Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Trends in Genetics : TIG|June 11, 2026
The SMN locus in the T2T era: Structure, gene conversion, and clinical implicationsDemi Gommers, Maria M Zwartkruis, W Ludo van der Pol, et al.
Frontiers in Molecular Neuroscience|March 16, 2019
An Intersectional Approach to Target Neural Circuits With Cell- and Projection-Type Specificity: Validation in the Mesolimbic Dopamine SystemNefeli Kakava-Georgiadou, Maria M Zwartkruis, Clara Bullich-Vilarrubias, et al.
Human Molecular Genetics|March 17, 2025
A de novo deletion underlying spinal muscular atrophy: implications for carrier testing and genetic counselingMaria M Zwartkruis, Mirjam S de Pagter, Demi Gommers, et al.
Molecular Therapy. Methods & Clinical Development|December 10, 2024
Patient-specific responses to SMN2 splice-modifying treatments in spinal muscular atrophy fibroblastsIlaria Signoria, Maria M Zwartkruis, Lotte Geerlofs, et al.
Iscience|May 19, 2025
Comprehensive analysis across SMN2 excludes DNA methylation as an epigenetic biomarker for spinal muscular atrophyMaria M Zwartkruis, Joris V Kortooms, Demi Gommers, et al.
Acta Neuropathologica Communications|September 17, 2024
Molecular pathology, developmental changes and synaptic dysfunction in (pre-) symptomatic human C9ORF72-ALS/FTD cerebral organoidsAstrid T van der Geest, Channa E Jakobs, Tijana Ljubikj, et al.
Pageof 1