Clinical phenotypes of MAGEL2 mutations and deletions

by Buiting, Karin, Di Donato, Nataliya, Beygo, Jasmin, Bens, Susanne, von der Hagen, Maja, Hackmann, Karl, Horsthemke, Bernhard
Published 2014

Universal Tre (uTre) recombinase specifically targets the majority of HIV-1 isolates

by Karpinski, Janet, Chemnitz, Jan, Hauber, Ilona, Abi-Ghanem, Josephine, Paszkowski-Rogacz, Maciej, Surendranath, Vineeth, Chakrabort, Debojyoti, Hackmann, Karl, Schröck, Evelin, Teresa Pisabarro, María, Hauber, Joachim, Buchholz, Frank
Published 2014

An unusual phenotype of MEN1 syndrome with a SI-NEN associated with a deletion of the MEN1 gene

by Manoharan, Jerena, Lopez, Caroline L, Hackmann, Karl, Albers, Max B, Pehl, Anika, Kann, Peter H, Slater, Emily P, Schröck, Evelin, Bartsch, Detlef K
Published 2016

Highly Significant Antiviral Activity of HIV-1 LTR-Specific Tre-Recombinase in Humanized Mice

by Hauber, Ilona, Hofmann-Sieber, Helga, Chemnitz, Jan, Dubrau, Danilo, Chusainow, Janet, Stucka, Rolf, Hartjen, Philip, Schambach, Axel, Ziegler, Patrick, Hackmann, Karl, Schröck, Evelin, Schumacher, Udo, Lindner, Christoph, Grundhoff, Adam, Baum, Christopher, Manz, Markus G., Buchholz, Frank, Hauber, Joachim
Published 2013

Novel CIC Point Mutations and an Exon-Spanning, Homozygous Deletion Identified in Oligodendroglial Tumors by a Comprehensive Genomic Approach Including Transcriptome Sequencing

by Eisenreich, Sophie, Abou-El-Ardat, Khalil, Szafranski, Karol, Campos Valenzuela, Jaime A., Rump, Andreas, Nigro, Janice M., Bjerkvig, Rolf, Gerlach, Eva-Maria, Hackmann, Karl, Schröck, Evelin, Krex, Dietmar, Kaderali, Lars, Schackert, Gabriele, Platzer, Matthias, Klink, Barbara
Published 2013

Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1

by Gregor, Anne, Albrecht, Beate, Bader, Ingrid, Bijlsma, Emilia K, Ekici, Arif B, Engels, Hartmut, Hackmann, Karl, Horn, Denise, Hoyer, Juliane, Klapecki, Jakub, Kohlhase, Jürgen, Maystadt, Isabelle, Nagl, Sandra, Prott, Eva, Tinschert, Sigrid, Ullmann, Reinhard, Wohlleber, Eva, Woods, Geoffrey, Reis, André, Rauch, Anita, Zweier, Christiane
Published 2011

Identification and Functional Testing of ERCC2 Mutations in a Multi-national Cohort of Patients with Familial Breast- and Ovarian Cancer

by Rump, Andreas, Benet-Pages, Anna, Schubert, Steffen, Kuhlmann, Jan Dominik, Janavičius, Ramūnas, Macháčková, Eva, Foretová, Lenka, Kleibl, Zdenek, Lhota, Filip, Zemankova, Petra, Betcheva-Krajcir, Elitza, Mackenroth, Luisa, Hackmann, Karl, Lehmann, Janin, Nissen, Anke, DiDonato, Nataliya, Opitz, Romy, Thiele, Holger, Kast, Karin, Wimberger, Pauline, Holinski-Feder, Elke, Emmert, Steffen, Schröck, Evelin, Klink, Barbara
Published 2016