Search research articles
Contact Us
Filters
Showing results (41-50 of 144) with videos related to
Page
of 15
Sort By:
Nature Genetics
|
May 1, 1992
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease
O Riess, A Noerremoelle, C Collins, et al.
Annals of Neurology
|
December 24, 1997
Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, et al.
Genomics
|
July 1, 1992
The human beta-subunit of rod photoreceptor cGMP phosphodiesterase: complete retinal cDNA sequence and evidence for expression in brain
C Collins, G Hutchinson, D Kowbel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation
L Schöls, G Amoiridis, J T Epplen, et al.
Fortschritte Der Neurologie-Psychiatrie
|
February 1, 1997
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities]
L Schöls, O Riess, G Amoiridis, et al.
Addiction Biology
|
June 26, 2010
The dopamine D2 receptor (DRD2) gene-a genetic risk factor in heavy smoking?
A Batra, G Gelfort, M Bartels, et al.
Neuroscience
|
July 21, 2012
Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein
V E L May, S Nuber, F Marxreiter, et al.
Cytogenetics and Cell Genetics
|
January 1, 1994
Characterization of a human chromosome 4 flow-sorted cosmid library
O Riess, I Siedlaczck, S Kredtke, et al.
Genes, Brain, and Behavior
|
October 15, 2013
A behavioral comparison of the common laboratory rat strains Lister Hooded, Lewis, Fischer 344 and Wistar in an automated homecage system
L E Clemens, E K H Jansson, E Portal, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 15, 2008
Novel TOR1A mutation p.Arg288Gln in early-onset dystonia (DYT1)
B Zirn, K Grundmann, P Huppke, et al.
Page
of 15
Search research articles
Search
Showing results (41-50 of 144) with videos related to
Sort By:
Page
of 15
Nature Genetics
|
May 1, 1992
Exclusion of DNA changes in the beta-subunit of the c-GMP phosphodiesterase gene as the cause for Huntington's disease
O Riess, A Noerremoelle, C Collins, et al.
Annals of Neurology
|
December 24, 1997
Autosomal dominant cerebellar ataxia: phenotypic differences in genetically defined subtypes?
L Schöls, G Amoiridis, T Büttner, et al.
Genomics
|
July 1, 1992
The human beta-subunit of rod photoreceptor cGMP phosphodiesterase: complete retinal cDNA sequence and evidence for expression in brain
C Collins, G Hutchinson, D Kowbel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 1, 1996
Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation
L Schöls, G Amoiridis, J T Epplen, et al.
Fortschritte Der Neurologie-Psychiatrie
|
February 1, 1997
[Genetic diagnosis, classification and clinical hereditary ataxia disease entities]
L Schöls, O Riess, G Amoiridis, et al.
Addiction Biology
|
June 26, 2010
The dopamine D2 receptor (DRD2) gene-a genetic risk factor in heavy smoking?
A Batra, G Gelfort, M Bartels, et al.
Neuroscience
|
July 21, 2012
Impaired olfactory bulb neurogenesis depends on the presence of human wild-type alpha-synuclein
V E L May, S Nuber, F Marxreiter, et al.
Cytogenetics and Cell Genetics
|
January 1, 1994
Characterization of a human chromosome 4 flow-sorted cosmid library
O Riess, I Siedlaczck, S Kredtke, et al.
Genes, Brain, and Behavior
|
October 15, 2013
A behavioral comparison of the common laboratory rat strains Lister Hooded, Lewis, Fischer 344 and Wistar in an automated homecage system
L E Clemens, E K H Jansson, E Portal, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 15, 2008
Novel TOR1A mutation p.Arg288Gln in early-onset dystonia (DYT1)
B Zirn, K Grundmann, P Huppke, et al.
Page
of 15