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M Beckmann

Showing results (211-220 of 220) with videos related to

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Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Nature Genetics|January 12, 2010
Genome-wide association study of PR intervalArne Pfeufer, Charlotte van Noord, Kristin D Marciante, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Physical Review Letters|February 3, 2004
Flavor decomposition of the sea-quark helicity distributions in the nucleon from semiinclusive deep inelastic scatteringA Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|March 14, 2003
Q2 dependence of nuclear transparency for exclusive rho0 productionA Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|April 12, 2003
Evidence for quark-hadron duality in the proton spin asymmetry A1A Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|February 9, 2005
Single-spin asymmetries in semi-inclusive deep-inelastic scattering on a transversely polarized hydrogen targetA Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|December 31, 2005
Measurement of the tensor structure function b1 of the deuteronA Airapetian, N Akopov, Z Akopov, et al.
Pageof 22

Showing results (211-220 of 220) with videos related to

Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 220 results.
Nature Genetics|July 23, 2013
Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac deathConnie R Bezzina, Julien Barc, Yuka Mizusawa, et al.
Nature Genetics|January 12, 2010
Genome-wide association study of PR intervalArne Pfeufer, Charlotte van Noord, Kristin D Marciante, et al.
Nature Genetics|February 23, 2010
Common variants in KCNN3 are associated with lone atrial fibrillationPatrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, et al.
Circulation|May 21, 2020
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT SyndromeNajim Lahrouchi, Rafik Tadros, Lia Crotti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 7, 2020
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controlsRoddy Walsh, Najim Lahrouchi, Rafik Tadros, et al.
Physical Review Letters|February 3, 2004
Flavor decomposition of the sea-quark helicity distributions in the nucleon from semiinclusive deep inelastic scatteringA Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|March 14, 2003
Q2 dependence of nuclear transparency for exclusive rho0 productionA Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|April 12, 2003
Evidence for quark-hadron duality in the proton spin asymmetry A1A Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|February 9, 2005
Single-spin asymmetries in semi-inclusive deep-inelastic scattering on a transversely polarized hydrogen targetA Airapetian, N Akopov, Z Akopov, et al.
Physical Review Letters|December 31, 2005
Measurement of the tensor structure function b1 of the deuteronA Airapetian, N Akopov, Z Akopov, et al.
Pageof 22