The multicellular interplay of microglia in health and disease: lessons from leukodystrophy
Berdowski, Woutje M, Sanderson, Leslie E, van Ham, Tjakko J
Published in Disease models & mechanisms (01.08.2021)
Published in Disease models & mechanisms (01.08.2021)
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Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy
Berdowski, Woutje M., van der Linde, Herma C., Breur, Marjolein, Oosterhof, Nynke, Beerepoot, Shanice, Sanderson, Leslie, Wijnands, Lieve I., de Jong, Patrick, Tsai-Meu-Chong, Elisa, de Valk, Walter, de Witte, Moniek, van IJcken, Wilfred F. J., Demmers, Jeroen, van der Knaap, Marjo S., Bugiani, Marianna, Wolf, Nicole I., van Ham, Tjakko J.
Published in Acta neuropathologica (01.08.2022)
Published in Acta neuropathologica (01.08.2022)
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Microglia in post-mortem brain tissue of patients with bipolar disorder are not immune activated
Sneeboer, Marjolein A M, Snijders, Gijsje J L J, Berdowski, Woutje M, Fernández-Andreu, Alba, van Mierlo, Hans C, Berdenis van Berlekom, Amber, Litjens, Manja, Kahn, René S, Hol, Elly M, de Witte, Lot D
Published in Translational psychiatry (24.05.2019)
Published in Translational psychiatry (24.05.2019)
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Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases
Perenthaler, Elena, Nikoncuk, Anita, Yousefi, Soheil, Berdowski, Woutje M., Alsagob, Maysoon, Capo, Ivan, van der Linde, Herma C., van den Berg, Paul, Jacobs, Edwin H., Putar, Darija, Ghazvini, Mehrnaz, Aronica, Eleonora, van IJcken, Wilfred F. J., de Valk, Walter G., Medici-van den Herik, Evita, van Slegtenhorst, Marjon, Brick, Lauren, Kozenko, Mariya, Kohler, Jennefer N., Bernstein, Jonathan A., Monaghan, Kristin G., Begtrup, Amber, Torene, Rebecca, Al Futaisi, Amna, Al Murshedi, Fathiya, Mani, Renjith, Al Azri, Faisal, Kamsteeg, Erik-Jan, Mojarrad, Majid, Eslahi, Atieh, Khazaei, Zaynab, Darmiyan, Fateme Massinaei, Doosti, Mohammad, Karimiani, Ehsan Ghayoor, Vandrovcova, Jana, Zafar, Faisal, Rana, Nuzhat, Kandaswamy, Krishna K., Hertecant, Jozef, Bauer, Peter, AlMuhaizea, Mohammed A., Salih, Mustafa A., Aldosary, Mazhor, Almass, Rawan, Al-Quait, Laila, Qubbaj, Wafa, Coskun, Serdar, Alahmadi, Khaled O., Hamad, Muddathir H. A., Alwadaee, Salem, Awartani, Khalid, Dababo, Anas M., Almohanna, Futwan, Colak, Dilek, Dehghani, Mohammadreza, Mehrjardi, Mohammad Yahya Vahidi, Gunel, Murat, Ercan-Sencicek, A. Gulhan, Passi, Gouri Rao, Cheema, Huma Arshad, Efthymiou, Stephanie, Houlden, Henry, Bertoli-Avella, Aida M., Brooks, Alice S., Retterer, Kyle, Maroofian, Reza, Kaya, Namik, van Ham, Tjakko J., Barakat, Tahsin Stefan
Published in Acta neuropathologica (01.03.2020)
Published in Acta neuropathologica (01.03.2020)
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Journal Article
Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform specific start-loss mutations of essential genes can cause genetic diseases
Perenthaler, Elena, Nikoncuk, Anita, Yousefi, Soheil, Berdowski, Woutje M, Capo, Ivan, Herma C Van Der Linde, Van Den Berg, Paul, Jacobs, Edwin H, Putar, Darija, Ghazvini, Mehrnaz, Aronica, Eleonora, Wilfred Fj Van Ijcken, De Valk, Walter G, Evita Medici-Van Den Herik, Marjon Van Slegtenhorst, Brick, Lauren, Kozenko, Mariya, Kohler, Jennefer N, Bernstein, Jonathan A, Monaghan, Kristin G, Begtrup, Amber, Torene, Rebecca, Amna Al Futaisi, Fathiya Al Murshedi, Mani, Renjith, Faisal Al Azri, Erik-Jan Kamsteeg, Mojarrad, Majid, Eslahi, Atieh, Khazaei, Zaynab, Darmiyan, Fateme Massinaei, Doosti, Mohammad, Ehsan Ghayoor Karimiani, Vandrovcova, Jana, Zafar, Faisal, Rana, Nuzhat, Kandaswamy, Krishna K, Hertecant, Jozef, Bauer, Peter, Efthymiou, Stephanie, Houlden, Henry, Bertoli-Avella, Aida M, Maroofian, Reza, Retterer, Kyle, Brooks, Alice S, Van Ham, Tjakko J, Barakat, Tahsin Stefan
Published in bioRxiv (10.10.2019)
Published in bioRxiv (10.10.2019)
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