Not logged in Reply to: “EFNB3 Frameshift Variant in Weimaraner Dogs with a Condition Resembling a Congenital Mirror Movement Disorder” Cleo Schwarz DVM; Florian Bartenschlager DVM, PhD, DECVP; Olivia Kershaw DVM, DECVP; Judith Braun DVM; Julien Guevar DVM, MVM, DECVN, MRCVS; Vidhya Jagannathan PhD; Jörg T. Epplen MD; Wencke Reineking DVM; Wolfgang Baumgärtner DVM, PhD, DECVP, DACVP (Hon.); Kailash P. Bhatia MD, FRCP; Achim D. Gruber DVM, PhD, DECVP; Tosso Leeb PhD Share Save
Share Save
Share Save
TPP2 mutation associated with sterile brain inflammation mimicking MS Reinthaler, Eva M.; Graf, Elisabeth; Zrzavy, Tobias; Wieland, Thomas; Hotzy, Christoph; Kopecky, Chantal; Pferschy, Sandra; Schmied, Christiane; Leutmezer, Fritz; Keilani, Mohammad; Lill, Christina M.; Hoffjan, Sabine; Epplen, Joerg T.; Zettl, Uwe K.; Hecker, Michael; Deutschlaender, Angela; Meuth, Sven G.; Ahram, Mamoun; Mustafa, Baha; El-Khateeb, Mohammed; Vilarino-Guell, Cartes; Sadovnick, Dessa; Zimprich, Fritz; Tomkinson, Birgitta; Strom, Tim; Kristoferitsch, Wolfgang; Lassmann, Hans; Zimprich, Alexander Share Save
Pathogenetic and Clinical Aspects of Anti-neutrophil Cytoplasmic Autoantibody-Associated vasculitides Lamprecht, Peter; Kerstein, Anja; Klapa, Sebastian; Schinke, Susanne; Karsten, Christian M.; Yu, Xinhua; Ehlers, Marc; Epplen, Joerg T.; Holl-Ulrich, Konstanze; Wiech, Thorsten; Kalies, Kathrin; Lange, Tanja; Laudien, Martin; Laskay, Tamas; Gemoll, Timo; Schumacher, Udo; Ullrich, Sebastian; Busch, Hauke; Ibrahim, Saleh; Fischer, Nicole; Hasselbacher, Katrin; Pries, Ralph; Petersen, Frank; Weppner, Gesche; Manz, Rudolf; Humrich, Jens Y.; Nieberding, Relana; Riemekasten, Gabriela; Mueller, Antje Share Save
Share Save
Epigenetic regulation of lateralized fetal spinal gene expression underlies hemispheric asymmetries Ocklenburg, Sebastian; Schmitz, Judith; Moinfar, Zahra; Moser, Dirk; Klose, Rena; Lor, Stephanie; Kunz, Georg; Tegenthoff, Martin; Faustmann, Pedro; Francks, Clyde; Epplen, Joerg T.; Kumsta, Robert; Guentuerkuen, Onur Share Save
Share Save
Share Save
Exome Sequencing Reveals AGBL5 as Novel Candidate Gene and Additional Variants for Retinitis Pigmentosa in Five Turkish Families Kastner, Simone; Thiemann, Ina-Janine; Dekomien, Gabriele; Petrasch-Parwez, Elisabeth; Schreiber, Sabrina; Akkad, Denis A.; Gerding, Wanda M.; Hoffjan, Sabine; Gunes, Sezgin; Gunes, Selcuk; Bagci, Hasan; Epplen, Joerg T. Share Save
Genome-wide significant association with seven novel multiple sclerosis risk loci Lill, Christina M.; Luessi, Felix; Alcina, Antonio; Sokolova, Ekaterina A.; Ugidos, Nerea; de la Hera, Belen; Guillot-Noel, Lena; Malhotra, Sunny; Reinthaler, Eva; Schjeide, Brit-Maren M.; Mescheriakova, Julia Y.; Mashychev, Andriy; Wohlers, Inken; Akkad, Denis A.; Aktas, Orhan; Alloza, Iraide; Antigueedad, Alfredo; Arroyo, Rafa; Astobiza, Ianire; Blaschke, Paul; Boyko, Alexei N.; Buttmann, Mathias; Chan, Andrew; Doerner, Thomas; Epplen, Joerg T.; Favorova, Olga O.; Fedetz, Maria; Fernandez, Oscar; Garcia-Martinez, Angel; Gerdes, Lisa-Ann; Graetz, Christiane; Hartung, Hans-Peter; Hoffjan, Sabine; Izquierdo, Guillermo; Korobko, Denis S.; Kroner, Antje; Kubisch, Christian; Kuempfel, Tania; Leyva, Laura; Lohse, Peter; Malkova, Nadezhda A.; Montalban, Xavier; Popova, Ekaterina V.; Rieckmann, Peter; Rozhdestvenskii, Alexei S.; Schmied, Christiane; Smagina, Inna V.; Tsareva, Ekaterina Y.; Winkelmann, Alexander; Zettl, Uwe K.; Binder, Harald; Cournu-Rebeix, Isabelle; Hintzen, Rogier; Zimprich, Alexander; Comabella, Manuel; Fontaine, Bertrand; Urcelay, Elena; Vandenbroeck, Koen; Filipenko, Maxim; Matesanz, Fuencisla; Zipp, Frauke; Bertram, Lars Share Save
Smaller caliber renal arteries are a novel feature of uromodulin-associated kidney disease Prejbisz, Aleksander; Sellin, Lorenz; Szwench-Pietrasz, Elzbieta; Woznowski, Magdalena; Michalowska, Ilona; Blondin, Dirk; Sajnaga, Dariusz; Epplen, Jorg T.; Litwin, Mieczyslaw; Dekomien, Gabriele; Januszewicz, Magdalena; Helmchen, Udo; Matuszkiewicz-Rowinska, Joanna; Adamczak, Marcin; Wiecek, Andrzej; Januszewicz, Andrzej; Rump, Lars C. Share Save
Share Save
Handedness and the X chromosome: The role of androgen receptor CAG-repeat length Arning, Larissa; Ocklenburg, Sebastian; Schulz, Stefanie; Ness, Vanessa; Gerding, Wanda M.; Hengstler, Jan G.; Falkenstein, Michael; Epplen, Joerg T.; Guentuerkuen, Onur; Beste, Christian Share Save
Share Save
Share Save
Genetics of toll like receptor 9 in ANCA associated vasculitides Husmann, C. A.; Holle, J. U.; Moosig, F.; Mueller, S.; Wilde, B.; Tervaert, J. W. Cohen; Harper, L.; Assmann, G.; Gross, W. L.; Epplen, J. T.; Wieczorek, S. Share Save
Share Save
Share Save
Growth rate of late passage sarcoma cells is independent of epigenetic events but dependent on the amount of chromosomal aberrations Becerikli, Mustafa; Jacobsen, Frank; Rittig, Andrea; Koehne, Wiebke; Nambiar, Sandeep; Mirmohammadsadegh, Alireza; Stricker, Ingo; Tannapfel, Andrea; Wieczorek, Stefan; Epplen, Joerg Thomas; Tilkorn, Daniel; Steinstraesser, Lars Share Save