Frontiers Lysosomal Diseases and Neuropsychiatry: Opportunities

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Last updated 09 novembro 2024
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
The Endo-lysosomal System in Parkinson's Disease: Expanding the Horizon - ScienceDirect
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers in Molecular Neuroscience
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers Ubiquitination-Dependent Regulation of Small GTPases in Membrane Trafficking: From Cell Biology to Human Diseases
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Neuronopathic Lysosomal Storage Diseases - Specific Neuronal Characteristics and Therapeutic Approaches
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Neurological manifestations of lysosomal disorders and emerging therapies targeting the CNS - The Lancet Child & Adolescent Health
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Lithium and Autophagy ACS Chemical Neuroscience
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Lysosomal storage diseases Nature Reviews Disease Primers
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers Dynamics of a model for the degradation mechanism of aggregated α-synuclein in Parkinson's disease
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Pharmaceutics, Free Full-Text
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Rare genetic disorders - List of Frontiers' open access articles
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers CNS-Targeting Therapies for Lysosomal Storage Diseases: Current Advances and Challenges
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers Exosomal noncoding RNAs in central nervous system diseases: biological functions and potential clinical applications
Frontiers  Lysosomal Diseases and Neuropsychiatry: Opportunities
Frontiers CRISPR-Cas9 Knock-In of T513M and G41S Mutations in the Murine β–Galactosyl-Ceramidase Gene Re-capitulates Early-Onset and Adult-Onset Forms of Krabbe Disease

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