TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia (Q28294001)

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

ALS: a disease of motor neurons and their nonneuronal neighbors

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Aggregation and Motor Neuron Toxicity of an ALS-Linked SOD1 Mutant Independent from Wild-Type SOD1

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Continuum of frontal lobe impairment in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Ubiquitin immunohistochemistry suggests classic motor neuron disease, motor neuron disease with dementia, and frontotemporal dementia of the motor neuron disease type represent a clinicopathologic spectrum.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutation within TARDBP leads to frontotemporal dementia without motor neuron disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Accumulation of TDP-43 and alpha-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

FUS mutations in amyotrophic lateral sclerosis: clinical, pathological, neurophysiological and genetic analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Genetic contribution of FUS to frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Structural diversity and functional implications of the eukaryotic TDP gene family

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 and FUS/TLS: emerging roles in RNA processing and neurodegeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Nuclear factor TDP-43 can affect selected microRNA levels

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Knockdown of transactive response DNA-binding protein (TDP-43) downregulates histone deacetylase 6

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 is a developmentally regulated protein essential for early embryonic development

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Cytosolic TDP-43 expression following axotomy is associated with caspase 3 activation in NFL-/- mice: support for a role for TDP-43 in the physiological response to neuronal injury.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Axonal ligation induces transient redistribution of TDP-43 in brainstem motor neurons

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Frontotemporal dementia and amyotrophic lateral sclerosis-associated disease protein TDP-43 promotes dendritic branching

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43-positive white matter pathology in frontotemporal lobar degeneration with ubiquitin-positive inclusions.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TAR DNA-binding protein 43 immunohistochemistry reveals extensive neuritic pathology in FTLD-U: a midwest-southwest consortium for FTLD study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 and ubiquitinated cytoplasmic aggregates in sporadic ALS are low frequency and widely distributed in the lower motor neuron columns independent of disease spread.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Clinical and pathological continuum of multisystem TDP-43 proteinopathies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43-immunoreactive neuronal and glial inclusions in the neostriatum in amyotrophic lateral sclerosis with and without dementia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 in differential diagnosis of motor neuron disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 neuropathology is similar in sporadic amyotrophic lateral sclerosis with or without TDP-43 mutations.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 mutation in familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Genetics of familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Fus gene mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Multiple system degeneration with basophilic inclusions in Japanese ALS patients with FUS mutation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Frontotemporal lobar degeneration: clinical and pathological relationships

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Neuronal intranuclear inclusions distinguish familial FTD-MND type from sporadic cases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions with progranulin gene (PGRN) mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

DCTN1 mutations in Perry syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Pallidonigral TDP-43 pathology in Perry syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutant dynactin in motor neuron disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Point mutations of the p150 subunit of dynactin (DCTN1) gene in ALS.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Hippocampal sclerosis dementia: a reappraisal

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Concomitant TAR-DNA-binding protein 43 pathology is present in Alzheimer disease and corticobasal degeneration but not in other tauopathies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Phosphorylated TDP-43 in Alzheimer's disease and dementia with Lewy bodies.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Concurrence of TDP-43, tau and alpha-synuclein pathology in brains of Alzheimer's disease and dementia with Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 A315T mutation in familial motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TARDBP in amyotrophic lateral sclerosis: identification of a novel variant but absence of copy number variation.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

The genetics of frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Recent insights into the molecular genetics of dementia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Progranulin locus deletion in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Serum biomarker for progranulin-associated frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Low plasma progranulin levels predict progranulin mutations in frontotemporal lobar degeneration.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Progranulin Leu271LeufsX10 is one of the most common FTLD and CBS associated mutations worldwide.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Prominent phenotypic variability associated with mutations in Progranulin

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Common variant in GRN is a genetic risk factor for hippocampal sclerosis in the elderly

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Progranulin genetic variability contributes to amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

GRN variability contributes to sporadic frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Genetic variability in progranulin contributes to risk for clinically diagnosed Alzheimer disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Proteolytic processing of TAR DNA binding protein-43 by caspases produces C-terminal fragments with disease defining properties independent of progranulin

