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Saima Riazuddin

Showing results (91-100 of 135) with videos related to

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Cell|June 1, 2010
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearingShin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, et al.
Communications Biology|July 8, 2024
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephalyAmama Ghaffar, Tehmeena Akhter, Petter Strømme, et al.
Pigment Cell & Melanoma Research|July 23, 2015
Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani populationMohsin Shahzad, Julia Sires Campos, Nabeela Tariq, et al.
International Journal of Molecular Sciences|February 26, 2025
A Novel <i>SLPI</i> Splice Variant Confers Susceptibility to Otitis Media in HumansChristina L Elling, Allen F Ryan, Talitha Karisse L Yarza, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channelsArnaud P J Giese, Wei-Hsiang Weng, Katie S Kindt, et al.
Elife|January 8, 2025
Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channelsArnaud P J Giese, Wei-Hsiang Weng, Katie S Kindt, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cellsCelia Zazo Seco, Arnaud P Giese, Sobia Shafique, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
American Journal of Human Genetics|July 7, 2009
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39Julie M Schultz, Shaheen N Khan, Zubair M Ahmed, et al.
Pageof 14

Showing results (91-100 of 135) with videos related to

Sort By:
Pageof 14
Cell|June 1, 2010
Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearingShin-ichiro Kitajiri, Takeshi Sakamoto, Inna A Belyantseva, et al.
Communications Biology|July 8, 2024
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephalyAmama Ghaffar, Tehmeena Akhter, Petter Strømme, et al.
Pigment Cell & Melanoma Research|July 23, 2015
Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani populationMohsin Shahzad, Julia Sires Campos, Nabeela Tariq, et al.
International Journal of Molecular Sciences|February 26, 2025
A Novel <i>SLPI</i> Splice Variant Confers Susceptibility to Otitis Media in HumansChristina L Elling, Allen F Ryan, Talitha Karisse L Yarza, et al.
Biorxiv : the Preprint Server for Biology|July 3, 2023
Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channelsArnaud P J Giese, Wei-Hsiang Weng, Katie S Kindt, et al.
Elife|January 8, 2025
Complexes of vertebrate TMC1/2 and CIB2/3 proteins form hair-cell mechanotransduction cation channelsArnaud P J Giese, Wei-Hsiang Weng, Katie S Kindt, et al.
European Journal of Human Genetics : EJHG|July 16, 2015
Novel and recurrent CIB2 variants, associated with nonsyndromic deafness, do not affect calcium buffering and localization in hair cellsCelia Zazo Seco, Arnaud P Giese, Sobia Shafique, et al.
Human Genetics|June 12, 2015
Mutation of ATF6 causes autosomal recessive achromatopsiaMuhammad Ansar, Regie Lyn P Santos-Cortez, Muhammad Arif Nadeem Saqib, et al.
American Journal of Human Genetics|February 9, 2010
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouseHana Odeh, Kristina L Hunker, Inna A Belyantseva, et al.
American Journal of Human Genetics|July 7, 2009
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39Julie M Schultz, Shaheen N Khan, Zubair M Ahmed, et al.
Pageof 14