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Nucleic Acid Therapeutics|June 1, 2021
Antisense Oligonucleotide-Induced Amyloid Precursor Protein Splicing Modulation as a Therapeutic Approach for Dutch-Type Cerebral Amyloid AngiopathyElena Daoutsali, Tsinatkeab T Hailu, Ronald A M Buijsen, et al.Stroke|October 26, 2018
Cerebral Amyloid Angiopathy With Vascular Iron Accumulation and CalcificationMarjolein Bulk, Laure Grand Moursel, Linda M van der Graaf, et al.Neurobiology of Disease|January 31, 2026
Impedance-based phenotypic profiling of metabotropic glutamate receptor ligand responses in SCA1 human iPSC-derived neuronal culturesLaurie M C Kerkhof, Ronald A M Buijsen, Stefan Hartman, et al.Circulation. Heart Failure|November 19, 2009
A new direction for cardiac regeneration therapy: application of synergistically acting epicardium-derived cells and cardiomyocyte progenitor cellsElizabeth M Winter, Angelique A M van Oorschot, Bianca Hogers, et al.Neurobiology of Disease|June 9, 2026
Loss of astrocytic markers and impaired metabolic function in spinocerebellar ataxia type 7 patient-derived neural culturesLinde F Bouwman, Ronald A M Buijsen, Linda M van der Graaf, et al.Stem Cell Research|April 18, 2026
Generation of an isogenic human induced pluripotent stem cell line for spinocerebellar ataxia type 1Laurie M C Kerkhof, Barry A Pepers, Linda M van der Graaf, et al.Stem Cell Research|April 16, 2018
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 stem cell lines LUMCi003-A and BRonald A M Buijsen, Sarah L Gardiner, Marga J Bouma, et al.Journal of Internal Medicine|April 8, 2021
Cerebrotendinous xanthomatosis without neurological involvementB M L Stelten, F J Raal, A D Marais, et al.Stem Cell Research|June 8, 2024
Generation of human induced pluripotent stem cell lines (LUMCi051-A,B and LUMCi052-A,B,C) of two patients with Spinocerebellar ataxia type 7Linde F Bouwman, Milou E M Joosen, Ronald A M Buijsen, et al.Brain Pathology (Zurich, Switzerland)|May 31, 2017
TGFβ pathway deregulation and abnormal phospho-SMAD2/3 staining in hereditary cerebral hemorrhage with amyloidosis-Dutch typeLaure Grand Moursel, Leon P Munting, Linda M van der Graaf, et al.Pageof 10