Semi-targeted proteomics on two ovarian cancer serum samples, F10 and F12, from the sample set of the FOLFOX-4 study
Semi-targeted Mass Spectrometry proteomics study to detect 12 selected proteins of two serum samples belonging to the FOLFOX-4 study on heavly-pretreated ovarian cancer patients. The two samples, F10 and F12, are basal samples collected at before the first FOLFOX-4 treatment cycle (T0) and were selected for this study because they show a different proteome profile.
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Semi-targeted proteomics FOLFOX-4_Ovarian cancer_V5.docx
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Created: 11th Apr 2021 at 04:22
Last updated: 27th Jun 2021 at 18:13
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Version 4 (latest) Created 27th Jun 2021 at 18:13 by Maria Paola Costi
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Version 3 Created 3rd May 2021 at 21:04 by Maria Paola Costi
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Projects: NMTrypI - New Medicines for Trypanosomatidic Infections, Mass spectrometry proteomics for biomarker discovery, Thymidylate synthase dimer dissociation, BioTarget Database, Compound Data, Giulia Malpezzi PhD raw data, Defining the role of fibroblasts in skin expansion, Thymidylate synthase dimer disrupters induce DNA damage, halt cell growth and overcome drug resistance in colorectal cancer
Institutions: Università degli Studi di Modena e Reggio Emilia (UNIMORE), Life Science, University of Modena and Reggio Emilia
https://orcid.org/0000-0002-0443-5402
Projects: Mass spectrometry proteomics for biomarker discovery, TEAD-(YAP) structure, function and inhibition, Thymidylate synthase dimer dissociation
Web page: Not specified
Programme: Cancer drug discovery preclinical research
Public web page: Not specified
