Pick's disease associated with the novel Tau gene mutation K369I. (Q48744508)

15 February 2018

title

Pick's disease associated with the novel Tau gene mutation K369I. (English)

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15 February 2018

author name string

Neumann M

1

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Schulz-Schaeffer W

2

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Crowther RA

3

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Smith MJ

4

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Spillantini MG

5

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Goedert M

6

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Kretzschmar HA

7

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publication date

1 October 2001

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15 February 2018

published in

Annals of Neurology

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15 February 2018

volume

50

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issue

4

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page(s)

503-513

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

cites work

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

21 January 2018

1 reference

A distinct familial presenile dementia with a novel missense mutation in the tau gene

21 January 2018

1 reference

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.

21 January 2018

1 reference

5' splice site mutations in tau associated with the inherited dementia FTDP-17 affect a stem-loop structure that regulates alternative splicing of exon 10.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Tau gene mutation in familial progressive subcortical gliosis

21 January 2018

1 reference

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

21 January 2018

1 reference

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

21 January 2018

1 reference

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Reduced binding of protein phosphatase 2A to tau protein with frontotemporal dementia and parkinsonism linked to chromosome 17 mutations

21 January 2018

1 reference

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

21 January 2018

1 reference

Tau pathology in a family with dementia and a P301L mutation in tau.

21 January 2018

1 reference

Autosomal dominant dementia with widespread neurofibrillary tangles.

21 January 2018

1 reference

Phenotypic variation in hereditary frontotemporal dementia with tau mutations

21 January 2018

1 reference

Monoclonal antibody AT8 recognises tau protein phosphorylated at both serine 202 and threonine 205.

21 January 2018

1 reference

Sequential phosphorylation of Tau by glycogen synthase kinase-3beta and protein kinase A at Thr212 and Ser214 generates the Alzheimer-specific epitope of antibody AT100 and requires a paired-helical-filament-like conformation

21 January 2018

1 reference

Epitope mapping of monoclonal antibodies to the paired helical filaments of Alzheimer's disease: identification of phosphorylation sites in tau protein

21 January 2018

1 reference

Detection of Phosphorylated Ser262 in Fetal Tau, Adult Tau, and Paired Helical Filament Tau

21 January 2018

1 reference

Diagnostic criteria for sporadic Creutzfeldt-Jakob disease

21 January 2018

1 reference

Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms

21 January 2018

1 reference

Assembly of microtubule-associated protein tau into Alzheimer-like filaments induced by sulphated glycosaminoglycans

21 January 2018

1 reference

Straight and paired helical filaments in Alzheimer disease have a common structural unit

21 January 2018

1 reference

Pick's disease: hyperphosphorylated tau protein segregates to the somatoaxonal compartment

21 January 2018

1 reference

Vulnerable neuronal subsets in Alzheimer's and Pick's disease are distinguished by their tau isoform distribution and phosphorylation.

21 January 2018

1 reference

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

21 January 2018

1 reference

Isolation of the insoluble straight fibrils of Pick's disease

21 January 2018

1 reference

Immunocytochemical and ultrastructural studies of Pick's disease

21 January 2018

1 reference

Cognitive, neuroimaging, and pathological studies in a patient with Pick's disease

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/ANA.1223

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15 February 2018

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15 February 2018