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Author Correction: RGS7 is recurrently mutated in melanoma and promotes migration and invasion of human cancer cells

Year: 2019
Type: erratum
DOI: 10.1038/s41598-018-37932-6
Authors: Nouar Qutob, Ikuo Masuho, Michal Alon, Rafi Emmanuel, Isadora Cohen, Antonella Di Pizio, Jason Madore, Abdel Elkahloun, Tamar Ziv, Ronen Levy, Jared J. Gartner, Victoria K. Hill, Jimmy C. Lin, Yael Hevroni, Polina Greenberg, Alexandra Brodezki, Steven A. Rosenberg, Mickey Kosloff, Nicholas K. Hayward, Arie Admon, Masha Y. Niv, Richard A. Scolyer, Kirill A. Martemyanov, Yardena Samuels
Institutions: Weizmann Institute of Science, Scripps Research Institute, Hebrew University of Jerusalem, The University of Sydney, Royal Prince Alfred Hospital, Melanoma Institute Australia, National Institutes of Health, National Human Genome Research Institute, Technion – Israel Institute of Technology, National Cancer Institute, University of Haifa, QIMR Berghofer Medical Research Institute
Language: English
Open Access status: gold
Estimated APC paid: $1,790
Funders: Minerva Foundation, Israel Science Foundation, National Institutes of Health, Medical Research Council, National Health and Medical Research Council, National Institute on Drug Abuse, FP7 Ideas: European Research Council
Awards: G2006664195, G3111619614, Molecular Basis of RGS Protein Function in the Striatum, Mutational and Functional Analysis of the Melanoma Genome, G4935591845, G5366983142, G5957486411, G7176579579, G7683164002, Regulation of Neuronal GPCR Signaling
OpenAlex ID: W2922301188
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Cited by: 1
Related to: 10