Spelling suggestions: "subject:"biomedical 3research"" "subject:"biomedical 1research""
101 |
Optimized Mouse Models for the Discovery of Novel Targets and Testing of Melanoma Preventative AgentsHennessey, Rebecca Coral January 2018 (has links)
No description available.
|
102 |
HER2 and Folate Receptor Targeted Therapy is Enhanced by NK Cell-Activating CytokinesJaime-Ramirez, Alena Cristina 05 July 2013 (has links)
No description available.
|
103 |
Glutathione Reductase, Redox Homeostasis, and Mitochondrial DysfunctionREN, PEI 22 April 2013 (has links)
No description available.
|
104 |
Brining A Monitoring System To MarketNaples, Colin James 23 August 2013 (has links)
No description available.
|
105 |
Use of Annular Coded Aperture in Nuclear ImagingAthawale, Samita S. 27 August 2010 (has links)
No description available.
|
106 |
Signal formulation, segmentation, and lesion volume estimation in magnetic resonance imagesStein, Benjamin Reece 01 January 2001 (has links)
In this dissertation we present a new approach to estimate the volume of ischermic stroke lesions using magnetic resonance imagery (MRI). The approach is hierarchical, regularized, and guided by statistical theory, resulting in a confidence map for the lesion itself and a confidence interval for the lesion volume. We test the procedure on synthetic data and real MRI, with estimates to within 6% of the volumes from physicians' hand segmentations. These results compare favorably to those from other Bayesian-based methods. Also, we present a formulation of the free induction decay signal for several MR pulse sequences, which allow for the classification of distinct tissue types in MRI.
|
107 |
Left ventricular volume estimation from three -dimensional echocardiographyShin, Il-Seop 01 January 2007 (has links)
The objective of this research is to extend the clinical utility of three-dimensional echocardiography (3DE) by developing automated means for left ventricular (LV) function estimation. This dissertation presents our work on a semi-automated algorithm that, without extensive supervision, tracks the LV boundary through the spatial and temporal sequences of two-dimensional frames that constitute a 3DE data set. The construction of the algorithm is based on a framework of factor graph representations and probability propagation. One key component is the derivation of "LV edge likelihoods" as image features that provide "soft" edge information rather than a "hard" edge map to make LV tracking more robust to frame-to-frame variations in feature sizes and intensity levels. The algorithm begins with the operator marking some highly visible landmark points along the LV boundary in a few spatially separated frames. This takes a few seconds to complete, and is the only operator input to initiate the procedure. Full boundary estimates in these initial frames are completed by spline fitting to the selected points. Using spatial continuity in the LV boundary, these estimates establish search regions for the intermediate frames, within which boundary points are specified as those having highest edge likelihood. A similar procedure, employing forward and backward tracking, is used for the temporal sequence of frames at each spatial location. LV volume as a function of time is calculated from the set of estimated boundaries using a modified version of planimetry. Our system's performance is tested on gated-rotational and real-time 3DE data from both normal and diseased hearts, obtained using Philips ultrasound systems. The results are validated by comparison to the "gold standard" of nuclear scan (Single Photon Emission Computed Tomography or SPECT) volumes for the same hearts. As a critical part of our algorithm, the development of a method for characterizing the mean square error (MSE) in LV volume estimates is presented, which serves as the quality indicator that can flag unreliable estimates. The utility of this self-verification information is also validated as part of the nuclear scan comparison studies. Preliminary results show that it does seem to distinguish between more and less reliable estimates.
|
108 |
Integrative Network and Transcriptomics Approach Enables Computational Drug Repurposing and Drug Combination Discovery in MelanomaRegan-Fendt, Kelly E. 27 July 2018 (has links)
No description available.
|
109 |
Tumor Commensal Microbiota Activates an S100A7-TLR4-STAT-3 Signaling to Induce Chronic Inflammation and Consequent Growth and Metastasis of Breast CancerWilkie, Tasha, Wilkie 27 July 2018 (has links)
No description available.
|
110 |
Activating lymphocyte reactions against chronic lymphocytic leukemiaYano, Max January 2021 (has links)
No description available.
|
Page generated in 0.0613 seconds