Search Results - "Aurade, Frederic"

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    Pax3 and Pax7 Play Essential Safeguard Functions against Environmental Stress-Induced Birth Defects by Zalc, Antoine, Rattenbach, Revital, Auradé, Frédéric, Cadot, Bruno, Relaix, Frédéric

    Published in Developmental cell (06-04-2015)
    “…Exposure to environmental teratogenic pollutant leads to severe birth defects. However, the biological events underlying these developmental abnormalities…”
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    Journal Article
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    SOXF factors regulate murine satellite cell self-renewal and function through inhibition of β-catenin activity by Alonso-Martin, Sonia, Auradé, Frédéric, Mademtzoglou, Despoina, Rochat, Anne, Zammit, Peter S, Relaix, Frédéric

    Published in eLife (08-06-2018)
    “…Muscle satellite cells are the primary source of stem cells for postnatal skeletal muscle growth and regeneration. Understanding genetic control of satellite…”
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    Journal Article
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    Samp1 is a component of TAN lines and is required for nuclear movement by Borrego-Pinto, Joana, Jegou, Thibaud, Osorio, Daniel S, Auradé, Frederic, Gorjánácz, Mátyás, Koch, Birgit, Mattaj, Iain W, Gomes, Edgar R

    Published in Journal of cell science (01-03-2012)
    “…The position of the nucleus is regulated in different developmental stages and cellular events. During polarization, the nucleus moves away from the future…”
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  4. 4

    Neural Crest Cell Lineage Restricts Skeletal Muscle Progenitor Cell Differentiation through Neuregulin1-ErbB3 Signaling by Ho, Andrew Tri Van, Hayashi, Shinichiro, Bröhl, Dominique, Auradé, Frédéric, Rattenbach, Révital, Relaix, Frédéric

    Published in Developmental cell (16-08-2011)
    “…Coordinating the balance between progenitor self-renewal and myogenic differentiation is required for a regulated expansion of the developing muscles. Previous…”
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    Pax3- and Pax7-mediated Dbx1 regulation orchestrates the patterning of intermediate spinal interneurons by Gard, Chris, Gonzalez Curto, Gloria, Frarma, Youcef El-Mokhtar, Chollet, Elodie, Duval, Nathalie, Auzié, Valentine, Auradé, Frédéric, Vigier, Lisa, Relaix, Frédéric, Pierani, Alessandra, Causeret, Frédéric, Ribes, Vanessa

    Published in Developmental biology (01-12-2017)
    “…Transcription factors are key orchestrators of the emergence of neuronal diversity within the developing spinal cord. As such, the two paralogous proteins Pax3…”
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    Generation of BAC transgenic tadpoles enabling live imaging of motoneurons by using the urotensin II-related peptide (ust2b) gene as a driver by Bougerol, Marion, Auradé, Frédéric, Lambert, François M, Le Ray, Didier, Combes, Denis, Thoby-Brisson, Muriel, Relaix, Frédéric, Pollet, Nicolas, Tostivint, Hervé

    Published in PloS one (06-02-2015)
    “…Xenopus is an excellent tetrapod model for studying normal and pathological motoneuron ontogeny due to its developmental morpho-physiological advantages. In…”
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  7. 7

    Gene Expression Profiling of Muscle Stem Cells Identifies Novel Regulators of Postnatal Myogenesis by Alonso-Martin, Sonia, Rochat, Anne, Mademtzoglou, Despoina, Morais, Jessica, de Reyniès, Aurélien, Auradé, Frédéric, Chang, Ted Hung-Tse, Zammit, Peter S, Relaix, Frédéric

    “…Skeletal muscle growth and regeneration require a population of muscle stem cells, the satellite cells, located in close contact to the myofiber. These cells…”
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  8. 8

    A p57 conditional mutant allele that allows tracking of p57‐expressing cells by Mademtzoglou, Despoina, Alonso‐Martin, Sonia, Chang, Ted Hung‐Tse, Bismuth, Keren, Drayton‐Libotte, Bernadette, Aurade, Frédéric, Relaix, Frédéric

