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Zubair M Ahmed

Showing results (1-10 of 145) with videos related to

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Physiological Genomics|September 12, 2013
Usher proteins in inner ear structure and functionZubair M Ahmed, Gregory I Frolenkov, Saima Riazuddin
Retina (Philadelphia, Pa.)|December 24, 2005
Usher syndrome type 1: genotype-phenotype relationshipsThomas B Friedman, Julie M Schultz, Zubair M Ahmed
Biomed Research International|May 17, 2021
Identification of Hearing Loss-Associated Variants of <i>PTPRQ</i>, <i>MYO15A</i>, and <i>SERPINB6</i> in Pakistani FamiliesUmair Mahmood, Shazia A Bukhari, Muhammad Ali, et al.
Genes|March 25, 2022
Identification of Frameshift Variants in <i>POLH</i> Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani FamiliesGhazala Y Zamani, Ranjha Khan, Noreen Karim, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 31, 2012
Gene therapy for Leber congenital amaurosis: advances and future directionsRobert B Hufnagel, Zubair M Ahmed, Zélia M Corrêa, et al.
Genes|December 15, 2019
Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani FamiliesMuhammad Noman, Rafaqat Ishaq, Shazia A Bukhari, et al.
Genes|November 2, 2018
Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle GlaucomaOsamah Saeedi, Sairah Yousaf, Joby Tsai, et al.
Human Genetics|July 27, 2007
In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndromeAnnie Rebibo-Sabbah, Igor Nudelman, Zubair M Ahmed, et al.
Genes|December 24, 2021
Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani KindredIrum Badshah Saleem, Muhammad Shareef Masoud, Muhammad Qasim, et al.
Ophthalmology|February 18, 2014
Planned preterm delivery and treatment of retinal neovascularization in Norrie diseaseRobert A Sisk, Robert B Hufnagel, Sindura Bandi, et al.
Pageof 15

Showing results (1-10 of 145) with videos related to

Sort By:
Pageof 15
Physiological Genomics|September 12, 2013
Usher proteins in inner ear structure and functionZubair M Ahmed, Gregory I Frolenkov, Saima Riazuddin
Retina (Philadelphia, Pa.)|December 24, 2005
Usher syndrome type 1: genotype-phenotype relationshipsThomas B Friedman, Julie M Schultz, Zubair M Ahmed
Biomed Research International|May 17, 2021
Identification of Hearing Loss-Associated Variants of <i>PTPRQ</i>, <i>MYO15A</i>, and <i>SERPINB6</i> in Pakistani FamiliesUmair Mahmood, Shazia A Bukhari, Muhammad Ali, et al.
Genes|March 25, 2022
Identification of Frameshift Variants in <i>POLH</i> Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani FamiliesGhazala Y Zamani, Ranjha Khan, Noreen Karim, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|May 31, 2012
Gene therapy for Leber congenital amaurosis: advances and future directionsRobert B Hufnagel, Zubair M Ahmed, Zélia M Corrêa, et al.
Genes|December 15, 2019
Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani FamiliesMuhammad Noman, Rafaqat Ishaq, Shazia A Bukhari, et al.
Genes|November 2, 2018
Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle GlaucomaOsamah Saeedi, Sairah Yousaf, Joby Tsai, et al.
Human Genetics|July 27, 2007
In vitro and ex vivo suppression by aminoglycosides of PCDH15 nonsense mutations underlying type 1 Usher syndromeAnnie Rebibo-Sabbah, Igor Nudelman, Zubair M Ahmed, et al.
Genes|December 24, 2021
Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani KindredIrum Badshah Saleem, Muhammad Shareef Masoud, Muhammad Qasim, et al.
Ophthalmology|February 18, 2014
Planned preterm delivery and treatment of retinal neovascularization in Norrie diseaseRobert A Sisk, Robert B Hufnagel, Sindura Bandi, et al.
Pageof 15