Showing results (1-10 of 15) with videos related to
Sort By:
Pageof 2
American Journal of Human Genetics|April 9, 2008
Mapping of small RNAs in the human ENCODE regionsChristelle Borel, Maryline Gagnebin, Corinne Gehrig, et al.American Journal of Human Genetics|August 2, 2007
Human microRNA-155 on chromosome 21 differentially interacts with its polymorphic target in the AGTR1 3' untranslated region: a mechanism for functional single-nucleotide polymorphisms related to phenotypesPraveen Sethupathy, Christelle Borel, Maryline Gagnebin, et al.Human Mutation|May 11, 2012
Tandem repeat sequence variation as causative cis-eQTLs for protein-coding gene expression variation: the case of CSTBChristelle Borel, Eugenia Migliavacca, Audrey Letourneau, et al.Human Molecular Genetics|October 28, 2005
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genesSamuel Deutsch, Robert Lyle, Emmanouil T Dermitzakis, et al.Stem Cell Research|December 25, 2013
Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modificationsAntonietta Coppola, Antonio Romito, Christelle Borel, et al.American Journal of Medical Genetics. Part A|July 16, 2008
Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: a complex series of eventsSophie Dahoun, Sarantis Gagos, Maryline Gagnebin, et al.American Journal of Human Genetics|August 2, 2007
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalancePaola Prandini, Samuel Deutsch, Robert Lyle, et al.Genome Research|December 15, 2010
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblastsChristelle Borel, Samuel Deutsch, Audrey Letourneau, et al.Plos One|September 7, 2012
Extensive natural variation for cellular hydrogen peroxide release is genetically controlledHoma Attar, Karen Bedard, Eugenia Migliavacca, et al.Journal of Medical Genetics|April 14, 2012
Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphaloceleUppala Radhakrishna, Swapan K Nath, Ken McElreavey, et al.Pageof 2