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  1. Article

    Open Access

    Dysfunctional mitochondria accumulate in a skeletal muscle knockout model of Smn1, the causal gene of spinal muscular atrophy

    The approved gene therapies for spinal muscular atrophy (SMA), caused by loss of survival motor neuron 1 (SMN1), greatly ameliorate SMA natural history but are not curative. These therapies primarily target mo...

    Francesco Chemello, Michela Pozzobon, Lorenza Iolanda Tsansizi… in Cell Death & Disease (2023)

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  2. Article

    Author Correction: The mitochondrial protein Opa1 promotes adipocyte browning that is dependent on urea cycle metabolites

    Camilla Bean, Matteo Audano, Tatiana Varanita, Francesca Favaretto… in Nature Metabolism (2022)

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  3. No Access

    Article

    The mitochondrial protein Opa1 promotes adipocyte browning that is dependent on urea cycle metabolites

    White to brown/beige adipocytes conversion is a possible therapeutic strategy to tackle the current obesity epidemics. While mitochondria are key for energy dissipation in brown fat, it is unknown if they can ...

    Camilla Bean, Matteo Audano, Tatiana Varanita, Francesca Favaretto… in Nature Metabolism (2021)