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Michael R Bowl

Showing results (11-20 of 51) with videos related to

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The Journal of Physiology|July 26, 2020
Pathophysiological changes in inner hair cell ribbon synapses in the ageing mammalian cochleaJing-Yi Jeng, Federico Ceriani, Jennifer Olt, et al.
Disease Models & Mechanisms|November 7, 2015
The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cellsAndrew Parker, Sally H Cross, Ian J Jackson, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2024
CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase patternArnaud P J Giese, Andrew Parker, Sakina Rehman, et al.
Disease Models & Mechanisms|March 14, 2025
CIB2 function is distinct from that of whirlin in the organization of sterocilia architectureArnaud P J Giese, Andrew Parker, Sakina Rehman, et al.
Neuron|April 2, 2026
TMEM145 is a principal component of outer hair cell stereociliaDennis Derstroff, Marisa Flook, Antonia Löhnes, et al.
Plos Genetics|January 31, 2022
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearingSherylanne Newton, Fanbo Kong, Adam J Carlton, et al.
The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.
Clinical Genetics|June 10, 2024
Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literatureAboulfazl Rad, Oliver Bartsch, Somayeh Bakhtiari, et al.
Genome Medicine|February 16, 2016
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repairJoffrey Mianné, Lauren Chessum, Saumya Kumar, et al.
Molecular and Cellular Biology|January 24, 2008
Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult micePengfei Wang, Michael R Bowl, Stephanie Bender, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
The Journal of Physiology|July 26, 2020
Pathophysiological changes in inner hair cell ribbon synapses in the ageing mammalian cochleaJing-Yi Jeng, Federico Ceriani, Jennifer Olt, et al.
Disease Models & Mechanisms|November 7, 2015
The goya mouse mutant reveals distinct newly identified roles for MAP3K1 in the development and survival of cochlear sensory hair cellsAndrew Parker, Sally H Cross, Ian J Jackson, et al.
Biorxiv : the Preprint Server for Biology|August 12, 2024
CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase patternArnaud P J Giese, Andrew Parker, Sakina Rehman, et al.
Disease Models & Mechanisms|March 14, 2025
CIB2 function is distinct from that of whirlin in the organization of sterocilia architectureArnaud P J Giese, Andrew Parker, Sakina Rehman, et al.
Neuron|April 2, 2026
TMEM145 is a principal component of outer hair cell stereociliaDennis Derstroff, Marisa Flook, Antonia Löhnes, et al.
Plos Genetics|January 31, 2022
Neuroplastin genetically interacts with Cadherin 23 and the encoded isoform Np55 is sufficient for cochlear hair cell function and hearingSherylanne Newton, Fanbo Kong, Adam J Carlton, et al.
The Journal of Clinical Investigation|September 17, 2005
An interstitial deletion-insertion involving chromosomes 2p25.3 and Xq27.1, near SOX3, causes X-linked recessive hypoparathyroidismMichael R Bowl, M Andrew Nesbit, Brian Harding, et al.
Clinical Genetics|June 10, 2024
Expanding the spectrum of phenotypes for MPDZ: Report of four unrelated families and review of the literatureAboulfazl Rad, Oliver Bartsch, Somayeh Bakhtiari, et al.
Genome Medicine|February 16, 2016
Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repairJoffrey Mianné, Lauren Chessum, Saumya Kumar, et al.
Molecular and Cellular Biology|January 24, 2008
Parafibromin, a component of the human PAF complex, regulates growth factors and is required for embryonic development and survival in adult micePengfei Wang, Michael R Bowl, Stephanie Bender, et al.
Pageof 6