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Jessica Varilh

Showing results (11-20 of 15) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Small-scale high-throughput sequencing-based identification of new therapeutic tools in cystic fibrosisJennifer Bonini, Jessica Varilh, Caroline Raynal, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 18, 2022
The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthroughIwona M Pranke, Jessica Varilh, Aurélie Hatton, et al.
Clinical Epigenetics|March 15, 2017
DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosisMilena Magalhães, Isabelle Rivals, Mireille Claustres, et al.
Brain : a Journal of Neurology|July 27, 2022
RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiologyMehdi Benkirane, Dylan Da Cunha, Cecilia Marelli, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 8, 2023
Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis childrenAnnalisa Orenti, Iwona Pranke, Caroline Faucon, et al.
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Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 9, 2015
Small-scale high-throughput sequencing-based identification of new therapeutic tools in cystic fibrosisJennifer Bonini, Jessica Varilh, Caroline Raynal, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|November 18, 2022
The U UGA C sequence provides a favorable context to ELX-02 induced CFTR readthroughIwona M Pranke, Jessica Varilh, Aurélie Hatton, et al.
Clinical Epigenetics|March 15, 2017
DNA methylation at modifier genes of lung disease severity is altered in cystic fibrosisMilena Magalhães, Isabelle Rivals, Mireille Claustres, et al.
Brain : a Journal of Neurology|July 27, 2022
RFC1 nonsense and frameshift variants cause CANVAS: clues for an unsolved pathophysiologyMehdi Benkirane, Dylan Da Cunha, Cecilia Marelli, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|July 8, 2023
Nonsense mutations accelerate lung disease and decrease survival of cystic fibrosis childrenAnnalisa Orenti, Iwona Pranke, Caroline Faucon, et al.
Pageof 2