Relevant bibliographies by topics / Spindle (Cell division) Cell migration

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

Academic literature on the topic 'Spindle (Cell division) Cell migration'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Spindle (Cell division) Cell migration"

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Wordeman, L., K. L. McDonald, and W. Z. Cande. "The distribution of cytoplasmic microtubules throughout the cell cycle of the centric diatom Stephanopyxis turris: their role in nuclear migration and positioning the mitotic spindle during cytokinesis." Journal of Cell Biology 102, no. 5 (1986): 1688–98. http://dx.doi.org/10.1083/jcb.102.5.1688.

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The cell cycle of the marine centric diatom Stephanopyxis turris consists of a series of spatially and temporally well-ordered events. We have used immunofluorescence microscopy to examine the role of cytoplasmic microtubules in these events. At interphase, microtubules radiate out from the microtubule-organizing center, forming a network around the nucleus and extending much of the length and breadth of the cell. As the cell enters mitosis, this network breaks down and a highly ordered mitotic spindle is formed. Peripheral microtubule bundles radiate out from each spindle pole and swing out a
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Gönczy, Pierre, Heinke Schnabel, Titus Kaletta, Ana Duran Amores, Tony Hyman, and Ralf Schnabel. "Dissection of Cell Division Processes in the One Cell Stage Caenorhabditis elegans Embryo by Mutational Analysis." Journal of Cell Biology 144, no. 5 (1999): 927–46. http://dx.doi.org/10.1083/jcb.144.5.927.

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To identify novel components required for cell division processes in complex eukaryotes, we have undertaken an extensive mutational analysis in the one cell stage Caenorhabditis elegans embryo. The large size and optical properties of this cell permit observation of cell division processes with great detail in live specimens by simple differential interference contrast (DIC) microscopy. We have screened an extensive collection of maternal-effect embryonic lethal mutations on chromosome III with time-lapse DIC video microscopy. Using this assay, we have identified 48 mutations in 34 loci which
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Sun, Shao-Chen, and Nam-Hyung Kim. "Molecular Mechanisms of Asymmetric Division in Oocytes." Microscopy and Microanalysis 19, no. 4 (2013): 883–97. http://dx.doi.org/10.1017/s1431927613001566.

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AbstractIn contrast to symmetric division in mitosis, mammalian oocyte maturation is characterized by asymmetric cell division that produces a large egg and a small polar body. The asymmetry results from oocyte polarization, which includes spindle positioning, migration, and cortical reorganization, and this process is critical for fertilization and the retention of maternal components for early embryo development. Although actin dynamics are involved in this process, the molecular mechanism underlying this remained unclear until the use of confocal microscopy and live cell imaging became wide
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de Saint Phalle, Brigitte, and William Sullivan. "Spindle Assembly and Mitosis without Centrosomes in Parthenogenetic Sciara Embryos." Journal of Cell Biology 141, no. 6 (1998): 1383–91. http://dx.doi.org/10.1083/jcb.141.6.1383.

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In Sciara, unfertilized embryos initiate parthenogenetic development without centrosomes. By comparing these embryos with normal fertilized embryos, spindle assembly and other microtubule-based events can be examined in the presence and absence of centrosomes. In both cases, functional mitotic spindles are formed that successfully proceed through anaphase and telophase, forming two daughter nuclei separated by a midbody. The spindles assembled without centrosomes are anastral, and it is likely that their microtubules are nucleated at or near the chromosomes. These spindles undergo anaphase B a
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Sutradhar, Sabyasachi, Vikas Yadav, Shreyas Sridhar, et al. "A comprehensive model to predict mitotic division in budding yeasts." Molecular Biology of the Cell 26, no. 22 (2015): 3954–65. http://dx.doi.org/10.1091/mbc.e15-04-0236.

