Bibliografías temáticas / Cellular Migration

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Literatura académica sobre el tema "Cellular Migration"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 16 de noviembre de 2024

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Artículos de revistas sobre el tema "Cellular Migration"

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Mcclay, D. "Cellular migration." Reproductive Toxicology 11, no. 2-3 (June 1997): 321–29. http://dx.doi.org/10.1016/s0890-6238(96)00215-8.

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Schönfisch, Birgitt, and Claude Lacoursière. "Migration in cellular automata." Physica D: Nonlinear Phenomena 103, no. 1-4 (April 1997): 537–53. http://dx.doi.org/10.1016/s0167-2789(96)00284-9.

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Zhao, Jieling, Youfang Cao, Luisa A. DiPietro, and Jie Liang. "Dynamic cellular finite-element method for modelling large-scale cell migration and proliferation under the control of mechanical and biochemical cues: a study of re-epithelialization." Journal of The Royal Society Interface 14, no. 129 (April 2017): 20160959. http://dx.doi.org/10.1098/rsif.2016.0959.

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Computational modelling of cells can reveal insight into the mechanisms of the important processes of tissue development. However, current cell models have limitations and are challenged to model detailed changes in cellular shapes and physical mechanics when thousands of migrating and interacting cells need to be modelled. Here we describe a novel dynamic cellular finite-element model (DyCelFEM), which accounts for changes in cellular shapes and mechanics. It also models the full range of cell motion, from movements of individual cells to collective cell migrations. The transmission of mechan
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Kravets, E. A., A. I. Yemets, and Ya B. Blume. "Cellular mechanisms of nuclear migration." Cytology and Genetics 51, no. 3 (May 2017): 192–201. http://dx.doi.org/10.3103/s0095452717030069.

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Vaughan, Douglas E. "PAI-1 and Cellular Migration." Arteriosclerosis, Thrombosis, and Vascular Biology 22, no. 10 (October 2002): 1522–23. http://dx.doi.org/10.1161/01.atv.0000037901.89736.0a.

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Chang, Stephanie S., Andrew D. Rape, Stephanie A. Wong, Wei-hui Guo, and Yu-li Wang. "Migration regulates cellular mechanical states." Molecular Biology of the Cell 30, no. 26 (December 15, 2019): 3104–11. http://dx.doi.org/10.1091/mbc.e19-02-0099.

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Cell migration has a profound effect on the generation of traction forces and the phosphorylation of focal adhesion proteins. The mechanism may involve the dynamic turnover of focal adhesions during cell migration and mechanical interactions between nascent and preexisting focal adhesions.
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Verdoorn, Cornelis. "Cellular Migration, Proliferation, and Contraction." Archives of Ophthalmology 104, no. 8 (August 1, 1986): 1216. http://dx.doi.org/10.1001/archopht.1986.01050200122064.

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Nagayama, M., H. Haga, M. Takahashi, and K. Kawabata. "Cellular migration coordinated by cortical tension." Seibutsu Butsuri 43, supplement (2003): S108. http://dx.doi.org/10.2142/biophys.43.s108_3.

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SCHUBERT, THOMAS, ALEXANDRA E. DENK, ANKE RUEDEL, SIMONE KAUFMANN, ELISABETH HUSTERT, PATRIZIA BASTONE, and ANJA K. BOSSERHOFF. "Fragments of SLIT3 inhibit cellular migration." International Journal of Molecular Medicine 30, no. 5 (August 20, 2012): 1133–37. http://dx.doi.org/10.3892/ijmm.2012.1098.

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Reyes-Aldasoro, C. C., D. Biram, G. M. Tozer, and C. Kanthou. "Measuring cellular migration with image processing." Electronics Letters 44, no. 13 (2008): 791. http://dx.doi.org/10.1049/el:20080943.

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Tesis sobre el tema "Cellular Migration"

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Dimchev, Georgi Aleksandrov. "Cellular regulators of myoblast migration and myogenesis." Thesis, Manchester Metropolitan University, 2012. http://e-space.mmu.ac.uk/315695/.

