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Methods in Molecular Biology (Clifton, N.J.)|May 28, 2018
Dopaminergic Neuron-Specific Autophagy-Deficient MiceShigeto Sato, Nobutaka HattoriParkinson'S Disease|August 24, 2011
Genetic mutations and mitochondrial toxins shed new light on the pathogenesis of Parkinson's diseaseShigeto Sato, Nobutaka HattoriNeuropathology : Official Journal of the Japanese Society of Neuropathology|November 21, 2007
Animal models of Parkinson's disease: similarities and differences between the disease and modelsNobutaka Hattori, Shigeto SatoJournal of Neural Transmission (Vienna, Austria : 1996)|November 25, 2024
Mitochondrial dysfunction in Parkinson's diseaseNobutaka Hattori, Shigeto SatoNeuroscience Research|May 4, 2020
Pathogenic insights to Parkin-linked model miceShigeto Sato, Sachiko Noda, Nobutaka HattoriJournal of Neural Transmission (Vienna, Austria : 1996)|September 13, 2017
Lysosomal defects in ATP13A2 and GBA associated familial Parkinson's diseaseShigeto Sato, Yuanzhe Li, Nobutaka HattoriJournal of Neurology, Neurosurgery, and Psychiatry|December 6, 2011
Molecular pathogenesis of Parkinson's disease: updateShinji Saiki, Shigeto Sato, Nobutaka HattoriNeurology|March 23, 2005
Urinary 8-hydroxydeoxyguanosine levels as a biomarker for progression of Parkinson diseaseShigeto Sato, Yoshikuni Mizuno, Nobutaka HattoriTrends in Pharmacological Sciences|July 26, 2011
Genetic mutations and functions of PINK1Sumihiro Kawajiri, Shinji Saiki, Shigeto Sato, et al.Journal of Neurochemistry|September 29, 2009
Pathogenesis of familial Parkinson's disease: new insights based on monogenic forms of Parkinson's diseaseTaku Hatano, Shin-ichiro Kubo, Shigeto Sato, et al.Pageof 96