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High-fidelity chromosome segregation during cell division depends on a series of concerted interdependent interactions. Using a systems biology approach, we built a robust minimal computational model to comprehend mitotic events in dividing budding yeasts of two major phyla: Ascomycota and Basidiomycota. This model accurately reproduces experimental observations related to spindle alignment, nuclear migration, and microtubule (MT) dynamics during cell division in these yeasts. The model converges to the conclusion that biased nucleation of cytoplasmic microtubules (cMTs) is essential for direc
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Telley, Ivo A., Imre Gáspár, Anne Ephrussi, and Thomas Surrey. "Aster migration determines the length scale of nuclear separation in the Drosophila syncytial embryo." Journal of Cell Biology 197, no. 7 (2012): 887–95. http://dx.doi.org/10.1083/jcb.201204019.

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In the early embryo of many species, comparatively small spindles are positioned near the cell center for subsequent cytokinesis. In most insects, however, rapid nuclear divisions occur in the absence of cytokinesis, and nuclei distribute rapidly throughout the large syncytial embryo. Even distribution and anchoring of nuclei at the embryo cortex are crucial for cellularization of the blastoderm embryo. The principles underlying nuclear dispersal in a syncytium are unclear. We established a cell-free system from individual Drosophila melanogaster embryos that supports successive nuclear divisi
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Riparbelli, M. G., G. Callaini, and D. M. Glover. "Failure of pronuclear migration and repeated divisions of polar body nuclei associated with MTOC defects in polo eggs of Drosophila." Journal of Cell Science 113, no. 18 (2000): 3341–50. http://dx.doi.org/10.1242/jcs.113.18.3341.

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The meiotic spindle of Drosophila oocytes is acentriolar but develops an unusual central microtubule organising centre (MTOC) at the end of meiosis I. In polo oocytes, this common central pole for the two tandem spindles of meiosis II was poorly organised and in contrast to wild-type failed to maintain its associated Pav-KLP motor protein. Furthermore, the polar body nuclei failed to arrest at metaphase, and the four products of female meiosis all underwent repeated haploid division cycles on anastral spindles. This was linked to a failure to form the astral array of microtubules with which th
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Zhang, Yu, Xiang Wan, Hong-Hui Wang, Meng-Hao Pan, Zhen-Nan Pan, and Shao-Chen Sun. "RAB35 depletion affects spindle formation and actin-based spindle migration in mouse oocyte meiosis." MHR: Basic science of reproductive medicine 25, no. 7 (2019): 359–72. http://dx.doi.org/10.1093/molehr/gaz027.

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Abstract Mammalian oocyte maturation involves a unique asymmetric cell division, in which meiotic spindle formation and actin filament-mediated spindle migration to the oocyte cortex are key processes. Here, we report that the vesicle trafficking regulator, RAB35 GTPase, is involved in regulating cytoskeleton dynamics in mouse oocytes. RAB35 GTPase mainly accumulated at the meiotic spindle periphery and cortex during oocyte meiosis. Depletion of RAB35 by morpholino microinjection led to aberrant polar body extrusion and asymmetric division defects in almost half the treated oocytes. We also fo
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Liu, Xiaoyu, Xiaoyun Liu, Dandan Chen, Xiuying Jiang, and Wei Ma. "PLD2 regulates microtubule stability and spindle migration in mouse oocytes during meiotic division." PeerJ 5 (May 16, 2017): e3295. http://dx.doi.org/10.7717/peerj.3295.

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Phospholipase D2 (PLD2) is involved in cytoskeletal reorganization, cell migration, cell cycle progression, transcriptional control and vesicle trafficking. There is no evidence about PLD2 function in oocytes during meiosis. Herein, we analyzed PLD2 expression and its relationship with spindle formation and positioning in mouse oocyte meiosis. High protein level of PLD2 was revealed in oocytes by Western blot, which remained consistently stable from prophase I with intact germinal vesicle (GV) up to metaphase II (MII) stage. Immunofluorescence showed that PLD2 appeared and gathered around the
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Gholkar, Ankur A., Keith Cheung, Kevin J. Williams, et al. "Fatostatin Inhibits Cancer Cell Proliferation by Affecting Mitotic Microtubule Spindle Assembly and Cell Division." Journal of Biological Chemistry 291, no. 33 (2016): 17001–8. http://dx.doi.org/10.1074/jbc.c116.737346.

