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Age of major depression onset, depressive symptoms, and risk for subsequent dementia: results of the German Study on Ageing, Cognition, and Dementia in Primary Care Patients (AgeCoDe)

Psychological medicine, 2013-08, Vol.43 (8), p.1597-1610

2013

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Activation of nuclear factor-kappa B signalling promotes cellular senescence

Oncogene, 2011-05, Vol.30 (20), p.2356-2366

2011

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Psoriasis-like skin disease and arthritis caused by inducible epidermal deletion of Jun proteins

Nature, 2005-09, Vol.437 (7057), p.369-375

2005

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

Nature genetics, 2005-08, Vol.37 (8), p.806-808

2005

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Serotonin—more than a neurotransmitter: transglutaminase-mediated serotonylation of C6 glioma cells and fibronectin

Neurochemistry international, 2010-08, Vol.57 (1), p.67-75

2010

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HTT-lowering reverses Huntington's disease immune dysfunction caused by NFκB pathway dysregulation

Brain (London, England : 1878), 2014-03, Vol.137 (Pt 3), p.819-833

2014

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Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Human molecular genetics, 2012-04, Vol.21 (8), p.1897-1906

2012

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Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport

Science (American Association for the Advancement of Science), 2003-05, Vol.300 (5620), p.808-812

2003

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A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure

The New England journal of medicine, 2009-11, Vol.361 (21), p.2056-2065

2009

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Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases

Neurology, 2012-07, Vol.79 (2), p.127-131

2012

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A dopamine transporter mutation associated with bipolar affective disorder causes inhibition of transporter cell surface expression

Molecular psychiatry, 2005-12, Vol.10 (12), p.1104-1109

2005

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Identification of novel AP-1 target genes in fibroblasts regulated during cutaneous wound healing

Oncogene, 2004-09, Vol.23 (42), p.7005-7017

2004

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Identification of novel oligodendroglioma‐associated candidate tumor suppressor genes in 1p36 and 19q13 using microarray‐based expression profiling

International journal of cancer, 2006-08, Vol.119 (4), p.792-800

2006

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Down-regulation of the rat serotonin transporter upon exposure to a selective serotonin reuptake inhibitor

Neuroreport, 2001-07, Vol.12 (10), p.2181-2184

2001

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Functional coupling of serotonin and noradrenaline transporters

Journal of neurochemistry, 2003-08, Vol.86 (4), p.958-965

2003

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DASB –in vitro binding characteristics on human recombinant monoamine transporters with regard to its potential as positron emission tomography (PET) tracer

Journal of neurochemistry, 2004-09, Vol.90 (5), p.1218-1226

2004

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A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse

Neurogenetics, 2010-05, Vol.11 (2), p.185-191

2010

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A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Cell, 1993-03, Vol.72 (6), p.971-983

1993

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Structure and expression of the Huntington's disease gene : evidence against simple inactivation due to an expanded CAG repeat

Somatic cell and molecular genetics, 1994, Vol.20 (1), p.27-38

1994

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Modulation of cytochrome P450 1A1 by food-derived heterocyclic aromatic amines

Toxicology (Amsterdam), 2004-07, Vol.199 (2), p.231-240

2004

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A 500-kb sequence-ready cosmid contig and transcript map of the MEN1 region on 11q13

Genomics (San Diego, Calif.), 1999, Vol.55 (1), p.49-56

1999

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A Sequence-Ready 3-Mb PAC Contig Covering 16 Breakpoints of the Wilms Tumor/Anirida Region of Human Chromosome 11p13

Genomics (San Diego, Calif.), 1998-10, Vol.53 (2), p.155-163

1998

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Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996

Cytogenetic and genome research, 1996, Vol.74 (1-2), p.1-20

1996

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B-Cell Lymphoma Involving the Biliary Tree

Endoscopy, 1996-10, Vol.28 (8), p.731-732

1996

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Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene

Human molecular genetics, 1994-01, Vol.3 (1), p.73-78

1994

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Age of major depression onset, depressive symptoms, and risk for subsequent dementia: results of the German Study on Ageing, Cognition, and Dementia in Primary Care Patients (AgeCoDe)

Activation of nuclear factor-kappa B signalling promotes cellular senescence

Psoriasis-like skin disease and arthritis caused by inducible epidermal deletion of Jun proteins

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

Serotonin—more than a neurotransmitter: transglutaminase-mediated serotonylation of C6 glioma cells and fibronectin

HTT-lowering reverses Huntington's disease immune dysfunction caused by NFκB pathway dysregulation

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP

Mutations in Dynein Link Motor Neuron Degeneration to Defects in Retrograde Transport

A Novel Protective Prion Protein Variant that Colocalizes with Kuru Exposure

Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases

A dopamine transporter mutation associated with bipolar affective disorder causes inhibition of transporter cell surface expression

Identification of novel AP-1 target genes in fibroblasts regulated during cutaneous wound healing

Identification of novel oligodendroglioma‐associated candidate tumor suppressor genes in 1p36 and 19q13 using microarray‐based expression profiling

Down-regulation of the rat serotonin transporter upon exposure to a selective serotonin reuptake inhibitor

Functional coupling of serotonin and noradrenaline transporters

DASB –in vitro binding characteristics on human recombinant monoamine transporters with regard to its potential as positron emission tomography (PET) tracer

A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

Structure and expression of the Huntington's disease gene : evidence against simple inactivation due to an expanded CAG repeat

Modulation of cytochrome P450 1A1 by food-derived heterocyclic aromatic amines

A 500-kb sequence-ready cosmid contig and transcript map of the MEN1 region on 11q13

A Sequence-Ready 3-Mb PAC Contig Covering 16 Breakpoints of the Wilms Tumor/Anirida Region of Human Chromosome 11p13

Report of the Fifth International Workshop on Human Chromosome 11 Mapping 1996

B-Cell Lymphoma Involving the Biliary Tree

Distribution of trinucleotide repeat sequences across a 2 Mbp region containing the Huntington's disease gene

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