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1. Augmentation of scleral glycolysis promotes myopia through histone lactylation

3. A new polygenic score for refractive error improves detection of children at risk of high myopia but not the prediction of those at risk of myopic macular degeneration

6. Near work induces myopia in Guinea pigs

7. Sustained abnormality with recovery of COVID-19 convalescents: a 2-year follow-up study

9. Common Postzygotic Mutational Signatures in Healthy Adult Tissues Related to Embryonic Hypoxia

10. Near Work Induces Myopia in Guinea Pigs

11. Identification of novel loci influencing refractive error in East Asian populations using an extreme phenotype design

12. Declines in PDE4B activity promote myopia progression through downregulation of scleral collagen expression

14. Identification of Novel Loci Influencing Refractive Error in East Asian Populations Using an Extreme Phenotype Design

15. Up-Regulation of Matrix Metalloproteinase-2 by Scleral Monocyte–Derived Macrophages Contributes to Myopia Development

17. Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis

18. Optic nerve crush modulates refractive development of the C57BL/6 mouse by changing multiple ocular dimensions

25. Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese families

28. Genetic Variants at 13q12.12 Are Associated with High Myopia in the Han Chinese Population

29. Leber's Hereditary Optic Neuropathy Is Associated with the T12338C Mutation in Mitochondrial ND5 Gene in Six Han Chinese Families

30. Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation

31. Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families

46. The mitochondrial tRNAGlu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber’s hereditary optic neuropathy

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