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The sterol regulatory element-binding protein (SREBP) transcription factors have become attractive targets for pharmacological inhibition in the treatment of metabolic diseases and cancer. SREBPs are critical for the production and metabolism of lipids and cholesterol, which are essential for cellular homeostasis and cell proliferation. Fatostatin was recently discovered as a specific inhibitor of SREBP cleavage-activating protein (SCAP), which is required for SREBP activation. Fatostatin possesses antitumor properties including the inhibition of cancer cell proliferation, invasion, and migrat
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Dissertations / Theses on the topic "Spindle (Cell division) Cell migration"

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Nestor-Bergmann, Alexander. "Relating cell shape, mechanical stress and cell division in epithelial tissues." Thesis, University of Manchester, 2018. https://www.research.manchester.ac.uk/portal/en/theses/relating-cell-shape-mechanical-stress-and-cell-division-in-epithelial-tissues(ebf1bce8-ca35-4f5a-8be9-f2e19c96e20d).html.

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The development and maintenance of tissues and organs depend on the careful regulation and coordinated motion of large numbers of cells. There is substantial evidence that many complex tissue functions, such as cell division, collective cell migration and gene expression, are directly regulated by mechanical forces. However, relatively little is known about how mechanical stress is distributed within a tissue and how this may guide biochemical signalling. Working in the framework of a popular vertex-based model, we derive expressions for stress tensors at the cell and tissue level to build ana
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Chanasakulniyom, Mayuree. "Single cell devices for migration and division studies." Thesis, University of Glasgow, 2014. http://theses.gla.ac.uk/5072/.

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Microfluidic technologies and devices now provide powerful tools for many biological studies to gain knowledge and insight into cell behaviour because of their potential to control the local in vitro environment. This thesis aims to develop microfluidic devices for the single cell proliferation and migration studies that are fundamental in determining cell and tissue behaviour. There are two designs of microfluidic devices that have been used in this project. The first one is hydrodynamic single cell trap device having a bagatelle- like structure. The bagatelle-like devices were used to trap m
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Stewart, Neil Padilla Pamela Ann Fox. "Identifying genetic interactions of the spindle checkpoint in Caenorhabditis elegans." [Denton, Tex.] : University of North Texas, 2009. http://digital.library.unt.edu/ark:/67531/metadc12203.

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Golub, Ognjen. "Molecular Mechanisms Regulating Subcellular Localization and Function of Mitotic Spindle Orientation Determinants." Thesis, University of Oregon, 2016. http://hdl.handle.net/1794/20711.

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Proper orientation of the mitotic spindle is essential during animal development for the generation of cell diversity and organogenesis. To understand the molecular mechanisms regulating this process, genetic studies have implicated evolutionarily conserved proteins that function in diverse cell types to align the spindle along an intrinsic cellular polarity axis. This activity is achieved through physical contacts between astral microtubules of the spindle and a distinct domain of force generating proteins on the cell cortex. In this work, I shed light on how these proteins form distinct cort
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Joslin, Elizabeth Jane. "Quantitative studies of EGFR autocrine induced cell signaling and migration." Thesis, Massachusetts Institute of Technology, 2007. http://hdl.handle.net/1721.1/39910.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2007.<br>Includes bibliographical references.<br>Epidermal growth factor (EGF) receptor autocrine and/or paracrine signaling plays an important role in normal epithelial cell proliferation, survival, adhesion and migration. Aberrant expression of the EGF receptor and its cognate ligands have been implicated in various types of cancers, hence EGF receptor autocrine activation is thought to also be involved in tumorigenesis. EGF family ligands are synthesized as membrane-anchored proteins requiring proteolyt
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Chu, Calvin School of Biomedical Engineering UNSW. "Development of a semi-automatic method for cellular migration and division analysis." Awarded by:University of New South Wales. School of Biomedical Engineering, 2005. http://handle.unsw.edu.au/1959.4/20543.

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Binary image processing algorithms have been implemented in this study to create a background subtraction mask for the segmentation of cellular time lapse images. The complexity in the development of the background subtraction mask stems from the inherent difficulties in contrast resolution at the cellular boundaries. Coupling the background subtraction mask with the path reconstruction method via superposition of overlapping binary segmented objects in sequential time lapse images produces a semi-automatic method for cellular tracking. In addition to the traditional center of mass or centroid
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Reschen, Richard Frederick. "The roles of Dgp71WD at the centrosome and spindle in Drosophila." Thesis, University of Cambridge, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.609808.

