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amyotrophic lateral sclerosis (15) 15
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Neuron, ISSN 0896-6273, 05/2016, Volume 90, Issue 3, pp. 535 - 550
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 12/2013, Volume 126, Issue 6, pp. 829 - 844
Journal Article
Journal Article
Neuron, ISSN 0896-6273, 12/2015, Volume 88, Issue 5, pp. 892 - 901
Noncoding expansions of a hexanucleotide repeat (GGGGCC) in the gene are the most common cause of familial amyotrophic lateral sclerosis and frontotemporal... 
DEMENTIA | EXPANDED C9ORF72 | DIPEPTIDE-REPEAT PROTEINS | EXPANSIONS | AMYOTROPHIC-LATERAL-SCLEROSIS | FRONTOTEMPORAL LOBAR DEGENERATION | TRANSLATION | HEXANUCLEOTIDE REPEAT | NEUROSCIENCES | GGGGCC REPEAT | RNA FOCI | Muscle Strength - genetics | Spinal Cord - metabolism | Age Factors | Amyotrophic Lateral Sclerosis - physiopathology | DNA Repeat Expansion - genetics | Humans | Psychomotor Performance - physiology | Brain - metabolism | Chromosomes, Artificial, Bacterial - genetics | Spinal Cord - pathology | Chromosomes, Artificial, Bacterial - metabolism | Neuromuscular Junction - genetics | C9orf72 Protein | Neurons - drug effects | Neuromuscular Junction - pathology | Disease Models, Animal | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Frontotemporal Dementia - physiopathology | Glutamic Acid - pharmacology | Amyotrophic Lateral Sclerosis - genetics | Cells, Cultured | Mice, Transgenic | Proteins - genetics | Motor Activity - genetics | Amyotrophic Lateral Sclerosis - pathology | Animals | Brain - pathology | Mice | Neurosciences | Genetic engineering | RNA | Dementia | Medical colleges | Peptides | Proteins | Brain research | Transgenic animals | Neurodegeneration | Laboratories | Rodents | Amyotrophic lateral sclerosis | Genomes | Artificial chromosomes | Alzheimers disease | Experiments | Patients
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 10/2014, Volume 128, Issue 4, pp. 505 - 524
The occurrence of repeat-associated non-ATG (RAN) translation, an atypical form of translation of expanded repeats that results in the synthesis of... 
Pathology | Neurosciences | Medicine & Public Health | Expanded repeat | Repeat-associated non-ATG translation | ER stress | Amyotrophic lateral sclerosis | Frontotemporal dementia | C9ORF72 | Poly(GA) proteins | Proteasome activity | UBIQUITIN-PROTEASOME SYSTEM | CHEMICAL CHAPERONES | COGNITIVE IMPAIRMENT | ENDOPLASMIC-RETICULUM STRESS | AMYOTROPHIC-LATERAL-SCLEROSIS | PATHOLOGY | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | CLINICAL NEUROLOGY | CELL-DEATH | C9ORF72 HEXANUCLEOTIDE REPEAT | RNA FOCI | Cholagogues and Choleretics - pharmacology | DNA Repeat Expansion - genetics | Embryo, Mammalian | Humans | Middle Aged | Male | DNA Repeat Expansion - immunology | Endoplasmic Reticulum Stress - genetics | Brain - metabolism | Frontotemporal Dementia - metabolism | Cell Nucleolus - metabolism | Cell Nucleolus - ultrastructure | Brain - ultrastructure | HEK293 Cells | Aged, 80 and over | Adult | Female | C9orf72 Protein | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Endoplasmic Reticulum Stress - drug effects | Protein Structure, Secondary | Amyotrophic Lateral Sclerosis - genetics | Cells, Cultured | Antibodies - pharmacology | Gene Expression Regulation - drug effects | Nerve Tissue Proteins - metabolism | Amyotrophic Lateral Sclerosis - pathology | Animals | Proteins - metabolism | Amyotrophic Lateral Sclerosis - metabolism | Brain - pathology | Gene Expression Regulation - radiation effects | Aged | Mice | Proteins - chemistry | Endoplasmic Reticulum Stress - physiology | Proteins | Health aspects | Dementia | Index Medicus | Original Paper
Journal Article
Neuron, ISSN 0896-6273, 12/2015, Volume 88, Issue 5, pp. 902 - 909
A non-coding hexanucleotide repeat expansion in the gene is the most common mutation associated with familial amyotrophic lateral sclerosis (ALS) and... 
RAN translation | transgenic mice | Amyotrophic lateral sclerosis (ALS) | frontotemporal dementia (FTD) | neurodegeneration | microRNA | repeat expansions | C9ORF72 | RNA foci | Repeat expansions | MicroRNA | Neurodegeneration | Transgenic mice | Frontotemporal dementia (FTD) | DEMENTIA | ALS | AMYOTROPHIC-LATERAL-SCLEROSIS | SPECTRUM | MODEL | FRONTOTEMPORAL LOBAR DEGENERATION | TRANSLATION | SENSE | NEUROSCIENCES | PATHOLOGICAL FEATURES | Age Factors | Amyotrophic Lateral Sclerosis - physiopathology | DNA Repeat Expansion - genetics | Humans | MicroRNAs - metabolism | Frontotemporal Dementia - mortality | Cerebral Cortex - cytology | Brain - metabolism | Chromosomes, Artificial, Bacterial - genetics | Chromosomes, Artificial, Bacterial - metabolism | Neurons - physiology | C9orf72 Protein | Dipeptides - metabolism | Neurons - drug effects | Disease Models, Animal | Frontotemporal Dementia - pathology | Frontotemporal Dementia - genetics | Frontotemporal Dementia - physiopathology | Gene Expression Regulation - genetics | Amyotrophic Lateral Sclerosis - genetics | Cells, Cultured | Genotype | Mice, Transgenic | Amyotrophic Lateral Sclerosis - mortality | Nerve Tissue Proteins - metabolism | Proteins - genetics | Amyotrophic Lateral Sclerosis - pathology | Animals | Brain - pathology | In Vitro Techniques | Dipeptides - genetics | Proteins | Neurosciences | Proline | Genetic engineering | Glycine | Dementia | Analysis | Genetic translation | Plasmids | Neurons | Rodents | Cloning | Amyotrophic lateral sclerosis | Behavior | Artificial chromosomes | Expansion
Journal Article
Nature Neuroscience, ISSN 1097-6256, 05/2016, Volume 19, Issue 5, pp. 668 - 677
Journal Article
Molecular neurodegeneration, ISSN 1750-1326, 02/2019, Volume 14, Issue 1, pp. 9 - 9
Journal Article
Nature Medicine, ISSN 1078-8956, 08/2018, Volume 24, Issue 8, pp. 1136 - 1142
Journal Article
Science, ISSN 0036-8075, 08/2016, Volume 353, Issue 6300, pp. 708 - 712
Journal Article