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Stephanie A Mauriac

Showing results (1-10 of 7) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 18, 2025
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic TargetsShelby E Redfield, Stephanie A Mauriac, Gwenaëlle S Géléoc, et al.
Medrxiv : the Preprint Server for Health Sciences|March 10, 2025
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic TargetsShelby E Redfield, Stephanie A Mauriac, Gwenaëlle S Géléoc, et al.
Cells|December 23, 2022
Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing LossStephanie A Mauriac, Thibault Peineau, Aamir Zuberi, et al.
Nature Communications|May 26, 2018
Author Correction: Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Nature Communications|April 8, 2017
Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 26, 2018
Gαi Proteins are Indispensable for HearingSandra Beer-Hammer, Sze Chim Lee, Stephanie A Mauriac, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 25, 2025
AAV-mediated exon skipping therapy for Usher syndrome, type 2AStephanie A Mauriac, Jiyoon Lee, Jingyuan Zhang, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 18, 2025
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic TargetsShelby E Redfield, Stephanie A Mauriac, Gwenaëlle S Géléoc, et al.
Medrxiv : the Preprint Server for Health Sciences|March 10, 2025
A Genomic Analysis of Usher Syndrome: Population-Scale Prevalence and Therapeutic TargetsShelby E Redfield, Stephanie A Mauriac, Gwenaëlle S Géléoc, et al.
Cells|December 23, 2022
Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing LossStephanie A Mauriac, Thibault Peineau, Aamir Zuberi, et al.
Nature Communications|May 26, 2018
Author Correction: Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Nature Communications|April 8, 2017
Defective Gpsm2/Gα<sub>i3</sub> signalling disrupts stereocilia development and growth cone actin dynamics in Chudley-McCullough syndromeStephanie A Mauriac, Yeri E Hien, Jonathan E Bird, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|June 26, 2018
Gαi Proteins are Indispensable for HearingSandra Beer-Hammer, Sze Chim Lee, Stephanie A Mauriac, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|September 25, 2025
AAV-mediated exon skipping therapy for Usher syndrome, type 2AStephanie A Mauriac, Jiyoon Lee, Jingyuan Zhang, et al.
Pageof 1