Novel Treatments for Rare Cancers: The U.S. Orphan Drug Act Is Delivering—A Cross-Sectional Analysis

بواسطة Stockklausner, Clemens, Lampert, Anette, Hoffmann, Georg F., Ries, Markus
الحاوية / القاعدة Oncologist (2016)

The uORF-containing thrombopoietin mRNA escapes nonsense-mediated decay (NMD)

بواسطة Stockklausner, Clemens, Breit, Stephen, Neu-Yilik, Gabriele, Echner, Nicole, Hentze, Matthias W., Kulozik, Andreas E., Gehring, Niels H.
منشور في 2006

DNA methylation in PRDM8 is indicative for dyskeratosis congenita

بواسطة Weidner, Carola I., Lin, Qiong, Birkhofer, Carina, Gerstenmaier, Uwe, Kaifie, Andrea, Kirschner, Martin, Bruns, Heiko, Balabanov, Stefan, Trummer, Arne, Stockklausner, Clemens, Höchsmann, Britta, Schrezenmeier, Hubert, Wlodarski, Marcin, Panse, Jens, Brümmendorf, Tim H., Beier, Fabian, Wagner, Wolfgang
الحاوية / القاعدة Oncotarget (2016)

A novel autosomal recessive TERT T1129P mutation in a dyskeratosis congenita family leads to cellular senescence and loss of CD34+ hematopoietic stem cells not reversible by mTOR-i...

بواسطة Stockklausner, Clemens, Raffel, Simon, Klermund, Julia, Bandapalli, Obul Reddy, Beier, Fabian, Brümmendorf, Tim H., Bürger, Friederike, Sauer, Sven W., Hoffmann, Georg F., Lorenz, Holger, Tagliaferri, Laura, Nowak, Daniel, Hofmann, Wolf-Karsten, Buergermeister, Rebecca, Kerber, Carolin, Rausch, Tobias, Korbel, Jan O., Luke, Brian, Trumpp, Andreas, Kulozik, Andreas E.
الحاوية / القاعدة Aging (Albany NY) (2015)

Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin

بواسطة Seo, Aaron, Ben-Harosh, Miri, Sirin, Mehtap, Stein, Jerry, Dgany, Orly, Kaplelushnik, Joseph, Hoenig, Manfred, Pannicke, Ulrich, Lorenz, Myriam, Schwarz, Klaus, Stockklausner, Clemens, Walsh, Tom, Gulsuner, Suleyman, Lee, Ming K., Sendamarai, Anoop, Sanchez-Bonilla, Marilyn, King, Mary-Claire, Cario, Holger, Kulozik, Andreas E., Debatin, Klaus-Michael, Schulz, Ansgar, Tamary, Hannah, Shimamura, Akiko
الحاوية / القاعدة Blood (2017)