Search Results - "Rüegg, Markus A."

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    Hepatic mTORC2 Activates Glycolysis and Lipogenesis through Akt, Glucokinase, and SREBP1c by Hagiwara, Asami, Cornu, Marion, Cybulski, Nadine, Polak, Pazit, Betz, Charles, Trapani, Francesca, Terracciano, Luigi, Heim, Markus H., Rüegg, Markus A., Hall, Michael N.

    Published in Cell metabolism (02-05-2012)
    “…Mammalian target of rapamycin complex 2 (mTORC2) phosphorylates and activates AGC kinase family members, including Akt, SGK1, and PKC, in response to…”
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    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.

    Published in Cell metabolism (07-05-2013)
    “…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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    WNT7B promotes bone formation in part through mTORC1 by Chen, Jianquan, Tu, Xiaolin, Esen, Emel, Joeng, Kyu Sang, Lin, Congxin, Arbeit, Jeffrey M, Rüegg, Markus A, Hall, Michael N, Ma, Liang, Long, Fanxin

    Published in PLoS genetics (01-01-2014)
    “…WNT signaling has been implicated in both embryonic and postnatal bone formation. However, the pertinent WNT ligands and their downstream signaling mechanisms…”
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    Activated mTORC1 promotes long-term cone survival in retinitis pigmentosa mice by Venkatesh, Aditya, Ma, Shan, Le, Yun Z, Hall, Michael N, Rüegg, Markus A, Punzo, Claudio

    Published in The Journal of clinical investigation (01-04-2015)
    “…Retinitis pigmentosa (RP) is an inherited photoreceptor degenerative disorder that results in blindness. The disease is often caused by mutations in genes that…”
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    BDNF is a mediator of glycolytic fiber-type specification in mouse skeletal muscle by Delezie, Julien, Weihrauch, Martin, Maier, Geraldine, Tejero, Rocío, Ham, Daniel J., Gill, Jonathan F., Karrer-Cardel, Bettina, Rüegg, Markus A., Tabares, Lucía, Handschin, Christoph

    “…Brain-derived neurotrophic factor (BDNF) influences the differentiation, plasticity, and survival of central neurons and likewise, affects the development of…”
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    Fast, multiplexable and efficient somatic gene deletions in adult mouse skeletal muscle fibers using AAV-CRISPR/Cas9 by Thürkauf, Marco, Lin, Shuo, Oliveri, Filippo, Grimm, Dirk, Platt, Randall J., Rüegg, Markus A.

    Published in Nature communications (30-09-2023)
    “…Molecular screens comparing different disease states to identify candidate genes rely on the availability of fast, reliable and multiplexable systems to…”
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    mTORC1 and mTORC2 regulate skin morphogenesis and epidermal barrier formation by Ding, Xiaolei, Bloch, Wilhelm, Iden, Sandra, Rüegg, Markus A., Hall, Michael N., Leptin, Maria, Partridge, Linda, Eming, Sabine A.

    Published in Nature communications (27-10-2016)
    “…Mammalian target of rapamycin (mTOR), a regulator of growth in many tissues, mediates its activity through two multiprotein complexes, mTORC1 or mTORC2. The…”
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    Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I by Brockhoff, Marielle, Rion, Nathalie, Chojnowska, Kathrin, Wiktorowicz, Tatiana, Eickhorst, Christopher, Erne, Beat, Frank, Stephan, Angelini, Corrado, Furling, Denis, Rüegg, Markus A, Sinnreich, Michael, Castets, Perrine

    Published in The Journal of clinical investigation (01-02-2017)
    “…Myotonic dystrophy type I (DM1) is a disabling multisystemic disease that predominantly affects skeletal muscle. It is caused by expanded CTG repeats in the…”
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    Activation of mTORC1 in skeletal muscle regulates whole-body metabolism through FGF21 by Guridi, Maitea, Tintignac, Lionel A, Lin, Shuo, Kupr, Barbara, Castets, Perrine, Rüegg, Markus A

