Výsledky vyhledávání - Barbara D′haene
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Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain Autor 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
Vydáno 2013Artigo -
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Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G) Autor 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
Vydáno 2010Artigo -
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Disease-Causing 7.4 kb Cis-Regulatory Deletion Disrupting Conserved Non-Coding Sequences and Their Interaction with the FOXL2 Promotor: Implications for Mutation Screening Autor 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
Vydáno 2009Artigo -
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Expanding the Spectrum of<i>FOXC1</i>and<i>PITX2</i>Mutations and Copy Number Changes in Patients with Anterior Segment Malformations Autor 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
Vydáno 2010Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Computational biology
Copy-number variation
Gene expression
Genome
Mutation
Computer science
Operating system
Profiling (computer programming)
Andrology
Anthropology
Base sequence
Breakpoint
Cancer research
Chromosomal translocation
Coding region
Comparative genomic hybridization
Conserved sequence
Context (archaeology)
DNA
DNA sequencing
Data mining
Database
Dysgenesis
Exon
Gene expression profiling
Germline mutation
Granulosa cell