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Simone Silberman

Researcher at Loyola University Chicago

Publications -  11
Citations -  634

Simone Silberman is an academic researcher from Loyola University Chicago. The author has contributed to research in topics: Cell culture & Gentamicin protection assay. The author has an hindex of 9, co-authored 11 publications receiving 628 citations.

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Journal Article

Inhibition by Human Recombinant Tissue Inhibitor of Metalloproteinases of Human Amnion Invasion and Lung Colonization by Murine B16-F10 Melanoma Cells

TL;DR: The inhibition of lung colonization in C57BL/6 mice by rTIMP is one of the first examples showing an antimetastatic effect of a selective metalloproteinase inhibitor in a mammalian animal model, and supports an essential role for metalliproteinase(s) in the extravasation and invasion of tumor cells during lung colonization by blood-borne tumor cells.
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Immediate centrifugation of oxygenator contents after cardiopulmonary bypass. Role in maximum blood conservation.

TL;DR: Centrifugation of oxygenator contents was found to be safe, sterile, and effective in concentrating red cells without damage and serves as a means of minimizing the consequences of fluid overload after cardiopulmonary bypass.
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Role of Mitogen-activated Protein Kinases and c-Jun/AP-1 trans-Activating Activity in the Regulation of Protease mRNAs and the Malignant Phenotype in NIH 3T3 Fibroblasts

TL;DR: It is concluded that high ERK activity is required for both protease Phenotypes, whereas the JNK pathway and c-Jun/AP-1 activity are not required for transformation but regulate a switch between uPA and CL protease phenotypes in both transformed and untransformed cells.
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Characterization of Downstream Ras Signals That Induce Alternative Protease-dependent Invasive Phenotypes

TL;DR: The JNK pathway acts as a switch between two distinct protease phenotypes that are redundant in their abilities to grow tumors and metastasize.
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Acute megakaryoblastic leukemia in Down's syndrome: report of a case and review of cytogenetic findings.

TL;DR: Serial cytogenetic studies using banding techniques at various stages during the course of the disease showed several chromosomal abnormalities (unbalanced translocation between chromosomes 1 and 4 leading to trisomy 1q,trisomy 7q, monosomy 7p, and a reciprocal translocated between chromosomes 10 and 16).