(Q37039451)

17 August 2017

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title

TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis (English)

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17 August 2017

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3

John Q Trojanowski

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17 August 2017

Linda K Kwong

1

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17 August 2017

Kunihiro Uryu

series ordinal

2

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17 August 2017

Virginia M-Y Lee

series ordinal

4

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17 August 2017

publication date

5 December 2007

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17 August 2017

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17 August 2017

volume

16

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17 August 2017

issue

1

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17 August 2017

page(s)

41-51

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The prevalence and causes of dementia in people under the age of 65 years

17 August 2017

cites work

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

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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

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Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

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Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

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Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: a functional link with disease penetrance

21 January 2018

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cis-requirement for the maintenance of round spermatid-specific transcription

21 January 2018

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Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene.

21 January 2018

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Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function

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TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing

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Structural diversity and functional implications of the eukaryotic TDP gene family

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hnRNP proteins and the biogenesis of mRNA

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Higher order arrangement of the eukaryotic nuclear bodies

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TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

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TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

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Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

21 January 2018

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21 January 2018

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Mutant valosin-containing protein causes a novel type of frontotemporal dementia

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Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

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21 January 2018

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A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology

21 January 2018

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TDP-43 immunoreactivity in hippocampal sclerosis and Alzheimer's disease

21 January 2018

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

21 January 2018

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TDP-43 proteinopathy: the neuropathology underlying major forms of sporadic and familial frontotemporal lobar degeneration and motor neuron disease

21 January 2018

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TDP-43 proteinopathy in frontotemporal lobar degeneration and amyotrophic lateral sclerosis: protein misfolding diseases without amyloidosis

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000109758

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17 August 2017

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