The molecular basis of frontotemporal dementia (Q37564674)

21 August 2017

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title

The molecular basis of frontotemporal dementia (English)

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21 August 2017

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frontotemporal dementia

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2

Markus Tolnay

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Manuela Neumann

series ordinal

1

object named as

Manuela Neumann

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21 August 2017

Markus Tolnay

2

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PubMed ID

19638255

21 August 2017

Ian R A Mackenzie

series ordinal

3

1 reference

21 August 2017

29 July 2009

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Expert Reviews in Molecular Medicine

21 August 2017

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21 August 2017

11

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21 August 2017

e23

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Mutations in progranulin explain atypical phenotypes with variants in MAPT.

21 August 2017

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Pick bodies in a family with presenilin-1 Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaques.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Invited article: the Alzheimer disease-frontotemporal lobar degeneration spectrum

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

100 years and counting: prospects for defeating Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Tau gene mutations and their effects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Hereditary frontotemporal dementia caused by Tau gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Hippocampal sclerosis dementia: a reappraisal

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Hippocampal sclerosis: a common pathological feature of dementia in very old (> or = 80 years of age) humans.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

White matter tauopathy with globular glial inclusions: a distinct sporadic frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontal lobe dementia with novel tauopathy: sporadic multiple system tauopathy with dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neurofibrillary tangle-predominant dementia: comparison with classical Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Clinical and pathological evidence for a frontal variant of Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Argyrophilic grain disease is a sporadic 4-repeat tauopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Biochemical analysis of tau proteins in argyrophilic grain disease, Alzheimer's disease, and Pick's disease : a comparative study

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Distribution of cerebral cortical lesions in Pick's disease with Pick bodies: a clinicopathological study of six autopsy cases showing unusual clinical presentations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Argyrophilic grain disease presenting with frontotemporal dementia: a neuropsychological and pathological study of an autopsied case with presenile onset.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Motor neurone disease-inclusion dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Ubiquitin-positive intraneuronal inclusions in the extramotor cortices of presenile dementia patients with motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Hippocampal and neocortical ubiquitin-immunoreactive inclusions in amyotrophic lateral sclerosis with dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Presenilin mutations associated with fronto-temporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal lobar degeneration: current concepts in the light of recent advances

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Clinical characteristics of dementia associated with argyrophilic grain disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Argyrophilic grain disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Argyrophilic thorny astrocyte clusters in association with Alzheimer's disease pathology in possible primary progressive aphasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Dementia as the most common presentation of cortical-basal ganglionic degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Alzheimer and frontotemporal pathology in subsets of primary progressive aphasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Corticodentatonigral Degeneration With Neuronal Achromasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal dementia: clinicopathological correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

The evolution and pathology of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Adult-onset neuronal intranuclear hyaline inclusion disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Progressive supranuclear palsy: pathology and genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Insights into the dynamics of hereditary diffuse leukoencephalopathy with axonal spheroids

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Progressive supranuclear palsy with dementia: cortical pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

PROGRESSIVE SUPRANUCLEAR PALSY. A HETEROGENEOUS DEGENERATION INVOLVING THE BRAIN STEM, BASAL GANGLIA AND CEREBELLUM WITH VERTICAL GAZE AND PSEUDOBULBAR PALSY, NUCHAL DYSTONIA AND DEMENTIA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neuropathologic, biochemical, and molecular characterization of the frontotemporal dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Sporadic Pick's disease: a tauopathy characterized by a spectrum of pathological tau isoforms in gray and white matter

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Mutation analysis of patients with neuronal intermediate filament inclusion disease (NIFID).

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

alpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Functions of intermediate filaments in neuronal development and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Tau, a biological marker of neurodegenerative diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neurodegenerative tauopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

The neuropathological spectrum of neurodegenerative tauopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neurofilament proteins in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

A century of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Heterogeneous inclusions in neurofilament inclusion disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Structure and novel exons of the human tau gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neuronal intranuclear inclusions are ultrastructurally and immunologically distinct from cytoplasmic inclusions of neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

A common inversion under selection in Europeans

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Patients with a novel neurofilamentopathy: dementia with neurofilament inclusions.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

A protein factor essential for microtubule assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Extending the clinicopathological spectrum of neurofilament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Purification of tau, a microtubule-associated protein that induces assembly of microtubules from purified tubulin

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neurofilament inclusion body disease: a new proteinopathy?

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

TDP-43 A315T mutation in familial motor neuron disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Neurodegeneration with features of NIFID and ALS--extended clinical and neuropathological spectrum.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Screening for neurofilament inclusion disease using alpha-internexin immunohistochemistry

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Inheritance of frontotemporal dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

TDP-43 M311V mutation in familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

TDP-43 mutation in familial amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Familial aggregation in frontotemporal dementia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Epidemiology and genetics of frontotemporal dementia/Pick's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Clinical and pathological continuum of multisystem TDP-43 proteinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

Higher order arrangement of the eukaryotic nuclear bodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Extrapyramidal symptoms in Frontotemporal Dementia: prevalence and clinical correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

The neuropathology and clinical phenotype of FTD with progranulin mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Progranulin is a mediator of the wound response

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Progranulin functions as a neurotrophic factor to regulate neurite outgrowth and enhance neuronal survival

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Progranulin (granulin-epithelin precursor, PC-cell-derived growth factor, acrogranin) mediates tissue repair and tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Clinical and Pathological Heterogeneity of Neuronal Intermediate Filament Inclusion Disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

A Canadian Cohort Study of Cognitive Impairment and Related Dementias (ACCORD): Study Methods and Baseline Results

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

No association of TDP-43 with sporadic frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Cortical and subcortical argyrophilic grains characterize a disease associated with adult onset dementia

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

TDP-43 gene analysis in frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Contribution of TARDBP mutations to sporadic amyotrophic lateral sclerosis.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Expression of the gene for the neuronal intermediate filament protein alpha-internexin coincides with the onset of neuronal differentiation in the developing rat nervous system

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Clinical and neuropathological criteria for frontotemporal dementia. The Lund and Manchester Groups

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Argyrophilic grain disease and Alzheimer's disease are distinguished by their different distribution of tau protein isoforms

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Two novel presenilin 1 gene mutations connected with frontotemporal dementia-like clinical phenotype: Genetic and bioinformatic assessment

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Progranulin in frontotemporal lobar degeneration and neuroinflammation

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

A new case of frontotemporal dementia and parkinsonism resulting from an intron 10 +3-splice site mutation in the tau gene: clinical and pathological features

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Argyrophilic grain disease mimicking temporal Pick's disease: a clinical, radiological, and pathological study of an autopsy case with a clinical course of 15 years.

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Dementia lacking distinctive histology (DLDH) revisited

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Neuropathologic features of frontotemporal lobar degeneration with ubiquitin-positive inclusions visualized with ubiquitin-binding protein p62 immunohistochemistry

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

Tau-mediated neurodegeneration in Alzheimer's disease and related disorders

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1017%2FS1462399409001136

7 January 2021

10.1017/S1462399409001136

Identifiers

DOI

1 reference

21 August 2017

1 reference

PubMed ID

19638255