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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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Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

Cerebellum (London, England), 2014-04, Vol.13 (2), p.269-302

2014

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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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Transgenic rat model of Huntington's disease

Human molecular genetics, 2003-03, Vol.12 (6), p.617-624

2003

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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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Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein

Neuroscience, 2012-10, Vol.222, p.343-355

2012

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Metabolic and Type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of Huntington disease

Experimental neurology, 2011-06, Vol.229 (2), p.440-449

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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Stem Cell Quiescence in the Hippocampal Neurogenic Niche Is Associated With Elevated Transforming Growth Factor-β Signaling in an Animal Model of Huntington Disease

Journal of neuropathology and experimental neurology, 2010-07, Vol.69 (7), p.717-728

2010

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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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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

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B-Raf and Ha-ras mutations in chemically induced mouse liver tumors

Oncogene, 2005-02, Vol.24 (7), p.1290-1295

2005

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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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Adult neural precursor cells unaffected in animal models of DYT1 dystonia

Neuroreport, 2009-11, Vol.20 (17), p.1529-1533

2009

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Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease

Brain research, 2009-02, Vol.1256, p.19-33

2009

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Characterization of the rat spinocerebellar ataxia type 3 gene

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

1997

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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

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

Consensus Paper: Pathological Mechanisms Underlying Neurodegeneration in Spinocerebellar Ataxias

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)

Transgenic rat model of Huntington's disease

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

Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein

Metabolic and Type 1 cannabinoid receptor imaging of a transgenic rat model in the early phase of 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

Stem Cell Quiescence in the Hippocampal Neurogenic Niche Is Associated With Elevated Transforming Growth Factor-β Signaling in an Animal Model of Huntington Disease

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

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

B-Raf and Ha-ras mutations in chemically induced mouse liver tumors

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

Adult neural precursor cells unaffected in animal models of DYT1 dystonia

Microarray expression analysis of human dopaminergic neuroblastoma cells after RNA interference of SNCA — A key player in the pathogenesis of Parkinson's disease

Characterization of the rat spinocerebellar ataxia type 3 gene

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

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