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

VCP disease associated with myopathy, Paget disease of bone and frontotemporal dementia: review of a unique disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Transgenic mice expressing mutant forms VCP/p97 recapitulate the full spectrum of IBMPFD including degeneration in muscle, brain and bone.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Three families with amyotrophic lateral sclerosis and frontotemporal dementia with evidence of linkage to chromosome 9p.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Identification of 2 Loci at chromosomes 9 and 14 in a multiplex family with frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 depletion induces neuronal cell damage through dysregulation of Rho family GTPases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Gain and loss of function of ALS-related mutations of TARDBP (TDP-43) cause motor deficits in vivo

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

A yeast TDP-43 proteinopathy model: Exploring the molecular determinants of TDP-43 aggregation and cellular toxicity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Phosphorylated and cleaved TDP-43 in ALS, FTLD and other neurodegenerative disorders and in cellular models of TDP-43 proteinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

A Drosophila model for TDP-43 proteinopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 transgenic mice develop spastic paralysis and neuronal inclusions characteristic of ALS and frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mimicking aspects of frontotemporal lobar degeneration and Lou Gehrig's disease in rats via TDP-43 overexpression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Transgenic rat model of neurodegeneration caused by mutation in the TDP gene.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43 mutant transgenic mice develop features of ALS and frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TLS, EWS and TAF15: a model for transcriptional integration of gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Rules for nuclear localization sequence recognition by karyopherin beta 2

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Identification and characterization of the nuclear localization/retention signal in the EWS proto-oncoprotein

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

The multifunctional FUS, EWS and TAF15 proto-oncoproteins show cell type-specific expression patterns and involvement in cell spreading and stress response

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

EWS-ETS oncoproteins: the linchpins of Ewing tumors

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

The RNA binding protein TLS is translocated to dendritic spines by mGluR5 activation and regulates spine morphology.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TLS facilitates transport of mRNA encoding an actin-stabilizing protein to dendritic spines

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Fus deficiency in mice results in defective B-lymphocyte development and activation, high levels of chromosomal instability and perinatal death.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Male sterility and enhanced radiation sensitivity in TLS(-/-) mice

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

A new subtype of frontotemporal lobar degeneration with FUS pathology

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

FALS with FUS mutation in Japan, with early onset, rapid progress and basophilic inclusion.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Caudate atrophy on MRI is a characteristic feature of FTLD-FUS

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Classic and generalized variants of Pick's disease: A clinicopathological, ultrastructural, and immunocytochemical comparative study

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Basophilic cytoplasmic inclusions in a case of sporadic juvenile amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Basophilic inclusions in sporadic juvenile amyotrophic lateral sclerosis: an immunocytochemical and ultrastructural study.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Sporadic juvenile amyotrophic lateral sclerosis. A clinicopathological study of a case with neuronal cytoplasmic inclusions containing RNA.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Immunohistochemical identification of messenger RNA-related proteins in basophilic inclusions of adult-onset atypical motor neuron disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

An autopsy case of frontotemporal dementia with severe dysarthria and motor neuron disease showing numerous basophilic inclusions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

FUS pathology in basophilic inclusion body disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Neurofilament inclusion body disease: a new proteinopathy?

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

The RNA-binding protein FUS/TLS is a common aggregate-interacting protein in polyglutamine diseases

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

FUS-immunoreactive intranuclear inclusions in neurodegenerative disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

De novo truncating FUS gene mutation as a cause of sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

The occurrence of mutations inFUSin a Belgian cohort of patients with familial ALS

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Two Italian kindreds with familial amyotrophic lateral sclerosis due to FUS mutation

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutations in FUS cause FALS and SALS in French and French Canadian populations

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Novel missense and truncating mutations in FUS/TLS in familial ALS

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Occurrence of basophilic inclusions and FUS-immunoreactive neuronal and glial inclusions in a case of familial amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Identification and characterization of FUS/TLS as a new target of ATM.

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Identifying and quantifying in vivo methylation sites by heavy methyl SILAC

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Detection of arginine dimethylated peptides by parallel precursor ion scanning mass spectrometry in positive ion mode

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Protein arginine methylation in mammals: who, what, and why

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Regulation of heterogenous nuclear ribonucleoprotein A1 transport by phosphorylation in cells stressed by osmotic shock

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

Mutations of optineurin in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2810%2970195-2

7 January 2021

10.1016/S1474-4422(10)70195-2

Identifiers

DOI

1 reference

Consolidated OpenCitations Corpus – April 2017

1832250

1832250

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference