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O Riess

Showing results (31-40 of 144) with videos related to

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Epilepsy Research|March 27, 1999
Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsyT Sander, L Schölz, D Janz, et al.
Electrophoresis|May 1, 1995
Indirect DNA/gene diagnoses via electrophoresis--an obsolete principle?J T Epplen, J Buitkamp, C Epplen, et al.
Human Molecular Genetics|June 1, 1993
(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3B Weber, O Riess, H Daneshvar, et al.
Nucleic Acids Research|April 11, 1991
A polymorphic DNA marker at the D8S131 locusB Weber, O Riess, C N Kreklywich, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|June 6, 2006
Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's diseaseT Franck, R Krueger, D Woitalla, et al.
American Journal of Human Genetics|October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosaO Riess, A Noerremoelle, B Weber, et al.
Human Genetics|April 1, 1988
Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic RepublicO Riess, A Michel, A Speer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998
Spinocerebellar ataxia type 6: genotype and phenotype in German kindredsL Schöls, R Krüger, G Amoiridis, et al.
Brain Research. Molecular Brain Research|June 23, 2004
Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathwaysM Bonin, S Poths, H Osaka, et al.
Human Molecular Genetics|March 1, 1996
cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 geneM Gossen, I Schmitt, K Obst, et al.
Pageof 15

Showing results (31-40 of 144) with videos related to

Sort By:
Pageof 15
Epilepsy Research|March 27, 1999
Length variation of a polyglutamine array in the gene encoding a small-conductance, calcium-activated potassium channel (hKCa3) and susceptibility to idiopathic generalized epilepsyT Sander, L Schölz, D Janz, et al.
Electrophoresis|May 1, 1995
Indirect DNA/gene diagnoses via electrophoresis--an obsolete principle?J T Epplen, J Buitkamp, C Epplen, et al.
Human Molecular Genetics|June 1, 1993
(CA)n-dinucleotide repeat at the PDEB locus in 4p16.3B Weber, O Riess, H Daneshvar, et al.
Nucleic Acids Research|April 11, 1991
A polymorphic DNA marker at the D8S131 locusB Weber, O Riess, C N Kreklywich, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|June 6, 2006
Mutation analysis of the seven in absentia homolog 1 (SIAH1) gene in Parkinson's diseaseT Franck, R Krueger, D Woitalla, et al.
American Journal of Human Genetics|October 1, 1992
The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosaO Riess, A Noerremoelle, B Weber, et al.
Human Genetics|April 1, 1988
Linkage disequilibrium between RFLP haplotype 2 and the affected PAH allele in PKU families from the Berlin area of the German Democratic RepublicO Riess, A Michel, A Speer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|January 22, 1998
Spinocerebellar ataxia type 6: genotype and phenotype in German kindredsL Schöls, R Krüger, G Amoiridis, et al.
Brain Research. Molecular Brain Research|June 23, 2004
Microarray expression analysis of gad mice implicates involvement of Parkinson's disease associated UCH-L1 in multiple metabolic pathwaysM Bonin, S Poths, H Osaka, et al.
Human Molecular Genetics|March 1, 1996
cDNA cloning and expression of rsca1, the rat counterpart of the human spinocerebellar ataxia type 1 geneM Gossen, I Schmitt, K Obst, et al.
Pageof 15