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Januar 2014 / Am J Hum Genet Reponse to De Leeuw and Houge A.K. Arndt C.A. Macrae S. Klaassen 16. November 2013 / Mol Vis Retinal pigment epithelium protein of 65 kDA gene-linked retinal degeneration is not modulated by chicken acidic leucine-rich epidermal growth factor-like domain containing brain protein/Neuroglycan C/chondroitin sulfate proteoglycan 5 S. Cottet R. Jüttner N. Voirol P. Chambon F.G. Rathjen D.F. Schorderet P. Escher 06. Januar 2014 / PLoS ONE Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot V. Bansal C. Dorn M. Grunert S. Klaassen R. Hetzer F. Berger S.R. Sperling 15. Januar 2014 / J Neurosci Bifurcation of axons from cranial sensory neurons is disabled in the absence of Npr2-induced cGMP signaling G. Ter-Avetisyan F.G. Rathjen H. Schmidt 03. Februar 2014 / J Clin Invest Changes in neural network homeostasis trigger neuropsychiatric symptoms A. Winkelmann N. Maggio J. Eller G. Caliskan M. Semtner U. Häussler R. Jüttner T. Dugladze B. Smolinsky S. Kowalczyk E. Chronowska G. Schwarz F.G. Rathjen G. Rechavi C.A. Haas A. Kulik T. Gloveli U. Heinemann J.C. Meier 15. Juni 2014 / Hum Mol Genet Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot M. Grunert C. Dorn M. Schueler I. Dunkel J. Schlesinger S. Mebus V. Alexi-Meskishvili A. Perrot K. Wassilew B. Timmermann R. Hetzer F. Berger S.R. Sperling 01. Januar 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 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 »
16. November 2013 / Mol Vis Retinal pigment epithelium protein of 65 kDA gene-linked retinal degeneration is not modulated by chicken acidic leucine-rich epidermal growth factor-like domain containing brain protein/Neuroglycan C/chondroitin sulfate proteoglycan 5 S. Cottet R. Jüttner N. Voirol P. Chambon F.G. Rathjen D.F. Schorderet P. Escher
06. Januar 2014 / PLoS ONE Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with tetralogy of fallot V. Bansal C. Dorn M. Grunert S. Klaassen R. Hetzer F. Berger S.R. Sperling
15. Januar 2014 / J Neurosci Bifurcation of axons from cranial sensory neurons is disabled in the absence of Npr2-induced cGMP signaling G. Ter-Avetisyan F.G. Rathjen H. Schmidt
03. Februar 2014 / J Clin Invest Changes in neural network homeostasis trigger neuropsychiatric symptoms A. Winkelmann N. Maggio J. Eller G. Caliskan M. Semtner U. Häussler R. Jüttner T. Dugladze B. Smolinsky S. Kowalczyk E. Chronowska G. Schwarz F.G. Rathjen G. Rechavi C.A. Haas A. Kulik T. Gloveli U. Heinemann J.C. Meier
15. Juni 2014 / Hum Mol Genet Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot M. Grunert C. Dorn M. Schueler I. Dunkel J. Schlesinger S. Mebus V. Alexi-Meskishvili A. Perrot K. Wassilew B. Timmermann R. Hetzer F. Berger S.R. Sperling
01. Januar 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
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