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 TitleAuthors / EditorsDate
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Serial genomic inversions induce tissue-specific architectural stripes, gene misexpression and congenital malformations Kraft, Katerina; Magg, Andreas; Heinrich, Verena; Riemenschneider, Christina; ... Mundlos, Stefan 2019
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Preformed chromatin topology assists transcriptional robustness of Shh during limb development Paliou, Christina; Guckelberger, Philine; Schöpflin, Robert; Heinrich, Verena; ... Andrey, Guillaume 2019
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Characterization of glycosylphosphatidylinositol biosynthesis defects by clinical features, flow cytometry, and automated image analysis Knaus, Alexej; Pantel, Jean Tori; Pendziwiat, Manuela; Hajjir, Nurulhuda; ... Krawitz, Peter M 2018
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Dynamic 3D chromatin architecture contributes to enhancer specificity and limb morphogenesis Kragesteen, Bjørt K; Spielmann, Malte; Visel, Axel; Mundlos, Stefan; Andrey, Guillaume 2018
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Polymer physics predicts the effects of structural variants on chromatin architecture Bianco, Simona; Lupiáñez, Darío G; Chiariello, Andrea M; Annunziatella, Carlo; ... Nicodemi, Mario 2018
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The three-dimensional genome: regulating gene expression during pluripotency and development Andrey, Guillaume; Mundlos, Stefan 2017
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Characterization of hundreds of regulatory landscapes in developing limbs reveals two regimes of chromatin folding Andrey, Guillaume; Schöpflin, Robert; Jerković, Ivana; Heinrich, Verena; ... Mundlos, Stefan 2017
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Formation of new chromatin domains determines pathogenicity of genomic duplications Franke, Martin; Ibrahim, Daniel M; Andrey, Guillaume; Schwarzer, Wibke; ... Mundlos, Stefan 2016
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Deletions, Inversions, Duplications: Engineering of Structural Variants using CRISPR/Cas in Mice Kraft, Katerina; Geuer, Sinje; Will, Anja J; Chan, Wing Lee; ... Andrey, Guillaume 2015
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Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion Klopocki, Eva; Lohan, Silke; Doelken, Sandra C; Stricker, Sigmar; ... Mundlos, Stefan 2012
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Primary ciliary dyskinesia associated with normal axoneme ultrastructure is caused by DNAH11 mutations Schwabe, Georg C.; Hoffmann, Katrin; Loges, Niki Tomas; Birker, Daniel; ... Bartoloni, Lucia 2008