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Morag A Lewis

Showing results (21-30 of 40) with videos related to

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Scientific Reports|March 19, 2016
Exploring regulatory networks of miR-96 in the developing inner earMorag A Lewis, Annalisa Buniello, Jennifer M Hilton, et al.
BMC Medical Genomics|September 6, 2018
Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genesMorag A Lewis, Lisa S Nolan, Barbara A Cadge, et al.
Plos One|January 23, 2023
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner earChiara Chiereghin, Michela Robusto, Morag A Lewis, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing lossMorag A Lewis, Jennifer Schulte, Lois Matthews, et al.
Hearing Research|November 15, 2020
Translational and interdisciplinary insights into presbyacusis: A multidimensional diseaseMark A Eckert, Kelly C Harris, Hainan Lang, et al.
Genome Medicine|October 21, 2024
Pathological mechanisms and candidate therapeutic approaches in the hearing loss of mice carrying human MIR96 mutationsMorag A Lewis, Maria Lachgar-Ruiz, Francesca Di Domenico, et al.
Plos Genetics|November 27, 2023
Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing lossMorag A Lewis, Jennifer Schulte, Lois Matthews, et al.
Disease Models & Mechanisms|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variantsMaría Lachgar-Ruiz, Matías Morín, Elisa Martelletti, et al.
Scientific Reports|July 8, 2016
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouseNeil J Ingham, Francesca Carlisle, Selina Pearson, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutationWenliang Zhu, Wan Du, Arun Prabhu Rameshbabu, et al.
Pageof 4

Showing results (21-30 of 40) with videos related to

Sort By:
Pageof 4
Scientific Reports|March 19, 2016
Exploring regulatory networks of miR-96 in the developing inner earMorag A Lewis, Annalisa Buniello, Jennifer M Hilton, et al.
BMC Medical Genomics|September 6, 2018
Whole exome sequencing in adult-onset hearing loss reveals a high load of predicted pathogenic variants in known deafness-associated genes and identifies new candidate genesMorag A Lewis, Lisa S Nolan, Barbara A Cadge, et al.
Plos One|January 23, 2023
In-depth genetic and molecular characterization of diaphanous related formin 2 (DIAPH2) and its role in the inner earChiara Chiereghin, Michela Robusto, Morag A Lewis, et al.
Medrxiv : the Preprint Server for Health Sciences|May 10, 2023
Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing lossMorag A Lewis, Jennifer Schulte, Lois Matthews, et al.
Hearing Research|November 15, 2020
Translational and interdisciplinary insights into presbyacusis: A multidimensional diseaseMark A Eckert, Kelly C Harris, Hainan Lang, et al.
Genome Medicine|October 21, 2024
Pathological mechanisms and candidate therapeutic approaches in the hearing loss of mice carrying human MIR96 mutationsMorag A Lewis, Maria Lachgar-Ruiz, Francesca Di Domenico, et al.
Plos Genetics|November 27, 2023
Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing lossMorag A Lewis, Jennifer Schulte, Lois Matthews, et al.
Disease Models & Mechanisms|May 11, 2023
Insights into the pathophysiology of DFNA44 hearing loss associated with CCDC50 frameshift variantsMaría Lachgar-Ruiz, Matías Morín, Elisa Martelletti, et al.
Scientific Reports|July 8, 2016
S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouseNeil J Ingham, Francesca Carlisle, Selina Pearson, et al.
Biorxiv : the Preprint Server for Biology|November 14, 2023
Targeted genome editing restores auditory function in adult mice with progressive hearing loss caused by a human microRNA mutationWenliang Zhu, Wan Du, Arun Prabhu Rameshbabu, et al.
Pageof 4