G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth von Pasternack, Sandra M, Molderings, Gerhard J, Voss, Katrin, Betz, Regina C, Nöthen, Markus M, Aboud, Khalid Al, Lee, Young-Ae, Hillmer, Axel M, Ramirez, Alfredo, Rüschendorf, Franz, Nürnberg, Peter, Franz, Thomas, von Kügelgen, Ivar

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Acoustic communication in noise: regulation of call characteristics in a New World monkey von Brumm, Henrik, Voss, Katrin, Köllmer, Ireen, Todt, Dietmar

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Maps of open chromatin highlight cell type-restricted patterns of regulatory sequence variation at hematological trait loci von Paul, Dirk S, Albers, Cornelis A, Rendon, Augusto, Voss, Katrin, Stephens, Jonathan, van der Harst, Pim, Chambers, John C, Soranzo, Nicole, Ouwehand, Willem H, Deloukas, Panos

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A GWAS sequence variant for platelet volume marks an alternative DNM3 promoter in megakaryocytes near a MEIS1 binding site von Nürnberg, Sylvia T., Rendon, Augusto, Smethurst, Peter A., Paul, Dirk S., Voss, Katrin, Thon, Jonathan N., Lloyd-Jones, Heather, Sambrook, Jennifer G., Tijssen, Marloes R., Italiano, Joseph E., Deloukas, Panos, Gottgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H.

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Inhibition of Notch signaling biases rat thymocyte development towards the NK cell lineage von van den Brandt, Jens, Voss, Katrin, Schott, Melanie, Hünig, Thomas, Wolfe, Michael S., Reichardt, Holger M.

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Transcriptional diversity during lineage commitment of human blood progenitors von Chen, Lu, Kostadima, Myrto, Martens, Joost H. A., Canu, Giovanni, Garcia, Sara P., Turro, Ernest, Downes, Kate, Macaulay, Iain C., Bielczyk-Maczynska, Ewa, Coe, Sophia, Farrow, Samantha, Poudel, Pawan, Burden, Frances, Jansen, Sjoert B. G., Astle, William J., Attwood, Antony, Bariana, Tadbir, de Bono, Bernard, Breschi, Alessandra, Chambers, John C., Consortium, BRIDGE, Choudry, Fizzah A., Clarke, Laura, Coupland, Paul, van der Ent, Martijn, Erber, Wendy N., Jansen, Joop H., Favier, Rémi, Fenech, Matthew E., Foad, Nicola, Freson, Kathleen, van Geet, Chris, Gomez, Keith, Guigo, Roderic, Hampshire, Daniel, Kelly, Anne M., Kerstens, Hindrik H. D., Kooner, Jaspal S., Laffan, Michael, Lentaigne, Claire, Labalette, Charlotte, Martin, Tiphaine, Meacham, Stuart, Mumford, Andrew, Nürnberg, Sylvia, Palumbo, Emilio, van der Reijden, Bert A., Richardson, David, Sammut, Stephen J., Slodkowicz, Greg, Tamuri, Asif U., Vasquez, Louella, Voss, Katrin, Watt, Stephen, Westbury, Sarah, Flicek, Paul, Loos, Remco, Goldman, Nick, Bertone, Paul, Read, Randy J., Richardson, Sylvia, Cvejic, Ana, Soranzo, Nicole, Ouwehand, Willem H., Stunnenberg, Hendrik G., Frontini, Mattia, Rendon, Augusto

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Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome von Albers, Cornelis A, Ouwehand, Willem H, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross N W, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita

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New gene functions in megakaryopoiesis and platelet formation von Gieger, Christian, Radhakrishnan, Aparna, Cvejic, Ana, Tang, Weihong, Pistis, Giorgio, Serbanovic-Canic, Jovana, Elling, Ulrich, Goodall, Alison H., Labrune, Yann, Lopez, Lorna M., Meacham, Stuart, Sorice, Rossella, Teumer, Alexander, Ramirez-Solis, Ramiro, Ellinghaus, David, Gögele, Martin, Hottenga, Jouke-Jan, Langenberg, Claudia, Kovacs, Peter, O’Reilly, Paul F., Shin, So-Youn, Murgia, Federico, Parsa, Afshin, Stephens, Jonathan, Ellen van der Schoot, C., Allayee, Hooman, Attwood, Antony, Baumeister, Sebastian E., Biino, Ginevra, Cambien, François, Cucca, Francesco, de Boer, Rudolf A., Erdmann, Jeanette, Evans, David M., Falchi, Mario, Feng, Wei, Folsom, Aaron R., Frazer, Ian H., Gibson, Quince D., Glazer, Nicole L., Hartikainen, Anna-Liisa, Heckbert, Susan R., Hersch, Micha, Illig, Thomas, Kühnel, Brigitte, Lagou, Vasiliki, Lloyd-Jones, Heather, Lumley, Thomas, Maschio, Andrea, Mateo Leach, Irene, McKnight, Barbara, Memari, Yasin, Montgomery, Grant W., Nakamura, Yusuke, Nauck, Matthias, Nöthlings, Ute, Nolte, Ilja M., Pouta, Anneli, Ruggiero, Daniela, Sala, Cinzia, Sambrook, Jennifer, Schlessinger, David, Scott, James, Smith, Nicholas L., Snieder, Harold, Starr, John M., Stumvoll, Michael, Wilson Tang, W. H., Tenesa, Albert, Uda, Manuela, Visscher, Peter M., Völker, Uwe, Willemsen, Gonneke, Yang, Tsun-Po, Zitting, Paavo, Dedoussis, George V., Metspalu, Andres, Shuldiner, Alan R., Joost van Pelt, L., Zwaginga, Jaap-Jan, Franke, Andre, Froguel, Philippe, Jarvelin, Marjo-Riitta, Martin, Nicholas G., Meisinger, Christa, Psaty, Bruce M., Spector, Timothy D., Wareham, Nicholas J., Akkerman, Jan-Willem N., Ciullo, Marina, Deloukas, Panos, Jupe, Steve, Khadake, Jyoti, Kooner, Jaspal S., Penninger, Josef, Stemple, Derek, Wernisch, Lorenz, Sanna, Serena, Rendon, Augusto, Soranzo, Nicole

