Gotowe bibliografie tematyczne / In vivo bioluminescence imaging

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Gotowa bibliografia na temat „In vivo bioluminescence imaging”

Autor: Grafiati
Data publikacji: 3 czerwca 2025
Data aktualizacji: 31 lipca 2025

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Artykuły w czasopismach na temat "In vivo bioluminescence imaging"

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Liu, Tracy W., Seth T. Gammon, David Fuentes, and David Piwnica-Worms. "Multi-Modal Multi-Spectral Intravital Macroscopic Imaging of Signaling Dynamics in Real Time during Tumor–Immune Interactions." Cells 10, no. 3 (2021): 489. http://dx.doi.org/10.3390/cells10030489.

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A major obstacle in studying the interplay between cancer cells and the immune system has been the examination of proposed biological pathways and cell interactions in a dynamic, physiologically relevant system in vivo. Intravital imaging strategies are one of the few molecular imaging techniques that can follow biological processes at cellular resolution over long periods of time in the same individual. Bioluminescence imaging has become a standard preclinical in vivo optical imaging technique with ever-expanding versatility as a result of the development of new emission bioluminescent report
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Wiles, Siouxsie, Karen M. Pickard, Katian Peng, Thomas T. MacDonald, and Gad Frankel. "In Vivo Bioluminescence Imaging of the Murine Pathogen Citrobacter rodentium." Infection and Immunity 74, no. 9 (2006): 5391–96. http://dx.doi.org/10.1128/iai.00848-06.

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ABSTRACT Citrobacter rodentium is a natural mouse pathogen related to enteropathogenic and enterohemorrhagic Escherichia coli. We have previously utilized bioluminescence imaging (BLI) to determine the in vivo colonization dynamics of C. rodentium. However, due to the oxygen requirement of the bioluminescence system and the colonic localization of C. rodentium, in vivo localization studies were performed using harvested organs. Here, we report the detection of bioluminescent C. rodentium and commensal E. coli during colonization of the gastrointestinal tract in intact living animals. Biolumine
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Brovko, Lubov Y., and Mansel W. Griffiths. "Illuminating Cellular Physiology: Recent Developments." Science Progress 90, no. 2-3 (2007): 129–60. http://dx.doi.org/10.3184/003685007x215986.

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Bioluminescent methods are gaining more and more attention among scientists due to their sensitivity, selectivity and simplicity; coupled with the fact that the bioluminescence can be monitored both in vitro and in vivo. Since the discovery of bioluminescence in the 19th century, enzymes involved in the bioluminescent process have been isolated and cloned. The bioluminescent reactions in several different organisms have also been fully characterized and used as reporters in a wide variety of biochemical assays. From the 1990s it became clear that bioluminescence can be detected and quantified
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Jawhara, Samir, and Serge Mordon. "In Vivo Imaging of Bioluminescent Escherichia coli in a Cutaneous Wound Infection Model for Evaluation of an Antibiotic Therapy." Antimicrobial Agents and Chemotherapy 48, no. 9 (2004): 3436–41. http://dx.doi.org/10.1128/aac.48.9.3436-3441.2004.

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ABSTRACT A rapid, continuous method for noninvasively monitoring the effectiveness of several antibacterial agents in real time by using a model of wound infection was developed. This study was divided into three steps: (i) construction of a plasmid to transform Escherichia coli into a bioluminescent variant, (ii) study of the bioluminescent E. coli in vitro as a function of temperature and pH, and (iii) determination of the MIC and the minimal bactericidal concentration of sulfamethoxazole-trimethoprim (SMX-TMP). Finally, the efficacy of SMX-TMP was monitored in vivo in a cutaneous wound mode
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Pesnel, Sabrina, Smaïl Akkoul, Roger Ledée, et al. "Use of an Image Restoration Process to Improve Spatial Resolution in Bioluminescence Imaging." Molecular Imaging 10, no. 6 (2011): 7290.2011.00012. http://dx.doi.org/10.2310/7290.2011.00012.

