Common fragile sites are conserved features of human and mouse chromosomes and relate to large active genes

Por Helmrich, Anne, Stout-Weider, Karen, Hermann, Klaus, Schrock, Evelin, Heiden, Thomas
Publicado em 2006

A mosaic maternal splice donor mutation in the EHMT1 gene leads to aberrant transcripts and to Kleefstra syndrome in the offspring

Por Rump, Andreas, Hildebrand, Laura, Tzschach, Andreas, Ullmann, Reinhard, Schrock, Evelin, Mitter, Diana
Publicado em 2013

Glioblastomas with Oligodendroglial Component – Common Origin of the Different Histological Parts and Genetic Subclassification

Por Klink, Barbara, Schlingelhof, Ben, Klink, Martin, Stout-Weider, Karen, Patt, Stephan, Schrock, Evelin
Publicado no Anal Cell Pathol (Amst) (2010)

Survivin safeguards chromosome numbers and protects from aneuploidy independently from p53

Por Wiedemuth, Ralf, Klink, Barbara, Töpfer, Katrin, Schröck, Evelin, Schackert, Gabriele, Tatsuka, Masaaki, Temme, Achim
Publicado em 2014

Specific Chromosomal Aberrations and Amplification of the AIB1 Nuclear Receptor Coactivator Gene in Pancreatic Carcinomas

Por Ghadimi, B. Michael, Schröck, Evelin, Walker, Robert L., Wangsa, Danny, Jauho, Annukka, Meltzer, Paul S., Ried, Thomas
Publicado em 1999

Frequent translocation t(4;14)(p16.3;q32.3) in multiple myeloma is associated with increased expression and activating mutations of fibroblast growth factor receptor 3

Por Chesi, Marta, Nardini, Elena, Brents, Leslie A., Schröck, Evelin, Ried, Thomas, Kuehl, W. Michael, Bergsagel, P. Leif
Publicado em 1997

An unusual case of Cowden syndrome associated with ganglioneuromatous polyposis

Por Pistorius, Steffen, Klink, Barbara, Pablik, Jessica, Rump, Andreas, Aust, Daniela, Garzarolli, Marlene, Schröck, Evelin, Schackert, Hans K.
Publicado no Hered Cancer Clin Pract (2016)

Centrosome Amplification and Instability Occurs Exclusively in Aneuploid, But Not in Diploid Colorectal Cancer Cell Lines, and Correlates With Numerical Chromosomal Aberrations

Por Ghadimi, B. Michael, Sackett, Dan L., Difilippantonio, Michael J., Schröck, Evelin, Neumann, Thomas, Jauho, Annukka, Auer, Gert, Ried, Thomas
Publicado no Genes Chromosomes Cancer (2000)

Partial deletion of GLRB and GRIA2 in a patient with intellectual disability

Por Hackmann, Karl, Matko, Sarah, Gerlach, Eva-Maria, von der Hagen, Maja, Klink, Barbara, Schrock, Evelin, Rump, Andreas, Di Donato, Nataliya
Publicado em 2013

Identification and characterisation of a novel constitutional PIK3CA mutation in a child lacking the typical segmental overgrowth of “PIK3CA-Related Overgrowth Spectrum” (PROS)

Por Di Donato, Nataliya, Rump, Andreas, Mirzaa, Ghayda M., Alcantara, Diana, Oliver, Antony, Schrock, Evelin, Dobyns, William B., O’Driscoll, Mark
Publicado no Hum Mutat (2015)

Comprehensive molecular cytogenetic investigation of chromosomal abnormalities in human medulloblastoma cell lines and xenograft.

Por Aldosari, Naji, Wiltshire, Rodney N., Dutra, Amalia, Schrock, Evelin, McLendon, Roger E., Friedman, Henry S., Bigner, Darell D., Bigner, Sandra H.
Publicado em 2002

The contribution of homology arms to nuclease-assisted genome engineering

Por Baker, Oliver, Tsurkan, Sarah, Fu, Jun, Klink, Barbara, Rump, Andreas, Obst, Mandy, Kranz, Andrea, Schröck, Evelin, Anastassiadis, Konstantinos, Stewart, A. Francis
Publicado no Nucleic Acids Res (2017)

The conjugated antimetabolite 5-FdU-ECyd and its cellular and molecular effects on platinum-sensitive vs. -resistant ovarian cancer cells in vitro

Por Schott, Sarah, Wimberger, Pauline, Klink, Barbara, Grützmann, Konrad, Puppe, Julian, Wauer, Ulrike Sophie, Klotz, Daniel Martin, Schröck, Evelin, Kuhlmann, Jan Dominik
Publicado no Oncotarget (2017)

Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer

Por Kast, Karin, Neuhann, Teresa M, Görgens, Heike, Becker, Kerstin, Keller, Katja, Klink, Barbara, Aust, Daniela, Distler, Wolfgang, Schröck, Evelin, Schackert, Hans K
Publicado em 2012

Telomere Dysfunction and DNA-PKcs Deficiency: characterization and consequence

Por Williams, Eli S., Klingler, Rebekah, Ponnaiya, Brian, Hardt, Tanja, Schrock, Evelin, Lees-Miller, Susan P., Meek, Katheryn, Ullrich, Robert L., Bailey, Susan M.
Publicado em 2009

Stromelysin-3 over-expression enhances tumourigenesis in MCF-7 and MDA-MB-231 breast cancer cell lines: involvement of the IGF-1 signalling pathway

Por Kasper, Grit, Reule, Matthias, Tschirschmann, Miriam, Dankert, Niels, Stout-Weider, Karen, Lauster, Roland, Schrock, Evelin, Mennerich, Detlev, Duda, Georg N, Lehmann, Kerstin E
Publicado em 2007

Side population in human glioblastoma is non-tumorigenic and characterizes brain endothelial cells

Por Golebiewska, Anna, Bougnaud, Sébastien, Stieber, Daniel, Brons, Nicolaas H. C., Vallar, Laurent, Hertel, Frank, Klink, Barbara, Schröck, Evelin, Bjerkvig, Rolf, Niclou, Simone P.
Publicado em 2013

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

Por Manoharan, Jerena, Lopez, Caroline L, Hackmann, Karl, Albers, Max B, Pehl, Anika, Kann, Peter H, Slater, Emily P, Schröck, Evelin, Bartsch, Detlef K
Publicado no Endocrinol Diabetes Metab Case Rep (2016)

Functional Restoration of gp91phox-Oxidase Activity by BAC Transgenesis and Gene Targeting in X-linked Chronic Granulomatous Disease iPSCs

Por Laugsch, Magdalena, Rostovskaya, Maria, Velychko, Sergiy, Richter, Cornelia, Zimmer, Ariane, Klink, Barbara, Schröck, Evelin, Haase, Michael, Neumann, Katrin, Thieme, Sebastian, Roesler, Joachim, Brenner, Sebastian, Anastassiadis, Konstantinos
Publicado no Mol Ther (2016)

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

Por 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
Publicado no J Int AIDS Soc (2014)