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Seventy-five genetic loci influencing the human red blood cell von Zhang, Weihua, Sehmi, Joban, Paul, Dirk S., Allayee, Hooman, Li, Xinzhong, Tan, Sian-Tsung, Voss, Katrin, Weichenberger, Christian X., Asselbergs, Folkert W., Franke, Lude, Gögele, Martin, Holm, Hilma, Hottenga, Jouke-Jan, Kleber, Marcus E., Lagou, Vasiliki, Langenberg, Claudia, Lopez, Lorna M., Lyytikäinen, Leo-Pekka, Melander, Olle, Murgia, Federico, Nolte, Ilja M., Porcu, Eleonora, Portas, Laura, Prokopenko, Inga, Ulivi, Sheila, Westra, Harm-Jan, Hua Zhao, Jing, Anni, Franco, Abdellaoui, Abdel, Attwood, Antony, Bastardot, François, Das, Debashish, Döring, Angela, Engström, Gunnar, Ingi Eyjolfsson, Gudmundur, Ferrucci, Luigi, Fischer, Krista, Garner, Stephen F., Gibson, Quince D., Girotto, Giorgia, Fannar Gudbjartsson, Daniel, Hastie, Claire E., Hedblad, Bo, Illig, Thomas, Jolley, Jennifer, Kema, Ido P., Lloyd-Jones, Heather, Meisinger, Christa, Memari, Yasin, Mihailov, Evelin, Nauck, Matthias, Nutile, Teresa, Parracciani, Debora, Penninx, Brenda W., Perseu, Lucia, Piga, Antonio, Pistis, Giorgio, Puc, Ursula, Ring, Susan M., Robino, Antonietta, Saint-Pierre, Aude, Salumets, Andres, Schepers, Hein, Smit, Johannes H., Starr, John M., Stephens, Jonathan, Sulem, Patrick, Tanaka, Toshiko, Tragante, Vinicius, van Gilst, Wiek H., Joost van Pelt, L., van Veldhuisen, Dirk J., Winkelmann, Bernhard R., Cucca, Francesco, Elliott, Paul, Fortina, Paolo, Froguel, Philippe, Gasparini, Paolo, Maerz, Winfried, Moore, Carmel, Pirastu, Mario, Ramirez-Solis, Ramiro, Schadt, Eric, Shuldiner, Alan R., Davey Smith, George, Gustav Smith, J., Sorice, Rossella, Spector, Tim D., Stefansson, Kari, Tönjes, Anke, Wolffenbuttel, Bruce H. R., Boomsma, Dorret I., Dedoussis, George V., Deloukas, Panos, Ferreira, Manuel A., Martin Penninger, Josef, Gieger, Christian, Kooner, Jaspal S., Ouwehand, Willem H., Soranzo, Nicole

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CCM3 interacts with CCM2 indicating common pathogenesis for cerebral cavernous malformations von VOSS, Katrin, STAHL, Sonja, SCHLEIDER, Elisa, ULLRICH, Sybille, NICKEL, Joachim, MUELLER, Thomas D, FELBOR, Ute

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Competencies for virtual teamwork : Development and validation of a web-based selection tool for members of distributed teams von HERTEL, Guido, KONRADT, Udo, VOSS, Katrin

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Functional analyses of human and zebrafish 18-amino acid in-frame deletion pave the way for domain mapping of the cerebral cavernous malformation 3 protein von Voss, Katrin, Stahl, Sonja, Hogan, Benjamin M, Reinders, Joerg, Schleider, Elisa, Schulte-Merker, Stefan, Felbor, Ute

