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

11

1 reference

18 August 2017

1473-1478

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