Torthaí cuardaigh - Pascal Brouillard

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  1. 1
    Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect

    Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effect de réir Pascal Brouillard

    Foilsithe / Cruthaithe 2005
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  2. 2
    Genetics of lymphatic anomalies

    Genetics of lymphatic anomalies de réir Pascal Brouillard, Laurence M. Boon, Miikka Vikkula

    Foilsithe / Cruthaithe 2014
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    Revisão
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  3. 3
    Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3

    Loss of ADAMTS3 activity causes Hennekam lymphangiectasia–lymphedema syndrome 3 de réir Pascal Brouillard, Laura Dupont, Raphaël Helaers, Richard Coulie, George E. Tiller, Joseph Peeden, Alain Colige, Miikka Vikkula

    Foilsithe / Cruthaithe 2017
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  4. 4
    Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1

    Efficient activation of the lymphangiogenic growth factor VEGF-C requires the C-terminal domain of VEGF-C and the N-terminal domain of CCBE1 de réir Sawan Kumar Jha, Khushbu Rauniyar, Terhi Kärpänen, Veli‐Matti Leppänen, Pascal Brouillard, Miikka Vikkula, Kari Alitalo, Michael Jeltsch

    Foilsithe / Cruthaithe 2017
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  5. 5
    KRAS-driven model of Gorham-Stout disease effectively treated with trametinib

    KRAS-driven model of Gorham-Stout disease effectively treated with trametinib de réir Nassim Homayun Sepehr, Anna McCarter, Raphaël Helaers, Christine Galant, Laurence M. Boon, Pascal Brouillard, Miikka Vikkula, Michael T. Dellinger

    Foilsithe / Cruthaithe 2021
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  6. 6
    A Gene for Inherited Cutaneous Venous Anomalies (“Glomangiomas”) Localizes to Chromosome 1p21-22

    A Gene for Inherited Cutaneous Venous Anomalies (“Glomangiomas”) Localizes to Chromosome 1p21-22 de réir Laurence M. Boon, Pascal Brouillard, Alexandre Irrthum, Leena Karttunen, Matthew L. Warman, Ross Rudolph, John B. Mulliken, Bjørn R. Olsen, Miikka Vikkula

    Foilsithe / Cruthaithe 1999
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  7. 7
    Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”)

    Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”) de réir Pascal Brouillard, Laurence M. Boon, John B. Mulliken, O Enjolras, Michella Ghassibe‐Sabbagh, Matthew L. Warman, Oon Tian Tan, Bjørn R. Olsen, Miikka Vikkula

    Foilsithe / Cruthaithe 2002
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  8. 8
    Association of <i>PDGFRB</i> Mutations With Pediatric Myofibroma and Myofibromatosis

    Association of <i>PDGFRB</i> Mutations With Pediatric Myofibroma and Myofibromatosis de réir Guillaume Dachy, Ronald R. de Krijger, Sylvie Fraïtag, Ivan Théate, Bénédicte Brichard, Suma B. Hoffman, Louis Libbrecht, Florence A. Arts, Pascal Brouillard, Miikka Vikkula, Nisha Limaye, Jean‐Baptiste Demoulin

    Foilsithe / Cruthaithe 2019
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  9. 9
    Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations

    Somatic Uniparental Isodisomy Explains Multifocality of Glomuvenous Malformations de réir Mustapha Amyere, Virginie Aerts, Pascal Brouillard, Brendan A.S. McIntyre, François P. Duhoux, Michel Wassef, O Enjolras, John B. Mulliken, Olivier Devuyst, Hélène Antoine‐Poirel, Laurence M. Boon, Miikka Vikkula

    Foilsithe / Cruthaithe 2013
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  10. 10
    Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation

    Blockade of VEGF-C signaling inhibits lymphatic malformations driven by oncogenic PIK3CA mutation de réir Inés Martínez‐Corral, Yan Zhang, Milena Petkova, Henrik Ortsäter, Sofie Sjöberg, Sandra D. Castillo, Pascal Brouillard, Louis Libbrecht, Dieter Saur, Mariona Graupera, Kari Alitalo, Laurence M. Boon, Miikka Vikkula, Taija Mäkinen

    Foilsithe / Cruthaithe 2020
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  11. 11
    Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema

    Mutations in the VEGFR3 Signaling Pathway Explain 36% of Familial Lymphedema de réir Antonella Mendola, Matthieu J. Schlögel, Arash Ghalamkarpour, Alexandre Irrthum, Ha‐Long Nguyen, Elodie Fastré, Anette Bygum, Cees van der Vleuten, Christina Fagerberg, Eulàlia Baselga, I. Quéré, John B. Mulliken, Laurence M. Boon, Pascal Brouillard, Miikka Vikkula

    Foilsithe / Cruthaithe 2013
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  12. 12
    Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations

    Non-hotspot PIK3CA mutations are more frequent in CLOVES than in common or combined lymphatic malformations de réir Pascal Brouillard, Matthieu J. Schlögel, Nassim Homayun Sepehr, Raphaël Helaers, Angela Queisser, Elodie Fastré, Simon Boutry, Sandra Schmitz, Philippe Clapuyt, Frank Hammer, A. Dompmartin, Annamaria Weitz-Tuoretmaa, Jussi Laranne, L. Pasquesoone, Catheline Vilain, Laurence M. Boon, Miikka Vikkula

    Foilsithe / Cruthaithe 2021
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  13. 13
    Preliminary results of the European multicentric phase III trial regarding sirolimus in slow-flow vascular malformations

    Preliminary results of the European multicentric phase III trial regarding sirolimus in slow-flow vascular malformations de réir Emmanuel Seront, An Van Damme, Catherine Legrand, Annouk Bisdorff-Bresson, Philippe Orcel, Thomas Funck‐Brentano, Marie‐Antoinette Sevestre, A. Dompmartin, I. Quéré, Pascal Brouillard, Nicole Revençu, Martina De Bortoli, Frank Hammer, Philippe Clapuyt, Dana Dumitriu, Miikka Vikkula, Laurence M. Boon

    Foilsithe / Cruthaithe 2023
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  14. 14
    Genotypes and Phenotypes of 162 Families with a &lt;b&gt;&lt;i&gt;Glomulin&lt;/i&gt;&lt;/b&gt; Mutation

    Genotypes and Phenotypes of 162 Families with a &lt;b&gt;&lt;i&gt;Glomulin&lt;/i&gt;&lt;/b&gt; Mutation de réir Pascal Brouillard, Laurence M. Boon, Nicole Revençu, J. Berg, A. Dompmartin, Josée Dubois, Maria C. Garzón, Simon Holden, Loshan Kangesu, Christine Labrèze, Sally Ann Lynch, C McKeown, Raimundas Meškauskas, I. Quéré, Samira Syed, P. Vabres, Michel Wassef, John B. Mulliken, Miikka Vikkula

    Foilsithe / Cruthaithe 2013
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  15. 15
    An endothelial SOX18-mevalonate pathway axis enables repurposing of statins for infantile hemangioma

    An endothelial SOX18-mevalonate pathway axis enables repurposing of statins for infantile hemangioma de réir Annegret Holm, Matthew S. Graus, Jill Wylie‐Sears, J. Tan, Maya Alvarez-Harmon, Luke Borgelt, Sana Nasim, Long Hoa Chung, Ashish Jain, Mingwei Sun, Liang Sun, Pascal Brouillard, Ramrada Lekwuttikarn, Yanfei Qi, Joyce Teng, Miikka Vikkula, Harry P. Kozakewich, John B. Mulliken, Mathias François, Joyce Bischoff

    Foilsithe / Cruthaithe 2025
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