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To improve spatial resolution in in vivo bioluminescence imaging, a photon scattering correction, image restoration method was tested. The chosen algorithm was tested on in vivo bioluminescent images acquired on three representative tumor models: subcutaneous, pulmonary, and disseminated peritoneal. Tumor size was chosen as a quantitative criterion, such that the tumor reference measurements (determined photographically or by computed tomography) were compared to those derived from bioluminescent images, before and after restoration. This technique allowed a significant reduction to be achieve
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Simonyan, Hayk, Chansol Hurr, and Colin N. Young. "A synthetic luciferin improves in vivo bioluminescence imaging of gene expression in cardiovascular brain regions." Physiological Genomics 48, no. 10 (2016): 762–70. http://dx.doi.org/10.1152/physiolgenomics.00055.2016.

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Bioluminescence imaging is an effective tool for in vivo investigation of molecular processes. We have demonstrated the applicability of bioluminescence imaging to spatiotemporally monitor gene expression in cardioregulatory brain nuclei during the development of cardiovascular disease, via incorporation of firefly luciferase into living animals, combined with exogenous d-luciferin substrate administration. Nevertheless, d-luciferin uptake into the brain tissue is low, which decreases the sensitivity of bioluminescence detection, particularly when considering small changes in gene expression i
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Liu, Tracy W., Seth T. Gammon, and David Piwnica-Worms. "Multi-Modal Multi-Spectral Intravital Microscopic Imaging of Signaling Dynamics in Real-Time during Tumor–Immune Interactions." Cells 10, no. 3 (2021): 499. http://dx.doi.org/10.3390/cells10030499.

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Intravital microscopic imaging (IVM) allows for the study of interactions between immune cells and tumor cells in a dynamic, physiologically relevant system in vivo. Current IVM strategies primarily use fluorescence imaging; however, with the advances in bioluminescence imaging and the development of new bioluminescent reporters with expanded emission spectra, the applications for bioluminescence are extending to single cell imaging. Herein, we describe a molecular imaging window chamber platform that uniquely combines both bioluminescent and fluorescent genetically encoded reporters, as well
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Kudo, Ayane, Haruka Osedo, Rahmawati Aisyah, et al. "Serum Amyloid A3 Promoter-Luciferase Reporter Mice Are Useful for Early Drug-Induced Nephrotoxicity Detection." International Journal of Molecular Sciences 25, no. 10 (2024): 5124. http://dx.doi.org/10.3390/ijms25105124.

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Early detection of drug-induced kidney injury is essential for drug development. In this study, multiple low-dose aristolochic acid (AA) and cisplatin (Cis) injections increased renal mRNA levels of inflammation, fibrosis, and renal tubule injury markers. We applied a serum amyloid A3 (Saa3) promoter-driven luciferase reporter (Saa3 promoter-luc mice) to these two tubulointerstitial nephritis models and performed in vivo bioluminescence imaging to monitor early renal pathologies. The bioluminescent signals from renal tissues with AA or CIS injections were stronger than those from normal kidney
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Rajashekara, Gireesh, David A. Glover, Menachem Banai, David O'Callaghan, and Gary A. Splitter. "Attenuated Bioluminescent Brucella melitensis Mutants GR019 (virB4), GR024 (galE), and GR026 (BMEI1090-BMEI1091) Confer Protection in Mice." Infection and Immunity 74, no. 5 (2006): 2925–36. http://dx.doi.org/10.1128/iai.74.5.2925-2936.2006.

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ABSTRACT In vivo bioluminescence imaging is a persuasive approach to investigate a number of issues in microbial pathogenesis. Previously, we have applied bioluminescence imaging to gain greater insight into Brucella melitensis pathogenesis. Endowing Brucella with bioluminescence allowed direct visualization of bacterial dissemination, pattern of tissue localization, and the contribution of Brucella genes to virulence. In this report, we describe the pathogenicity of three attenuated bioluminescent B. melitensis mutants, GR019 (virB4), GR024 (galE), and GR026 (BMEI1090-BMEI1091), and the dynam
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Zhang, Shuang, Chengcai Leng, Hongbo Liu, Kun Wang, and Jie Tian. "Fast in vivo bioluminescence tomography using a novel pure optical imaging technique." Journal of Innovative Optical Health Sciences 10, no. 03 (2017): 1750003. http://dx.doi.org/10.1142/s1793545817500031.

