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pro vyhledávání: '"Michaela, Schneider"'
Akademický článek
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Autor:
Gerald Biebersdorf, Melanie Dworaczek, Werner Gritzbach, Nadine Hasse, Sascha Ihns, Patricia Kämpf, Lydia Ranke, Michaela Schneider, Susanne Schramm, Hanadi Siering, Kai Simmerl, The Magnificent Travellers, Ev Tsakiridou, Andrea Weil, Sabrina Wendling
edinburgh – the beauty in the north. Edinburgh. Nestled in an idyllic natural landscape between the shores of the Firth of Forth and the volcanic hills that are the gateway to the Scottish Highlands. A small capital, on the fringe of Europe – but
Autor:
Harald, Welter, Nicole, Kreitmair, Michaela, Schneider, Carola, Herrmann, Nina, Schmid, Youli, Stepanov, Thomas, Fröhlich, Frank-Michael, Köhn, Ulrich, Pickl, Matthias, Trottmann, Artur, Mayerhofer
Publikováno v:
Journal of Clinical Medicine; Aug2024, Vol. 13 Issue 15, p4357, 13p
Autor:
Julia Würtemberger, Daria Tchessalova, Carla Regina, Christoph Bauer, Michaela Schneider, Amy J Wagers, Simone Hettmer
Publikováno v:
PLoS ONE, Vol 15, Iss 9, p e0238572 (2020)
Functional genomic screening of KRAS-driven mouse sarcomas was previously employed to identify proliferation-relevant genes. Genes identified included Ubiquitin-conjugating enzyme E2 (Ube2c), Centromere Protein E (Cenpe), Hyaluronan Synthase 2 (Has2)
Externí odkaz:
https://doaj.org/article/d715d757ec6e43f9b37584e4e9597793
Autor:
Jakob Siebert, Michaela Schneider, Daniela Reuter‐Schmitt, Julia Würtemberger, Annette Neubüser, Wolfgang Driever, Simone Hettmer, Friedrich G. Kapp
Publikováno v:
Pediatric Blood & Cancer. 70
Rhabdomyosarcomas (RMS) are the most common pediatric soft tissue sarcomas. High-risk and metastatic disease continues to be associated with very poor prognosis. RMS model systems that faithfully recapitulate the human disease and provide rapid, cost
Autor:
Klara‐Maria Hanft, Ebrahem Hamed, Max Kaiser, Julia Würtemberger, Michaela Schneider, Torsten Pietsch, Ursula Feige, Frank Meiss, Sven Krengel, Charlotte Niemeyer, Simone Hettmer
Publikováno v:
Pediatric Blood & Cancer. 69
Congenital melanocytic nevus (CMN) syndrome represents a mosaic RASopathy, typically caused by postzygotic NRAS codon 61 mutations, which originate in ectodermal precursor cells and result in melanocyte deposits in the skin and central nervous system
Autor:
Simone Hettmer, Anna C Schinzel, Daria Tchessalova, Michaela Schneider, Christina L Parker, Roderick T Bronson, Nigel GJ Richards, William C Hahn, Amy J Wagers
Publikováno v:
eLife, Vol 4 (2015)
Current therapies for sarcomas are often inadequate. This study sought to identify actionable gene targets by selective targeting of the molecular networks that support sarcoma cell proliferation. Silencing of asparagine synthetase (ASNS), an amidotr
Externí odkaz:
https://doaj.org/article/02c860c99dd149119671592902b66edd
Autor:
Michaela Schneider
Publikováno v:
Allergo Journal. 30:8-9
Autor:
Michaela Schneider
Publikováno v:
hautnah dermatologie. 38:51-51
Publikováno v:
Haematologica, Vol 95, Iss 4 (2010)
Externí odkaz:
https://doaj.org/article/6697d5361a6e4777bf20d1eca6632bda