Academic literature on the topic 'Histology|Biomedical engineering'

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Journal articles on the topic "Histology|Biomedical engineering":

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do Amaral, Ronaldo J. F. C., Kátia D. Arcanjo, Márcia C. El-Cheikh, and Felipe L. de Oliveira. "The Peritoneum: Health, Disease, and Perspectives regarding Tissue Engineering and Cell Therapies." Cells Tissues Organs 204, no. 5-6 (2017): 211–17. http://dx.doi.org/10.1159/000479924.

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There are several pathologies associated with the peritoneum, such as mesothelioma and peritonitis. Moreover, the peritoneum is widely used in ultrafiltration procedures, i.e., peritoneal dialysis, presenting advantages over hemodialysis. On the other hand, ultrafiltration failure may lead to dialysis-induced fibrosis and hypervolemia. Therefore, the pathophysiological study of this tissue is of extreme biomedical importance. Studies investigating the biology of the cells dwelling in the peritoneum wall provide evidence of their plasticity and progenitor features. For instance, both mesothelial and submesothelial cells present characteristics similar to mesenchymal stem cells, including osteogenic and adipogenic differentiation potential, support of extramedullary hematopoiesis, modulation of inflammatory responses, and regulation of tumor progression. Indeed, the participation of each cell type in peritoneal pathological and physiological phenomena is still under debate, especially regarding a possible differentiation pathway connecting these peritoneal cells. The primary aim of this review is to raise this discussion. In order to do so, we will firstly provide an overview of the peritoneum anatomy, histology, and ontology, and finally we will address how a better understanding of peritoneal cell biology may contribute to future cell therapy and tissue engineering approaches.
2

Pinto, Joana F., Hugo Plácido da Silva, Francisco Melo, and Ana Fred. "ScientIST: Biomedical Engineering Experiments Supported by Mobile Devices, Cloud and IoT." Signals 1, no. 2 (September 7, 2020): 110–20. http://dx.doi.org/10.3390/signals1020006.

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Currently, mobile devices such as smartphones or tablets are widespread within the student community. However, their potential to be used in classrooms is yet to be fully explored. Our work proposes an approach that benefits from the ease of access to mobile devices, and combines it with state-of-the-art software and hardware. This approach builds upon previous developments from our team on biosignal acquisition and analysis, and is designed towards the enrichment of the teaching experience for students, namely in what concerns laboratory activities in the field of biomedical engineering. The implementation of such methodology aims at involving students more actively in the learning process, using case studies and emerging educational approaches such as project-based, active and research-based learning. It also provides an effective option for remote teaching, as recently required by the COVID-19 outbreak. In our approach (ScientIST) we explore the use of the Arduino MKR WIFI 1010, a variant of the popular electronic platform, recently launched for prototyping Internet of Things (IoT) applications, and the Google Science Journal (GSJ), a digital notebook created by Google, to support laboratory activities using mobile devices. This approach has shown promising results in two case studies, namely, documenting a Histology laboratory class and a Photoplethysmography (PPG) data acquisition and processing experiment. The System Usability Scale (SUS) was used in the evaluation of the students’ experience, revealing an overall score of 78.68%.
3

Grebenyuk, Sergei, and Adrian Ranga. "Engineering Organoid Vascularization." Frontiers in Bioengineering and Biotechnology 7 (March 19, 2019). http://dx.doi.org/10.3389/fbioe.2019.00039.

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Phummirat, Pisrut, Nicholas Mann, and Daryl Preece. "Applications of Optically Controlled Gold Nanostructures in Biomedical Engineering." Frontiers in Bioengineering and Biotechnology 8 (January 20, 2021). http://dx.doi.org/10.3389/fbioe.2020.602021.

