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E Seidman

Showing results (381-390 of 533) with videos related to

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Anesthesiology|January 13, 2015
Using next-generation RNA sequencing to examine ischemic changes induced by cold blood cardioplegia on the human left ventricular myocardium transcriptomeJochen D Muehlschlegel, Danos C Christodoulou, David McKean, et al.
Nature Genetics|November 7, 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.
JCI Insight|July 1, 2020
BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathyAndrew Antolic, Hiroko Wakimoto, Zhe Jiao, et al.
Circulation Research|April 10, 2010
Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathyAdam J Saltzman, Debora Mancini-DiNardo, Chumei Li, et al.
JACC. Heart Failure|December 30, 2014
Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expressionCarolyn Y Ho, Neal K Lakdawala, Allison L Cirino, et al.
Iscience|January 6, 2022
Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndromeAnna B Meier, Sarala Raj Murthi, Hilansi Rawat, et al.
Circulation Research|May 21, 2021
CalTrack: High-Throughput Automated Calcium Transient Analysis in CardiomyocytesYiangos Psaras, Francesca Margara, Marcelo Cicconet, et al.
Circulation. Genomic and Precision Medicine|September 28, 2023
Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart TransplantationYuri Kim, Oddný Brattberg Gunnarsdóttir, Anissa Viveiros, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathyAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Human Mutation|March 13, 2018
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errorsKathryn B Manheimer, Nihir Patel, Felix Richter, et al.
Pageof 54

Showing results (381-390 of 533) with videos related to

Sort By:
Pageof 54
Anesthesiology|January 13, 2015
Using next-generation RNA sequencing to examine ischemic changes induced by cold blood cardioplegia on the human left ventricular myocardium transcriptomeJochen D Muehlschlegel, Danos C Christodoulou, David McKean, et al.
Nature Genetics|November 7, 1998
Mutations in a novel cochlear gene cause DFNA9, a human nonsyndromic deafness with vestibular dysfunctionN G Robertson, L Lu, S Heller, et al.
JCI Insight|July 1, 2020
BET bromodomain proteins regulate transcriptional reprogramming in genetic dilated cardiomyopathyAndrew Antolic, Hiroko Wakimoto, Zhe Jiao, et al.
Circulation Research|April 10, 2010
Short communication: the cardiac myosin binding protein C Arg502Trp mutation: a common cause of hypertrophic cardiomyopathyAdam J Saltzman, Debora Mancini-DiNardo, Chumei Li, et al.
JACC. Heart Failure|December 30, 2014
Diltiazem treatment for pre-clinical hypertrophic cardiomyopathy sarcomere mutation carriers: a pilot randomized trial to modify disease expressionCarolyn Y Ho, Neal K Lakdawala, Allison L Cirino, et al.
Iscience|January 6, 2022
Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndromeAnna B Meier, Sarala Raj Murthi, Hilansi Rawat, et al.
Circulation Research|May 21, 2021
CalTrack: High-Throughput Automated Calcium Transient Analysis in CardiomyocytesYiangos Psaras, Francesca Margara, Marcelo Cicconet, et al.
Circulation. Genomic and Precision Medicine|September 28, 2023
Genetic Contribution to End-Stage Cardiomyopathy Requiring Heart TransplantationYuri Kim, Oddný Brattberg Gunnarsdóttir, Anissa Viveiros, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 3, 2018
Genome sequencing as a first-line genetic test in familial dilated cardiomyopathyAndre E Minoche, Claire Horvat, Renee Johnson, et al.
Human Mutation|March 13, 2018
Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errorsKathryn B Manheimer, Nihir Patel, Felix Richter, et al.
Pageof 54