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Nature Communications
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February 22, 2023
Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub
Marc P Forrest, Marc Dos Santos, Nicolas H Piguel, et al.
Cell
|
July 22, 2025
In vivo prime editing rescues alternating hemiplegia of childhood in mice
Alexander A Sousa, Markus Terrey, Holt A Sakai, et al.
JAMA Cardiology
|
August 11, 2021
Genomic Autopsy of Sudden Deaths in Young Individuals
Gregory Webster, Megan J Puckelwartz, Lorenzo L Pesce, et al.
The Journal of Clinical Investigation
|
May 20, 2024
Susceptibility to innate immune activation in genetically mediated myocarditis
Daniel F Selgrade, Dominic E Fullenkamp, Ivana A Chychula, et al.
Molecular Oncology
|
August 7, 2013
SPARCL1 suppresses metastasis in prostate cancer
Yuzhu Xiang, Qingchao Qiu, Ming Jiang, et al.
Circulation. Arrhythmia and Electrophysiology
|
April 15, 2017
Azithromycin Causes a Novel Proarrhythmic Syndrome
Zhenjiang Yang, Joseph K Prinsen, Kevin R Bersell, et al.
The Journal of Biological Chemistry
|
October 4, 2012
Identification and characterization of a compound that protects cardiac tissue from human Ether-à-go-go-related gene (hERG)-related drug-induced arrhythmias
Franck Potet, Amanda N Lorinc, Sebastien Chaigne, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
High Throughput Screening Identifies a Small Molecule Trafficking Corrector for Long-QT Syndrome Associated KCNQ1 Variants
Katherine R Clowes Moster, Carlos G Vanoye, Ana C Chang-Gonzalez, et al.
Psychiatric Research and Clinical Practice
|
October 18, 2022
Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor-Treated Women
Gabrielle A Mesches, Jody D Ciolino, Catherine S Stika, et al.
JCI Insight
|
January 8, 2026
High throughput screening identifies a trafficking corrector for long-QT syndrome associated KCNQ1 variants
Katherine R Clowes Moster, Carlos G Vanoye, Ana C Chang-Gonzalez, et al.
Page
of 27
Search research articles
Search
Showing results (231-240 of 270) with videos related to
Sort By:
Page
of 27
Nature Communications
|
February 22, 2023
Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub
Marc P Forrest, Marc Dos Santos, Nicolas H Piguel, et al.
Cell
|
July 22, 2025
In vivo prime editing rescues alternating hemiplegia of childhood in mice
Alexander A Sousa, Markus Terrey, Holt A Sakai, et al.
JAMA Cardiology
|
August 11, 2021
Genomic Autopsy of Sudden Deaths in Young Individuals
Gregory Webster, Megan J Puckelwartz, Lorenzo L Pesce, et al.
The Journal of Clinical Investigation
|
May 20, 2024
Susceptibility to innate immune activation in genetically mediated myocarditis
Daniel F Selgrade, Dominic E Fullenkamp, Ivana A Chychula, et al.
Molecular Oncology
|
August 7, 2013
SPARCL1 suppresses metastasis in prostate cancer
Yuzhu Xiang, Qingchao Qiu, Ming Jiang, et al.
Circulation. Arrhythmia and Electrophysiology
|
April 15, 2017
Azithromycin Causes a Novel Proarrhythmic Syndrome
Zhenjiang Yang, Joseph K Prinsen, Kevin R Bersell, et al.
The Journal of Biological Chemistry
|
October 4, 2012
Identification and characterization of a compound that protects cardiac tissue from human Ether-à-go-go-related gene (hERG)-related drug-induced arrhythmias
Franck Potet, Amanda N Lorinc, Sebastien Chaigne, et al.
Biorxiv : the Preprint Server for Biology
|
November 24, 2025
High Throughput Screening Identifies a Small Molecule Trafficking Corrector for Long-QT Syndrome Associated KCNQ1 Variants
Katherine R Clowes Moster, Carlos G Vanoye, Ana C Chang-Gonzalez, et al.
Psychiatric Research and Clinical Practice
|
October 18, 2022
Trajectories of Depressive and Anxiety Symptoms Across Pregnancy and Postpartum in Selective Serotonin Reuptake Inhibitor-Treated Women
Gabrielle A Mesches, Jody D Ciolino, Catherine S Stika, et al.
JCI Insight
|
January 8, 2026
High throughput screening identifies a trafficking corrector for long-QT syndrome associated KCNQ1 variants
Katherine R Clowes Moster, Carlos G Vanoye, Ana C Chang-Gonzalez, et al.
Page
of 27