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Bijun Zhang

Showing results (11-20 of 45) with videos related to

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Journal of Chemical Information and Modeling|November 29, 2012
Systematic assessment of compound series with SAR transfer potentialBijun Zhang, Anne Mai Wassermann, Martin Vogt, et al.
Journal of Computer-Aided Molecular Design|November 10, 2015
Erratum to: design of chemical space networks using a Tanimoto similarity variant based upon maximum common substructuresBijun Zhang, Martin Vogt, Gerald M Maggiora, et al.
Journal of Computer-Aided Molecular Design|June 8, 2015
Comparison of bioactive chemical space networks generated using substructure- and fingerprint-based measures of molecular similarityBijun Zhang, Martin Vogt, Gerald M Maggiora, et al.
Kidney & Blood Pressure Research|July 28, 2021
Renal NKCC2 Is Dual Regulated by the Synergy of 20-HETE and High-Fat Diet in CYP4F2 Transgenic MiceJingjing Wu, Guangrui Lai, Fangjie Chen, et al.
Experimental Cell Research|March 17, 2020
Neddylation-mediated Nedd4-2 activation regulates ubiquitination modification of renal NBCe1Jianqiao Tu, Bijun Zhang, Guicun Fang, et al.
Molecular Genetics & Genomic Medicine|March 4, 2020
Nonsense suppression induced readthrough of a novel PAX6 mutation in patient-derived cells of congenital aniridiaXiaoliang Liu, Yuanyuan Zhang, Bijun Zhang, et al.
Prostaglandins & Other Lipid Mediators|August 16, 2017
20-HETE regulated PSMB5 expression via TGF-β/Smad signaling pathwayGuangrui Lai, Ru Sun, Jingjing Wu, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 16, 2021
Nedd4-2 haploinsufficiency in mice causes increased seizure susceptibility and impaired Kir4.1 ubiquitinationXiaoliang Liu, Hebo Zhang, Bijun Zhang, et al.
Molecular Medicine Reports|October 18, 2017
20-Hydroxyeicosatetraenoic acid regulates the expression of Nedd4‑2 in kidney and liver through a neddylation modification pathwayJianzhu Zhao, Bijun Zhang, Guangrui Lai, et al.
Orphanet Journal of Rare Diseases|March 13, 2025
Identification of ETFDH gene c. 487 + 2 T > A pathogenic variant and mechanisms for polycystic kidney in neonatal onset MADDBijun Zhang, Dongyang Zhang, Feiyue Sun, et al.
Pageof 5

Showing results (11-20 of 45) with videos related to

Sort By:
Pageof 5
Journal of Chemical Information and Modeling|November 29, 2012
Systematic assessment of compound series with SAR transfer potentialBijun Zhang, Anne Mai Wassermann, Martin Vogt, et al.
Journal of Computer-Aided Molecular Design|November 10, 2015
Erratum to: design of chemical space networks using a Tanimoto similarity variant based upon maximum common substructuresBijun Zhang, Martin Vogt, Gerald M Maggiora, et al.
Journal of Computer-Aided Molecular Design|June 8, 2015
Comparison of bioactive chemical space networks generated using substructure- and fingerprint-based measures of molecular similarityBijun Zhang, Martin Vogt, Gerald M Maggiora, et al.
Kidney & Blood Pressure Research|July 28, 2021
Renal NKCC2 Is Dual Regulated by the Synergy of 20-HETE and High-Fat Diet in CYP4F2 Transgenic MiceJingjing Wu, Guangrui Lai, Fangjie Chen, et al.
Experimental Cell Research|March 17, 2020
Neddylation-mediated Nedd4-2 activation regulates ubiquitination modification of renal NBCe1Jianqiao Tu, Bijun Zhang, Guicun Fang, et al.
Molecular Genetics & Genomic Medicine|March 4, 2020
Nonsense suppression induced readthrough of a novel PAX6 mutation in patient-derived cells of congenital aniridiaXiaoliang Liu, Yuanyuan Zhang, Bijun Zhang, et al.
Prostaglandins & Other Lipid Mediators|August 16, 2017
20-HETE regulated PSMB5 expression via TGF-β/Smad signaling pathwayGuangrui Lai, Ru Sun, Jingjing Wu, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|March 16, 2021
Nedd4-2 haploinsufficiency in mice causes increased seizure susceptibility and impaired Kir4.1 ubiquitinationXiaoliang Liu, Hebo Zhang, Bijun Zhang, et al.
Molecular Medicine Reports|October 18, 2017
20-Hydroxyeicosatetraenoic acid regulates the expression of Nedd4‑2 in kidney and liver through a neddylation modification pathwayJianzhu Zhao, Bijun Zhang, Guangrui Lai, et al.
Orphanet Journal of Rare Diseases|March 13, 2025
Identification of ETFDH gene c. 487 + 2 T > A pathogenic variant and mechanisms for polycystic kidney in neonatal onset MADDBijun Zhang, Dongyang Zhang, Feiyue Sun, et al.
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