5 results match your criteria: "Clark Center E-150[Affiliation]"
J Biomed Mater Res A
August 2016
Department of Orthopaedic Surgery, Stanford University School of Medicine, Clark Center E-150, 300 Pasteur Drive, Edwards R105, MC5341, Stanford, California, 94305.
Scaffold-mediated gene delivery holds great promise for tissue regeneration. However, previous attempts to induce bone regeneration using scaffold-mediated non-viral gene delivery rarely resulted in satisfactory healing. We report a novel platform with sustained release of minicircle DNA (MC) from PLGA scaffolds to accelerate bone repair.
View Article and Find Full Text PDFMol Imaging Biol
April 2015
Molecular Imaging Program at Stanford, Departments of Radiology and Bioengineering, Bio-X Program, Stanford University, 318 Campus Dr., Clark Center E-150, Stanford, CA, USA.
Purpose: To develop novel positron emission tomography (PET) agents for visualization and therapy monitoring of bacterial infections.
Procedures: It is known that maltose and maltodextrins are energy sources for bacteria. Hence, (18)F-labelled maltose derivatives could be a valuable tool for imaging bacterial infections.
J Biomed Opt
July 2011
Stanford University School of Medicine, Department of Pediatrics, Clark Center E-150, 318 Campus Drive, Stanford, California 94305-5427, USA.
Induction of heat shock protein (Hsp) expression correlates with cytoprotection, reduced tissue damage, and accelerated healing in animal models. Since Hsps are transcriptionally activated in response to stress, they can act as stress indicators in burn injury or surgical procedures that produce heat and thermal change. A fast in vivo readout for induction of Hsp transcription in tissues would allow for the study of these proteins as therapeutic effect mediators and reporters of thermal stress∕damage.
View Article and Find Full Text PDFJ Biomed Opt
May 2011
Department of Pediatrics, Stanford University School of Medicine, Clark Center E-150, 318 Campus Drive, Stanford, California 94305-5427, USA.
The cytoprotective response to thermal injury is characterized by transcriptional activation of "heat shock proteins" (hsp) and proinflammatory proteins. Expression of these proteins may predict cellular survival. Microarray analyses were performed to identify spatially distinct gene expression patterns responding to thermal injury.
View Article and Find Full Text PDFJ Nucl Med
May 2005
Molecular Imaging Program at Stanford, Department of Radiology, and Bio-X Program, Stanford University, 318 Campus Drive, Clark Center E-150, Stanford, CA 94305, USA.
Unlabelled: Numerous new molecular targets for diseases are rapidly being identified and validated in the postgenomic era, urging scientists to explore novel techniques for accelerating molecular probe development. In this study, matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS) was investigated as a potential tool for high-throughput screening and characterization of molecular imaging probes. Specifically, MALDI-TOF-MS was used to screen a small library of phosphonium cations for their ability to accumulate in cells.
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