Quality Prediction in Directed Energy Deposition Using Artificial Neural Networks Based on Process Signals von Marko, Angelina, Bähring, Stefan, Raute, Julius, Biegler, Max, Rethmeier, Michael

Volltext

Transferability of ANN-generated parameter sets from welding tracks to 3D-geometries in Directed Energy Deposition von Marko, Angelina, Bähring, Stefan, Raute, Julius, Biegler, Max, Rethmeier, Michael

Volltext

PDE3A mutations cause autosomal dominant hypertension with brachydactyly von Maass, Philipp G, Aydin, Atakan, Luft, Friedrich C, Schächterle, Carolin, Weise, Anja, Stricker, Sigmar, Lindschau, Carsten, Vaegler, Martin, Qadri, Fatimunnisa, Toka, Hakan R, Schulz, Herbert, Krawitz, Peter M, Parkhomchuk, Dmitri, Hecht, Jochen, Hollfinger, Irene, Wefeld-Neuenfeld, Yvette, Bartels-Klein, Eireen, Mühl, Astrid, Kann, Martin, Schuster, Herbert, Chitayat, David, Bialer, Martin G, Wienker, Thomas F, Ott, Jürg, Rittscher, Katharina, Liehr, Thomas, Jordan, Jens, Plessis, Ghislaine, Tank, Jens, Mai, Knut, Naraghi, Ramin, Hodge, Russell, Hopp, Maxwell, Hattenbach, Lars O, Busjahn, Andreas, Rauch, Anita, Vandeput, Fabrice, Gong, Maolian, Rüschendorf, Franz, Hübner, Norbert, Haller, Hermann, Mundlos, Stefan, Bilginturan, Nihat, Movsesian, Matthew A, Klussmann, Enno, Toka, Okan, Bähring, Sylvia

Volltext

KCND2 variants associated with global developmental delay differentially impair Kv4.2 channel gating von Zhang, Yongqiang, Tachtsidis, Georgios, Schob, Claudia, Koko, Mahmoud, Hedrich, Ulrike B S, Lerche, Holger, Lemke, Johannes R, van Haeringen, Arie, Ruivenkamp, Claudia, Prescott, Trine, Tveten, Kristian, Gerstner, Thorsten, Pruniski, Brianna, DiTroia, Stephanie, VanNoy, Grace E, Rehm, Heidi L, McLaughlin, Heather, Bolz, Hanno J, Zechner, Ulrich, Bryant, Emily, McDonough, Tiffani, Kindler, Stefan, Bähring, Robert

Volltext

Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity von Kalm, Tassja, Schob, Claudia, Völler, Hanna, Gardeitchik, Thatjana, Gilissen, Christian, Pfundt, Rolph, Klöckner, Chiara, Platzer, Konrad, Klabunde-Cherwon, Annick, Ries, Markus, Syrbe, Steffen, Beccaria, Francesca, Madia, Francesca, Scala, Marcello, Zara, Federico, Hofstede, Floris, Simon, Marleen E H, van Jaarsveld, Richard H, Oegema, Renske, van Gassen, Koen L I, Holwerda, Sjoerd J B, Barakat, Tahsin Stefan, Bouman, Arjan, van Slegtenhorst, Marjon, Álvarez, Sara, Fernández-Jaén, Alberto, Porta, Javier, Accogli, Andrea, Mancardi, Margherita Maria, Striano, Pasquale, Iacomino, Michele, Chae, Jong-Hee, Jang, SeSong, Kim, Soo Y, Chitayat, David, Mercimek-Andrews, Saadet, Depienne, Christel, Kampmeier, Antje, Kuechler, Alma, Surowy, Harald, Bertini, Enrico Silvio, Radio, Francesca Clementina, Mancini, Cecilia, Pizzi, Simone, Tartaglia, Marco, Gauthier, Lucas, Genevieve, David, Tharreau, Mylène, Azoulay, Noy, Zaks-Hoffer, Gal, Gilad, Nesia K, Orenstein, Naama, Bernard, Geneviève, Thiffault, Isabelle, Denecke, Jonas, Herget, Theresia, Kortüm, Fanny, Kubisch, Christian, Bähring, Robert, Kindler, Stefan

Volltext

Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity von Kalm, Tassja, Schob, Claudia, Völler, Hanna, Gardeitchik, Thatjana, Gilissen, Christian, Pfundt, Rolph, Klöckner, Chiara, Platzer, Konrad, Klabunde-Cherwon, Annick, Ries, Markus, Syrbe, Steffen, Beccaria, Francesca, Madia, Francesca, Scala, Marcello, Zara, Federico, Hofstede, Floris, Simon, Marleen E.H., van Jaarsveld, Richard H., Oegema, Renske, van Gassen, Koen L.I., Holwerda, Sjoerd J.B., Barakat, Tahsin Stefan, Bouman, Arjan, van Slegtenhorst, Marjon, Álvarez, Sara, Fernández-Jaén, Alberto, Porta, Javier, Accogli, Andrea, Mancardi, Margherita Maria, Striano, Pasquale, Iacomino, Michele, Chae, Jong-Hee, Jang, SeSong, Kim, Soo Y., Chitayat, David, Mercimek-Andrews, Saadet, Depienne, Christel, Kampmeier, Antje, Kuechler, Alma, Surowy, Harald, Bertini, Enrico Silvio, Radio, Francesca Clementina, Mancini, Cecilia, Pizzi, Simone, Tartaglia, Marco, Gauthier, Lucas, Genevieve, David, Tharreau, Mylène, Azoulay, Noy, Zaks-Hoffer, Gal, Gilad, Nesia K., Orenstein, Naama, Bernard, Geneviève, Thiffault, Isabelle, Denecke, Jonas, Herget, Theresia, Kortüm, Fanny, Kubisch, Christian, Bähring, Robert, Kindler, Stefan

Volltext

Inositol-1,4,5-trisphosphate 3-kinase A regulates dendritic morphology and shapes synaptic Ca2+ transients von Windhorst, Sabine, Minge, Daniel, Bähring, Robert, Hüser, Svenja, Schob, Claudia, Blechner, Christine, Lin, Hong-Ying, Mayr, Georg W., Kindler, Stefan

Volltext

Single nucleotide polymorphism map of five long-QT genes von Aydin, Atakan, Bähring, Sylvia, Dahm, Stefan, Guenther, Ulf P, Uhlmann, Regina, Busjahn, Andreas, Luft, Friedrich C

Volltext

Single nucleotide polymorphism map of five long-QT genes von AYDIN, Atakan, BÄHRING, Sylvia, DAHM, Stefan, GUENTHER, Ulf P, UHLMANN, Regina, BUSJAHN, Andreas, LUFT, Friedrich C

Volltext