(Q48236600)

9 February 2018

title

Tau gene mutation in familial progressive subcortical gliosis. (English)

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9 February 2018

author

Shu Chen

4

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9 February 2018

Piero Parchi

5

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9 February 2018

Dennis W. Dickson

10

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9 February 2018

Pierluigi Gambetti

12

object named as

Gambetti P

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9 February 2018

Massimo Tabaton

6

object named as

Tabaton M

1 reference

9 February 2018

Kirk Wilhelmsen

9

object named as

Wilhelmsen KC

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9 February 2018

author name string

Goedert M

1

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9 February 2018

Spillantini MG

2

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9 February 2018

Crowther RA

3

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9 February 2018

Lanska DJ

7

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9 February 2018

Markesbery WR

8

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9 February 2018

Petersen RB

11

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9 February 2018

language of work or name

English

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publication date

1 April 1999

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9 February 2018

published in

Nature Medicine

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9 February 2018

volume

5

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9 February 2018

page(s)

454-457

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9 February 2018

issue

4

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9 February 2018

https://scigraph.springernature.com/pub.10.1038/7454

exact match

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cites work

Progressive subcortical gliosis, a rare form of presenile dementia

1 reference

Familial progressive subcortical gliosis.

21 January 2018

1 reference

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

21 January 2018

1 reference

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

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

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

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

Prion in progressive subcortical gliosis revisited.

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

Structure and novel exons of the human tau gene

21 January 2018

1 reference

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

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 mutations cause frontotemporal dementias.

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

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Familial progressive subcortical gliosis: presence of prions and linkage to chromosome 17

21 January 2018

1 reference

7 January 2021

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

1 reference

7 January 2021

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

1 reference

7 January 2021

Tau proteins with FTDP-17 mutations have a reduced ability to promote microtubule assembly

1 reference

7 January 2021

Identifiers

DOI

10.1038/7454

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9 February 2018

PubMed ID

10202939

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9 February 2018