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Since their inception, optical tweezers have proven to be a useful tool for improving human understanding of the microscopic world with wide-ranging applications across science. In recent years, they have found many particularly appealing applications in the field of biomedical engineering which harnesses the knowledge and skills in engineering to tackle problems in biology and medicine. Notably, metallic nanostructures like gold nanoparticles have proven to be an excellent tool for OT-based micromanipulation due to their large polarizability and relatively low cytotoxicity. In this article, we review the progress made in the application of optically trapped gold nanomaterials to problems in bioengineering. After an introduction to the basic methods of optical trapping, we give an overview of potential applications to bioengineering specifically: nano/biomaterials, microfluidics, drug delivery, biosensing, biophotonics and imaging, and mechanobiology/single-molecule biophysics. We highlight the recent research progress, discuss challenges, and provide possible future directions in this field.
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Montero-Morales, Laura, and Herta Steinkellner. "Advanced Plant-Based Glycan Engineering." Frontiers in Bioengineering and Biotechnology 6 (June 14, 2018). http://dx.doi.org/10.3389/fbioe.2018.00081.

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Hickey, Ryan J., and Andrew E. Pelling. "Cellulose Biomaterials for Tissue Engineering." Frontiers in Bioengineering and Biotechnology 7 (March 22, 2019). http://dx.doi.org/10.3389/fbioe.2019.00045.

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Boys, Alexander J., Sarah L. Barron, Damyan Tilev, and Roisin M. Owens. "Building Scaffolds for Tubular Tissue Engineering." Frontiers in Bioengineering and Biotechnology 8 (December 10, 2020). http://dx.doi.org/10.3389/fbioe.2020.589960.

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Hollow organs and tissue systems drive various functions in the body. Many of these hollow or tubular systems, such as vasculature, the intestines, and the trachea, are common targets for tissue engineering, given their relevance to numerous diseases and body functions. As the field of tissue engineering has developed, numerous benchtop models have been produced as platforms for basic science and drug testing. Production of tubular scaffolds for different tissue engineering applications possesses many commonalities, such as the necessity for producing an intact tubular opening and for formation of semi-permeable epithelia or endothelia. As such, the field has converged on a series of manufacturing techniques for producing these structures. In this review, we discuss some of the most common tissue engineered applications within the context of tubular tissues and the methods by which these structures can be produced. We provide an overview of the general structure and anatomy for these tissue systems along with a series of general design criteria for tubular tissue engineering. We categorize methods for manufacturing tubular scaffolds as follows: casting, electrospinning, rolling, 3D printing, and decellularization. We discuss state-of-the-art models within the context of vascular, intestinal, and tracheal tissue engineering. Finally, we conclude with a discussion of the future for these fields.
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Tsuchiya, Tomoshi, Ryoichiro Doi, Tomohiro Obata, Go Hatachi, and Takeshi Nagayasu. "Lung Microvascular Niche, Repair, and Engineering." Frontiers in Bioengineering and Biotechnology 8 (February 21, 2020). http://dx.doi.org/10.3389/fbioe.2020.00105.

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Ledesma-Amaro, Rodrigo, Pablo I. Nikel, and Francesca Ceroni. "Editorial: Synthetic Biology-Guided Metabolic Engineering." Frontiers in Bioengineering and Biotechnology 8 (March 20, 2020). http://dx.doi.org/10.3389/fbioe.2020.00221.

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Moysidou, Chrysanthi-Maria, Chiara Barberio, and Róisín Meabh Owens. "Advances in Engineering Human Tissue Models." Frontiers in Bioengineering and Biotechnology 8 (January 28, 2021). http://dx.doi.org/10.3389/fbioe.2020.620962.

