Pages that link to "Q36274060"
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The following pages link to Irish setter dogs affected with rod/cone dysplasia contain a nonsense mutation in the rod cGMP phosphodiesterase beta-subunit gene (Q36274060):
Displaying 50 items.
- A frameshift mutation in golden retriever dogs with progressive retinal atrophy endorses SLC4A3 as a candidate gene for human retinal degenerations (Q21135317) (← links)
- The Finnish lapphund retinal atrophy locus maps to the centromeric region of CFA9 (Q21203578) (← links)
- Cloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptors (Q24319495) (← links)
- Mutation spectrum of the gene encoding the beta subunit of rod phosphodiesterase among patients with autosomal recessive retinitis pigmentosa (Q24564816) (← links)
- Screening of the arrestin gene in dogs afflicted with generalized progressive retinal atrophy (Q24798554) (← links)
- Lentiviral expression of retinal guanylate cyclase-1 (RetGC1) restores vision in an avian model of childhood blindness (Q27307727) (← links)
- Autosomal recessive retinitis pigmentosa caused by mutations in the alpha subunit of rod cGMP phosphodiesterase (Q28118318) (← links)
- Recessive mutations in the gene encoding the beta-subunit of rod phosphodiesterase in patients with retinitis pigmentosa (Q28118750) (← links)
- Heterozygous missense mutation in the rod cGMP phosphodiesterase beta-subunit gene in autosomal dominant stationary night blindness (Q28247337) (← links)
- Restoration of vision in the pde6β-deficient dog, a large animal model of rod-cone dystrophy (Q28271734) (← links)
- A novel mutation in exon 17 of the beta-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family (Q28272966) (← links)
- Photoreceptor cell rescue in retinal degeneration (rd) mice by in vivo gene therapy (Q28279907) (← links)
- Recent advances in understanding the spectrum of canine generalised progressive retinal atrophy (Q28285794) (← links)
- Review: the history and role of naturally occurring mouse models with Pde6b mutations (Q28304672) (← links)
- Genetic and phenotypic variations of inherited retinal diseases in dogs: the power of within- and across-breed studies (Q28658209) (← links)
- Man's best friend becomes biology's best in show: genome analyses in the domestic dog (Q28730686) (← links)
- Restoration of visual function by expression of a light-gated mammalian ion channel in retinal ganglion cells or ON-bipolar cells (Q30612156) (← links)
- Comprehensive analysis of photoreceptor gene expression and the identification of candidate retinal disease genes (Q30716734) (← links)
- Assessment of Rod, Cone, and Intrinsically Photosensitive Retinal Ganglion Cell Contributions to the Canine Chromatic Pupillary Response (Q30834824) (← links)
- Molecular cloning, characterization and expression of a novel retinal clusterin-like protein cDNA. (Q30839227) (← links)
- Progressive retinal atrophy in the Border Collie: a new XLPRA. (Q33322223) (← links)
- Molecular ophthalmology: an update on animal models for retinal degenerations and dystrophies (Q33975506) (← links)
- Nrl and Sp nuclear proteins mediate transcription of rod-specific cGMP-phosphodiesterase beta-subunit gene: involvement of multiple response elements (Q34082975) (← links)
- Gene therapy and retinitis pigmentosa: advances and future challenges (Q34084443) (← links)
- The rod cGMP-phosphodiesterase beta-subunit promoter is a specific target for Sp4 and is not activated by other Sp proteins or CRX. (Q34123053) (← links)
- A novel form of progressive retinal atrophy in Swedish vallhund dogs (Q34149777) (← links)
- Identification of genetic variation and haplotype structure of the canine ABCA4 gene for retinal disease association studies (Q34197079) (← links)
- Pathways to photoreceptor cell death in inherited retinal degenerations (Q34312941) (← links)
- Zebrafish mutants: behavioral genetic studies of visual system defects. (Q34334398) (← links)
- Rod photoreceptor-specific gene expression in human retinoblastoma cells (Q34403702) (← links)
- The genetics of eye disorders in the dog (Q34495471) (← links)
- Animal models in research on retinal degenerations: past progress and future hope (Q34537525) (← links)
- Transcriptional Activation of the Human Rod cGMP-Phosphodiesterase -Subunit Gene Is Mediated by an Upstream AP-1 Element (Q34637047) (← links)
- Evaluation of lateral spread of transgene expression following subretinal AAV-mediated gene delivery in dogs (Q34656341) (← links)
- Gene therapy for retinal and choroidal diseases (Q34701404) (← links)
- Genetic animal models for retinal degeneration (Q34772735) (← links)
- Regulatory sequences in the 3' untranslated region of the human cGMP-phosphodiesterase beta-subunit gene (Q34945443) (← links)
- The Domestic Cat as a Large Animal Model for Characterization of Disease and Therapeutic Intervention in Hereditary Retinal Blindness (Q34961635) (← links)
- A large animal model for CNGB1 autosomal recessive retinitis pigmentosa (Q34973721) (← links)
- Canine inherited retinal degenerations: update on molecular genetic research and its clinical application (Q34980394) (← links)
- RAS-converting enzyme 1-mediated endoproteolysis is required for trafficking of rod phosphodiesterase 6 to photoreceptor outer segments (Q35008463) (← links)
- Up-regulation of tumor necrosis factor superfamily genes in early phases of photoreceptor degeneration (Q35075904) (← links)
- Altered miRNA expression in canine retinas during normal development and in models of retinal degeneration. (Q35104863) (← 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)
- Increased expression of MERTK is associated with a unique form of canine retinopathy (Q35527147) (← links)
- Generation of an inbred miniature pig model of retinitis pigmentosa. (Q35797314) (← links)
- How to keep photoreceptors alive (Q35844688) (← links)
- Assessment of hereditary retinal degeneration in the English springer spaniel dog and disease relationship to an RPGRIP1 mutation (Q35894226) (← links)
- Photoreceptor proliferation and dysregulation of cell cycle genes in early onset inherited retinal degenerations (Q35954761) (← links)
- Strong upregulation of inflammatory genes accompanies photoreceptor demise in canine models of retinal degeneration. (Q36367039) (← links)