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1

1961-, Duijn Bert van y Wiltink Anneke 1961-, eds. Signal transduction--single cell techniques. Berlin: Springer, 1998.

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2

Richard, McIntosh J., ed. Cellular electron microscopy. Amsterdam: Elsevier/Academic Press, 2007.

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3

Cheville, Norman F. Ultrastructural pathology: An introduction to interpretation. Ames: Iowa State University Press, 1994.

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4

Ammasi, Periasamy, ed. Methods in cellular imaging. Oxford: Published for the American Physiological Society by Oxford University Press, 2001.

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5

László, Módis. Organization of the extracellular matrix: A polarization microscopic approach. Boca Raton, Fla: CRC Press, 1991.

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6

L, Shorte Spencer y Frischknecht Friedrich, eds. Imaging cellular and molecular biological functions. Berlin: Springer, 2007.

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7

Robert, Jacques. Signalisation cellulaire et cancer: Un manuel pour les étudiants et les oncologues. Paris: Springer-Verlag Paris, 2010.

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8

L, Shorte Spencer y Frischknecht Friedrich, eds. Imaging cellular and molecular biological functions. Berlin: Springer, 2007.

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9

Culling, C. F. A. Cellular pathology technique. 4a ed. London: Butterworths, 1985.

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10

T, Allison R., Barr W. T y Culling C. F. A, eds. Cellular pathology technique. 4a ed. London: Butterworths, 1985.

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11

Jena, Bhanu P. NanoCellBiology of Secretion: Imaging Its Cellular and Molecular Underpinnings. Boston, MA: Springer US, 2012.

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12

Chevanne, Marta y Riccardo Caldini. Immagini di Istopatologia. Florence: Firenze University Press, 2007. http://dx.doi.org/10.36253/978-88-5518-023-8.

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This collection of images of Histopathology is the fruit of the authors' thirty years' experience in the performance of practical exercises in General Pathology. It is aimed at students attending lessons of General Pathology on the Degree Courses in Medical Surgery and Biological Sciences. It does not aspire either to be complete from the point of view of the various organic pathologies, or to replace direct and personal observation of the histological preparations through the microscope, but is rather intended as an aid to students preparing for the exam. It does not include the rudiments of cytology and microscopic anatomy, which it is assumed have already been mastered by those approaching General Histopathology, nor are histopathological phenomena systematically addressed, for which the reader is referred to textbooks on General Pathology. The 44 preparations presented here have been grouped in line with the main arguments of General Pathology: Cellular Degeneration, Inflammation, Neoplasia both benign and malign, and Vascular Pathology. They have been selected for their didactic significance and the simplicity and clarity of the lesions present, without taking into account the information to be derived from the clinical case history. The images of the preparations, in which the best possible quality of reproduction has been sought, are presented in progressive enlargements and are accompanied by brief descriptions comprising the explanations essential for identification of the characteristic aspects of the elementary lesion, as well as any eventual defects in the preparations themselves. Effectively, the objective of the work is to enable the student to exercise his understanding of the images. For this reason the casuistics included is as essential as possible, and the method of presentation utilised is designed to avoid mere visual memorisation, stimulating first analysis and then synthesis, and the development of individual logical skills so as to indicate whether aspects of cellular pathology, inflammation or neoplasia are present.
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13

Li, Mi. Investigations of Cellular and Molecular Biophysical Properties by Atomic Force Microscopy Nanorobotics. Singapore: Springer Singapore, 2018. http://dx.doi.org/10.1007/978-981-10-6829-4.

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14

Mandriota, Nicola. The relationship between intracellular forces and cellular stiffness investigated by atomic force microscopy. [New York, N.Y.?]: [publisher not identified], 2016.

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15

G, Toner P., ed. Subcellular taxonomy: An ultrastructural classification system with diagnostic applications. Washington: Hemisphere Pub. Corp., 1985.

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16

service), ScienceDirect (Online, ed. Cryo-EM: Sample preparation and data collection. San Diego, Calif: Academic Press/Elsevier, 2010.

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17

Stumpf, Walter E. Drug localization in tissues and cells: Receptor microscopic autoradiography : a basis for tissue and cellular pharmacokinetics, drug targeting, delivery, and prediction. Chapel Hill, NC: IDDC-Press, 2003.

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18

C, Mothersill y Austin B. 1951-, eds. Aquatic invertebrate cell culture. London: Springer, 2000.

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19

Cellular Analysis by Atomic Force Microscopy. Taylor & Francis Group, 2017.

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20

Lekka, Malgorzata. Cellular Analysis by Atomic Force Microscopy. Jenny Stanford Publishing, 2017.

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21

New Concepts in Blood Formation Cell Generation in Malignant & Benign Tissues: Adult & Embryonic Tissues from Humans & Animals in Chronic Ischemic Con. Diagnostic & Cell Research Institute, 1995.

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22

Cellular Electron Microscopy. Elsevier, 2007. http://dx.doi.org/10.1016/s0091-679x(06)x7900-1.

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23

Ober, Raimund J., Jerry Chao y E. S. Ward. Modern Cellular Microscopy. Taylor & Francis Group, 2020.

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24

McIntosh, J. Richard. Cellular Electron Microscopy. Elsevier Science & Technology Books, 2011.

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25

Cellular Imaging Techniques For Neuroscience And Beyond. Academic Press, 2012.

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26

Wouterlood, Floris G. Cellular Imaging Techniques for Neuroscience and Beyond. Elsevier Science & Technology Books, 2012.

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27

Li, Mi. Investigations of Cellular and Molecular Biophysical Properties by Atomic Force Microscopy Nanorobotics. Springer, 2019.