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Migration of myogenic cells is an important step in myogenesis and skeletal muscle repair. Migration is required for the cells to reach the site of damage, for their alignment and subsequent fusion. Limited migration is also one of the limitations of proposed therapies of diseases, such as Duchenne Muscular Dystrophy (DMD). Therefore, revealing the regulators of myogenic cell migration is important for improving our knowledge of myogenesis, but could also be applied in therapies for conditions, associated with loss of muscle mass and muscle weakness. In this thesis, extracellular and intracell
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Corvaglia, Valentina. "pna - assisted cellular migration on patterned surfaces." Doctoral thesis, Università degli studi di Trieste, 2013. http://hdl.handle.net/10077/8646.

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2011/2012<br>ABSTRACT - The ability to control the cellular microenvironment, such as cell-substrate and cell-cell interactions at the micro- and nanoscale, is important for advances in several fields such as medicine and immunology, biochemistry, biomaterials, and tissue engineering. In order to undergo fundamental biological processes, most mammalian cells must adhere to the underlying extracellular matrix (ECM), eliciting cell adhesion and migration processes that are critical to embryogenesis, angiogenesis, wound healing, tissue repair, and immunity response, to cite few. For instance, upo
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Hennig, Katharina. "Dynamique des forces motiles et brisure de symétrie chez la cellule migrante." Thesis, Université Grenoble Alpes (ComUE), 2018. http://www.theses.fr/2018GREAY040/document.

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La motilité cellulaire directionnelle au cours du développement de l'organisme et des tissus, l'homéostasie et la maladie nécessite une rupture de symétrie. Ce processus repose sur la capacité des cellules individuelles à établir une polarité avant-arrière, et peut se produire en l'absence de signaux externes. L'initiation de la migration a été attribuée à la polarisation spontanée des composants du cytosquelette, tandis que l'évolution spatio-temporelle des forces du cytosquelette résultant de l'interaction mécanique cellule-substrat continue n'a pas encore été résolue. Ici, nous établissons
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English, Jane Louise. "Cellular regulation of matrix metalloproteinase function." Thesis, University of East Anglia, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.247107.

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Ashrafzadeh, Parham. "Exploring Cellular Dynamics : From Vesicle Tethering to Cell Migration." Doctoral thesis, Uppsala universitet, Institutionen för medicinsk cellbiologi, 2016. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-306174.

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Cells in the body communicate with each other in order to cooperate efficiently. This communication is in part achieved by regulated secretion of signaling molecules, which when released from a cell may activate receptors present at the plasma membrane of an adjacent cell. Such signals affect both cell fate and behavior. Dysregulated signaling may lead to disease, including cancer. This thesis is focused on how exocytosis and subsequent activation and trafficking of receptors can be regulated, and what the consequences of this regulation may be for cell migration. Actin filaments are important
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Rodriguez, Marbelys. "Two Adaptation Mechanisms Regulate Cellular Migration in Dictyostelium discouideum." FIU Digital Commons, 2014. http://digitalcommons.fiu.edu/etd/1144.

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Dictyostelium discoideum is a simple model widely used to study many cellular functions, including differentiation, gene regulation, cellular trafficking and directional migration. Adaptation mechanisms are essential in the regulation of these cellular processes. The misregulation of adaptation components often results in persistent activation of signaling pathways and aberrant cellular responses. Studying adaptation mechanisms regulating cellular migration will be crucial in the treatment of many pathological conditions in which motility plays a central role, such as tumor metastasis and acut
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Petrolli, Vanni. "Confinement induced transition between wave-like cellular migration modes." Thesis, Université Grenoble Alpes (ComUE), 2019. http://www.theses.fr/2019GREAY056.

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La capacité des cellules à générer spontanément de l'ordre a l’échelle supra cellulaire repose sur l'interaction de signaux mécaniques et biochimiques. Si le consensus général est que la signalisation chimique est le régulateur principal du comportement cellulaire, il est aujourd’hui bien établi que l'impact des facteurs mécaniques est primordial sur des processus fondamentaux de la physiologie cellulaire tel que la différenciation, la prolifération, la motilité et qu’une dérégulation des paramètres mécaniques du microenvironnement des cellules sont impliqués dans un grand nombre de pathologie
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da, Silva Barbara Luisa. "Glioblastoma cell behaviour : a study of chemically-induced cellular connectivity and 3D modelling of cellular migration." Thesis, University of Leeds, 2018. http://etheses.whiterose.ac.uk/22479/.

