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Thomas L Edwards

Showing results (31-40 of 62) with videos related to

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Human Molecular Genetics|December 13, 2005
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partnersChristopher M Sanderson, James W Connell, Thomas L Edwards, et al.
Clinical & Experimental Optometry|March 10, 2021
An optometrist's guide to the top candidate inherited retinal diseases for gene therapyFleur O'Hare, Thomas L Edwards, Monica L Hu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
The safety and efficacy of gene therapy treatment for monogenic retinal and optic nerve diseases: A systematic reviewAlexis Ceecee Britten-Jones, Rui Jin, Sena A Gocuk, et al.
Survey of Ophthalmology|October 1, 2023
Adaptive optics imaging in inherited retinal diseases: A scoping review of the clinical literatureAlexis Ceecee Britten-Jones, Lawrence Thai, Jeremy P M Flanagan, et al.
Clinical & Experimental Ophthalmology|April 10, 2025
Retinal Gene Therapy: Perceptions of Ophthalmologists in Australia and New ZealandJohn O T Britton, Heather G Mack, Andrea L Vincent, et al.
American Journal of Ophthalmology|November 17, 2021
First-in-Human Robot-Assisted Subretinal Drug Delivery Under Local AnesthesiaJasmina Cehajic-Kapetanovic, Kanmin Xue, Thomas L Edwards, et al.
Clinical & Experimental Ophthalmology|May 12, 2012
Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutationsThomas L Edwards, Benjamin O Burt, Graeme C M Black, et al.
Human Molecular Genetics|July 22, 2009
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signallingHilda T H Tsang, Thomas L Edwards, Xinnan Wang, et al.
Genome Research|September 16, 2024
Measuring X-Chromosome inactivation skew for X-linked diseases with adaptive nanopore sequencingSena A Gocuk, James Lancaster, Shian Su, et al.
Scientific Reports|March 13, 2025
Retrospective audit reviewing accuracy of clinical diagnosis of geographic atrophy in a single centre private tertiary retinal practice in AustraliaDemi Markakis, Alexis Ceecee Britten-Jones, Robyn H Guymer, et al.
Pageof 7

Showing results (31-40 of 62) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|December 13, 2005
Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partnersChristopher M Sanderson, James W Connell, Thomas L Edwards, et al.
Clinical & Experimental Optometry|March 10, 2021
An optometrist's guide to the top candidate inherited retinal diseases for gene therapyFleur O'Hare, Thomas L Edwards, Monica L Hu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
The safety and efficacy of gene therapy treatment for monogenic retinal and optic nerve diseases: A systematic reviewAlexis Ceecee Britten-Jones, Rui Jin, Sena A Gocuk, et al.
Survey of Ophthalmology|October 1, 2023
Adaptive optics imaging in inherited retinal diseases: A scoping review of the clinical literatureAlexis Ceecee Britten-Jones, Lawrence Thai, Jeremy P M Flanagan, et al.
Clinical & Experimental Ophthalmology|April 10, 2025
Retinal Gene Therapy: Perceptions of Ophthalmologists in Australia and New ZealandJohn O T Britton, Heather G Mack, Andrea L Vincent, et al.
American Journal of Ophthalmology|November 17, 2021
First-in-Human Robot-Assisted Subretinal Drug Delivery Under Local AnesthesiaJasmina Cehajic-Kapetanovic, Kanmin Xue, Thomas L Edwards, et al.
Clinical & Experimental Ophthalmology|May 12, 2012
Familial retinal detachment associated with COL2A1 exon 2 and FZD4 mutationsThomas L Edwards, Benjamin O Burt, Graeme C M Black, et al.
Human Molecular Genetics|July 22, 2009
The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signallingHilda T H Tsang, Thomas L Edwards, Xinnan Wang, et al.
Genome Research|September 16, 2024
Measuring X-Chromosome inactivation skew for X-linked diseases with adaptive nanopore sequencingSena A Gocuk, James Lancaster, Shian Su, et al.
Scientific Reports|March 13, 2025
Retrospective audit reviewing accuracy of clinical diagnosis of geographic atrophy in a single centre private tertiary retinal practice in AustraliaDemi Markakis, Alexis Ceecee Britten-Jones, Robyn H Guymer, et al.
Pageof 7