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Relevant bibliographies by topics / Molecular Imaging

Academic literature on the topic 'Molecular Imaging'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2024

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Dissertations / Theses
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Journal articles on the topic "Molecular Imaging"

1

Bury, Bob. "Molecular imaging." South African Journal of Radiology 14, no. 4 (December 7, 2010): 82. http://dx.doi.org/10.4102/sajr.v14i4.449.

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Sperryn, Clive. "Molecular Imaging." South African Journal of Radiology 14, no. 4 (December 7, 2010): 126. http://dx.doi.org/10.4102/sajr.v14i4.463.

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Editorial, Article. "MOLECULAR IMAGING." Diagnostic radiology and radiotherapy 12, no. 1S (April 4, 2021): 144–49. http://dx.doi.org/10.22328/2079-5343-2021-12-s-144-149.

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Editorial, Article. "MOLECULAR IMAGING." Diagnostic radiology and radiotherapy, no. 1S (May 24, 2019): 116–24. http://dx.doi.org/10.22328/2079-5343-2019-s-1-116-124.

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Editorial, Artiсle. "MOLECULAR IMAGING." Diagnostic radiology and radiotherapy, no. 1S (April 22, 2020): 168–79. http://dx.doi.org/10.22328/2079-5343-2020-11-1s-168-179.

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UEDA, Masashi. "Molecular Imaging." Analytical Sciences 37, no. 6 (June 10, 2021): 797–98. http://dx.doi.org/10.2116/analsci.highlights2106.

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Editorial, Article. "MOLECULAR IMAGING." Diagnostic radiology and radiotherapy 13, no. 1S (April 14, 2022): 142–54. http://dx.doi.org/10.22328/2079-5343-2022-13-s-142-154.

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Fenderson, Bruce A. "MOLECULAR IMAGING." Shock 25, no. 3 (March 2006): 317. http://dx.doi.org/10.1097/01.shk.0000214139.49166.1b.

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Zheng, Gang, and Zhifei Dai. "Molecular Imaging." Bioconjugate Chemistry 31, no. 2 (February 19, 2020): 157–58. http://dx.doi.org/10.1021/acs.bioconjchem.0c00044.

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Pomper, Martin G. "Molecular Imaging." Academic Radiology 8, no. 11 (November 2001): 1141–53. http://dx.doi.org/10.1016/s1076-6332(03)80728-6.

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Dissertations / Theses on the topic "Molecular Imaging"

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DE, BIASIO VALERIA. "Nanosystems for molecular imaging." Doctoral thesis, Università del Piemonte Orientale, 2014. http://hdl.handle.net/11579/45958.

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Zotti, Linda Angela. "Molecular ordering and STM imaging of functionalized organic molecules." Thesis, University of Liverpool, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.479082.

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Somoza, Eduardo A. Jr. "UTILIZATION OF FLUORESCENCE MOLECULAR IMAGING TO OPTIMIZE RADIONUCLIDE IMAGING." Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1338904705.

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Talvik, Mirjam. "Clinical molecular imaging of schizophrenia /." Stockholm, 2003. http://diss.kib.ki.se/2003/91-7349-587-5/.

