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C X Li

Showing results (111-120 of 174) with videos related to

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Nanotechnology|July 7, 2011
Biofunctionalization of CeF(3):Tb(3+) nanoparticlesD Y Kong, Z L Wang, C K Lin, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 6, 2015
A novel mutation in the COL7A1 gene results in a unique phenotype of epidermolysis bullosa pruriginosaC Ni, J Zhang, H Zhang, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|December 30, 2020
[Clinical efficacy and prognostic factors analysis following curative hepatectomy for hepatocellular carcinoma patients with different China Liver Cancer Staging]C X Li, H Zhang, X F Wu, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 15, 1991
Evidence that thymocyte-activating molecule is mouse CD26 (dipeptidyl peptidase IV)I Vivier, D Marguet, P Naquet, et al.
Clinical and Experimental Dermatology|September 25, 2016
A sporadic case of Nagashima-type palmoplantar keratosis caused by gene mutation in SERPINB7C-X Li, S-Q Zhang, J Wen, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|April 22, 2026
[Genetic characteristics analysis of the VP1 region of coxsackievirus A2 in Guangdong Province, 2008-2024]M Y Zhou, Y Long, W Zhang, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 17, 2015
S159P mutation of keratin 10 gene causes severe form of epidermolytic hyperkeratosisP-J Chen, C-X Li, J Wen, et al.
Genetics and Molecular Research : GMR|November 25, 2015
Serum levels of S-100β correlate with the clinical status and severity of hypoxic-ischemic encephalopathy in neonatesL H Shi, Y Zhou, M F Guo, et al.
The Journal of Nutrition, Health & Aging|June 9, 2016
Hyperhomocysteinemia Is Associated with Vitamin B-12 Deficiency: A Cross-sectional Study in a Rural, Elderly Population of Shanxi ChinaJ Zhang, T-T Liu, W Zhang, et al.
Clinical and Experimental Dermatology|January 30, 2009
Mutation of GJB2 in a Chinese patient with keratitis-ichthyosis-deafness syndrome and brain malformationX-B Zhang, S-C Wei, C-X Li, et al.
Pageof 18

Showing results (111-120 of 174) with videos related to

Sort By:
Pageof 18
Nanotechnology|July 7, 2011
Biofunctionalization of CeF(3):Tb(3+) nanoparticlesD Y Kong, Z L Wang, C K Lin, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|January 6, 2015
A novel mutation in the COL7A1 gene results in a unique phenotype of epidermolysis bullosa pruriginosaC Ni, J Zhang, H Zhang, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|December 30, 2020
[Clinical efficacy and prognostic factors analysis following curative hepatectomy for hepatocellular carcinoma patients with different China Liver Cancer Staging]C X Li, H Zhang, X F Wu, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 15, 1991
Evidence that thymocyte-activating molecule is mouse CD26 (dipeptidyl peptidase IV)I Vivier, D Marguet, P Naquet, et al.
Clinical and Experimental Dermatology|September 25, 2016
A sporadic case of Nagashima-type palmoplantar keratosis caused by gene mutation in SERPINB7C-X Li, S-Q Zhang, J Wen, et al.
Zhonghua Liu Xing Bing Xue Za Zhi = Zhonghua Liuxingbingxue Zazhi|April 22, 2026
[Genetic characteristics analysis of the VP1 region of coxsackievirus A2 in Guangdong Province, 2008-2024]M Y Zhou, Y Long, W Zhang, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 17, 2015
S159P mutation of keratin 10 gene causes severe form of epidermolytic hyperkeratosisP-J Chen, C-X Li, J Wen, et al.
Genetics and Molecular Research : GMR|November 25, 2015
Serum levels of S-100β correlate with the clinical status and severity of hypoxic-ischemic encephalopathy in neonatesL H Shi, Y Zhou, M F Guo, et al.
The Journal of Nutrition, Health & Aging|June 9, 2016
Hyperhomocysteinemia Is Associated with Vitamin B-12 Deficiency: A Cross-sectional Study in a Rural, Elderly Population of Shanxi ChinaJ Zhang, T-T Liu, W Zhang, et al.
Clinical and Experimental Dermatology|January 30, 2009
Mutation of GJB2 in a Chinese patient with keratitis-ichthyosis-deafness syndrome and brain malformationX-B Zhang, S-C Wei, C-X Li, et al.
Pageof 18