Atypical 22q11.2 Microduplication with “Typical” Signs and Overgrowth von Fischer, Matthias, Klopocki, Eva

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Catch Bonds Govern Adhesion through L-Selectin at Threshold Shear von Yago, Tadayuki, Wu, Jianhua, Wey, C. Diana, Klopocki, Arkadiusz G., Zhu, Cheng, McEver, Rodger P.

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Circulating soluble P-selectin must dimerize to promote inflammation and coagulation in mice von Panicker, Sumith R., Mehta-D'souza, Padmaja, Zhang, Nan, Klopocki, Arkadiusz G., Shao, Bojing, McEver, Rodger P.

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Disruptions of Topological Chromatin Domains Cause Pathogenic Rewiring of Gene-Enhancer Interactions von Lupiáñez, Darío G., Kraft, Katerina, Heinrich, Verena, Krawitz, Peter, Brancati, Francesco, Klopocki, Eva, Horn, Denise, Kayserili, Hülya, Opitz, John M., Laxova, Renata, Santos-Simarro, Fernando, Gilbert-Dussardier, Brigitte, Wittler, Lars, Borschiwer, Marina, Haas, Stefan A., Osterwalder, Marco, Franke, Martin, Timmermann, Bernd, Hecht, Jochen, Spielmann, Malte, Visel, Axel, Mundlos, Stefan

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Low Force Decelerates L-selectin Dissociation from P-selectin Glycoprotein Ligand-1 and Endoglycan von Sarangapani, Krishna K., Yago, Tadayuki, Klopocki, Arkadiusz G., Lawrence, Michael B., Fieger, Claudia B., Rosen, Steven D., McEver, Rodger P., Zhu, Cheng

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CNVs of noncoding cis -regulatory elements in human disease von Spielmann, Malte, Klopocki, Eva

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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis von Kortüm, Fanny, Das, Soma, Flindt, Max, Morris-Rosendahl, Deborah J, Stefanova, Irina, Goldstein, Amy, Horn, Denise, Klopocki, Eva, Kluger, Gerhard, Martin, Peter, Rauch, Anita, Roumer, Agathe, Saitta, Sulagna, Walsh, Laurence E, Wieczorek, Dagmar, Uyanik, Gökhan, Kutsche, Kerstin, Dobyns, William B

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Negative enrichment by immunomagnetic nanobeads for unbiased characterization of circulating tumor cells from peripheral blood of cancer patients von Liu, Zhian, Fusi, Alberto, Klopocki, Eva, Schmittel, Alexander, Tinhofer, Ingeborg, Nonnenmacher, Anika, Keilholz, Ulrich

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Generation of a CRISPR/Cas9-edited Plakoglobin (JUP) knock-out (JMUi001-A-4) iPSC line to model the cardiac phenotype of arrhythmogenic cardiomyopathy von Walz, Katharina, Janz, Anna, Klopocki, Eva, Gerull, Brenda

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Glycan Bound to the Selectin Low Affinity State Engages Glu-88 to Stabilize the High Affinity State under Force von Mehta-D'souza, Padmaja, Klopocki, Arkadiusz G., Oganesyan, Vaheh, Terzyan, Simon, Mather, Timothy, Li, Zhenhai, Panicker, Sumith R., Zhu, Cheng, McEver, Rodger P.

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Composition and dosage of a multipartite enhancer cluster control developmental expression of Ihh (Indian hedgehog) von Will, Anja J, Cova, Giulia, Osterwalder, Marco, Chan, Wing-Lee, Wittler, Lars, Brieske, Norbert, Heinrich, Verena, de Villartay, Jean-Pierre, Vingron, Martin, Klopocki, Eva, Visel, Axel, Lupiáñez, Darío G, Mundlos, Stefan

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Copy-Number Variations, Noncoding Sequences, and Human Phenotypes von Klopocki, Eva, Mundlos, Stefan

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Investigation of alpl expression and Tnap-activity in zebrafish implies conserved functions during skeletal and neuronal development von Ohlebusch, Barbara, Borst, Angela, Frankenbach, Tina, Klopocki, Eva, Jakob, Franz, Liedtke, Daniel, Graser, Stephanie

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DFNB16 is a frequent cause of congenital hearing impairment: implementation of STRC mutation analysis in routine diagnostics von Vona, B., Hofrichter, M.A.H., Neuner, C., Schröder, J., Gehrig, A., Hennermann, J.B., Kraus, F., Shehata-Dieler, W., Klopocki, E., Nanda, I., Haaf, T.

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On the traces of tcf12: Investigation of the gene expression pattern during development and cranial suture patterning in zebrafish (Danio rerio) von Blümel, Rabea, Zink, Miriam, Klopocki, Eva, Liedtke, Daniel

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Microarray expression profiling of fndc3a zebrafish mutants von Liedtke, Daniel, Klopocki, Eva

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E-selectin engages PSGL-1 and CD44 through a common signaling pathway to induce integrin αLβ2-mediated slow leukocyte rolling von Yago, Tadayuki, Shao, Bojing, Miner, Jonathan J., Yao, Longbiao, Klopocki, Arkadiusz G., Maeda, Kenichiro, Coggeshall, K. Mark, McEver, Rodger P.

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Generation of induced pluripotent stem cell line (UKWNLi008) derived from a patient carrying a c.1678C>G variant in the transient receptor potential cation channel subfamily A memb... von Schottmann, Nicole Michelle, Klug, Katharina, Klopocki, Eva, Üçeyler, Nurcan

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P18-08 Identification of transcriptional biomarkers of nephrotoxicity in zebrafish larvae von Bauer, B., Liedtke, D., Unsöld, J., Klopocki, E., Mally, A.

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Generation of two induced pluripotent stem cell lines UKWNLi006 and UKWNLi007 derived from two patients with an active site GLA mutation leading to a pain and no pain phenotype in... von Klug, Katharina, Breyer, Maximilian, Klopocki, Eva, Üçeyler, Nurcan

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