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Research in cell biology greatly relies on cell-based in vitro assays and models that facilitate the investigation and understanding of specific biological events and processes under different conditions. The quality of such experimental models and particularly the level at which they represent cell behavior in the native tissue, is of critical importance for our understanding of cell interactions within tissues and organs. Conventionally, in vitro models are based on experimental manipulation of mammalian cells, grown as monolayers on flat, two-dimensional (2D) substrates. Despite the amazing progress and discoveries achieved with flat biology models, our ability to translate biological insights has been limited, since the 2D environment does not reflect the physiological behavior of cells in real tissues. Advances in 3D cell biology and engineering have led to the development of a new generation of cell culture formats that can better recapitulate the in vivo microenvironment, allowing us to examine cells and their interactions in a more biomimetic context. Modern biomedical research has at its disposal novel technological approaches that promote development of more sophisticated and robust tissue engineering in vitro models, including scaffold- or hydrogel-based formats, organotypic cultures, and organs-on-chips. Even though such systems are necessarily simplified to capture a particular range of physiology, their ability to model specific processes of human biology is greatly valued for their potential to close the gap between conventional animal studies and human (patho-) physiology. Here, we review recent advances in 3D biomimetic cultures, focusing on the technological bricks available to develop more physiologically relevant in vitro models of human tissues. By highlighting applications and examples of several physiological and disease models, we identify the limitations and challenges which the field needs to address in order to more effectively incorporate synthetic biomimetic culture platforms into biomedical research.

Dissertations / Theses on the topic "Histology|Biomedical engineering":

1

Lin, Sally. "Characterization of histological changes in the microvasculature of rat skeletal muscle after spinal cord injury." Thesis, Marquette University, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10243099.

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The purpose of this study was to determine whether there are histological changes in the microvasculature of rat skeletal muscle following chronic spinal cord injury both above and below the level of injury. This study is important because microvascular structure likely impacts muscle performance and cardiovascular health. To the best of our knowledge, this is the only study to investigate microvascular structure within rat skeletal muscle after spinal cord injury. We hypothesized structural remodeling would occur in both the myofibers and microvasculature, which would then manifest in differences in myofiber cross sectional area and microvascular diameter, wall thickness, wall to lumen ratio, and wall cross sectional area.

Changes in sympathetic tone and reduced muscular activity following spinal cord injury may induce microvascular structural remodeling. Initially after injury, sympathetic activity below the level of injury is diminished. Over time, neuroplasticity results in recovery of sympathetic tone, which increases vascular smooth muscle contraction and may lead to alterations in vasculature structure. In addition, the spinal lesion leads to loss of descending drive, which causes physical deconditioning below the level of injury. Physical deconditioning is known to induce vascular remodeling, and effects may be opposite of those associated with increased sympathetic tone.

We conducted a test of vascular remodeling in a rat contusion model of spinal cord injury. Ten adult female rats were evenly divided into control and spinal cord injury groups. Severe spinal cord injury was induced using a controlled weight drop onto the spinal cord, resulting in a contusion injury. After a 90 day survival period, the biceps brachii, triceps brachii, tibialis cranialis, and soleus muscles were removed, processed, and stained with Verhoeff van Gieson elastin and hematoxylin and eosin stains for histological analysis. Ultrastructural features of the myofibers and non-capillary microvessels were quantified. There was no significant difference between spinal cord injury and control skeletal muscles with regards to muscle cross sectional area, myofiber cross sectional area, microvascular diameter, wall thickness, wall to lumen ratio, or wall cross sectional area. Results indicated similar myofiber integrity and microvascular structure between control and spinal cord injury groups above and below level of injury.

While results did not support our original hypothesis, the findings also did not contradict previous studies. Following chronic spinal cord injury, recovery of spontaneous muscle activation and sympathetic activity may maintain integrity of skeletal muscle and associated microvasculature. Future research could assess microvascular function post spinal cord injury and identify an alternate animal model to study effects of spinal cord injury on muscle atrophy and associated microvasculature changes.

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Prabhu, David. "Automated Plaque Characterization of Intravascular Optical Coherence Tomography (IVOCT) Images Using 3D Cryo-image/Histology Validation." Case Western Reserve University School of Graduate Studies / OhioLINK, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1556293860943414.

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Nun, Nicholas. "Improving Skin Wound Healing Using Functional Electrospun Wound Dressings and 3D Printed Tissue Engineering Constructs." University of Akron / OhioLINK, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=akron1617985844538101.

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Deshmukh, Abhay S. "Histological Characterization of Inter Ictal Epileptiform Discharges Generating Brain Regions using a Preclinical Model of Focal Cortical Dysplasia." FIU Digital Commons, 2015. http://digitalcommons.fiu.edu/etd/2316.

