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Polymorphisms of the α-synuclein promoter: expression analyses and association studies in Parkinson's disease

Journal of Neural Transmission, 2003, Vol.110 (1), p.67-76

2003

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Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)

Annals of neurology, 2003-09, Vol.54 (3), p.367-375

2003

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Genetic influence on the development of Parkinson's disease

Journal of neurology, 2000-04, Vol.247 Suppl 2 (S2), p.II69-II74

2000

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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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DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

Neurology, 1999-09, Vol.53 (4), p.801

1999

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Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

Neurology, 1997-09, Vol.49 (3), p.842

1997

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Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds

Journal of neurology, neurosurgery and psychiatry, 2010-11, Vol.81 (11), p.1229-1232

2010

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2.018 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

Parkinsonism & related disorders, 2007, Vol.13, p.S90-S90

2007

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2.304 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

Parkinsonism & related disorders, 2007, Vol.13, p.S122-S122

2007

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Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families

Neurology, 1999-03, Vol.52 (4), p.849

1999

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Practical importance of neuroprotection in Parkinson's disease

Journal of neurology, 2002-10, Vol.249 Suppl 3, p.III/53-1

2002

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Specification of 14-3-3 proteins in Lewy bodies

Annals of neurology, 2003-07, Vol.54 (1), p.135-135

2003

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Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Annals of neurology, 1997-12, Vol.42 (6), p.924-932

1997

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Haploinsufficiency at the -synuclein gene underlies phenotypic severity in familial Parkinson's disease

Brain (London, England : 1878), 2003-01, Vol.126 (1), p.32-42

2003

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Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Nature genetics, 1999-12, Vol.23 (4), p.391-392

1999

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New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14

Annals of neurology, 2005-11, Vol.58 (5), p.720-729

2005

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Protein surveillance machinery in brains with spinocerebellar ataxia type 3: Redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions

Annals of neurology, 2002-03, Vol.51 (3), p.302-310

2002

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Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathways

Brain research. Molecular brain research., 2004-07, Vol.126 (1), p.88-97

2004

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Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation

Journal of neurochemistry, 2005-08, Vol.94 (3), p.639-650

2005

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Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

Annals of neurology, 1999-05, Vol.45 (5), p.611-617

1999

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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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Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

Movement disorders, 2005-09, Vol.20 (9), p.1191-1194

2005

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An Isoform of Ataxin-3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients

Brain pathology (Zurich, Switzerland), 1998-10, Vol.8 (4), p.669-679

1998

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Do CTG expansions at the SCA8 locus cause ataxia?

Annals of neurology, 2003-07, Vol.54 (1), p.110-115

2003

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Polymorphisms of the α-synuclein promoter: expression analyses and association studies in Parkinson's disease

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17)

Genetic influence on the development of Parkinson's disease

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

DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland

Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6

Spinocerebellar ataxia type 11 (SCA11) is an uncommon cause of dominant ataxia among French and German kindreds

2.018 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

2.304 Neuropathology of conditional alpha-synuclein transgenic mouse models of Parkinson's disease

Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families

Practical importance of neuroprotection in Parkinson's disease

Specification of 14-3-3 proteins in Lewy bodies

Autosomal dominant cerebellar ataxia: Phenotypic differences in genetically defined subtypes?

Haploinsufficiency at the -synuclein gene underlies phenotypic severity in familial Parkinson's disease

Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

New mutations in protein kinase Cγ associated with spinocerebellar ataxia type 14

Protein surveillance machinery in brains with spinocerebellar ataxia type 3: Redistribution and differential recruitment of 26S proteasome subunits and chaperones to neuronal intranuclear inclusions

Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathways

Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation

Increased susceptibility to sporadic Parkinson's disease by a certain combined α-synuclein/apolipoprotein E genotype

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

Alpha-synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patients

An Isoform of Ataxin-3 Accumulates in the Nucleus of Neuronal Cells in Affected Brain Regions of SCA3 Patients

Do CTG expansions at the SCA8 locus cause ataxia?

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