Relevant bibliographies by topics / In vivo characterization

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'In vivo characterization'

Author: Grafiati
Published: 4 June 2021
Last updated: 6 February 2022

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Journal articles on the topic "In vivo characterization"

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Sharma, Rakesh Kumar, and Anil Kumar Midda. "Preparation of Sustained Release Microspheres of Aceclofenac: Characterization & in-vivo studies." International Journal of Research and Development in Pharmacy & Life Sciences 6, no. 7 (December 2017): 2862–66. http://dx.doi.org/10.21276/ijrdpl.2278-0238.2017.6(7).2862-2866.

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Loiola, Bruna R., Luiz A. S. Abreu, and Helcio R. B. Orlande. "Thermal Characterization of Ex Vivo Tissue." Critical Reviews in Biomedical Engineering 48, no. 2 (2020): 111–24. http://dx.doi.org/10.1615/critrevbiomedeng.2020034068.

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Appay, Victor, John J. Zaunders, Laura Papagno, Julian Sutton, Angel Jaramillo, Anele Waters, Philippa Easterbrook, et al. "Characterization of CD4+CTLs Ex Vivo." Journal of Immunology 168, no. 11 (June 1, 2002): 5954–58. http://dx.doi.org/10.4049/jimmunol.168.11.5954.

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Keduka, Etsuko, Yukiko K. Hayashi, Sherine Shalaby, Hiroaki Mitsuhashi, Satoru Noguchi, Ikuya Nonaka, and Ichizo Nishino. "In Vivo Characterization of Mutant Myotilins." American Journal of Pathology 180, no. 4 (April 2012): 1570–80. http://dx.doi.org/10.1016/j.ajpath.2011.12.040.

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Ko, Match W. L., Leo K. K. Leung, David C. C. Lam, and Christopher K. S. Leung. "Characterization of corneal tangent modulusin vivo." Acta Ophthalmologica 91, no. 4 (January 22, 2013): e263-e269. http://dx.doi.org/10.1111/aos.12066.

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Trani, Jose L., Howard K. Song, Susan M. Lerner, Hooman Noorchashm, Joseph W. Markmann, Jing Wang, Clyde F. Barker, Ali Naji, and James F. Markmann. "IN VIVO CHARACTERIZATION OF CELLULAR XENOIMMUNITY." Transplantation 67, no. 9 (May 1999): S554. http://dx.doi.org/10.1097/00007890-199905150-00072.

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Miyoshi, Ko, Masato Asanuma, Ikuko Miyazaki, Shinsuke Matsuzaki, Masaya Tohyama, and Norio Ogawa. "Characterization of pericentrin isoforms in vivo." Biochemical and Biophysical Research Communications 351, no. 3 (December 2006): 745–49. http://dx.doi.org/10.1016/j.bbrc.2006.10.101.

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Piñero, David P., and Natividad Alcón. "In vivo characterization of corneal biomechanics." Journal of Cataract & Refractive Surgery 40, no. 6 (June 2014): 870–87. http://dx.doi.org/10.1016/j.jcrs.2014.03.021.

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Faramarzalian, Ali, David Prabhu, Ahmad Abdul-Aziz, Wei Wang, Daniel Chamie, Hirosada Yamamoto, Yusuke Fujino, et al. "Ex Vivo Cryoimaging for Plaque Characterization." JACC: Cardiovascular Imaging 7, no. 4 (April 2014): 430–32. http://dx.doi.org/10.1016/j.jcmg.2013.08.017.

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Humeniuk, Rachel E., Jennifer Ong, David I. B. Kerr, and Jason M. White. "Characterization of GABAB ligands in vivo." General Pharmacology: The Vascular System 26, no. 2 (March 1995): 417–24. http://dx.doi.org/10.1016/0306-3623(94)00175-m.

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Dissertations / Theses on the topic "In vivo characterization"

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Cayer, Christian. ""In vivo" Behavorial Characterization of Anxiolytic Botanicals." Thèse, Université d'Ottawa / University of Ottawa, 2011. http://hdl.handle.net/10393/20473.

