(Q38442790)

3 September 2017

title

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

1 reference

3 September 2017

1 reference

Rizzini C

1

1 reference

3 September 2017

Goedert M

2

1 reference

3 September 2017

Hodges JR

3

1 reference

3 September 2017

Smith MJ

4

1 reference

3 September 2017

Jakes R

5

1 reference

3 September 2017

Hills R

6

1 reference

3 September 2017

Xuereb JH

7

1 reference

3 September 2017

Crowther RA

8

1 reference

3 September 2017

Spillantini MG

9

1 reference

3 September 2017

publication date

1 November 2000

1 reference

Journal of Neuropathology & Experimental Neurology

3 September 2017

published in

1 reference

3 September 2017

volume

59

1 reference

3 September 2017

issue

11

1 reference

3 September 2017

page(s)

990-1001

1 reference

Tau is a candidate gene for chromosome 17 frontotemporal dementia

3 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

A68: a major subunit of paired helical filaments and derivatized forms of normal Tau.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Tau gene mutation in familial progressive subcortical gliosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Autosomal dominant dementia with widespread neurofibrillary tangles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Phenotypic variation in hereditary frontotemporal dementia with tau mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Re-examination of a family with Pick's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Monoclonal antibody PHF-1 recognizes tau protein phosphorylated at serine residues 396 and 404.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Characterization of mAb AP422, a novel phosphorylation-dependent monoclonal antibody against tau protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Tau mutations cause frontotemporal dementias

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Filamentous aggregates in Pick's disease, progressive supranuclear palsy, and Alzheimer's disease share antigenic determinants with microtubule-associated protein, tau.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Phosphorylated serine422 on tau proteins is a pathological epitope found in several diseases with neurofibrillary degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Pick's disease immunohistochemistry: new alterations and Alzheimer's disease comparisons.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Tau protein is phosphorylated by cyclic AMP-dependent protein kinase and calcium/calmodulin-dependent protein kinase II within its microtubule-binding domains at Ser-262 and Ser-356.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

MARK, a novel family of protein kinases that phosphorylate microtubule-associated proteins and trigger microtubule disruption

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Stable expression in Chinese hamster ovary cells of mutated tau genes causing frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Different distribution of phosphorylated tau protein isoforms in Alzheimer's and Pick's diseases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Isolation of the insoluble straight fibrils of Pick's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

Mutations in tau reduce its microtubule binding properties in intact cells and affect its phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FJNEN%2F59.11.990

21 January 2018

Identifiers

DOI

10.1093/JNEN/59.11.990

1 reference

3 September 2017

1 reference