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(6) Klix, Sabrina (1) Kobelt, Dennis Dr. (3) Kofahl, Bente Dr. (1) Kopp, Joachim Dr. (1) Kowenz-Leutz, Elisabeth Dr. (3) Krüger, Kerstin (2) Ku, Min-Chi Dr. (2) Kudryashev, Mikhail Prof. Dr. (2) Kühn, Ralf Dr. (6) Lacadie, Scott Allen Dr. (2) Lafuente, Dana (1) Landthaler, Markus Prof. Dr. (9) Langnick, Claudia (1) Lee, Young-Ae Prof. Dr. (5) Leisegang, Matthias Prof. Dr. rer. nat. (2) Leutz, Achim Prof. Dr. (9) Lewin, Gary Prof. Dr. (9) Lisewski, Ulrike Dr. (2) Löber, Ulrike Dr. (2) Lorenz, Felix Dr. (1) Ludwig, Leif S. Dr. med. Dr. rer. nat. 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August 2016 / Curr Drug Targets Pharmacological interference with protein-protein interactions of A-kinase anchoring proteins as a strategy for the treatment of disease V.A. Deák E. Klussmann 09. September 2016 / J Biol Chem The A-kinase anchoring protein (AKAP) glycogen synthase kinase 3β interaction protein (GSKIP) regulates β-catenin through its interactions with both protein kinase A (PKA) and GSK3β A. Dema M.F. Schröter E. Perets P. Skroblin M.C. Moutty V.A. Deàk W. Birchmeier E. Klussmann 01. August 2004 / Am J Hum Genet Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease B. Uhlenberg M. Schuelke F. Rueschendorf N. Ruf A.M. Kaindl M. Henneke H. Thiele G. Stoltenburg-Didinger F. Aksu H. Topaloglu P. Nuernberg C. Huebner B. Weschke J. Gaertner 01. Januar 2004 / Nat Genet Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy A.R. Janecke D.A. Thompson G. Utermann C. Becker C.A. Huebner E. Schmid C.L. McHenry A.R. Nair F. Rueschendorf J. Heckenlively B. Wissinger P. Nuernberg A. Gal 01. Januar 2004 / J Clin Endocrinol Metab Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter Y. Bayer S. Neumann B. Meyer F. Rueschendorf A. Reske T. Brix L. Hegedues P. Langer P. Nuernberg R. Paschke 01. Januar 2004 / J Med Genet Missense mutations of ACTA1 cause dominant congenital myopathy with cores A.M. Kaindl F. Rueschendorf S. Krause H.H. Goebel K. Koehler C. Becker D. Pongratz J. Mueller-Hoecker P. Nuernberg G. Stoltenburg-Didinger H. Lochmueller A. Huebner 01. Januar 2004 / J Med Genet Molecular karyotyping using an SNP array for genomewide genotyping A. Rauch F. Rueschendorf J. Huang U. Trautmann C. Becker C. Thiel K.W. Jones A. Reis P. Nuernberg 01. Januar 2004 / J Evol Biol Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus U. Zechner W. Shi M. Hemberger H. Himmelbauer S. Otto A. Orth V. Kalscheuer U. Fischer R. Elango A. Reis W. Vogel H. Ropers F. Rueschendorf R. Fundele 01. Januar 2004 / Endocr Res Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2 L.A. Metherell S. Cooray A. Huebner F. Rueschendorf D. Naville M. Begeot A.J.L. Clark 01. Januar 2016 / Bioessays Pluripotency and the endogenous retrovirus HERVH: Conflict or serendipity? Z. Izsvák J. Wang M. Singh D.L. Mager L.D. Hurst Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Nächste Seite Next › Letzte Seite Last »
01. August 2016 / Curr Drug Targets Pharmacological interference with protein-protein interactions of A-kinase anchoring proteins as a strategy for the treatment of disease V.A. Deák E. Klussmann
09. September 2016 / J Biol Chem The A-kinase anchoring protein (AKAP) glycogen synthase kinase 3β interaction protein (GSKIP) regulates β-catenin through its interactions with both protein kinase A (PKA) and GSK3β A. Dema M.F. Schröter E. Perets P. Skroblin M.C. Moutty V.A. Deàk W. Birchmeier E. Klussmann
01. August 2004 / Am J Hum Genet Mutations in the gene encoding gap junction protein alpha 12 (connexin 46.6) cause Pelizaeus-Merzbacher-like disease B. Uhlenberg M. Schuelke F. Rueschendorf N. Ruf A.M. Kaindl M. Henneke H. Thiele G. Stoltenburg-Didinger F. Aksu H. Topaloglu P. Nuernberg C. Huebner B. Weschke J. Gaertner
01. Januar 2004 / Nat Genet Mutations in RDH12 encoding a photoreceptor cell retinol dehydrogenase cause childhood-onset severe retinal dystrophy A.R. Janecke D.A. Thompson G. Utermann C. Becker C.A. Huebner E. Schmid C.L. McHenry A.R. Nair F. Rueschendorf J. Heckenlively B. Wissinger P. Nuernberg A. Gal
01. Januar 2004 / J Clin Endocrinol Metab Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter Y. Bayer S. Neumann B. Meyer F. Rueschendorf A. Reske T. Brix L. Hegedues P. Langer P. Nuernberg R. Paschke
01. Januar 2004 / J Med Genet Missense mutations of ACTA1 cause dominant congenital myopathy with cores A.M. Kaindl F. Rueschendorf S. Krause H.H. Goebel K. Koehler C. Becker D. Pongratz J. Mueller-Hoecker P. Nuernberg G. Stoltenburg-Didinger H. Lochmueller A. Huebner
01. Januar 2004 / J Med Genet Molecular karyotyping using an SNP array for genomewide genotyping A. Rauch F. Rueschendorf J. Huang U. Trautmann C. Becker C. Thiel K.W. Jones A. Reis P. Nuernberg
01. Januar 2004 / J Evol Biol Divergent genetic and epigenetic post-zygotic isolation mechanisms in Mus and Peromyscus U. Zechner W. Shi M. Hemberger H. Himmelbauer S. Otto A. Orth V. Kalscheuer U. Fischer R. Elango A. Reis W. Vogel H. Ropers F. Rueschendorf R. Fundele
01. Januar 2004 / Endocr Res Mutations in a novel gene, encoding a single transmembrane domain protein are associated with familial glucocorticoid deficiency type 2 L.A. Metherell S. Cooray A. Huebner F. Rueschendorf D. Naville M. Begeot A.J.L. Clark
01. Januar 2016 / Bioessays Pluripotency and the endogenous retrovirus HERVH: Conflict or serendipity? Z. Izsvák J. Wang M. Singh D.L. Mager L.D. Hurst