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Cell & Bioscience|January 1, 2020
Drosophila Prominin-like, a homolog of CD133, interacts with ND20 to maintain mitochondrial functionXuexiang Wang, Huimei Zheng, Zexiao Jia, et al.Frontiers in Genetics|November 8, 2019
A Novel Compound Heterozygous CYP17A1 Variant Causes 17α-Hydroxylase/17, 20-Lyase DeficiencyHong Chen, Ke Yuan, Bingtao Zhang, et al.Langmuir : the ACS Journal of Surfaces and Colloids|December 27, 2013
Formic acid-assisted synthesis of palladium nanocrystals and their electrocatalytic propertiesQinchao Wang, Yiqian Wang, Peizhi Guo, et al.Fish & Shellfish Immunology|July 15, 2018
Bitter peptides from enzymatically hydrolyzed protein increase the number of leucocytes and lysozyme activity of large yellow croaker (Larimichthys crocea)Cheng Luo, Blessing Gwekwe, Phares Choto, et al.Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi = Zhonghua Laodong Weisheng Zhiyebing Zazhi = Chinese Journal of Industrial Hygiene and Occupational Diseases|March 2, 2018
[Analysis of the impact of job characteristics and organizational support for workplace violence]M L Li, P Chen, F H Zeng, et al.The Journal of Physical Chemistry Letters|September 24, 2016
Capacitance of Nanoporous Carbon-Based Supercapacitors Is a Trade-Off between the Concentration and the Separability of the IonsRyan Burt, Konrad Breitsprecher, Barbara Daffos, et al.Plos One|March 6, 2014
Mechanistic study on the nuclear modifier gene MSS1 mutation suppressing neomycin sensitivity of the mitochondrial 15S rRNA C1477G mutation in Saccharomyces cerevisiaeQiyin Zhou, Wei Wang, Xiangyu He, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|July 2, 2024
NF2 regulates IP3R-mediated Ca2+ signal and apoptosis in meningiomasZhaoying Lei, Jie Niu, Huajian Cai, et al.Gene|July 5, 2012
Mitochondrial ND5 12338T>C variant is associated with maternally inherited hypertrophic cardiomyopathy in a Chinese pedigreeZhong Liu, Yanrui Song, Shulian Gu, et al.Journal of Medical Genetics|December 25, 2013
The novel mitochondrial 16S rRNA 2336T>C mutation is associated with hypertrophic cardiomyopathyZhong Liu, Yanrui Song, Dan Li, et al.Pageof 31