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This thesis studied three plants traditionally used for treating a variety of anxiety related conditions. The three species were Roseroot, Rhodiola rosea from Nunavik, Cordonsillo, Piper amalago from Belize and “Sin Susto”, Souroubea sympetala from Costa Rica. The main objective of this research project was to investigate effects on behavior of these traditionally used native plants. It was found that the crude ethanol extracts derived from these plants administered intragastrically had measurable anxiolytic effects in male Sprague Dawley rats. Rats treated with extracts of these plants were then tested in several behavioral paradigms: elevated plus maze (EPM), social interaction (SI), conditioned emotional response (CER) and fear potentiated startle FPS. “Sin susto” produced significant anti-anxiety effects in several paradigms. Its active principle, betulinic acid, was significantly active in the EPM and FPS at a dose of 0.5mg/kg. Cordonsillo had strong activity in the SI paradigm and Roseroot in the CER paradigm. The results suggest that traditional use is based on pharmacological activity of the plants.
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Biasiolli, Luca. "In-vivo MRI characterization of atherosclerotic plaques." Thesis, University of Oxford, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.558196.

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Acute ischemic events associated with atherosclerosis are most often caused by rupture or erosion of unstable plaques. Clinical studies have demonstrated that in-vivo multi- contrast MRI can characterize plaque morphology and composition to evaluate the vulnerability of atherosclerotic plaques. The standard protocol for carotid imaging uses the Double-Inversion-Recovery (DIR) Fast-Spin-Echo (FSE) pulse sequence to acquire black-blood 2D high-resolution cross-sectional T\W, PDW and T2W images. With the addition of bright-blood Time-of-Flight images, it was demonstrated that in-vivo multi- contrast MRI could discriminate the major plaque components: lipid-rich necrotic core, intra-plaque haemorrhage, fibrous tissue and calcification. Given the nature and the large amount of multi-contrast MRI data, clinical studies of atherosclerosis would benefit from the availability of reliable and accurate automated techniques for image registration, segmentation and plaque classification. Recent multi-contrast MRI studies presented automatic plaque characterization methods that showed promising results under ex-vivo and in-vivo conditions. This thesis investigates some weaknesses in the current image acquisition and analysis techniques, which can affect the results of in- vivo MRI plaque characterization, and then proposes novel methods to advance the understanding of atherosclerosis in the carotid arteries. An automated multi -contrast registration algorithm that corrects for misalignments between carotid images caused by patient motion using sub-pixel accuracy and different similarity metrics was developed and validated. This project also used an alternative in-vivo carotid imaging approach based on the DIR Multi-Echo-Spin-Echo (Multi-SE) pulse sequence that acquired a series of black-blood 2D high-resolution cross-sectional images at different echo times. Quantitative T2 maps and synthetic multi-contrast images of carotid arteries were calculated from the Multi-SE images. T2 maps were automatically segmented and classified to provide in-vivo T2 measurements of the main plaque components, while Multi-SE synthetic images were compared with FSE images to demonstrate that the FSE acquisition strategy causes a significant loss of vessel edge sharpness.
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Liu, Zhen. "In Vivo Three-Dimensional Characterization of mRNA Nuclear Export." Bowling Green State University / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1353608190.

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Raju, Balasundara I. (Balasundara Iyyavu) 1972. "High frequency ultrasonic characterization of human skin In vivo." Thesis, Massachusetts Institute of Technology, 2002. http://hdl.handle.net/1721.1/29232.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Electrical Engineering and Computer Science, 2002.
Includes bibliographical references (p. 144-161).
High frequency (>20 MHz) ultrasound has numerous potential applications in dermatology because of its ability to penetrate several millimeters into the skin and provide information at a spatial resolution of tens of microns. However, conventional B-scan images of skin tissues often lack the capability to characterize and differentiate various skin tissues. In this work, quantitative ultrasonic methods using the attenuation coefficient, backscatter coefficient, and echo envelope statistics were studied for their potential to characterize human skin tissues in vivo. A high frequency ultrasound system was developed using polymer transducers, a pulser/receiver, high-speed digitizer, 3-axis scanning system, and a PC. Data collected using three different transducers with center frequencies of 28, 30 and 44 MHz were processed to determine the characteristics of normal human dermis and subcutaneous fat. Attenuation coefficients were obtained by computing spectral slopes vs. depth, with the transducers axially translated to minimize diffraction effects. Backscatter coefficients were obtained by compensating recorded backscatter spectra for system-dependent effects, and additionally for one transducer, using the reference phantom technique. Good agreement was seen between the results from the different transducers/methods. The attenuation coefficients were well described by a linear frequency dependence whose slope showed significant differences between the forearm and fingertip dermis, but not between the forearm dermis and fat. The backscatter coefficient of the dermis showed an increasing trend with frequency and was significantly higher than that of fat.
(cont.) A maximum likelihood fit of six probability distributions (Rayleigh, Rician, K, Nakagami, Weibull, and Generalized Gamma) to fluctuations in echo envelope data showed that the Generalized Gamma distribution modeled the envelope better than the other distributions. Fat was seen to exhibit significantly more pre-Rayleigh behavior than the dermis. Data were also obtained from the skin of patients patch-tested for contact dermatitis. A significant increase in skin thickness, decrease in mean backscatter of the upper dermis, and decrease in attenuation coefficient slope was found at the affected sites compared to normal skin. However, no differences in terms of echo statistics were found in the mid-dermis. These results indicate that a combination of ultrasonic parameters have the potential to non-invasively characterize skin tissues.
by Balasundara I. Raju.
Ph.D.
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Babina, Arianne M. "In vivo characterization of RNA cis-regulators in bacteria." Thesis, Boston College, 2017. http://hdl.handle.net/2345/bc-ir:107922.

