Resultats de la cerca - Jérémie Vitte

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  1. 1
    Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development

    Timing of Smarcb1 and Nf2 inactivation determines schwannoma versus rhabdoid tumor development per Jérémie Vitte, Fuying Gao, Giovanni Coppola, Alexander R. Judkins, Marco Giovannini

    Publicat 2017
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  2. 2
    Refined Characterization of the Expression and Stability of the SMN Gene Products

    Refined Characterization of the Expression and Stability of the SMN Gene Products per Jérémie Vitte, Coralie Fassier, Francesco Danilo Tiziano, Cécile Dalard, Sabrina Soave, Natacha Roblot, Christine Brahe, Pascale Saugier‐Veber, Jean‐Paul Bonnefont, Judith Melki

    Publicat 2007
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  3. 3
    Deletion of Murine Smn Exon 7 Directed to Liver Leads to Severe Defect of Liver Development Associated with Iron Overload

    Deletion of Murine Smn Exon 7 Directed to Liver Leads to Severe Defect of Liver Development Associated with Iron Overload per Jérémie Vitte, Bénédicte Davoult, Natacha Roblot, M. Mayer, Vandana Joshi, Sabrina Courageot, François Tronche, Jacqueline Vadrot, Marie Helene Moreau, F Kémény, Judith Melki

    Publicat 2004
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  4. 4
    mTORC1 inhibition delays growth of neurofibromatosis type 2 schwannoma

    mTORC1 inhibition delays growth of neurofibromatosis type 2 schwannoma per Marco Giovannini, N.-X. Bonne, Jérémie Vitte, Fabrice Chareyre, Karo Tanaka, Rocky Adams, Laurel M. Fisher, L. Valeyrie‐Allanore, P. Wolkenstein, Stéphane Goutagny, Michel Kalamarides

    Publicat 2014
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  5. 5
    Expanding the mutational spectrum of LZTR1 in schwannomatosis

    Expanding the mutational spectrum of LZTR1 in schwannomatosis per Irene Paganini, Vivian Y. Chang, Gabriele Lorenzo Capone, Jérémie Vitte, Matteo Benelli, Lorenzo Barbetti, Roberta Sestini, Eva Trevisson, Theo J.M. Hulsebos, Marco Giovannini, Stanley F. Nelson, Laura Papi

    Publicat 2014
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  6. 6
    A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition

    A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition per Anne Couturier‐Tarrade, Coralie Fassier, Sabrina Courageot, Delphine Charvin, Jérémie Vitte, Leticia Peris, Alain Thorel, Étienne Mouisel, Núria Fonknechten, Natacha Roblot, Danielle Seilhean, Andrée Dierich, Jean Jacques Hauw, Judith Melki

    Publicat 2006
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  7. 7
    Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria

    Update from the 2011 International Schwannomatosis Workshop: From genetics to diagnostic criteria per Scott R. Plotkin, Jaishri O. Blakeley, D. Gareth Evans, C. Oliver Hanemann, Theo J.M. Hulsebos, Kim Hunter‐Schaedle, Ganjam V. Kalpana, Bruce R. Korf, Ludwine Messiaen, Laura Papi, Nancy Ratner, Larry S. Sherman, Miriam J. Smith, Anat Stemmer‐Rachamimov, Jérémie Vitte, Marco Giovannini

    Publicat 2013
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  8. 8
    Genetically engineered minipigs model the major clinical features of human neurofibromatosis type 1

    Genetically engineered minipigs model the major clinical features of human neurofibromatosis type 1 per Sara Isakson, Anthony E. Rizzardi, Alexander Coutts, Daniel F. Carlson, Mark N. Kirstein, James Fisher, Jérémie Vitte, Kyle Williams, G. Elizabeth Pluhar, Sonika Dahiya, Brigitte C. Widemann, Eva Dombi, Tilat A. Rizvi, Nancy Ratner, Ludwine Messiaen, Anat Stemmer‐Rachamimov, Scott C. Fahrenkrug, David H. Gutmann, Marco Giovannini, Christopher L. Moertel, David A. Largaespada, Adrienne L. Watson

    Publicat 2018
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