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Slusarczyk, Adrian L. (Adrian Lukas). "Molecular imaging with engineered physiology." Thesis, Massachusetts Institute of Technology, 2016. http://hdl.handle.net/1721.1/104229.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biological Engineering, 2016.
Cataloged from PDF version of thesis.
Includes bibliographical references (pages 125-133).
Using molecular imaging in vivo, biomolecular and cellular phenomena can be investigated within their relevant physiological context, addressing a central challenge for 21st century biomedicine and basic research. To advance neuroscience in particular, molecular-level measurements across the brain inside the intact organism are required. However, existing imaging strategies and available probes have been limited by serious constraints. Magnetic resonance imaging (MRI) provides deeper tissue penetration depth than optical imaging and better spatial resolution and greater versatility in sensor design than radioactive probes. The most important drawback for MRI probes has been the need for high concentrations in the micromolar to millimolar range, leading to analyte sequestration, complications for noninvasive brain delivery, and toxicity. Efforts to address the sensitivity problem, such as nuclear hyperpolarization, introduce their own technical constraints and so far lack generality. Here, we introduce a conceptually novel molecular imaging technique based on artificially induced physiological perturbations, enabling molecular MRI with nanomolar sensitivity. In this imaging strategy, we take advantage of blood as an abundant endogenous source of contrast compatible with multiple imaging modalities including MRI and optical imaging to decouple the concentration requirement for molecular sensing from the concentration requirement for imaging contrast. Highly potent vasoactive peptides are engineered to respond to specific biomolecular phenomena of interest at nanomolar concentrations by inducing dilation of the microvasculature, increased local bloodflow, and consequently, large changes in T₂*-weighted MRI contrast. This principle is exploited to design activatable probes for protease activity based on the calcitonin gene-related peptide (CGRP) and validate them for brain imaging in live rats; to use CGRP as a genetic reporter for cell tracking; and to create fusions of a vasoactive peptide from flies to previously characterized antibodies capable of crossing the blood-brain barrier (BBB), suggesting the possibility of minimally invasive brain delivery of such probes. We demonstrate the feasibility of highly sensitive molecular MRI with vasoactive probes at concentrations compatible with in situ expression of probes and delivery across the BBB, and show that vasoactive peptides are a versatile platform for MRI probe design which promises unprecedented in vivo molecular insights for biomedicine and neuroscience.
by Adrian L. Slusarczyk.
Ph. D.

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Keasberry, Natasha Ann. "Functionalised nanoparticles for molecular imaging." Thesis, Imperial College London, 2014. http://hdl.handle.net/10044/1/42886.

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This thesis describes the synthesis of iron oxide nanoparticles for use as contrast agents in biomedical imaging, specifically for MRI. The limitations of single imaging modalities can be overcome by the synergistic combination of two or more imaging techniques, e.g. the low sensitivity but high resolution of MRI complements the high sensitivity but low resolution of PET. The large surface area of superparamagnetic iron oxide nanoparticles (SPION) allows relatively simple functionalisation. The large size of a single combined nanoparticle MRI/PET probe would slow down in vivo movement, diminishing radioactivity before reaching its target. Pre-targeting using a magnetic nanoparticle followed by the injection of the radio-labelled molecule at the correct time will ensure radioactivity remains sufficiently high. Thus, the investigation of dual-modality probe development is also a focus of the thesis. Chapter 2 discusses the preparation of iron oxide nanoparticles with a core diameter of 6 nm via the high temperature thermal decomposition of iron salts. Direct modification to the surface of the nanoparticles was carried out using various small molecules with differing anchoring groups, the most successful being sodium alendronate, a bisphosphonate ligand. Chapter 3 describes the further functionalisation of the nanoparticles. One way this was achieved was by the incorporation of PEG chains of different lengths to increase water solubility and biocompatibility. Functionalisation with a strained alkyne for eventual in vitro/in vivo copper-free cycloaddition with an azide group was also achieved. The PET moiety was designed to be a 68Ga-azido-DOTA complex. Prior to radiolabelling with gallium-68, the copper-free cyclised resultant nanoparticles were characterised by the use of lanthanide analogues (Eu, Tb and Gd). Eu and Tb allowed for fluorescence spectroscopy, while the Gd allowed for relaxivity measurements to be carried out. Unexpected fluorescence results were observed for the Eu and Tb analogues. The Gd-NP conjugates are further investigated in Chapter 4. Combination of both a T1 and T2 moiety results in changes to the relaxivity of the resultant nanoparticle which can act as a dual-weighted MRI probe. The relaxivities are found to vary with modifications to the nanoparticle construct. Finally, preliminary in vitro experiments with macrophages were carried out to investigate whether there was significant preferential uptake between M1 and M2 macrophages. A single-chain variable fragment (scFv) specific to Fractalkine, a chemokine important in the progression of atherosclerosis was prepared, for use as a targeting moiety towards the imaging of vulnerable plaque.

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Strand, Joanna. "Affibody Molecules for PET Imaging." Doctoral thesis, Uppsala universitet, Institutionen för immunologi, genetik och patologi, 2015. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-259410.

