Rezultati - Schanze, Denny

GPFrontend and GPGraphics: graphical analysis tools for genetic association studies od Uebe, Steffen, Pasutto, Francesca, Krumbiegel, Mandy, Schanze, Denny, Ekici, Arif B, Reis, André

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Profiling of the Bacterial Microbiota along the Murine Alimentary Tract od Vilchez-Vargas, Ramiro, Salm, Franz, Znalesniak, Eva B., Haupenthal, Katharina, Schanze, Denny, Zenker, Martin, Link, Alexander, Hoffmann, Werner

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CTLA-4-mediated posttranslational modifications direct cytotoxic T-lymphocyte differentiation od Lingel, Holger, Wissing, Josef, Arra, Aditya, Schanze, Denny, Lienenklaus, Stefan, Klawonn, Frank, Pierau, Mandy, Zenker, Martin, Jänsch, Lothar, Brunner-Weinzierl, Monika C

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Insulin-signaling abnormalities in drug-naïve first-episode schizophrenia: Transduction protein analyses in extracellular vesicles of putative neuronal origin od Kapogiannis, Dimitrios, Dobrowolny, Henrik, Tran, Joyce, Mustapic, Maja, Frodl, Thomas, Meyer-Lotz, Gabriela, Schiltz, Kolja, Schanze, Denny, Rietschel, Marcella, Bernstein, Hans-Gert, Steiner, Johann

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Synaptic activity controls localization and function of CtBP1 via binding to Bassoon and Piccolo od Ivanova, Daniela, Dirks, Anika, Montenegro-Venegas, Carolina, Schöne, Cornelia, Altrock, Wilko D, Marini, Claudia, Frischknecht, Renato, Schanze, Denny, Zenker, Martin, Gundelfinger, Eckart D, Fejtova, Anna

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Behavioral and Neural Manifestations of Reward Memory in Carriers of Low-Expressing versus High-Expressing Genetic Variants of the Dopamine D2 Receptor od Richter, Anni, Barman, Adriana, Wüstenberg, Torsten, Soch, Joram, Schanze, Denny, Deibele, Anna, Behnisch, Gusalija, Assmann, Anne, Klein, Marieke, Zenker, Martin, Seidenbecher, Constanze, Schott, Björn H.

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Corrigendum: Valenced action/inhibition learning in humans is modulated by a genetic variant linked to dopamine D2 receptor expression od Richter, Anni, Guitart-Masip, Marc, Barman, Adriana, Libeau, Catherine, Behnisch, Gusalija, Czerney, Sophia, Schanze, Denny, Assmann, Anne, Klein, Marieke, Düzel, Emrah, Zenker, Martin, Seidenbecher, Constanze, Schott, Björn H.

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Valenced action/inhibition learning in humans is modulated by a genetic variant linked to dopamine D2 receptor expression od Richter, Anni, Guitart-Masip, Marc, Barman, Adriana, Libeau, Catherine, Behnisch, Gusalija, Czerney, Sophia, Schanze, Denny, Assmann, Anne, Klein, Marieke, Düzel, Emrah, Zenker, Martin, Seidenbecher, Constanze I., Schott, Björn H.

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Multiple Small Supernumerary Marker Chromosomes Resulting from Maternal Meiosis I or II Errors od Hochstenbach, Ron, Nowakowska, Beata, Volleth, Marianne, Ummels, Amber, Kutkowska-Kaźmierczak, Anna, Obersztyn, Ewa, Ziemkiewicz, Kamila, Gerloff, Claudia, Schanze, Denny, Zenker, Martin, Muschke, Petra, Schanze, Ina, Poot, Martin, Liehr, Thomas

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Gut microbial similarity in twins is driven by shared environment and aging od Vilchez-Vargas, Ramiro, Skieceviciene, Jurgita, Lehr, Konrad, Varkalaite, Greta, Thon, Cosima, Urba, Mindaugas, Morkūnas, Egidijus, Kucinskas, Laimutis, Bauraite, Karolina, Schanze, Denny, Zenker, Martin, Malfertheiner, Peter, Kupcinskas, Juozas, Link, Alexander

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Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy od Altmüller, Franziska, Pothula, Santosh, Annamneedi, Anil, Nakhaei-Rad, Saeideh, Montenegro-Venegas, Carolina, Pina-Fernández, Eneko, Marini, Claudia, Santos, Monica, Schanze, Denny, Montag, Dirk, Ahmadian, Mohammad R., Stork, Oliver, Zenker, Martin, Fejtova, Anna

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Correction: Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy od Altmüller, Franziska, Pothula, Santosh, Annamneedi, Anil, Nakhaei-Rad, Saeideh, Montenegro-Venegas, Carolina, Pina-Fernández, Eneko, Marini, Claudia, Santos, Monica, Schanze, Denny, Montag, Dirk, Ahmadian, Mohammad R., Stork, Oliver, Zenker, Martin, Fejtova, Anna

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Requirements Analysis and Specification for a Molecular Tumor Board Platform Based on cBioPortal od Buechner, Philipp, Hinderer, Marc, Unberath, Philipp, Metzger, Patrick, Boeker, Martin, Acker, Till, Haller, Florian, Mack, Elisabeth, Nowak, Daniel, Paret, Claudia, Schanze, Denny, von Bubnoff, Nikolas, Wagner, Sebastian, Busch, Hauke, Boerries, Melanie, Christoph, Jan

