(Q57306362)

5

object named as

Leonard Petrucelli

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author name string

Casey Cook

1

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Yong-jie Zhang

2

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Ya-fei Xu

Expert Opinion on Biological Therapy

3

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language of work or name

English

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publication date

July 2008

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published in

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volume

8

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issue

7

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page(s)

969-78

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cites work

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

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Structural diversity and functional implications of the eukaryotic TDP gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP43 is a human low molecular weight neurofilament (hNFL) mRNA-binding protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Characterization and functional implications of the RNA binding properties of nuclear factor TDP-43, a novel splicing regulator of CFTR exon 9

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43, the signature protein of FTLD-U, is a neuronal activity-responsive factor

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

The prevalence of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

21 January 2018

Frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Frontal lobe dementia and motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Frontotemporal dementia: clinicopathological correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Neurofilament inclusion body disease: a new proteinopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: a comparative clinicopathological study

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43 in the ubiquitin pathology of frontotemporal dementia with VCP gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTD

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43: a novel neurodegenerative proteinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Molecular biology of amyotrophic lateral sclerosis: insights from genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Genetics of familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Are amyotrophic lateral sclerosis patients cognitively normal?

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43 A315T mutation in familial motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Extra neurofilament NF-L subunits rescue motor neuron disease caused by overexpression of the human NF-H gene in mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Mutant copper-zinc superoxide dismutase binds to and destabilizes human low molecular weight neurofilament mRNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43 in differential diagnosis of motor neuron disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

TDP-43 immunoreactivity in anoxic, ischemic and neoplastic lesions of the central nervous system.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Missense mutations in the progranulin gene linked to frontotemporal lobar degeneration with ubiquitin-immunoreactive inclusions reduce progranulin production and secretion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

HDAC6 rescues neurodegeneration and provides an essential link between autophagy and the UPS

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Trehalose, a novel mTOR-independent autophagy enhancer, accelerates the clearance of mutant huntingtin and alpha-synuclein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

Disturbance of nuclear and cytoplasmic TAR DNA-binding protein (TDP-43) induces disease-like redistribution, sequestration, and aggregate formation

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855963

Classification and description of frontotemporal dementias.

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855963

Cloning and characterization of a novel cellular protein, TDP-43, that binds to human immunodeficiency virus type 1 TAR DNA sequence motifs

2 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855963

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

2 November 2018

1 reference

https://api.crossref.org/works/10.1517%2F14712598.8.7.969

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2855963

Novel ubiquitin neuropathology in frontotemporal dementia with valosin-containing protein gene mutations

30 November 2018

1 reference

12 December 2020

TDP-43 gene analysis in frontotemporal lobar degeneration

1 reference

12 December 2020

Lack of TDP-43 abnormalities in mutant SOD1 transgenic mice shows disparity with ALS

1 reference

12 December 2020

Selective loss of trans-acting instability determinants of neurofilament mRNA in amyotrophic lateral sclerosis spinal cord

1 reference

12 December 2020

Pathological TDP-43 in parkinsonism-dementia complex and amyotrophic lateral sclerosis of Guam

1 reference

12 December 2020

Evidence that TDP-43 is not the major ubiquitinated target within the pathological inclusions of amyotrophic lateral sclerosis

1 reference

12 December 2020

Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model

1 reference

12 December 2020

No association of TDP-43 with sporadic frontotemporal dementia

1 reference

12 December 2020

Dementia lacking distinctive histology (DLDH) revisited

1 reference

12 December 2020

Quantitative evidence for neurofilament heavy subunit aggregation in motor neurons of spinal cords of patients with amyotrophic lateral sclerosis

1 reference

12 December 2020