Marie-Tooth neuropathy von Atkinson, Derek, Nikodinovic Glumac, Jelena, Asselbergh, Bob, Ermanoska, Biljana, Blocquel, David, Steiner, Regula, Estrada-Cuzcano, Alejandro, Peeters, Kristien, Ooms, Tinne, De Vriendt, Els, Yang, Xiang-Lei, Hornemann, Thorsten, Milic Rasic, Vedrana, Jordanova, Albena

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Resistance to Botrytis cinerea in sitiens, an Abscisic Acid-Deficient Tomato Mutant, Involves Timely Production of Hydrogen Peroxide and Cell Wall Modifications in the Epidermis von Asselbergh, Bob, Curvers, Katrien, França, Soraya C, Audenaert, Kris, Vuylsteke, Marnik, Van Breusegem, Frank, Höfte, Monica

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Transcriptional dysregulation by a nucleus-localized aminoacyl-tRNA synthetase associated with Charcot-Marie-Tooth neuropathy von Bervoets, Sven, Wei, Na, Erfurth, Maria-Luise, Yusein-Myashkova, Shazie, Ermanoska, Biljana, Mateiu, Ligia, Asselbergh, Bob, Blocquel, David, Kakad, Priyanka, Penserga, Tyrone, Thomas, Florian P, Guergueltcheva, Velina, Tournev, Ivailo, Godenschwege, Tanja, Jordanova, Albena, Yang, Xiang-Lei

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Tyrosyl-tRNA synthetase has a noncanonical function in actin bundling von Ermanoska, Biljana, Asselbergh, Bob, Morant, Laura, Petrovic-Erfurth, Maria-Luise, Hosseinibarkooie, Seyyedmohsen, Leitão-Gonçalves, Ricardo, Almeida-Souza, Leonardo, Bervoets, Sven, Sun, Litao, Lee, LaTasha, Atkinson, Derek, Khanghahi, Akram, Tournev, Ivaylo, Callaerts, Patrick, Verstreken, Patrik, Yang, Xiang-Lei, Wirth, Brunhilde, Rodal, Avital A., Timmerman, Vincent, Goode, Bruce L., Godenschwege, Tanja A., Jordanova, Albena

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Rare missense mutations in ABCA7 might increase Alzheimer's disease risk by plasma membrane exclusion von Bossaerts, Liene, Hendrickx Van de Craen, Elisabeth, Cacace, Rita, Asselbergh, Bob, Van Broeckhoven, Christine

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Regulation of human microglial gene expression and function via RNAase-H active antisense oligonucleotides in vivo in Alzheimer's disease von Vandermeulen, Lina, Geric, Ivana, Fumagalli, Laura, Kreir, Mohamed, Lu, Ashley, Nonneman, Annelies, Premereur, Jessie, Wolfs, Leen, Policarpo, Rafaela, Fattorelli, Nicola, De Bondt, An, Van Den Wyngaert, Ilse, Asselbergh, Bob, Fiers, Mark, De Strooper, Bart, d'Ydewalle, Constantin, Mancuso, Renzo

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Charcot–Marie–Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments von Holmgren, Anne, Bouhy, Delphine, De Winter, Vicky, Asselbergh, Bob, Timmermans, Jean-Pierre, Irobi, Joy, Timmerman, Vincent

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Human Rab7 mutation mimics features of Charcot–Marie–Tooth neuropathy type 2B in Drosophila von Janssens, Katrien, Goethals, Sofie, Atkinson, Derek, Ermanoska, Biljana, Fransen, Erik, Jordanova, Albena, Auer-Grumbach, Michaela, Asselbergh, Bob, Timmerman, Vincent

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Diffusion kurtosis imaging to detect amyloidosis in an APP/PS1 mouse model for Alzheimer's disease von Vanhoutte, Greetje, Pereson, Sandra, Delgado y Palacios, Rafael, Guns, Pieter-Jan, Asselbergh, Bob, Veraart, Jelle, Sijbers, Jan, Verhoye, Marleen, Van Broeckhoven, Christine, Van der Linden, Annemie

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Contribution of rare homozygous and compound heterozygous VPS13C missense mutations to dementia with Lewy bodies and Parkinson's disease von Smolders, Stefanie, Philtjens, Stéphanie, Crosiers, David, Sieben, Anne, Hens, Elisabeth, Heeman, Bavo, Van Mossevelde, Sara, Pals, Philippe, Asselbergh, Bob, Dos Santos Dias, Roberto, Vermeiren, Yannick, Vandenberghe, Rik, Engelborghs, Sebastiaan, De Deyn, Peter Paul, Martin, Jean-Jacques, Cras, Patrick, Annaert, Wim, Van Broeckhoven, Christine

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CMT-associated mutations in glycyl- and tyrosyl-tRNA synthetases exhibit similar pattern of toxicity and share common genetic modifiers in Drosophila von Ermanoska, Biljana, Motley, William W, Leitão-Gonçalves, Ricardo, Asselbergh, Bob, Lee, LaTasha H, De Rijk, Peter, Sleegers, Kristel, Ooms, Tinne, Godenschwege, Tanja A, Timmerman, Vincent, Fischbeck, Kenneth H, Jordanova, Albena

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