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151. ERG Alteration Due to the rd8 Mutation of the Crb1 Gene in Cln3 +/+ rd8−/rd8- Mice

152. PRCD Is a Small Disc-Specific Rhodopsin-Binding Protein of Unknown Function

153. RPE65 Palmitoylation: A Tale of Lipid Posttranslational Modification

155. New Insights into Endothelin Signaling and Its Diverse Roles in the Retina

156. Analysis of ATP-Induced Ca2+ Responses at Single Cell Level in Retinal Pigment Epithelium Monolayers

157. No Difference Between Age-Matched Male and Female C57BL/6J Mice in Photopic and Scotopic Electroretinogram a- and b-Wave Amplitudes or in Peak Diurnal Outer Segment Phagocytosis by the Retinal Pigment Epithelium

158. Postmitotic Cone Migration Mechanisms in the Mammalian Retina

159. Sildenafil Administration in Dogs Heterozygous for a Functional Null Mutation in Pde6a: Suppressed Rod-Mediated ERG Responses and Apparent Retinal Outer Nuclear Layer Thinning

160. The Dynamic and Complex Role of the Joubert Syndrome-Associated Ciliary Protein, ADP-Ribosylation Factor-Like GTPase 13B (ARL13B) in Photoreceptor Development and Maintenance

161. Prominin-1 and Photoreceptor Cadherin Localization in Xenopus laevis: Protein-Protein Relationships and Function

162. Critical Role of Trophic Factors in Protecting Müller Glia: Implications to Neuroprotection in Age-Related Macular Degeneration, Diabetic Retinopathy, and Anti-VEGF Therapies

163. The Role of the Prph2 C-Terminus in Outer Segment Morphogenesis

164. AMPK May Play an Important Role in the Retinal Metabolic Ecosystem

165. Signaling Mechanisms Involved in PEDF-Mediated Retinoprotection

167. Analysis of Damage and Wound Healing in the Retinal Pigmented Epithelium

168. The Resveratrol Prodrug JC19 Delays Retinal Degeneration in rd10 Mice

169. Initial Assessment of Lactate as Mediator of Exercise-Induced Retinal Protection

170. Release of Retinal Extracellular Vesicles in a Model of Retinitis Pigmentosa

171. GSK-3 Inhibitors: From the Brain to the Retina and Back Again

172. Bestrophin1: A Gene that Causes Many Diseases

173. HDAC Inhibition Prevents Primary Cone Degeneration Even After the Onset of Degeneration

174. Hypoxia-Regulated MicroRNAs in the Retina

175. Live Imaging of Organelle Motility in RPE Flatmounts

176. Role of the PNPLA2 Gene in the Regulation of Oxidative Stress Damage of RPE

177. Pathomechanisms of ATF6-Associated Cone Photoreceptor Diseases

178. Pathoconnectome Analysis of Müller Cells in Early Retinal Remodeling

180. Intravitreal Injection of Amyloid β1–42 Activates the Complement System and Induces Retinal Inflammatory Responses and Malfunction in Mouse

181. Persistent Activation of STAT3 Pathway in the Retina Induced Vision Impairment and Retinal Degenerative Changes in Ageing Mice

182. Bisretinoids: More than Meets the Eye

183. Oxidative Stress, Diabetic Retinopathy, and Superoxide Dismutase 3

184. Inner Blood-Retinal Barrier Regulation in Retinopathies

185. Parthanatos as a Cell Death Pathway Underlying Retinal Disease

186. Retinal Bioenergetics: New Insights for Therapeutics

187. Peroxisomal Disorders and Retinal Degeneration

188. Analysis of the ABCA4 c.[2588G>C;5603A>T] Allele in the Australian Population

189. cAMP and Photoreceptor Cell Death in Retinal Degeneration

190. Differential Contribution of Calcium-Activated Proteases and ER-Stress in Three Mouse Models of Retinitis Pigmentosa Expressing P23H Mutant RHO

191. Lipid Signaling in Retinal Pigment Epithelium Cells Exposed to Inflammatory and Oxidative Stress Conditions. Molecular Mechanisms Underlying Degenerative Retinal Diseases

192. RD Genes Associated with High Photoreceptor cGMP-Levels (Mini-Review)

193. Light Intensity-Dependent Dysregulation of Retinal Reference Genes

194. Applications of Genomic Technologies in Retinal Degenerative Diseases

195. Update on Inherited Retinal Disease in South Africa: Encouraging Diversity in Molecular Genetics

196. The Enigma of CRB1 and CRB1 Retinopathies

197. Emerging Drug Therapies for Inherited Retinal Dystrophies

198. The Role of Caveolin-1 in Retinal Inflammation

199. Naturally Occurring Inherited Forms of Retinal Degeneration in Vertebrate Animal Species: A Comparative and Evolutionary Perspective

200. Mutations in VSX2, SOX2, and FOXE3 Identified in Patients with Micro-/Anophthalmia

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