(Q36130911)

12 August 2017

Novel tau polymorphisms, tau haplotypes, and splicing in familial and sporadic frontotemporal dementia (English)

1 reference

12 August 2017

frontotemporal dementia

1 reference

2

Bruce L Miller

1 reference

12 August 2017

10

Jeffrey L Cummings

1 reference

12 August 2017

12

Daniel H Geschwind

1 reference

12 August 2017

9

Kirk C Wilhelmsen

1 reference

12 August 2017

Maria-Jesús Sobrido

1

1 reference

12 August 2017

Necat Havlioglu

3

1 reference

12 August 2017

Victoria Zhukareva

4

1 reference

12 August 2017

Zhihong Jiang

5

1 reference

12 August 2017

Ziad S Nasreddine

6

1 reference

12 August 2017

Virginia M-Y Lee

7

1 reference

12 August 2017

Tiffany W Chow

8

1 reference

12 August 2017

Jane Y Wu

11

1 reference

12 August 2017

1 May 2003

1 reference

12 August 2017

Archives of Neurology

1 reference

12 August 2017

60

1 reference

12 August 2017

698-702

1 reference

12 August 2017

5

1 reference

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

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

The extended haplotype of the microtubule associated protein tau gene is not associated with Pick's disease.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

Inheritance of frontotemporal dementia

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

The apolipoprotein E epsilon4 allele is not a significant risk factor for frontotemporal dementia.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

Tau gene polymorphisms and apolipoprotein E epsilon4 may interact to increase risk for Alzheimer's disease.

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

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

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

Tau is a candidate gene for chromosome 17 frontotemporal dementia

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

A study of the Lund-Manchester research criteria for frontotemporal dementia: clinical and single-photon emission CT correlations.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

Genetic evidence for the involvement of tau in progressive supranuclear palsy

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2072863

Corticobasal degeneration shares a common genetic background with progressive supranuclear palsy

23 September 2018

1 reference

12 December 2020

Frequency of tau gene mutations in familial and sporadic cases of non-Alzheimer dementia

1 reference

12 December 2020

Possible association of the tau H1/H1 genotype with primary progressive aphasia

1 reference

12 December 2020

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

1 reference

12 December 2020

Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia

1 reference

12 December 2020

10.1001/ARCHNEUR.60.5.698

Identifiers

DOI

1 reference

12 August 2017

1 reference

12 August 2017

1 reference