Latest papers

Membrane-binding and enzymatic properties of RPE65.

Long-term 12 year follow-up of X-linked congenital retinoschisis.

The pigment epithelial-derived factor gene loaded in PLGA nanoparticles for therapy of colon carcinoma.

[The role of chromosomal regions anchored to the nuclear envelope in the functional organization of chromosomes].

Sumoylation of bZIP transcription factor NRL modulates target gene expression during photoreceptor differentiation.

Facilitated DNA Search by Multidomain Transcription Factors: Cross Talk via a Flexible Linker

Identification of a prevalent founder mutation in an Israeli Muslim Arab village confirms the role of PRCD in the aetiology of retinitis pigmentosa in humans.

Choroidal neovascularization associated with cancer-associated retinopathy.

Brr2p RNA helicase with a split personality: insights into structure and function.

Focus on Molecules: Nuclear hormone receptor Nr2e3: Impact on retinal development and disease

Cleavage of the retinal pigment epithelium-specific protein RPE65 under oxidative stress

tgAAG76, an adeno-associated virus delivered gene therapy for the potential treatment of vision loss caused by RPE65 gene abnormalities.

Blockade of interleukin-6 signaling suppresses experimental autoimmune uveoretinitis by the inhibition of inflammatory Th17 responses

The role of TLR4 in photoreceptor {alpha}a crystallin upregulation during early experimental autoimmune uveitis.

Retinal very long-chain PUFAs: new insights from studies on ELOVL4 protein.

Glial cell line-derived neurotrophic factor enhances neurogenin3 gene expression and beta-cell proliferation in the developing mouse pancreas.

Self-complementary AAV-mediated gene therapy restores cone function and prevents cone degeneration in two models of Rpe65 deficiency.

Gene expression within the amacrine cell layer of chicks after myopic and hyperopic defocus.

Bestrophins and retinopathies.

Retinal degeneration and failure of photoreceptor outer segment formation in mice with targeted deletion of the Joubert syndrome gene, Ahi1.