Showing results (1-10 of 49) with videos related to
Sort By:
Pageof 5
Current Opinion in Neurology|August 7, 2025
Genetics of ALS - genes and modifierSonja Menge, Lorena Decker, Axel FreischmidtMolecular Neurobiology|March 29, 2023
The Fragile X Protein Family in Amyotrophic Lateral SclerosisSarah Mueller, Lorena Decker, Sonja Menge, et al.Cellular and Molecular Life Sciences : CMLS|October 21, 2025
Comparing loss of individual fragile X proteins suggests strong links to cellular senescence and agingSonja Menge, Inmaculada Segura, Max Hartmann, et al.Brain : a Journal of Neurology|December 11, 2025
Somatic gene mutations in the motor cortex of patients with sporadic amyotrophic lateral sclerosisÓscar González-Velasco, Rosanna Parlato, Rüstem Yilmaz, et al.Current Opinion in Neurology|August 9, 2022
Update on genetics of amyotrophic lateral sclerosisDavid Brenner, Axel FreischmidtJournal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|March 12, 2014
FXN GAA repeat expansions in amyotrophic lateral sclerosisNaji Rizik, Axel Freischmidt, Albert C Ludolph, et al.Human Molecular Genetics|April 27, 2024
An integrative miRNA-mRNA expression analysis identifies miRNA signatures associated with SOD1 and TARDBP patient-derived motor neuronsBanaja P Dash, Axel Freischmidt, Jochen H Weishaupt, et al.Biotechnology Letters|November 13, 2012
Enhanced in vitro translation at reduced temperatures using a cold-shock RNA motifAxel Freischmidt, Johannes Hiltl, Hans Robert Kalbitzer, et al.Acta Neuropathologica Communications|November 21, 2013
Systemic dysregulation of TDP-43 binding microRNAs in amyotrophic lateral sclerosisAxel Freischmidt, Kathrin Müller, Albert C Ludolph, et al.International Journal of Molecular Sciences|September 9, 2022
Downstream Effects of Mutations in SOD1 and TARDBP Converge on Gene Expression Impairment in Patient-Derived Motor NeuronsBanaja P Dash, Axel Freischmidt, Jochen H Weishaupt, et al.Pageof 5