(Q34566547)

3 August 2017

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title

Frontotemporal dementia and tauopathy (English)

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3 August 2017

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frontotemporal dementia

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3

Trojanowski JQ

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3 August 2017

Yoshiyama Y

1

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3 August 2017

Lee VM

series ordinal

2

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3 August 2017

publication date

1 September 2001

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Current Neurology and Neuroscience Reports

3 August 2017

published in

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3 August 2017

volume

1

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3 August 2017

issue

5

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3 August 2017

page(s)

413-421

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Neurofilament protein levels in CSF are increased in dementia.

3 August 2017

cites work

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https://api.crossref.org/works/10.1007%2FS11910-001-0100-0

Tau gene mutation K257T causes a tauopathy similar to Pick's disease

21 January 2018

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https://api.crossref.org/works/10.1007%2FS11910-001-0100-0

A lack of the R406W tau mutation in progressive supranuclear palsy and corticobasal degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-001-0100-0

Prominent axonopathy in the brain and spinal cord of transgenic mice overexpressing four-repeat human tau protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-001-0100-0

Transgenic expression of the shortest human tau affects its compartmentalization and its phosphorylation as in the pretangle stage of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-001-0100-0

Age-dependent induction of congophilic neurofibrillary tau inclusions in tau transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11910-001-0100-0

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

21 January 2018

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12 December 2020

A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies.

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12 December 2020

The tau gene A0 polymorphism in progressive supranuclear palsy and related neurodegenerative diseases.

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12 December 2020

Accelerated filament formation from tau protein with specific FTDP-17 missense mutations.

1 reference

12 December 2020

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

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12 December 2020

Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein

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12 December 2020

A novel mutation at position +12 in the intron following exon 10 of the tau gene in familial frontotemporal dementia (FTD-Kumamoto)

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12 December 2020

Familial frontotemporal dementia with ubiquitin-positive, tau-negative inclusions

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12 December 2020

Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion

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12 December 2020

High prevalence of mutations in the microtubule-associated protein tau in a population study of frontotemporal dementia in the Netherlands

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12 December 2020

Loss of brain tau defines novel sporadic and familial tauopathies with frontotemporal dementia

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12 December 2020

In vitro polymerization of tau protein monitored by laser light scattering: method and application to the study of FTDP-17 mutants

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12 December 2020

Defects in axonal elongation and neuronal migration in mice with disrupted tau and map1b genes

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12 December 2020

Characterization of pathology in transgenic mice over-expressing human genomic and cDNA tau transgenes

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12 December 2020

Overexpression of four-repeat tau mRNA isoforms in progressive supranuclear palsy but not in Alzheimer's disease

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12 December 2020

Age-Dependent Emergence and Progression of a Tauopathy in Transgenic Mice Overexpressing the Shortest Human Tau Isoform

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12 December 2020

Familial frontotemporal dementia with ubiquitin inclusion bodies and without motor neuron disease

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12 December 2020

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

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12 December 2020

Muscle weakness, hyperactivity, and impairment in fear conditioning in tau-deficient mice.

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12 December 2020

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

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12 December 2020

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

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12 December 2020

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

1 reference

12 December 2020

FTDP-17 mutations N279K and S305N in tau produce increased splicing of exon 10

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12 December 2020

Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

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12 December 2020

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

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12 December 2020

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

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12 December 2020

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

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12 December 2020

Quantitative neurohistological features of frontotemporal degeneration.

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12 December 2020

Aberrant splicing of tau pre-mRNA caused by intronic mutations associated with the inherited dementia frontotemporal dementia with parkinsonism linked to chromosome 17.

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12 December 2020

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17

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12 December 2020

Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene

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12 December 2020

Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein

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12 December 2020

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

1 reference

12 December 2020

Effects of frontotemporal dementia FTDP-17 mutations on heparin-induced assembly of tau filaments

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12 December 2020

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

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12 December 2020

Tau filament formation in transgenic mice expressing P301L tau.

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12 December 2020

Phenotypic variation in hereditary frontotemporal dementia with tau mutations

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12 December 2020

The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian cases

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12 December 2020

Pick's disease is associated with mutations in the tau gene.

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12 December 2020

Cytoskeleton proteins in CSF distinguish frontotemporal dementia from AD

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12 December 2020

Mutation-dependent aggregation of tau protein and its selective depletion from the soluble fraction in brain of P301L FTDP-17 patients.

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12 December 2020

Glycogen synthase kinase-3beta phosphorylates protein tau and rescues the axonopathy in the central nervous system of human four-repeat tau transgenic mice.

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12 December 2020

Frontotemporal dementia with novel tau pathology and a Glu342Val tau mutation.

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12 December 2020

Semantic dementia with ubiquitin-positive tau-negative inclusion bodies.

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12 December 2020

10.1007/S11910-001-0100-0

Identifiers

DOI

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Dimensions Publication ID

3 August 2017

1044854510

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