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Current clinical practice of resective surgery in focal epilepsy involves electroencephalogram (EEG) brain source imaging to localize irritative brain areas from where Inter-ictal epileptiform discharges (IEDs) emerge, useful to localize the seizures-onset zones. Unfortunately, there are no previous systematic studies to characterize the pathophysiological mechanisms and abnormal cellular substrates in these irritative areas since histological data are available only from the final resective zones. To address this issue we applied a combination of EEG brain imaging described by Bae et al. (2015) using cutting-edge technology for high-density scalp EEG in rodents and histological analysis on a chronic rat model of focal cortical dysplasia. Post-mortem brain sections were stained for anatomical, functional and inflammatory biomarkers. Abnormal anatomical structures and increased expression of inflammatory biomarkers were found in the irritative regions. We conclude that IED-based brain source imaging can help to localize abnormal tissues highly prospective for epileptogenesis.
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Varghai, Daniel. "Tubular Tissue Engineered Scaffold-Free High-Cell-Density Mesenchymal Condensations For Femoral Defect Regeneration." Case Western Reserve University School of Graduate Studies / OhioLINK, 2017. http://rave.ohiolink.edu/etdc/view?acc_num=case1497222797338966.

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Bodnyk, Kyle Anthony Bodnyk. "The Long-Term Residual Effects of Low Intensity Vibration Therapy on Skeletal Health." The Ohio State University, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1530797834329838.

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Peruzzo, Angela Maria. "Avaliação mecânica e histológica de pericárdio bovino descelularizado submetido à pressão." Universidade Tecnológica Federal do Paraná, 2013. http://repositorio.utfpr.edu.br/jspui/handle/1/985.

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O pericárdio bovino é um tecido biológico utilizado na fabricação de vários produtos para a saúde e também em válvulas cardíacas desde o início da década de setenta, porém, ainda requer estudos mais aprofundados no que diz respeito às mudanças que os tratamentos químicos utilizados para confecção das válvulas ocasionam. Atualmente a engenharia de tecidos estuda a descelularização do pericárdio bovino como um processo para retirar os componentes celulares, mantendo intacta a matriz extracelular (MEC), preservando a integridade do colágeno e também pode atuar como anticalcificante. Porém, é necessário saber qual o impacto que o tratamento químico trará nas propriedades mecânicas do tecido, como tensão máxima, deformação específica e alongamento. Nos trabalhos observados, os testes mecânicos realizados nos pericárdios bovinos descelularizados foram feitos no tecido sem serem submetidos a uma pré-tensão, a qual é necessária na maioria das vezes, para formação das cúspides durante a confecção das válvulas cardíacas ou outro dispositivo médico. Por essa razão, foi realizado um estudo do efeito na propriedade mecânica que uma determinada pressão exerce sobre o pericárdio bovino, que passou pelo processo de descelularização. Em paralelo também foi feito uma avaliação histológica do tecido para verificar a ausência de células e a preservação das fibras de colágeno no tecido descelularizado. Foram preparados quatro grupos diferentes para a realização dos testes. O grupo I chamado de grupo controle. O grupo II, onde os pericárdios foram descelularizados com o método PUC I. O grupo III foi tratado como o grupo I, porém sob pressão de 240 mmHg. Já o grupo IV, os pericárdios foram descelularizados e em seguida submetidos à mesma pressão utilizando solução de glutaraldeído 0,2% e 0,5%. Após os tratamentos dos grupos, todas as amostras foram tingidas em solução de azul de metileno 0,03% para melhor visualização das fibras do tecido. Em seguida os tecidos foram cortados a laser para obtenção dos corpos de prova e submetidos ao ensaio de tração. Obteve-se a partir do ensaio, a tensão máxima das amostras, a deformação específica e o alongamento na ruptura. Foi observado que nos grupos onde foram submetidos à pressão tiveram uma tensão máxima menor do que os grupos sem pressão e um maior alongamento. Verificou-se que o efeito da pressão diminuiu a espessura dos tecidos. O processo de descelularização se mostrou eficaz uma vez que foi demonstrada a ausência de células e a preservação das fibras de colágeno após técnica utilizada.
The pericardium is a biological tissue used in the manufacture of various products for medical advices and manufacture of heart valves since the early seventies, however, it still requires further study with regard to the changes that the chemical treatments used to manufacture the valves cause. Several studies show that the tissue often undergoes a process of calcification generated by mechanical stress of opening and closing of the leaflets, damaging the hydrodynamics making valvular replacement necessary. Currently tissue engineering study decellularization process of the bovine pericardium to remove cellular components while preserving the extracellular the matrix (ECM), preserving the integrity of collagen it and can also act as anti-calcification. However, one must know the impact that chemical treatment will bring on the mechanical properties of the tissue, such as tensile strength, strain and elongation percentage. In examined studies, the mechanical tests performed on bovine pericardium decellularized tissue was made without being subjected to a pre-tension which is necessary in most cases for formation of the leaflets during the manufacturing of heart valves. For this reason, a study of the effect on mechanical property that a certain pressure exerts on the pericardium, which passed the decellularization process was made. In parallel it was also made a histological evaluation of the tissue to verify the absence of cells and preservation of collagen fibers in decellularized tissue. Four different groups were prepared for test. The group I was called a control group. In group II, the pericardia were decellularized with the PUC method I. Group III was treated as group I, but under pressure of 240 mmHg. The group IV, the pericardia were decellularized and then subjected to pressure using glutaraldehyde 0.2% and 0.5%. After treatment of the groups, all samples were stained in a solution of blue methylene 0.03% for better visualization of the fibers of the tissue. Then the tissues were cut by laser to obtain the specimens and subjected to tensile test. It was obtained from the test, the tensile strength of the samples, the strain and elongation percentage at break. It is observed that the groups which underwent pressure had a lower tensile strength than those without pressure and on the other hand showed a greater elongation percentage. Thus, it can be verified that the effect of the pressure decreased the thickness of the tissues. The decellularization process has show efficient since it has demonstrated the absence of cells and preservation of collagen fibers after technique.
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Miller, Robert M. "Mechanobiological Investigation of Periosteum Through Finite Element Modeling and Histology." Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1307732052.

