Publications

BibTex format

@article{Angelopoulos:2016:10.1016/j.dib.2016.03.024,
author = {Angelopoulos, N and Stebbing, J and Xu, Y and Giamas, G and Zhang, H},
doi = {10.1016/j.dib.2016.03.024},
journal = {Data in Brief},
pages = {740--746},
title = {Proteome-wide dataset supporting functional study of tyrosine kinases in breast cancer.},
url = {http://dx.doi.org/10.1016/j.dib.2016.03.024},
volume = {7},
year = {2016}
}

Download

RIS format (EndNote, RefMan)

TY  - JOUR
AB  - Tyrosine kinases (TKs) play an essential role in regulating various cellular activities and dysregulation of TK signaling contributes to oncogenesis. However, less than half of the TKs have been thoroughly studied. Through a combined use of RNAi and stable isotope labeling with amino acids in cell culture (SILAC)-based quantitative proteomics, a global functional proteomic landscape of TKs in breast cancer was recently revealed highlighting a comprehensive and highly integrated signaling network regulated by TKs (Stebbing et al., 2015) [1]. We collate the enormous amount of the proteomic data in an open access platform, providing a valuable resource for studying the function of TKs in cancer and benefiting the science community. Here we present a detailed description related to this study (Stebbing et al., 2015) [1] and the raw data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the identifier PXD002065.
AU  - Angelopoulos,N
AU  - Stebbing,J
AU  - Xu,Y
AU  - Giamas,G
AU  - Zhang,H
DO  - 10.1016/j.dib.2016.03.024
EP  - 746
PY  - 2016///
SN  - 2352-3409
SP  - 740
TI  - Proteome-wide dataset supporting functional study of tyrosine kinases in breast cancer.
T2  - Data in Brief
UR  - http://dx.doi.org/10.1016/j.dib.2016.03.024
UR  - http://hdl.handle.net/10044/1/30925
VL  - 7
ER  -

Download

DrGeorgiosGiamas

Contact

Location

Summary

Citation

BibTex format

RIS format (EndNote, RefMan)