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Optimization of Affibody molecules would allow for high contrast imaging of cancer associated surface receptors using molecular imaging. The primary aim of the thesis was to develop Affibody-based PET imaging agents to provide the highest possible sensitivity of RTK detection in vivo. The thesis evaluates the effect of radiolabelling chemistry on biodistribution and targeting properties of Affibody molecules directed against HER2 and PDGFRβ. The thesis is based on five published papers (I-V). Paper I. The targeting properties of maleimido derivatives of DOTA and NODAGA for site-specific labelling of a recombinant HER2-binding Affibody molecule radiolabelled with 68Ga were compared in vivo. Favourable in vivo properties were seen for the Affibody molecule with the combination of 68Ga with NODAGA. Paper II. The aim was to compare the biodistribution of 68Ga- and 111In-labelled HER2-targeting Affibody molecules containing DOTA, NOTA and NODAGA at the N-terminus. This paper also demonstrated favourable in vivo properties for Affibody molecules in combination with 68Ga and NODAGA placed on the N-terminus. Paper III. The influence of chelator positioning on the synthetic anti-HER2 affibody molecule labelled with 68Ga was investigated. The chelator DOTA was conjugated either at the N-terminus, the middle of helix-3 or at the C-terminus of the Affibody molecules. The N-terminus placement provided the highest tumour uptake and tumour-to-organ ratios. Paper IV. The aim of this study was to evaluate if the 68Ga labelled PDGFRβ-targeting Affibody would provide an imaging agent suitable for PDGFRβ visualization using PET. The 68Ga labelled conjugate provided high-contrast imaging of PDGFRβ-expressing tumours in vivo using microPET as early as 2h after injection. Paper V. This paper investigated if the replacement of IHPEM with IPEM as a linker molecule for radioiodination of Affibody molecules would reduce renal retention of radioactivity. Results showed that the use of the more lipophilic linker IPEM reduced the renal radioactivity retention for radioiodinated Affibody molecules. In conclusion, this thesis clearly demonstrates that the labelling strategy is of great importance with a substantial influence on the targeting properties of Affibody molecules and should be taken under serious considerations when developing new imaging agents.

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Rogers, Leon John. "Photofragment ion imaging." Thesis, University of Bristol, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.266958.

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Danfors, Torsten. "11C Molecular Imaging in Focal Epilepsy." Doctoral thesis, Uppsala universitet, Neurologi, 2012. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-179954.

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Epilepsy is a common neurological disease affecting 6 million people in Europe. Early prevention and accurate diagnosis and treatment are of importance to obtain seizure freedom. In this thesis new applications of carbon-11-labelled tracers in PET and autoradiographic studies were explored in focal epilepsy. Patients with low-grade gliomas often experience epileptic seizures. A retrospective PET-study assessing seizure activity, metabolic rate measured with 11C-methionine and other known prognostic factors was performed in patients with glioma. No correlation was found between seizure activity and uptake of methionine. The presence and termination of early seizures was a favourable prognostic factor. Activation of the neurokinin-1 (NK1) receptor by substance P (SP) induces epileptic activity. PET with the NK1 receptor antagonist GR205171 was performed in patients with temporal lobe epilepsy (TLE) and healthy controls. In TLE patients an increased NK1 receptor availability was found in both hemispheres, most pronounced in anterior cingulate gyrus ipsilateral to seizure onset. A positive correlation between NK1 receptors and seizure frequency was observed in ipsilateral medial structures consistent with an intrinsic network using the NK1-SP receptor system for transmission of seizure activity. The uptake of 18F-fluoro-deoxy-glucose (FDG) is related to cerebral blood flow (CBF). Previously, methods to estimate blood flow from dynamic PET data have been described. A retrospective study was conducted in 15 patients undergoing epilepsy surgery investigation, including PET with 11C-FDG and 11C-Flumazenil (FMZ). The dynamic FMZ dataset and pharmacokinetic modeling with a multilinear reference tissue model were used to determine images of relative CBF. Agreement between data of FDG and CBF was analyzed showing a close association between interictal brain metabolism and relative CBF. Epilepsy often occurs after traumatic brain injuries. Changes in glia and inhibitory neuronal cells contribute to the chain of events leading to seizures. Autoradiography with 11C-PK11195, 11C-L-deprenyl and 11C-Flumazenil in an animal model of posttraumatic epilepsy studied the temporal and spatial distribution of microglia, astrocytes and GABAergic neurons. Results showed an instant increase in microglial activity that subsequently normalized, a late formation of astrogliosis and an instant and prolonged decease in GABA binding. The model can be used to visualize pathophysiological events during the epileptogenesis.

