Evelin Schröck

RAPID COMMUNICATION Frequent Dysregulation of the c-maf Proto-Oncogene at 16q23 by Translocation to an Ig Locus in Multiple Myeloma (2007)

Marta Chesi, P. Leif Bergsagel, Oluwatoyin O. Shonukan, Maria Luisa Martelli, Leslie A. Brents, Theresa Chen, ...

Dysregulation of oncogenes by translocation to an IgH (14q32) or IgL (�, 2p11 or �, 22q11) locus is a frequent event in the pathogenesis of B-cell tumors. Translocations involving an IgH locus...

Multicolor fluorescence in situ hybridization on metaphase chromosomes and interphase Halo-preparations using cosmid and YAC clones for the simultaneous high resolution mapping of deletions in the dystrophin gene (1994)

Tocharoentanaphol, Chintana, Cremer, Marion, Schröck, Evelin, Blonden, Lau, Kilian, Karin, Cremer, Thomas, ...

We report on multicolor fluorescence in situ hybridization protocols for the simultaneous visualization of deletion-prone regions for carrier detection of Duchenne/ Becker (DMD/BMD) muscular...

Mapping of Multiple DNA Gains and Losses in Primary Small Cell Lung Carcinomas by Comparative Genomic Hybridization (1994)

Ried, Thomas, Petersen, Iver, Holtgreve-Grez, Heidi, Speicher, Michael R., Schröck, Evelin, Manoir, Stanislas Du, ...

Comparative genomic hybridization was applied for a comprehensive screening of under- and overrepresentation of genetic material in 13 autoptic small cell lung cancer specimens. The most abundant...

Comparative Genomic Hybridization of Human Malignant Gliomas Reveals Multiple Amplification Sites and Nonrandom Chromosomal Gains and Losses (1994)

Schröck, Evelin, Thiel, G., Lozonova, T., Manoir, Stanislas Du, Meffert, M. C., Jauch, Anna, ...

Nine human malignant gliomas (2 astrocytomas grade III and 7 glioblastomas) were analyzed using comparative genomic hybridization (CGH). In addition to the amplification of the EGFR gene at 7p12 in 4...

Specific loss of chromosomes 1, 2, 6, 10, 13, 17, and 21 in chromophobe renal cell carcinomas revealed by comparative genomic hybridization (1994)

Speicher, Michael R., Schoell, B., Manoir, Stanislas Du, Schröck, Evelin, Ried, Thomas, Cremer, Thomas, ...

We analyzed 19 chromophobe renal cell carcinomas by means of comparative genomic hybridization. Two tumors revealed no numerical abnormalities. In the remaining 17 cases we found loss of entire...

3D-Voronoi Diagramme zur quantitativen Bildanalyse in der Interphase-Cytogenetik (1994)

Eils, R., Dietzel, S., Bertin, E., Schröck, Evelin, Usson, Y., Robert-Nicoud, Michel, ...

Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization (1993)

Manoir, Stanislas Du, Speicher, Michael R., Joos, Stefan, Schröck, Evelin, Popp, Susanne, Döhner, Hartmut, ...

Comparative genomic in situ hybridization (CGH) provides a new possibility for searching genomes for imbalanced genetic material. Labeled genomic test DNA, prepared from clinical or tumor specimens,...

The role of chromosome territories in the funtional compartmentalization of the cell nucleus (1993)

Cremer, Thomas, Kurz, A., Zirbel, R. M., Dietzel, S., Rinke, B., Schröck, Evelin, ...

Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification (1993)

Speicher, Michael R., Manoir, Stanislas Du, Schröck, Evelin, Holtgreve-Grez, Heidi, Schoell, B., Lengauer, Christoph, ...

We present a technique which allows the detection and chromosomal localization of DNA sequence copy number changes in solid tumor genomes from frozen sections and paraffin embedded, formalin fixed...

Detection of genetic imbalances in tumor genomes by fluorescence in situ hybridization with tumor genomic DNA and subregional DNA probes (1993)

Cremer, Thomas, Lichter, Peter, Popp, Susanne, Schröck, Evelin, Jauch, Anna, Manoir, Stanislas Du, ...

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

Ghadimi, B. Michael, Schröck, Evelin, Walker, Robert L., Wangsa, Danny, Jauho, Annukka, Meltzer, Paul S., ...

To screen pancreatic carcinomas for chromosomal aberrations we have applied molecular cytogenetic techniques, including fluorescent in situ hybridization, comparative genomic hybridization, and...