The use of primary human fibroblasts for monitoring mitochondrial phenotypes in the field of Parkinson's disease

Keyphrases

• Parkinson's Disease 100%
• Primary Fibroblasts 100%
• Neurodegeneration 28%
• Mitochondrial Function 28%
• Pathological Features 28%
• Human Fibroblasts 28%
• Cancer Cells 14%
• Human Disease 14%
• In Vitro Model 14%
• Ex Vivo Model 14%
• Parkinsonism 14%
• Risk Factors 14%
• Molecular Pathways 14%
• Motor Symptoms 14%
• Mitochondrial Dynamics 14%
• Protein Folding 14%
• Aging 14%
• Mitochondria 14%
• Lysosome 14%
• Mitochondrial Morphology 14%
• Skin Biopsy 14%
• Detailed Protocol 14%
• Colocalization 14%
• Movement Disorders 14%
• Pathogenesis-related Proteins 14%
• Disease-causing mutations 14%
• Microscopic Techniques 14%
• Pathway Alteration 14%
• New Therapeutic Approaches 14%
• Common Movements 14%
• Early Signs 14%
• Gene Carrier 14%
• Artificial Cells 14%
• Human Disease Genes 14%
• Dysfunctional Mitochondria 14%
• Protein Degradation Systems 14%
• Lysosomal Pathway 14%

Neuroscience

• Parkinson's Disease 100%
• Fibroblast 100%
• Mitochondrial Function 28%
• Mitochondrion 28%
• Neurodegeneration 28%
• Lysosome 14%
• In Vitro 14%
• Stereotypic Movement Disorder 14%
• Parkinsonism 14%
• Protein Folding 14%
• Risk Factor 14%

Biochemistry, Genetics and Molecular Biology

• Fibroblast 100%
• Mitochondrion 50%
• Protein Catabolism 25%
• Lysosome 25%
• Cancer Cell 25%
• Protein Folding 25%
• Colocalization 25%