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Raphael Rubin

Researcher at Thomas Jefferson University

Publications -  103
Citations -  7535

Raphael Rubin is an academic researcher from Thomas Jefferson University. The author has contributed to research in topics: Growth factor & Liver transplantation. The author has an hindex of 45, co-authored 102 publications receiving 7413 citations. Previous affiliations of Raphael Rubin include Thomas Jefferson University Hospital & University of Nebraska Medical Center.

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Simian virus 40 large tumor antigen is unable to transform mouse embryonic fibroblasts lacking type 1 insulin-like growth factor receptor.

TL;DR: Results demonstrate that signaling via the IGF-I receptor is an indispensable component of the SV40 transformation pathway, and is further supported from the results of antisense RNA experiments with tumor cell lines showing that interference with the function of the IGF -I receptor has a profound effect on anchorage-independent growth, even under conditions that only modestly affect growth in monolayers.
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Effect of a null mutation of the insulin-like growth factor I receptor gene on growth and transformation of mouse embryo fibroblasts.

TL;DR: Reintroduction into R- cells (or their derivatives) of a plasmid expressing the human insulin-like growth factor I receptor RNA and protein restores their ability to grow with purified growth factors or in soft agar.
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The Insulin-like Growth Factor I Receptor Protects Tumor Cells from Apoptosis in Vivo

TL;DR: It is concluded that the IGF-IR activated by its ligands plays a very important protective role in programmed cell death, and that its protective action is even more striking in vivo than in vitro.
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A functional insulin-like growth factor i receptor is required for the mitogenic and transforming activities of the epidermal growth factor receptor

TL;DR: The results indicate that at least in mouse embryo fibroblasts, the EGFR requires the presence of a functional IGF-I receptor for its mitogenic and transforming activities.
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Rat Glioblastoma Cells Expressing an Antisense RNA to the Insulin-like Growth Factor-1 (IGF-1) Receptor Are Nontumorigenic and Induce Regression of Wild-Type Tumors

TL;DR: The fact that the injection of C6 cells expressing an antisense RNA to IGF-1R RNA leads to regression of already established wild-type C6 tumors suggests the possibility of practical applications and demonstrates the critical importance of the IGF- 1R in glioblastoma cell growth, clonogenicity, and tumorigenicity.