Antisense Oligonucleotide-Mediated Removal of the Polyglutamine Repeat in Spinocerebellar Ataxia Type 3 Mice by Lodewijk J.A. Toonen, Frank Rigo, Haico van Attikum, Willeke M.C. van Roon-Mom

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Co-expression patterns of microglia markers Iba1, TMEM119 and P2RY12 in Alzheimer's disease by Boyd Kenkhuis, Antonios Somarakis, Lynn R.T. Kleindouwel, Willeke M.C. van Roon-Mom, Thomas Höllt, Louise van der Weerd

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Antisense-mediated RNA targeting: versatile and expedient genetic manipulation in the brain by Ioannis eZalachoras, Melvin M Evers, Willeke M C van Roon-Mom, Annemieke M Aartsma-Rus, Onno C Meijer

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Therapeutic Strategies for Spinocerebellar Ataxia Type 1 by Laurie M. C. Kerkhof, Bart P. C. van de Warrenburg, Willeke M. C. van Roon-Mom, Ronald A. M. Buijsen

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Exploring the transcriptome of ciliated cells using in silico dissection of human tissues. by Alexander E Ivliev, Peter A C 't Hoen, Willeke M C van Roon-Mom, Dorien J M Peters, Marina G Sergeeva

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Generation of a gene-corrected human isogenic line (UAMi006-A) from propionic acidemia patient iPSC with an homozygous mutation in the PCCB gene using CRISPR/Cas9 technology by Alejandro Fulgencio-Covián, Mar Álvarez, Barry A. Pepers, Arístides López-Márquez, Magdalena Ugarte, Belén Pérez, Willeke M.C. van Roon-Mom, Lourdes R. Desviat, Eva Richard

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Machine learning in Huntington’s disease: exploring the Enroll-HD dataset for prognosis and driving capability prediction by Jasper Ouwerkerk, Stephanie Feleus, Kasper F. van der Zwaan, Yunlei Li, Marco Roos, Willeke M. C. van Roon-Mom, Susanne T. de Bot, Katherine J. Wolstencroft, Eleni Mina

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Amyloid beta accumulations and enhanced neuronal differentiation in cerebral organoids of Dutch-type cerebral amyloid angiopathy patients by Elena Daoutsali, Barry A. Pepers, Stavros Stamatakis, Linda M. van der Graaf, Gisela M. Terwindt, David A. Parfitt, Ronald A. M. Buijsen, Willeke M. C. van Roon-Mom

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Ataxin-3 protein modification as a treatment strategy for spinocerebellar ataxia type 3: Removal of the CAG containing exon by Melvin M. Evers, Hoang-Dai Tran, Ioannis Zalachoras, Barry A. Pepers, Onno C. Meijer, Johan T. den Dunnen, Gert-Jan B. van Ommen, Annemieke Aartsma-Rus, Willeke M.C. van Roon-Mom

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GLUT-1 changes in paediatric Huntington disease brain cortex and fibroblasts: an observational case-control studyResearch in context by Antonella Tramutola, Hannah S. Bakels, Federica Perrone, Michela Di Nottia, Tommaso Mazza, Maria Pia Abruzzese, Martina Zoccola, Sara Pagnotta, Rosalba Carrozzo, Susanne T. de Bot, Marzia Perluigi, Willeke M.C. van Roon-Mom, Ferdinando Squitieri

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Generation of 3 spinocerebellar ataxia type 1 (SCA1) patient-derived induced pluripotent stem cell lines LUMCi002-A, B, and C and 2 unaffected sibling control induced pluripotent s... by Ronald A.M. Buijsen, Sarah L. Gardiner, Marga J. Bouma, Linda M. van der Graaf, Merel W. Boogaard, Barry A. Pepers, Bert Eussen, Annelies de Klein, Christian Freund, Willeke M.C. van Roon-Mom

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Molecular investigation of TBP allele length: by Suzanne J. Reid, Mark I. Rees, Willeke M.C. van Roon-Mom, A.Lesley Jones, Marcy E. MacDonald, Greg Sutherland, Matthew J. During, Richard L.M. Faull, Michael J. Owen, Mike Dragunow, Russell G. Snell

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Co-expression Patterns between ATN1 and ATXN2 Coincide with Brain Regions Affected in Huntington’s Disease by Arlin Keo, Arlin Keo, N. Ahmad Aziz, Oleh Dzyubachyk, Jeroen van der Grond, Willeke M. C. van Roon-Mom, Boudewijn P. F. Lelieveldt, Boudewijn P. F. Lelieveldt, Boudewijn P. F. Lelieveldt, Marcel J. T. Reinders, Marcel J. T. Reinders, Ahmed Mahfouz, Ahmed Mahfouz

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Generation of 3 human induced pluripotent stem cell lines LUMCi005-A, B and C from a Hereditary Cerebral Hemorrhage with Amyloidosis-Dutch type patient by Elena Daoutsali, Ronald A.M. Buijsen, Simone van de Pas, Anke 't Jong, Harald Mikkers, Tom Brands, Bert Eussen, Annelies de Klein, Linda M. van der Graaf, Barry A. Pepers, Christian Freund, Gisela M. Terwindt, Valeria V. Orlova, Willeke M.C. van Roon-Mom

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Transcriptional profiling and biomarker identification reveal tissue specific effects of expanded ataxin-3 in a spinocerebellar ataxia type 3 mouse model by Lodewijk J. A. Toonen, Maurice Overzier, Melvin M. Evers, Leticia G. Leon, Sander A. J. van der Zeeuw, Hailiang Mei, Szymon M. Kielbasa, Jelle J. Goeman, Kristina M. Hettne, Olafur Th. Magnusson, Marion Poirel, Alexandre Seyer, Peter A. C. ‘t Hoen, Willeke M. C. van Roon-Mom

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Generation of genetically matched hiPSC lines from two mosaic facioscapulohumeral dystrophy type 1 patients by Erik van der Wal, Bianca den Hamer, Patrick J. van der Vliet, Merve Tok, Tom Brands, Bert Eussen, Richard J.L.F. Lemmers, Christian Freund, Annelies de Klein, Ronald A.M. Buijsen, Willeke M.C. van Roon-Mom, Rabi Tawil, Silvère M. van der Maarel, Jessica C. de Greef

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Brain Transcriptomic Analysis of Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type by Laure Grand Moursel, Laure Grand Moursel, Willeke M. C. van Roon-Mom, Szymon M. Kiełbasa, Hailiang Mei, Henk P. J. Buermans, Linda M. van der Graaf, Linda M. van der Graaf, Kristina M. Hettne, Emile J. de Meijer, Sjoerd G. van Duinen, Jeroen F. J. Laros, Jeroen F. J. Laros, Mark A. van Buchem, Peter A. C. ‘t Hoen, Silvère M. van der Maarel, Louise van der Weerd, Louise van der Weerd

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