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Stewart, Neil. "Identifying genetic interactions of the spindle checkpoint in Caenorhabditis elegans." Thesis, University of North Texas, 2009. https://digital.library.unt.edu/ark:/67531/metadc12203/.

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Faithful segregation of chromosomes is ensured by the spindle checkpoint. If a kinetochore does not correctly attach to a microtubule the spindle checkpoint stops cell cycle progression until all chromosomes are attached to microtubules or tension is experienced while pulling the chromosomes. The C. elegans gene, san-1, is required for spindle checkpoint function and anoxia survival. To further understand the role of san-1 in the spindle checkpoint, an RNAi screen was conducted to identify genetic interactions with san-1. The kinetochore gene hcp-1 identified in this screen, was known to have
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Kosmin, Alan Simon. "Cell proliferation, apoptosis and migration within the human fetal retina." Thesis, University of Liverpool, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366488.

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Hung, Hui-Fang. "Roles of the Mother Centriole Appendage Protein Cenexin in Microtubule Organization during Cell Migration and Cell Division: A Dissertation." eScholarship@UMMS, 2016. https://escholarship.umassmed.edu/gsbs_diss/842.

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Epithelial cells are necessary building blocks of the organs they line. Their apicalbasolateral polarity, characterized by an asymmetric distribution of cell components along their apical-basal axis, is a requirement for normal organ function. Although the centrosome, also known as the microtubule organizing center, is important in establishing cell polarity the mechanisms through which it achieves this remain unclear. It has been suggested that the centrosome influences cell polarity through microtubule cytoskeleton organization and endosome trafficking. In the first chapter of this thesis, I
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Books on the topic "Spindle (Cell division) Cell migration"

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Tazawa, M. Cell Dynamics: Cytoplasmic Streaming Cell Movement-Contraction and Migration Cell and Organelle Division Phototaxis of Cell and Cell Organelle. Springer Vienna, 1989.

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Laboratory, Cold Spring Harbor, ed. The cell surface. Cold Spring Harbor Laboratory Press, 1992.

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M, Tazawa, ed. Cell dynamics. Springer-Verlag, 1989.

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(Editor), Robert E. Palazzo, and Trisha N. Davis (Editor), eds. Centrosomes and Spindle Pole Bodies (Methods in Cell Biology, Volume 67) (Methods in Cell Biology). Academic Press, 2001.

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Laboratory, Cold Spring Harbor, ed. The Cell surface. Cold Spring Harbor Laboratory, 1992.

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Symposia on Quantitative Biology Vol. LVII, 1992. Cold Spring Harbor Laboratory Press, 1993.

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Book chapters on the topic "Spindle (Cell division) Cell migration"

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Geymonat, Marco, and Marisa Segal. "Intrinsic and Extrinsic Determinants Linking Spindle Pole Fate, Spindle Polarity, and Asymmetric Cell Division in the Budding Yeast S. cerevisiae." In Results and Problems in Cell Differentiation. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53150-2_3.

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Smith, Prestina, Mark Azzam, and Lindsay Hinck. "Extracellular Regulation of the Mitotic Spindle and Fate Determinants Driving Asymmetric Cell Division." In Results and Problems in Cell Differentiation. Springer International Publishing, 2017. http://dx.doi.org/10.1007/978-3-319-53150-2_16.

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Gönczy, Pierre, Stephan Grill, Ernst H. K. Stelzer, Matthew Kirkham, and Anthony A. Hyman. "Spindle Positioning during the Asymmetric First Cell Division of Caenorhabditis elegans Embroyos." In Novartis Foundation Symposia. John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/0470846666.ch13.

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Yao, Li, and Yongchao Li. "Electric Field-Guided Cell Migration, Polarization, and Division: An Emerging Therapy in Neural Regeneration." In Glial Cell Engineering in Neural Regeneration. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-030-02104-7_5.

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Gazea, R. M., and W. E. Watson. "Cell Division and Migration in the Brain After Optic Nerve Lesions." In Novartis Foundation Symposia. John Wiley & Sons, Ltd., 2008. http://dx.doi.org/10.1002/9780470719633.ch5.

