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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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Hagith Yonath

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NEJM Evidence|March 24, 2026

West Nile Virus-Neutralizing Plasma for West Nile Virus DiseaseGili Regev-Yochay, Noam Barda, Yonatan Shusterman, et al.

Journal of the American Society of Nephrology : JASN|April 7, 2017

A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations <i>via</i> Dysregulation of Retinoic Acid SignalingAsaf Vivante, Nina Mann, Hagith Yonath, et al.

Scientific Reports|September 28, 2021

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomaliesBen Pode-Shakked, Ortal Barel, Amihood Singer, et al.

Journal of the American College of Cardiology|December 3, 2016

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic CardiomyopathiesMartín F Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, et al.

American Journal of Human Genetics|September 26, 2023

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defectsFlorence Petit, Mauro Longoni, Julie Wells, et al.

American Journal of Human Genetics|April 18, 2023

SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disabilityElke Bogaert, Aurore Garde, Thierry Gautier, et al.

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Search research articles

Showing results (31-40 of 36) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 36 results.

NEJM Evidence|March 24, 2026

West Nile Virus-Neutralizing Plasma for West Nile Virus DiseaseGili Regev-Yochay, Noam Barda, Yonatan Shusterman, et al.

Journal of the American Society of Nephrology : JASN|April 7, 2017

A Dominant Mutation in Nuclear Receptor Interacting Protein 1 Causes Urinary Tract Malformations <i>via</i> Dysregulation of Retinoic Acid SignalingAsaf Vivante, Nina Mann, Hagith Yonath, et al.

Scientific Reports|September 28, 2021

A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomaliesBen Pode-Shakked, Ortal Barel, Amihood Singer, et al.

Journal of the American College of Cardiology|December 3, 2016

Truncating FLNC Mutations Are Associated With High-Risk Dilated and Arrhythmogenic CardiomyopathiesMartín F Ortiz-Genga, Sofía Cuenca, Matteo Dal Ferro, et al.

American Journal of Human Genetics|September 26, 2023

PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defectsFlorence Petit, Mauro Longoni, Julie Wells, et al.

American Journal of Human Genetics|April 18, 2023

SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disabilityElke Bogaert, Aurore Garde, Thierry Gautier, et al.

Pageof 4