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2010 | 1 |
2017 | 1 |
2020 | 1 |
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OPA1 disease alleles causing dominant optic atrophy have defects in cardiolipin-stimulated GTP hydrolysis and membrane tubulation.
Hum Mol Genet. 2010 Jun 1;19(11):2113-22. doi: 10.1093/hmg/ddq088. Epub 2010 Feb 25.
Hum Mol Genet. 2010.
PMID: 20185555
Free PMC article.
Molecular basis of selective mitochondrial fusion by heterotypic action between OPA1 and cardiolipin.
Ban T, Ishihara T, Kohno H, Saita S, Ichimura A, Maenaka K, Oka T, Mihara K, Ishihara N.
Ban T, et al.
Nat Cell Biol. 2017 Jul;19(7):856-863. doi: 10.1038/ncb3560. Epub 2017 Jun 19.
Nat Cell Biol. 2017.
PMID: 28628083
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Cryo-EM structures of S-OPA1 reveal its interactions with membrane and changes upon nucleotide binding.
Zhang D, Zhang Y, Ma J, Zhu C, Niu T, Chen W, Pang X, Zhai Y, Sun F.
Zhang D, et al.
Elife. 2020 Mar 31;9:e50294. doi: 10.7554/eLife.50294.
Elife. 2020.
PMID: 32228866
Free PMC article.
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