(Q37187152)

18 August 2017

Role of the tau gene region chromosome inversion in progressive supranuclear palsy, corticobasal degeneration, and related disorders (English)

1 reference

progressive supranuclear palsy

18 August 2017

1 reference

3

Stephen Bonasera

1 reference

18 August 2017

4

Adam Boxer

1 reference

18 August 2017

6

Kirk C Wilhelmsen

1 reference

18 August 2017

Amy Webb

1

1 reference

PMCID

2680206

18 August 2017

Bruce Miller

series ordinal

2

1 reference

PMCID

2680206

18 August 2017

Anna Karydas

series ordinal

5

1 reference

18 August 2017

1 November 2008

1 reference

18 August 2017

Archives of Neurology

1 reference

18 August 2017

65

1 reference

18 August 2017

1473-1478

1 reference

18 August 2017

11

1 reference

Untangling the tau gene association with neurodegenerative disorders.

18 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

Tauopathies: classification and clinical update on neurodegenerative diseases associated with microtubule-associated protein tau

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

A common inversion under selection in Europeans

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

The role of tau (MAPT) in frontotemporal dementia and related tauopathies

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

Pick Complex: an integrative approach to frontotemporal dementia: primary progressive aphasia, corticobasal degeneration, and progressive supranuclear palsy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

The MAPT H1c risk haplotype is associated with increased expression of tau and especially of 4 repeat containing transcripts

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

14 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

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

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

Genetic evidence for the involvement of tau in progressive supranuclear palsy

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

3 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2680206

Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region

4 December 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19001166

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Frontotemporal dementia

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19001166

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1001/ARCHNEUR.65.11.1473

1 reference

18 August 2017

1 reference

18 August 2017

1 reference

PMCID

2680206