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C B Lücking

Showing results (1-10 of 19) with videos related to

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Cellular and Molecular Life Sciences : CMLS|February 24, 2001
Alpha-synuclein and Parkinson's diseaseC B Lücking, A Brice
Biochemical and Biophysical Research Communications|June 15, 1995
Absence of the mitochondrial A7237T mutation in Parkinson's diseaseC B Lücking, S Kösel, P Mehraein, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 1996
Nonradioactive PCR sequencing using digoxigeninS Kösel, C B Lücking, R Egensperger, et al.
Journal of Neuroscience Research|April 15, 1996
Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonismS Kösel, C B Lücking, R Egensperger, et al.
Neurology|September 12, 2001
Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutationsC B Lücking, V Bonifati, M Periquet, et al.
Neurology|September 20, 2000
[18 F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutationsE Broussolle, C B Lücking, N Ginovart, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2001
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonismV Bonifati, C B Lücking, E Fabrizio, et al.
Journal of Neurology|March 14, 2008
Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's diseaseC B Lücking, P Lichtner, M Dichgans, et al.
Neurobiology of Aging|April 26, 2008
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern GermanyC B Lücking, P Lichtner, E R Kramer, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|October 14, 2004
Ultrastructural localization of parkin in the rat brainstem, thalamus and basal gangliaA Mouatt-Prigent, M-P Muriel, W-J Gu, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Cellular and Molecular Life Sciences : CMLS|February 24, 2001
Alpha-synuclein and Parkinson's diseaseC B Lücking, A Brice
Biochemical and Biophysical Research Communications|June 15, 1995
Absence of the mitochondrial A7237T mutation in Parkinson's diseaseC B Lücking, S Kösel, P Mehraein, et al.
Methods in Molecular Biology (Clifton, N.J.)|January 1, 1996
Nonradioactive PCR sequencing using digoxigeninS Kösel, C B Lücking, R Egensperger, et al.
Journal of Neuroscience Research|April 15, 1996
Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonismS Kösel, C B Lücking, R Egensperger, et al.
Neurology|September 12, 2001
Pseudo-dominant inheritance and exon 2 triplication in a family with parkin gene mutationsC B Lücking, V Bonifati, M Periquet, et al.
Neurology|September 20, 2000
[18 F]-dopa PET study in patients with juvenile-onset PD and parkin gene mutationsE Broussolle, C B Lücking, N Ginovart, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 19, 2001
Three parkin gene mutations in a sibship with autosomal recessive early onset parkinsonismV Bonifati, C B Lücking, E Fabrizio, et al.
Journal of Neurology|March 14, 2008
Polymorphisms in the proteasomal subunit alpha4 are not associated with Parkinson's diseaseC B Lücking, P Lichtner, M Dichgans, et al.
Neurobiology of Aging|April 26, 2008
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern GermanyC B Lücking, P Lichtner, E R Kramer, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|October 14, 2004
Ultrastructural localization of parkin in the rat brainstem, thalamus and basal gangliaA Mouatt-Prigent, M-P Muriel, W-J Gu, et al.
Pageof 2