Reasonability of Frequent Laboratory Analyses during Therapy with Nivolumab and Nivolumab+Ipilimumab in Patients with Advanced or Metastatic Renal Cell Carcinoma during the Phase 2... von Franke, Klara, Foller, Susan, Rosero Moreno, Michele Estephania, Ali, Nalyan, Leistritz, Lutz, Leucht, Katharina, Grimm, Marc-Oliver

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Efficient removal of per- and polyfluoroalkyl substances (PFASs) in drinking water treatment: nanofiltration combined with active carbon or anion exchange von Franke, Vera, McCleaf, Philip, Lindegren, Klara, Ahrens, Lutz

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A Two-in-One Antibody against HER3 and EGFR Has Superior Inhibitory Activity Compared with Monospecific Antibodies von Schaefer, Gabriele, Haber, Lauric, Crocker, Lisa M., Shia, Steven, Shao, Lily, Dowbenko, Donald, Totpal, Klara, Wong, Anne, Lee, Chingwei V., Stawicki, Scott, Clark, Robyn, Fields, Carter, Lewis Phillips, Gail D., Prell, Rodney A., Danilenko, Dimitry M., Franke, Yvonne, Stephan, Jean-Philippe, Hwang, Jiyoung, Wu, Yan, Bostrom, Jenny, Sliwkowski, Mark X., Fuh, Germaine, Eigenbrot, Charles

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finDr: A web server for in silico D-peptide ligand identification von Engel, Helena, Guischard, Felix, Krause, Fabian, Nandy, Janina, Kaas, Paulina, Höfflin, Nico, Köhn, Maja, Kilb, Normann, Voigt, Karsten, Wolf, Steffen, Aslan, Tahira, Baezner, Fabian, Hahne, Salomé, Ruckes, Carolin, Weygant, Joshua, Zinina, Alisa, Akmeriç, Emir Bora, Antwi, Enoch B., Dombrovskij, Dennis, Franke, Philipp, Lesch, Klara L., Vesper, Niklas, Weis, Daniel, Gensch, Nicole, Di Ventura, Barbara, Öztürk, Mehmet Ali

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Exploring Hornstedtia scyphifera: an extensive multimethod phytochemical investigation reveals the chemical composition and bioactive potential von Kappen, Jonas, David, Andreea, Pieplow, Klara, Wujtschik, Annika, Ware, Ismail, Dhar, Dipendu, Wagner, Christoph, Davari, Mehdi D., Franke, Katrin, Wessjohann, Ludger A.

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology (vol 53, pg 1636... von van, Rheenen W, van, der Spek RAA, Bakker, MK, van, Vugt JJFA, Hop, PJ, Zwamborn, RAJ, de, Klein N, Westra, H-J, Bakker, OB, Deelen, P

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von van Rheenen, Wouter, van der Spek, Rick a A, Bakker, Mark K, van Vugt, Joke J F A, Hop, Paul J, Zwamborn, Ramona a J, de Klein, Niek, Westra, Harm-Jan, Bakker, Olivier B, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H P, van Eijk, Kristel R, Kooyman, Maarten, Byrne, Ross P, Doherty, Mark, Heverin, Mark, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley N, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke J, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, d'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'H, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stéphanie, Meininger, Vincent, Salachas, François, Mora Pardina, Jesus S, Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine a M, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia

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Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von van Rheenen, Wouter, van der Spek, Rick A.A, Bakker, Mark K, van Vugt, Joke J.F.A, Hop, Paul J, Zwamborn, Ramona A.J, de Klein, Niek, Westra, Harm-Jan, Bakker, Olivier B, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot M, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H.P, van Eijk, Kristel R, Kooyman, Maarten, Byrne, Ross P, Doherty, Mark, Heverin, Mark, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley N, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen E, Shaw, Pamela J, Hardy, John, Orrell, Richard W, Sendtner, Michael, Meyer, Thomas, Basak, Nazli, van der Kooi, Anneke J, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D'Alfonso, Sandra, Soraru, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chio, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert H, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stephanie, Meininger, Vincent, Salachas, Francois, Mora Pardina, Jesus S, Assialioui, Abdelilah, Rojas-Garcia, Ricardo, Dion, Patrick A, Ross, Jay P, Ludolph, Albert C, Weishaupt, Jochen H, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine A.M, Saker-Delye, Safa, Wood, Nicholas W, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia

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The Red Blood Cell NOS System after Blood Donation and Re-infusion in Moderately Trained Subjects von Willkomm, Lena, Polzer, Eric, Konou, Thierry, Balakirski, Galina, Bloch, Wilhelm, Franke, Julia, Marek, Eike, Hawener, Ina, Mank, Dennis, Hinrichs, Timo, Brixius, Klara, Platen, Petra

