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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Andrea Nagy

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Genes & Development|October 16, 2020

PRIM1 deficiency causes a distinctive primordial dwarfism syndromeDavid A Parry, Lukas Tamayo-Orrego, Paula Carroll, et al.

BMC Biology|April 1, 2022

A versatile transposon-based technology to generate loss- and gain-of-function phenotypes in the mouse liverAnna Georgina Kopasz, Dávid Zsolt Pusztai, Réka Karkas, et al.

Molecular Therapy. Methods & Clinical Development|April 7, 2023

Prolonged activity of the transposase helper may raise safety concerns during DNA transposon-based gene therapyGergely Imre, Bertalan Takács, Erik Czipa, et al.

JACC. Clinical Electrophysiology|November 20, 2025

Characterizing Sustained Arrhythmias in Patients With Arrhythmic Mitral Valve Prolapse: Insights From the SAVE-MVP collaborationAvi Sabbag, Nina Ajmone-Marsan, Fatima Ezzeddine, et al.

Pageof 7

Search research articles

Showing results (61-70 of 64) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 64 results.

Genes & Development|October 16, 2020

PRIM1 deficiency causes a distinctive primordial dwarfism syndromeDavid A Parry, Lukas Tamayo-Orrego, Paula Carroll, et al.

BMC Biology|April 1, 2022

A versatile transposon-based technology to generate loss- and gain-of-function phenotypes in the mouse liverAnna Georgina Kopasz, Dávid Zsolt Pusztai, Réka Karkas, et al.

Molecular Therapy. Methods & Clinical Development|April 7, 2023

Prolonged activity of the transposase helper may raise safety concerns during DNA transposon-based gene therapyGergely Imre, Bertalan Takács, Erik Czipa, et al.

JACC. Clinical Electrophysiology|November 20, 2025

Characterizing Sustained Arrhythmias in Patients With Arrhythmic Mitral Valve Prolapse: Insights From the SAVE-MVP collaborationAvi Sabbag, Nina Ajmone-Marsan, Fatima Ezzeddine, et al.

Pageof 7