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Thesis advisor: Michelle M. Meyer
Bacteria commonly utilize cis-acting mRNA structures that bind specific molecules to control gene expression in response to changing cellular conditions. Examples of these ligand-sensing RNA cis-regulators are found throughout the bacterial world and include riboswitches, which interact with small metabolites to modulate the expression of fundamental metabolic genes, and the RNA structures that bind select ribosomal proteins to regulate entire ribosomal protein operons. Despite advances in both non-coding RNA discovery and validation, many predicted regulatory RNA motifs remain uncharacterized and little work has examined how RNA cis-regulators behave within their physiological context in the cell. Furthermore, it is not well understood how structured RNA regulators emerge and are maintained within bacterial genomes. In this thesis, I validate the biological function of a conserved RNA cis-regulator of ribosomal protein synthesis previously discovered by my group using bioinformatic approaches. I then investigate how bacteria respond to the loss of two different cis-regulatory RNA structures. Using Bacillus subtilis as a model organism, I introduce point mutations into the native loci of the ribosomal protein L20-interacting RNA cis-regulator and the tandem glycine riboswitch and assay the strains for fitness defects. I find that disrupting these regulatory RNA structures results in severe mutant phenotypes, especially under harsh conditions such as low temperatures or high glycine concentrations. Together, this body of work highlights the advantages of examining RNA behavior within its biological context and emphasizes the important role RNA cis-regulators play in overall organismal viability. My studies shed light on the selective pressures that impact structured RNA evolution in vivo and reinforce the potential of cis-regulatory RNAs as novel antimicrobial targets
Thesis (PhD) — Boston College, 2017
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Biology
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Rahman, Md Mominur. "In vivo characterization of Hsp104 variants in Saccharomyces cerevisiae." Thesis, Högskolan i Skövde, Institutionen för biovetenskap, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-20187.

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Cell stress, caused by misfolded or aggregated proteins or exposure to certain environmental stressors, activates stress detectors and selected analysis processes within the cell, resulting intranscriptional regulation and synthesis of factors that influence appropriate folding or removal of misaligned proteins to recover proteostasis. Yeasts are given a sophisticated and interconnected system to restore from the disruption of proteostasis, which involves molecular chaperones and protein degradation pathways as significant participants. Hsp104 is a stress response protein that, through an unknown mechanism, stimulates the reactivation of heatdamaged proteins in yeast. The aim of this thesis study is to learn more about Hsp104 function and location in young and old yeast cells. On the one hand, we aim to see how Hsp104 wildtype vs. mutant forms are distributed in young vs. elderly yeast cells. As a negative control, we employed the mutant variant of this protein. We also wanted to stress Hsp104 wildtype and mutant versions to see whether there are any variations in behaviour or protein levels. All research was carried out in yeast, with biochemical tests and high-throughput technologies like flow cytometry. Hsp104GFP signal were increased in the nucleus of Hsp104 wildtype cells with the increasing of cellular age. As well as, after heatshock treatment the Hsp104GFP aggregation was raised in Hsp104 wildtype and mutant forms. The results data demonstrated that Hsp104 protein levels were increased with cellular age and heatshock treatment enhanced the Hsp104 aggregation in Hsp104 wildtype and mutant forms.
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Liapis, Stephen Constantine. "Discovery and In Vivo Characterization of Long Noncoding RNAs." Thesis, Harvard University, 2016. http://nrs.harvard.edu/urn-3:HUL.InstRepos:33493297.

