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Daniel Robyr

Showing results (11-20 of 17) with videos related to

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Plos One|January 6, 2011
A systematic enhancer screen using lentivector transgenesis identifies conserved and non-conserved functional elements at the Olig1 and Olig2 locusMarc Friedli, Isabelle Barde, Mélanie Arcangeli, et al.
Cancer Research|December 4, 2012
A single-nucleotide substitution mutator phenotype revealed by exome sequencing of human colon adenomasSergey I Nikolaev, Sotirios K Sotiriou, Ioannis S Pateras, et al.
Human Molecular Genetics|February 22, 2015
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)Elisa Giorgio, Daniel Robyr, Malte Spielmann, et al.
Nature Genetics|December 27, 2011
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanomaSergey I Nikolaev, Donata Rimoldi, Christian Iseli, et al.
Nature|December 4, 2015
Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndromeAudrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature|April 18, 2014
Domains of genome-wide gene expression dysregulation in Down's syndromeAudrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature|September 8, 2012
Landscape of transcription in human cellsSarah Djebali, Carrie A Davis, Angelika Merkel, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Plos One|January 6, 2011
A systematic enhancer screen using lentivector transgenesis identifies conserved and non-conserved functional elements at the Olig1 and Olig2 locusMarc Friedli, Isabelle Barde, Mélanie Arcangeli, et al.
Cancer Research|December 4, 2012
A single-nucleotide substitution mutator phenotype revealed by exome sequencing of human colon adenomasSergey I Nikolaev, Sotirios K Sotiriou, Ioannis S Pateras, et al.
Human Molecular Genetics|February 22, 2015
A large genomic deletion leads to enhancer adoption by the lamin B1 gene: a second path to autosomal dominant adult-onset demyelinating leukodystrophy (ADLD)Elisa Giorgio, Daniel Robyr, Malte Spielmann, et al.
Nature Genetics|December 27, 2011
Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanomaSergey I Nikolaev, Donata Rimoldi, Christian Iseli, et al.
Nature|December 4, 2015
Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndromeAudrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature|April 18, 2014
Domains of genome-wide gene expression dysregulation in Down's syndromeAudrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature|September 8, 2012
Landscape of transcription in human cellsSarah Djebali, Carrie A Davis, Angelika Merkel, et al.
Pageof 2