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(46) de la Rosa, Kathrin Prof. Dr. (2) Diebolder, Christoph Dr. (2) Diecke, Sebastian Dr. (10) Di Virgilio, Michela Prof. Dr. (2) Dörr, Jan Rafael (1) Escobar Fernandez, Helena Dr. (1) Estebanez, Luc Dr. (1) Fälber, Katja Dr. (2) Falcke, Martin Prof. Dr. (8) Falk, Kirsten Dr. (4) Fielitz, Jens Dr. (7) Fischer, Christian (5) Forslund, Sofia Dr. (5) Frahm, Silke Dr. (2) Gargiulo, Gaetano Dr. (4) Gerlach, Kerstin (2) Gorski, Stan Dr. (3) Gösele, Claudia Dr. (1) Gotthardt, Michael Prof. Dr. (12) Gouti, Mina Dr. (2) Graf, Robin Dr. (1) Grobe, Jenny (1) Grossmann, Katja Dr. (4) Grosswendt, Stefanie Dr. (2) Grybowski, Andrea (1) Haas, Simon Dr. rer. nat. (4) Haase, Nadine Dr. (3) Hammes-Lewin, Annette Dr. (3) Hänig, Christian (1) Harabula, Izabela-Cezara (1) Haseleu, Julia Dr. (1) Haucke, Volker Professor (5) Hedtrich, Sarah Prof. Dr. (12) Heinemann, Udo Prof. Dr. (25) Henssen, Anton Prof. Dr. med. 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(2) Leutz, Achim Prof. Dr. (22) Lewin, Gary Prof. Dr. (26) Lisewski, Ulrike Dr. (2) Lisowski, Pawel Dr. (1) Ludwig, Leif S. Dr. med. Dr. rer. nat. (1) Luft, Friedrich Prof. Dr. (216) Luganskaja, Tatjana (1) Lupianez Garcia, Dario Jesus Dr. (3) Lusatis, Simone (1) Lutter, Steffen (1) Maatz, Henrike Dr. (2) Mahmoodzadeh, Shokoufeh PD Dr. (4) Marenholz, Ingo Dr. (7) Marg, Andreas Dr. (2) Marko, Lajos Dr. (7) Mastrobuoni, Guido Dr. (4) Mathas, Stephan Dr. (8) Mekle, Ralf (1) Mertins, Philipp Dr. (11) Metzger, Jakob Johannes Dr. (4) Meyer, Irmtraud Margret Prof. Dr. (4) Millward, Jason Dr. (5) Morano, Ingo Prof. Dr. (20) Müller, Dominik Prof. Dr. (40) Müller, Gerd Dr. (4) Müller, Thomas Dr. (5) Münchberg, Stefanie (1) Na, Il-Kang Dr. (10) Neuendorf, Nancy (1) Nguyen, Tam Hoai Dr. (1) Niendorf, Thoralf Prof. Dr. (47) Nimptsch, Katharina Dr. (7) Niquet, Sylvia (1) Nolte, Christiane Dr. (4) Obermayer-Wasserscheid, Benedikt Dr. (7) Ofenbauer, Andreas Dr. (1) Ohler, Uwe Prof. Dr. (22) Panakova, Daniela Dr. (3) Patone, Giannino Dr. (4) Paul, Friedemann Prof. Dr. med. (68) Perrot, Andreas (15) Pezzutto, Antonio Prof. Dr. (15) Piazza, Ilaria Dr. (2) Pilz, Bernhard Dr. (3) Pischon, Tobias Prof. Dr. (43) Pombo, Ana Prof. Dr. (12) Popova, Elena Dr. (5) Potente, Michael Prof. Dr. (4) Poulet, James Prof. Dr. (6) Preibisch, Stephan Dr. (4) Qadri, Fatimunnisa Dr. (8) Quedenau, Claudia (1) Quensel, Christina Dr. (1) Rademann, Joerg Prof. Dr. (2) Radke, Michael Dr. (2) Rahn, Hans-Peter Dr. (3) Rajewsky, Klaus Prof. Dr. (15) Rajewsky, Nikolaus Prof. Dr. (25) Rehm, Armin Dr. (4) Rhein, Simone Dr. (1) Robson, Michael Dr. (2) Rocks, Oliver Dr. (13) Rosenthal, Walter Prof. Dr. (6) Roske, Yvette Dr. (4) Rother, Franziska Dr. (1) Rousselle, Anthony (3) Rybak-Wolf, Agnieszka Dr. (4) Saar, Kathrin Dr. (15) Sander, Maike Prof. Dr. (16) Sattentau, Quentin James Prof. Dr. (16) Sawamiphak, Suphansa Dr. (2) Schäfer, Gesa Dr. (1) Scheidereit, Claus Prof. Dr. (18) Schiattarella, Gabriele G. Dr. (16) Schlag, Peter M. Prof. Dr. (77) Schlegel, Wolfgang-Peter (2) Schmidt, Deborah (2) Schmidt, Willi Dr. (1) Schmidt-Krüger, Vanessa Dr. (4) Schmidt-Ullrich, Ruth Dr. (5) Schmitt, Clemens Prof. Dr. (7) Schreiber, Adrian PD Dr. med. 