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Bioluminescence tomography (BLT) is a novel optical molecular imaging technique that advanced the conventional planar bioluminescence imaging (BLI) into a quantifiable three-dimensional (3D) approach in preclinical living animal studies in oncology. In order to solve the inverse problem and reconstruct tumor lesions inside animal body accurately, the prior structural information is commonly obtained from X-ray computed tomography (CT). This strategy requires a complicated hybrid imaging system, extensive post imaging analysis and involvement of ionizing radiation. Moreover, the overall robustn
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Rozprawy doktorskie na temat "In vivo bioluminescence imaging"

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Adams, Spencer T. Jr. "Deconstructing bioluminescence: from molecular detail to in vivo imaging." eScholarship@UMMS, 2020. https://escholarship.umassmed.edu/gsbs_diss/1064.

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Bioluminescence is the chemical production of light that results when a luciferase enzyme catalyzes the luminogenic oxidation of a small-molecule luciferin substrate. The numerous luciferases and luciferins nature has evolved can be used to illuminate biological processes, from in vitro assays to imaging processes in live animals. However, we can improve the utility of bioluminescence through modification of these enzymes and substrates. My thesis work focuses on developing reporters that expand the bioluminescent toolkit and improving our understanding of how bioluminescence works on a molecu
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Stowe, Cassandra. "Development of firefly luciferase bioluminescence for in vivo optical imaging." Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10041771/.

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Firefly luciferase is ubiquitously used as a genetic reporter for the non-invasive bioluminescence imaging of small animal models. This widespread use of Firefly luciferase in vivo has been facilitated by genetic engineering producing mutants which are extremely stable at physiological conditions. In addition, the red-shifting of bioluminescence has resulted in the enhanced penetration of light emission through biological tissue. However, the use of bioluminescence in vivo is still largely limited to the tracking of single events within a model. This is due to the differential attenuation of l
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Belarbi, Essia. "Etude de la physiopathologie des infections à alphavirus arthritogènes par une approche d’imagerie in vivo." Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS073.

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Les alphavirus arthritogènes de la rivière Ross (RRV) et du chikungunya (CHIKV) sont des arbovirus à l’origine de maladies inflammatoires musculosquelettiques chez l'homme. Ils sont largement distribués dans le monde et provoquent périodiquement des épidémies explosives. Les principaux signes cliniques lors d’une infection par un alphavirus arthritogène sont les myalgies, polyarthrites et arthralgies intenses pouvant persister plusieurs mois après l'infection. Les mécanismes de développement de l’infection et des manifestations persistantes sont peu connus. Pour étudier la pathogenèse de l'inf
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Maiwald, Gelja. "In vivo bioluminescence imaging for monitoring of siRNA mediated luciferase knockdown in tumor models." kostenfrei, 2009. http://d-nb.info/1001449320/34.

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Maiwald, Gelja. "In vivo bioluminescence imaging for monitoring of siRNA mediated luciferase knockdown in tumor models." Diss., lmu, 2010. http://nbn-resolving.de/urn:nbn:de:bvb:19-113028.

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Bolin, Celeste, Caleb Sutherland, Ken Tawara, Jim Moselhy, and Cheryl Jorcyk. "Novel mouse mammary cell lines for in vivo bioluminescence imaging (BLI) of bone metastasis." BioMed Central, 2012. http://hdl.handle.net/10150/610032.

