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(46) de la Rosa, Kathrin Prof. Dr. (4) 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-Barske, 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. (2) Herse, Florian PD Dr. (8) Herzog, Margareta (3) Heuser, Arnd Dr. (4) Hinz, Michael Dr. (2) Hofstätter, Maria (3) Höpken, Uta Elisabeth PD Dr. (9) Hörnberg, Hanna Dr. (2) Hübner, Norbert Prof. Dr. (48) Hummel, Oliver (7) Infante Duarte, Carmen (8) Ittermann, Bernd Dr. (1) Ivics, Zoltan Dr. (23) Izsvak, Zsuzsanna Dr. (26) Janke, Jürgen Dr. (8) Janz, Martin Dr. (7) Jarosch, Ernst Dr. (6) Jentsch, Thomas Prof. Dr. (42) Jouhanneau, Jean-Sebastien Dr. (1) Jung, Simone (1) Junker, Jan Philipp Prof. Dr. (5) Jüttner, Rene Dr. (4) Kainmüller, Dagmar Prof. Dr. (4) Kamer, Ilona (1) Kaminski, Michael Dr. (1) Kammertöns, Thomas Dr. (7) Keller, Ulrich Dr. med. 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(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) Prigione, Alessandro Prof. Dr. (8) 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. 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Januar 2014 / Am J Hum Genet Reponse to De Leeuw and Houge A.K. Arndt C.A. Macrae S. Klaassen 09. Juli 2001 / J Cell Biol Targeted ablation of NrCAM or ankyrin-B results in disorganized lens fibers leading to cataract formation M.I. More F.P. Kirsch F.G. Rathjen 24. Februar 1997 / J Cell Biol Chicken acidic leucine-rich EGF-like domain containing brain protein (CALEB), a neural member of the EGF family of differentiation factors, is implicated in neurite formation S. Schumacher H. Volkmer F. Buck A. Otto A. Tarnok S. Roth F.G. Rathjen 01. Januar 2001 / J Neurocytol Tenascin-R associates extracellularly with parvalbumin immunoreactive neurones but is synthesised by another neuronal population in the adult rat cerebral cortex E.S. Wintergerst F.G. Rathjen B. Schwaller P. Eggli M.R. Celio 03. April 2014 / Am J Hum Genet Rare variants in NR2F2 cause congenital heart defects in humans S. Al Turki A.K. Manickaraj C.L. Mercer S.S. Gerety M.P. Hitz S. Lindsay L.C.A. D'Alessandro G.J. Swaminathan J. Bentham A.K. Arndt J. Low J. Breckpot M. Gewillig B. Thienpont H. Abdul-Khaliq C. Harnack K. Hoff H.H. Kramer S. Schubert R. Siebert O. Toka C. Cosgrove H. Watkins A.M. Lucassen I.M. O'Kelly A.P. Salmon F.A. Bu'Lock J. Granados-Riveron K. Setchfield C. Thornborough J.D. Brook B. Mulder S. Klaassen S. Bhattacharya K. Devriendt D.F. Fitzpatrick D.I. Wilson S. Mital M.E. Hurles 29. April 2014 / BMC Med Genet Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2) S. Froehler M. Kieslich C. Langnick M. Feldkamp B. Opgen-Rhein F. Berger J.C. Will W. Chen 01. Juni 2013 / Neurochem Res Regulation of adhesion by flexible ectodomains of IgCAMs H. Volkmer J. Schreiber F.G. Rathjen 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 01. 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 01. 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 Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 … Nächste Seite Next › Letzte Seite Last »
09. Juli 2001 / J Cell Biol Targeted ablation of NrCAM or ankyrin-B results in disorganized lens fibers leading to cataract formation M.I. More F.P. Kirsch F.G. Rathjen
24. Februar 1997 / J Cell Biol Chicken acidic leucine-rich EGF-like domain containing brain protein (CALEB), a neural member of the EGF family of differentiation factors, is implicated in neurite formation S. Schumacher H. Volkmer F. Buck A. Otto A. Tarnok S. Roth F.G. Rathjen
01. Januar 2001 / J Neurocytol Tenascin-R associates extracellularly with parvalbumin immunoreactive neurones but is synthesised by another neuronal population in the adult rat cerebral cortex E.S. Wintergerst F.G. Rathjen B. Schwaller P. Eggli M.R. Celio
03. April 2014 / Am J Hum Genet Rare variants in NR2F2 cause congenital heart defects in humans S. Al Turki A.K. Manickaraj C.L. Mercer S.S. Gerety M.P. Hitz S. Lindsay L.C.A. D'Alessandro G.J. Swaminathan J. Bentham A.K. Arndt J. Low J. Breckpot M. Gewillig B. Thienpont H. Abdul-Khaliq C. Harnack K. Hoff H.H. Kramer S. Schubert R. Siebert O. Toka C. Cosgrove H. Watkins A.M. Lucassen I.M. O'Kelly A.P. Salmon F.A. Bu'Lock J. Granados-Riveron K. Setchfield C. Thornborough J.D. Brook B. Mulder S. Klaassen S. Bhattacharya K. Devriendt D.F. Fitzpatrick D.I. Wilson S. Mital M.E. Hurles
29. April 2014 / BMC Med Genet Exome sequencing helped the fine diagnosis of two siblings afflicted with atypical Timothy syndrome (TS2) S. Froehler M. Kieslich C. Langnick M. Feldkamp B. Opgen-Rhein F. Berger J.C. Will W. Chen
01. Juni 2013 / Neurochem Res Regulation of adhesion by flexible ectodomains of IgCAMs H. Volkmer J. Schreiber F.G. Rathjen
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
01. 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
01. 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