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TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis

Data up to Jan 2025

Published2008
Citations2,514
References28

Total Citations Per Year

Abstract

References (28)

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Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases

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Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3

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A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia

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TDP-43 is deposited in the Guam parkinsonism-dementia complex brains

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Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration

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Identification of Two Novel Loci for Dominantly Inherited Familial Amyotrophic Lateral Sclerosis

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A Novel CpG-free Vertebrate Insulator Silences the Testis-specific SP-10 Gene in Somatic Tissues

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Two Families with Familial Amyotrophic Lateral Sclerosis Are Linked to a Novel Locus on Chromosome 16q

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Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS

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TAR-DNA Binding Protein 43 in Pick Disease

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TDP-43 gene analysis in frontotemporal lobar degeneration

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No association of TDP-43 with sporadic frontotemporal dementia

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Truncated wild-type SOD1 and FALS-linked mutant SOD1 cause neural cell death in the chick embryo spinal cord

2005 • 28 citations

No association of chromatin-modifying protein 2B with sporadic frontotemporal dementia

2006 • 18 citations

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