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Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington disease

Neurobiology of disease, 2019-05, Vol.125, p.219-231

2019

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Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1

Cell death & disease, 2014-04, Vol.5 (4), p.e1180-e1180

2014

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Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3)

Human molecular genetics, 2013-02, Vol.22 (3), p.508-518

2013

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Behavioral and in vivo electrophysiological evidence for presymptomatic alteration of prefrontostriatal processing in the transgenic rat model for huntington disease

The Journal of neuroscience, 2011-06, Vol.31 (24), p.8986-8997

2011

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Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice

Cellular and molecular life sciences : CMLS, 2010-09, Vol.67 (18), p.3173-3186

2010

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14-3-3 proteins in the nervous system

Nature reviews. Neuroscience, 2003-09, Vol.4 (9), p.752-762

2003

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Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition

Proceedings of the National Academy of Sciences - PNAS, 2018-09, Vol.115 (37), p.E8765-E8774

2018

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LRRK2 guides the actin cytoskeleton at growth cones together with ARHGEF7 and Tropomyosin 4

Biochimica et biophysica acta, 2013-12, Vol.1832 (12), p.2352-2367

2013

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Nuclear Localization of Ataxin-3 Is Required for the Manifestation of Symptoms in SCA3: In Vivo Evidence

The Journal of neuroscience, 2007-07, Vol.27 (28), p.7418-7428

2007

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Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat

Brain research bulletin, 2006-04, Vol.69 (3), p.306-310

2006

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Ubiquitylation of Synphilin-1 and α-Synuclein by SIAH and Its Presence in Cellular Inclusions and Lewy Bodies Imply a Role in Parkinson's Disease

Proceedings of the National Academy of Sciences - PNAS, 2004-04, Vol.101 (15), p.5500-5505

2004

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Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarker

Neurotoxicity research, 2006-01, Vol.9 (1), p.1-13

2006

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Neurobehavioral tests in rat models of degenerative brain diseases

Methods in molecular biology (Clifton, N.J.), 2010-01, Vol.597, p.333

2010

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Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during development

Human molecular genetics, 1995-07, Vol.4 (7), p.1173-1182

1995

Volltextzugriff (PDF)

Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: Restoration by the neuroprotective compound CEP-1347

Molecular and cellular neuroscience, 2008-09, Vol.39 (1), p.1-7

2008

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Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging

Journal of Parkinson's disease, 2014, Vol.4 (3), p.483

2014

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Genetic causes of Parkinson’s disease: extending the pathway

Journal of neural transmission. Supplementum, 2006 (70), p.181-189

2006

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Characterization of the rat spinocerebellar ataxia type 3 gene

Neurogenetics, 1997-11, Vol.1 (2), p.103-112

1997

Volltextzugriff (PDF)

Parkinson's disease: one biochemical pathway to fit all genes?

Trends in Molecular Medicine, 2002-05, Vol.8 (5), p.236-240

2002

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Human Txk: genomic organization, structure and contiguous physical linkage with the Tec gene

Oncogene, 1996-02, Vol.12 (4), p.937-942

1996

Volltextzugriff (PDF)

The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis

Molecular genetics and metabolism, 2005-05, Vol.85 (1), p.12-20

2005

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Characterization of a human chromosome 4 flow-sorted cosmid library

Cytogenetics and cell genetics, 1994, Vol.65 (4), p.238

1994

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Overexpression of human wildtype torsinA and human DeltaGAG torsinA in a transgenic mouse model causes phenotypic abnormalities

Neurobiology of disease, 2007-08, Vol.27 (2), p.190-206

2007

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Characterization of a cosmid library from flow-sorted chromosomes 11

Chromosome research, 1994-05, Vol.2 (3), p.201-207

1994

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Isolation and characterization of the rat huntingtin promoter

Biochemical journal, 1998-11, Vol.336 ( Pt 1) (1), p.227-234

1998

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Olfactory bulb atrophy and caspase activation observed in the BACHD rat models of Huntington disease

Mitochondrial proteolytic stress induced by loss of mortalin function is rescued by Parkin and PINK1

Calpain-mediated ataxin-3 cleavage in the molecular pathogenesis of spinocerebellar ataxia type 3 (SCA3)

Behavioral and in vivo electrophysiological evidence for presymptomatic alteration of prefrontostriatal processing in the transgenic rat model for huntington disease

Induction of STAT3-related genes in fast degenerating cone photoreceptors of cpfl1 mice

14-3-3 proteins in the nervous system

Early postnatal behavioral, cellular, and molecular changes in models of Huntington disease are reversible by HDAC inhibition

LRRK2 guides the actin cytoskeleton at growth cones together with ARHGEF7 and Tropomyosin 4

Nuclear Localization of Ataxin-3 Is Required for the Manifestation of Symptoms in SCA3: In Vivo Evidence

Normal sensitivity to excitotoxicity in a transgenic Huntington's disease rat

Ubiquitylation of Synphilin-1 and α-Synuclein by SIAH and Its Presence in Cellular Inclusions and Lewy Bodies Imply a Role in Parkinson's Disease

Disturbance of iron metabolism in Parkinson's disease -- ultrasonography as a biomarker

Neurobehavioral tests in rat models of degenerative brain diseases

Expression of the Huntington disease gene in rodents: cloning the rat homologue and evidence for downregulation in non-neuronal tissues during development

Blood level of brain-derived neurotrophic factor mRNA is progressively reduced in rodent models of Huntington's disease: Restoration by the neuroprotective compound CEP-1347

Behavioral deficits and striatal DA signaling in LRRK2 p.G2019S transgenic rats: a multimodal investigation including PET neuroimaging

Genetic causes of Parkinson’s disease: extending the pathway

Characterization of the rat spinocerebellar ataxia type 3 gene

Parkinson's disease: one biochemical pathway to fit all genes?

Human Txk: genomic organization, structure and contiguous physical linkage with the Tec gene

The pathogenesis of molybdenum cofactor deficiency, its delay by maternal clearance, and its expression pattern in microarray analysis

Characterization of a human chromosome 4 flow-sorted cosmid library

Overexpression of human wildtype torsinA and human DeltaGAG torsinA in a transgenic mouse model causes phenotypic abnormalities

Characterization of a cosmid library from flow-sorted chromosomes 11

Isolation and characterization of the rat huntingtin promoter

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