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Alan Renton

neuroscientist

Alan Renton

British neuroscientist (born 1976)

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About Alan Renton

Also known as Alan Edward Mayo Renton, Alan E. Renton, Alan E Renton

About Alan Renton

British neuroscientist (born 1976)

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Occupation: neuroscientist
Born: 1976

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Nicholas Renton Caroline Harrow

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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD State of play in amyotrophic lateral sclerosis genetics Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis PINK1 cleavage at position A103 by the mitochondrial protease PARL.Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress response Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophy

Occupation: neuroscientist
Born: 1976

Family

Nicholas Rentonfather Caroline Harrowmother

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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDknown for State of play in amyotrophic lateral sclerosis geneticsknown for Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional studyknown for Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisknown for PINK1 cleavage at position A103 by the mitochondrial protease PARL.known for Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.known for Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress responseknown for Genetic variants of the alpha-synuclein gene SNCA are associated with multiple system atrophyknown for