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Molecular Medicine Reports
|
September 18, 2020
Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA
Jiewen Fu, Jingliang Cheng, Qi Zhou, et al.
Molecules (Basel, Switzerland)
|
May 7, 2025
A Study on the Separation of Nitric Acid and Acetic Acid from Simulated Reprocessing Waste by TBP Extraction
Hongbin Lv, Xiao Ge, Tiansheng He, et al.
Ophthalmic Research
|
September 28, 2022
Automated Detection of Epiretinal Membranes in OCT Images Using Deep Learning
Yong Tang, Xiaorong Gao, Weijia Wang, et al.
Journal of Cellular and Molecular Medicine
|
August 31, 2018
A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosis
Jiewen Fu, Lu Ma, Jingliang Cheng, et al.
Frontiers in Genetics
|
May 20, 2020
Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the <i>CDH23</i> Gene Causing Usher Syndrome Type ID in a Chinese Patient
Lianmei Zhang, Jingliang Cheng, Qi Zhou, et al.
Photodiagnosis and Photodynamic Therapy
|
September 16, 2024
The lack of causal link between myopia and intraocular pressure: Insights from cross-sectional analysis and Mendelian randomization study
Bo Deng, Mo Zhou, Xiangmei Kong, et al.
Translational Vision Science & Technology
|
March 22, 2024
Sirt3 Protects Retinal Pigment Epithelial Cells From High Glucose-Induced Injury by Promoting Mitophagy Through the AMPK/mTOR/ULK1 Pathway
Wei Yang, Chen Qiu, Hongbin Lv, et al.
3 Biotech
|
April 30, 2021
Novel compound heterozygous missense variants (c.G955A and c.A1822C) of <i>CACNA2D4</i> likely causing autosomal recessive retinitis pigmentosa in a Chinese patient
Jingliang Cheng, Qi Zhou, Jiewen Fu, et al.
International Journal of Biological Macromolecules
|
March 22, 2026
SP1-induced TUG1 promotes vascular injury in diabetic retinopathy via epigenetic silencing of KLF2
Min Tian, Zheng Li, Simeng Yi, et al.
BMC Medical Genetics
|
June 13, 2018
A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing
Chunli Wei, Lisha Yang, Jingliang Cheng, et al.
Page
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Search research articles
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Showing results (61-70 of 82) with videos related to
Sort By:
Page
of 9
Molecular Medicine Reports
|
September 18, 2020
Novel compound heterozygous nonsense variants, p.L150* and p.Y3565*, of the USH2A gene in a Chinese pedigree are associated with Usher syndrome type IIA
Jiewen Fu, Jingliang Cheng, Qi Zhou, et al.
Molecules (Basel, Switzerland)
|
May 7, 2025
A Study on the Separation of Nitric Acid and Acetic Acid from Simulated Reprocessing Waste by TBP Extraction
Hongbin Lv, Xiao Ge, Tiansheng He, et al.
Ophthalmic Research
|
September 28, 2022
Automated Detection of Epiretinal Membranes in OCT Images Using Deep Learning
Yong Tang, Xiaorong Gao, Weijia Wang, et al.
Journal of Cellular and Molecular Medicine
|
August 31, 2018
A novel, homozygous nonsense variant of the CDHR1 gene in a Chinese family causes autosomal recessive retinal dystrophy by NGS-based genetic diagnosis
Jiewen Fu, Lu Ma, Jingliang Cheng, et al.
Frontiers in Genetics
|
May 20, 2020
Targeted Next-Generation Sequencing Identified Novel Compound Heterozygous Variants in the <i>CDH23</i> Gene Causing Usher Syndrome Type ID in a Chinese Patient
Lianmei Zhang, Jingliang Cheng, Qi Zhou, et al.
Photodiagnosis and Photodynamic Therapy
|
September 16, 2024
The lack of causal link between myopia and intraocular pressure: Insights from cross-sectional analysis and Mendelian randomization study
Bo Deng, Mo Zhou, Xiangmei Kong, et al.
Translational Vision Science & Technology
|
March 22, 2024
Sirt3 Protects Retinal Pigment Epithelial Cells From High Glucose-Induced Injury by Promoting Mitophagy Through the AMPK/mTOR/ULK1 Pathway
Wei Yang, Chen Qiu, Hongbin Lv, et al.
3 Biotech
|
April 30, 2021
Novel compound heterozygous missense variants (c.G955A and c.A1822C) of <i>CACNA2D4</i> likely causing autosomal recessive retinitis pigmentosa in a Chinese patient
Jingliang Cheng, Qi Zhou, Jiewen Fu, et al.
International Journal of Biological Macromolecules
|
March 22, 2026
SP1-induced TUG1 promotes vascular injury in diabetic retinopathy via epigenetic silencing of KLF2
Min Tian, Zheng Li, Simeng Yi, et al.
BMC Medical Genetics
|
June 13, 2018
A novel homozygous variant of GPR98 causes usher syndrome type IIC in a consanguineous Chinese family by next generation sequencing
Chunli Wei, Lisha Yang, Jingliang Cheng, et al.
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of 9