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Showing results (441-450 of 493) with videos related to

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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.
Molecular Vision|December 24, 2010
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3qNamerah Sabir, S Amer Riazuddin, Tariq Butt, et al.
Advances in Experimental Medicine and Biology|May 4, 2018
Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two PedigreesKari Branham, Aditya A Guru, Igor Kozak, et al.
Molecular Vision|September 1, 2015
Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani familiesShahid Y Khan, Shahbaz Ali, Muhammad Asif Naeem, et al.
Investigative Ophthalmology & Visual Science|December 23, 2011
GNAT1 associated with autosomal recessive congenital stationary night blindnessMuhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, et al.
Science Bulletin|July 27, 2025
Synergy-optimized spin support for reinforced intermediate supply in ultrafast water splittingChao Meng, Deyu Kong, Yue Zhou, et al.
Journal of the American Chemical Society|August 22, 2020
Conformational Flexibility of Hybrid [3]- and [4]-RotaxanesSelena J Lockyer, Selina Nawaz, Adam Brookfield, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 21, 2018
Room Temperature Uniaxial Magnetic Anisotropy Induced By Fe-Islands in the InSe Semiconductor Van Der Waals CrystalFabrizio Moro, Mahabub A Bhuiyan, Zakhar R Kudrynskyi, et al.
Molecular Vision|April 21, 2010
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1Afshan Yasmeen, S Amer Riazuddin, Haiba Kaul, et al.
Molecular Vision|December 3, 2015
Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindnessMuhammad Asif Naeem, Alexander D H Gottsch, Inayat Ullah, et al.
Pageof 50

Showing results (441-450 of 493) with videos related to

Sort By:
Pageof 50
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.
Molecular Vision|December 24, 2010
Mapping of a new locus associated with autosomal recessive congenital cataract to chromosome 3qNamerah Sabir, S Amer Riazuddin, Tariq Butt, et al.
Advances in Experimental Medicine and Biology|May 4, 2018
Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two PedigreesKari Branham, Aditya A Guru, Igor Kozak, et al.
Molecular Vision|September 1, 2015
Splice-site mutations identified in PDE6A responsible for retinitis pigmentosa in consanguineous Pakistani familiesShahid Y Khan, Shahbaz Ali, Muhammad Asif Naeem, et al.
Investigative Ophthalmology & Visual Science|December 23, 2011
GNAT1 associated with autosomal recessive congenital stationary night blindnessMuhammad Asif Naeem, Venkata R M Chavali, Shahbaz Ali, et al.
Science Bulletin|July 27, 2025
Synergy-optimized spin support for reinforced intermediate supply in ultrafast water splittingChao Meng, Deyu Kong, Yue Zhou, et al.
Journal of the American Chemical Society|August 22, 2020
Conformational Flexibility of Hybrid [3]- and [4]-RotaxanesSelena J Lockyer, Selina Nawaz, Adam Brookfield, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|July 21, 2018
Room Temperature Uniaxial Magnetic Anisotropy Induced By Fe-Islands in the InSe Semiconductor Van Der Waals CrystalFabrizio Moro, Mahabub A Bhuiyan, Zakhar R Kudrynskyi, et al.
Molecular Vision|April 21, 2010
Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1Afshan Yasmeen, S Amer Riazuddin, Haiba Kaul, et al.
Molecular Vision|December 3, 2015
Mutations in GRM6 identified in consanguineous Pakistani families with congenital stationary night blindnessMuhammad Asif Naeem, Alexander D H Gottsch, Inayat Ullah, et al.
Pageof 50