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The noncoding genome, or the portion of the genome that does not encode for proteins, encompasses >95% of the human genome. It has been found that the majority of disease-associated genetic variants identified by genome-wide association studies (GWAS) are located in this noncoding 95%, where they have the potential to affect regions that control transcription (promoters, enhancers) and noncoding RNAs that also can influence gene expression. The discovery of these alterations has already contributed to a better understanding of the etiology of human diseases and has begun to yield insight into the function of these noncoding loci I am interested in studying how the noncoding genome functions and contributes to human development and disease pathology, especially when it is considered that our understanding of human disease is almost entirely contained within the realm of the <5% of the genome that is protein coding. Toward this end, I have focused my studies on one part of the noncoding genome, long noncoding RNAs. In order to identify whether long noncoding RNAs are important for mammalian development and disease, our lab created a set of lincRNA knockout animal models in which a cassette expressing beta-galactosidase (lacZ) replaces the lincRNA DNA sequence. I have used these models for the in vivo characterization of several lincRNAs, including Fendrr in the lungs, Brn1b in the brain, Tug1 in the testes, and Cox2 in the innate immune system. Each of these studies reveals perturbations in development induced by loss of function of the respective lincRNA locus, and demonstrates promising potential for further examination of the role these molecules play in human disease.
Biology, Molecular and Cellular
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Yadav, Nitin. "In Vivo characterization of Epileptic Tissue with Optical Spectroscopy." FIU Digital Commons, 2012. http://digitalcommons.fiu.edu/etd/728.

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For children with intractable seizures, surgical removal of epileptic foci, if identifiable and feasible, can be an effective way to reduce or eliminate seizures. The success of this type of surgery strongly hinges upon the ability to identify and demarcate those epileptic foci. The ultimate goal of this research project is to develop an effective technology for detection of unique in vivo pathophysiological characteristics of epileptic cortex and, subsequently, to use this technology to guide epilepsy surgery intraoperatively. In this PhD dissertation the feasibility of using optical spectroscopy to identify unique in vivo pathophysiological characteristics of epileptic cortex was evaluated and proven using the data collected from children undergoing epilepsy surgery. In this first in vivo human study, static diffuse reflectance and fluorescence spectra were measured from the epileptic cortex, defined by intraoperative ECoG, and its surrounding tissue from pediatric patients undergoing epilepsy surgery. When feasible, biopsy samples were taken from the investigated sites for the subsequent histological analysis. Using the histological data as the gold standard, spectral data was analyzed with statistical tools. The results of the analysis show that static diffuse reflectance spectroscopy and its combination with static fluorescence spectroscopy can be used to effectively differentiate between epileptic cortex with histopathological abnormalities and normal cortex in vivo with a high degree of accuracy. To maximize the efficiency of optical spectroscopy in detecting and localizing epileptic cortex intraoperatively, the static system was upgraded to investigate histopathological abnormalities deep within the epileptic cortex, as well as to detect unique temporal pathophysiological characteristics of epileptic cortex. Detection of deep abnormalities within the epileptic cortex prompted a redesign of the fiberoptic probe. A mechanical probe holder was also designed and constructed to maintain the probe contact pressure and contact point during the time dependent measurements. The dynamic diffuse reflectance spectroscopy system was used to characterize in vivo pediatric epileptic cortex. The results of the study show that some unique wavelength dependent temporal characteristics (e.g., multiple horizontal bands in the correlation coefficient map g(λref = 800 nm, λcomp,t)) can be found in the time dependent recordings of diffuse reflectance spectra from epileptic cortex defined by ECoG.
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Ryan, de Medeiros Anna Katharina [Verfasser], and Katja Elisabeth [Akademischer Betreuer] Odening. "In vivo und ex vivo Charakterisierung des arrhythmogenen Phänotyps transgener SQT1 Kaninchen = In vivo and ex vivo characterization of the arrhythmic phenotype of transgenic SQT1 rabbits." Freiburg : Universität, 2018. http://d-nb.info/1150643420/34.

