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Vincent Plagnol

Showing results (11-20 of 189) with videos related to

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American Journal of Human Genetics|March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenitaAmanda J Walne, Tom Vulliamy, Michael Kirwan, et al.
Genetics|November 22, 2005
Relative influences of crossing over and gene conversion on the pattern of linkage disequilibrium in Arabidopsis thalianaVincent Plagnol, Badri Padhukasahasram, Jeffrey D Wall, et al.
Plos Genetics|May 22, 2007
A method to address differential bias in genotyping in large-scale association studiesVincent Plagnol, Jason D Cooper, John A Todd, et al.
Archives of Oral Biology|April 16, 2015
A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesisShurog AlFawaz, Vincent Plagnol, Ferranti S L Wong, et al.
Biostatistics (Oxford, England)|November 29, 2008
Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13Vincent Plagnol, Deborah J Smyth, John A Todd, et al.
BMC Medical Genomics|May 28, 2017
Quantitative analysis of cryptic splicing associated with TDP-43 depletionJack Humphrey, Warren Emmett, Pietro Fratta, et al.
Journal of Medical Genetics|October 12, 2012
Use of targeted exome sequencing as a diagnostic tool for Familial HypercholesterolaemiaMarta Futema, Vincent Plagnol, Ros A Whittall, et al.
Neuroscience Letters|May 8, 2012
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1Arianna Tucci, Gavin Charlesworth, Una-Marie Sheerin, et al.
Plos One|August 14, 2008
Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analysesVincent Plagnol, Elif Uz, Chris Wallace, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 7, 2007
Interactions between Idd5.1/Ctla4 and other type 1 diabetes genesKara Hunter, Dan Rainbow, Vincent Plagnol, et al.
Pageof 19

Showing results (11-20 of 189) with videos related to

Sort By:
Pageof 19
American Journal of Human Genetics|March 5, 2013
Constitutional mutations in RTEL1 cause severe dyskeratosis congenitaAmanda J Walne, Tom Vulliamy, Michael Kirwan, et al.
Genetics|November 22, 2005
Relative influences of crossing over and gene conversion on the pattern of linkage disequilibrium in Arabidopsis thalianaVincent Plagnol, Badri Padhukasahasram, Jeffrey D Wall, et al.
Plos Genetics|May 22, 2007
A method to address differential bias in genotyping in large-scale association studiesVincent Plagnol, Jason D Cooper, John A Todd, et al.
Archives of Oral Biology|April 16, 2015
A novel frameshift MSX1 mutation in a Saudi family with autosomal dominant premolar and third molar agenesisShurog AlFawaz, Vincent Plagnol, Ferranti S L Wong, et al.
Biostatistics (Oxford, England)|November 29, 2008
Statistical independence of the colocalized association signals for type 1 diabetes and RPS26 gene expression on chromosome 12q13Vincent Plagnol, Deborah J Smyth, John A Todd, et al.
BMC Medical Genomics|May 28, 2017
Quantitative analysis of cryptic splicing associated with TDP-43 depletionJack Humphrey, Warren Emmett, Pietro Fratta, et al.
Journal of Medical Genetics|October 12, 2012
Use of targeted exome sequencing as a diagnostic tool for Familial HypercholesterolaemiaMarta Futema, Vincent Plagnol, Ros A Whittall, et al.
Neuroscience Letters|May 8, 2012
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1Arianna Tucci, Gavin Charlesworth, Una-Marie Sheerin, et al.
Plos One|August 14, 2008
Extreme clonality in lymphoblastoid cell lines with implications for allele specific expression analysesVincent Plagnol, Elif Uz, Chris Wallace, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 7, 2007
Interactions between Idd5.1/Ctla4 and other type 1 diabetes genesKara Hunter, Dan Rainbow, Vincent Plagnol, et al.
Pageof 19