Torthaí cuardaigh - Barbara D′haene

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  1. 1
    Accurate and objective copy number profiling using real-time quantitative PCR

    Accurate and objective copy number profiling using real-time quantitative PCR de réir Barbara D′haene, Jo Vandesompele, Jan Hellemans

    Foilsithe / Cruthaithe 2010
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  2. 2
    miRNA Expression Profiling: From Reference Genes to Global Mean Normalization

    miRNA Expression Profiling: From Reference Genes to Global Mean Normalization de réir Barbara D′haene, Pieter Mestdagh, Jan Hellemans, Jo Vandesompele

    Foilsithe / Cruthaithe 2011
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    Artigo
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  3. 3
    Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain

    Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain de réir Hannah Verdin, Barbara D′haene, Diane Beysen, Yana Novikova, Björn Menten, Tom Sante, Pablo Lapunzina, Julián Nevado, Claudia M.B. Carvalho, James R. Lupski, Elfride De Baere

    Foilsithe / Cruthaithe 2013
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    Artigo
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  4. 4
    Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G)

    Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) de réir Bérénice A. Benayoun, Sandrine Caburet, Aurélie Dipietromaria, Adrien Georges, Barbara D′haene, Eswari P. J. Pandaranayaka, David L’Hôte, Anne‐Laure Todeschini, S. Krishnaswamy, Marc Fellous, Elfride De Baere, Reiner A. Veitia

    Foilsithe / Cruthaithe 2010
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    Artigo
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  5. 5
    Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening

    Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening de réir Barbara D′haene, Catia Attanasio, Diane Beysen, Josée Dostie, Edmond G. Lemire, Philippe Bouchard, Michael Field, Kristie Jones, Birgit Lorenz, Björn Menten, Karen Buysse, Filip Pattyn, Marc Friedli, Catherine Ucla, Colette Rossier, Carine Wyss, Frank Speleman, Anne De Paepe, Job Dekker, Stylianos E. Antonarakis, Elfride De Baere

    Foilsithe / Cruthaithe 2009
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  6. 6
    Expanding the Spectrum of<i>FOXC1</i>and<i>PITX2</i>Mutations and Copy Number Changes in Patients with Anterior Segment Malformations

    Expanding the Spectrum of<i>FOXC1</i>and<i>PITX2</i>Mutations and Copy Number Changes in Patients with Anterior Segment Malformations de réir Barbara D′haene, Françoise Meire, Ilse Claerhout, Hester Y. Kroes, Astrid S. Plomp, Yvonne Arens, Thomy de Ravel, Ingele Casteels, Sarah De Jaegere, Sally Hooghe, Wim Wuyts, Jenneke van den Ende, Françoise Roulez, Hermine E. Veenstra‐Knol, Rogier A. Oldenburg, Jacques C. Giltay, Johanna B. G. M. Verheij, Jan-Tjeerd de Faber, Björn Menten, Anne De Paepe, Philippe Kestelyn, Bart P. Leroy, Elfride De Baere

    Foilsithe / Cruthaithe 2010
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