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

5

1 reference

12 August 2017

698-702

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