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Mobed, Maryam. "In-vitro and in-vivo characterization of carboxymethylchitin-coated liposomes." Thesis, McGill University, 1996. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=42098.

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The survival of red blood cells in circulation has been correlated to a negative surface charge in the membrane due to the presence of N-acetyl neuraminic acid (NANA) residues. In this study, biodegradable NANA analogs such as the polyelectrolytes Carboxymethylchitin (CMC) and Carboxymethyl/Glycolchitin (CO) have been adsorbed by physical adsorption onto the surface of positive and neutral liposomes. The dye Alcian Blue has been used to standardize the initial polymer concentration between unequally substituted polymer batches of the same molecular weight. The amount of polymer adsorbed on the surface of the liposomes can be quantified using chitinase from Streptomyces griseus (EC 3.2.1.14), provided that the polymeric substrate is first desorbed from the surface of the liposomes. A Factorial Design is used to optimize the adsorption conditions of CMC and CO onto 0.22 $ mu$m diameter liposomes in phosphate buffer saline (PBS, $ kappa$ = 154 mM, pH = 7.4). The molecular weight of the polymer ranges from $5.00 times 10 sp4$ to $1.20 times 10 sp6.$ Increasing the liposome diameter from 0.22 to 0.45 $ mu$m reduces the extent of polymer-induced aggregation in PBS buffer. Polymer adsorption results in disaggregation of liposome suspensions for all polymer-coated suspensions in plasma and blood. The theoretical stability ratios (W) obtained using the classical DLVO theory show that the CMC-coated liposomes are more stable than the CO-coated and stealth (DSPC:CHOL:DSPE-PEG2000,5:4:1) liposomes. Meanwhile, experimental values of W prove that the lipid-grafted stealth is the most stable suspension. Results of simulations of liposome-macrophage interactions show that the polymer-coated liposomes are not prone to uptake by macrophages prior and after plasma incubation. Measurements of zeta potential, calorimetry and plasma protein adsorption on stealth, polymer-coated and (DSPC:CHOL:DMPG, 5:4:1) ( (-)) liposomes show that for the polymer-coated liposomes the change in zeta p
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Books on the topic "In vivo characterization"

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Karaskov, Elizabeta. In vivo characterization of ordered factor recruitment at CIITA inducible promoter IV. Ottawa: National Library of Canada, 2003.

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Müller, Rainer H. Colloidal carriers for controlled drug delivery and targeting: Modification, characterization, and in vivo distribution. Stuttgart: Wissenschaftliche Verlagsgesellschaft, 1991.

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Joshi, Mital. Development and characterization of a graded, in vivo, compressive, murine model of spinal cord injury. Ottawa: National Library of Canada, 2000.

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Kroeker, Randall Murray. In vivo characterization of NMR relaxation times. 1987.

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Juliette, Lisa Yvonne. In vivo and in vitro characterization of ammonia monooxygenase in Nitrosomonas europaea. 1995.

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Rahman, Mohammad Mohsin. In-vivo and in-vitro characterization of a human ependymoma-derived cell line. 1985.

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Griffiths, Emily Kathleen. Characterization of the in vivo roles of the adapter proteins ADAP and CBL-3. 2002.

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Characterization of rat glomerular epithelial cells in culture: A comparison to rat glomeruli in vivo. Ottawa: National Library of Canada = Bibliothèque nationale du Canada, 1993.

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Dymarkowski, Steven. In Vivo Analysis & Characterization of Myocardial Ischemia & Infarction: Experimental Mri-Studies (Acta Biomedica Lovaniensia, 288). Leuven Univ Pr, 2003.

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Lahooti, Shahab. In vitro and in vivo characterization of genetically engineered cells microencapsulated in a HEMA-MMA copolymer. 1999.

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Book chapters on the topic "In vivo characterization"

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Ophir, J., I. Cespedes, N. Maklad, and H. Ponnekanti. "Elastography: A Method for Imaging the Elastic Properties of Tissue in vivo." In Ultrasonic Tissue Characterization, 95–123. Tokyo: Springer Japan, 1996. http://dx.doi.org/10.1007/978-4-431-68382-7_7.

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Liu, Guofeng, Jianhui Sheng, and Yanli Zhao. "In Vivo Near-Infrared Fluorescence Imaging." In Nanotechnology Characterization Tools for Biosensing and Medical Diagnosis, 67–125. Berlin, Heidelberg: Springer Berlin Heidelberg, 2018. http://dx.doi.org/10.1007/978-3-662-56333-5_2.

