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Simon C. Watkins

Researcher at University of Pittsburgh

Publications -  999
Citations -  75771

Simon C. Watkins is an academic researcher from University of Pittsburgh. The author has contributed to research in topics: Apoptosis & Immune system. The author has an hindex of 135, co-authored 950 publications receiving 68358 citations. Previous affiliations of Simon C. Watkins include Harvard University & Children's National Medical Center.

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Sequential delivery of interferon-alpha gene and DCs to intracranial gliomas promotes an effective antitumor response

TL;DR: In vitro migration assays revealed the ability of DCs to migrate toward the tumor, suggesting that i.t. injected DCs migrate through the glioma, and this combination of gene therapy and cellular immunotherapy may be an effective future strategy for treating human gliomas.
Journal Article

Intercellular and Intracellular Events Following the MHC-Unrestricted TCR Recognition of a Tumor-Specific Peptide Epitope on the Epithelial Antigen MUC1

TL;DR: MHC-unrestricted TCR triggering, therefore, involves similar intercellular and intracellular events that participate in the conventional, MHC-restricted Ag recognition.
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alpha-actinin-2 is a new component of the dystrophin-glycoprotein complex.

TL;DR: It is proposed that dystrophin forms lateral, multicontact association with actin and that binding of alpha-actinin-2 to the carboxyl-terminus of dystrophicin is the communication link between the integrins and the dystphin/dystroph in-glycoprotein complex.
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Caveolae-dependent and -independent uptake of albumin in cultured rodent pulmonary endothelial cells.

TL;DR: A portion of overall uptake in pulmonary endothelial cells is cav-1 insensitive and appears to involve clathrin-mediated endocytosis and macropinocytotic-like process, in addition to the well described caveolar-dependent pulmonary endothelium cell endocyTosis of albumin.
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Pharmacological Rescue of the Mutant Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Detected by Use of a Novel Fluorescence Platform

TL;DR: A fluorescence detection platform using fluorogen-activating proteins (FAPs) is developed to directly detect FAP-CFTR trafficking to the cell surface using a cell-impermeant probe, indicating that this approach should be useful as a screening assay in diseases that impair protein trafficking toThe cell surface.