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Xu Ma

Showing results (371-380 of 1,039) with videos related to

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Nature Communications|February 15, 2024
Tunable templating of photonic microparticles via liquid crystal order-guided adsorption of amphiphilic polymers in emulsionsXu Ma, Yucen Han, Yan-Song Zhang, et al.
Molecular Vision|October 30, 2008
A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataractsXu Ma, Fei-Feng Li, Shu-Zhen Wang, et al.
The Journal of Headache and Pain|January 17, 2017
The status of diagnosis and treatment to intracranial hypotension, including SIHJin-Ping Lin, Shu-Dong Zhang, Fei-Fang He, et al.
Applied Optics|August 12, 2025
Design of on-chip coded X-ray sensors for high-confidence super-resolution radiological imagingTianyi Mao, Lei Wang, Yuqi Jiang, et al.
Molecular Vision|February 1, 2006
A missense mutation in the gammaD-crystallin gene CRYGD associated with autosomal dominant congenital cataract in a Chinese familyFeng Gu, Rong Li, Xi Xin Ma, et al.
Journal of Hazardous Materials|July 7, 2026
Atomistic insights into the As(V) and trace divalent metal co-stabilization in scorodite via precipitation and screening mechanismXu Ma, Haoze Wu, Jia Chen, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 16, 2011
Novel beta-crystallin gene mutations in Chinese families with nuclear cataractsKai Jie Wang, Bin Bin Wang, Fengju Zhang, et al.
Biochemical and Biophysical Research Communications|September 30, 2016
Cited2 participates in cardiomyocyte apoptosis and maternal diabetes-induced congenital heart abnormalityDongmei Su, Jun-Xian Song, Qianqian Gao, et al.
Zhonghua Shao Shang Za Zhi = Zhonghua Shaoshang Zazhi = Chinese Journal of Burns|August 18, 2004
[Experimental and clinical study on the treatment of ischemic skin flap with topical application of PGE1]Chi Li, Dong-Ning Yu, Hao Wang, et al.
Journal of Cellular Physiology|September 6, 2012
Abnormality of maternal-to-embryonic transition contributes to MEHP-induced mouse 2-cell blockDa-Peng Chu, Shi Tian, Lu Qi, et al.
Pageof 104

Showing results (371-380 of 1,039) with videos related to

Sort By:
Pageof 104
Nature Communications|February 15, 2024
Tunable templating of photonic microparticles via liquid crystal order-guided adsorption of amphiphilic polymers in emulsionsXu Ma, Yucen Han, Yan-Song Zhang, et al.
Molecular Vision|October 30, 2008
A new mutation in BFSP2 (G1091A) causes autosomal dominant congenital lamellar cataractsXu Ma, Fei-Feng Li, Shu-Zhen Wang, et al.
The Journal of Headache and Pain|January 17, 2017
The status of diagnosis and treatment to intracranial hypotension, including SIHJin-Ping Lin, Shu-Dong Zhang, Fei-Fang He, et al.
Applied Optics|August 12, 2025
Design of on-chip coded X-ray sensors for high-confidence super-resolution radiological imagingTianyi Mao, Lei Wang, Yuqi Jiang, et al.
Molecular Vision|February 1, 2006
A missense mutation in the gammaD-crystallin gene CRYGD associated with autosomal dominant congenital cataract in a Chinese familyFeng Gu, Rong Li, Xi Xin Ma, et al.
Journal of Hazardous Materials|July 7, 2026
Atomistic insights into the As(V) and trace divalent metal co-stabilization in scorodite via precipitation and screening mechanismXu Ma, Haoze Wu, Jia Chen, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|March 16, 2011
Novel beta-crystallin gene mutations in Chinese families with nuclear cataractsKai Jie Wang, Bin Bin Wang, Fengju Zhang, et al.
Biochemical and Biophysical Research Communications|September 30, 2016
Cited2 participates in cardiomyocyte apoptosis and maternal diabetes-induced congenital heart abnormalityDongmei Su, Jun-Xian Song, Qianqian Gao, et al.
Zhonghua Shao Shang Za Zhi = Zhonghua Shaoshang Zazhi = Chinese Journal of Burns|August 18, 2004
[Experimental and clinical study on the treatment of ischemic skin flap with topical application of PGE1]Chi Li, Dong-Ning Yu, Hao Wang, et al.
Journal of Cellular Physiology|September 6, 2012
Abnormality of maternal-to-embryonic transition contributes to MEHP-induced mouse 2-cell blockDa-Peng Chu, Shi Tian, Lu Qi, et al.
Pageof 104