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Showing results (1071-1080 of 1,089) with videos related to

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European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
Environment International|May 11, 2018
Critical knowledge gaps and research needs related to the environmental dimensions of antibiotic resistanceD G Joakim Larsson, Antoine Andremont, Johan Bengtsson-Palme, et al.
Trials|May 16, 2022
Reduced anticoagulation targets in extracorporeal life support (RATE): study protocol for a randomized controlled trialOlivier van Minnen, Annemieke Oude Lansink-Hartgring, Bas van den Boogaard, et al.
Nature Cell Biology|June 25, 2013
TRF2 inhibits a cell-extrinsic pathway through which natural killer cells eliminate cancer cellsAnnamaria Biroccio, Julien Cherfils-Vicini, Adeline Augereau, et al.
European Heart Journal|May 15, 2024
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk lociTaisuke Ishikawa, Tatsuo Masuda, Tsuyoshi Hachiya, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 21, 2011
Dickkopf-1 regulates bone formation in young growing rodents and upon traumatic injuryXiaodong Li, Mario Grisanti, Wei Fan, et al.
Nature Genetics|August 25, 2015
Genetic association analyses highlight biological pathways underlying mitral valve prolapseChristian Dina, Nabila Bouatia-Naji, Nathan Tucker, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
JAMA Cardiology|September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular PathwaysHildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.
Ebiomedicine|April 3, 2026
Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus casesMaud Tusseau, Samira Khaldi-Plassart, Audrey Labalme, et al.
Pageof 109

Showing results (1071-1080 of 1,089) with videos related to

Sort By:
Pageof 109
European Heart Journal|May 23, 2019
RRAD mutation causes electrical and cytoskeletal defects in cardiomyocytes derived from a familial case of Brugada syndromeNadjet Belbachir, Vincent Portero, Zeina R Al Sayed, et al.
Environment International|May 11, 2018
Critical knowledge gaps and research needs related to the environmental dimensions of antibiotic resistanceD G Joakim Larsson, Antoine Andremont, Johan Bengtsson-Palme, et al.
Trials|May 16, 2022
Reduced anticoagulation targets in extracorporeal life support (RATE): study protocol for a randomized controlled trialOlivier van Minnen, Annemieke Oude Lansink-Hartgring, Bas van den Boogaard, et al.
Nature Cell Biology|June 25, 2013
TRF2 inhibits a cell-extrinsic pathway through which natural killer cells eliminate cancer cellsAnnamaria Biroccio, Julien Cherfils-Vicini, Adeline Augereau, et al.
European Heart Journal|May 15, 2024
Brugada syndrome in Japan and Europe: a genome-wide association study reveals shared genetic architecture and new risk lociTaisuke Ishikawa, Tatsuo Masuda, Tsuyoshi Hachiya, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|July 21, 2011
Dickkopf-1 regulates bone formation in young growing rodents and upon traumatic injuryXiaodong Li, Mario Grisanti, Wei Fan, et al.
Nature Genetics|August 25, 2015
Genetic association analyses highlight biological pathways underlying mitral valve prolapseChristian Dina, Nabila Bouatia-Naji, Nathan Tucker, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
JAMA Cardiology|September 4, 2024
Genome-Wide Association Study of Accessory Atrioventricular PathwaysHildur M Aegisdottir, Laura Andreasen, Rosa B Thorolfsdottir, et al.
Ebiomedicine|April 3, 2026
Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus casesMaud Tusseau, Samira Khaldi-Plassart, Audrey Labalme, et al.
Pageof 109