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Alex Matter

Researcher at Agency for Science, Technology and Research

Publications -  56
Citations -  4190

Alex Matter is an academic researcher from Agency for Science, Technology and Research. The author has contributed to research in topics: Cytotoxic T cell & Antibody. The author has an hindex of 24, co-authored 56 publications receiving 3948 citations. Previous affiliations of Alex Matter include University of Geneva & École Normale Supérieure.

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Glivec (STI571, imatinib), a rationally developed, targeted anticancer drug

TL;DR: This work describes how this drug discovery programme led to the discovery and continuing development of Glivec (Gleevec in the United States), the first selective tyrosine-kinase inhibitor to be approved for the treatment of a cancer.
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A derivative of staurosporine (CGP 41 251) shows selectivity for protein kinase C inhibition and In vitro anti‐proliferative as well as In vivo anti‐tumor activity

TL;DR: An association between PKC inhibition and anti‐proliferative and anti-tumor activity is suggested and staurosporine and CGP 41 251 exerted growth inhibition in the human bladder carcinoma line T‐24, human promyelocytic leukemia line HL‐60 and bovine corneal endothelial cells at concentrations which correlated well with in vitroPKC inhibition.
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Wnt addiction of genetically defined cancers reversed by PORCN inhibition

TL;DR: A novel potent, orally available PORCN inhibitor, ETC-1922159, that blocks the secretion and activity of all Wnts is developed that is remarkably effective in treating RSPO-translocation bearing colorectal cancer patient-derived xenografts.
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Markers of tumor angiogenesis and proteolysis independently define high- and low-risk subsets of node-negative breast cancer patients.

TL;DR: Separate primary and validating clinical studies concur that tumor VEGF level is the most important prognostic parameter among several markers of tumor angiogenesis and proteolysis.
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Mouse thymus-independent and thymus-derived lymphoid cells : i. immunofluorescent and functional studies

TL;DR: The simultaneous use on mouse lymphoid suspensions of heterologous antisera directed against thymus-derived (T) cell mouse-specific lymphocyte antigen and brain-associated theta antigen and MBLA surface antigens allowed direct proof of the different specificity of these antisona by double immunofluorescence (IF) staining with selective visualization of fluorochromes.