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Shijing Wu

Showing results (31-40 of 73) with videos related to

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Scientific Reports|April 27, 2026
nnLoGoNet: a hybrid local-global network for retinal vessel segmentation with Skeleton Recall LossHaixia Bai, Fuquan Wu, Yushuai Zhou, et al.
Stem Cell Research|April 15, 2021
Generation of a human induced pluripotent stem cell line from a Bietti crystalline corneoretinal dystrophy patient with CYP4V2 mutationsShijing Wu, Tian Zhu, Zixi Sun, et al.
Brain and Cognition|February 4, 2021
The only-child effect in the neural and behavioral signatures of trust revealed by fNIRS hyperscanningShijing Wu, Shenggang Cai, Guanxing Xiong, et al.
Retina (Philadelphia, Pa.)|January 11, 2020
CLINICAL CHARACTERISTICS AND MOLECULAR GENETIC ANALYSIS OF A COHORT OF CHINESE PATIENTS WITH CHOROIDEREMIAXiaoxu Han, Shijing Wu, Hui Li, et al.
Stem Cell Research|January 15, 2022
Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutationXiaoxu Han, Shijing Wu, Zixi Sun, et al.
Journal of Alzheimer'S Disease : JAD|October 10, 2022
Excretion of Amyloid-β in the Gastrointestinal Tract and Regulation by the Gut MicrobiotaShijing Wu, Li Hu, Jiajing Lin, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2021
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophyShijing Wu, Zhisheng Yuan, Zixi Sun, et al.
Ophthalmic Genetics|August 20, 2020
Variants at codon 838 in the <i>GUCY2D</i> gene result in different phenotypes of cone rod dystrophyZixi Sun, Shijing Wu, Tian Zhu, et al.
Ophthalmic Genetics|February 29, 2024
Novel <i>ATF6</i> homozygous variant in a Chinese patient with achromatopsiaShijing Wu, Yinhui Yu, Yao Wang, et al.
Stem Cell Research|August 22, 2021
Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variantsTian Zhu, Shijing Wu, Zixi Sun, et al.
Pageof 8

Showing results (31-40 of 73) with videos related to

Sort By:
Pageof 8
Scientific Reports|April 27, 2026
nnLoGoNet: a hybrid local-global network for retinal vessel segmentation with Skeleton Recall LossHaixia Bai, Fuquan Wu, Yushuai Zhou, et al.
Stem Cell Research|April 15, 2021
Generation of a human induced pluripotent stem cell line from a Bietti crystalline corneoretinal dystrophy patient with CYP4V2 mutationsShijing Wu, Tian Zhu, Zixi Sun, et al.
Brain and Cognition|February 4, 2021
The only-child effect in the neural and behavioral signatures of trust revealed by fNIRS hyperscanningShijing Wu, Shenggang Cai, Guanxing Xiong, et al.
Retina (Philadelphia, Pa.)|January 11, 2020
CLINICAL CHARACTERISTICS AND MOLECULAR GENETIC ANALYSIS OF A COHORT OF CHINESE PATIENTS WITH CHOROIDEREMIAXiaoxu Han, Shijing Wu, Hui Li, et al.
Stem Cell Research|January 15, 2022
Generation of a human induced pluripotent stem cell line PUMCHi017-A from a Choroideremia patient with CHM mutationXiaoxu Han, Shijing Wu, Zixi Sun, et al.
Journal of Alzheimer'S Disease : JAD|October 10, 2022
Excretion of Amyloid-β in the Gastrointestinal Tract and Regulation by the Gut MicrobiotaShijing Wu, Li Hu, Jiajing Lin, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|August 24, 2021
A novel tandem duplication of PRDM13 in a Chinese family with North Carolina macular dystrophyShijing Wu, Zhisheng Yuan, Zixi Sun, et al.
Ophthalmic Genetics|August 20, 2020
Variants at codon 838 in the <i>GUCY2D</i> gene result in different phenotypes of cone rod dystrophyZixi Sun, Shijing Wu, Tian Zhu, et al.
Ophthalmic Genetics|February 29, 2024
Novel <i>ATF6</i> homozygous variant in a Chinese patient with achromatopsiaShijing Wu, Yinhui Yu, Yao Wang, et al.
Stem Cell Research|August 22, 2021
Generation of two human induced pluripotent stem cell lines from patients with biallelic USH2A variantsTian Zhu, Shijing Wu, Zixi Sun, et al.
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