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Volker Ruppert

Showing results (61-70 of 66) with videos related to

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Basic Research in Cardiology|June 27, 2020
Deficiency of Nucleotide-binding oligomerization domain-containing proteins (NOD) 1 and 2 reduces atherosclerosisAnn-Kathrin Vlacil, Jutta Schuett, Volker Ruppert, et al.
Frontiers in Genetics|August 11, 2023
Comparative analysis of full-length 16s ribosomal RNA genome sequencing in human fecal samples using primer sets with different degrees of degeneracyChristian Waechter, Leon Fehse, Marius Welzel, et al.
Basic Research in Cardiology|September 17, 2008
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathyAndreas Perrot, Shwan Hussein, Volker Ruppert, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 7

Showing results (61-70 of 66) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 66 results.
Basic Research in Cardiology|June 27, 2020
Deficiency of Nucleotide-binding oligomerization domain-containing proteins (NOD) 1 and 2 reduces atherosclerosisAnn-Kathrin Vlacil, Jutta Schuett, Volker Ruppert, et al.
Frontiers in Genetics|August 11, 2023
Comparative analysis of full-length 16s ribosomal RNA genome sequencing in human fecal samples using primer sets with different degrees of degeneracyChristian Waechter, Leon Fehse, Marius Welzel, et al.
Basic Research in Cardiology|September 17, 2008
Identification of mutational hot spots in LMNA encoding lamin A/C in patients with familial dilated cardiomyopathyAndreas Perrot, Shwan Hussein, Volker Ruppert, et al.
European Heart Journal|April 5, 2011
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathyEric Villard, Claire Perret, Françoise Gary, et al.
European Heart Journal|July 16, 2013
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathyBenjamin Meder, Frank Rühle, Tanja Weis, et al.
European Heart Journal|March 7, 2021
Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23Sophie Garnier, Magdalena Harakalova, Stefan Weiss, et al.
Pageof 7