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Morley, Nicholas Christopher Donald. "Molecular targeting for clinical cancer imaging." Thesis, University of Edinburgh, 2015. http://hdl.handle.net/1842/15880.

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Modern cancer treatment makes extensive use of clinical imaging methods for diagnosis and response assessment. To this end, there is increasing desire to non-invasively measure various drugs and biomarkers inside a patient on a centimetre scale. Despite undeniable preclinical progress and evaluation of many techniques, few new imaging drugs are emerging into pragmatic clinical cancer imaging. There are many drug targeting strategies, including target-affinity and activation-by-target. Affinity selections can identify binders from combinatorial libraries of heteropolymers such as nucleic-acid sequences and peptides. Using this approach, in combination with next-generation DNA sequencing, I identified sequences as binders of putative cancer biomarkers. In addition, I investigated a target-activated fluorescent probe as a reporter of cancer-associated enzyme activation. Messenger RNA levels for Leucine-rich-repeat containing 15 (LRRC15) are reported to be elevated in human, breast-cancer samples. I analysed a new antibody to LRRC15, which locates this protein in genetically triggered murine breast tumours and in their lysates on Western blot. Antibody staining also showed a distinct pattern in sections of normal murine kidney, and protein expression in human breast-cancer samples. LRRC15 affinity selection of phage peptide and aptamer libraries was performed with immunopurified protein, and this identified consensus sequences. However, specific binding of the peptides or aptamers to the target was not demonstrable. Alpha folate receptor overexpression has been described in many human tumours, particularly ovarian cancer. Cell-lines to enable whole-cell selection of binders to the folate receptor were developed. Specific staining with a folate-fluorophore compound validated these. Selection of peptide and aptamer binders showed early emergence of spurious dominant sequences, triggering abandonment of this approach. The cell-lines were used to test a folate-quantum dot conjugate, with disappointing results. Matrix Metalloproteinase-9 (MMP-9) activity in cancer has previously been described and pursued as a therapeutic target. A novel probe to report activity of MMP-9 was tested using fragments of murine tissue, successfully differentiating normal murine fat pad from pieces of murine mammary tumour. Significant off-target activation was also observed, particularly with kidney. Recombinant proteins based on human MMP-2 and -13 also activated the probe. Expression and activity of equivalent enzymes in the murine tissues and tumours were assessed using RT-PCR, Western blot, immunohistochemistry and zymography, but the basis of spurious activation remains obscure. In conclusion, a new antibody identifies LRRC15 in both human and murine breast cancers, and in the murine kidney. Library affinity selections with LRRC15 and the alpha folate receptor developed consensus sequences, but were unsuccessful. An MMP-9 activated probe successfully differentiated breast tumour from normal tissue but also showed significant off-target activation. Non-invasive detection and measurement of cancer biomarkers remains an important topic, likely to see much progress in coming decades. Some of the practical difficulties in developing reagents to achieve this are discussed.

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Books on the topic "Molecular Imaging"

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Vallabhajosula, Shankar. Molecular Imaging. Berlin, Heidelberg: Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-540-76735-0.

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Tian, Jie. Molecular Imaging. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-34303-2.

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Shah, Khalid, ed. Molecular Imaging. Totowa, NJ: Humana Press, 2011. http://dx.doi.org/10.1007/978-1-60761-901-7.

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W, Semmler, and Schwaiger Markus, eds. Molecular imaging. Berlin: Springer, 2008.

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W, Semmler, and Schwaiger Markus, eds. Molecular imaging. Berlin: Springer, 2008.

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Semmler, Wolfhard, and Markus Schwaiger, eds. Molecular Imaging I. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-72718-7.

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Semmler, Wolfhard, and Markus Schwaiger, eds. Molecular Imaging II. Berlin, Heidelberg: Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-77496-9.

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Targeted molecular imaging. Boca Raton: Taylor & Francis, 2012.

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Welch, Michael J., and William C. Eckelman. Targeted molecular imaging. Boca Raton: Taylor & Francis, 2012.

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Chen, Xiaoyuan, ed. Nanoplatform-Based Molecular Imaging. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2011. http://dx.doi.org/10.1002/9780470767047.