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Schmidt G. Ter-Avetisyan F.G. Rathjen September 2013 / J Tissue Eng Regen Med Teratoma formation of human embryonic stem cells in three-dimensional perfusion culture bioreactors H. Stachelscheid A. Wulf-Goldenberg K. Eckert J. Jensen J. Edsbagge P. Bjoerquist M. Rivero R. Strehl J. Jozefczuk A. Prigione J. Adjaye T. Urbaniak P. Bussmann K. Zeilinger J.C. Gerlach 11. Juli 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen November 2013 / Eur J Neurosci Impaired presynaptic function and elimination of synapses at premature stages during postnatal development of the cerebellum in the absence of CALEB (CSPG5/neuroglycan C) R. Jüttner D. Montag R.B. Craveiro A. Babich P. Vetter F.G. Rathjen August 2013 / Am J Med Genet C Semin Med Genet Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7 A.M. Vermeer K. van Engelen A.V. Postma M.J. Baars I. Christiaans S. De Haij S. Klaassen B.J. Mulder B. Keavney Juni 2013 / Neurochem Res Regulation of adhesion by flexible ectodomains of IgCAMs H. Volkmer J. Schreiber F.G. Rathjen 09. April 2014 / Commun Integr Biol Tissue guidance without filopodia A. Wacker H. Gerhardt L.K. Phng 06. Oktober 2014 / J R Soc Interface Computer simulations reveal complex distribution of haemodynamic forces in a mouse retina model of angiogenesis M.O. Bernabeu M.L. Jones J.H. Nielsen T. Krüger R.W. Nash D. Groen S. Schmieschek J. Hetherington H. Gerhardt C.A. Franco P.V. Coveney 01. Dezember 2014 / Hum Mol Genet Lack of CCM1 induces hypersprouting and impairs response to flow T.M. Mleynek A.C. Chan M. Redd C.C. Gibson C.T. Davis D.S. Shi T. Chen K.L. Carter J. Ling R. Blanco H. Gerhardt K. Whitehead D.Y. Li Januar 2014 / Development Crim1 maintains retinal vascular stability during development by regulating endothelial cell Vegfa autocrine signaling J. Fan V.G. Ponferrada T. Sato S. Vemaraju M. Fruttiger H. Gerhardt N. Ferrara R. A. Lang Seitennummerierung Erste Seite « First Vorherige Seite ‹ Previous … Seite 2 Aktuelle Seite 3 Seite 4 Seite 5 … Nächste Seite Next › Letzte Seite Last »
2013 / Methods Mol Biol A genetic strategy for the analysis of individual axon morphologies in cGMP signalling mutant mice H. Schmidt G. Ter-Avetisyan F.G. Rathjen
September 2013 / J Tissue Eng Regen Med Teratoma formation of human embryonic stem cells in three-dimensional perfusion culture bioreactors H. Stachelscheid A. Wulf-Goldenberg K. Eckert J. Jensen J. Edsbagge P. Bjoerquist M. Rivero R. Strehl J. Jozefczuk A. Prigione J. Adjaye T. Urbaniak P. Bussmann K. Zeilinger J.C. Gerlach
11. Juli 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen
November 2013 / Eur J Neurosci Impaired presynaptic function and elimination of synapses at premature stages during postnatal development of the cerebellum in the absence of CALEB (CSPG5/neuroglycan C) R. Jüttner D. Montag R.B. Craveiro A. Babich P. Vetter F.G. Rathjen
August 2013 / Am J Med Genet C Semin Med Genet Ebstein anomaly associated with left ventricular noncompaction: an autosomal dominant condition that can be caused by mutations in MYH7 A.M. Vermeer K. van Engelen A.V. Postma M.J. Baars I. Christiaans S. De Haij S. Klaassen B.J. Mulder B. Keavney
Juni 2013 / Neurochem Res Regulation of adhesion by flexible ectodomains of IgCAMs H. Volkmer J. Schreiber F.G. Rathjen
09. April 2014 / Commun Integr Biol Tissue guidance without filopodia A. Wacker H. Gerhardt L.K. Phng
06. Oktober 2014 / J R Soc Interface Computer simulations reveal complex distribution of haemodynamic forces in a mouse retina model of angiogenesis M.O. Bernabeu M.L. Jones J.H. Nielsen T. Krüger R.W. Nash D. Groen S. Schmieschek J. Hetherington H. Gerhardt C.A. Franco P.V. Coveney
01. Dezember 2014 / Hum Mol Genet Lack of CCM1 induces hypersprouting and impairs response to flow T.M. Mleynek A.C. Chan M. Redd C.C. Gibson C.T. Davis D.S. Shi T. Chen K.L. Carter J. Ling R. Blanco H. Gerhardt K. Whitehead D.Y. Li
Januar 2014 / Development Crim1 maintains retinal vascular stability during development by regulating endothelial cell Vegfa autocrine signaling J. Fan V.G. Ponferrada T. Sato S. Vemaraju M. Fruttiger H. Gerhardt N. Ferrara R. A. Lang