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Barbara Canlon

Showing results (91-100 of 98) with videos related to

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NPJ Genomic Medicine|November 30, 2022
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitusAlvaro Gallego-Martinez, Alba Escalera-Balsera, Natalia Trpchevska, et al.
Ebiomedicine|April 4, 2021
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype studySana Amanat, Alvaro Gallego-Martinez, Joseph Sollini, et al.
Journal of the Association for Research in Otolaryngology : JARO|December 11, 2023
Screening for Circulating Inflammatory Proteins Does Not Reveal Plasma Biomarkers of Constant TinnitusChristopher R Cederroth, Mun-Gwan Hong, Maxim B Freydin, et al.
Science Translational Medicine|June 28, 2023
Delivery of gene therapy through a cerebrospinal fluid conduit to rescue hearing in adult miceBarbara K Mathiesen, Leo M Miyakoshi, Christopher R Cederroth, et al.
Cell Metabolism|August 8, 2019
Medicine in the Fourth DimensionChristopher R Cederroth, Urs Albrecht, Joseph Bass, et al.
Cell Reports|September 30, 2021
A cell-type-specific atlas of the inner ear transcriptional response to acoustic traumaBeatrice Milon, Eldad D Shulman, Kathy S So, et al.
Frontiers in Aging Neuroscience|January 30, 2018
Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) PerspectiveWinfried Schlee, Deborah A Hall, Barbara Canlon, et al.
American Journal of Human Genetics|May 17, 2022
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing lossNatalia Trpchevska, Maxim B Freidin, Linda Broer, et al.
Pageof 10

Showing results (91-100 of 98) with videos related to

Sort By:
Pageof 10
You have reached the last page of results.This site can display upto 98 results.
NPJ Genomic Medicine|November 30, 2022
Using coding and non-coding rare variants to target candidate genes in patients with severe tinnitusAlvaro Gallego-Martinez, Alba Escalera-Balsera, Natalia Trpchevska, et al.
Ebiomedicine|April 4, 2021
Burden of rare variants in synaptic genes in patients with severe tinnitus: An exome based extreme phenotype studySana Amanat, Alvaro Gallego-Martinez, Joseph Sollini, et al.
Journal of the Association for Research in Otolaryngology : JARO|December 11, 2023
Screening for Circulating Inflammatory Proteins Does Not Reveal Plasma Biomarkers of Constant TinnitusChristopher R Cederroth, Mun-Gwan Hong, Maxim B Freydin, et al.
Science Translational Medicine|June 28, 2023
Delivery of gene therapy through a cerebrospinal fluid conduit to rescue hearing in adult miceBarbara K Mathiesen, Leo M Miyakoshi, Christopher R Cederroth, et al.
Cell Metabolism|August 8, 2019
Medicine in the Fourth DimensionChristopher R Cederroth, Urs Albrecht, Joseph Bass, et al.
Cell Reports|September 30, 2021
A cell-type-specific atlas of the inner ear transcriptional response to acoustic traumaBeatrice Milon, Eldad D Shulman, Kathy S So, et al.
Frontiers in Aging Neuroscience|January 30, 2018
Innovations in Doctoral Training and Research on Tinnitus: The European School on Interdisciplinary Tinnitus Research (ESIT) PerspectiveWinfried Schlee, Deborah A Hall, Barbara Canlon, et al.
American Journal of Human Genetics|May 17, 2022
Genome-wide association meta-analysis identifies 48 risk variants and highlights the role of the stria vascularis in hearing lossNatalia Trpchevska, Maxim B Freidin, Linda Broer, et al.
Pageof 10