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Book chapters on the topic "Molecular Imaging"

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Haedicke, Katja, Susanne Kossatz, Thomas Reiner, and Jan Grimm. "Molecular Imaging and Molecular Imaging Technologies." In Imaging and Metabolism, 3–27. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-61401-4_1.

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Thukkani, Arun K., and Farouc A. Jaffer. "Molecular Imaging." In Atherosclerosis, 503–16. Hoboken, NJ: John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118828533.ch39.

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Morgan, Michael M., MacDonald J. Christie, Thomas Steckler, Ben J. Harrison, Christos Pantelis, Christof Baltes, Thomas Mueggler, et al. "Molecular Imaging." In Encyclopedia of Psychopharmacology, 791. Berlin, Heidelberg: Springer Berlin Heidelberg, 2010. http://dx.doi.org/10.1007/978-3-540-68706-1_3404.

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Patel, Nisha R., Michael L. Wong, Anthony E. Dragun, Stephan Mose, Bernadine R. Donahue, Jay S. Cooper, Filip T. Troicki, et al. "Molecular Imaging." In Encyclopedia of Radiation Oncology, 504. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-540-85516-3_494.

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Cervenka, Simon, and Lars Farde. "Molecular Imaging." In Neuroimaging in Schizophrenia, 145–59. Cham: Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-35206-6_8.

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Bäuerle, Tobias, and Wolfhard Semmler. "Molecular Imaging." In Encyclopedia of Cancer, 1–5. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27841-9_3813-6.

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Saha, Gopal B. "Molecular Imaging." In Fundamentals of Nuclear Pharmacy, 341–55. New York, NY: Springer New York, 2010. http://dx.doi.org/10.1007/978-1-4419-5860-0_14.

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Bäuerle, Tobias, and Wolfhard Semmler. "Molecular Imaging." In Encyclopedia of Cancer, 2898–901. Berlin, Heidelberg: Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-662-46875-3_3813.

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Saha, Gopal B. "Molecular Imaging." In Fundamentals of Nuclear Pharmacy, 355–71. Cham: Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-57580-3_14.

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Wu, Hubing, DeWei Tang, XiaoPing Zhao, Gengbiao Yuan, and Xinhui Su. "Molecular Imaging." In Nuclear Medicine in Oncology, 153–76. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-7458-6_11.

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Conference papers on the topic "Molecular Imaging"

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Ntziachristos, Vasilis. "Molecular imaging." In Frontiers in Optics. Washington, D.C.: OSA, 2004. http://dx.doi.org/10.1364/fio.2004.fthk1.

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Phelps, Michael. ""Molecular Imaging"." In Conference Proceedings. Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE, 2006. http://dx.doi.org/10.1109/iembs.2006.259771.

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Villa, Anna Maria, Paola Fusi, Chiara Pozzi, Marco Valtorta, Giulia Amicarelli, Daniel Adlerstein, and Silvia Maria Doglia. "Ethidium bromide as a probe of mtDNA replication in living cells." In Molecular Imaging. SPIE, 2007. http://dx.doi.org/10.1117/12.728243.

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Ntziachristos, Vasilis, and Jorge Ripoll. "Optical molecular imaging." In SPIE Proceedings, edited by Valery V. Tuchin. SPIE, 2004. http://dx.doi.org/10.1117/12.578304.

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Kiser, Jr., William L., Daniel Reinecke, Timothy DeGrado, Sibaprasad Bhattacharyya, and Robert A. Kruger. "Photoacoustic molecular imaging." In Biomedical Optics (BiOS) 2007, edited by Alexander A. Oraevsky and Lihong V. Wang. SPIE, 2007. http://dx.doi.org/10.1117/12.705136.

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Smith, Jason T., Enagnon Aguénounon, Sylvain Gioux, and Xavier Intes. "Depth-resolved macroscopic fluorescence lifetime imaging improved though spatial frequency domain imaging." In Molecular-Guided Surgery: Molecules, Devices, and Applications VII, edited by Summer L. Gibbs, Brian W. Pogue, and Sylvain Gioux. SPIE, 2021. http://dx.doi.org/10.1117/12.2578495.

