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Pingping Jiang

Showing results (201-210 of 228) with videos related to

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Journal of Agricultural and Food Chemistry|May 25, 2026
Modification of Micellar Casein Isolate Alters Protein Degradation Pathways and Peptide Generation during In Vivo Gastrointestinal DigestionMengjia Li, Kristine Holgersen, Anita Phuong Vy Le, et al.
Investigative Ophthalmology & Visual Science|May 12, 2012
Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese FamiliesXiangtian Zhou, Yaping Qian, Juanjuan Zhang, et al.
Investigative Ophthalmology & Visual Science|May 14, 2016
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic NeuropathyYanchun Ji, Min Liang, Juanjuan Zhang, et al.
Scientific Reports|July 20, 2017
A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosisJuanjuan Zhang, Xiaoling Liu, Xiaoyang Liang, et al.
Heliyon|November 29, 2023
The mechanism of Shenbing Decoction II against IgA nephropathy renal fibrosis revealed by UPLC-MS/MS, network pharmacology and experimental verificationHuaxi Liu, Weijie Chen, Chunyang Tian, et al.
Innate Immunity|July 18, 2017
Elevated levels of circulating cell-free DNA and neutrophil proteins are associated with neonatal sepsis and necrotizing enterocolitis in immature mice, pigs and infantsDuc Ninh Nguyen, Allan Stensballe, Jacqueline Cy Lai, et al.
Zoo Biology|October 29, 2009
Seasonal shifts in giant panda feeding behavior: relationships to bamboo plant part consumptionRachel L Hansen, Meghan M Carr, Carolyn J Apanavicius, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigreesHong Chen, Jing Zheng, Ling Xue, et al.
Mitochondrion|August 22, 2016
Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertensionLing Xue, Meng Wang, Haiying Li, et al.
Circulation Research|April 2, 2011
Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese familyShiwen Wang, Ronghua Li, Andrea Fettermann, et al.
Pageof 23

Showing results (201-210 of 228) with videos related to

Sort By:
Pageof 23
Journal of Agricultural and Food Chemistry|May 25, 2026
Modification of Micellar Casein Isolate Alters Protein Degradation Pathways and Peptide Generation during In Vivo Gastrointestinal DigestionMengjia Li, Kristine Holgersen, Anita Phuong Vy Le, et al.
Investigative Ophthalmology & Visual Science|May 12, 2012
Leber's hereditary optic neuropathy is associated with the T3866C mutation in mitochondrial ND1 gene in three Han Chinese FamiliesXiangtian Zhou, Yaping Qian, Juanjuan Zhang, et al.
Investigative Ophthalmology & Visual Science|May 14, 2016
Mitochondrial ND1 Variants in 1281 Chinese Subjects With Leber's Hereditary Optic NeuropathyYanchun Ji, Min Liang, Juanjuan Zhang, et al.
Scientific Reports|July 20, 2017
A novel ADOA-associated OPA1 mutation alters the mitochondrial function, membrane potential, ROS production and apoptosisJuanjuan Zhang, Xiaoling Liu, Xiaoyang Liang, et al.
Heliyon|November 29, 2023
The mechanism of Shenbing Decoction II against IgA nephropathy renal fibrosis revealed by UPLC-MS/MS, network pharmacology and experimental verificationHuaxi Liu, Weijie Chen, Chunyang Tian, et al.
Innate Immunity|July 18, 2017
Elevated levels of circulating cell-free DNA and neutrophil proteins are associated with neonatal sepsis and necrotizing enterocolitis in immature mice, pigs and infantsDuc Ninh Nguyen, Allan Stensballe, Jacqueline Cy Lai, et al.
Zoo Biology|October 29, 2009
Seasonal shifts in giant panda feeding behavior: relationships to bamboo plant part consumptionRachel L Hansen, Meghan M Carr, Carolyn J Apanavicius, et al.
European Journal of Human Genetics : EJHG|February 10, 2012
The 12S rRNA A1555G mutation in the mitochondrial haplogroup D5a is responsible for maternally inherited hypertension and hearing loss in two Chinese pedigreesHong Chen, Jing Zheng, Ling Xue, et al.
Mitochondrion|August 22, 2016
Mitochondrial tRNA mutations in 2070 Chinese Han subjects with hypertensionLing Xue, Meng Wang, Haiying Li, et al.
Circulation Research|April 2, 2011
Maternally inherited essential hypertension is associated with the novel 4263A>G mutation in the mitochondrial tRNAIle gene in a large Han Chinese familyShiwen Wang, Ronghua Li, Andrea Fettermann, et al.
Pageof 23