(Q50547594)

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Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family.

scientific article published on 15 May 2008

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scholarly article

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family. (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

frontotemporal dementia

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based on heuristic

inferred from title

author name string

S G Lindquist

1

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

H Braedgaard

2

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

K Svenstrup

3

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

A M Isaacs

4

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

J E Nielsen

5

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

FReJA Consortium

6

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

publication date

15 May 2008

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

European Journal of Neurology

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

15

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Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

7

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

667-670

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

Inheritance of frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Neuropsychiatric studies in a family with presenile dementia different from Alzheimer and Pick disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Familial non-specific dementia maps to chromosome 3

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

A protein's final ESCRT.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

CHMP2B mutations are not a common cause of frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Functional multivesicular bodies are required for autophagic clearance of protein aggregates associated with neurodegenerative disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Macroautophagy--a novel Beta-amyloid peptide-generating pathway activated in Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Genetic Variability in CHMP2B and Frontotemporal Dementia

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02144.X

21 January 2018

Identifiers

10.1111/J.1468-1331.2008.02144.X

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 March 2018

http://europepmc.org/abstract/MED/18484988

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