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Lovegrove, Holly E., and Dan T. Bergstralh. "Cell Division | Spindle Positioning." In Encyclopedia of Biological Chemistry III. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-819460-7.00294-2.

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INOUÉ, SHINYA. "Cell Division and the Mitotic Spindle." In Collected Works of Shinya Inoué. WORLD SCIENTIFIC, 2008. http://dx.doi.org/10.1142/9789812790866_0035.

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Caillaud, Marie-Cécile, Laetitia Paganelli, Philippe Lecomte, et al. "Spindle Assembly Checkpoint Protein Dynamics and Roles in Plant Cell Division." In Plant Physiology. Apple Academic Press, 2011. http://dx.doi.org/10.1201/b12221-9.

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Wynshaw-Boris, Anthony J. "Microtubule Motors: Intracellular Transport, Cell Division, Ciliary Movement, and Nuclear Migration." In Epstein's Inborn Errors of Development. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199934522.003.0184.

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Grisar, Thierry, Bernard Lakaye, Laurence de Nijs, Joseph J. LoTurco, Andrea Daga, and Antonio V. Delgado-Escueta. "Myoclonin1/EFHC1 in Cell Division, Neuroblast Migration, and Synapse/Dendrite Formation in Juvenile Myoclonic Epilepsy." In Jasper's Basic Mechanisms of the Epilepsies. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199746545.003.0067.

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Conference papers on the topic "Spindle (Cell division) Cell migration"

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Li, Zhehan, David Grace, and Paul Mitchell. "Cell division, migration and death for energy efficient 5G ultra-small cell networks." In 2014 IEEE Globecom Workshops (GC Wkshps). IEEE, 2014. http://dx.doi.org/10.1109/glocomw.2014.7063554.

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Hashimoto, Shigehiro, and Kiyoshi Yoshinaka. "Migration Velocity of Cell under Shear Flow Field: After and Before Division." In 2020 IEEE 20th International Conference on Bioinformatics and Bioengineering (BIBE). IEEE, 2020. http://dx.doi.org/10.1109/bibe50027.2020.00033.

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Kraning-Rush, Casey M., Shawn P. Carey, and Cynthia A. Reinhart-King. "Molded Collagen Microchannels for the Study of Cancer Cell Invasion." In ASME 2012 10th International Conference on Nanochannels, Microchannels, and Minichannels collocated with the ASME 2012 Heat Transfer Summer Conference and the ASME 2012 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/icnmm2012-73093.

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Metastasis is the cause of 90% of cancer-related deaths and yet the precise mechanism of metastasis is poorly understood[1]. To metastasize, cells break free from the primary tumor, migrate through the surrounding tissue, and enter the vascular system to move to a secondary site. To migrate through the stroma, cell can both degrade the tissue and use physical force to move the tissue from its path. However, the relative roles of matrix degradation and cellular force are not well-understood. Previous work has shown that as cell move through the matrix, they create channels that other cells can
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Dangaria, Jhanvi H., and Peter J. Butler. "Interaction of Shear Stress, Myosin II, and Actin in Dynamic Modulation of Endothelial Cell Microrheology." In ASME 2008 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2008. http://dx.doi.org/10.1115/sbc2008-192947.

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The endothelial cell (EC) cytoskeleton mediates several biological functions such as adhesion, migration, phagocytosis, cell division, and mechanosensitivity. These functions are carried out in part through dynamic cytoskeletal polymerization, modulation of crosslinking, and development of tension between intracellular organelles and the extracellular matrix via focal adhesion plaques. One important component of the cytoskeleton is actin which polymerizes into filaments and is thought to be prestressed by virtue of crosslinking proteins such as α-actinin, filamin and myosin II molecular motors
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Kumar, G. Naga Siva, Sushanta K. Mitra, and Subir Bhattacharjee. "Dielectrophoretic Mixing With Novel Electrode Geometry." In ASME 2009 Fluids Engineering Division Summer Meeting. ASMEDC, 2009. http://dx.doi.org/10.1115/fedsm2009-78260.

