TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis (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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PubMed ID

18097159

17 August 2017

Kunihiro Uryu

series ordinal

2

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PubMed ID

18097159

17 August 2017

Virginia M-Y Lee

series ordinal

4

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17 August 2017

5 December 2007

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17 August 2017

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17 August 2017

16

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17 August 2017

1

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17 August 2017

41-51

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

17 August 2017

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The prevalence of frontotemporal dementia

21 January 2018

1 reference

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

Frontotemporal dementia: clinicopathological correlations

21 January 2018

1 reference

The role of hypothermia in the management of severe brain injury: a meta-analysis.

21 January 2018

1 reference

Clinicopathological correlates in frontotemporal dementia

21 January 2018

1 reference

Frontotemporal lobar degeneration: demographic characteristics of 353 patients

21 January 2018

1 reference

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

21 January 2018

1 reference

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

21 January 2018

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

Neurodegenerative diseases: new concepts of pathogenesis and their therapeutic implications

21 January 2018

1 reference

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

21 January 2018

1 reference

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

21 January 2018

1 reference

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

21 January 2018

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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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Structural diversity and functional implications of the eukaryotic TDP gene family

21 January 2018

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hnRNP proteins and the biogenesis of mRNA

21 January 2018

1 reference

Higher order arrangement of the eukaryotic nuclear bodies

21 January 2018

1 reference

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

21 January 2018

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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

1 reference

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

21 January 2018

1 reference

Frontotemporal lobar degeneration: clinical and pathological relationships

21 January 2018

1 reference

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

21 January 2018

1 reference

Gene expression analysis of frontotemporal lobar degeneration of the motor neuron disease type with ubiquitinated inclusions.

21 January 2018

1 reference

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

21 January 2018

1 reference

Genetics of familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

Recent advances in the genetics of amyotrophic lateral sclerosis and frontotemporal dementia: common pathways in neurodegenerative disease.

21 January 2018

1 reference

Ubiquitin-immunoreactive intraneuronal inclusions in amyotrophic lateral sclerosis. Morphology, distribution, and specificity.

21 January 2018

1 reference

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

21 January 2018

1 reference

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.

21 January 2018

1 reference

TDP-43 in differential diagnosis of motor neuron disorders

21 January 2018

1 reference

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

21 January 2018

1 reference

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

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000109758

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17 August 2017

1 reference

PubMed ID

18097159