Publication

Dissection of the BCR-ABL signaling network using highly specific monobody inhibitors to the SHP2 SH2 domains

Related publications (38)

About
Privacy
Disclaimer

Graph Chatbot

Chat with Graph Search

Ask any question about EPFL courses, lectures, exercises, research, news, etc. or try the example questions below.

DISCLAIMER: The Graph Chatbot is not programmed to provide explicit or categorical answers to your questions. Rather, it transforms your questions into API requests that are distributed across the various IT services officially administered by EPFL. Its purpose is solely to collect and recommend relevant references to content that you can explore to help you answer your questions.

Dissection of the BCR-ABL signaling network using highly specific monobody inhibitors to the SHP2 SH2 domains

Graph Chatbot

Chat with Graph Search

Nanomechanics of multidomain neuronal cell adhesion protein contactin revealed by single molecule AFM and SMD

Unpaired extracellular cysteine mutations of CSF3R mediate gain or loss of function

Allosteric regulation and targeting of Abl SH2-kinase interface and other cytoplasmic tyrosine kinases

HRD Motif as the Central Hub of the Signaling Network for Activation Loop Autophosphorylation in Abl Kinase

Allosteric Inhibition of Bcr-Abl Kinase by High Affinity Monobody Inhibitors Directed to the Src Homology 2 (SH2)-Kinase Interface

Identification and functional characterization of protein kinases that modulate Notch signaling under physiological conditions and in cancer

Identification of genetic interactors of ypa2 in Schizosaccharomyces pombe

Functional Perturbation of the Gab2 Multiprotein Complex by High-affinity SH2-binding Monobodies in Chronic Myelogenous Leukemia

Crystal structure of an SH2-kinase construct of c-Abl and effect of the SH2 domain on kinase activity

The SH2 domain of Abl kinases regulates kinase autophosphorylation by controlling activation loop accessibility