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European Journal of Medicinal Chemistry|September 9, 2018
Structure-based design of allosteric calpain-1 inhibitors populating a novel bioactivity spaceLeen Kalash, Joel Cresser-Brown, Johnny Habchi, et al.Frontiers in Computational Neuroscience|May 14, 2023
Stability of mental motor-imagery classification in EEG depends on the choice of classifier model and experiment design, but not on signal preprocessingMartin Justinus Rosenfelder, Myra Spiliopoulou, Burkhard Hoppenstedt, et al.Neuro-Oncology Advances|March 6, 2026
The glioblastoma GBMdrug1000 dataset resource provides directions for future small molecule drug discoveryLavinia-Lorena Pruteanu, Olivier J M Béquignon, Yoran Broersma, et al.The Journal of Steroid Biochemistry and Molecular Biology|March 27, 2016
Vitamin D production in UK Caucasian and South Asian women following UVR exposureOhood A Hakim, Kathryn Hart, Patrick McCabe, et al.Archives of Physical Medicine and Rehabilitation|December 3, 2014
Diagnosis and decision making for patients with disorders of consciousness: a survey among family membersRalf J Jox, Katja Kuehlmeyer, Anke-Maria Klein, et al.Drug Discovery Today|September 12, 2015
Modelling of compound combination effects and applications to efficacy and toxicity: state-of-the-art, challenges and perspectivesKrishna C Bulusu, Rajarshi Guha, Daniel J Mason, et al.Movement Disorders : Official Journal of the Movement Disorder Society|July 21, 2010
Tongue force analysis assesses motor phenotype in premanifest and symptomatic Huntington's diseaseRalf Reilmann, Stefan Bohlen, Thomas Klopstock, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 7, 2010
Grasping premanifest Huntington's disease - shaping new endpoints for new trialsRalf Reilmann, Stefan Bohlen, Thomas Klopstock, et al.Journal of Neurology|July 8, 2008
Dopaminergic midbrain neurons are the prime target for mitochondrial DNA deletionsAndreas Bender, Rachel-Maria Schwarzkopf, Anja McMillan, et al.Neuromuscular Disorders : NMD|May 18, 2010
The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotypeCharlotte L Alston, Andreas Bender, Iain P Hargreaves, et al.Pageof 48