Search research articles
Contact Us
Filters
Showing results (11-20 of 17) with videos related to
Page
of 2
Sort By:
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 locus
Marc 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 adenomas
Sergey 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 melanoma
Sergey I Nikolaev, Donata Rimoldi, Christian Iseli, et al.
Nature
|
December 4, 2015
Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndrome
Audrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature
|
April 18, 2014
Domains of genome-wide gene expression dysregulation in Down's syndrome
Audrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature
|
September 8, 2012
Landscape of transcription in human cells
Sarah Djebali, Carrie A Davis, Angelika Merkel, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 17) with videos related to
Sort By:
Page
of 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 locus
Marc 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 adenomas
Sergey 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 melanoma
Sergey I Nikolaev, Donata Rimoldi, Christian Iseli, et al.
Nature
|
December 4, 2015
Corrigendum: Domains of genome-wide gene expression dysregulation in Down's syndrome
Audrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature
|
April 18, 2014
Domains of genome-wide gene expression dysregulation in Down's syndrome
Audrey Letourneau, Federico A Santoni, Ximena Bonilla, et al.
Nature
|
September 8, 2012
Landscape of transcription in human cells
Sarah Djebali, Carrie A Davis, Angelika Merkel, et al.
Page
of 2