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International Journal of Biological Sciences
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January 22, 2024
Loss of MTX2 causes mitochondrial dysfunction, podocyte injury, nephrotic proteinuria and glomerulopathy in mice and patients
Ting Li, Ying Bao, Yu Xia, et al.
BMC Genomics
|
August 29, 2014
Marked methylation changes in intestinal genes during the perinatal period of preterm neonates
Fei Gao, Juyong Zhang, Pingping Jiang, et al.
Human Molecular Genetics
|
June 6, 2013
Coronary heart disease is associated with a mutation in mitochondrial tRNA
Zidong Jia, Xinjian Wang, Yanwen Qin, et al.
Investigative Ophthalmology & Visual Science
|
June 22, 2021
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations
Xiaofen Jin, Juanjuan Zhang, Qiuzi Yi, et al.
Journal of the American Heart Association
|
January 29, 2014
Mitochondrial tRNA variants in Chinese subjects with coronary heart disease
Yanwen Qin, Ling Xue, Pingping Jiang, et al.
Scientific Reports
|
August 17, 2025
FEN1 plays a key role in the transition from HSIL to CSCC
Fengxian Zhang, Xiaomei Chen, Chenyang Chu, et al.
Chemistry, an Asian Journal
|
September 26, 2019
Highly Dispersed and Small-Sized Nickel(II) Hydroxide Co-Catalyst Prepared by Photodeposition for Hydrogen Production
Feiyan Zhang, Yuming Dong, Pingping Jiang, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University
|
December 31, 2015
[Association between the risk of sub-health and health promotion lifestyle: a nested case-control study]
Shengwei Wu, Xiaomin Sun, Liuguo Wu, et al.
Biochemical Pharmacology
|
July 10, 2025
Dapagliflozin improves diabetic nephropathy by regulating autophagy and ferroptosis through CYP450s/ROS pathway
Huiyu Liang, Shujuan Chen, Jingying Zhong, et al.
International Journal of Legal Medicine
|
November 21, 2015
Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population
Qianhao Zhao, Yili Chen, Longlun Peng, et al.
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of 23
Search research articles
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Showing results (151-160 of 228) with videos related to
Sort By:
Page
of 23
International Journal of Biological Sciences
|
January 22, 2024
Loss of MTX2 causes mitochondrial dysfunction, podocyte injury, nephrotic proteinuria and glomerulopathy in mice and patients
Ting Li, Ying Bao, Yu Xia, et al.
BMC Genomics
|
August 29, 2014
Marked methylation changes in intestinal genes during the perinatal period of preterm neonates
Fei Gao, Juyong Zhang, Pingping Jiang, et al.
Human Molecular Genetics
|
June 6, 2013
Coronary heart disease is associated with a mutation in mitochondrial tRNA
Zidong Jia, Xinjian Wang, Yanwen Qin, et al.
Investigative Ophthalmology & Visual Science
|
June 22, 2021
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations
Xiaofen Jin, Juanjuan Zhang, Qiuzi Yi, et al.
Journal of the American Heart Association
|
January 29, 2014
Mitochondrial tRNA variants in Chinese subjects with coronary heart disease
Yanwen Qin, Ling Xue, Pingping Jiang, et al.
Scientific Reports
|
August 17, 2025
FEN1 plays a key role in the transition from HSIL to CSCC
Fengxian Zhang, Xiaomei Chen, Chenyang Chu, et al.
Chemistry, an Asian Journal
|
September 26, 2019
Highly Dispersed and Small-Sized Nickel(II) Hydroxide Co-Catalyst Prepared by Photodeposition for Hydrogen Production
Feiyan Zhang, Yuming Dong, Pingping Jiang, et al.
Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University
|
December 31, 2015
[Association between the risk of sub-health and health promotion lifestyle: a nested case-control study]
Shengwei Wu, Xiaomin Sun, Liuguo Wu, et al.
Biochemical Pharmacology
|
July 10, 2025
Dapagliflozin improves diabetic nephropathy by regulating autophagy and ferroptosis through CYP450s/ROS pathway
Huiyu Liang, Shujuan Chen, Jingying Zhong, et al.
International Journal of Legal Medicine
|
November 21, 2015
Identification of rare variants of DSP gene in sudden unexplained nocturnal death syndrome in the southern Chinese Han population
Qianhao Zhao, Yili Chen, Longlun Peng, et al.
Page
of 23