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  1. Molecular Bases of Neurodegenerative Disorders of the Retina
  2. Long-term rescue of cone photoreceptor degeneration in retinitis pigmentosa 2 ( RP2 )-knockout mice by gene replacement therapy
  3. Loss of retinitis pigmentosa 2 (RP2) protein affects cone photoreceptor sensory cilium elongation in mice
  4. Ablation of retinal ciliopathy protein RPGR results in altered photoreceptor ciliary composition
  5. Role of small GTPases in polarized vesicle transport to primary cilium
  6. Cilia in photoreceptors
  7. Loss of Raf-1 Kinase Inhibitory Protein Delays Early-Onset Severe Retinal Ciliopathy inCep290rd16Mouse
  8. Ablation of the X-Linked Retinitis Pigmentosa 2 (Rp2) Gene in Mice Results in Opsin Mislocalization and Photoreceptor Degeneration
  9. New mechanisms and treatment modalities for retinal degenerative diseases
  10. Retina ciliopathies: From genes to mechanisms and treatment
  11. Ciliary signaling cascades in photoreceptors
  12. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis
  13. Ciliary transition zone (TZ) proteins RPGR and CEP290: role in photoreceptor cilia and degenerative diseases
  14. Rd9 Is a Naturally Occurring Mouse Model of a Common Form of Retinitis Pigmentosa Caused by Mutations in RPGR-ORF15
  15. Combining Cep290 and Mkks ciliopathy alleles in mice rescues sensory defects and restores ciliogenesis
  16. Tackling Primary Cilia Dysfunction in Photoreceptor Degenerative Diseases of the Eye
  17. Expression and Functional Roles of Caspase-5 in Inflammatory Responses of Human Retinal Pigment Epithelial Cells
  18. Functional Analysis of Retinitis Pigmentosa 2 (RP2) Protein Reveals Variable Pathogenic Potential of Disease-Associated Missense Variants
  19. Accumulation of the Raf-1 Kinase Inhibitory Protein (Rkip) Is Associated with Cep290-mediated Photoreceptor Degeneration in Ciliopathies
  20. XIAP Therapy Increases Survival of Transplanted Rod Precursors in a Degenerating Host Retina
  21. Expression and localization of the ciliary disease protein retinitis pigmentosa GTPase regulator in mammalian kidney
  22. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy
  23. Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy
  24. Multiprotein Complexes of Retinitis Pigmentosa GTPase Regulator (RPGR), a Ciliary Protein Mutated in X-Linked Retinitis Pigmentosa (XLRP)
  25. RPGR-containing protein complexes in syndromic and non-syndromic retinal degeneration due to ciliary dysfunction
  26. Widespread expression of the Supv3L1 mitochondrial RNA helicase in the mouse
  27. A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies
  28. CP110 Suppresses Primary Cilia Formation through Its Interaction with CEP290, a Protein Deficient in Human Ciliary Disease
  29. FGF19 Exhibits Neuroprotective Effects on Adult Mammalian Photoreceptors In Vitro
  30. Retinitis Pigmentosa GTPase Regulator (RPGR) protein isoforms in mammalian retina: Insights into X-linked Retinitis Pigmentosa and associated ciliopathies
  31. Mutations in TOPORS Cause Autosomal Dominant Retinitis Pigmentosa with Perivascular Retinal Pigment Epithelium Atrophy
  32. Centrosomal-ciliary geneCEP290/NPHP6 mutations result in blindness with unexpected sparing of photoreceptors and visual brain: implications for therapy of Leber congenital amaurosis
  33. The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
  34. Nephrocystin-5, a ciliary IQ domain protein, is mutated in Senior-Loken syndrome and interacts with RPGR and calmodulin
  35. Role of residues constituting the 2β1 strand of domain II in the biological activity of anthrax protective antigen
  36. Anthrax‐toxin‐mediated delivery of a 19 kDa antigen of Mycobacterium tuberculosis into the cytosol of mammalian cells
  37. Participation of Residue F552 in Domain III of the Protective Antigen in the Biological Activity of Anthrax Lethal Toxin
  38. Anthrax toxin-mediated delivery of cholera toxin-A subunit into the cytosol of mammalian cells