(Q39811341)

14 September 2017

Cytoplasmic accumulation of TDP-43 in circulating lymphomonocytes of ALS patients with and without TARDBP mutations (English)

1 reference

amyotrophic lateral sclerosis

14 September 2017

1 reference

12

Adriano Chiò

1 reference

14 September 2017

4

Cristina Moglia

1 reference

14 September 2017

Giovanni De Marco

1

1 reference

14 September 2017

Elisa Lupino

2

1 reference

14 September 2017

Andrea Calvo

3

1 reference

14 September 2017

Barbara Buccinnà

5

1 reference

14 September 2017

Silvia Grifoni

6

1 reference

14 September 2017

Cristina Ramondetti

7

1 reference

14 September 2017

Annarosa Lomartire

8

1 reference

14 September 2017

Maria Teresa Rinaudo

9

1 reference

14 September 2017

Marco Piccinini

10

1 reference

14 September 2017

Maria Teresa Giordana

11

1 reference

14 September 2017

1 December 2010

1 reference

14 September 2017

Acta Neuropathologica

1 reference

14 September 2017

121

1 reference

14 September 2017

5

1 reference

14 September 2017

611-622

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-010-0786-7

14 September 2017

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Structural determinants of the cellular localization and shuttling of TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Cytoplasmic mislocalization of TDP-43 is toxic to neurons and enhanced by a mutation associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Genetic studies of amyotrophic lateral sclerosis: controversies and perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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/10.1007%2FS00401-010-0786-7

Prognostic factors in ALS: A critical review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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/10.1007%2FS00401-010-0786-7

TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43: a novel neurodegenerative proteinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer's disease and frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Global analysis of TDP-43 interacting proteins reveals strong association with RNA splicing and translation machinery.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Review: transactive response DNA-binding protein 43 (TDP-43): mechanisms of neurodegeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Evidence of multisystem disorder in whole-brain map of pathological TDP-43 in amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 redistribution is an early event in sporadic amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Genetics of familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Expression of TDP-43 C-terminal Fragments in Vitro Recapitulates Pathological Features of TDP-43 Proteinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Enrichment of C-terminal fragments in TAR DNA-binding protein-43 cytoplasmic inclusions in brain but not in spinal cord of frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 is intrinsically aggregation-prone, and amyotrophic lateral sclerosis-linked mutations accelerate aggregation and increase toxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Rethinking ALS: the FUS about TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

ALS and FTLD: two faces of TDP-43 proteinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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/10.1007%2FS00401-010-0786-7

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Nitroproteomics of peripheral blood mononuclear cells from patients and a rat model of ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Molecular neuropathology of TDP-43 proteinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Characterization of alternative isoforms and inclusion body of the TAR DNA-binding protein-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Truncation and pathogenic mutations facilitate the formation of intracellular aggregates of TDP-43.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Pregnancy induces molecular alterations reflecting impaired insulin control over glucose oxidative pathways that only in women with a family history of Type 2 diabetes last beyond pregnancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Current hypotheses for the underlying biology of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 in cerebrospinal fluid of patients with frontotemporal lobar degeneration and amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 M337V mutation in familial amyotrophic lateral sclerosis in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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/10.1007%2FS00401-010-0786-7

Detergent-insoluble glycosphingolipid/cholesterol microdomains of the myelin membrane

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Protein aggregation and defective RNA metabolism as mechanisms for motor neuron damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Recent advances in the genetics of amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

Structural diversity and functional implications of the eukaryotic TDP gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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://api.crossref.org/works/10.1007%2FS00401-010-0786-7

TDP-43 mutation in familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00401-010-0786-7

10.1007/S00401-010-0786-7

21 January 2018

Identifiers

DOI

1 reference

14 September 2017

1 reference