Retinal degenerations such as retinitis pigmentosa (RP) or glaucoma are a major cause of blindness in humans. Understanding the mechanisms underlying the various types of retinal degeneration is a pre-requisite for the development of rational therapies for these diseases. Activation of the calcium dependent protease, calpain, has been suggested to play an important role in cell death in various neuronal tissues including the retina. Improved detection and analysis of calpain activity during degenerative processes is likely to expand the list of pathological conditions with calpain involvement. We give a short overview of the methods available for the detection of calpain activity, and briefly discuss properties of calpain inhibitors. We the...
Axonal injury and degeneration, whether primary or secondary, contribute to the morbidity and mortal...
The ubiquitous, Ca2+-dependent, neutral proteases mu-calpain and m-calpain are heterodimeric regulat...
The cellular mechanisms underlying hereditary photoreceptor degeneration are still poorly understood...
Calpains are a family of calcium-activated proteases involved in numerous disorders. Notably, previo...
P>Photoreceptor degeneration is the hallmark of a group of inherited blinding diseases collectively ...
Recent advances in molecular genetic studies have revealed many of the causative genes of retinitis ...
Photoreceptor degeneration is the hallmark of a group of inherited blinding diseases collectively te...
Fluxes of calcium ions (Ca2+) in rod photoreceptors are major regulators of steady-state and light-e...
Calpain-mediated proteolysis has been implicated as a major process in neuronal cell death in both a...
Fluxes of calcium ions (Ca2+) in rod photoreceptors are major regulators of steady-state and light-e...
The mechanisms of neuronal cell death are still only poorly understood, which has hindered the advan...
Retinitis pigmentosa (RP) is a genetic degenerative disease causing blindness in later life. About 5...
The majority of mutations in rhodopsin (RHO) cause misfolding of the protein and has been linked to ...
Retinitis pigmentosa (RP) is a heterogeneous group of inherited neurodegenerative diseases affecting...
This study tested the hypothesis that diabetes promotes a greater than normal cytosolic calcium leve...
Axonal injury and degeneration, whether primary or secondary, contribute to the morbidity and mortal...
The ubiquitous, Ca2+-dependent, neutral proteases mu-calpain and m-calpain are heterodimeric regulat...
The cellular mechanisms underlying hereditary photoreceptor degeneration are still poorly understood...
Calpains are a family of calcium-activated proteases involved in numerous disorders. Notably, previo...
P>Photoreceptor degeneration is the hallmark of a group of inherited blinding diseases collectively ...
Recent advances in molecular genetic studies have revealed many of the causative genes of retinitis ...
Photoreceptor degeneration is the hallmark of a group of inherited blinding diseases collectively te...
Fluxes of calcium ions (Ca2+) in rod photoreceptors are major regulators of steady-state and light-e...
Calpain-mediated proteolysis has been implicated as a major process in neuronal cell death in both a...
Fluxes of calcium ions (Ca2+) in rod photoreceptors are major regulators of steady-state and light-e...
The mechanisms of neuronal cell death are still only poorly understood, which has hindered the advan...
Retinitis pigmentosa (RP) is a genetic degenerative disease causing blindness in later life. About 5...
The majority of mutations in rhodopsin (RHO) cause misfolding of the protein and has been linked to ...
Retinitis pigmentosa (RP) is a heterogeneous group of inherited neurodegenerative diseases affecting...
This study tested the hypothesis that diabetes promotes a greater than normal cytosolic calcium leve...
Axonal injury and degeneration, whether primary or secondary, contribute to the morbidity and mortal...
The ubiquitous, Ca2+-dependent, neutral proteases mu-calpain and m-calpain are heterodimeric regulat...
The cellular mechanisms underlying hereditary photoreceptor degeneration are still poorly understood...