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Glioblastoma multiforme (GBM) is the most common and deadliest brain cancer in adults. Despite considerable efforts at both bench and bedside, the average survival for GBM patients is only 14-15 months. This dismal prognosis stems from challenges in treatment and a malignant tumour biology. A key need in addressing GBM is to better understand and therapeutically target GBM cell invasion into the surrounding healthy brain tissue. Cytoskeletal remodelling and dynamics, mediated by ROCK effector proteins, play an important role in the ability of GBM cells to migrate. ROCK inhibition is being cons
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Kumar, Arun. "Cellular and molecular mechanism controlling collective glial cell migration in drosophila." Thesis, Strasbourg, 2013. http://www.theses.fr/2013STRAJ071/document.

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Le bon fonctionnement des réseaux neuronaux dépend des interactions entre les neurones et les cellules gliales. Alors que de nombreux efforts ont été faits pour comprendre les interactions entre les neurones, moins est connu sur la nature des interactions entre les cellules gliales ; ceci est due à la complexité du système nerveux des vertébrés, qui comprend plus de cellules gliales que de neurones. Cependant, le système nerveux de la drosophile à un rapport neurones-cellules gliales faible, ce qui fait de cet animal simple un modèle idéal pour évaluer ce concept. J’ai utilisé des approches gé
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Myer, Nicole M. "CLASP1 Regulated Endothelial Cell Branching Morphology and Directed Migration." Thesis, University of the Sciences in Philadelphia, 2017. http://pqdtopen.proquest.com/#viewpdf?dispub=10631484.

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<p> The eukaryotic cytoskeleton is composed of varying proteinaceous filaments and is responsible for intracellular transport, cell proliferation, cell morphogenesis, and cell motility. Microtubules are one of three cytoskeletal components and have a unique polymer structure. The hollow cylinders undergo rapid polymerization and depolymerization events (<i>i.e.</i> dynamic instability) to promote assembly at the leading edge of the cell and disassembly in the rear of the cell to drive the cell front forward and facilitate directional migration. High-resolution light microscopy and automated tr
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Libros sobre el tema "Cellular Migration"

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Nguyen, Laurent, and Simon Hippenmeyer, eds. Cellular and Molecular Control of Neuronal Migration. Dordrecht: Springer Netherlands, 2014. http://dx.doi.org/10.1007/978-94-007-7687-6.

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1949-, Husband Alan J., ed. Migration and homing of lymphoid cells. Boca Raton, Fla: CRC Press, 1988.

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Laboratory, Cold Spring Harbor, ed. The Cell surface. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory, 1992.

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Laboratory, Cold Spring Harbor, ed. The cell surface. Plainview, N.Y: Cold Spring Harbor Laboratory Press, 1992.

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Cellular Migration and Formation of Neuronal Connections. Elsevier, 2013. http://dx.doi.org/10.1016/c2011-0-07731-1.

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Nguyen, Laurent, and Simon Hippenmeyer. Cellular and Molecular Control of Neuronal Migration. Springer, 2016.

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Nguyen, Laurent, and Simon Hippenmeyer. Cellular and Molecular Control of Neuronal Migration. Springer London, Limited, 2013.

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Cellular And Molecular Control Of Neuronal Migration. Springer, 2013.

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Nguyen, Laurent, and Simon Hippenmeyer. Cellular and Molecular Control of Neuronal Migration. Springer, 2013.

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Cellular Migration and Formation of Axons and Dendrites. Elsevier, 2020. http://dx.doi.org/10.1016/c2017-0-00859-5.

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Capítulos de libros sobre el tema "Cellular Migration"

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Wagstaff, John. "Lymphocyte Migration Studies in Man." In Radiolabeled Cellular Blood Elements, 319–42. Boston, MA: Springer US, 1985. http://dx.doi.org/10.1007/978-1-4684-4922-8_16.

