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TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

Lancet neurology, 2010-10, Vol.9 (10), p.995-1007

2010

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Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers

Acta neuropathologica, 2015-12, Vol.130 (6), p.845-861

2015

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The neuropathology associated with repeat expansions in the C9ORF72 gene

Acta neuropathologica, 2014-03, Vol.127 (3), p.347-357

2014

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A harmonized classification system for FTLD-TDP pathology

Acta neuropathologica, 2011-07, Vol.122 (1), p.111-113

2011

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Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS

Acta neuropathologica, 2016-04, Vol.131 (4), p.587-604

2016

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hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

Acta neuropathologica, 2013-03, Vol.125 (3), p.413-423

2013

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Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

Acta neuropathologica, 2011-07, Vol.122 (1), p.87-98

2011

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A new subtype of frontotemporal lobar degeneration with FUS pathology

Brain (London, England : 1878), 2009-11, Vol.132 (11), p.2922-2931

2009

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Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Acta neuropathologica, 2010-01, Vol.119 (1), p.1-4

2010

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Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

Acta neuropathologica, 2009-11, Vol.118 (5), p.605-616

2009

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FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2595-2609

2011

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Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p

Acta neuropathologica, 2012-03, Vol.123 (3), p.409-417

2012

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Phosphorylated TDP-43 in Alzheimer’s disease and dementia with Lewy bodies

Acta neuropathologica, 2009-02, Vol.117 (2), p.125-136

2009

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Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects

Acta neuropathologica, 2012-09, Vol.124 (3), p.373-382

2012

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Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers

Acta neuropathologica communications, 2018-08, Vol.6 (1), p.72-72, Article 72

2018

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

Acta neuropathologica, 2007-07, Vol.114 (1), p.5-22

2007

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Progranulin: normal function and role in neurodegeneration

Journal of neurochemistry, 2008-01, Vol.104 (2), p.287-297

2008

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Early dipeptide repeat pathology in a frontotemporal dementia kindred with C9ORF72 mutation and intellectual disability

Acta neuropathologica, 2014-03, Vol.127 (3), p.451-458

2014

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Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

Acta neuropathologica, 2009-01, Vol.117 (1), p.15-18

2009

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Distinct pathological subtypes of FTLD-FUS

Acta neuropathologica, 2011-02, Vol.121 (2), p.207-218

2011

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

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3081-3090

2006

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Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations

Acta neuropathologica, 2012-11, Vol.124 (5), p.705-716

2012

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Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

Brain (London, England : 1878), 2008-05, Vol.131 (5), p.1282-1293

2008

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TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

Acta neuropathologica, 2008-08, Vol.116 (2), p.147-157

2008

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Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons

Nature neuroscience, 2013-10, Vol.16 (10), p.1383-1391

2013

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TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia

Quantitative analysis and clinico-pathological correlations of different dipeptide repeat protein pathologies in C9ORF72 mutation carriers

The neuropathology associated with repeat expansions in the C9ORF72 gene

A harmonized classification system for FTLD-TDP pathology

Monomethylated and unmethylated FUS exhibit increased binding to Transportin and distinguish FTLD-FUS from ALS-FUS

hnRNP A3 binds to GGGGCC repeats and is a constituent of p62-positive/TDP43-negative inclusions in the hippocampus of patients with C9orf72 mutations

Pathological heterogeneity in amyotrophic lateral sclerosis with FUS mutations: two distinct patterns correlating with disease severity and mutation

A new subtype of frontotemporal lobar degeneration with FUS pathology

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations

Clinical and pathological features of amyotrophic lateral sclerosis caused by mutation in the C9ORF72 gene on chromosome 9p

Phosphorylated TDP-43 in Alzheimer’s disease and dementia with Lewy bodies

Mechanisms of disease in frontotemporal lobar degeneration: gain of function versus loss of function effects

Novel antibodies reveal presynaptic localization of C9orf72 protein and reduced protein levels in C9orf72 mutation carriers

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

Progranulin: normal function and role in neurodegeneration

Early dipeptide repeat pathology in a frontotemporal dementia kindred with C9ORF72 mutation and intellectual disability

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

Distinct pathological subtypes of FTLD-FUS

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

Transportin 1 accumulates specifically with FET proteins but no other transportin cargos in FTLD-FUS and is absent in FUS inclusions in ALS with FUS mutations

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

Interaction of FUS and HDAC1 regulates DNA damage response and repair in neurons

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