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VAZQUEZ, JORGE ARTURO. "NERVE FIBER DIAMETER MEASUREMENTS USING HEMATOXYLIN AND EOSIN STAINING AND BRIGHTFIELD MICROSCOPY TO ASSESS THE NOVEL METHOD OF CHARACTERIZING PERIPHERAL NERVE FIBER DISTRIBUTIONS BY GROUP DELAY." DigitalCommons@CalPoly, 2014. https://digitalcommons.calpoly.edu/theses/1293.

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Peripheral neuropathies are a set of common diseases that affect the peripheral nervous system, causing damage to vital connections between various parts of the body and the brain and spinal cord. Different clinical conditions are known to selectively impact various size nerve fibers, which often makes it difficult to diagnose which peripheral neuropathy a patient might have. The nerve conduction velocity diagnostic test provides clinically useful information in the diagnosis of some peripheral neuropathies. This method is advantageous because it tends to be minimally invasive yet it provides valuable diagnostic information. However, this test does not determine characteristics of peripheral nerve fiber size distributions, and therefore does not show any detailed information regarding the nerve fibers within the nerve trunk. Being able to determine which nerve fibers are contributing to the evoked potential within a nerve trunk could provide additional information to clinicians for the diagnosis of specific pathologies of the peripheral nervous system, such as chronic inflammatory demyelinating polyneuropathy or early diabetic peripheral neuropathy. In this study, three rat sciatic nerves are sectioned and stained with hematoxylin and eosin in order to measure the nerve fiber diameters within the nerve trunk. Stained samples are viewed using brightfield microscopy and images are analyzed using ImageJ. Histograms were created to show the frequency of various nerve fiber diameters. The nerve fiber diameters measured during this research are consistent with the range of previously published diameter values and will be used to support continuing research for a novel method to characterize peripheral nerve fiber size distributions using group delay.
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Valiallah, Hasti. "Validation in-vivo des techniques d’élastographie ultrasonore, invasive et non-invasive, à l’aide d’un modèle porcin." Thèse, 2012. http://hdl.handle.net/1866/8945.

