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Lancet Neurology, The, ISSN 1474-4422, 2016, Volume 15, Issue 2, pp. 133 - 135
  [...]although many questions remain, stem cells have great potential to enhance our understanding of the molecular basis of Alzheimer's disease and provide a... 
Neurology | INTRACELLULAR A-BETA | CLINICAL NEUROLOGY | DEMENTIA | Stem Cell Transplantation | Genetic Therapy | Alzheimer Disease | Humans | Care and treatment | Transplantation | Drug therapy | Alzheimer's disease | Stem cells | Studies | Pathology | Transplants & implants | Bone marrow | Clinical trials | Alzheimers disease | Gene expression | Index Medicus
Journal Article
Nature Neuroscience, ISSN 1097-6256, 08/2016, Volume 19, Issue 8, pp. 1085 - 1092
Tau protein can transfer between neurons transneuronally and trans-synaptically, which is thought to explain the progressive spread of tauopathy observed in... 
PLURIPOTENT STEM-CELLS | PROTEIN | HYPEREXCITABILITY | ALZHEIMERS-DISEASE | AMYLOID-BETA | MOUSE MODEL | TAUOPATHY | CEREBROSPINAL-FLUID | NEUROSCIENCES | BRAIN | TRANSGENIC MICE | Brain - metabolism | tau Proteins - metabolism | Mice, Transgenic | Tauopathies - metabolism | Animals | Synapses - metabolism | Usage | Research | Neurons | Microfluidics | Tau proteins | Index Medicus
Journal Article
Nature Neuroscience, ISSN 1097-6256, 09/2013, Volume 16, Issue 9, pp. 1257 - 1265
Compelling evidence indicates that two autosomal recessive Parkinson's disease genes, PINK1 (PARK6) and Parkin (PARK2), cooperate to mediate the autophagic... 
CELLS | PINK1 | COMPLEX | MONITORING AUTOPHAGY | MITOCHONDRIAL PATHOLOGY | PROTEASOME | PYRAMIDAL SYNDROME | TARGETING SEQUENCES | NEUROSCIENCES | F-BOX PROTEIN | DROSOPHILA | Physiological aspects | Mitochondria | Genetic aspects | Parkinson's disease | Research | Gene expression | Index Medicus
Journal Article
Alzheimer's Research & Therapy, ISSN 1758-9193, 12/2017, Volume 9, Issue 1, pp. 1 - 17
Abstract A major challenge to our understanding of the molecular mechanisms of Alzheimer’s disease (AD) has been the lack of physiologically relevant in vitro... 
Neuronal differentiation | Alzheimer’s disease | Induced pluripotent stem cells | 3D cerebral organoids
Journal Article
Neuron, ISSN 0896-6273, 04/2013, Volume 78, Issue 1, pp. 57 - 64
Valosin-containing protein (VCP) is a highly expressed member of the type II AAA+ ATPase family. mutations are the cause of inclusion body myopathy, Paget’s... 
