Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Deepak Ben Vangala"'
Autor:
Verena Nilius-Eliliwi, Marco Tembrink, Wanda Maria Gerding, Krzystof P. Lubieniecki, Joanna M. Lubieniecka, Stefanie Kankel, Thomas Liehr, Thomas Mika, Fotios Dimopoulos, Konstanze Döhner, Roland Schroers, Hoa Huu Phuc Nguyen, Deepak Ben Vangala
Publikováno v:
Frontiers in Oncology, Vol 12 (2022)
In acute myeloid leukemia (AML), treatment decisions are currently made according to the risk classification of the European LeukemiaNet (ELN), which is based on genetic alterations. Recently, optical genome mapping (OGM) as a novel method proved to
Externí odkaz:
https://doaj.org/article/239df1092c224ff3a861dde340cd6900
Autor:
Marco Tembrink, Wanda Maria Gerding, Stefan Wieczorek, Thomas Mika, Roland Schroers, Huu Phuc Nguyen, Deepak Ben Vangala, Verena Nilius-Eliliwi
Publikováno v:
Cancers; Volume 15; Issue 11; Pages: 2942
Optical genome mapping (OGM) recently has demonstrated the potential to improve genetic diagnostics in acute myeloid leukemia (AML). In this study, OGM was utilized as a tool for the detection of genome-wide structural variants and disease monitoring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::630c49de649ec722db6b20ac2554ece4
https://doi.org/10.3390/cancers15112942
https://doi.org/10.3390/cancers15112942
Autor:
Sabine Seidel, Verena Nilius-Eliliwi, Thomas Kowalski, Deepak Ben Vangala, Uwe Schlegel, Roland Schroers
Publikováno v:
Cancers; Volume 14; Issue 9; Pages: 2100
High-dose chemotherapy with autologous stem cell transplantation (HCT-ASCT) is reportedly an effective treatment strategy in relapsed or refractory primary CNS lymphoma (r/r PCNSL); however, only selected patients are eligible for this treatment. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ccb422e2f44ed29d05aa24e8de243b0b
Autor:
Lisa-Marie Vieler, Verena Nilius-Eliliwi, Roland Schroers, Deepak Ben Vangala, Huu Phuc Nguyen, Wanda Maria Gerding
Publikováno v:
Genes; Volume 14; Issue 3; Pages: 686
(1) Background: In acute lymphoblastic leukemia (ALL) the genetic characterization remains challenging. Due to the genetic heterogeneity of mutations in adult patients, only a small proportion of aberrations can be analyzed with standard routine diag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::459205a5b7af64feed4d029bedb02a97
https://doi.org/10.3390/genes14030686
https://doi.org/10.3390/genes14030686