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Bo Gong

Showing results (331-340 of 430) with videos related to

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Scientific Reports|September 28, 2016
Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosaYin Yang, Yeming Yang, Lulin Huang, et al.
Journal of Pharmaceutical Analysis|October 6, 2025
Pathogenesis and treatment strategies for infectious keratitis: Exploring antibiotics, antimicrobial peptides, nanotechnology, and emerging therapiesMan Yu, Ling Li, Yijun Liu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 22, 2025
A Silk Fibroin Nanoparticle Hydrogel Loaded With NK1R Antagonist Has Synergistic Anti-Inflammatory and Reparative Effects on Dry Eye DiseaseBo Gong, Yi Liu, Huan Li, et al.
Molecular Medicine Reports|July 20, 2019
Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosaXiaoxin Guo, Jie Li, Qingwei Wang, et al.
Ophthalmic Genetics|August 23, 2017
Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese populationBo Gong, Yi Shi, Chao Qu, et al.
Iranian Journal of Allergy, Asthma, and Immunology|September 6, 2011
β-arrestin2 stimulates interleukin-17 production and expression of CD4+ T lymphocytes in a murine asthma modelYi Liu, Gu-Yi Wang, Shao-Kun Liu, et al.
The Science of the Total Environment|March 3, 2020
Determination of the response characteristics of anaerobic ammonium oxidation bioreactor disturbed by temperature change with the spectral fingerprintGui-Feng Li, Bao-Cheng Huang, Ya-Fei Cheng, et al.
Journal of the American Chemical Society|July 3, 2008
Detection of innersphere interactions between magnesium hydrate and the phosphate backbone of the HDV ribozyme using Raman crystallographyBo Gong, Yuanyuan Chen, Eric L Christian, et al.
Ophthalmic Genetics|June 15, 2018
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridiaXiaoqi Liu, Yaqi Wu, Zequn Miao, et al.
Stem Cell Research|February 12, 2026
Generation and characterization of iPSC lines (SPPHIi005-A, SPPHIi006-A, SPPHIi007-A) from a CRB1-mutation associated retinitis pigmentosa familyNing Xiao, Weijia Wu, Lingxue Gong, et al.
Pageof 43

Showing results (331-340 of 430) with videos related to

Sort By:
Pageof 43
Scientific Reports|September 28, 2016
Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosaYin Yang, Yeming Yang, Lulin Huang, et al.
Journal of Pharmaceutical Analysis|October 6, 2025
Pathogenesis and treatment strategies for infectious keratitis: Exploring antibiotics, antimicrobial peptides, nanotechnology, and emerging therapiesMan Yu, Ling Li, Yijun Liu, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|February 22, 2025
A Silk Fibroin Nanoparticle Hydrogel Loaded With NK1R Antagonist Has Synergistic Anti-Inflammatory and Reparative Effects on Dry Eye DiseaseBo Gong, Yi Liu, Huan Li, et al.
Molecular Medicine Reports|July 20, 2019
Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosaXiaoxin Guo, Jie Li, Qingwei Wang, et al.
Ophthalmic Genetics|August 23, 2017
Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese populationBo Gong, Yi Shi, Chao Qu, et al.
Iranian Journal of Allergy, Asthma, and Immunology|September 6, 2011
β-arrestin2 stimulates interleukin-17 production and expression of CD4+ T lymphocytes in a murine asthma modelYi Liu, Gu-Yi Wang, Shao-Kun Liu, et al.
The Science of the Total Environment|March 3, 2020
Determination of the response characteristics of anaerobic ammonium oxidation bioreactor disturbed by temperature change with the spectral fingerprintGui-Feng Li, Bao-Cheng Huang, Ya-Fei Cheng, et al.
Journal of the American Chemical Society|July 3, 2008
Detection of innersphere interactions between magnesium hydrate and the phosphate backbone of the HDV ribozyme using Raman crystallographyBo Gong, Yuanyuan Chen, Eric L Christian, et al.
Ophthalmic Genetics|June 15, 2018
A novel deletion downstream of the PAX6 gene identified in a Chinese family with congenital aniridiaXiaoqi Liu, Yaqi Wu, Zequn Miao, et al.
Stem Cell Research|February 12, 2026
Generation and characterization of iPSC lines (SPPHIi005-A, SPPHIi006-A, SPPHIi007-A) from a CRB1-mutation associated retinitis pigmentosa familyNing Xiao, Weijia Wu, Lingxue Gong, et al.
Pageof 43