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Kusuhara, Hiroyuki, Kenta Yoshida, and Yuichi Sugiyama. "In Vivo Characterization of Interactions on Transporters." In Transporters in Drug Development, 67–97. New York, NY: Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-8229-1_4.

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Hodges, Lee Ann. "In Vivo Characterization of Oral Multiparticulate Systems." In Advances in Delivery Science and Technology, 359–86. New York, NY: Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7012-4_14.

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Rascio, Federica, Chiara Divella, and Giuseppe Grandaliano. "CTL and Transplantation: Tissue In Vivo Characterization." In Methods in Molecular Biology, 283–94. New York, NY: Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1158-5_16.

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Mittal, Vikas, and Nadejda B. Matsko. "Macromolecular Distributions in Biological Organisms In Vivo." In Analytical Imaging Techniques for Soft Matter Characterization, 31–47. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-30400-2_3.

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Mittal, Vikas, and Nadejda B. Matsko. "Cellular Dynamics (Protein Transport, Mineralization In vivo)." In Analytical Imaging Techniques for Soft Matter Characterization, 77–83. Berlin, Heidelberg: Springer Berlin Heidelberg, 2012. http://dx.doi.org/10.1007/978-3-642-30400-2_6.

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Herranz, F., M. P. Morales, I. Rodríguez, and J. Ruiz-Cabello. "Iron Oxide Nanoparticle-Based MRI Contrast Agents: Characterization and In Vivo Use." In Magnetic Characterization Techniques for Nanomaterials, 85–120. Berlin, Heidelberg: Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-52780-1_3.

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Wagnières, Georges A., Seiichi Iinuma, Kevin T. Schomacker, Tom Deutsch, and Tayyaba Hasan. "In Vivo Tissue Characterization Using Environmentally Sensitive Fluorochromes." In Fluorescence Microscopy and Fluorescent Probes, 203–9. Boston, MA: Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1866-6_30.

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Laugier, Pascal. "Quantitative Ultrasound Instrumentation for Bone In Vivo Characterization." In Bone Quantitative Ultrasound, 47–71. Dordrecht: Springer Netherlands, 2010. http://dx.doi.org/10.1007/978-94-007-0017-8_3.

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Conference papers on the topic "In vivo characterization"

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Iliev, Blagoy P., Gheorghe A. M. Pop, and Gerard C. M. Meijer. "In-vivo Blood Characterization System." In IEEE Instrumentation and Measurement Technology Conference. IEEE, 2006. http://dx.doi.org/10.1109/imtc.2006.328249.

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Blagoy P. Iliev. "In-vivo Blood Characterization System." In 2006 IEEE Instrumentation and Measurement Technology. IEEE, 2006. http://dx.doi.org/10.1109/imtc.2006.235367.

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Puppels, Gerwin J., Matthijs van Aken, Rolf Wolthuis, Peter J. Caspers, Tom C. Bakker Schut, Hajo A. Bruining, Tjeerd J. Roemer, Hendrik P. J. Buschman, Michael L. Wach, and J. S. Robinson, Jr. "In-vivo tissue characterization by Raman spectroscopy." In BiOS '98 International Biomedical Optics Symposium, edited by Henry H. Mantsch and Michael Jackson. SPIE, 1998. http://dx.doi.org/10.1117/12.306086.

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Crawford, Bridget M., Pietro Strobbia, Hsin-Neng Wang, Rodolfo Zentella, Maxim I. Boyanov, Zhen-Ming Pei, Tai-Ping Sun, Kenneth M. Kemner, and Tuan Vo-Dinh. "In vivo detection of microRNA within plants using plasmonic nanosensors." In Plasmonics: Design, Materials, Fabrication, Characterization, and Applications XVII, edited by Takuo Tanaka and Din Ping Tsai. SPIE, 2019. http://dx.doi.org/10.1117/12.2529818.

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Bulykina, Anastasiia B., Victoria A. Ryzhova, and Valery V. Korotaev. "In vivo skin surface study by scattered ellipsometry method." In Optical Methods for Inspection, Characterization, and Imaging of Biomaterials IV, edited by Pietro Ferraro, Monika Ritsch-Marte, Simonetta Grilli, and Christoph K. Hitzenberger. SPIE, 2019. http://dx.doi.org/10.1117/12.2527625.