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Kras(P34R) and Kras(T58I) mutations induce distinct RASopathy phenotypes in mice od Wong, Jasmine C., Perez-Mancera, Pedro A., Huang, Tannie Q., Kim, Jangkyung, Grego-Bessa, Joaquim, del pilar Alzamora, Maria, Kogan, Scott C., Sharir, Amnon, Keefe, Susan H., Morales, Carolina E., Schanze, Denny, Castel, Pau, Hirose, Kentaro, Huang, Guo N., Zenker, Martin, Sheppard, Dean, Klein, Ophir D., Tuveson, David A., Braun, Benjamin S., Shannon, Kevin

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The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered od Brinkmann, Julia, Lissewski, Christina, Pinna, Valentina, Vial, Yoann, Pantaleoni, Francesca, Lepri, Francesca, Daniele, Paola, Burnyte, Birute, Cuturilo, Goran, Fauth, Christine, Gezdirici, Alper, Kotzot, Dieter, Güleç, Elif Yılmaz, Iotova, Violeta, Schanze, Denny, Ramond, Francis, Havlovicová, Markéta, Utine, Gulen Eda, Simsek-Kiper, Pelin Ozlem, Stoyanova, Milena, Verloes, Alain, De Luca, Alessandro, Tartaglia, Marco, Cavé, Hélène, Zenker, Martin

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Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1 od Slavotinek, Anne M, Baranzini, Sergio E, Schanze, Denny, Labelle-Dumais, Cassandre, Short, Kieran M, Chao, Ryan, Yahyavi, Mani, Bijlsma, Emilia K, Chu, Catherine, Musone, Stacey, Wheatley, Ashleigh, Kwok, Pui-Yan, Marles, Sandra, Fryns, Jean-Pierre, Maga, A Murat, Hassan, Mohamed G, Gould, Douglas B, Madireddy, Lohith, Li, Chumei, Cox, Timothy C, Smyth, Ian, Chudley, Albert E, Zenker, Martin

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Neu-Laxova Syndrome Is a Heterogeneous Metabolic Disorder Caused by Defects in Enzymes of the L-Serine Biosynthesis Pathway od Acuna-Hidalgo, Rocio, Schanze, Denny, Kariminejad, Ariana, Nordgren, Ann, Kariminejad, Mohamad Hasan, Conner, Peter, Grigelioniene, Giedre, Nilsson, Daniel, Nordenskjöld, Magnus, Wedell, Anna, Freyer, Christoph, Wredenberg, Anna, Wieczorek, Dagmar, Gillessen-Kaesbach, Gabriele, Kayserili, Hülya, Elcioglu, Nursel, Ghaderi-Sohi, Siavash, Goodarzi, Payman, Setayesh, Hamidreza, van de Vorst, Maartje, Steehouwer, Marloes, Pfundt, Rolph, Krabichler, Birgit, Curry, Cynthia, MacKenzie, Malcolm G., Boycott, Kym M., Gilissen, Christian, Janecke, Andreas R., Hoischen, Alexander, Zenker, Martin

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NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease od Martin, Paige B., Kigoshi-Tansho, Yu, Sher, Roger B., Ravenscroft, Gianina, Stauffer, Jennifer E., Kumar, Rajesh, Yonashiro, Ryo, Müller, Tina, Griffith, Christopher, Allen, William, Pehlivan, Davut, Haral, Tamar, Zenker, Martin, Howting, Denise, Schanze, Denny, Faqeih, Eissa A., Almontashiri, Naif A. M., Maroofian, Reza, Houlden, Henry, Mazaheri, Neda, Galehdari, Hamid, Douglas, Ganka, Posey, Jennifer E., Ryan, Monique, Lupski, James R., Laing, Nigel G., Joazeiro, Claudio A. P., Cox, Gregory A.

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Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease od Martin, Paige B., Kigoshi-Tansho, Yu, Sher, Roger B., Ravenscroft, Gianina, Stauffer, Jennifer E., Kumar, Rajesh, Yonashiro, Ryo, Müller, Tina, Griffith, Christopher, Allen, William, Pehlivan, Davut, Harel, Tamar, Zenker, Martin, Howting, Denise, Schanze, Denny, Faqeih, Eissa A., Almontashiri, Naif A. M., Maroofian, Reza, Houlden, Henry, Mazaheri, Neda, Galehdari, Hamid, Douglas, Ganka, Posey, Jennifer E., Ryan, Monique, Lupski, James R., Laing, Nigel G., Joazeiro, Claudio A. P., Cox, Gregory A.

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Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome od Capri, Yline, Flex, Elisabetta, Krumbach, Oliver H.F., Carpentieri, Giovanna, Cecchetti, Serena, Lißewski, Christina, Rezaei Adariani, Soheila, Schanze, Denny, Brinkmann, Julia, Piard, Juliette, Pantaleoni, Francesca, Lepri, Francesca R., Goh, Elaine Suk-Ying, Chong, Karen, Stieglitz, Elliot, Meyer, Julia, Kuechler, Alma, Bramswig, Nuria C., Sacharow, Stephanie, Strullu, Marion, Vial, Yoann, Vignal, Cédric, Kensah, George, Cuturilo, Goran, Kazemein Jasemi, Neda S., Dvorsky, Radovan, Monaghan, Kristin G., Vincent, Lisa M., Cavé, Hélène, Verloes, Alain, Ahmadian, Mohammad R., Tartaglia, Marco, Zenker, Martin

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