07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
Später ansehen07.05.24 | Vollzeit | Worms | Deutsches Krebsforschungszentrum DKFZBut options to target cell surface proteins and receptors remain limited. We recently developed ROTACs, bispecific Wnt and BMP signaling disabled R-spondin (RSPO) chimeras, which leverage the specificity of these stem cell growth factors for ZNRF3/RNF43 E3 transmembrane ligases, to target degradation
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