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Xu, G., Z. Meng, J. Lin, C. Deng, P. Carson, J. Fowlkes, S. Tomlins, et al. "In vivo biopsy by photoacousticUS based tissue characterization." In 2015 IEEE International Ultrasonics Symposium (IUS). IEEE, 2015. http://dx.doi.org/10.1109/ultsym.2015.0216.

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Demir, A. Fatih, Qammer H. Abbasi, Z. Esad Ankarali, Erchin Serpedin, and Huseyin Arslan. "Numerical characterization of in vivo wireless communication channels." In 2014 IEEE MTT-S International Microwave Workshop Series on RF and Wireless Technologies for Biomedical and Healthcare Applications (IMWS-BIO). IEEE, 2014. http://dx.doi.org/10.1109/imws-bio.2014.7032392.

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Demir, A. Fatih, Qammer H. Abbasi, Z. Esat Ankarali, Marwa Qaraqe, Erchin Serpedin, and Huseyin Arslan. "Experimental Characterization of In Vivo Wireless Communication Channels." In 2015 IEEE 82nd Vehicular Technology Conference (VTC Fall). IEEE, 2015. http://dx.doi.org/10.1109/vtcfall.2015.7390942.

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Pal, Saswati, Nabiul Islam, Sudip Misra, and Sasitharan Balasubramaniam. "In Vivo Channel Characterization for Dengue Virus Infection." In NANOCOM '19: The Sixth Annual ACM International Conference on Nanoscale Computing and Communication. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3345312.3345480.

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Lin, W. C., J. Ragheb, S. Bhatia, Mahlon Johnson, D. Sandberg, A. Fernandez, G. Morrison, M. Duchowny, and P. Jayakar. "In vivo optical characterization of pediatric epileptogenic lesions." In Biomedical Optics (BiOS) 2007, edited by Nikiforos Kollias, Bernard Choi, Haishan Zeng, Reza S. Malek, Brian J. Wong, Justus F. R. Ilgner, Kenton W. Gregory, Guillermo J. Tearney, Henry Hirschberg, and Steen J. Madsen. SPIE, 2007. http://dx.doi.org/10.1117/12.700717.

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Reports on the topic "In vivo characterization"

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DE Belle, Ian. Cloning and Characterization of Active Egr-1 Target Genes by In Vivo Crosslinking. Fort Belvoir, VA: Defense Technical Information Center, May 2001. http://dx.doi.org/10.21236/ada395170.

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DE Belle, Ian. Cloning and Characterization of Active Egr-1 Target Genes by In Vivo Crosslinking. Fort Belvoir, VA: Defense Technical Information Center, May 2000. http://dx.doi.org/10.21236/ada382458.

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Ya Wang. Characterization of the role of Fhit in maintenance of genomic integrity following low dose radiation, in vivo and in vitro. Office of Scientific and Technical Information (OSTI), May 2010. http://dx.doi.org/10.2172/990617.

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Wang, Ya. Characterization of the role of Fhit in maintenance of genomic integrity following low dose radiation, in vivo and in vitro. Office of Scientific and Technical Information (OSTI), May 2010. http://dx.doi.org/10.2172/1073626.

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Rosenberg, Avi Z. In-Vivo Characterization of Mammalian Polarity Genes as Novel Tumor Suppressors Involved in Breast Cancer Development and Progression in a Mouse Model. Fort Belvoir, VA: Defense Technical Information Center, March 2006. http://dx.doi.org/10.21236/ada462385.

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Sadar, Marianne D. Characterization of a New In Vivo Prostate Tumor Model that Progresses to Androgen-Independence and its Application in Determining Changes in Gene Expression. Fort Belvoir, VA: Defense Technical Information Center, November 2002. http://dx.doi.org/10.21236/ada413293.

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Cai, Lingshuang, Jacek A. Koziel, Jeremiah Davis, Yin-Cheung Lo, and Hongwei Xin. Characterization of Volatile Organic Compounds and Odors by in vivo Sampling of Beef Cattle Rumen Gas Using Solid Phase Microextraction and Gas Chromatography-Mass Spectrometry-Olfactometry. Ames (Iowa): Iowa State University, January 2007. http://dx.doi.org/10.31274/ans_air-180814-58.

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