724 results on '"Ali, Robin"'
Search Results
102. The Cholesterol, Hypertension, and Glucose Education (CHANGE) study for African Americans with diabetes: Study design and methodology
103. Gene therapy for retinitis pigmentosa and Leber congenital amaurosis caused by defects in AIPL1: effective rescue of mouse models of partial and complete Aipl1 deficiency using AAV2/2 and AAV2/8 vectors
104. Gene therapy for inherited childhood blindness shows promise
105. Letter to the Editor
106. Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector
107. Permanent phenotypic correction of hemophilia B in immunocompetent mice by prenatal gene therapy
108. Minocycline delays photoreceptor death in the rds mouse through a microglia-independent mechanism
109. Myeloid-Derived Vascular Endothelial Growth Factor and Hypoxia-Inducible Factor Are Dispensable for Ocular Neovascularization—Brief Report
110. Molecular therapy in ocular wound healing
111. Isolation of human photoreceptor precursors via a cell surface marker panel from stem cell-derived retinal organoids and fetal retinae
112. Additional file 1: of Use of bioreactors for culturing human retinal organoids improves photoreceptor yields
113. Development of a Gene Therapy Vector for RDH12-Associated Retinal Dystrophy
114. Stabilization of myeloid-derived HIFs promotes vascular regeneration in retinal ischemia
115. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease
116. Transcriptional regulation of cone photoreceptor development
117. Highly Differentiated Human Fetal RPE Cultures Are Resistant to the Accumulation and Toxicity of Lipofuscin-Like Material
118. Modulation of Contact Inhibition by ZO-1/ZONAB Gene Transfer—A New Strategy to Increase the Endothelial Cell Density of Corneal Grafts
119. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease
120. Detailed clinical characterisation, unique features and natural history of autosomal recessive RDH12-associated retinal degeneration
121. Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease.
122. Unlocking the Potential for Endogenous Repair to Restore Sight
123. Sustained and Widespread Gene Delivery to the Corneal Epithelium viaIn SituTransduction of Limbal Epithelial Stem Cells, Using Lentiviral and Adeno-Associated Viral Vectors
124. Assessment of AAV Vector Tropisms for Mouse and Human Pluripotent Stem Cell–Derived RPE and Photoreceptor Cells
125. Regenerating Eye Tissues to Preserve and Restore Vision
126. A novel adeno-associated virus capsid with enhanced neurotropism corrects a lysosomal transmembrane enzyme deficiency
127. Prevention of Photoreceptor Cell Loss in a Cln6 Mouse Model of Batten Disease Requires CLN6 Gene Transfer to Bipolar Cells
128. Retinal gene therapy
129. Isolation of Human Photoreceptor Precursors via a Cell Surface Marker Panel from Stem Cell-Derived Retinal Organoids and Fetal Retinae
130. Gene therapy for Leber congenital amaurosis
131. Late neuroprogenitors contribute to normal retinal vascular development in a Hif2a-dependent manner
132. Human iPSC-Derived RPE and Retinal Organoids Reveal Impaired Alternative Splicing of Genes Involved in Pre-mRNA Splicing in PRPF31 Autosomal Dominant Retinitis Pigmentosa Type 11
133. Human iPSC-derived RPE and retinal organoids reveal impaired alternative splicing of genes involved in pre-mRNA splicing in PRPF31 autosomal dominant retinitis pigmentosa
134. Human stem cell-derived retinal epithelial cells activate complement via collectin 11 in response to stress
135. Multimodal analysis of ocular inflammation using the endotoxin-induced uveitis mouse model
136. Additional file 1: of Investigation of SLA4A3 as a candidate gene for human retinal disease
137. Human stem cell-derived retinal epithelial cells activate complement via collectin 11 in response to stress
138. Celebrating 25 Years of the European Society of Gene and Cell Therapy
139. The Future Looks Brighter After 25 Years of Retinal Gene Therapy
140. Augmenting Endogenous Levels of Retinal Annexin A1 Suppresses Uveitis in Mice
141. Recapitulation of Human Retinal Development from Human Pluripotent Stem Cells Generates Transplantable Populations of Cone Photoreceptors
142. Early-Onset Progressive Degeneration of the Area Centralis in RPE65-Deficient Dogs
143. Accelerated oxygen-induced retinopathy is a reliable model of ischemia-induced retinal neovascularization
144. Differentiation and Transplantation of Embryonic Stem Cell-Derived Cone Photoreceptors into a Mouse Model of End-Stage Retinal Degeneration
145. Hypoxia inducible factors are dispensable for myeloid cell migration into the inflamed mouse eye
146. Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179
147. Dark-adaptation functions in molecularly confirmed achromatopsia and the implications for assessment in retinal therapy trials
148. Collectin 11 expression by hypoxia-stressed iPSC-derived RPE cells is linked to complement activation
149. Flow cytometric analysis of inflammatory and resident myeloid populations in mouse ocular inflammatory models
150. Impact of BREXIT on UK Gene and Cell Therapy: The Need for Continued Pan-European Collaboration
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.