Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
5 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Microglia in post-mortem brain tissue of patients with bipolar disorder are not immune activated.
Transl Psychiatry. 2019 May 24;9(1):153. doi: 10.1038/s41398-019-0490-x.
Transl Psychiatry. 2019.
PMID: 31127084
Free PMC article.
Colony-Stimulating Factor 1 Receptor (CSF1R) Regulates Microglia Density and Distribution, but Not Microglia Differentiation In Vivo.
Oosterhof N, Kuil LE, van der Linde HC, Burm SM, Berdowski W, van Ijcken WFJ, van Swieten JC, Hol EM, Verheijen MHG, van Ham TJ.
Oosterhof N, et al.
Cell Rep. 2018 Jul 31;24(5):1203-1217.e6. doi: 10.1016/j.celrep.2018.06.113.
Cell Rep. 2018.
PMID: 30067976
Free article.
Item in Clipboard
The multicellular interplay of microglia in health and disease: lessons from leukodystrophy.
Berdowski WM, Sanderson LE, van Ham TJ.
Berdowski WM, et al.
Dis Model Mech. 2021 Aug 1;14(8):dmm048925. doi: 10.1242/dmm.048925. Epub 2021 Jul 20.
Dis Model Mech. 2021.
PMID: 34282843
Free PMC article.
Review.
Item in Clipboard
Dominant-acting CSF1R variants cause microglial depletion and altered astrocytic phenotype in zebrafish and adult-onset leukodystrophy.
Berdowski WM, van der Linde HC, Breur M, Oosterhof N, Beerepoot S, Sanderson L, Wijnands LI, de Jong P, Tsai-Meu-Chong E, de Valk W, de Witte M, van IJcken WFJ, Demmers J, van der Knaap MS, Bugiani M, Wolf NI, van Ham TJ.
Berdowski WM, et al.
Acta Neuropathol. 2022 Aug;144(2):211-239. doi: 10.1007/s00401-022-02440-5. Epub 2022 Jun 17.
Acta Neuropathol. 2022.
PMID: 35713703
Free PMC article.
Item in Clipboard
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 E, Nikoncuk A, Yousefi S, Berdowski WM, Alsagob M, Capo I, van der Linde HC, van den Berg P, Jacobs EH, Putar D, Ghazvini M, Aronica E, van IJcken WFJ, de Valk WG, Medici-van den Herik E, van Slegtenhorst M, Brick L, Kozenko M, Kohler JN, Bernstein JA, Monaghan KG, Begtrup A, Torene R, Al Futaisi A, Al Murshedi F, Mani R, Al Azri F, Kamsteeg EJ, Mojarrad M, Eslahi A, Khazaei Z, Darmiyan FM, Doosti M, Karimiani EG, Vandrovcova J, Zafar F, Rana N, Kandaswamy KK, Hertecant J, Bauer P, AlMuhaizea MA, Salih MA, Aldosary M, Almass R, Al-Quait L, Qubbaj W, Coskun S, Alahmadi KO, Hamad MHA, Alwadaee S, Awartani K, Dababo AM, Almohanna F, Colak D, Dehghani M, Mehrjardi MYV, Gunel M, Ercan-Sencicek AG, Passi GR, Cheema HA, Efthymiou S, Houlden H, Bertoli-Avella AM, Brooks AS, Retterer K, Maroofian R, Kaya N, van Ham TJ, Barakat TS.
Perenthaler E, et al. Among authors: berdowski wm.
Acta Neuropathol. 2020 Mar;139(3):415-442. doi: 10.1007/s00401-019-02109-6. Epub 2019 Dec 9.
Acta Neuropathol. 2020.
PMID: 31820119
Free PMC article.
Item in Clipboard
Cite
Cite