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Novel CCM1, CCM2, and CCM3 mutations in patients with cerebral cavernous malformations: in-frame deletion in CCM2 prevents formation of a CCM1/CCM2/CCM3 protein complex von Stahl, Sonja, Gaetzner, Sabine, Voss, Katrin, Brackertz, Bettina, Schleider, Elisa, Sürücü, Oguzkan, Kunze, Ekkehard, Netzer, Christian, Korenke, Christoph, Finckh, Ulrich, Habek, Mario, Poljakovic, Zdravka, Elbracht, Miriam, Rudnik-Schöneborn, Sabine, Bertalanffy, Helmut, Sure, Ulrich, Felbor, Ute

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Transcriptional diversity during lineage commitment of human blood progenitors von Chen, Lu, Kostadima, Myrto, Martens, Joost H.A, Canu, Giovanni, Garcia, Sara P, Turro, Ernest, Downes, Kate, Macaulay, Iain C, Bielczyk-Maczynska, Ewa, Coe, Sophia, Farrow, Samantha, Poudel, Pawan, Burden, Frances, Jansen, Sjoert B.G, Astle, William J, Attwood, Antony, Bariana, Tadbir, de Bono, Bernard, Breschi, Alessandra, Chambers, John C, BRIDGE Consortium, Choudry, Fizzah A, Clarke, Laura, Coupland, Paul, van der Ent, Martijn, Erber, Wendy N, Jansen, Joop H, Favier, Rémi, Fenech, Matthew E, Foad, Nicola, Freson, Kathleen, Van Geet, Chris, Gomez, Keith, Guigo, Roderic, Hampshire, Daniel, Kelly, Anne M, Kerstens, Hindrik H.D, Kooner, Jaspal S, Laffan, Michael, Lentaigne, Claire, Labalette, Charlotte, Martin, Tiphaine, Meacham, Stuart, Mumford, Andrew, Nürnberg, Sylvia, Palumbo, Emilio, van der Reijden, Bert A, Richardson, David, Sammut, Stephen J, Slodkowicz, Greg, Tamuri, Asif U, Vasquez, Louella, Voss, Katrin, Watt, Stephen, Westbury, Sarah, Flicek, Paul, Loos, Remco, Goldman, Nick, Bertone, Paul, Read, Randy J, Richardson, Sylvia, Cvejic, Ana, Soranzo, Nicole, Ouwehand, Willem H, Stunnenberg, Hendrik G, Frontini, Mattia, Rendon, Augusto

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Exome sequencing identifies NBEAL2 as the causative genefor gray platelet syndrome von Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross N W, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H

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Competencies for virtual teamwork: Developmentand validation of a web-based selection tool for members of distributed teams von Hertel, Guido, Konradt, Udo, Voss, Katrin

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Identifizierung und Charakterisierung von Interaktiopnspartnern des humanen CCM3-Proteins von Voß, Katrin

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Transcriptional diversity during lineage commitment of human blood progenitors von Chen, Lu, Kostadima, Myrto, Martens, Joost HA, Canu, Giovanni, Garcia, Sara P, Turro, Ernest, Downes, Kate, Macaulay, Iain C, Bielczyk-Maczynska, Ewa, Coe, Sophia, Farrow, Samantha, Poudel, Pawan, Burden, Frances, Jansen, Sjoert BG, Astle, William J, Attwood, Antony, Bariana, Tadbir, de Bono, Bernard, Breschi, Alessandra, Chambers, John C, Consortium, Bridge, Choudry, Fizzah A, Clarke, Laura, Coupland, Paul, van der Ent, Martijn, Erber, Wendy N, Jansen, Joop H, Favier, Rémi, Fenech, Matthew E, Foad, Nicola, Freson, Kathleen, van Geet, Chris, Gomez, Keith, Guigo, Roderic, Hampshire, Daniel, Kelly, Anne M, Kerstens, Hindrik HD, Kooner, Jaspal S, Laffan, Michael, Lentaigne, Claire, Labalette, Charlotte, Martin, Tiphaine, Meacham, Stuart, Mumford, Andrew, Nürnberg, Sylvia, Palumbo, Emilio, van der Reijden, Bert A, Richardson, David, Sammut, Stephen J, Slodkowicz, Greg, Tamuri, Asif U, Vasquez, Louella, Voss, Katrin, Watt, Stephen, Westbury, Sarah, Flicek, Paul, Loos, Remco, Goldman, Nick, Bertone, Paul, Read, Randy J, Richardson, Sylvia, Cvejic, Ana, Soranzo, Nicole, Ouwehand, Willem H, Stunnenberg, Hendrik G, Frontini, Mattia, Rendon, Augusto

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Exome sequencing identifies NBEAL2 as the causative gene for gray platelet syndrome von Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H

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Experten erwarten weitere Preiserhöhungen bei Strom, Gas und Öl von Voss, Katrin

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