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Fengguo Zhang

Showing results (1-10 of 35) with videos related to

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International Journal of Biological Sciences|March 28, 2022
Alterations in synaptonemal complex coding genes and human infertilityFengguo Zhang, Mengfei Liu, Jinmin Gao
Acta Oto-Laryngologica|May 21, 2019
Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, ChinaMeng Zhang, Yuechen Han, Fengguo Zhang, et al.
Inflammation|June 27, 2015
Fusion Peptides CPU1 and CPU2 Inhibit Matrix Metalloproteinases and Protect Mice from Endotoxin Shock Within a Strict Time WindowZheng Qiu, Fengguo Zhang, Chengxin Gong, et al.
Journal of Biochemistry|July 1, 2010
Site-specific modification of anti-angiogenesis peptide HM-3 by polyethylene glycol molecular weight of 20 kDaBeili Zhu, Han-Mei Xu, Liming Zhao, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 30, 2024
HMG-3 contributes to meiotic chromosome maintenance and inhibits reproductive aging in C. elegansFengguo Zhang, Yuanyuan Liu, Yanmei Li, et al.
Optics Express|June 9, 2009
Emittance of a radar absorber coated with an infrared layer in the 3~5microm windowLingyun Liu, Rongzhou Gong, Yongshan Cheng, et al.
Neural Plasticity|June 1, 2018
Three <i>MYO15A</i> Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing LossFengguo Zhang, Lei Xu, Yun Xiao, et al.
BMC Medical Genetics|July 27, 2020
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing lossMingming Wang, Yicui Zhou, Fengguo Zhang, et al.
Biomed Research International|October 16, 2020
Corrigendum to "Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families"Xiaohui Bai, Chi Zhang, Fengguo Zhang, et al.
Micron (Oxford, England : 1993)|March 18, 2019
Strain measurement of particle-reinforced composites at the microscale: An approach towards concurrent characterization of strain and microstructureFengguo Zhang, Zhe Chen, Shengyi Zhong, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
International Journal of Biological Sciences|March 28, 2022
Alterations in synaptonemal complex coding genes and human infertilityFengguo Zhang, Mengfei Liu, Jinmin Gao
Acta Oto-Laryngologica|May 21, 2019
Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, ChinaMeng Zhang, Yuechen Han, Fengguo Zhang, et al.
Inflammation|June 27, 2015
Fusion Peptides CPU1 and CPU2 Inhibit Matrix Metalloproteinases and Protect Mice from Endotoxin Shock Within a Strict Time WindowZheng Qiu, Fengguo Zhang, Chengxin Gong, et al.
Journal of Biochemistry|July 1, 2010
Site-specific modification of anti-angiogenesis peptide HM-3 by polyethylene glycol molecular weight of 20 kDaBeili Zhu, Han-Mei Xu, Liming Zhao, et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao|August 30, 2024
HMG-3 contributes to meiotic chromosome maintenance and inhibits reproductive aging in C. elegansFengguo Zhang, Yuanyuan Liu, Yanmei Li, et al.
Optics Express|June 9, 2009
Emittance of a radar absorber coated with an infrared layer in the 3~5microm windowLingyun Liu, Rongzhou Gong, Yongshan Cheng, et al.
Neural Plasticity|June 1, 2018
Three <i>MYO15A</i> Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing LossFengguo Zhang, Lei Xu, Yun Xiao, et al.
BMC Medical Genetics|July 27, 2020
A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing lossMingming Wang, Yicui Zhou, Fengguo Zhang, et al.
Biomed Research International|October 16, 2020
Corrigendum to "Five Novel Mutations in LOXHD1 Gene Were Identified to Cause Autosomal Recessive Nonsyndromic Hearing Loss in Four Chinese Families"Xiaohui Bai, Chi Zhang, Fengguo Zhang, et al.
Micron (Oxford, England : 1993)|March 18, 2019
Strain measurement of particle-reinforced composites at the microscale: An approach towards concurrent characterization of strain and microstructureFengguo Zhang, Zhe Chen, Shengyi Zhong, et al.
Pageof 4