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Il est maintenant admis que la composition de la plaque athérosclérotique est un déterminant majeur de sa vulnérabilité à se rompre. Vu que la composition de la plaque affecte ses propriétés mécaniques, l'évaluation locale des propriétés mécaniques de la plaque d'athérome peut nous informer sur sa vulnérabilité. L'objectif est de comparer les techniques d’élastographie ultrasonores endovasculaire (EVE) et non-invasive (NIVE) en fonction de leur potentiel à identifier les composantes calcifiées et lipidiques de la plaque. Les acquisitions intravasculaire et extravasculaire ont été effectuées sur les artères carotidiennes de neuf porcs hypercholestérolémiques à l’aide d’un cathéter de 20 MHz et d'une sonde linéaire de 7.5 MHz, respectivement. Les valeurs de déformation radiale et axiale, rapportés par EVE et NIVE, ont été corrélées avec le pourcentage des zones histologiques calcifiées et lipidiques pour cinq plaques. Nos résultats démontrent une bonne corrélation positive entre les déformations et les composantes calcifiées (r2 = 0.82, P = 0.034 valeur par EVE et r2 = 0.80, P = 0.041 valeur par NIVE). Une forte corrélation entre les déformations axiales et les contenus lipidiques par NIVE (r2 = 0.92, P-value = 0.010) a été obtenue. En conclusion, NIVE et EVE sont des techniques potentielles pour identifier les composants de la plaque et aider les médecins à diagnostiquer précocement les plaques vulnérables.
It is now widely accepted that plaque composition is a major determinant of plaque’s vulnerability to rupture. Since composition of the plaque affects its mechanical properties, the local assessment of mechanical properties of atherosclerotic plaque may inform us about plaque’s vulnerability. The objective is to compare ultrasonic endovascular elastography (EVE) versus non-invasive vascular elastography (NIVE) according to their potential to identify plaque contents. Intravascular and extravascular acquisitions were performed on carotid arteries of nine hypercholesterolemic minipigs with a 20 MHz catheter and a 7.5 MHz standard probe, respectively. Radial and axial strain values, reported by EVE and NIVE respectively, were correlated with histological area of lipid and calcium for five plaques. Our results demonstrate a good positive correlation between strains and calcified contents (r2=0.82, P-value=0.034 by EVE and r2=0.80, P-value= 0.041 by NIVE). Additionally, there is a strong correlation between axial strains and lipid contents by NIVE (r2=0.92, P-value= 0.010). In conclusion, NIVE and EVE are the potential techniques to identify plaque components and to help physicians to early diagnose the vulnerable plaques.

Books on the topic "Histology|Biomedical engineering":

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Palsson, Bernhard. Tissue engineering. Upper Saddle River, N.J: Pearson Prentice Hall, 2004.

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Higer, H. Peter. Tissue Characterization in MR Imaging: Clinical and Technical Approaches. Berlin, Heidelberg: Springer Berlin Heidelberg, 1990.

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Payan, Yohan. Soft tissue biomechanical modeling for computer assisted surgery. Heidelberg: Springer, 2012.

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Xu, Feng. Introduction to Skin Biothermomechanics and Thermal Pain. Berlin, Heidelberg: Springer-Verlag Berlin Heidelberg, 2011.

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Palsson, Bernhard O., and Sangeeta N. Bhatia. Tissue Engineering. Prentice Hall, 2003.

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(Editor), Klaus-Peter Wilhelm, Peter Elsner (Editor), Enzo Berardesca (Editor), and Howard I. Maibach (Editor), eds. Bioengineering of the Skin: Skin Surface Imaging and Analysis, Volume IV. CRC, 1996.