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BACKGROUND:Tumor cell lines that can be tracked in vivo during tumorigenesis and metastasis provide vital tools for studying the specific cellular mechanisms that mediate these processes as well as investigating therapeutic targets to inhibit them. The goal of this study was to engineer imageable mouse mammary tumor cell lines with discrete propensities to metastasize to bone in vivo. Two novel luciferase expressing cell lines were developed and characterized for use in the study of breast cancer metastasis to bone in a syngeneic mouse model.RESULTS:The 4 T1.2 luc3 and 66c14 luc2 cell lines we
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Pinel, Karine. "Imagerie in vivo du contrôle de l’inhibition génique et de l’électroporation d’ARN." Thesis, Bordeaux 2, 2012. http://www.theses.fr/2012BOR22004/document.

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Ces travaux de thèse d’imagerie moléculaire et translationnelle proposent, sur des modèles murins, deux approches innovantes pour les thérapies géniques. La plupart des cancers sont associés à des dérégulations de l’expression génique et certains gènes sont surexprimés. L’utilisation de microARN (miARN) permet d’envisager une réduction de l’expression d’un gène spécifique mais il est nécessaire de limiter cette inhibition au tissu pathologique. L’utilisation des promoteurs thermo-inductibles couplés à un dépôt local de chaleur autorise un contrôle spatial et temporel de l’expression génique in
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Rettig, Garrett Richard. "Strategies to test nuclear localization of non-viral gene delivery vectors in vitro and in vivo." Diss., University of Iowa, 2008. https://ir.uiowa.edu/etd/212.

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Non-viral gene delivery is plagued by low transfection levels compared to viral delivery. The nuclear envelope presents a significant obstacle for non-viral vectors. A peptide-based nuclear localizing sequence has been incorporated into non-viral vectors to traverse the nuclear envelope. Here, we selected a photo-chemical method for covalently labeling the peptide onto plasmid DNA. The hypothesis of this work was to incorporate a nuclear localizing sequence into a non-viral delivery vector, demonstrate increased nuclear uptake and show a subsequent increase in transgene expression both in vitr
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Lin, Yuan. "In Vivo Imaging of Engraftment and Enrichment of Lentiviral Transduced Hematopoietic Bone Marrow Cells Under MGMT-P140K Mediated Selection." Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1295039430.

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Pesnel, Sabrina. "Développement de modalités d'imagerie in vivo pour l'oncologie expérimentale." Phd thesis, Université d'Orléans, 2010. http://tel.archives-ouvertes.fr/tel-00597262.

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L'imagerie in vivo du petit animal est de plus en plus utilisée en pharmacologie pour identifier et caractériser l'activité de nouveaux agents anticancéreux.La première partie de ma thèse a consisté à développer des outils pour améliorer la quantification enbioluminescence. Une méthode, basée sur les caractéristiques spectrales des photons émis, a été établie pour corriger l'absorption tissulaire. La seconde, faisant appel aux méthodes de restauration d'images, avait pour but de corriger la diffusion pour augmenter la résolution. Dans un second temps, j'ai mis en place des modèles in vivo de t
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Książki na temat "In vivo bioluminescence imaging"

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Brovko, Lubov. Bioluminescence and fluorescence for in vivo imaging. SPIE Press, 2010.

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Bai, Mingfeng, ed. In Vivo Fluorescence Imaging. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3721-9.

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Schröder, Leif, and Cornelius Faber, eds. In vivo NMR Imaging. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-219-9.

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Ntziachristos, Vasilis, Anne Leroy-Willig, and Bertrand Tavitian, eds. Textbook ofin vivo Imaging in Vertebrates. John Wiley & Sons, Ltd, 2006. http://dx.doi.org/10.1002/9780470029596.

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Shields, Anthony F., and Pat Price, eds. In Vivo Imaging of Cancer Therapy. Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-341-7.

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1965-, Ahrens Eric T., ed. In vivo cellular and molecular imaging. Elsevier Academic Press, 2005.

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R, Eaton Gareth, Eaton Sandra S, and Ohno Keiicho, eds. EPR imaging and in vivo EPR. CRC Press, 1991.

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D, Frostig Ron, ed. In vivo optical imaging of brain function. 2nd ed. Taylor & Francis, 2009.

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Hoffman, Robert M., ed. In Vivo Cellular Imaging Using Fluorescent Proteins. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-797-2.