LIPID-PEROXIDATION | SPINAL-CORD PATHOLOGY | MOUSE MODEL | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | DYSFUNCTION | BONE | NEUROSCIENCES | PAGET-DISEASE | TRANSGENIC MICE | REVEALS | RNA, Small Interfering - genetics | Humans | Middle Aged | Male | Frontotemporal Dementia - metabolism | Neurons - ultrastructure | Muscular Dystrophies, Limb-Girdle - genetics | Adenosine Triphosphate - metabolism | Membrane Potential, Mitochondrial - genetics | Muscular Dystrophies, Limb-Girdle - pathology | NAD - metabolism | Fibroblasts - metabolism | Animals, Newborn | Frontotemporal Dementia - genetics | Magnesium - metabolism | Mitochondria - pathology | Fibroblasts - pathology | Mutation - genetics | Myositis, Inclusion Body - genetics | Osteitis Deformans - pathology | Muscular Dystrophies, Limb-Girdle - metabolism | Analysis of Variance | Luminescent Proteins - genetics | Adenosine Triphosphatases - genetics | Mice | Lipid Peroxidation - genetics | RNA, Small Interfering - metabolism | Valosin Containing Protein | Osteitis Deformans - metabolism | Family Health | Cerebral Cortex - cytology | Case-Control Studies | Osteitis Deformans - genetics | Transfection | Mitochondria - genetics | Cell Cycle Proteins - genetics | Myositis, Inclusion Body - pathology | Adult | Female | Neuroblastoma - pathology | Frontotemporal Dementia - pathology | Adenosine Triphosphatases - deficiency | Mice, Inbred C57BL | Cells, Cultured | Cell Cycle Proteins - deficiency | Mitochondria - metabolism | Animals | Oxygen Consumption - genetics | Myositis, Inclusion Body - metabolism | Aged | Nervous system diseases | Neurosciences | Genes | Amyotrophic lateral sclerosis | Genetic aspects | Adenosine triphosphatase | Dementia | Proteins | Medical research | Phosphorylation | Biomedical research | Disease | Rodents | Respiration | Experiments | Patients | Index Medicus | Report
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2017, Volume 12, Issue 9, pp. e0184104 - e0184104
Mutations in PANK2 lead to neurodegeneration with brain iron accumulation. PANK2 has a role in the biosynthesis of coenzyme A (CoA) from dietary vitamin B5,... 
PANTOTHENATE | PANK2 | METABOLISM | MULTIDISCIPLINARY SCIENCES | BRAIN IRON ACCUMULATION | UPDATE | COENZYME-A | INSIGHTS | Reactive Oxygen Species - metabolism | Humans | Male | Brain - metabolism | NAD - chemistry | Pantothenate Kinase-Associated Neurodegeneration - physiopathology | Karyotyping | Membrane Potential, Mitochondrial | Female | Cell Differentiation | Neurons - metabolism | Induced Pluripotent Stem Cells - cytology | Child | Fibroblasts - metabolism | Induced Pluripotent Stem Cells - metabolism | Acetyl Coenzyme A - chemistry | Iron - chemistry | Pantothenic Acid - chemistry | Phosphotransferases (Alcohol Group Acceptor) - genetics | Mitochondria - pathology | Coenzyme A - metabolism | Plasmids - metabolism | Phosphotransferases (Alcohol Group Acceptor) - metabolism | Phenotype | Biopsy | Adolescent | Mutation | Lipid Peroxidation | Mitochondrial Diseases - physiopathology | Gene mutations | Stem cells | Physiological aspects | Nervous system | Genetic aspects | Degeneration | Research | Brain | Reactive oxygen species | Neurosciences | Phosphorylation | Disease | Childrens health | Homeostasis | Lipid peroxidation | Iron | Biosynthesis | Accumulation | Mitochondria | NADH | Publishing | Neurodegeneration | Rodents | Chelation | Fibroblasts | Coenzyme A | Membrane potential | Peroxidation | Neurons | Cortex | Light emitting diodes | Metabolism | Neurology | Oxidative phosphorylation | Insects | Diet | Nicotinamide adenine dinucleotide | Electron transport | Molecular biology | Pluripotency | Inhibitory postsynaptic potentials | Index Medicus
Journal Article
Frontiers in Psychiatry, ISSN 1664-0640, 2010, Volume 1, pp. 150 - 150
Parkinson's disease (PD) represents a major challenge for health care systems around the world: it is the most common degenerative movement disorder of old... 
Tau | Parkinson's disease | Genome wide association study | Synuclein | tau | genome wide association study | synuclein
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 8855 - 8855
The discovery of mutations within genes associated with autosomal recessive Parkinson's disease allowed for the identification of PINK1/Parkin regulated... 
OUTER-MEMBRANE | PARKIN | STEM-CELLS | MTORC2 | AKT/PKB | PHOSPHORYLATION | UBIQUITIN | MULTIDISCIPLINARY SCIENCES | MITOCHONDRIAL DYSFUNCTION | AUTOPHAGY | DROSOPHILA-PINK1
Journal Article