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The Red Blood Cells Nos System After Blood Donation And Re-infusion In Moderately Trained Subjects: 2980 Board #279 June 3 3:30 PM - 5:00 PM von Willkomm, Lena, Polzer, Eric, Konou, Thierry, Balakirski, Galina, Wilden, Maike, Bloch, Wilhelm, Franke, Julia, Marek, Eike, Hawener, Ina, Mank, Dennis, Hinrichs, Timo, Brixius, Klara, Platen, Petra

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The Red Blood Cells NOS System After Blood Donation And Re-infusion In Moderately Trained Subjects: 987 June 4 4:15 PM - 4:30 PM von Platen, Petra, Franke, Julia, Marek, Eike, Willkomm, Lena, Polzer, Eric, Hawener, Ina, Mank, Dennis, Hinrichs, Timo, Bloch, Wilhelm, Brixius, Klara

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Transforming the Hybrid Cloud for Emerging AI Workloads von Chen, Deming, Youssef, Alaa, Pendse, Ruchi, Schleife, André, Clark, Bryan K, Hamann, Hendrik, He, Jingrui, Laino, Teodoro, Varshney, Lav, Wang, Yuxiong, Sil, Avirup, Jabbarvand, Reyhaneh, Xu, Tianyin, Kindratenko, Volodymyr, Costa, Carlos, Adve, Sarita, Mendis, Charith, Zhang, Minjia, Núñez-Corrales, Santiago, Ganti, Raghu, Srivatsa, Mudhakar, Kim, Nam Sung, Torrellas, Josep, Huang, Jian, Seelam, Seetharami, Nahrstedt, Klara, Abdelzaher, Tarek, Eilam, Tamar, Zhao, Huimin, Manica, Matteo, Iyer, Ravishankar, Hirzel, Martin, Adve, Vikram, Marinov, Darko, Franke, Hubertus, Tong, Hanghang, Ainsworth, Elizabeth, Zhao, Han, Vasisht, Deepak, Do, Minh, Oliveira, Fabio, Pacifici, Giovanni, Puri, Ruchir, Nagpurkar, Priya

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Similarity Visualization for the Grouping of Forensic Speech Recordings von Weiand, Klara A., Bouten, Jos S., Veenman, Cor J.

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Transforming the Hybrid Cloud for Emerging AI Workloads von Chen, Deming, Youssef, Alaa, Pendse, Ruchi, Schleife, André, Clark, Bryan K, Hamann, Hendrik, He, Jingrui, Laino, Teodoro, Varshney, Lav, Wang, Yuxiong, Sil, Avirup, Jabbarvand, Reyhaneh, Xu, Tianyin, Kindratenko, Volodymyr, Costa, Carlos, Adve, Sarita, Mendis, Charith, Zhang, Minjia, Núñez-Corrales, Santiago, Ganti, Raghu, Srivatsa, Mudhakar, Nam Sung Kim, Torrellas, Josep, Huang, Jian, Seelam, Seetharami, Nahrstedt, Klara, Abdelzaher, Tarek, Eilam, Tamar, Zhao, Huimin, Manica, Matteo, Iyer, Ravishankar, Hirzel, Martin, Adve, Vikram, Marinov, Darko, Franke, Hubertus, Tong, Hanghang, Ainsworth, Elizabeth, Zhao, Han, Vasisht, Deepak, Do, Minh, Oliveira, Fabio, Pacifici, Giovanni, Puri, Ruchir, Nagpurkar, Priya

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Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Rheenen, Wouter van, Spek, Rick van der, Bakker, Mark, Berg, Leonard van den, Veldink, Jan, Vugt, Joke van, Hop, Paul, Zwamborn, Ramona, Klein, Niek de, Westra, Harm-Jan, Bakker, Olivier, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs, Eijk, Kristel van, Kooyman, Maarten, Byrne, Ross, Doherty, Mark, Heverin, Mark, Khleifat, Ahmad Al, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen, Shaw, Pamela, Hardy, John, Orrell, Richard, Sendtner, Michael, Meyer, Thomas, Basak, Nazli, Kooi, Anneke van der, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Pinter, Guiseppe Lauria, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D'Alfonso, Sandra, Soraru, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chio, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert, Bell, Shaugn, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stephanie, Meininger, Vincent, Salachas, Francois, Pardina, Jesus Mora, Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick, Ross, Jay, Ludolph, Albert, Weishaupt, Jochen, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Durr, Alexandra, Payan, Christine, Saker-Delye, Safa, Wood, Nicholas, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan

