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JACC. Basic to Translational Science
|
July 30, 2025
Single Ascending-Dose Study of Selective ErbB4 Agonist JK07 in Heart Failure With Reduced Ejection Fraction
W H Wilson Tang, Johannes Steiner, Mahwash Kassi, et al.
Nature Immunology
|
August 31, 2004
The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses
David L Boone, Emre E Turer, Eric G Lee, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)
|
September 27, 2021
Cardiopulmonary Exercise Testing With Echocardiography to Assess Recovery in Patients With Ventricular Assist Devices
Jeffrey W Christle, Kegan J Moneghetti, Sebastien Duclos, et al.
Progress in Cardiovascular Diseases
|
January 7, 2015
Personalized preventive medicine: genetics and the response to regular exercise in preventive interventions
Claude Bouchard, Ligia M Antunes-Correa, Euan A Ashley, et al.
Open Heart
|
June 21, 2019
Improving risk stratification in heart failure with preserved ejection fraction by combining two validated risk scores
Kalyani Anil Boralkar, Yukari Kobayashi, Kegan J Moneghetti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 8, 2022
A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network
Rebecca C Spillmann, Queenie K-G Tan, Chloe Reuter, et al.
Journal of Genetic Counseling
|
February 2, 2019
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students
Megan E Grove, Shana White, Dianna G Fisk, et al.
Circulation. Genomic and Precision Medicine
|
March 20, 2024
Regional Variation in Cardiovascular Genes Enables a Tractable Genome Editing Strategy
Vikki A Krysov, Rachel H Wilson, Nicholas S Ten, et al.
Future Cardiology
|
January 31, 2023
Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty <i>LMNA</i> gene
Calum A MacRae, Matthew Rg Taylor, Luisa Mestroni, et al.
Cold Spring Harbor Molecular Case Studies
|
January 5, 2017
Exome sequencing identifies de novo pathogenic variants in <i>FBN1</i> and <i>TRPS1</i> in a patient with a complex connective tissue phenotype
Diane B Zastrow, Patricia A Zornio, Annika Dries, et al.
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of 19
Search research articles
Search
Showing results (81-90 of 190) with videos related to
Sort By:
Page
of 19
JACC. Basic to Translational Science
|
July 30, 2025
Single Ascending-Dose Study of Selective ErbB4 Agonist JK07 in Heart Failure With Reduced Ejection Fraction
W H Wilson Tang, Johannes Steiner, Mahwash Kassi, et al.
Nature Immunology
|
August 31, 2004
The ubiquitin-modifying enzyme A20 is required for termination of Toll-like receptor responses
David L Boone, Emre E Turer, Eric G Lee, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)
|
September 27, 2021
Cardiopulmonary Exercise Testing With Echocardiography to Assess Recovery in Patients With Ventricular Assist Devices
Jeffrey W Christle, Kegan J Moneghetti, Sebastien Duclos, et al.
Progress in Cardiovascular Diseases
|
January 7, 2015
Personalized preventive medicine: genetics and the response to regular exercise in preventive interventions
Claude Bouchard, Ligia M Antunes-Correa, Euan A Ashley, et al.
Open Heart
|
June 21, 2019
Improving risk stratification in heart failure with preserved ejection fraction by combining two validated risk scores
Kalyani Anil Boralkar, Yukari Kobayashi, Kegan J Moneghetti, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 8, 2022
A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network
Rebecca C Spillmann, Queenie K-G Tan, Chloe Reuter, et al.
Journal of Genetic Counseling
|
February 2, 2019
Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students
Megan E Grove, Shana White, Dianna G Fisk, et al.
Circulation. Genomic and Precision Medicine
|
March 20, 2024
Regional Variation in Cardiovascular Genes Enables a Tractable Genome Editing Strategy
Vikki A Krysov, Rachel H Wilson, Nicholas S Ten, et al.
Future Cardiology
|
January 31, 2023
Plain Language Summary of Publication of the safety and efficacy of ARRY-371797 in people with dilated cardiomyopathy and a faulty <i>LMNA</i> gene
Calum A MacRae, Matthew Rg Taylor, Luisa Mestroni, et al.
Cold Spring Harbor Molecular Case Studies
|
January 5, 2017
Exome sequencing identifies de novo pathogenic variants in <i>FBN1</i> and <i>TRPS1</i> in a patient with a complex connective tissue phenotype
Diane B Zastrow, Patricia A Zornio, Annika Dries, et al.
Page
of 19