Search Results - "Bonezzi, Paul"

Photoreceptor deficits appear at eye opening in Rs1 mutant mouse models of X-linked retinoschisis by Tarchick, Matthew J., Beight, Craig, Bonezzi, Paul B., Peachey, Neal S., Renna, Jordan M.

“…X-linked retinoschisis (XLRS) is an early onset degenerative retinal disease characterized by cystic lesions in the middle layers of the retina. These…”
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Light drives the developmental progression of outer retinal function by Bonezzi, Paul J, Tarchick, Matthew J, Moore, Brittney D, Renna, Jordan M

“…The complex nature of rod and cone photoreceptors and the light-evoked responsivity of bipolar cells in the mature rodent retina have been well characterized…”
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Ex vivo electroretinograms made easy: performing ERGs using 3D printed components by Bonezzi, Paul J., Tarchick, Matthew J., Renna, Jordan M.

“…Key points Rod and cone photoreceptors convert light into electrochemical signals that are transferred to second order cells, initiating image‐forming visual…”
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The Development of Mid-Wavelength Photoresponsivity in the Mouse Retina by Bonezzi, Paul J., Stabio, Maureen E., Renna, Jordan M.

“…Purpose: Photoreceptors in the mouse retina express much of the molecular machinery necessary for phototransduction and glutamatergic transmission prior to eye…”
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Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells by Chung, Doug D, Chen, Angela C, Choo, Charlene H, Zhang, Wenlin, Williams, Dominic, Griffis, Christopher G, Bonezzi, Paul, Jatavallabhula, Kavya, Sampath, Alapakkam P, Aldave, Anthony J

“…Mutations in the solute linked carrier family 4 member 11 (SLC4A11) gene are associated with congenital hereditary endothelial dystrophy (CHED) and Fuchs…”
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The Development of Outer Retinal Photoresponsivity and the Effects of Sensory Deprivation by Bonezzi, Paul

“…Visual processing begins with phototransduction when rod and cone photoreceptors in the outer retina transform incident photons into electrochemical…”
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Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells by Doug D Chung, Angela C Chen, Charlene H Choo, Wenlin Zhang, Dominic Williams, Christopher G Griffis, Paul Bonezzi, Kavya Jatavallabhula, Alapakkam P Sampath, Anthony J Aldave

“…Mutations in the solute linked carrier family 4 member 11 (SLC4A11) gene are associated with congenital hereditary endothelial dystrophy (CHED) and Fuchs…”
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