Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Vivien Boldt"'
Autor:
Sophia Gross, Jana Ihlow, Leonie Busack, Kacper Adamiak, Jens Schrezenmeier, Julia Jesse, Michaela Schwarz, Anne Flörcken, Lam Giang Vuong, Kathrin Rieger, Jan Krönke, Philipp le Coutre, Vivien Boldt, Ann-Christin von Brünneck, David Horst, Thomas Burmeister, Igor-Wolfgang Blau, Ulrich Keller, Lars Bullinger, Jörg Westermann
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-10 (2024)
Abstract Therapy-related acute myeloid leukemia (t-AML) often exhibits adverse (genetic) features. There is ongoing discussion on the impact of t-AML on long-term outcome in AML. Therefore, we retrospectively analyzed clinical and biological characte
Externí odkaz:
https://doaj.org/article/23f631a9266149929a52a8ab90a8f749
Autor:
Reinhard Ullmann, Helmut Popper, Iris Halbwedl, Fattaneh A. Tavassoli, Vivien Boldt, Farid Moinfar, Sebastian Leibl, Elvira Stacher
Publikováno v:
Histopathology. 59:549-555
Stacher E, Boldt V, Leibl S, Halbwedl I, Popper H H, Ullmann R, Tavassoli F A & Moinfar F (2011) Histopathology59, 549–555 Chromosomal aberrations as detected by array comparative genomic hybridization in early low-grade intraepithelial neoplasias
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e90c3cb7ec31b1807265d36449cdf3d8
https://doi.org/10.1111/j.1365-2559.2011.03918.x
https://doi.org/10.1111/j.1365-2559.2011.03918.x
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:
Elvira, Stacher, Vivien, Boldt, Sebastian, Leibl, Iris, Halbwedl, Helmut H, Popper, Reinhard, Ullmann, Fattaneh A, Tavassoli, Farid, Moinfar
Publikováno v:
Histopathology. 59(3)
Low-grade flat ductal intraepithelial neoplasia (DIN1a, flat epithelial atypia) is one of the earliest morphologically recognizable neoplastic lesions of the breast. Frequently, it occurs concomitantly with lobular intraepithelial neoplasia (LIN). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5a09e4e1056f45f68ee74f94fea9d82f
https://pubmed.ncbi.nlm.nih.gov/21906127
https://pubmed.ncbi.nlm.nih.gov/21906127
Autor:
Elvira Stacher, Iris Halbwedl, Claus Hultschig, Reinhard Ullmann, Fattaneh A. Tavassoli, Farid Moinfar, Helmut Popper, Vivien Boldt
Publikováno v:
Genes, Chromosomes and Cancer.
Lobular intraepithelial neoplasia Grade 3 (LIN3) is a recently recognized variant of intraepithelial lobular neoplasia (LIN) of the breast composed of either uniform, generally small cells with massive lobular distension, pleomorphic cells, signet-ri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7a5d098b1eee615e1c654fc56f6df55
https://doi.org/10.1002/gcc.20756
https://doi.org/10.1002/gcc.20756
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