Search Results - "Di Fulvio, Sabrina"

Sustained Activation of mTORC1 in Skeletal Muscle Inhibits Constitutive and Starvation-Induced Autophagy and Causes a Severe, Late-Onset Myopathy by Castets, Perrine, Lin, Shuo, Rion, Nathalie, Di Fulvio, Sabrina, Romanino, Klaas, Guridi, Maitea, Frank, Stephan, Tintignac, Lionel A., Sinnreich, Michael, Rüegg, Markus A.

“…Autophagy is a catabolic process that ensures homeostatic cell clearance and is deregulated in a growing number of myopathological conditions. Although FoxO3…”
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Dysferlin interacts with tubulin and microtubules in mouse skeletal muscle by Azakir, Bilal A, Di Fulvio, Sabrina, Therrien, Christian, Sinnreich, Michael

“…Dysferlin is a type II transmembrane protein implicated in surface membrane repair in muscle. Mutations in dysferlin lead to limb girdle muscular dystrophy 2B,…”
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Characterization of Lipid Binding Specificities of Dysferlin C2 Domains Reveals Novel Interactions with Phosphoinositides by Therrien, Christian, Di Fulvio, Sabrina, Pickles, Sarah, Sinnreich, Michael

“…Dysferlin is a type II transmembrane protein implicated in Ca2+-dependent sarcolemmal membrane repair. Dysferlin has seven C2 domains, which are lipid and…”
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Dysferlin interacts with histone deacetylase 6 and increases alpha-tubulin acetylation by Di Fulvio, Sabrina, Azakir, Bilal A, Therrien, Christian, Sinnreich, Michael

“…Dysferlin is a multi-C2 domain transmembrane protein involved in a plethora of cellular functions, most notably in skeletal muscle membrane repair, but also in…”
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Withdrawal: Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells by Azakir, Bilal A., Di Fulvio, Sabrina, Kinter, Jochen, Sinnreich, Michael

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Proteasomal inhibition restores biological function of mis-sense mutated dysferlin in patient-derived muscle cells by Azakir, Bilal A, Di Fulvio, Sabrina, Kinter, Jochen, Sinnreich, Michael

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Withdrawal: Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules by Azakir, Bilal A., Di Fulvio, Sabrina, Salomon, Steven, Brockhoff, Marielle, Therrien, Christian, Sinnreich, Michael

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PGC-1α modulates necrosis, inflammatory response, and fibrotic tissue formation in injured skeletal muscle by Dinulovic, Ivana, Furrer, Regula, Di Fulvio, Sabrina, Ferry, Arnaud, Beer, Markus, Handschin, Christoph

“…Skeletal muscle tissue has an enormous regenerative capacity that is instrumental for a successful defense against muscle injury and wasting. The peroxisome…”
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Proteasomal Inhibition Restores Biological Function of Mis-sense Mutated Dysferlin in Patient-derived Muscle Cells by Azakir, Bilal A., Di Fulvio, Sabrina, Kinter, Jochen, Sinnreich, Michael

“…Dysferlin is a transmembrane protein implicated in surface membrane repair of muscle cells. Mutations in dysferlin cause the progressive muscular dystrophies…”
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Modular dispensability of dysferlin C2 domains reveals rational design for mini-dysferlin molecules by Azakir, Bilal A, Di Fulvio, Sabrina, Salomon, Steven, Brockhoff, Marielle, Therrien, Christian, Sinnreich, Michael

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Proteasome inhibitors increase missense mutated dysferlin in patients with muscular dystrophy by Azakir, Bilal A, Erne, Beat, Di Fulvio, Sabrina, Stirnimann, Guido, Sinnreich, Michael

“…No treatment is available for patients affected by the recessively inherited, progressive muscular dystrophies caused by a deficiency in the muscle membrane…”
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Modular Dispensability of Dysferlin C2 Domains Reveals Rational Design for Mini-dysferlin Molecules by Azakir, Bilal A., Di Fulvio, Sabrina, Salomon, Steven, Brockhoff, Marielle, Therrien, Christian, Sinnreich, Michael

“…Dysferlin is a large transmembrane protein composed of a C-terminal transmembrane domain, two DysF domains, and seven C2 domains that mediate lipid- and…”
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PGC-1Alpha modulates necrosis, inflammatory response, and fibrotic tissue formation in injured skeletal muscle by Dinulovic, Ivana, Furrer, Regula, Sabrina Di Fulvio, Ferry, Arnaud, Beer, Markus, Handschin, Christoph

“…Background Skeletal muscle tissue has an enormous regenerative capacity that is instrumental for a successful defense against muscle injury and wasting. The…”
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Characterization of dysferlin's C2 domains reveals novel binding specificities to phospholipids and alpha-tubulin by Di Fulvio, Sabrina

“…Mutations in the dysferlin gene lead to a form of limb girdle muscular dystrophy (LGMD2B). Dysferlin is a transmembrane protein consisting of seven C2 domains…”
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