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Your search keyword '"Zhou, Xiangtian"' showing total 473 results

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473 results on '"Zhou, Xiangtian"'

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1. Efficient Pyramid Channel Attention Network for Pathological Myopia Recognition

2. Influencing factors of the approval of the Young Scientists Fund of National Natural Science Foundation of China: a case study of Shanghai Jiao Tong University School of Medicine

3. IMI—The Dynamic Choroid: New Insights, Challenges, and Potential Significance for Human Myopia

8. PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

9. 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

20. Scleral hypoxia is a target for myopia control

22. Myopia

24. Novel loci for ocular axial length identified through extreme-phenotype genome-wide association study in Chinese populations

25. Choroidal vasculature act as predictive biomarkers of long-term ocular elongation in myopic children treated with orthokeratology: a prospective cohort study

29. 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

31. Novel loci for ocular axial length identified through extreme-phenotype genome-wide association study in Chinese populations

34. Rare variant analyses across multiethnic cohorts identify novel genes for refractive error

35. Near work induces myopia in Guinea pigs

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

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

45. PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population

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

48. The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leberʼs hereditary optic neuropathy-associated mitochondrial DNA mutation

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