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Ntziachristos, Vasilis. Textbook of in vivo imaging in vertebrates. J. Wiley, 2007.

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Części książek na temat "In vivo bioluminescence imaging"

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Conway, Michael, Tingting Xu, Amelia Brumbaugh, Anna Young, Dan Close, and Steven Ripp. "Bioluminescence." In Imaging from Cells to Animals In Vivo. CRC Press, 2020. http://dx.doi.org/10.1201/9781315174662-6.

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Wu, Wenxiao, Laizhong Chen, Jing Li, Lupei Du, and Minyong Li. "Bioluminogenic Imaging of AminopeptidaseN In Vitro and In Vivo." In Bioluminescence. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3813-1_7.

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Degenfeld, Georges, Tom S. Wehrman, and Helen M. Blau. "Imaging β-Galactosidase Activity In Vivo Using Sequential Reporter-Enzyme Luminescence." In Bioluminescence. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-321-3_20.

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Mastraccio, Kate E., Celeste Huaman, Eric D. Laing, Christopher C. Broder, and Brian C. Schaefer. "Longitudinal Tracing of Lyssavirus Infection in Mice via In Vivo Bioluminescence Imaging." In Bioluminescence. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2453-1_30.

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Sanaki-Matsumiya, Marina, and Ryoichiro Kageyama. "Time-Lapse Bioluminescence Imaging of Hes7 Expression In Vitro and Ex Vivo." In Bioluminescence. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2473-9_25.

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Yamada, Kentaro, and Akira Nishizono. "In Vivo Bioluminescent Imaging of Rabies Virus Infection and Evaluation of Antiviral Drug." In Bioluminescence. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2453-1_28.

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Gangadaran, Prakash, Ji Min Oh, Ramya Lakshmi Rajendran, and Byeong-Cheol Ahn. "In Vivo Bioluminescent Imaging of Bone Marrow-Derived Mesenchymal Stem Cells in Mice." In Bioluminescence. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2473-9_21.

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Rettig, Garrett R., and Kevin G. Rice. "Quantitative In Vivo Imaging of Non-viral-Mediated Gene Expression and RNAi-Mediated Knockdown." In Bioluminescence. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-321-3_13.

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Barbier, Mariette, Justin Bevere, and F. Heath Damron. "In Vivo Bacterial Imaging Using Bioluminescence." In Methods in Molecular Biology. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7860-1_7.

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Ohta, Yasuyuki, Emi Nomura, Shinae Kizaka-Kondoh, and Koji Abe. "In Vivo Imaging of Oxidative and Hypoxic Stresses in Mice Model of Amyotrophic Lateral Sclerosis." In Bioluminescence. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-2473-9_22.

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Streszczenia konferencji na temat "In vivo bioluminescence imaging"

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Cong, Wenxiang, Durairaj Kumar, Yubin Kang, et al. "In vivo tomographic imaging based on bioluminescence." In Optical Science and Technology, the SPIE 49th Annual Meeting, edited by Ulrich Bonse. SPIE, 2004. http://dx.doi.org/10.1117/12.560522.

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Wang, Ken Kang-Hsin, Xiangkun Xu, Zijian Deng, et al. "Optical tomography-guided system for pre-clinical radiotherapy research." In Digital Holography and Three-Dimensional Imaging. Optica Publishing Group, 2023. http://dx.doi.org/10.1364/dh.2023.hm2e.3.

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We advance the in vivo cancer imaging capability of small animal irradiators to include bioluminescence and fluorescence tomography. The imaging system is expected to enhance preclinical radiation guidance and assessment for anatomical and functional targets.
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Liu, Kai, Jie Tian, Sr., Chenghu Qin, et al. "In vivo heterogeneous tomographic bioluminescence imaging via a higher-order approximation forward model." In SPIE Medical Imaging, edited by John B. Weaver and Robert C. Molthen. SPIE, 2011. http://dx.doi.org/10.1117/12.878040.

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Troy, T. L., D. G. Stearns, D. N. Nilson, and B. W. Rice. "Development of a 3D optical imaging system for in vivo detection of bioluminescence." In Biomedical Topical Meeting. OSA, 2002. http://dx.doi.org/10.1364/bio.2002.tud4.

