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Long-term in vivo imaging of fibrillar tau in the retina of P301S transgenic mice

PloS one, 2012-12, Vol.7 (12), p.e53547-e53547

2012

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The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS

Science (American Association for the Advancement of Science), 2013-03, Vol.339 (6125), p.1335-1338

2013

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Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations

Acta neuropathologica, 2013-12, Vol.126 (6), p.859-879

2013

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MicroRNA-125b induces tau hyperphosphorylation and cognitive deficits in Alzheimer's disease

The EMBO journal, 2014-08, Vol.33 (15), p.1667-1680

2014

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Age-Dependent Levels of 5-Methyl-, 5-Hydroxymethyl-, and 5-Formylcytosine in Human and Mouse Brain Tissues

Angewandte Chemie International Edition, 2015-10, Vol.54 (42), p.12511-12514

International ed. in English, 2015

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DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex

Epigenetics & chromatin, 2018-07, Vol.11 (1), p.41-41, Article 41

2018

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

Acta neuropathologica, 2006-10, Vol.112 (4), p.389-404

2006

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Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

Acta neuropathologica, 2013-12, Vol.126 (6), p.881-893

2013

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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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Altered Long Noncoding RNA Expression Precedes the Course of Parkinson’s Disease—a Preliminary Report

Molecular neurobiology, 2017-05, Vol.54 (4), p.2869-2877

2017

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Synapse Formation and Function Is Modulated by the Amyloid Precursor Protein

The Journal of neuroscience, 2006-07, Vol.26 (27), p.7212-7221

2006

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Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis

Acta neuropathologica, 2014-06, Vol.127 (6), p.845-860

2014

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Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Science (American Association for the Advancement of Science), 2006-10, Vol.314 (5796), p.130-133

2006

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Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future

Acta neuropathologica, 2011-01, Vol.121 (1), p.91-112

2011

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

Acta neuropathologica, 2009-02, Vol.117 (2), p.137-149

2009

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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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Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer's disease

Nature neuroscience, 2010-04, Vol.13 (4), p.411-413

2010

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Sox2 Requirement in Sonic Hedgehog-Associated Medulloblastoma

Cancer research (Chicago, Ill.), 2013-06, Vol.73 (12), p.3796-3807

2013

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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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Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

Nature genetics, 2012-02, Vol.44 (2), p.200-205

2012

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The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication

The EMBO journal, 2011-05, Vol.30 (10), p.2057-2070

2011

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Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

Acta neuropathologica, 2012-10, Vol.124 (4), p.517-529

2012

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First symptom and initial diagnosis in sporadic CJD patients in Germany

Journal of neurology, 2014-09, Vol.261 (9), p.1811-1817

2014

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Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

Acta neuropathologica, 2024-10, Vol.148 (1), p.48, Article 48

2024

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Low values of 5-hydroxymethylcytosine (5hmC), the "sixth base," are associated with anaplasia in human brain tumors

International journal of cancer, 2012-10, Vol.131 (7), p.1577-1590

2012

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Long-term in vivo imaging of fibrillar tau in the retina of P301S transgenic mice

The C9orf72 GGGGCC Repeat Is Translated into Aggregating Dipeptide-Repeat Proteins in FTLD/ALS

Dipeptide repeat protein pathology in C9ORF72 mutation cases: clinico-pathological correlations

MicroRNA-125b induces tau hyperphosphorylation and cognitive deficits in Alzheimer's disease

Age-Dependent Levels of 5-Methyl-, 5-Hydroxymethyl-, and 5-Formylcytosine in Human and Mouse Brain Tissues

DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex

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

Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

A new subtype of frontotemporal lobar degeneration with FUS pathology

Altered Long Noncoding RNA Expression Precedes the Course of Parkinson’s Disease—a Preliminary Report

Synapse Formation and Function Is Modulated by the Amyloid Precursor Protein

Common pathobiochemical hallmarks of progranulin-associated frontotemporal lobar degeneration and neuronal ceroid lipofuscinosis

Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

Phenotypic variability of sporadic human prion disease and its molecular basis: past, present, and future

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

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

Microglial Cx3cr1 knockout prevents neuron loss in a mouse model of Alzheimer's disease

Sox2 Requirement in Sonic Hedgehog-Associated Medulloblastoma

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

Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids

The cellular prion protein mediates neurotoxic signalling of β-sheet-rich conformers independent of prion replication

Consensus classification of human prion disease histotypes allows reliable identification of molecular subtypes: an inter-rater study among surveillance centres in Europe and USA

First symptom and initial diagnosis in sporadic CJD patients in Germany

Correction to: Bidirectional transcripts of the expanded C9orf72 hexanucleotide repeat are translated into aggregating dipeptide repeat proteins

Low values of 5-hydroxymethylcytosine (5hmC), the "sixth base," are associated with anaplasia in human brain tumors

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