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Electrokinetic mixing of analytes at micro-scale is important in several biochemical applications like cell activation, DNA hybridization, protein folding, immunoassays and enzyme reactions. This paper deals with the modeling and numerical simulation of micromixing of two different types of colloidal suspensions based on principle of dielectrophoresis (DEP). A mathematical model is developed based on Laplace, Navier-Stokes, and convection-diffusion-migration equations to calculate electric field, velocity, and concentration distributions, respectively. Mixing of two colloidal suspensions is si
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Melbye, Julie A., and Yechun Wang. "Droplet Dynamics in Constricted Return Bends of Microfluidic Channels." In ASME 2020 Fluids Engineering Division Summer Meeting collocated with the ASME 2020 Heat Transfer Summer Conference and the ASME 2020 18th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2020. http://dx.doi.org/10.1115/fedsm2020-20406.

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Abstract Microfluidic delivery systems have been employed to facilitate cell seeding procedures in drug development for personalized medicine for cancer patients. Despite of the high-throughput nature and potential impact on clinical outcomes of these systems, the efficiency in cell trapping remains a challenge in the operation. Droplet-based microfluidics became one of the solutions due to the large size of the cell-enclosing droplets and their interfacial properties. This study is focused on the motion of the cell-enclosing droplet in a constricted return bends that help to restrict the rele
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Tseng, Peter, Jack W. Judy, and Dino Di Carlo. "Dynamic Manipulation and Precision Localization of Nanoparticles Internal to Cells." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13272.

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Spatial localization of signals is commonplace within cells and allows for a variety of integral biological processes, including cell migration and polarization in development, neural synapse strengthening in learning, and correct cell division to avoid cancer development and progression. Despite the importance, few general tools have been developed to understand and probe spatial localization. We present a technique that translates the centimeter scale motions of an external magnet into nanometer scale motions of superparamagnetic nanoparticles internalized within cells growing on specially p
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Buehler, Markus J., and Je´re´mie Bertaud. "Hierarchical Structure Controls Nanomechanical Properties of Vimentin Intermediate Filaments." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13103.

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Intermediate filaments (often abbreviated as IFs), in addition to microtubules and microfilaments, are one of the three major components of the cytoskeleton in eukaryotic cells (Figure 1). It has been suggested that intermediate filaments are crucial in defining key mechanical functions of cells such as cell migration, cell division and mechanotransduction, and have also been referred to as the “safety belts of cells” reflecting their role in preventing exceedingly large cell stretch [1, 2]. Vimentin is a specific type of this protein filament found in fibroblasts, leukocytes, and blood vessel
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Richardson, William J., Dennis D. van der Voort, and James E. Moore. "A Device to Subject Cells to Longitudinal Stretch Gradients on a Tube In Vitro." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80941.

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In the US, cardiovascular disease accounts for more than 800,000 deaths and an economic burden of nearly $300 billion per year. A major pathology afflicting the cardiovascular system is atherosclerosis, characterized by intraluminal plaque formation, producing a stenosis and obstructing flow. Balloon angioplasty, often coupled with the implantation of either a bare-metal or drug-eluting stent, has become a standard treatment of atherosclerosis. However, the host tissue’s response to stenting is frequently maladaptive, leading to intimal hyperplasia via smooth muscle cell (SMC) division and mig
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Gheisari, Reza, and Parisa Mirbod. "Experimental Study of Non-Colloidal Mono and Polydisperse Suspension in Taylor-Couette Flow." In ASME 2014 4th Joint US-European Fluids Engineering Division Summer Meeting collocated with the ASME 2014 12th International Conference on Nanochannels, Microchannels, and Minichannels. American Society of Mechanical Engineers, 2014. http://dx.doi.org/10.1115/fedsm2014-21570.

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Monodisperse and polydisperse suspension flows form an extensive section of natural and technological flows. These flow structures can be categorized to sedimenting or neutrally buoyant suspensions considering the density ratio between particle phase to dispersion phase. Biological systems, food processing, ceramic injection, dynamic filtration and air conditioning are examples of areas that such flows arise. Various complicated interparticle interactions and their inevitable influence on and from the continuous phase result in some interesting phenomena which are challenging to justify. This
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