SK channel activation is neuroprotective in conditions of enhanced ER–mitochondrial coupling

por Honrath, Birgit, Krabbendam, Inge E., IJsebaart, Carmen, Pegoretti, Valentina, Bendridi, Nadia, Rieusset, Jennifer, Schmidt, Martina, Culmsee, Carsten, Dolga, Amalia M.
Publicado 2018

Gsta4 controls apoptosis of differentiating adult oligodendrocytes during homeostasis and remyelination via the mitochondria-associated Fas-Casp8-Bid-axis

por Carlström, Karl E., Zhu, Keying, Ewing, Ewoud, Krabbendam, Inge E., Harris, Robert A., Falcão, Ana Mendanha, Jagodic, Maja, Castelo-Branco, Gonçalo, Piehl, Fredrik
Publicado 2020

Plasma hsa‐mir‐19b is a potential LevoDopa therapy marker

por Chis, Aimee Rodica, Moatar, Alexandra Ioana, Dijmarescu, Cristina, Rosca, Cecilia, Vorovenci, Ruxandra Julia, Krabbendam, Inge, Dolga, Amalia, Bejinar, Cristina, Marian, Catalin, Sirbu, Ioan Ovidiu, Simu, Mihaela
Publicado 2021

Fibril polymorphism affects immobilized non-amyloid flanking domains of huntingtin exon1 rather than its polyglutamine core

por Lin, Hsiang-Kai, Boatz, Jennifer C., Krabbendam, Inge E., Kodali, Ravindra, Hou, Zhipeng, Wetzel, Ronald, Dolga, Amalia M., Poirier, Michelle A., van der Wel, Patrick C. A.
Publicado 2017

Negative modulation of mitochondrial calcium uniporter complex protects neurons against ferroptosis

por Marmolejo-Garza, Alejandro, Krabbendam, Inge E., Luu, Minh Danh Anh, Brouwer, Famke, Trombetta-Lima, Marina, Unal, Osman, O’Connor, Shane J., Majerníková, Naďa, Elzinga, Carolina R. S., Mammucari, Cristina, Schmidt, Martina, Madesh, Muniswamy, Boddeke, Erik, Dolga, Amalia M.
Publicado 2023

SK channel-mediated metabolic escape to glycolysis inhibits ferroptosis and supports stress resistance in C. elegans

por Krabbendam, Inge E., Honrath, Birgit, Dilberger, Benjamin, Iannetti, Eligio F., Branicky, Robyn S., Meyer, Tammo, Evers, Bernard, Dekker, Frank J., Koopman, Werner J. H., Beyrath, Julien, Bano, Daniele, Schmidt, Martina, Bakker, Barbara M., Hekimi, Siegfried, Culmsee, Carsten, Eckert, Gunter P., Dolga, Amalia M.
Publicado 2020

ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia

por Bouwkamp, Christian G., Afawi, Zaid, Fattal-Valevski, Aviva, Krabbendam, Inge E., Rivetti, Stefano, Masalha, Rafik, Quadri, Marialuisa, Breedveld, Guido J., Mandel, Hanna, Tailakh, Muhammad Abu, Beverloo, H. Berna, Stevanin, Giovanni, Brice, Alexis, van IJcken, Wilfred F.J., Vernooij, Meike W., Dolga, Amalia M., de Vrij, Femke M.S., Bonifati, Vincenzo, Kushner, Steven A.
Publicado 2018