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J Beynon

Showing results (441-450 of 459) with videos related to

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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.
Journal of Proteome Research|June 16, 2020
PEPPI-MS: Polyacrylamide-Gel-Based Prefractionation for Analysis of Intact Proteoforms and Protein Complexes by Mass SpectrometryAyako Takemori, David S Butcher, Victoria M Harman, et al.
Hearing Research|January 24, 2013
Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusisA M M Oonk, J M Leijendeckers, E M Lammers, et al.
Plos One|August 16, 2014
Increased expression of chemerin in squamous esophageal cancer myofibroblasts and role in recruitment of mesenchymal stromal cellsJ Dinesh Kumar, Chris Holmberg, Sandhir Kandola, et al.
Molecular & Cellular Proteomics : MCP|September 21, 2011
Absolute quantification of the glycolytic pathway in yeast: deployment of a complete QconCAT approachKathleen M Carroll, Deborah M Simpson, Claire E Eyers, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2ADirk H Wijn, Mirthe L A Fehrmann, Sybren M M Robijn, et al.
Ear and Hearing|January 1, 2014
Similar phenotypes caused by mutations in OTOG and OTOGLAnne M M Oonk, Joop M Leijendeckers, Patrick L M Huygen, et al.
Clinical Genetics|April 21, 2018
Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophyM Wesdorp, V Schreur, A J Beynon, et al.
Scientific Reports|December 4, 2019
Landscape of heart proteome changes in a diet-induced obesity modelDanielle F Vileigas, Victoria M Harman, Paula P Freire, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2009
ATP8B1 is essential for maintaining normal hearingJanneke M Stapelbroek, Theo A Peters, Denis H A van Beurden, et al.
Pageof 46

Showing results (441-450 of 459) with videos related to

Sort By:
Pageof 46
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|March 12, 2021
A Novel COCH Mutation Affects the vWFA2 Domain and Leads to a Relatively Mild DFNA9 PhenotypeJeroen J Smits, Eline van Beelen, Nicole J D Weegerink, et al.
Journal of Proteome Research|June 16, 2020
PEPPI-MS: Polyacrylamide-Gel-Based Prefractionation for Analysis of Intact Proteoforms and Protein Complexes by Mass SpectrometryAyako Takemori, David S Butcher, Victoria M Harman, et al.
Hearing Research|January 24, 2013
Progressive hereditary hearing impairment caused by a MYO6 mutation resembles presbyacusisA M M Oonk, J M Leijendeckers, E M Lammers, et al.
Plos One|August 16, 2014
Increased expression of chemerin in squamous esophageal cancer myofibroblasts and role in recruitment of mesenchymal stromal cellsJ Dinesh Kumar, Chris Holmberg, Sandhir Kandola, et al.
Molecular & Cellular Proteomics : MCP|September 21, 2011
Absolute quantification of the glycolytic pathway in yeast: deployment of a complete QconCAT approachKathleen M Carroll, Deborah M Simpson, Claire E Eyers, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|February 23, 2026
From Sound to Stability: Lessons Learned From the CRUSH Study on Hearing Loss Progression and Vestibular Phenotype in Usher Syndrome Type 2ADirk H Wijn, Mirthe L A Fehrmann, Sybren M M Robijn, et al.
Ear and Hearing|January 1, 2014
Similar phenotypes caused by mutations in OTOG and OTOGLAnne M M Oonk, Joop M Leijendeckers, Patrick L M Huygen, et al.
Clinical Genetics|April 21, 2018
Further audiovestibular characterization of DFNB77, caused by deleterious variants in LOXHD1, and investigation into the involvement of Fuchs corneal dystrophyM Wesdorp, V Schreur, A J Beynon, et al.
Scientific Reports|December 4, 2019
Landscape of heart proteome changes in a diet-induced obesity modelDanielle F Vileigas, Victoria M Harman, Paula P Freire, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 30, 2009
ATP8B1 is essential for maintaining normal hearingJanneke M Stapelbroek, Theo A Peters, Denis H A van Beurden, et al.
Pageof 46