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Brain Pathology, ISSN 1015-6305, 04/2014, Volume 24, Issue 3, pp. 311 - 312
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2017, Volume 1523, pp. 361 - 368
Aggregates of hyperphosphorylated tau can be observed in the human brain affected by various neurodegenerative disorders. The development of a noninvasive... 
Tauopathies | FSB | P301S mutant mice | Tau protein | Confocal scanning laser ophthalmoscopy | Retina - metabolism | Tauopathies - genetics | Humans | Tauopathies - pathology | tau Proteins - metabolism | Mice, Transgenic | Mutation - genetics | Diagnostic Imaging - methods | Tauopathies - metabolism | Animals | Mice | Retina - pathology | Disease Models, Animal
Journal Article
Journal Article
BRAIN PATHOLOGY, ISSN 1015-6305, 04/2014, Volume 24, Issue 3, pp. 311 - 312
Journal Article
Neurobiology of Aging, ISSN 0197-4580, 11/2013, Volume 34, Issue 11, pp. 2517 - 2524
Cholinergic basal forebrain (BF) neurons source one of the largest modulator systems of the brain, supplying acetylcholine to the entire cerebral mantle. Ample... 
Acetylcholine
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 3/2013, Volume 125, Issue 3, pp. 413 - 423
Genetic analysis revealed the hexanucleotide repeat expansion GGGGCC within the regulatory region of the gene C9orf72 as the most common cause of familial... 
Pathology | hnRNP A3 | Neurosciences | Medicine & Public Health | Neurodegeneration | TDP-43 | FTLD | ALS | C9orf72 | DEMENTIA | PROTEIN | EXPANSIONS | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | FRONTOTEMPORAL LOBAR DEGENERATION | NEUROSCIENCES | MASS-SPECTROMETRY | CLINICAL NEUROLOGY | GENE | HEXANUCLEOTIDE REPEAT | Frontotemporal Lobar Degeneration - pathology | Gene Expression Regulation - genetics | Sequestosome-1 Protein | Amyotrophic Lateral Sclerosis - genetics | Humans | Repetitive Sequences, Nucleic Acid - physiology | Heterogeneous-Nuclear Ribonucleoprotein Group A-B - metabolism | Hippocampus - pathology | Chromatography, High Pressure Liquid | Mutation - genetics | DNA-Binding Proteins - metabolism | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Transfection | Frontotemporal Lobar Degeneration - metabolism | Mass Spectrometry | Amyotrophic Lateral Sclerosis - metabolism | HEK293 Cells | Inclusion Bodies - pathology | C9orf72 Protein | Frontotemporal Lobar Degeneration - genetics | Adaptor Proteins, Signal Transducing - metabolism | Inclusion Bodies - metabolism | RNA, Small Interfering - metabolism | Immunohistochemistry | Brain | RNA | Analysis | Physiological aspects | Amyotrophic lateral sclerosis | Genetic aspects | Binding proteins | Genetic translation | Protein binding | Index Medicus | Translation | Toxicity | Regulatory sequences | Metabolism | RNA-binding protein | Autopsy | Inclusion bodies | Genetic analysis | Mutation | Frontotemporal dementia | Hippocampus
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 7/2015, Volume 130, Issue 1, pp. 1 - 19
Synaptic failure is an immediate cause of cognitive decline and memory dysfunction in Alzheimer’s disease. Dendritic spines are specialized structures on... 
Medicine & Public Health | Pathology | Neurosciences | Review
Journal Article
Journal Article