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Journal of Neurology|September 10, 2018
Sensor-based gait analysis of individualized improvement during apomorphine titration in Parkinson's diseaseFranz Marxreiter, Heiko Gaßner, Olga Borozdina, et al.
Nutrients|November 26, 2022
Neurometabolic Dysfunction in SPG11 Hereditary Spastic ParaplegiaMartin Regensburger, Laura Krumm, Manuel Alexander Schmidt, et al.
Human Molecular Genetics|November 27, 2018
Human SPG11 cerebral organoids reveal cortical neurogenesis impairmentFrancesc Pérez-Brangulí, Isabel Y Buchsbaum, Tatyana Pozner, et al.
Journal of Neurochemistry|January 29, 2024
Sex-specific pleiotropic changes in emotional behavior and alcohol consumption in human α-synuclein A53T transgenic mice during early adulthoodLiubov S Kalinichenko, Zacharias Kohl, Christiane Mühle, et al.
Journal of Neuropathology and Experimental Neurology|June 11, 2010
Stem cell quiescence in the hippocampal neurogenic niche is associated with elevated transforming growth factor-beta signaling in an animal model of Huntington diseaseMahesh Kandasamy, Sebastien Couillard-Despres, Kerstin A Raber, et al.
Stem Cell Reports|September 1, 2015
Pattern of Functional TTX-Resistant Sodium Channels Reveals a Developmental Stage of Human iPSC- and ESC-Derived NociceptorsEsther Eberhardt, Steven Havlicek, Diana Schmidt, et al.
Cell Stem Cell|July 7, 2018
Th17 Lymphocytes Induce Neuronal Cell Death in a Human iPSC-Based Model of Parkinson's DiseaseAnnika Sommer, Franz Marxreiter, Florian Krach, et al.
Human Molecular Genetics|May 6, 2014
Dysfunction of spatacsin leads to axonal pathology in SPG11-linked hereditary spastic paraplegiaFrancesc Pérez-Brangulí, Himanshu K Mishra, Iryna Prots, et al.
Scientific Reports|November 23, 2018
Need for high-resolution Genetic Analysis in iPSC: Results and Lessons from the ForIPS ConsortiumBernt Popp, Mandy Krumbiegel, Janina Grosch, et al.
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