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Priska Binner

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

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Herz|September 20, 2005
[Hypertrophic cardiomyopathy]Thomas Scheffold, Priska Binner, Jeanette Erdmann, et al.
Clinical Chemistry|February 9, 2008
Array-based resequencing assay for mutations causing hypertrophic cardiomyopathyStephan Waldmüller, Melanie Müller, Kirsten Rackebrandt, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissectionsSabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, et al.
International Journal of Cancer|January 30, 2004
MHC class I antigen processing pathway defects, ras mutations and disease stage in colorectal carcinomaDerek Atkins, Aldona Breuckmann, Gerd E Schmahl, et al.
Scientific Reports|October 15, 2021
FH ALERT: efficacy of a novel approach to identify patients with familial hypercholesterolemiaFelix Fath, Andreas Bengeser, Mathias Barresi, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variantsUrsula Kassner, Bastian Salewsky, Marion Wühle-Demuth, et al.
BMC Cardiovascular Disorders|October 10, 2009
Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary interventionSilke Kullmann, Priska Binner, Kirsten Rackebrandt, et al.
Molecular and Cellular Probes|November 13, 2012
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissectionsUshanthine Kathiravel, Britta Keyser, Sabine Hoffjan, et al.
Journal of Lipid Research|July 5, 2024
Clinical characterization and mutation spectrum of patients with hypertriglyceridemia in a German outpatient clinicFrieda Bardey, Lorenz Rieck, Dominik Spira, et al.
BMC Cardiovascular Disorders|March 10, 2011
Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registryThomas Scheffold, Silke Kullmann, Andreas Huge, et al.
Pageof 2

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

Sort By:
Pageof 2
Herz|September 20, 2005
[Hypertrophic cardiomyopathy]Thomas Scheffold, Priska Binner, Jeanette Erdmann, et al.
Clinical Chemistry|February 9, 2008
Array-based resequencing assay for mutations causing hypertrophic cardiomyopathyStephan Waldmüller, Melanie Müller, Kirsten Rackebrandt, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Three novel mutations in the ACTA2 gene in German patients with thoracic aortic aneurysms and dissectionsSabine Hoffjan, Stephan Waldmüller, Wulf Blankenfeldt, et al.
International Journal of Cancer|January 30, 2004
MHC class I antigen processing pathway defects, ras mutations and disease stage in colorectal carcinomaDerek Atkins, Aldona Breuckmann, Gerd E Schmahl, et al.
Scientific Reports|October 15, 2021
FH ALERT: efficacy of a novel approach to identify patients with familial hypercholesterolemiaFelix Fath, Andreas Bengeser, Mathias Barresi, et al.
European Journal of Human Genetics : EJHG|January 15, 2015
Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variantsUrsula Kassner, Bastian Salewsky, Marion Wühle-Demuth, et al.
BMC Cardiovascular Disorders|October 10, 2009
Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary interventionSilke Kullmann, Priska Binner, Kirsten Rackebrandt, et al.
Molecular and Cellular Probes|November 13, 2012
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissectionsUshanthine Kathiravel, Britta Keyser, Sabine Hoffjan, et al.
Journal of Lipid Research|July 5, 2024
Clinical characterization and mutation spectrum of patients with hypertriglyceridemia in a German outpatient clinicFrieda Bardey, Lorenz Rieck, Dominik Spira, et al.
BMC Cardiovascular Disorders|March 10, 2011
Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registryThomas Scheffold, Silke Kullmann, Andreas Huge, et al.
Pageof 2