about
Lentiviral gene transfer of RPE65 rescues survival and function of cones in a mouse model of Leber congenital amaurosisFAM161A, associated with retinitis pigmentosa, is a component of the cilia-basal body complex and interacts with proteins involved in ciliopathiesRapid cohort generation and analysis of disease spectrum of large animal model of cone dystrophyRetinal degeneration progression changes lentiviral vector cell targeting in the retinaGene therapy regenerates protein expression in cone photoreceptors in Rpe65(R91W/R91W) mice.Rai1 frees mice from the repression of active wake behaviors by light.Bmi1 loss produces an increase in astroglial cells and a decrease in neural stem cell population and proliferation.Reduction of choroidal neovascularization in mice by adeno-associated virus-delivered anti-vascular endothelial growth factor short hairpin RNA.Amyloid Precursor-Like Protein 2 deletion-induced retinal synaptopathy related to congenital stationary night blindness: structural, functional and molecular characteristicsHyperactivation of retina by light in mice leads to photoreceptor cell death mediated by VEGF and retinal pigment epithelium permeabilityAdamts18 deletion results in distinct developmental defects and provides a model for congenital disorders of lens, lung, and female reproductive tract development.Animal modelling for inherited central vision loss.Evaluation of tolerance to lentiviral LV-RPE65 gene therapy vector after subretinal delivery in nonhuman primates.Activity analysis of housekeeping promoters using self-inactivating lentiviral vector delivery into the mouse retina.Isolation and characterization of sixteen novel p53 response genes.Multigenic lentiviral vectors for combined and tissue-specific expression of miRNA- and protein-based antiangiogenic factorsDetermination of Rod and Cone Influence to the Early and Late Dynamic of the Pupillary Light Response.Remaining rod activity mediates visual behavior in adult Rpe65-/- mice.Notch signaling in the pigmented epithelium of the anterior eye segment promotes ciliary body development at the expense of iris formation.Delivery of ciliary neurotrophic factor via lentiviral-mediated transfer protects axotomized retinal ganglion cells for an extended period of time.Use of human MAR elements to improve retroviral vector production.Lentiviral vectors containing a retinal pigment epithelium specific promoter for leber congenital amaurosis gene therapy. Lentiviral gene therapy for LCA.Isolation of multipotent neural precursors residing in the cortex of the adult human brain.[Gene therapy for hereditary eye diseases: where are we?].Maturation of the Pupil Light Reflex Occurs Until Adulthood in MiceLentiviral mediated RPE65 gene transfer in healthy hiPSCs-derived retinal pigment epithelial cells markedly increased RPE65 mRNA, but modestly protein level
P50
Q21144697-1D045C71-2EB7-4CAC-BAFC-B0232C7CD3CBQ24297877-81EA4591-AF5E-40FB-BA62-1DC6123A0D23Q27309443-C2F6ADDD-99CC-483F-8907-D29ADE4814F2Q28741007-4DAE217D-48C7-48A8-9E18-E2E2792ED3E8Q30999247-7D1CA382-F437-4421-8793-C9EEBF1775D6Q33779025-5B48CBF6-553D-425B-A16F-D0220E9AB9AFQ34426800-AA70F1AF-5F10-487B-B2D8-101A15F37D88Q34451693-0CC8995A-018F-4D07-97E6-1084DD8A1811Q36980803-7A614410-C7D1-47E9-837D-BFA48273508EQ37148310-B22D059A-E3B5-45DD-B04D-6B584FAB0F19Q37502202-861C67A3-888F-4CBA-BEF1-DA686B52E0D0Q38589892-BF8BE94E-8BA3-4804-AFDC-926F3C8722C2Q40103624-1BB76416-2D2E-4E2F-AB78-165A68C03E64Q40592978-4CAA5E0E-69AA-4AC6-AE46-4C1FD5118B46Q40858501-D12AB3D8-1540-4157-8C13-0BFBB1A2A6E0Q41373392-413DA950-CC85-4C32-B7F1-C5CE48472DF1Q42786166-F076B739-FCA4-4647-A4B4-943832E51BC7Q42940194-BD73F699-4CD3-4ED8-BB92-67C1AAC8051AQ43989095-8BD34090-F1FE-40B4-BAE4-BEADC56B127DQ44340109-376BB31A-4F92-4865-A1F1-5EE01C7FBB39Q45863292-A72C2A16-D0A4-43C1-93D0-A31D78939506Q45865415-B1A4568B-855A-4A49-B57A-68AA5995B645Q45878110-E2D69DEB-F418-4D49-BAEF-17BA26923EA5Q46111426-5A7C19D2-0D6F-47A5-9473-8333106B2650Q61800064-04DDB866-BD93-4823-BE4C-56491CBCD462Q96126980-8E0C5497-0A6A-4E53-AA98-06229FC71339
P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0003-1006-9733
@en
name
Corinne Kostic
@ast
Corinne Kostic
@en
Corinne Kostic
@es
Corinne Kostic
@nl
type
label
Corinne Kostic
@ast
Corinne Kostic
@en
Corinne Kostic
@es
Corinne Kostic
@nl
prefLabel
Corinne Kostic
@ast
Corinne Kostic
@en
Corinne Kostic
@es
Corinne Kostic
@nl
P106
P31
P496
0000-0003-1006-9733