Pages that link to "Q72650885"
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The following pages link to The effects of dystrophin gene mutations on the ERG in mice and humans (Q72650885):
Displaying 28 items.
- Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness (Q21710708) (← links)
- Pikachurin interaction with dystroglycan is diminished by defective O-mannosyl glycosylation in congenital muscular dystrophy models and rescued by LARGE overexpression (Q24602380) (← links)
- Visual impairment in the absence of dystroglycan (Q24622370) (← links)
- Post-translational Maturation of Dystroglycan Is Necessary for Pikachurin Binding and Ribbon Synaptic Localization (Q24634095) (← links)
- The dynamic architecture of photoreceptor ribbon synapses: cytoskeletal, extracellular matrix, and intramembrane proteins (Q26865168) (← links)
- Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness (Q33676559) (← links)
- Mechanisms of resistance to pathogenesis in muscular dystrophies (Q33680413) (← links)
- New dystrophin/dystroglycan interactors control neuron behavior in Drosophila eye. (Q34029179) (← links)
- Abnormal electroretinogram associated with developmental brain anomalies (Q34211157) (← links)
- The negative ERG is not synonymous with nightblindness (Q34331164) (← links)
- Normal photoresponses and altered b-wave responses to APB in the mdx(Cv3) mouse isolated retina ERG supports role for dystrophin in synaptic transmission (Q34693791) (← links)
- Electrophysiological analysis of visual function in mutant mice. (Q35195026) (← links)
- Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafness (Q35299420) (← links)
- ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy (Q35432074) (← links)
- Red-green color vision impairment in Duchenne muscular dystrophy (Q35788517) (← links)
- Gene regulation induced in the C57BL/6J mouse retina by hyperoxia: a temporal microarray study (Q36965795) (← links)
- Characterization of a Dmd (EGFP) reporter mouse as a tool to investigate dystrophin expression (Q37064342) (← links)
- The roles of the dystrophin-associated glycoprotein complex at the synapse (Q37629726) (← links)
- Mouse b-wave mutants (Q38176282) (← links)
- The Transduction Cascade in Retinal ON-Bipolar Cells: Signal Processing and Disease (Q38429824) (← links)
- Correlation between electroretinogram findings and molecular analysis in the Duchenne muscular dystrophy phenotype. (Q39704029) (← links)
- Retinal signal transmission in Duchenne muscular dystrophy: evidence for dysfunction in the photoreceptor/depolarizing bipolar cell pathway (Q40336962) (← links)
- Molecular characterization of the 5'-UTR of retinal dystrophin reveals a cryptic intron that regulates translational activity. (Q41109988) (← links)
- Synapse formation is arrested in retinal photoreceptors of the zebrafish nrc mutant. (Q42501579) (← links)
- Dystrophin Dp71 is critical for the clustered localization of potassium channels in retinal glial cells. (Q44012207) (← links)
- Comparisons of the amplitude size and the reproducibility of three different electrodes to record the corneal flash electroretinogram in rodents (Q47231893) (← links)
- Presynaptic dystroglycan-pikachurin complex regulates the proper synaptic connection between retinal photoreceptor and bipolar cells. (Q51787587) (← links)
- Rescue of Defective Electroretinographic Responses in Dp71-Null Mice With AAV-Mediated Reexpression of Dp71 (Q89675952) (← links)