about
Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS).Serum miRNAs miR-206, 143-3p and 374b-5p as potential biomarkers for amyotrophic lateral sclerosis (ALS).Neuronal DNA damage response-associated dysregulation of signalling pathways and cholesterol metabolism at the earliest stages of Alzheimer-type pathologyA distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK seriesAnalysis of European case-control studies suggests that common inherited variation in mitochondrial DNA is not involved in susceptibility to amyotrophic lateral sclerosis.Concurrence of multiple sclerosis and amyotrophic lateral sclerosis in patients with hexanucleotide repeat expansions of C9ORF72.Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis.Large-scale pathways-based association study in amyotrophic lateral sclerosis.Oligogenic inheritance of optineurin (OPTN) and C9ORF72 mutations in ALS highlights localisation of OPTN in the TDP-43-negative inclusions of C9ORF72-ALS.
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description
hulumtuese
@sq
onderzoeker
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researcher
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հետազոտող
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name
Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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type
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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Emily F. Goodall
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0000-0002-1002-6541