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2021Mitochondrial dysfunction caused by novel ATAD3A mutations., Mol Genet Metab ; 131(1-2): 107-113.
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2019Loss of the mitochondrial -AAA protease YME1L leads to ocular dysfunction and spinal axonopathy, EMBO Mol Med 2019 Jan;11(1).
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2017Lung ultrasound as a translational approach for non-invasive assessment of heart failure with reduced or preserved ejection fraction in mice, Cardiovasc. Res. 2017 Aug;113(10):1113-1123.
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2016The membrane scaffold SLP2 anchors a proteolytic hub in mitochondria containing PARL and the i-AAA protease YME1L, EMBO Rep. 2016 12;17(12):1844-1856.
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2016Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentation, Elife 2016 08;5.
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2016Mitochondrial Dynamics and Metabolic Regulation, Trends Endocrinol. Metab. 2016 Feb;27(2):105-117.
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2015Imbalanced OPA1 processing and mitochondrial fragmentation cause heart failure in mice, Science 2015 Dec;350(6265):aad0116.
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2015SLIRP Regulates the Rate of Mitochondrial Protein Synthesis and Protects LRPPRC from Degradation, PLoS Genet. 2015 Aug;11(8):e1005423.
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2015Stomatin-like protein 2 is required for in vivo mitochondrial respiratory chain supercomplex formation and optimal cell function, Mol. Cell. Biol. 2015 May;35(10):1838-47.
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2015The Mitochondrial Metallochaperone SCO1 Is Required to Sustain Expression of the High-Affinity Copper Transporter CTR1 and Preserve Copper Homeostasis, Cell Rep 2015 Feb;.
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