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Brain : a Journal of Neurology|September 22, 2018
UBA1/GARS-dependent pathways drive sensory-motor connectivity defects in spinal muscular atrophyHannah K Shorrock, Dinja van der Hoorn, Penelope J Boyd, et al.Nature Communications|July 11, 2014
The intracellular redox protein MICAL-1 regulates the development of hippocampal mossy fibre connectionsEljo Y Van Battum, Rou-Afza F Gunput, Suzanne Lemstra, et al.Science Signaling|April 15, 2025
Dynamic modulation of the motor neuron translatome during developmental synapse eliminationDinja van der Hoorn, Fabio Lauria, Helena Chaytow, et al.Human Molecular Genetics|July 10, 2020
Pre-natal manifestation of systemic developmental abnormalities in spinal muscular atrophyAnna A L Motyl, Kiterie M E Faller, Ewout J N Groen, et al.Journal of the Peripheral Nervous System : JPNS|March 26, 2024
A 21-bp deletion in the complement regulator CD55 promotor region is associated with multifocal motor neuropathy and its disease courseJeroen W Bos, Ewout J N Groen, Henny G Otten, et al.Cell Reports|October 26, 2017
In Vivo Translatome Profiling in Spinal Muscular Atrophy Reveals a Role for SMN Protein in Ribosome BiologyPaola Bernabò, Toma Tebaldi, Ewout J N Groen, et al.Cell Reports|October 26, 2018
Active Ribosome Profiling with RiboLaceMassimiliano Clamer, Toma Tebaldi, Fabio Lauria, et al.Neurology. Genetics|June 25, 2021
<i>SMN1</i> Duplications Are Associated With Progressive Muscular Atrophy, but Not With Multifocal Motor Neuropathy and Primary Lateral SclerosisJeroen W Bos, Ewout J N Groen, Renske I Wadman, et al.Brain Communications|September 21, 2020
Intragenic and structural variation in the <i>SMN</i> locus and clinical variability in spinal muscular atrophyRenske I Wadman, Marc D Jansen, Marloes Stam, et al.Plos One|June 26, 2018
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker studyWouter van Rheenen, Frank P Diekstra, Oliver Harschnitz, et al.Pageof 6