Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Katrin Tebel"'
Autor:
Grit, Ebert, Anne, Steininger, Robert, Weißmann, Vivien, Boldt, Allan, Lind-Thomsen, Jana, Grune, Stefan, Badelt, Melanie, Heßler, Matthias, Peiser, Manuel, Hitzler, Lars R, Jensen, Ines, Müller, Hao, Hu, Peter F, Arndt, Andreas W, Kuss, Katrin, Tebel, Reinhard, Ullmann
Publikováno v:
BMC Genomics
Background Segmental duplications (SDs) are not evenly distributed along chromosomes. The reasons for this biased susceptibility to SD insertion are poorly understood. Accumulation of SDs is associated with increased genomic instability, which can le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::780cf09ab0de42740eecfa96249f76a2
https://pubmed.ncbi.nlm.nih.gov/24973960
https://pubmed.ncbi.nlm.nih.gov/24973960
Autor:
Artur Muradyan, Vivien Boldt, Anne Steininger, Stephanie Stabentheiner, Katrin Tebel, Jürgen Kreutzberger, Ines Müller, Hannelore Madle, Helmut H. Popper, Reinhard Ullmann
Publikováno v:
Archives of pathologylaboratory medicine. 132(10)
The accumulation of chromosomal aberrations is a characteristic feature of tumor development. However, an understanding of tumorigenesis that assumes that changes in DNA copy number always cause equivalent changes in the corresponding RNA and protein
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6542c1b60128d644c6a751b4cdd3bfe
https://pubmed.ncbi.nlm.nih.gov/18834209
https://pubmed.ncbi.nlm.nih.gov/18834209
Publikováno v:
BMC Bioinformatics
Background The analysis of DNA copy number variants (CNV) has increasing impact in the field of genetic diagnostics and research. However, the interpretation of CNV data derived from high resolution array CGH or NGS platforms is complicated by the co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6cf5d947dcfe1e161954ba82c188aa6