    Published in Genesis (New York, N.Y. : 2000) (01-04-2017)
    “…p57Kip2 (p57) is a maternally expressed imprinted gene regulating growth arrest which belongs to the CIP/KIP family of cyclin‐dependent kinase inhibitors…”
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  9. 9

    Aurora B is dispensable for megakaryocyte polyploidization, but contributes to the endomitotic process by Lordier, Larissa, Chang, Yunhua, Jalil, Abdelali, Aurade, Frédéric, Garçon, Loïc, Lécluse, Yann, Larbret, Frédéric, Kawashima, Toshiyuki, Kitamura, Toshio, Larghero, Jérôme, Debili, Najet, Vainchenker, William

    Published in Blood (30-09-2010)
    “…Polyploidization of megakaryocytes (MKs), the platelet precursors, occurs by endomitosis, a mitotic process that fails at late stages of cytokinesis…”
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  10. 10

    Proteasome inhibitor bortezomib impairs both myelofibrosis and osteosclerosis induced by high thrombopoietin levels in mice by Wagner-Ballon, Orianne, Pisani, Didier F., Gastinne, Thomas, Tulliez, Micheline, Chaligné, Ronan, Lacout, Catherine, Auradé, Frédéric, Villeval, Jean-Luc, Gonin, Patrick, Vainchenker, William, Giraudier, Stéphane

    Published in Blood (01-07-2007)
    “…Primary myelofibrosis (PMF) is the most serious myeloproliferative disorder, characterized by clonal myeloproliferation associated with cytokine-mediated bone…”
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    Megakaryocyte endomitosis is a failure of late cytokinesis related to defects in the contractile ring and Rho/Rock signaling by Lordier, Larissa, Jalil, Abdelali, Aurade, Fréderic, Larbret, Fréderic, Larghero, Jerôme, Debili, Najet, Vainchenker, William, Chang, Yunhua

    Published in Blood (15-10-2008)
    “…Megakaryocyte (MK) is the naturally polyploid cell that gives rise to platelets. Polyploidization occurs by endomitosis, which was a process considered to be…”
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    Proplatelet formation is regulated by the Rho/ROCK pathway by Chang, Yunhua, Auradé, Frédéric, Larbret, Frédéric, Zhang, Yanyan, Le Couedic, Jean-Pierre, Momeux, Laurence, Larghero, Jerôme, Bertoglio, Jacques, Louache, Fawzia, Cramer, Elisabeth, Vainchenker, William, Debili, Najet

    Published in Blood (15-05-2007)
    “…Platelets are released by megakaryocytes (MKs) via cytoplasmic extensions called proplatelets, which require profound changes in the microtubule and actin…”
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    A de novo synonymous variant in EFTUD2 disrupts normal splicing and causes mandibulofacial dysostosis with microcephaly: case report by Jacob, Arthur, Pasquier, Jennifer, Carapito, Raphael, Auradé, Frédéric, Molitor, Anne, Froguel, Philippe, Fakhro, Khalid, Halabi, Najeeb, Viot, Géraldine, Bahram, Seiamak, Rafii, Arash

    Published in BMC medical genetics (17-09-2020)
    “…Mandibulofacial dysostosis with microcephaly (MFDM) is a rare autosomal dominant genetic disease characterized by intellectual and growth retardations, as well…”
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    Generation of BAC Transgenic Tadpoles Enabling Live Imaging of Motoneurons by Using the Urotensin II-Related Peptide (ust2b) Gene as a Driver: e0117370 by Bougerol, Marion, Aurade, Frederic, Lambert, Francois M, Ray, Didier Le, Combes, Denis, Thoby-Brisson, Muriel, Relaix, Frederic, Pollet, Nicolas, Tostivint, Herve

    Published in PloS one (01-02-2015)
    “…Xenopus is an excellent tetrapod model for studying normal and pathological motoneuron ontogeny due to its developmental morpho-physiological advantages. In…”
    Get full text
    Journal Article