scholarly article | Q13442814 |
P2093 | author name string | Li T | |
Dryja TP | |||
Davidson BL | |||
Berson EL | |||
Roessler BJ | |||
Adamian M | |||
Roof DJ | |||
P433 | issue | 5 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Adenoviridae | Q193447 |
P304 | page(s) | 2543-2549 | |
P577 | publication date | 1994-04-01 | |
P1433 | published in | Investigative Ophthalmology Visual Science | Q6060707 |
P1476 | title | In vivo transfer of a reporter gene to the retina mediated by an adenoviral vector | |
P478 | volume | 35 |
Q35864616 | A "humanized" green fluorescent protein cDNA adapted for high-level expression in mammalian cells |
Q98177383 | A Review of Gene, Drug and Cell-Based Therapies for Usher Syndrome |
Q42762084 | Adenovirus-mediated delivery of catalase to retinal pigment epithelial cells protects neighboring photoreceptors from photo-oxidative stress |
Q33397385 | Alternate serotype adenovector provides long-term therapeutic gene expression in the eye. |
Q26767086 | Clinical Trials in Retinal Dystrophies |
Q33947904 | Correction of the retinal dystrophy phenotype of the RCS rat by viral gene transfer of Mertk |
Q45855882 | Efficient in vivo catheter-based pericardial gene transfer mediated by adenoviral vectors. |
Q36242842 | Efficient photoreceptor-targeted gene expression in vivo by recombinant adeno-associated virus |
Q41677858 | Gene therapy for inherited retinal degeneration |
Q36147481 | Gene therapy of inherited retinopathies: a long and successful road from viral vectors to patients |
Q93016526 | Has retinal gene therapy come of age? From bench to bedside and back to bench |
Q58779270 | Human Vascular Endothelial Growth Factor A Expression Induces the Mouse Model of Neovascular Age-Related Macular Degeneration |
Q60215437 | Intraocular gene transfer of ciliary neurotrophic factor prevents death and increases responsiveness of rod photoreceptors in the retinal degeneration slow mouse |
Q34063520 | My career path for developing gene therapy for blinding diseases: the importance of mentors, collaborators, and opportunities |
Q41987307 | Neural retina limits the nonviral gene transfer to retinal pigment epithelium in an in vitro bovine eye model |
Q33985663 | Nonneurotropic adenovirus: a vector for gene transfer to the brain and gene therapy of neurological disorders |
Q36175279 | Normal retina releases a diffusible factor stimulating cone survival in the retinal degeneration mouse |
Q34000123 | Phenotype correction in retinal pigment epithelium in murine mucopolysaccharidosis VII by adenovirus-mediated gene transfer |
Q36014895 | Prolonged delivery of brain-derived neurotrophic factor by adenovirus-infected Müller cells temporarily rescues injured retinal ganglion cells |
Q27007079 | Promising and delivering gene therapies for vision loss |
Q36569912 | Regulatable gene expression systems for gene therapy |
Q36157542 | Regulatable gene expression systems for gene therapy applications: progress and future challenges |
Q39551137 | Rescue from photoreceptor degeneration in the rd mouse by human immunodeficiency virus vector-mediated gene transfer |
Q42208596 | Retinal transduction profiles by high-capacity viral vectors |
Q36586077 | Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector |
Q35908639 | Variable phenotypic expressivity in inbred retinal degeneration mouse lines: A comparative study of C3H/HeOu and FVB/N rd1 mice |
Q34561531 | Vector platforms for gene therapy of inherited retinopathies. |
Q40648820 | Vitreous is a barrier in nonviral gene transfer by cationic lipids and polymers |
Q42828777 | beta-Galactosidase transgene expression in transplanted rabbit retinal pigment epithelial cells in vivo |
Search more.