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Marcel Grunert

Showing results (1-10 of 14) with videos related to

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Briefings in Functional Genomics|October 8, 2013
Application of high-throughput sequencing for studying genomic variations in congenital heart diseaseCornelia Dorn, Marcel Grunert, Silke R Sperling
Advances in Experimental Medicine and Biology|June 17, 2024
Cardiac Transcription Factors and Regulatory NetworksMarcel Grunert, Cornelia Dorn, Silke Rickert-Sperling
Journal of Cardiovascular Development and Disease|December 5, 2020
The Needle in the Haystack-Searching for Genetic and Epigenetic Differences in Monozygotic Twins Discordant for Tetralogy of FallotMarcel Grunert, Sandra Appelt, Paul Grossfeld, et al.
Advances in Experimental Medicine and Biology|June 17, 2024
Human Genetics of Tetralogy of Fallot and Double-Outlet Right VentricleCornelia Dorn, Andreas Perrot, Marcel Grunert, et al.
Scientific Reports|December 15, 2019
Altered microRNA and target gene expression related to Tetralogy of FallotMarcel Grunert, Sandra Appelt, Ilona Dunkel, et al.
Bioinformatics (Oxford, England)|November 3, 2009
MicroRazerS: rapid alignment of small RNA readsAnne-Katrin Emde, Marcel Grunert, David Weese, et al.
Plos One|January 9, 2014
Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of FallotVikas Bansal, Cornelia Dorn, Marcel Grunert, et al.
Advances in Experimental Medicine and Biology|June 17, 2024
Technologies to Study Genetics and Molecular PathwaysMarcel Grunert, Cornelia Dorn, Ana Dopazo, et al.
Scientific Reports|July 4, 2020
Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiationMarcel Grunert, Sandra Appelt, Sophia Schönhals, et al.
Cardiovascular Research|August 7, 2016
Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseasesMarcel Grunert, Cornelia Dorn, Huanhuan Cui, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Briefings in Functional Genomics|October 8, 2013
Application of high-throughput sequencing for studying genomic variations in congenital heart diseaseCornelia Dorn, Marcel Grunert, Silke R Sperling
Advances in Experimental Medicine and Biology|June 17, 2024
Cardiac Transcription Factors and Regulatory NetworksMarcel Grunert, Cornelia Dorn, Silke Rickert-Sperling
Journal of Cardiovascular Development and Disease|December 5, 2020
The Needle in the Haystack-Searching for Genetic and Epigenetic Differences in Monozygotic Twins Discordant for Tetralogy of FallotMarcel Grunert, Sandra Appelt, Paul Grossfeld, et al.
Advances in Experimental Medicine and Biology|June 17, 2024
Human Genetics of Tetralogy of Fallot and Double-Outlet Right VentricleCornelia Dorn, Andreas Perrot, Marcel Grunert, et al.
Scientific Reports|December 15, 2019
Altered microRNA and target gene expression related to Tetralogy of FallotMarcel Grunert, Sandra Appelt, Ilona Dunkel, et al.
Bioinformatics (Oxford, England)|November 3, 2009
MicroRazerS: rapid alignment of small RNA readsAnne-Katrin Emde, Marcel Grunert, David Weese, et al.
Plos One|January 9, 2014
Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of FallotVikas Bansal, Cornelia Dorn, Marcel Grunert, et al.
Advances in Experimental Medicine and Biology|June 17, 2024
Technologies to Study Genetics and Molecular PathwaysMarcel Grunert, Cornelia Dorn, Ana Dopazo, et al.
Scientific Reports|July 4, 2020
Induced pluripotent stem cells of patients with Tetralogy of Fallot reveal transcriptional alterations in cardiomyocyte differentiationMarcel Grunert, Sandra Appelt, Sophia Schönhals, et al.
Cardiovascular Research|August 7, 2016
Comparative DNA methylation and gene expression analysis identifies novel genes for structural congenital heart diseasesMarcel Grunert, Cornelia Dorn, Huanhuan Cui, et al.
Pageof 2