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Saima Riazuddin

Showing results (61-70 of 135) with videos related to

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Scientific Reports|March 8, 2017
Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani populationMohsin Shahzad, Sairah Yousaf, Yar M Waryah, et al.
Scientific Data|October 14, 2020
Whole genome sequencing data of multiple individuals of Pakistani descentShahid Y Khan, Muhammad Ali, Mei-Chong W Lee, et al.
Human Molecular Genetics|November 10, 2022
Syntaxin 4 is essential for hearing in human and zebrafishIsabelle Schrauwen, Amama Ghaffar, Thashi Bharadwaj, et al.
Journal of Medical Genetics|February 7, 2006
Mutations of human TMHS cause recessively inherited non-syndromic hearing lossM I Shabbir, Z M Ahmed, S Y Khan, et al.
Biorxiv : the Preprint Server for Biology|July 18, 2023
Calcium and Integrin-binding protein 2 (CIB2) controls force sensitivity of the mechanotransducer channels in cochlear outer hair cellsIsabel Aristizábal-Ramírez, Abigail K Dragich, Arnaud P J Giese, et al.
Elife|November 9, 2021
Proposed therapy, developed in a <i>Pcdh15</i>-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.
Human Mutation|January 18, 2007
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locusShahid Y Khan, Zubair M Ahmed, Muhammad I Shabbir, et al.
Molecular Vision|March 2, 2019
Identities and frequencies of variants in <i>CYP1B1</i> causing primary congenital glaucoma in PakistanMuhammad Rashid, Sairah Yousaf, Shakeel A Sheikh, et al.
American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.
American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.
Pageof 14

Showing results (61-70 of 135) with videos related to

Sort By:
Pageof 14
Scientific Reports|March 8, 2017
Molecular outcomes, clinical consequences, and genetic diagnosis of Oculocutaneous Albinism in Pakistani populationMohsin Shahzad, Sairah Yousaf, Yar M Waryah, et al.
Scientific Data|October 14, 2020
Whole genome sequencing data of multiple individuals of Pakistani descentShahid Y Khan, Muhammad Ali, Mei-Chong W Lee, et al.
Human Molecular Genetics|November 10, 2022
Syntaxin 4 is essential for hearing in human and zebrafishIsabelle Schrauwen, Amama Ghaffar, Thashi Bharadwaj, et al.
Journal of Medical Genetics|February 7, 2006
Mutations of human TMHS cause recessively inherited non-syndromic hearing lossM I Shabbir, Z M Ahmed, S Y Khan, et al.
Biorxiv : the Preprint Server for Biology|July 18, 2023
Calcium and Integrin-binding protein 2 (CIB2) controls force sensitivity of the mechanotransducer channels in cochlear outer hair cellsIsabel Aristizábal-Ramírez, Abigail K Dragich, Arnaud P J Giese, et al.
Elife|November 9, 2021
Proposed therapy, developed in a <i>Pcdh15</i>-deficient mouse, for progressive loss of vision in human Usher syndromeSaumil Sethna, Wadih M Zein, Sehar Riaz, et al.
Human Mutation|January 18, 2007
Mutations of the RDX gene cause nonsyndromic hearing loss at the DFNB24 locusShahid Y Khan, Zubair M Ahmed, Muhammad I Shabbir, et al.
Molecular Vision|March 2, 2019
Identities and frequencies of variants in <i>CYP1B1</i> causing primary congenital glaucoma in PakistanMuhammad Rashid, Sairah Yousaf, Shakeel A Sheikh, et al.
American Journal of Human Genetics|December 23, 2006
Tricellulin is a tight-junction protein necessary for hearingSaima Riazuddin, Zubair M Ahmed, Alan S Fanning, et al.
American Journal of Human Genetics|August 4, 2009
Molecular basis of DFNB73: mutations of BSND can cause nonsyndromic deafness or Bartter syndromeSaima Riazuddin, Saima Anwar, Martin Fischer, et al.
Pageof 14