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Yinan Ma

Showing results (41-50 of 53) with videos related to

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Clinical Genetics|July 26, 2024
A de novo novel variant in the MT-TD gene is associated with prominent extra-neurologic manifestationsLiuyu Sun, Yali Ren, Yinan Ma, et al.
The Journal of Pediatrics|October 7, 2021
Mitochondrial DNA Copy Number in Rett Syndrome Caused by Methyl-CpG-Binding Protein-2 VariantsSiwen Liu, Pei Pei, Lin Li, et al.
Journal of the Neurological Sciences|February 13, 2010
Clinical features of mitochondrial DNA m.3243A>G mutation in 47 Chinese familiesYinan Ma, Fang Fang, Yanyan Cao, et al.
Chinese Journal of Natural Medicines|March 4, 2026
Mitochondrial dysfunction: a new target for traditional Chinese medicine in the treatment of chronic heart failureFuyun Jia, Yadong Wang, Shengwei Gao, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 7, 2025
EC-Less High-Entropy Electrolytes Enabling High-Safety and Durable Ni-Rich Lithium-Ion BatteriesJunxian Hou, Yinan Ma, Daihua Cao, et al.
Oncology Reports|December 6, 2017
Diallyl disulfide inhibits the metastasis of type Ⅱ esophageal‑gastric junction adenocarcinoma cells via NF-κB and PI3K/AKT signaling pathways in vitroXiaoran Yin, Cheng Feng, Lili Han, et al.
Clinical Case Reports|January 19, 2017
Experience of Mowat-Wilson syndrome prenatal diagnosis for a Chinese familyQian Jiang, Xiaoxiao Zhang, Yinan Ma, et al.
Plos One|May 30, 2015
Deletion of a 4977-bp Fragment in the Mitochondrial Genome Is Associated with Mitochondrial Disease SeverityYanchun Zhang, Yinan Ma, Dingfang Bu, et al.
Zhonghua Yi Xue Za Zhi|January 28, 2016
[Analysis of the relationship between mitochondrial DNA deletion and clinical complexity of mitochondrial disease]Yanchun Zhang, Yinan Ma, Dingfang Bu, et al.
Mitochondrion|February 4, 2010
Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathiesYanyan Cao, Yinan Ma, Ying Zhang, et al.
Pageof 6

Showing results (41-50 of 53) with videos related to

Sort By:
Pageof 6
Clinical Genetics|July 26, 2024
A de novo novel variant in the MT-TD gene is associated with prominent extra-neurologic manifestationsLiuyu Sun, Yali Ren, Yinan Ma, et al.
The Journal of Pediatrics|October 7, 2021
Mitochondrial DNA Copy Number in Rett Syndrome Caused by Methyl-CpG-Binding Protein-2 VariantsSiwen Liu, Pei Pei, Lin Li, et al.
Journal of the Neurological Sciences|February 13, 2010
Clinical features of mitochondrial DNA m.3243A>G mutation in 47 Chinese familiesYinan Ma, Fang Fang, Yanyan Cao, et al.
Chinese Journal of Natural Medicines|March 4, 2026
Mitochondrial dysfunction: a new target for traditional Chinese medicine in the treatment of chronic heart failureFuyun Jia, Yadong Wang, Shengwei Gao, et al.
Small (Weinheim an Der Bergstrasse, Germany)|November 7, 2025
EC-Less High-Entropy Electrolytes Enabling High-Safety and Durable Ni-Rich Lithium-Ion BatteriesJunxian Hou, Yinan Ma, Daihua Cao, et al.
Oncology Reports|December 6, 2017
Diallyl disulfide inhibits the metastasis of type Ⅱ esophageal‑gastric junction adenocarcinoma cells via NF-κB and PI3K/AKT signaling pathways in vitroXiaoran Yin, Cheng Feng, Lili Han, et al.
Clinical Case Reports|January 19, 2017
Experience of Mowat-Wilson syndrome prenatal diagnosis for a Chinese familyQian Jiang, Xiaoxiao Zhang, Yinan Ma, et al.
Plos One|May 30, 2015
Deletion of a 4977-bp Fragment in the Mitochondrial Genome Is Associated with Mitochondrial Disease SeverityYanchun Zhang, Yinan Ma, Dingfang Bu, et al.
Zhonghua Yi Xue Za Zhi|January 28, 2016
[Analysis of the relationship between mitochondrial DNA deletion and clinical complexity of mitochondrial disease]Yanchun Zhang, Yinan Ma, Dingfang Bu, et al.
Mitochondrion|February 4, 2010
Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathiesYanyan Cao, Yinan Ma, Ying Zhang, et al.
Pageof 6