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28

Li, Mi. Investigations of Cellular and Molecular Biophysical Properties by Atomic Force Microscopy Nanorobotics. Springer, 2017.

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29

Periasamy, Ammasi. Methods in Cellular Imaging. Springer, 2013.

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30

(Editor), Valtere Evangelista, Laura Barsanti (Editor), Vincenzo Passarelli (Editor) y Paolo Gualtieri (Editor), eds. From Cells to Proteins: Imaging Nature across Dimensions: Proceedings of the NATO Advanced Study Institute, held in Pisa, Italy, 12-23 September 2004. Springer, 2005.

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31

Lekka, Malgorzata. Cellular Analysis by Atomic Force Microscopy. Jenny Stanford Publishing, 2017.

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32

Succi, Sauro. Lattice Gas-Cellular Automata. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780199592357.003.0011.

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This chapter discusses the ancestor of the Lattice Boltzmann, the Boolean formulation of hydrodynamics known as lattice Gas Cellular Automata. In 1986, Uriel Frisch, Brosl Hasslacher and Yves Pomeau sent big waves across the fluid dynamics community: a simple cellular automaton obeying nothing but conservation laws at a microscopic level was able to reproduce the complexity of real fluid flows. This discovery spurred great excitement in the fluid dynamics community. The prospects were tantalizing: around free, intrinsically parallel computational paradigm for fluid flows. However, a few serious problems were quickly recognized and addressed with great intensity in the following years.
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33

Shorte, Spencer L. y Friedrich Frischknecht. Imaging Cellular and Molecular Biological Functions. Springer London, Limited, 2007.

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34

Allison, R. T., W. T. Barr y C. F. A. Culling. Cellular Pathology Technique. Elsevier Science & Technology Books, 2014.

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35

Martin, Francis L. y Hubert M. Pollock. Microspectroscopy as a tool to discriminate nanomolecular cellular alterations in biomedical research. Editado por A. V. Narlikar y Y. Y. Fu. Oxford University Press, 2017. http://dx.doi.org/10.1093/oxfordhb/9780199533053.013.8.

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This article considers the use of microspectroscopy for discriminating nanomolecular cellular alterations in biomedical research. It begins with an overview of some existing mid-infrared microspectroscopy techniques, including FTIR microspectroscopy and Raman microspectroscopy. It then discusses near-field techniques such as scanning near-field optical microscopy, near-field Raman microscopy, and photothermal microspectroscopy (PTMS). It also examines promising alternative sources of IR light, possible advantages of using normal atomic force microscopy probes, experimental procedures for PTMS, and prospects for high spatial resolution in near-field FTIR spectroscopy. Finally, it describes the spectroscopic detection of small particles, along with the use of the analysis paradigm to discriminate nanomolecular cellular alterations in biomedical research.
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36

Newberger, Alfonzo. Cannabis at the Cellular and Molecular Level : a Microscopic World with Sub-Cellular Detail: Marijuana. Independently Published, 2021.

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37

High-Resolution Imaging of Cellular Proteins: Methods and Protocols. Humana, 2018.

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38

High-Resolution Imaging of Cellular Proteins: Methods and Protocols. Springer New York, 2016.

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39

McIntosh, J. Richard. Cellular Electron Microscopy, Volume 79 (Methods in Cell Biology). Academic Press, 2007.

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40

McIntosh, J. Richard. Cellular Electron Microscopy, Volume 79 (Methods in Cell Biology). Academic Press, 2007.

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41

Toner, Peter G. y Arthur L. C. Mclay. Subcelluar Taxonomy: An Ultrastructural Classification System with Diagnostic Applications (An Ultrastructural Pathology Publication). Hemisphere Publishing/McGraw-Hill, 1985.

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42

(Editor), Spencer L. Shorte y Friedrich Frischknecht (Editor), eds. Imaging Cellular and Molecular Biological Functions (Principles and Practice) (Principles and Practice). Springer, 2007.

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43

Moore, Sarah y Kasipathy Kailasapathy. Cellular Interactions of Probiotic Bacteria with Intestinal and Immune Cells. Nova Science Publishers, Incorporated, 2017.

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44

Viral Cytopathology. Taylor & Francis Group, 2017.

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45

Malherbe. Viral Cytopathology. Taylor & Francis Group, 2018.

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46

Malherbe. Viral Cytopathology. Taylor & Francis Group, 2018.

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47

Malherbe. Viral Cytopathology. Taylor & Francis Group, 2018.

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48

Malherbe. Viral Cytopathology. Taylor & Francis Group, 2018.

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49

König, Karsten, Thérèse Baldeweck, Mihaela Balu, Ana Batista y Wolfgang Vecker. Multiphoton Microscopy and Fluorescence Lifetime Imaging: Applications in Biology and Medicine. de Gruyter GmbH, Walter, 2018.

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50

Harris, Brent T., Galam A. Khan y Saed Sadeghi. Amyotrophic Lateral Sclerosis. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0029.

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Although the basic gross and microscopic pathological changes in amyotrophic lateral sclerosis (ALS) have been known for more than 100 years, emerging technology and research into the cellular and molecular changes found in this disease are challenging our understanding about the pathogenesis and pathophysiology. All cell types of the CNS/PNS as well as circulating immune cells have been implicated in the pathology of ALS. Numerous genes, their proteins, and environmental factors have also been associated. However, we still do not understand the specific gene-environmental interactions that bring about and drive this devastating disease in most cases. This short chapter does not address the causal factors and molecular pathogeneses that have been hypothesized and actively researched in the pathology of ALS-as these are discussed in other sections of this text. Here, it shows and discusses the basic pathological changes at the tissue and cellular levels that help to establish the pathological diagnosis of ALS at autopsy.
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