    Published in Science signaling (10-11-2015)
    “…Skeletal muscle is the largest organ, comprising 40% of the total body lean mass, and affects whole-body metabolism in multiple ways. We investigated the…”
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    Chimeric protein repair of laminin polymerization ameliorates muscular dystrophy phenotype by McKee, Karen K, Crosson, Stephanie C, Meinen, Sarina, Reinhard, Judith R, Rüegg, Markus A, Yurchenco, Peter D

    Published in The Journal of clinical investigation (01-03-2017)
    “…Mutations in laminin α2-subunit (Lmα2, encoded by LAMA2) are linked to approximately 30% of congenital muscular dystrophy cases. Mice with a homozygous…”
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    Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive by Hall, Michael N, Jacinto, Estela, Loewith, Robbie, Schmidt, Anja, Lin, Shuo, Rüegg, Markus A, Hall, Alan

    Published in Nature cell biology (01-11-2004)
    “…The target of rapamycin (TOR) is a highly conserved protein kinase and a central controller of cell growth. In budding yeast, TOR is found in structurally and…”
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    Rescue of spinal muscular atrophy mouse models with AAV9-Exon-specific U1 snRNA by Donadon, Irving, Bussani, Erica, Riccardi, Federico, Licastro, Danilo, Romano, Giulia, Pianigiani, Giulia, Pinotti, Mirko, Konstantinova, Pavlina, Evers, Melvin, Lin, Shuo, Rüegg, Markus A, Pagani, Franco

    Published in Nucleic acids research (22-08-2019)
    “…Abstract Spinal Muscular Atrophy results from loss-of-function mutations in SMN1 but correcting aberrant splicing of SMN2 offers hope of a cure. However,…”
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    Ablation of the mTORC2 component rictor in brain or Purkinje cells affects size and neuron morphology by Thomanetz, Venus, Angliker, Nico, Cloëtta, Dimitri, Lustenberger, Regula M, Schweighauser, Manuel, Oliveri, Filippo, Suzuki, Noboru, Rüegg, Markus A

    Published in The Journal of cell biology (15-04-2013)
    “…The mammalian target of rapamycin (mTOR) assembles into two distinct multi-protein complexes called mTORC1 and mTORC2. Whereas mTORC1 is known to regulate cell…”
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    Impaired mTORC1-Dependent Expression of Homer-3 Influences SCA1 Pathophysiology by Ruegsegger, Céline, Stucki, David M., Steiner, Silvio, Angliker, Nico, Radecke, Julika, Keller, Eva, Zuber, Benoît, Rüegg, Markus A., Saxena, Smita

    Published in Neuron (Cambridge, Mass.) (06-01-2016)
    “…Spinocerebellar ataxia type 1 (SCA1), due to the expansion of a polyglutamine repeat within the ubiquitously expressed Ataxin-1 protein, leads to the premature…”
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    Mammalian Target of Rapamycin Complex 2 Controls CD8 T Cell Memory Differentiation in a Foxo1-Dependent Manner by Zhang, Lianjun, Tschumi, Benjamin O., Lopez-Mejia, Isabel C., Oberle, Susanne G., Meyer, Marten, Samson, Guerric, Rüegg, Markus A., Hall, Michael N., Fajas, Lluis, Zehn, Dietmar, Mach, Jean-Pierre, Donda, Alena, Romero, Pedro

    Published in Cell reports (Cambridge) (09-02-2016)
    “…Upon infection, antigen-specific naive CD8 T cells are activated and differentiate into short-lived effector cells (SLECs) and memory precursor cells (MPECs)…”
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    Differential localization and anabolic responsiveness of mTOR complexes in human skeletal muscle in response to feeding and exercise by Hodson, Nathan, McGlory, Chris, Oikawa, Sara Y, Jeromson, Stewart, Song, Zhe, Rüegg, Markus A, Hamilton, D Lee, Phillips, Stuart M, Philp, Andrew

    “…Mechanistic target of rapamycin (mTOR) resides as two complexes within skeletal muscle. mTOR complex 1 [mTORC1-regulatory associated protein of mTOR (Raptor)…”
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