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Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

The New England journal of medicine, 2000-05, Vol.342 (21), p.1560-1567

2000

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Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death

Human molecular genetics, 2003-03, Vol.12 (5), p.517-526

2003

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A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

Human molecular genetics, 1999-04, Vol.8 (4), p.567-574

1999

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Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations

Neurology, 2001-02, Vol.56 (4), p.555

2001

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Alpha-synuclein and Parkinson's disease

Cellular and molecular life sciences : CMLS, 2000-12, Vol.57 (13-14), p.1894-1908

2000

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Complex relationship between Parkin mutations and Parkinson disease

American journal of medical genetics, 2002-07, Vol.114 (5), p.584-591

2002

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Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

The Lancet (British edition), 1998-10, Vol.352 (9137), p.1355-1356

1998

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The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates

Neurobiology of disease, 2003-12, Vol.14 (3), p.357-364

2003

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Polymorphisms in the receptor for GDNF ( RET ) are not associated with Parkinson's disease in Southern Germany

Neurobiology of aging, 2010-01, Vol.31 (1), p.167-168

2010

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Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

Neurology, 2001-09, Vol.57 (5), p.924

2001

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Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

American journal of human genetics, 2001-03, Vol.68 (3), p.617-626

2001

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[18 F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations

Neurology, 2000-09, Vol.55 (6), p.877

2000

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New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

Neurology, 2003-04, Vol.60 (8), p.1378

2003

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Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism

Journal of neurology, neurosurgery and psychiatry, 2001-10, Vol.71 (4), p.531-534

2001

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Aspects of cytotoxic lignan biosynthesis in suspension cultures of Linum nodiflorum

Phytochemistry reviews, 2002-01, Vol.1 (1), p.37-43

2002

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Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

Movement disorders, 2003-08, Vol.18 (8), p.914-919

2003

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Advances in Experimental Medicine and Biology, Vol 541: Frontiers in Clinical Neuroscience: Neurodegeneration and Neuroprotection, Laszlo Vecsei (Ed.) Springer, New York, 2004 212 pp. Hardcover ISBN: 0-306-48038-7 EUR 128,80

Journal of neurology, 2005-11, Vol.252 (11), p.1425-1425

Lücking, Christoph B.

2005

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Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease

Neuroscience letters, 2005-05, Vol.379 (3), p.195-198

2005

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Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia

Journal of Neural Transmission, 2004-10, Vol.111 (10-11), p.1209-1218

2004

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Proteasomal inhibition reduces parkin mRNA in PC12 and SH-SY5Y cells

Parkinsonism & related disorders, 2009-03, Vol.15 (3), p.220-225

2009

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Semiquantitative PCR for the detection of exon rearrangements in the Parkin gene

Methods in molecular biology (Clifton, N.J.), 2003, Vol.217, p.13

2003

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The parkin gene and its phenotype

Neurological sciences, 2001-02, Vol.22 (1), p.51-52

2001

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Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease

Journal of neurology, 2008-03, Vol.255 (3), p.441-442

2008

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Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body Parkinsonism

Journal of neuroscience research, 1996-04, Vol.44 (2), p.174-183

1996

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Parkin modulates gene expression in control and ceramide-treated PC12 cells

Molecular biology reports, 2006-03, Vol.33 (1), p.13-32

2006

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Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene

Parkin prevents mitochondrial swelling and cytochrome c release in mitochondria-dependent cell death

A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe

Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutations

Alpha-synuclein and Parkinson's disease

Complex relationship between Parkin mutations and Parkinson disease

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

The C289G and C418R missense mutations cause rapid sequestration of human Parkin into insoluble aggregates

Polymorphisms in the receptor for GDNF ( RET ) are not associated with Parkinson's disease in Southern Germany

Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutations

Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

[18 F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutations

New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism

Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonism

Aspects of cytotoxic lignan biosynthesis in suspension cultures of Linum nodiflorum

Mutation analysis of the parkin gene in Russian families with autosomal recessive juvenile parkinsonism

Advances in Experimental Medicine and Biology, Vol 541: Frontiers in Clinical Neuroscience: Neurodegeneration and Neuroprotection, Laszlo Vecsei (Ed.) Springer, New York, 2004 212 pp. Hardcover ISBN: 0-306-48038-7 EUR 128,80

Mutations in the pantothenate kinase gene PANK2 are not associated with Parkinson disease

Ultrastructural localization of parkin in the rat brainstem, thalamus and basal ganglia

Proteasomal inhibition reduces parkin mRNA in PC12 and SH-SY5Y cells

Semiquantitative PCR for the detection of exon rearrangements in the Parkin gene

The parkin gene and its phenotype

Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's disease

Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body Parkinsonism

Parkin modulates gene expression in control and ceramide-treated PC12 cells

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