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Wylie, C. C., D. Stott, and P. J. Donovan. "Primordial Germ Cell Migration." In The Cellular Basis of Morphogenesis, 433–48. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2141-5_11.

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Solursh, Michael. "Migration of Sea Urchin Primary Mesenchyme Cells." In The Cellular Basis of Morphogenesis, 391–431. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2141-5_10.

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Sanders, Esmond J. "Mesoderm Migration in the Early Chick Embryo." In The Cellular Basis of Morphogenesis, 449–80. Boston, MA: Springer US, 1986. http://dx.doi.org/10.1007/978-1-4613-2141-5_12.

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Deutsch, Andreas, and Sabine Dormann. "Cell Migration in Heterogeneous Environments." In Cellular Automaton Modeling of Biological Pattern Formation, 141–58. Boston, MA: Birkhäuser Boston, 2017. http://dx.doi.org/10.1007/978-1-4899-7980-3_6.

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Irianto, Jerome, Irena L. Ivanovska, Joe Swift, and Dennis E. Discher. "The Nuclear Lamina: From Mechanosensing in Differentiation to Cancer Cell Migration." In Molecular and Cellular Mechanobiology, 175–95. New York, NY: Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-5617-3_9.

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Bosanquet, David C., Keith G. Harding, and Wen G. Jiang. "ECIS, Cellular Adhesion and Migration in Keratinocytes." In Electric Cell-Substrate Impedance Sensing and Cancer Metastasis, 217–37. Dordrecht: Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-94-007-4927-6_12.

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McCarthy, James B., Daryl F. Sas, and Leo T. Furcht. "Mechanisms of Parenchymal Cell Migration into Wounds." In The Molecular and Cellular Biology of Wound Repair, 281–319. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4615-1795-5_13.

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McCarthy, James B., Joji Iida, and Leo T. Furcht. "Mechanisms of Parenchymal Cell Migration into Wounds." In The Molecular and Cellular Biology of Wound Repair, 373–90. Boston, MA: Springer US, 1988. http://dx.doi.org/10.1007/978-1-4899-0185-9_12.

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DiMilla, P. A. "Receptor-Mediated Adhesive Interactions at the Cytoskeleton/Substratum Interface During Cell Migration." In Cell Mechanics and Cellular Engineering, 490–514. New York, NY: Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4613-8425-0_27.

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Actas de conferencias sobre el tema "Cellular Migration"

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Trusiak, Maciej, Piotr Arcab, Mikołaj Rogalski, Piotr Rogujski, and Luiza Stanaszek. "Multiplexed label-free high-throughput holographic lensless method for live cell migration sensing." In Computational Optical Sensing and Imaging, CTu1B.3. Washington, D.C.: Optica Publishing Group, 2024. http://dx.doi.org/10.1364/cosi.2024.ctu1b.3.

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Cell migration plays crucial role in regeneration, morphogenesis and cancer metastasis. We present a novel hardware-software method for multiplexed (3-cameras) holographic lensless label-free full-culture live-cell quantitative migration sensing with single-cell sensitivity and sub-cellular motion precision.
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Gee, A. P. "Hematopoietic Stem Cell Engineering: The Magic Bullet of the Next Millenium?" In ASME 1997 International Mechanical Engineering Congress and Exposition, 95–96. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-1317.

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Abstract Hematopoietic stem cell [HSC] therapy has its origins as hematological rescue following marrow ablative high-dose therapy for refractory cancers and myelodysplastic syndromes. In its simplest form, bone marrow is collected from a tissue-matched related normal donor and intravenously infused into the patient who has usually received high-dose chemo/radiotherapy for his or her disease. The stem cells migrate to the marrow spaces, where they multiply and differentiate to restore blood cell-forming activity and immune defenses in the recipient Restrictions in the availability of tissue-ma
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Boppart, Stephen A., Brett E. Bouma, Costas Pitris, James F. Southern, Mark E. Brezinski, and James G. Fujimoto. "Optical Coherence Tomographic Imaging of In Vivo Cellular Dynamics." In Advances in Optical Imaging and Photon Migration. Washington, D.C.: OSA, 1998. http://dx.doi.org/10.1364/aoipm.1998.amc1.

