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P Holmans

Showing results (11-20 of 82) with videos related to

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Genetic Epidemiology|December 24, 2003
Bayesian trio models for association in the presence of genotyping errorsL Bernardinelli, C Berzuini, S Seaman, et al.
Annals of Human Genetics|September 6, 2005
Design of case-controls studies with unscreened controlsV Moskvina, P Holmans, K M Schmidt, et al.
Molecular Psychiatry|March 1, 1996
Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairsN Craddock, J Daniels, P Holmans, et al.
Lancet (London, England)|October 31, 1997
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's diseaseO Bandmann, J Vaughan, P Holmans, et al.
Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1994
No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairsN W Wood, P Holmans, D Clayton, et al.
Genetic Epidemiology|October 31, 2000
Clustering methods applied to allele sharing dataR J Neuman, N L Saccone, P Holmans, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 14, 2000
Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's diseaseO Bandmann, J R Vaughan, P Holmans, et al.
Genes, Brain, and Behavior|August 19, 2007
Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's diseaseA Hodges, G Hughes, S Brooks, et al.
Cellular Signalling|December 19, 2016
SMAD transcription factors are altered in cell models of HD and regulate HTT expressionK R Bowles, T Stone, P Holmans, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
Genetic Epidemiology|December 24, 2003
Bayesian trio models for association in the presence of genotyping errorsL Bernardinelli, C Berzuini, S Seaman, et al.
Annals of Human Genetics|September 6, 2005
Design of case-controls studies with unscreened controlsV Moskvina, P Holmans, K M Schmidt, et al.
Molecular Psychiatry|March 1, 1996
Increasing the efficiency of genomic searches for linkage in complex disorders by DNA pooling of affected sib-pairsN Craddock, J Daniels, P Holmans, et al.
Lancet (London, England)|October 31, 1997
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's diseaseO Bandmann, J Vaughan, P Holmans, et al.
Kidney International|July 20, 1999
Familial phenotype differences in PKD11N Hateboer, L P Lazarou, A J Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1994
No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairsN W Wood, P Holmans, D Clayton, et al.
Genetic Epidemiology|October 31, 2000
Clustering methods applied to allele sharing dataR J Neuman, N L Saccone, P Holmans, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 14, 2000
Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's diseaseO Bandmann, J R Vaughan, P Holmans, et al.
Genes, Brain, and Behavior|August 19, 2007
Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's diseaseA Hodges, G Hughes, S Brooks, et al.
Cellular Signalling|December 19, 2016
SMAD transcription factors are altered in cell models of HD and regulate HTT expressionK R Bowles, T Stone, P Holmans, et al.
Pageof 9