(Q36417377)

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Laminar distribution of the pathological changes in sporadic frontotemporal lobar degeneration with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy: a quantitative study using polynomial curve fitting

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

Laminar distribution of the pathological changes in sporadic frontotemporal lobar degeneration with transactive response (TAR) DNA-binding protein of 43 kDa (TDP-43) proteinopathy: a quantitative study using polynomial curve fitting (English)

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

frontotemporal lobar degeneration

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based on heuristic

inferred from title

5

object named as

N J Cairns

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

author name string

R A Armstrong

1

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

R L Hamilton

2

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

I R A Mackenzie

3

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

J Hedreen

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

publication date

1 June 2013

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Europe PubMed Central

PMC publication ID

14 August 2017

Neuropathology and Applied Neurobiology

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

39

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

4

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

335-347

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

National Institute on Aging-Alzheimer's Association guidelines for the neuropathologic assessment of Alzheimer's disease

1 reference

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

1 reference

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30 September 2017

A quantitative study of the neuropathology of 32 sporadic and familial cases of frontotemporal lobar degeneration with TDP-43 proteinopathy (FTLD-TDP).

1 reference

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30 September 2017

The propagation of prion-like protein inclusions in neurodegenerative diseases

1 reference

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30 September 2017

Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

1 reference

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TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

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30 September 2017

Phosphorylation of S409/410 of TDP-43 is a consistent feature in all sporadic and familial forms of TDP-43 proteinopathies

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30 September 2017

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

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30 September 2017

Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

1 reference

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TAR DNA-binding protein 43 immunohistochemistry reveals extensive neuritic pathology in FTLD-U: a midwest-southwest consortium for FTLD study

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TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

1 reference

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TDP-43 A315T mutation in familial motor neuron disease

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The genetics of frontotemporal lobar degeneration

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30 September 2017

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

Frontotemporal lobar degeneration: clinical and pathological relationships

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

Ubiquitinated pathological lesions in frontotemporal lobar degeneration contain the TAR DNA-binding protein, TDP-43.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

1 reference

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Staging of Alzheimer disease-associated neurofibrillary pathology using paraffin sections and immunocytochemistry

1 reference

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30 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3504185

30 September 2017

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

1 reference

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30 September 2017

Frontotemporal lobar degeneration--tau as a pied piper?

1 reference

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Tau-positive glial inclusions in progressive supranuclear palsy, corticobasal degeneration and Pick's disease

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The role of cortical connectivity in Alzheimer's disease pathogenesis: a review and model system.

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Subcortical neurofibrillary tangles, neuropil threads, and argentophilic glial inclusions in corticobasal degeneration.

1 reference

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Appearance of paired nucleated, Tau-positive glia in patients with progressive supranuclear palsy brain tissue

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Ultrastructural and immunohistochemical studies on ballooned cortical neurons in Creutzfeldt-Jakob disease: expression of alpha B-crystallin, ubiquitin and stress-response protein 27

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28 June 2018

Cortical ubiquitin-positive inclusions in frontotemporal dementia without motor neuron disease: a quantitative immunocytochemical study

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Absence of heterogeneous nuclear ribonucleoproteins and survival motor neuron protein in TDP-43 positive inclusions in frontotemporal lobar degeneration

1 reference

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1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2990.2012.01291.X

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The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

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https://api.crossref.org/works/10.1111%2FJ.1365-2990.2012.01291.X

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Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation

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TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies.

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TDP-43 pathology in familial British dementia.

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Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.

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Identifiers

10.1111/J.1365-2990.2012.01291.X

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

14 August 2017

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