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Boppart, Stephen A., Gary J. Tearney, Brett E. Bouma, James G. Fujimoto, and Mark E. Brezinski. "Optical Coherence Tomography of Embryonic Morphology During Cellular Differentiation." In Advances in Optical Imaging and Photon Migration. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/aoipm.1996.cit231.

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Improved imaging of morphological changes has the potential of offering new insight into the complex process of embryonic development. Optical coherence tomography (OCT), is a new imaging technique for performing in vivo cross-sectional imaging of architectural morphology by measuring backscattered infrared light. This study investigates the application of OCT for imaging developing structure in Xenopus laevis (African frog) and Brachydanio rerio (zebra fish), two developmental biology animal models. Images are compared to corresponding histological preparations. Cross sectional imaging can be
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Ng, Colin, and Amrinder Nain. "Cellular Dynamics on Aligned Fibrous PLGA Scaffolds." In ASME 2011 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2011. http://dx.doi.org/10.1115/sbc2011-54014.

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Understanding cellular dynamics is fundamental to increasing the healing and regenerative capacity of biomedical scaffolds. The ability to investigate environmental cues and cell-cell interactions in vitro with successful translation to in vivo therapies will enhance many tissue engineering technologies. Understanding the dynamics of a cell in response to external mechanical stimuli can help achieve directed cellular migration by varying cellular environment geometries. Customized scaffolds can then be designed to achieve desired cellular migration rates, cell-cell interaction pathways, increa
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Schmidt, Lars Henning, Tilmann Spieker, Julia Humberg, Alessandro Marra, Ludger Hillejan, Wolfgang E. Berdel, Carsten Muller-Tidow, and Rainer Wiewrodt. "MALAT-1 NcRNA Enhances Cellular Migration And Wound Healing." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a6369.

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Penney, C. M., D. N. Pattanayak, and W. T. Lotshaw. "Modeling the Wavelength Dependence of the Early Arriving Fraction of a Short Optical Pulse Transmitted Through a Highly Scattering Medium." In Advances in Optical Imaging and Photon Migration. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/aoipm.1996.trit87.

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The wavelength dependence of light transport parameters of human tissue are estimated using Mie calculations of scattering from a simple model of a distribution of single sized spherical scatterers in an otherwise homogeneous background medium. The results are consistent with a dominant contribution to tissue scattering from small cellular or intercellular constituents such as mitochondria. The early arriving transmitted fraction of short optical pulses is calculated using both a diffusion approximation, and a Monte Carlo solution of the transport problem. Both predict enhancement of this tran
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Jacques, Steven L. "Origins of Tissue Optical Properties in the UVA, Visible, and NIR Regions." In Advances in Optical Imaging and Photon Migration. Washington, D.C.: Optica Publishing Group, 1996. http://dx.doi.org/10.1364/aoipm.1996.opc364.

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This paper describes the relationship between the ultrastructure of biological tissues and the observed macroscopic optical scattering properties. A summary of the tissue absorption spectrum is also presented. The scattering of soft tissues (liver, prostate, etc.) and fibrous tissues such as dermis are considered. The scattering of soft tissues is attribued to membranous structures and modeled as Mie scattering from spheres in the 0.2-2-μm diameter range, where membrane lipids occupy about 1-20% of the cellular volume and the refractive index mismatch is 1.46/1.35. The scattering of dermis is
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Applewhite-Grosso, Terri, Nancy Davis Griffeth, Elisa Lannon, Uchenna Unachukwu, Stephen Redenti, and Naralys Batista. "A multi-scale, physics engine-based simulation of cellular migration." In 2015 Winter Simulation Conference (WSC). IEEE, 2015. http://dx.doi.org/10.1109/wsc.2015.7408248.

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Roddy, Meagan, John Rauch, Lindy O’Clair, and Daniel M. Appledorn. "Abstract 5084: Real-time, quantitative cellular analysis of migration and invasion." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-5084.

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