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C B Lücking

Showing results (11-20 of 19) with videos related to

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Molecular Biology Reports|April 26, 2006
Parkin modulates gene expression in control and ceramide-treated PC12 cellsP G Unschuld, J Dächsel, F Darios, et al.
Neurology|February 27, 2001
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutationsB P van de Warrenburg, M Lammens, C B Lücking, et al.
Lancet (London, England)|November 5, 1998
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study GroupC B Lücking, N Abbas, A Dürr, et al.
The New England Journal of Medicine|May 29, 2000
Association between early-onset Parkinson's disease and mutations in the parkin geneC B Lücking, A Dürr, V Bonifati, et al.
FEBS Letters|July 1, 2005
Parkin interacts with the proteasome subunit alpha4J C Dächsel, C B Lücking, S Deeg, et al.
Brain : a Journal of Neurology|May 29, 2000
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?J Tassin, A Dürr, A M Bonnet, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, et al.
Neurology|April 23, 2003
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonismN Rawal, M Periquet, E Lohmann, et al.
Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Molecular Biology Reports|April 26, 2006
Parkin modulates gene expression in control and ceramide-treated PC12 cellsP G Unschuld, J Dächsel, F Darios, et al.
Neurology|February 27, 2001
Clinical and pathologic abnormalities in a family with parkinsonism and parkin gene mutationsB P van de Warrenburg, M Lammens, C B Lücking, et al.
Lancet (London, England)|November 5, 1998
Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study GroupC B Lücking, N Abbas, A Dürr, et al.
The New England Journal of Medicine|May 29, 2000
Association between early-onset Parkinson's disease and mutations in the parkin geneC B Lücking, A Dürr, V Bonifati, et al.
FEBS Letters|July 1, 2005
Parkin interacts with the proteasome subunit alpha4J C Dächsel, C B Lücking, S Deeg, et al.
Brain : a Journal of Neurology|May 29, 2000
Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?J Tassin, A Dürr, A M Bonnet, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, et al.
Neurology|April 23, 2003
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonismN Rawal, M Periquet, E Lohmann, et al.
Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, et al.
Pageof 2