Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Dietrich Lueerssen"'
Autor:
Veronique Laloux, Jan K Larsen, Simon M. Hughes, Vikas Gupta, Dietrich Lueerssen, Olivier Biglia, Ferose Charifi, Sarah Lafi, Alexandre Bona, Juergen Lauber
Publikováno v:
Blood. 132:5272-5272
Introduction Somatic mutations acquired in key signalling pathway, transcription factor, spliceosome, epigenetic and tumor suppressor genes are of central importance in the development and progression of myeloid malignancies including myeloproliferat
Autor:
Simon M. Hughes, Alexander Burton, Andrew Robb, Leif Schauser, Nathan Dennison, Bodil Oester, Adam Burke, Vishal Kapoor, Kyriakos Ttavas, Dietrich Lueerssen, Lea Thoegerson, Richard Dyson, Juergen Lauber
Publikováno v:
Journal of Clinical Oncology. 36:e17536-e17536
e17536Background: Supported by strong clinical evidence, testing for germline mutations in BRCA1 and BRCA2 in suspected familial breast cancer cases has gradually become common practice, especially...
Autor:
Vikas Gupta, Paola Arzuffi, Simon M. Hughes, John Blood, Alexander Burton, Dietrich Lueerssen, Leif Schauser, Juergen Lauber
Publikováno v:
Journal of Clinical Oncology. 36:e21193-e21193
e21193Background: Lung cancer is the cause of 1 in 5 cancer deaths worldwide and is frequently driven by somatic mutations acquired in key genes. Targeted Next-Generation Sequencing (NGS) is a valu...
Autor:
David G. Barnes, Simon Hughes, Daniel Swan, Nicholas A. Athanasou, Udo Oppermann, Dietrich Lueerssen, Takeshi Kashima, A. B. Hassan, John Anson, E S Hookway
Publikováno v:
BMC Cancer
Barnes, D J, Hookway, E, Athanasou, N, Kashima, T, Oppermann, U, Hughes, S, Swan, D, Lueerssen, D, Anson, J & Hassan, A B 2016, ' A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy : a case report ', BMC Cancer, vol. 16, pp. 629 . https://doi.org/10.1186/s12885-016-2669-3
Barnes, D J, Hookway, E, Athanasou, N, Kashima, T, Oppermann, U, Hughes, S, Swan, D, Lueerssen, D, Anson, J & Hassan, A B 2016, ' A germline mutation of CDKN2A and a novel RPLP1-C19MC fusion detected in a rare melanotic neuroectodermal tumor of infancy : a case report ', BMC Cancer, vol. 16, pp. 629 . https://doi.org/10.1186/s12885-016-2669-3
Background Melanotic neuroectodermal tumor of infancy (MNTI) is exceptionally rare and occurs predominantly in the head and neck (92.8 % cases). The patient reported here is only the eighth case of MNTI presenting in an extremity, and the first repor
Publikováno v:
Frontiers in Optics 2004/Laser Science XXII/Diffractive Optics and Micro-Optics/Optical Fabrication and Testing.
The fiber or waveguide coupling efficiency of a packaged semiconductor optical amplifier can be quantified using thermal profiling in conjunction with a finite element total energy balance model. This technique does not rely on characterization prior