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J H Smith

Showing results (521-530 of 588) with videos related to

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Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
Nature Communications|February 18, 2011
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and humanNikoletta Charizopoulou, Andrea Lelli, Margit Schraders, et al.
American Journal of Human Genetics|February 24, 2009
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisIsabelle Schrauwen, Megan Ealy, Matthew J Huentelman, et al.
Iscience|March 4, 2025
Complement is primarily activated in the lung in a mouse model of severe COVID-19Peter J Szachowicz, Christine Wohlford-Lenane, Cobey J Donelson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 3, 2007
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell functionMartin Schwander, Anna Sczaniecka, Nicolas Grillet, et al.
Cell Metabolism|November 4, 2009
Dominant role of the p110beta isoform of PI3K over p110alpha in energy homeostasis regulation by POMC and AgRP neuronsHind Al-Qassab, Mark A Smith, Elaine E Irvine, et al.
Human Genetics|March 13, 2016
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing lossChristina M Sloan-Heggen, Amanda O Bierer, A Eliot Shearer, et al.
Human Mutation|October 9, 2007
An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing lossMichel Guipponi, Min-Yen Toh, Justin Tan, et al.
Frontiers in Immunology|June 2, 2025
Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathyAmanda K Slagle, Nicolo Ghiringhelli Borsa, Kai Wang, et al.
Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.
Pageof 59

Showing results (521-530 of 588) with videos related to

Sort By:
Pageof 59
Human Molecular Genetics|April 30, 2003
Prestin, a cochlear motor protein, is defective in non-syndromic hearing lossXue Zhong Liu, Xiao Mei Ouyang, Xia Juan Xia, et al.
Nature Communications|February 18, 2011
Gipc3 mutations associated with audiogenic seizures and sensorineural hearing loss in mouse and humanNikoletta Charizopoulou, Andrea Lelli, Margit Schraders, et al.
American Journal of Human Genetics|February 24, 2009
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisIsabelle Schrauwen, Megan Ealy, Matthew J Huentelman, et al.
Iscience|March 4, 2025
Complement is primarily activated in the lung in a mouse model of severe COVID-19Peter J Szachowicz, Christine Wohlford-Lenane, Cobey J Donelson, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 3, 2007
A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell functionMartin Schwander, Anna Sczaniecka, Nicolas Grillet, et al.
Cell Metabolism|November 4, 2009
Dominant role of the p110beta isoform of PI3K over p110alpha in energy homeostasis regulation by POMC and AgRP neuronsHind Al-Qassab, Mark A Smith, Elaine E Irvine, et al.
Human Genetics|March 13, 2016
Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing lossChristina M Sloan-Heggen, Amanda O Bierer, A Eliot Shearer, et al.
Human Mutation|October 9, 2007
An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing lossMichel Guipponi, Min-Yen Toh, Justin Tan, et al.
Frontiers in Immunology|June 2, 2025
Factor H-related 1 and heparan sulfate architecture contribute to complement dysregulation in C3 glomerulopathyAmanda K Slagle, Nicolo Ghiringhelli Borsa, Kai Wang, et al.
Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.
Pageof 59