8
results
for author:"Schupp I."
in Literature Citations
| Modeling ERBB receptor-regulated G1/S transition to find novel targets for de novo trastuzumab resistance. Sahin O., Frohlich H., Lobke C., Korf U., Burmester S., Majety M., Mattern J., Schupp I., Chaouiya C., Thieffry D. et al. BMC Syst Biol 3:1-1(2009) · Mapped (15) |
| The full-ORF clone resource of the German cDNA consortium. Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H. et al. BMC Genomics 8:399-399(2007) · UniProtKB (2,241) |
| Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism. Klauck S.M., Felder B., Kolb-Kokocinski A., Schuster C., Chiocchetti A., Schupp I., Wellenreuther R., Schmoetzer G., Poustka F., Breitenbach-Koller L. et al. Mol. Psychiatry 11:1073-1084(2006) · UniProtKB (1) |
| An anthropoid-specific segmental duplication on human chromosome 1q22. Kuryshev V.Y., Vorobyov E., Zink D., Schmitz J., Rozhdestvensky T.S., Muenstermann E., Ernst U., Wellenreuther R., Moosmayer P., Bechtel S. et al. |
| NIR is a novel INHAT repressor that modulates the transcriptional activity of p53. Hublitz P., Kunowska N., Mayer U.P., Muller J.M., Heyne K., Yin N., Fritzsche C., Poli C., Miguet L., Schupp I.W. et al. Genes Dev. 19:2912-2924(2005) · Mapped (7) |
| SMART amplification combined with cDNA size fractionation in order to obtain large full-length clones. German cDNA Consortium BMC Genomics 5:36-36(2004) · UniProtKB (1) |
| A point mutation in the IL-12R beta 2 gene underlies the IL-12 unresponsiveness of Lps-defective C57BL/10ScCr mice. Poltorak A., Merlin T., Nielsen P.J., Sandra O., Smirnova I., Schupp I., Boehm T., Galanos C., Freudenberg M.A. J. Immunol. 167:2106-2111(2001) · UniProtKB (1) · Mapped (33) |
| Predetermined chromosomal deletion encompassing the Nf-1 gene. Schlake T., Schupp I., Kutsche K., Mincheva A., Lichter P., Boehm T. Oncogene 18:6078-6082(1999) · Mapped (4) |
