Results 131 to 140 of about 3,353 (142)
Some of the next articles are maybe not open access.

The MFN2 gene is responsible for mitochondrial DNA instability and optic atrophy 'plus' phenotype.

Brain, 2012
Aline Cano   +2 more
exaly  

Low MFN2 expression related to ageing in granulosa cells is associated with assisted reproductive technology outcome

Reproductive BioMedicine Online, 2019
Lingjuan Wang, Wenpei Xiang, Xuemei Liu
exaly  

Melatonin prevents adverse myocardial infarction remodeling via Notch1/Mfn2 pathway

Free Radical Biology and Medicine, 2016
Lei He, Yongjian Yang, Erhe Gao
exaly  

Mitofusins Mfn1 and Mfn2 coordinately regulate mitochondrial fusion and are essential for embryonic development

Journal of Cell Biology, 2003
Erik E Griffin   +2 more
exaly  

Mfn2, Mfn2, and Mfn2 mutations drive Charcot-Marie-Tooth type 2A disease by inducing apoptosis and mitochondrial oxidative phosphorylation damage

International Journal of Biological Macromolecules
Hongsheng Ouyang   +2 more
exaly  

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