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Expression of C9orf72-related dipeptides impairs motor function in a vertebrate model

Human molecular genetics, 2018-05, Vol.27 (10), p.1754-1762

2018

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Identification of biological pathways regulated by PGRN and GRN peptide treatments using transcriptome analysis

The European journal of neuroscience, 2016-09, Vol.44 (5), p.2214-2225

2016

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The cellular expression and proteolytic processing of the amyloid precursor protein is independent of TDP-43

Bioscience reports, 2020-04, Vol.40 (4)

2020

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Pathogenesis/genetics of frontotemporal dementia and how it relates to ALS

Experimental neurology, 2014-12, Vol.262, p.84-90

2014

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C9orf72 dipeptides disrupt the nucleocytoplasmic transport machinery and cause TDP-43 mislocalisation to the cytoplasm

Scientific reports, 2022-03, Vol.12 (1), p.4799-4799, Article 4799

2022

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TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration

Acta neuropathologica, 2008-08, Vol.116 (2), p.141-146

2008

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Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.693-708

2012

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CRISPR/Cas9 does not facilitate stable expression of long C9orf72 dipeptides in mice

Neurobiology of aging, 2019-12, Vol.84, p.235.e1-235.e8

2019

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Modelling C9orf72 dipeptide repeat proteins of a physiologically relevant size

Human molecular genetics, 2016-12, Vol.25 (23), p.5069-5082

2016

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

Nature, 2006-08, Vol.442 (7105), p.916-919

2006

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Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

Neurobiology of aging, 2012-08, Vol.33 (8), p.1846.e5-1846.e6

2012

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Histone deacetylases (HDACs) in frontotemporal lobar degeneration

Neuropathology and applied neurobiology, 2015-02, Vol.41 (2), p.245-257

2015

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Progranulin and frontotemporal lobar degeneration

Acta neuropathologica, 2007-07, Vol.114 (1), p.39-47

Pickering-Brown, Stuart M

2007

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Progranulin Mediates Caspase-Dependent Cleavage of TAR DNA Binding Protein-43

The Journal of neuroscience, 2007-09, Vol.27 (39), p.10530-10534

2007

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Extracellular Vesicles Isolated from Human Induced Pluripotent Stem Cell-Derived Neurons Contain a Transcriptional Network

Neurochemical research, 2020-07, Vol.45 (7), p.1711-1728

2020

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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Human molecular genetics, 2006-10, Vol.15 (20), p.2988-3001

2006

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

Acta neuropathologica, 2007-05, Vol.113 (5), p.521-533

2007

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Patterns of microglial cell activation in frontotemporal lobar degeneration

Neuropathology and applied neurobiology, 2014-10, Vol.40 (6), p.686-696

2014

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

Acta neuropathologica, 2006-11, Vol.112 (5), p.539-549

2006

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TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

Acta neuropathologica, 2011-12, Vol.122 (6), p.703-713

2011

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Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel

Movement disorders, 2014-02, Vol.29 (2), p.245-251

2014

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An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies

Acta neuropathologica, 2006-04, Vol.111 (4), p.329-340

2006

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Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene

Neuropathology and applied neurobiology, 2015-08, Vol.41 (5), p.601-612

2015

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Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

Alzheimer's & dementia, 2016-08, Vol.12 (8), p.862-871

2016

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C9ORF72 DIPEPTIDE REPEAT PROTEINS DISRUPT NUCLEOCYTOPLASMIC TRANSPORT

Alzheimer's & dementia, 2017-07, Vol.13 (7), p.P242-P242

2017

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Expression of C9orf72-related dipeptides impairs motor function in a vertebrate model

Identification of biological pathways regulated by PGRN and GRN peptide treatments using transcriptome analysis

The cellular expression and proteolytic processing of the amyloid precursor protein is independent of TDP-43

Pathogenesis/genetics of frontotemporal dementia and how it relates to ALS

C9orf72 dipeptides disrupt the nucleocytoplasmic transport machinery and cause TDP-43 mislocalisation to the cytoplasm

TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

CRISPR/Cas9 does not facilitate stable expression of long C9orf72 dipeptides in mice

Modelling C9orf72 dipeptide repeat proteins of a physiologically relevant size

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

Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

Histone deacetylases (HDACs) in frontotemporal lobar degeneration

Progranulin and frontotemporal lobar degeneration

Progranulin Mediates Caspase-Dependent Cleavage of TAR DNA Binding Protein-43

Extracellular Vesicles Isolated from Human Induced Pluripotent Stem Cell-Derived Neurons Contain a Transcriptional Network

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

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

Patterns of microglial cell activation in frontotemporal lobar degeneration

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

TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

Genomewide association study in cervical dystonia demonstrates possible association with sodium leak channel

An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies

Accumulation of dipeptide repeat proteins predates that of TDP-43 in frontotemporal lobar degeneration associated with hexanucleotide repeat expansions in C9ORF72 gene

Genetic risk factors for the posterior cortical atrophy variant of Alzheimer's disease

C9ORF72 DIPEPTIDE REPEAT PROTEINS DISRUPT NUCLEOCYTOPLASMIC TRANSPORT

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