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Feroldi, Fabio, Margherita Vaselli, Mariska Verlaan, Helene Knaus, Valentina Davidoiu, Danielle Vugts, Carla Molthoff, Guus van Dongen, and Johannes F. de Boer. "Combined structural and molecular imaging using optical coherence tomography and immunofluorescence imaging (Conference Presentation)." In Molecular-Guided Surgery: Molecules, Devices, and Applications VI, edited by Summer L. Gibbs, Brian W. Pogue, and Sylvain Gioux. SPIE, 2020. http://dx.doi.org/10.1117/12.2545222.

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Zhao, Ming, Xuefeng Wang, and David Nolte. "Molecular interferometric imaging study of molecular interactions." In Biomedical Optics (BiOS) 2008, edited by Alexander N. Cartwright and Dan V. Nicolau. SPIE, 2008. http://dx.doi.org/10.1117/12.760783.

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Harris, T. D., J. J. Macklin, J. K. Trautman, and L. E. Brus. "Imaging and Time-Resolved Spectroscopy of Single Molecules." In Laser Applications to Chemical and Environmental Analysis. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/lacea.1996.lwd.5.

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Recent progress in the fluorescence detection of individual molecules [1-8] suggests that a single dye molecule can be a useful tool to probe chemical identity and activity. Measurement of fluorescence lifetime [5,6] and spectrum [6] can be augmented by knowledge of molecular orientation using polarized light [3], and triplet [2] and photoisomer excitation, as well as diffusion processes, via fluorescence-intensity correlation. Applications of fluorescent probes include the study of the dynamic conformation of membrane-bound proteins, transport of and signaling by messenger molecules, and the optical detection of the sequence of DNA. While molecules can be spatially located using near-field microscopy [5-8], near-field probes can perturb the molecule under study. We show here that molecular properties can be determined easily and in a non-perturbative manner using far-field illumination, and we obtain unperturbed spectral and lifetime data that cannot be extracted from an ensemble measurement.

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Angelo, Joseph P., Martijn van de Giessen, and Sylvain Gioux. "Real-time endoscopic oxygenation imaging using single snapshot of optical properties (SSOP) imaging (Conference Presentation)." In Molecular-Guided Surgery: Molecules, Devices, and Applications II, edited by Brian W. Pogue and Sylvain Gioux. SPIE, 2016. http://dx.doi.org/10.1117/12.2213117.

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Reports on the topic "Molecular Imaging"

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Chen, Xiaoyuan. Molecular Imaging of Ovarian Carcinoma Angiogenesis. Fort Belvoir, VA: Defense Technical Information Center, March 2007. http://dx.doi.org/10.21236/ada489876.

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Chen, Xiaoyuan. Molecular Imaging of Ovarian Carcinoma Angiogenesis. Fort Belvoir, VA: Defense Technical Information Center, March 2009. http://dx.doi.org/10.21236/ada588287.

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Wang, Lei. Molecular Probes for Pancreatic Cancer Imaging. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.3105.

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Ho, Wilson. Spectroscopic Imaging of Molecular Functions at Surfaces. Office of Scientific and Technical Information (OSTI), December 2018. http://dx.doi.org/10.2172/1485203.

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Landers, Allen. Imaging Multi-Particle Atomic and Molecular Dynamics. Office of Scientific and Technical Information (OSTI), February 2016. http://dx.doi.org/10.2172/1237839.

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Cai, Weibo. Molecular Imaging and Therapy of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2015. http://dx.doi.org/10.21236/ada630120.

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Bohn, Paul W., and Jonathan V. Sweedler. Three Dimensional Molecular Imaging for Lignocellulosic Materials. Office of Scientific and Technical Information (OSTI), June 2011. http://dx.doi.org/10.2172/1043043.

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Panchapakesan, Balaji. Integrated Molecular Imaging and Therapy for Breast Cancer. Fort Belvoir, VA: Defense Technical Information Center, August 2008. http://dx.doi.org/10.21236/ada494146.

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Resau, James H. Molecular Based Imaging Determination of Breast Cancer Prognosis. Fort Belvoir, VA: Defense Technical Information Center, June 2002. http://dx.doi.org/10.21236/ada407431.

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Hackel, Benjamin. Patient Stratification with a Novel Molecular Imaging Agent. Fort Belvoir, VA: Defense Technical Information Center, December 2014. http://dx.doi.org/10.21236/ada614487.

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