Zobrazeno 1 - 10
of 39
pro vyhledávání: '"Michael P Schroeder"'
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 12, Iss 4, p e5734 (2024)
Background:. Reported drug allergies are commonly encountered by surgeons and can lead to uncertainty in selecting an appropriate agent due to concerns of associated risks with related and cross-reactive drugs. This uncertainty can ultimately lead to
Externí odkaz:
https://doaj.org/article/86dd79e426d447469817b8d7de5a2e74
Autor:
Sven Liebig, Martin Neumann, Patricia Silva, Jutta Ortiz-Tanchez, Veronika Schulze, Konstandina Isaakidis, Cornelia Schlee, Michael P. Schroeder, Thomas Beder, Luc G. T. Morris, Timothy A. Chan, Lorenz Bastian, Thomas Burmeister, Stefan Schwartz, Nicola Gökbuget, Liliana H. Mochmann, Claudia D. Baldus
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract FAT atypical cadherin 1 (FAT1), a transmembrane protein, is frequently mutated in various cancer types and has been described as context-dependent tumor suppressor or oncogene. The FAT1 gene is mutated in 12–16% of T-cell acute leukemia (T
Externí odkaz:
https://doaj.org/article/73aaef34737c42fdadc2a0d1ed2b4094
Autor:
Lorenz Bartsch, Michael P. Schroeder, Sonja Hänzelmann, Lorenz Bastian, Juan Lázaro-Navarro, Cornelia Schlee, Jutta Ortiz Tanchez, Veronika Schulze, Konstandina Isaakidis, Michael A. Rieger, Nicola Gökbuget, Cornelia Eckert, Hubert Serve, Martin Horstmann, Martin Schrappe, Monika Brüggemann, Claudia D. Baldus, Martin Neumann
Publikováno v:
BMC Genomic Data, Vol 23, Iss 1, Pp 1-13 (2022)
Abstract Background B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is a genetically heterogenous malignancy with poor prognosis in relapsed adult patients. The genetic basis for relapse in aneuploid subtypes such as near haploid (NH) and hig
Externí odkaz:
https://doaj.org/article/09f3d7f0ee36410499c81781f4b8a802
Autor:
Alva Rani James, Michael P. Schroeder, Martin Neumann, Lorenz Bastian, Cornelia Eckert, Nicola Gökbuget, Jutta Ortiz Tanchez, Cornelia Schlee, Konstandina Isaakidis, Stefan Schwartz, Thomas Burmeister, Arend von Stackelberg, Michael A. Rieger, Stefanie Göllner, Martin Horstman, Martin Schrappe, Renate Kirschner-Schwabe, Monika Brüggemann, Carsten Müller-Tidow, Hubert Serve, Altuna Akalin, Claudia D. Baldus
Publikováno v:
Journal of Hematology & Oncology, Vol 12, Iss 1, Pp 1-16 (2019)
Abstract Background Long non-coding RNAs (lncRNAs) have emerged as a novel class of RNA due to its diverse mechanism in cancer development and progression. However, the role and expression pattern of lncRNAs in molecular subtypes of B cell acute lymp
Externí odkaz:
https://doaj.org/article/0239516c3301412db8a7d3731f5b8443
Autor:
David Tamborero, Carlota Rubio-Perez, Jordi Deu-Pons, Michael P. Schroeder, Ana Vivancos, Ana Rovira, Ignasi Tusquets, Joan Albanell, Jordi Rodon, Josep Tabernero, Carmen de Torres, Rodrigo Dienstmann, Abel Gonzalez-Perez, Nuria Lopez-Bigas
Publikováno v:
Genome Medicine, Vol 10, Iss 1, Pp 1-8 (2018)
Abstract While tumor genome sequencing has become widely available in clinical and research settings, the interpretation of tumor somatic variants remains an important bottleneck. Here we present the Cancer Genome Interpreter, a versatile platform th
Externí odkaz:
https://doaj.org/article/0e69b340b3c34623b79163ba6ddce679
Autor:
Michael J. Schroeder, MD, Nihaal Reddy, BS, Andrew Rust, BS, Andrew L. O’Brien, MD, MPH, Sonu A. Jain, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 9, Iss 10S, Pp 99-99 (2021)
Externí odkaz:
https://doaj.org/article/87d571fd3206497b9dc7ef1156eed467
Autor:
Michael W. Schroeder, Rebecca Smith
Publikováno v:
Discrete Mathematics & Theoretical Computer Science, Vol Vol. 18 no. 2, Permutation..., Iss Permutation Patterns (2017)
We consider a sorting machine consisting of two stacks in series where the first stack has the added restriction that entries in the stack must be in decreasing order from top to bottom. The class of permutations sortable by this machine are known to
Externí odkaz:
https://doaj.org/article/d9ddf14ef6e0468992586d32405e0ef0
Autor:
Claudia D. Baldus, Jana Hof, Helia J Pimentel-Gutiérrez, Seval Türkmen, Malwine J Pogodzinski, Stefanie Groeneveld-Krentz, Stefan Gattenlöhner, Michael Reiter, Leonid Karawajew, Cornelia Eckert, Christiane Chen-Santel, Arend von Stackelberg, Michael P Schroeder, Oskar A. Haas, Jutta Bradtke, Renia Vagkopoulou, Karin Nebral, Renate Kirschner-Schwabe
Publikováno v:
British Journal of Haematology. 185:266-283
Aneuploidy is common in paediatric B-cell precursor acute lymphoblastic leukaemia (ALL). Specific subgroups, such as high hyperdiploidy (>50 chromosomes or DNA Index ≥1·16) and hypodiploidy (
Autor:
Hubert Serve, Renate Kirschner-Schwabe, Alva Rani James, Cornelia Eckert, Carsten Müller-Tidow, Jutta Ortiz Tanchez, Claudia D. Baldus, Martin Schrappe, Stefanie Göllner, Konstandina Isaakidis, Arend von Stackelberg, Michael P Schroeder, Michael A. Rieger, Stefan Schwartz, Monika Brüggemann, Cornelia Schlee, Lorenz Bastian, Nicola Gökbuget, Martin Horstman, Altuna Akalin, Thomas Burmeister, Martin Neumann
Publikováno v:
Journal of Hematology & Oncology, Vol 12, Iss 1, Pp 1-16 (2019)
Journal of Hematology & Oncology
Journal of Hematology & Oncology
Recent studies implicated that long non-coding RNAs (lncRNAs) may play a role in the progression and development of acute lymphoblastic leukemia, however, this role is not yet clear. In order to unravel the role of lncRNAs associated with B-cell prec
Autor:
Nael Alakel, Folker Schneller, Jutta Ortiz Tanchez, Heiko Trautmann, Carsten Müller-Tidow, Martin Neumann, Cornelia Schlee, Lorenz Bastian, Mustafa Kondakci, Michael P Schroeder, Walter Fiedler, Nicola Goekbuget, Stefan Schwartz, A. Reichle, Philipp A. Greif, Sonja Hänzelmann, Monika Brüggemann, Lars Fransecky, Thomas Burmeister, Michael Starck, Alina Hartmann, Sebastian Vosberg, Claudia D. Baldus
Publikováno v:
Blood. 136:37-38
Introduction: In T-ALL, in contrast to BCP-ALL, molecular subgroups are less well defined. Molecular subgroups are based on aberrant expression of oncogenes often resting upon structural aberrations (chromosomal translocation, copy number variations,