David M Hunt

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 7

Top Topics

Particulate Matter

Diabetic Retinopathy

Age Related Macular Degeneration

Top Venues

Pflugers Archiv : European journal of physiology

Ophthalmic genetics

The Journal of comparative neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Xiaotian Jiang, Rabab Rashwan, Valentina Voigt, Jeanne M Nerbonne, David M Hunt, Livia S Carvalho
Molecular, Cellular and Functional Changes in the Retinas of Young Adult Mice Lacking the Voltage-Gated K+ Channel Subunits Kv8.2 and K2.1. International journal of molecular sciences 22 (9) (2021)
Rabab Rashwan, David M Hunt, Livia S Carvalho
The role of voltage-gated ion channels in visual function and disease in mammalian photoreceptors. Pflugers Archiv : European journal of physiology 473 (9) (2021)
Rachael E Warrington, Wayne I L Davies, Jan M Hemmi, Nathan S Hart, Ian C Potter, Shaun P Collin, David M Hunt
Visual opsin expression and morphological characterization of retinal photoreceptors in the pouched lamprey (Geotria australis, Gray). The Journal of comparative neurology 529 (9) (2020)
Jenna M Crowe-Riddell, Bruno F Simões, Julian C Partridge, David M Hunt, Steven Delean, Julian G Schwerdt, James Breen, Alastair Ludington, David J Gower, Kate L Sanders
Phototactic tails: Evolution and molecular basis of a novel sensory trait in sea snakes. Molecular ecology 28 (8) (2019)
Trevor D Lamb, Hardip R Patel, Aaron Chuah, David M Hunt
Evolution of the shut-off steps of vertebrate phototransduction. Open biology 8 (1) (2019)
Trevor D Lamb, David M Hunt
Evolution of the calcium feedback steps of vertebrate phototransduction. Open biology 8 (9) (2018)
Valentina Cipriani, Ambreen Kalhoro, Gavin Arno, Raquel Sofia Silva, Nikolas Pontikos, Virginie Puech, Michelle E McClements, David M Hunt, Veronica Van Heyningen, Michel Michaelides, Andrew R Webster, Anthony T Moore, Bernard Puech
Genome-wide linkage and haplotype sharing analysis implicates the MCDR3 locus as a candidate region for a developmental macular disorder in association with digit abnormalities. Ophthalmic genetics 38 (6) (2017)