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Bioengineering of the Skin: Skin Imaging & Analysis, 2nd Edition (Dermatology: Clinical & Basic Science). 2nd ed. Informa Healthcare, 2006.

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Higer, H. Peter, and Gernot Bielke. Tissue Characterization in MR Imaging: Clinical and Technical Approaches. Springer, 2011.

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Payan, Yohan. Soft Tissue Biomechanical Modeling for Computer Assisted Surgery. Springer, 2014.

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Maibach, Howard I., Peter Elsner, Enzo Berardesca, and Klaus-Peter Wilhelm. Bioengineering of the Skin: Methods and Instrumentation, Volume III. Taylor & Francis Group, 2020.

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Book chapters on the topic "Histology|Biomedical engineering":

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Sales, Fernando José Ribeiro, J. L. A. A. Falcão, P. A. Lemos, S. S. Furuie, R. M. G. Cabral, and R. C. Silva. "Post-Processing Analysis of Virtual Histology Images — A New Tool for Intra-Plaque Component Assessment." In IV Latin American Congress on Biomedical Engineering 2007, Bioengineering Solutions for Latin America Health, 377–80. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-74471-9_87.

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Meng, Tao, Mei-Ling Shyu, and Lin Lin. "Multimodal Information Integration and Fusion for Histology Image Classification." In Multimedia Data Engineering Applications and Processing, 35–50. IGI Global, 2013. http://dx.doi.org/10.4018/978-1-4666-2940-0.ch003.

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Biomedical imaging technology has become an important tool for medical research and clinical practice. A large amount of imaging data is generated and collected every day. Managing and analyzing these data sets require the corresponding development of the computer based algorithms for automatic processing. Histology image classification is one of the important tasks in the bio-image informatics field and has broad applications in phenotype description and disease diagnosis. This study proposes a novel framework of histology image classification. The original images are first divided into several blocks and a set of visual features is extracted for each block. An array of C-RSPM (Collateral Representative Subspace Projection Modeling) models is then built that each model is based on one block from the same location in original images. Finally, the C-Value Enhanced Majority Voting (CEWMV) algorithm is developed to derive the final classification label for each testing image. To evaluate this framework, the authors compare its performance with several well-known classifiers using the benchmark data available from IICBU data repository. The results demonstrate that this framework achieves promising performance and performs significantly better than other classifiers in the comparison.

Conference papers on the topic "Histology|Biomedical engineering":

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Ke, Jing, Yiqing Shen, Yi Guo, Jason D. Wright, and Xiaoyao Liang. "A Prediction Model of Microsatellite Status from Histology Images." In ICBET 2020: 2020 10th International Conference on Biomedical Engineering and Technology. New York, NY, USA: ACM, 2020. http://dx.doi.org/10.1145/3397391.3397442.

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Onder, Devrim, Sulen Sarioglu, and Bilge Karacali. "Automated classification of cancerous textures in histology images using quasi-supervised learning algorithm." In 2010 15th National Biomedical Engineering Meeting (BIYOMUT 2010). IEEE, 2010. http://dx.doi.org/10.1109/biyomut.2010.5479863.

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Onder, Devrim, and Bilge Karacali. "Automated clustering of histology slide texture using co-occurrence based grayscale image features and manifold learning." In 2009 14th National Biomedical Engineering Meeting. IEEE, 2009. http://dx.doi.org/10.1109/biyomut.2009.5130342.

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Wu, Shu-lian, Hui Li, Zheng-ying Xiao, and Zhi-fang Li. "Skin Response During Irradiation by Intense Pulsed Light Based on Optical Imaging Technology and Histology." In 2009 2nd International Conference on Biomedical Engineering and Informatics. IEEE, 2009. http://dx.doi.org/10.1109/bmei.2009.5305767.

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Pourakpour, Fattaneh, and Hassan Ghassemian. "Automated mitosis detection based on combination of effective textural and morphological features from breast cancer histology slide images." In 2015 22nd Iranian Conference on Biomedical Engineering (ICBME). IEEE, 2015. http://dx.doi.org/10.1109/icbme.2015.7404154.

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