Pages that link to "Q40168119"
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The following pages link to Rod-Cone Dysplasia in Irish Setters: A Defect in Cyclic GMP Metabolism in Visual Cells (Q40168119):
Displaying 50 items.
- Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa (Q24564816) (← links)
- Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase (Q28118318) (← links)
- Linkage mapping of the primary disease locus for collie eye anomaly (Q28179553) (← links)
- Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy (Q28271734) (← links)
- Recent advances in understanding the spectrum of canine generalised progressive retinal atrophy (Q28285794) (← links)
- Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies (Q28658209) (← links)
- Molecular cloning, characterization and expression of a novel retinal clusterin-like protein cDNA. (Q30839227) (← links)
- CREB1/ATF1 activation in photoreceptor degeneration and protection (Q33488875) (← links)
- Dopamine receptor loss of function is not protective of rd1 rod photoreceptors in vivo. (Q33552905) (← links)
- A genetic analysis of retinitis pigmentosa (Q33642650) (← links)
- Sildenafil (Viagra) and ophthalmology (Q33762855) (← links)
- Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies (Q33975506) (← links)
- Genes and diseases in man and models (Q34290615) (← links)
- Isolation of a candidate cDNA for the gene causing retinal degeneration in the rd mouse (Q34324848) (← links)
- Genetic analysis of patients with retinitis pigmentosa using a cloned cDNA probe for the human gamma subunit of cyclic GMP phosphodiesterase (Q34547155) (← links)
- Genetic animal models for retinal degeneration (Q34772735) (← links)
- A truncated form of rod photoreceptor PDE6 β-subunit causes autosomal dominant congenital stationary night blindness by interfering with the inhibitory activity of the γ-subunit (Q35156268) (← links)
- The search for mutations in the gene for the beta subunit of the cGMP phosphodiesterase (PDEB) in patients with autosomal recessive retinitis pigmentosa (Q35196035) (← links)
- A null mutation in the photoreceptor guanylate cyclase gene causes the retinal degeneration chicken phenotype (Q35803466) (← links)
- Dog star rising: the canine genetic system (Q35968436) (← links)
- Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene (Q36274060) (← links)
- Finding cardiovascular disease genes in the dog. (Q36574205) (← links)
- Calcium channel blockers inhibit retinal degeneration in the retinal-degeneration-B mutant of Drosophila (Q36779309) (← links)
- In vivo imaging of the photoreceptor mosaic in retinal dystrophies and correlations with visual function (Q36973449) (← links)
- Targeting gene expression to cones with human cone opsin promoters in recombinant AAV. (Q37304864) (← links)
- Retinal degeneration in the dog and cat. (Q37937795) (← links)
- A review of the role of cyclic GMP in neurological mutants with photoreceptor dysplasia (Q39495889) (← links)
- Gene Therapy in a Large Animal Model of PDE6A-Retinitis Pigmentosa (Q40135224) (← links)
- Molecular characterization and mapping of canine cGMP-phosphodiesterase delta subunit (PDE6D). (Q40934728) (← links)
- Increased incidence of abnormal nasal cilia in patients with retinitis pigmentosa (Q41644883) (← links)
- A review of research to elucidate the causes of thegeneralized progressive retinal atrophies (Q41696011) (← links)
- Criteria for development of animal models of diseases of the eye. (Q42017450) (← links)
- Reduced phosphoCREB in Müller glia during retinal degeneration in rd10 mice (Q42152649) (← links)
- Cyclic GMP phosphodiesterase from bovine retina. Evidence for interspecies conservation (Q42775485) (← links)
- Rod/cone dysplasia in Irish setters. Presence of an altered rhodopsin (Q42857792) (← links)
- Light-induced photoreceptor apoptosis in vivo requires neuronal nitric-oxide synthase and guanylate cyclase activity and is caspase-3-independent. (Q43559246) (← links)
- Extensive cerebral calcification and retinal changes in pseudohypoparathyroidism (Q43928233) (← links)
- Animal models of human retinal dystrophies (Q45889604) (← links)
- The nitric oxide-cGMP signaling pathway differentially regulates presynaptic structural plasticity in cone and rod cells. (Q46367970) (← links)
- Involvement of cyclic GMP phosphodiesterase activator in an hereditary retinal degeneration (Q47982265) (← links)
- Neurotoxicity of cGMP in the vertebrate retina: from the initial research on rd mutant mice to zebrafish genetic approaches (Q48232458) (← links)
- Retinal degeneration in the pcd cerebellar mutant mouse. II. Electron microscopic analysis (Q48859940) (← links)
- Effect of Photic Injury on the Retinal Tissues (Q52499107) (← links)
- Regulation of adenylyl cyclase in LTP (Q57417820) (← links)
- Diagnostic ophthalmology (Q57652503) (← links)
- Targeted disruption of the endogenous zebrafish locus as models of rapid rod photoreceptor degeneration (Q58700462) (← links)
- Retinal degenerations in the dog III abnormal cyclic nucleotide metabolism in rod-cone dysplasia (Q67255562) (← links)
- Calcium modulation of cyclic GMP synthesis in rat visual cells (Q67299807) (← links)
- Linkage studies and mutation analysis of the PDEB gene in 23 families with Leber congenital amaurosis (Q67510273) (← links)
- Erythrocyte and platelet fatty acids in retinitis pigmentosa (Q67947968) (← links)