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Reproducible grey matter patterns index a multivariate, global alteration of brain structure in schizophrenia and bipolar disorder von Schwarz, Emanuel, Doan, Nhat Trung, Pergola, Giulio, Westlye, Lars T, Kaufmann, Tobias, Wolfers, Thomas, Brecheisen, Ralph, Quarto, Tiziana, Ing, Alex J, Di Carlo, Pasquale, Gurholt, Tiril P, Harms, Robbert L, Noirhomme, Quentin, Moberget, Torgeir, Agartz, Ingrid, Andreassen, Ole A, Bellani, Marcella, Bertolino, Alessandro, Blasi, Giuseppe, Brambilla, Paolo, Buitelaar, Jan K, Cervenka, Simon, Flyckt, Lena, Frangou, Sophia, Franke, Barbara, Hall, Jeremy, Heslenfeld, Dirk J, Kirsch, Peter, McIntosh, Andrew M, Noethen, Markus M, Papassotiropoulos, Andreas, de Quervain, Dominique J-F, Rietschel, Marcella, Schumann, Gunter, Tost, Heike, Witt, Stephanie H, Zink, Mathias, Meyer-Lindenberg, Andreas, Bettella, Francesco, Brandt, Christine L, Clarke, Toni-Kim, Coynel, David, Degenhardt, Franziska, Djurovic, Srdjan, Eisenacher, Sarah, Fastenrath, Matthias, Fatouros-Bergman, Helena, Forstner, Andreas J, Frank, Josef, Gambi, Francesco, Gelao, Barbara, Geschwind, Leo, Di Giannantonio, Massimo, Di Giorgio, Annabella, Hartman, Catharina A, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hoekstra, Pieter J, Hoffmann, Per, Hoogman, Martine, Jonsson, Erik G, Loos, Eva, Maggioni, Eleonora, Oosterlaan, Jaap, Papalino, Marco, Rampino, Antonio, Romaniuk, Liana, Selvaggi, Pierluigi, Sepede, Gianna, Sonderby, Ida E, Spalek, Klara, Sussmann, Jessika E, Thompson, Paul M, Vasquez, Alejandro Arias, Vogler, Christian, Whalley, Heather, Farde, L, Flyckt, L, Engberg, G, Erhardt, S, Fatouros-Bergman, H, Cervenka, S, Schwieler, L, Agartz, I, Collste, K, Victorsson, P, Malmqvist, A, Hedberg, M, Orhan, F

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Common and rare variant association analyses in Amyotrophic Lateral Sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology von Rheenen, Wouter van, van der Spek, Rick A.A, Bakker, Mark, Vugt, Joke J.F.A. van, Hop, Paul, Zwamborn, Ramona A.J, Klein, Niek de, Westra, Harm-Jan, Bakker, Olivier, Deelen, Patrick, Shireby, Gemma, Hannon, Eilis, Moisse, Matthieu, Baird, Denis, Restuadi, Restuadi, Dolzhenko, Egor, Dekker, Annelot, Gawor, Klara, Westeneng, Henk-Jan, Tazelaar, Gijs H.P, van Eijk, Kristel, Kooyman, Maarten, Byrne, Ross, Doherty, Mark, Heverin, Mark, Khleifat, Ahmad Al, Iacoangeli, Alfredo, Shatunov, Aleksey, Ticozzi, Nicola, Cooper-Knock, Johnathan, Smith, Bradley, Gromicho, Marta, Chandran, Siddharthan, Pal, Suvankar, Morrison, Karen, Shaw, Pamela, Hardy, John, Orrell, Richard, Sendtner, Michael, Meyer, Thomas, Başak, Nazli, van der Kooi, Anneke, Ratti, Antonia, Fogh, Isabella, Gellera, Cinzia, Lauria Pinter, Giuseppe, Corti, Stefania, Cereda, Cristina, Sproviero, Daisy, D'Alfonso, Sandra, Sorarù, Gianni, Siciliano, Gabriele, Filosto, Massimiliano, Padovani, Alessandro, Chiò, Adriano, Calvo, Andrea, Moglia, Cristina, Brunetti, Maura, Canosa, Antonio, Grassano, Maurizio, Beghi, Ettore, Pupillo, Elisabetta, Logroscino, Giancarlo, Nefussy, Beatrice, Osmanovic, Alma, Nordin, Angelica, Lerner, Yossef, Zabari, Michal, Gotkine, Marc, Baloh, Robert, Bell, Shaughn, Vourc'h, Patrick, Corcia, Philippe, Couratier, Philippe, Millecamps, Stéphanie, Meininger, Vincent, Salachas, François, Pardina, Jesus Mora, Assialioui, Abdelilah, Rojas-García, Ricardo, Dion, Patrick, Ross, Jay, Ludolph, Albert, Weishaupt, Jochen, Brenner, David, Freischmidt, Axel, Bensimon, Gilbert, Brice, Alexis, Dürr, Alexandra, Payan, Christine A.M, Saker-Delye, Safa, Wood, Nicholas, Topp, Simon, Rademakers, Rosa, Tittmann, Lukas, Lieb, Wolfgang, Franke, Andre, Ripke, Stephan, Braun, Alice, Kraft, Julia

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Human genome-guided identification of memory-modulating drugs von Papassotiropoulos, Andreas

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Vooys. Jaargang 14 von [tijdschrift] Vooys

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