(Q42332631)

27 October 2017

TMEM106B: a strong FTLD disease modifier (English)

1 reference

27 October 2017

2

1 reference

27 October 2017

Yuetiva Deming

1

0 references

publication date

1 February 2014

1 reference

27 October 2017

Acta Neuropathologica

1 reference

27 October 2017

127

1 reference

27 October 2017

3

1 reference

27 October 2017

419-422

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-014-1249-3

27 October 2017

0 references

cites work

TMEM106B is a genetic modifier of frontotemporal lobar degeneration with C9orf72 hexanucleotide repeat expansions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

TMEM106B protects C9ORF72 expansion carriers against frontotemporal dementia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

TMEM106B p.T185S regulates TMEM106B protein levels: implications for frontotemporal dementia

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

TMEM106B, the risk gene for frontotemporal dementia, is regulated by the microRNA-132/212 cluster and affects progranulin pathways

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Association of TMEM106B gene polymorphism with age at onset in granulin mutation carriers and plasma granulin protein levels

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

TMEM106B regulates progranulin levels and the penetrance of FTLD in GRN mutation carriers.

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Risk genotypes at TMEM106B are associated with cognitive impairment in amyotrophic lateral sclerosis

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

29 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5494845

Effect of TMEM106B polymorphism on functional network connectivity in asymptomatic GRN mutation carriers

29 May 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24488309

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00401-014-1249-3

1 reference

27 October 2017

1 reference

PMC publication ID

5494845

27 October 2017

PubMed publication ID

24488309

1 reference

PMC publication ID

5494845