470 results on '"Zhou, Xiangtian"'
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102. Author Response: Concerning Manuscript “Bright Light Suppresses Form-Deprivation Myopia Development With Activation of Dopamine D1 Receptor Signaling in the ON Pathway in Retina”
103. Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia:The CREAM Consortium
104. The effect of topical administration of cyclopentolate on ocular biometry: An analysis for mouse and human models
105. A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosis
106. Changes in retinal metabolic profiles associated with form deprivation myopia development in guinea pigs
107. Bright Light Suppresses Form-Deprivation Myopia Development With Activation of Dopamine D1 Receptor Signaling in the ON Pathway in Retina
108. Conjunctival Microbiome Changes Associated With Soft Contact Lens and Orthokeratology Lens Wearing
109. AB007. Visual signals modulate refractive error development through dopamine receptor signaling
110. Developmental expression of three small GTPases in the mouse eye
111. Using Basement Membrane of Human Amniotic Membrane as a Cell Carrier for Cultivated Cat Corneal Endothelial Cell Transplantation
112. Abstracts from the 15th International Myopia Conference
113. The Role of Retinal Dopamine in C57BL/6 Mouse Refractive Development as Revealed by Intravitreal Administration of 6-Hydroxydopamine
114. Transient Expression of Fez Family Zinc Finger 2 Protein Regulates the Brn3b Gene in Developing Retinal Ganglion Cells
115. Research for Construction Process Monitoring System of Main Reflector System for FAST
116. Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees
117. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutation
118. Adenomatous Polyposis Coli Mutation Leads to Myopia Development in Mice
119. Prevalence of MitochondrialND4Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy
120. Daily Injection But Not Continuous Infusion of Apomorphine Inhibits Form-Deprivation Myopia in Mice
121. The suitability of guinea pigs as an experimental model for the study of human refractive errors
122. Effects of Dopaminergic Agents on Progression of Naturally Occurring Myopia in Albino Guinea Pigs (Cavia porcellus)
123. Effects of muscarinic receptor modulators on ocular biometry of guinea pigs
124. Mitochondrial haplogroup D4j specific variant m.11696G > a( MT-ND4 ) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigrees.
125. Activation of Dopamine D2 Receptor Is Critical for the Development of Form-Deprivation Myopia in the C57BL/6 Mouse
126. Association study of 15q14 and 15q25 with high myopia in the Han Chinese population
127. Frequency and Spectrum of MitochondrialND6Mutations in 1218 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy
128. The Role of cGMP in Ocular Growth and the Development of Form-Deprivation Myopia in Guinea Pigs
129. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families
130. cAMP Level Modulates Scleral Collagen Remodeling, a Critical Step in the Development of Myopia
131. Deciphering gene expression program of MAP3K1 in mouse eyelid morphogenesis
132. The Effect of Temporal and Spatial Stimuli on the Refractive Status of Guinea Pigs Following Natural Emmetropization
133. Preparation and characterization of film-forming raspberry-like polymer/silica nanocomposites via soap-free emulsion polymerization and the sol–gel process
134. Leber's Hereditary Optic Neuropathy Is Associated with the T3866C Mutation in MitochondrialND1Gene in Three Han Chinese Families
135. The altered activity of complex III may contribute to the high penetrance of Leber's hereditary optic neuropathy in a Chinese family carrying the ND4 G11778A mutation
136. Disruption of Emmetropization and High Susceptibility to Deprivation Myopia in Albino Guinea Pigs
137. Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population
138. Spontaneous High Myopia in One Eye Will Affect the Development of Form Deprivation Myopia in the Fellow Eye
139. Leber's Hereditary Optic Neuropathy Is Associated with the T12338C Mutation in Mitochondrial ND5 Gene in Six Han Chinese Families
140. A Comparative Transcriptomic Analysis of Uveal Melanoma and Normal Uveal Melanocyte
141. Gene Therapy Rescues Cone Structure and Function in the 3-Month-Oldrd12Mouse: A Model for Midcourse RPE65 Leber Congenital Amaurosis
142. Macroporous magnetic poly(styrene–divinylbenzene) nanocomposites prepared via magnetite nanoparticles-stabilized high internal phase emulsions
143. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation
144. Leber's Hereditary Optic Neuropathy Affects Only Female Matrilineal Relatives in Two Chinese Families
145. Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families
146. Genetic Deletion of the Adenosine A2AReceptor Confers Postnatal Development of Relative Myopia in Mice
147. Very high penetrance and occurrence of Leber’s hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation
148. Very low penetrance of Leber’s hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation
149. Low penetrance of Leber's hereditary optic neuropathy in ten Han Chinese families carrying the ND6 T11484C mutation
150. Relative Axial Myopia Induced by Prolonged Light Exposure in C57BL/6 Mice
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