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Jiabao Ren

Showing results (1-10 of 19) with videos related to

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The Journal of Prosthetic Dentistry|August 17, 2015
Determining color difference thresholds in denture base acrylic resinJiabao Ren, Hong Lin, Qingmei Huang, et al.
Bio-Medical Materials and Engineering|September 26, 2015
Color difference threshold determination for acrylic denture base resinsJiabao Ren, Hong Lin, Qingmei Huang, et al.
Frontiers in Rehabilitation Sciences|March 16, 2026
Effects of video game-based interventions on executive functions and motor skills in children and adolescents with neurodevelopmental disorders: a systematic review and meta-analysisMing Gao, Jiabao Ren, Askerbayi Kaulie, et al.
Physiologia Plantarum|April 20, 2026
Contrasting Coordination Among Photosynthesis, Growth, and Storage of Two Dominant Desert Shrubs in Response to DroughtShensi Liu, Guiqing Xu, Jiabao Ren, et al.
Frontiers in Neurology|February 5, 2026
Multidomain intervention for dementia prevention: a scoping reviewXindi Guo, Chenhui Fan, Jiabao Ren, et al.
Fitoterapia|March 25, 2026
Characterized polyphenols from Prunus cerasifera alleviated HFD-induced intestinal inflammation and barrier dysfunction in obese mice by remodeling the gut microbiota and short-chain fatty acid profileJiabao Ren, S U Heiyan-Perhat, Ming Gao, et al.
Frontiers in Cell and Developmental Biology|January 23, 2026
Transcriptome analysis identifies EDA1 variants disrupt FOSB-mediated regulation of odontogenic epithelial cell behaviors during dental germ developmentJing Zhang, Xuanting Kong, Yunyun Yuan, et al.
Molecular Genetics & Genomic Medicine|December 9, 2023
Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese familiesYa Zhao, Jiabao Ren, Lingqiang Meng, et al.
Archives of Oral Biology|July 9, 2023
Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia familyYa Zhao, Yifei Hou, Jiabao Ren, et al.
Medicine|November 12, 2021
Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasiaLiyuan Yang, Genqi Lu, Wenjing Shen, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
The Journal of Prosthetic Dentistry|August 17, 2015
Determining color difference thresholds in denture base acrylic resinJiabao Ren, Hong Lin, Qingmei Huang, et al.
Bio-Medical Materials and Engineering|September 26, 2015
Color difference threshold determination for acrylic denture base resinsJiabao Ren, Hong Lin, Qingmei Huang, et al.
Frontiers in Rehabilitation Sciences|March 16, 2026
Effects of video game-based interventions on executive functions and motor skills in children and adolescents with neurodevelopmental disorders: a systematic review and meta-analysisMing Gao, Jiabao Ren, Askerbayi Kaulie, et al.
Physiologia Plantarum|April 20, 2026
Contrasting Coordination Among Photosynthesis, Growth, and Storage of Two Dominant Desert Shrubs in Response to DroughtShensi Liu, Guiqing Xu, Jiabao Ren, et al.
Frontiers in Neurology|February 5, 2026
Multidomain intervention for dementia prevention: a scoping reviewXindi Guo, Chenhui Fan, Jiabao Ren, et al.
Fitoterapia|March 25, 2026
Characterized polyphenols from Prunus cerasifera alleviated HFD-induced intestinal inflammation and barrier dysfunction in obese mice by remodeling the gut microbiota and short-chain fatty acid profileJiabao Ren, S U Heiyan-Perhat, Ming Gao, et al.
Frontiers in Cell and Developmental Biology|January 23, 2026
Transcriptome analysis identifies EDA1 variants disrupt FOSB-mediated regulation of odontogenic epithelial cell behaviors during dental germ developmentJing Zhang, Xuanting Kong, Yunyun Yuan, et al.
Molecular Genetics & Genomic Medicine|December 9, 2023
Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese familiesYa Zhao, Jiabao Ren, Lingqiang Meng, et al.
Archives of Oral Biology|July 9, 2023
Phenotypic characteristics of taurodontism and a novel WNT10A variant in non-syndromic oligodontia familyYa Zhao, Yifei Hou, Jiabao Ren, et al.
Medicine|November 12, 2021
Whole-exome sequencing of a novel initiation codon mutation in RUNX2 in a Chinese family with cleidocranial dysplasiaLiyuan Yang, Genqi Lu, Wenjing Shen, et al.
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