Functional integrity of visual coding following advanced photoreceptor degeneration.
Rodgers J. et al, (2024), Curr Biol, 34, 224 - 233
A systematic comparison of optogenetic approaches to visual restoration
Gilhooley MJ. et al, (2022), Molecular Therapy - Methods and Clinical Development, 25, 111 - 123
Optogenetics for visual restoration: From proof of principle to translational challenges
HANKINS M. et al, (2022), Progress in Retinal and Eye Research
Zfhx3 modulates retinal sensitivity and circadian responses to light.
Hughes S. et al, (2021), FASEB J, 35
Chimeric human opsins as optogenetic light sensitisers
HANKINS M. et al, (2021), The Journal of Experimental Biology
ON-bipolar cell gene expression during retinal degeneration: Implications for optogenetic visual restoration.
Gilhooley MJ. et al, (2021), Exp Eye Res
The functional characteristics of optogenetic gene therapy for vision restoration
HANKINS M. et al, (2020), Cellular and Molecular Life Sciences
The functional characteristics of optogenetic gene therapy for vision restoration
HANKINS M. et al, (2020), Cellular and Molecular Life Sciences
Expression and localization of Kcne2 in the vertebrate retina
HANKINS M. et al, (2020), Investigative Ophthalmology and Visual Science
Melanopsin: targeted ectopic expression for optogenetic visual restoration
Gilhooley MJ. et al, (2019), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 60
Melanopsin: photoreceptors, physiology and potential
Palumaa T. et al, (2018), Current Opinion in Physiology, 5, 68 - 74
Differential roles for cryptochromes in the mammalian retinal clock.
Wong JCY. et al, (2018), FASEB J, 32, 4302 - 4314
Melanopsin regulates circadian rhythms in contrast sensitivity but not pupillary light responses
Wong JC-Y. et al, (2018), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 59
Retinal bipolar cell gene changes in the rd1 model of inherited retinal degeneration
Gilhooley MJ. et al, (2018), INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 59
Defining the impact of melanopsin missense polymorphisms using in vivo functional rescue.
Rodgers J. et al, (2018), Hum Mol Genet
Functional characterisation of naturally occurring mutations in human melanopsin.
Rodgers J. et al, (2018), Cell Mol Life Sci
Tropism of engineered and evolved recombinant AAV serotypes in the rd1 mouse and ex vivo primate retina.
Hickey DG. et al, (2017), Gene Ther, 24, 787 - 800
Long-term restoration of visual function in end-stage retinal degeneration using subretinal human melanopsin gene therapy.
De Silva SR. et al, (2017), Proc Natl Acad Sci U S A, 114, 11211 - 11216
Expression and localisation of two-pore domain (K2P) background leak potassium ion channels in the mouse retina.
Hughes S. et al, (2017), Sci Rep, 7