Search Results - "Franklin, John P"
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1
Occupational and Residential Exposure Assessment for Pesticides
Published 2005“…This timely publication concentrates on the exposure to pesticides by agricultural workers and residential users of pesticides through inhalation and physical…”
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2
Simultaneous ALS and SCA2 associated with an intermediate-length ATXN2 CAG-repeat expansion
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (02-10-2021)“…Spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS) share a common molecular basis: both are associated with CAG-repeat expansion of…”
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Journal Article -
3
Concurrent sodium channelopathies and amyotrophic lateral sclerosis supports shared pathogenesis
Published in Amyotrophic lateral sclerosis and frontotemporal degeneration (01-11-2020)“…Amyotrophic lateral sclerosis (ALS) is an invariably fatal adult-onset neurodegenerative disorder; approximately 10% of ALS is monogenic but all ALS exhibits…”
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Journal Article -
4
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene
Published in Cell reports (Cambridge) (02-02-2021)Get full text
Journal Article -
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Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene
Published in Cell reports (Cambridge) (01-12-2020)“…Amyotrophic lateral sclerosis (ALS) is an incurable neurodegenerative disease. CAV1 and CAV2 organize membrane lipid rafts (MLRs) important for cell signaling…”
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Journal Article -
6
Simultaneous ALS and SCA2 associated with an intermediate-length ATXN2 CAG-repeat expansion
Published in Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (02-10-2021)“…Spinocerebellar ataxia type 2 (SCA2) and amyotrophic lateral sclerosis (ALS) share a common molecular basis: both are associated with CAG-repeat expansion of…”
Get full text
Report -
7
Concurrent sodium channelopathies and amyotrophic lateral sclerosis supports shared pathogenesis
Published in Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration (01-10-2020)“…Amyotrophic lateral sclerosis (ALS) is an invariably fatal adult-onset neurodegenerative disorder; approximately 10% of ALS is monogenic but all ALS exhibits…”
Get full text
Report