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

Por Stockklausner, Clemens, Lampert, Anette, Hoffmann, Georg F., Ries, Markus
Publicado no Oncologist (2016)

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

Por Stockklausner, Clemens, Breit, Stephen, Neu-Yilik, Gabriele, Echner, Nicole, Hentze, Matthias W., Kulozik, Andreas E., Gehring, Niels H.
Publicado em 2006

DNA methylation in PRDM8 is indicative for dyskeratosis congenita

Por 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
Publicado no 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...

Por 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.
Publicado no Aging (Albany NY) (2015)

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

Por 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
Publicado no Blood (2017)