Risultati della ricerca - Timothée Revil

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  1. 1
    Heterogeneous Nuclear Ribonucleoprotein F/H Proteins Modulate the Alternative Splicing of the Apoptotic Mediator Bcl-x

    Heterogeneous Nuclear Ribonucleoprotein F/H Proteins Modulate the Alternative Splicing of the Apoptotic Mediator Bcl-x di Daniel Garneau, Timothée Revil, Jean‐François Fisette, Benoı̂t Chabot

    Pubblicazione 2005
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  2. 2
    Heterogeneous Nuclear Ribonucleoprotein K Represses the Production of Pro-apoptotic Bcl-xS Splice Isoform

    Heterogeneous Nuclear Ribonucleoprotein K Represses the Production of Pro-apoptotic Bcl-xS Splice Isoform di Timothée Revil, Jordan Pelletier, Johanne Toutant, Alexandre Cloutier, Benoı̂t Chabot

    Pubblicazione 2009
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  3. 3
    Antagonistic Effects of the SRp30c Protein and Cryptic 5 ′ Splice Sites on the Alternative Splicing of the Apoptotic Regulator Bcl-x

    Antagonistic Effects of the SRp30c Protein and Cryptic 5 ′ Splice Sites on the Alternative Splicing of the Apoptotic Regulator Bcl-x di Philippe Cloutier, Johanne Toutant, Lulzim Shkreta, Serge Goekjian, Timothée Revil, Benoı̂t Chabot

    Pubblicazione 2008
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  4. 4
    Protein Kinase C-Dependent Control of <i>Bcl-x</i> Alternative Splicing

    Protein Kinase C-Dependent Control of <i>Bcl-x</i> Alternative Splicing di Timothée Revil, Johanne Toutant, Lulzim Shkreta, Daniel Garneau, Philippe Cloutier, Benoı̂t Chabot

    Pubblicazione 2007
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  5. 5
    Alternative splicing is frequent during early embryonic development in mouse

    Alternative splicing is frequent during early embryonic development in mouse di Timothée Revil, Daniel J. Gaffney, Christel Dias, Jacek Majewski, Loydie A. Jerome‐Majewska

    Pubblicazione 2010
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  6. 6
    Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

    Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS di Donna M. McDonald‐McGinn, Somayyeh Fahiminiya, Timothée Revil, Beata Nowakowska, Joshua A. Suhl, Alice Bailey, Elisabeth E. Mlynarski, David R. Lynch, Albert C. Yan, Larissa T. Bilaniuk, Kathleen E. Sullivan, Stephen T. Warren, Beverly S. Emanuel, Joris Vermeesch, Elaine H. Zackai, Loydie A. Jerome‐Majewska

    Pubblicazione 2012
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  7. 7
    A Targetable EGFR-Dependent Tumor-Initiating Program in Breast Cancer

    A Targetable EGFR-Dependent Tumor-Initiating Program in Breast Cancer di Paul Savage, Alexis Blanchet-Cohen, Timothée Revil, Dunarel Badescu, Sadiq M.I. Saleh, Yu-Chang Wang, Dongmei Zuo, Leah Liu, Nicholas Bertos, Valentina Muñoz-Ramos, Mark Basik, Kevin Petrecca, Jamil Asselah, Sarkis Meterissian, Marie‐Christine Guiot, Atilla Ömeroğlu, Claudia L. Kleinman, Morag Park, Jiannis Ragoussis

    Pubblicazione 2017
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  8. 8
    Analysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancy

    Analysis of head and neck carcinoma progression reveals novel and relevant stage-specific changes associated with immortalisation and malignancy di Ratna Veeramachaneni, Thomas D. J. Walker, Timothée Revil, Antoine de Weck, Dunarel Badescu, James O’Sullivan, Catherine Higgins, Louise Elliott, Triantafillos Liloglou, Janet M. Risk, Richard Shaw, Lynne Hampson, Ian Hampson, Simon Dearden, Robert Woodwards, Stephen S. Prime, Keith D. Hunter, Eric Kenneth Parkinson, Jiannis Ragoussis, Nalin Thakker

    Pubblicazione 2019
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  9. 9
    High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome

    High-sensitivity sequencing reveals multi-organ somatic mosaicism causing DICER1 syndrome di Leanne de Kock, Yu Chang Wang, Timothée Revil, Dunarel Badescu, Bárbara Rivera, Nelly Sabbaghian, Mona K. Wu, Evan Weber, Claudio Sandoval, Saskia Hopman, Johannes H. M. Merks, Johanna M. van Hagen, Antonia H. Bouts, David A. Plager, Aparna Ramasubramanian, Linus Forsmark, Kristine L Doyle, Tonja Toler, Janine Callahan, Charlotte Engelenberg, Dorothée Bouron-Dal Soglio, John R. Priest, Jiannis Ragoussis, William D. Foulkes

    Pubblicazione 2015
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  10. 10
    Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome

    Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro–costo–mandibular syndrome di Danielle C. Lynch, Timothée Revil, Jeremy Schwartzentruber, Elizabeth Bhoj, A. Micheil Innes, Ryan E. Lamont, Edmond G. Lemire, Bernard N. Chodirker, Juliet Taylor, Elaine H. Zackai, D. Ross McLeod, Edwin P. Kirk, Julie Hoover‐Fong, Leah R. Fleming, Ravi Savarirayan, Kym M. Boycott, Alex MacKenzie, Michael Brudno, Dennis E. Bulman, David A. Dyment, Jacek Majewski, Loydie A. Jerome‐Majewska, Jillian S. Parboosingh, François Bernier

    Pubblicazione 2014
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  11. 11
    Whole‐exome sequencing of non‐ <i>BRCA1/BRCA2</i> mutation carrier cases at high‐risk for hereditary breast/ovarian cancer

    Whole‐exome sequencing of non‐ <i>BRCA1/BRCA2</i> mutation carrier cases at high‐risk for hereditary breast/ovarian cancer di Paula Silva Felicio, Rebeca Silveira Grasel, Natália Campacci, Andre Escremin de Paula, Henrique C.R. Galvão, Giovana Tardin Torrezan, Cristina S. Sabato, Gabriela Carvalho Fernandes, Cristiano de Pádua Souza, Rodrigo D. Michelli, Carlos Eduardo Mattos Cunha Andrade, Bruna Durães de Figueiredo Barros, Marcus Matsushita, Timothée Revil, Jiannis Ragoussis, Fergus J. Couch, Steven N. Hart, Rui Manuel Reis, Matias Eliseo Melendez, Patricia N. Tonin, Dirce Maria Carraro, Edenir Inêz Palmero

    Pubblicazione 2020
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  12. 12
    DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis

    DGCR8 microprocessor defect characterizes familial multinodular goiter with schwannomatosis di Bárbara Rivera, Javad Nadaf, Somayyeh Fahiminiya, María Apellániz-Ruiz, Avi Saskin, Anne‐Sophie Chong, Sahil Sharma, Rabea Wagener, Timothée Revil, Vincenzo Condello, Zineb Harra, Nancy Hamel, Nelly Sabbaghian, Karl Muchantef, Christian Thomas, Leanne de Kock, Marie‐Noëlle Hébert‐Blouin, Angelia V. Bassenden, Hannah Rabenstein, Özgür Mete, Ralf Paschke, Marc Pusztaszeri, Werner Paulus, Albert M. Berghuis, Jiannis Ragoussis, Yuri E. Nikiforov, Reiner Siebert, Steffen Albrecht, Robert Turcotte, Martin Hasselblatt, Marc R. Fabian, William D. Foulkes

    Pubblicazione 2019
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