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Gao, Yuan, Kun Wang, Hui Meng, Yu An, Shixin Jiang, and Jie Tian. "Bioluminescence tomography based on bilateral weight Laplace method for in vivo morphological imaging of glioma." In Imaging, Manipulation, and Analysis of Biomolecules, Cells, and Tissues XVII, edited by Daniel L. Farkas, James F. Leary, and Attila Tarnok. SPIE, 2019. http://dx.doi.org/10.1117/12.2508285.

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Tan, J. J., K. Furuya, F. Boudreault, E. Brochiero, and R. Grygorczyk. "Mechanisms of Inflation-Induced ATP Release in Ex Vivo Rat Lungs: A Bioluminescence Imaging Study." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a7245.

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Liu, Kai, Jie Tian, Xin Yang, et al. "A fast reconstruction algorithm based on parallel coordinate descent optimization for in vivo tomographic bioluminescence imaging." In 2011 8th IEEE International Symposium on Biomedical Imaging (ISBI 2011). IEEE, 2011. http://dx.doi.org/10.1109/isbi.2011.5872452.

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Foulke, John, Luping Chen, Alexei Miagkov, Elizabeth Turner-Gillies, Lysa-Anne Volpe, and Fang Tian. "Abstract 88: Stable luciferase expressing cell lines forin vivo xenograft and syngeneic tumor model bioluminescence imaging." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-88.

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Foulke, John, Luping Chen, Alexei Miagkov, Elizabeth Turner-Gillies, Lysa-Anne Volpe, and Fang Tian. "Abstract 88: Stable luciferase expressing cell lines forin vivo xenograft and syngeneic tumor model bioluminescence imaging." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-88.

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Alshetaiwi, Hamad, Sivasai Balivada, Marla Pyle, Tej B. Shrestha, Stefan H. Bossmann, and Deryl L. Troyer. "Abstract 738: Neutrophil tracking study on mammary tumors using bioluminescence imagingin vivo." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-738.

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Raporty organizacyjne na temat "In vivo bioluminescence imaging"

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Gruenhagen, Jason Alan. Bioanalytical Applications of Real-Time ATP Imaging Via Bioluminescence. Office of Scientific and Technical Information (OSTI), 2003. http://dx.doi.org/10.2172/822057.

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Synold, Timothy W. In Vivo Imaging of MDR1A Gene Expression. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada433034.

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Hsu, E. W. Imaging of Human Hepatic Stem Cells In Vivo. Office of Scientific and Technical Information (OSTI), 2006. http://dx.doi.org/10.2172/877135.

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CHATZIIOANNOU, ARION. DEVELOPMENT OF A DUAL MODALITY TOMOGRAPHIC IMAGING SYSTEM FOR BIOLUMINESCENCE AND PET. Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1031734.

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Greenwald, A. C. Compact Gamma-Ray Imager for In-Vivo Gene Imaging. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/833940.

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Han, Xiaoxing. Quantitative In Vivo Imaging of Breast Tumor Extracellular Matrix. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada541944.

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Han, Xiaoxing. Quantitative In Vivo Imaging of Breast Tumor Extracellular Matrix. Defense Technical Information Center, 2009. http://dx.doi.org/10.21236/ada549531.

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Han, Xiaoxing. Quantitative In Vivo Imaging of Breast Tumor Extracellular Matrix. Defense Technical Information Center, 2011. http://dx.doi.org/10.21236/ada552848.

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Piwnica-Worms, David, and Ken Blumer. Elucidating Mechanisms of Farnesyltransferase Inhibitor Action and Resistance in Breast Cancer by Bioluminescence Imaging. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada491469.

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Piwnica-Worms, David. Elucidating Mechanisms of Farnesyltransferase Inhibitor Action and Resistance in Breast Cancer by Bioluminescence Imaging. Defense Technical Information Center, 2010. http://dx.doi.org/10.21236/ada540951.

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