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Li Di

Showing results (141-150 of 293) with videos related to

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Lasers in Medical Science|October 8, 2017
A study on the clinical characteristics of treating nevus of Ota by Q-switched Nd:YAG laserLiu Yan, Li Di, Wang Weihua, et al.
Neuromuscular Disorders : NMD|June 14, 2017
Monoclonal gammopathy with both nemaline myopathy and amyloid myopathyMin Wang, Lin Lei, Hai Chen, et al.
Journal of Cell Science|March 17, 2005
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysisWei-Li Di, Yan Gu, John E A Common, et al.
The Review of Scientific Instruments|February 13, 2014
Feedback control of torsion balance in measurement of gravitational constant G with angular acceleration methodLi-Di Quan, Chao Xue, Cheng-Gang Shao, et al.
The Journal of Investigative Dermatology|July 22, 2019
Human Mesenchymal Stromal Cells Engineered to Express Collagen VII Can Restore Anchoring Fibrils in Recessive Dystrophic Epidermolysis Bullosa Skin Graft ChimerasAnastasia Petrova, Christos Georgiadis, Roland A Fleck, et al.
Journal of Molecular Neuroscience : MN|November 17, 2019
The Cannabinoid WIN 55,212-2 Reduces Delayed Neurologic Sequelae After Carbon Monoxide Poisoning by Promoting Microglial M2 Polarization Through ST2 SignalingJing-Jing Du, Zhi-Qin Liu, Yue Yan, et al.
Frontiers in Neuroscience|September 4, 2018
Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing AnalysisYan Lu, Yu-Wei Da, Yong-Biao Zhang, et al.
Frontiers in Neuroscience|June 7, 2018
Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing AnalysisYan Lu, Yu-Wei Da, Yong-Biao Zhang, et al.
Medicine|October 7, 2025
[194 + 2T>C;-215G>A] mutation of SPINK1 gene is associated with fibrocalculous pancreatic diabetes: A rare case reportYan Li, Qing-Hui Liao, Li-di Zhong, et al.
Cell Communication & Adhesion|December 19, 2003
Cellular mechanisms of mutant connexins in skin disease and hearing lossJohn E A Common, Wei-Li Di, Derek Davies, et al.
Pageof 30

Showing results (141-150 of 293) with videos related to

Sort By:
Pageof 30
Lasers in Medical Science|October 8, 2017
A study on the clinical characteristics of treating nevus of Ota by Q-switched Nd:YAG laserLiu Yan, Li Di, Wang Weihua, et al.
Neuromuscular Disorders : NMD|June 14, 2017
Monoclonal gammopathy with both nemaline myopathy and amyloid myopathyMin Wang, Lin Lei, Hai Chen, et al.
Journal of Cell Science|March 17, 2005
Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysisWei-Li Di, Yan Gu, John E A Common, et al.
The Review of Scientific Instruments|February 13, 2014
Feedback control of torsion balance in measurement of gravitational constant G with angular acceleration methodLi-Di Quan, Chao Xue, Cheng-Gang Shao, et al.
The Journal of Investigative Dermatology|July 22, 2019
Human Mesenchymal Stromal Cells Engineered to Express Collagen VII Can Restore Anchoring Fibrils in Recessive Dystrophic Epidermolysis Bullosa Skin Graft ChimerasAnastasia Petrova, Christos Georgiadis, Roland A Fleck, et al.
Journal of Molecular Neuroscience : MN|November 17, 2019
The Cannabinoid WIN 55,212-2 Reduces Delayed Neurologic Sequelae After Carbon Monoxide Poisoning by Promoting Microglial M2 Polarization Through ST2 SignalingJing-Jing Du, Zhi-Qin Liu, Yue Yan, et al.
Frontiers in Neuroscience|September 4, 2018
Corrigendum: Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing AnalysisYan Lu, Yu-Wei Da, Yong-Biao Zhang, et al.
Frontiers in Neuroscience|June 7, 2018
Identification of the CFTR c.1666A>G Mutation in Hereditary Inclusion Body Myopathy Using Next-Generation Sequencing AnalysisYan Lu, Yu-Wei Da, Yong-Biao Zhang, et al.
Medicine|October 7, 2025
[194 + 2T>C;-215G>A] mutation of SPINK1 gene is associated with fibrocalculous pancreatic diabetes: A rare case reportYan Li, Qing-Hui Liao, Li-di Zhong, et al.
Cell Communication & Adhesion|December 19, 2003
Cellular mechanisms of mutant connexins in skin disease and hearing lossJohn E A Common, Wei-Li Di, Derek Davies, et al.
Pageof 30