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Relevant bibliographies by topics / Cell division

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Academic literature on the topic 'Cell division'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Cell division"

1

Patterson, Dillon, Christopher D. Scharer, and Jeremy M. Boss. "IRF4 regulates the rate of cell cycle during B cell differentiation." Journal of Immunology 200, no. 1_Supplement (2018): 48.16. http://dx.doi.org/10.4049/jimmunol.200.supp.48.16.

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Abstract Cell division is required for the initiation of B cell differentiation, the regulation of isotype class switching, and ultimately entry of cells into the plasma cell (PC) lineage. Division coupled changes in the expression of transcription factors, such as interferon regulatory factor-4 (IRF4), that coordinate the PC transcriptional program also occur; however, little is known regarding how these factors coordinate cell division and exit from the cell cycle after differentiation. To begin to address this gap in knowledge, we assessed the cell division kinetics of wildtype (WT) B cells

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Scholey, Jonathan M., Ingrid Brust-Mascher, and Alex Mogilner. "Cell division." Nature 422, no. 6933 (2003): 746–52. http://dx.doi.org/10.1038/nature01599.

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Kawahigashi, Teiko, Shoya Iwanami, Munetomo Takahashi, Joydeep Bhadury, Shingo Iwami, and Satoshi Yamazaki. "Age-related changes in the hematopoietic stem cell pool revealed via quantifying the balance of symmetric and asymmetric divisions." PLOS ONE 19, no. 1 (2024): e0292575. http://dx.doi.org/10.1371/journal.pone.0292575.

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Hematopoietic stem cells (HSCs) are somatic stem cells that continuously generate lifelong supply of blood cells through a balance of symmetric and asymmetric divisions. It is well established that the HSC pool increases with age. However, not much is known about the underlying cause for these observed changes. Here, using a novel method combining single-cell ex vivo HSC expansion with mathematical modeling, we quantify HSC division types (stem cell—stem cell (S-S) division, stem cell—progenitor cell (S-P) division, and progenitor cell—progenitor cell (P-P) division) as a function of the aging

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Serra, Léo, and Sarah Robinson. "Plant cell divisions: variations from the shortest symmetric path." Biochemical Society Transactions 48, no. 6 (2020): 2743–52. http://dx.doi.org/10.1042/bst20200529.

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In plants, the spatial arrangement of cells within tissues and organs is a direct consequence of the positioning of the new cell walls during cell division. Since the nineteenth century, scientists have proposed rules to explain the orientation of plant cell divisions. Most of these rules predict the new wall will follow the shortest path passing through the cell centroid halving the cell into two equal volumes. However, in some developmental contexts, divisions deviate significantly from this rule. In these situations, mechanical stress, hormonal signalling, or cell polarity have been describ

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Sei, Yoshitatsu, Jianying Feng, Carson C. Chow, and Stephen A. Wank. "Asymmetric cell division-dominant neutral drift model for normal intestinal stem cell homeostasis." American Journal of Physiology-Gastrointestinal and Liver Physiology 316, no. 1 (2019): G64—G74. http://dx.doi.org/10.1152/ajpgi.00242.2018.

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The normal intestinal epithelium is continuously regenerated at a rapid rate from actively cycling Lgr5-expressing intestinal stem cells (ISCs) that reside at the crypt base. Recent mathematical modeling based on several lineage-tracing studies in mice shows that the symmetric cell division-dominant neutral drift model fits well with the observed in vivo growth of ISC clones and suggests that symmetric divisions are central to ISC homeostasis. However, other studies suggest a critical role for asymmetric cell division in the maintenance of ISC homeostasis in vivo. Here, we show that the stocha

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Biliński, Tomasz, and Grzegorz Bartosz. "Hypothesis: cell volume limits cell divisions." Acta Biochimica Polonica 53, no. 4 (2006): 833–35. http://dx.doi.org/10.18388/abp.2006_3313.

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Mammalian somatic cells and also cells of the yeast Saccharomyces cerevisiae are capable of undergoing a limited number of divisions. Reaching the division limit is referred to, apparently not very fortunately, as replicative aging. A common feature of S. cerevisiae cells and fibroblasts approaching the limit of cell divisions in vitro is attaining giant volumes. In yeast cells this phenomenon is an inevitable consequence of budding so it is not causally related to aging. Therefore, reaching a critically large cell volume may underlie the limit of cell divisions. A similar phenomenon may limit

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Venkei, Zsolt G., and Yukiko M. Yamashita. "Emerging mechanisms of asymmetric stem cell division." Journal of Cell Biology 217, no. 11 (2018): 3785–95. http://dx.doi.org/10.1083/jcb.201807037.

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The asymmetric cell division of stem cells, which produces one stem cell and one differentiating cell, has emerged as a mechanism to balance stem cell self-renewal and differentiation. Elaborate cellular mechanisms that orchestrate the processes required for asymmetric cell divisions are often shared between stem cells and other asymmetrically dividing cells. During asymmetric cell division, cells must establish asymmetry/polarity, which is guided by varying degrees of intrinsic versus extrinsic cues, and use intracellular machineries to divide in a desired orientation in the context of the as

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Hodgkin, P. D., J. H. Lee, and A. B. Lyons. "B cell differentiation and isotype switching is related to division cycle number." Journal of Experimental Medicine 184, no. 1 (1996): 277–81. http://dx.doi.org/10.1084/jem.184.1.277.

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The mature, resting immunoglobulin (Ig) M, IgD+ B lymphocyte can be induced by T cells to proliferate, switch isotype, and differentiate into Ig-secreting or memory cells. Furthermore, B cell activation results in the de novo expression or loss of a number of cell surface molecules that function in cell recirculation or further interaction with T cells. Here, a novel fluorescent technique reveals that T-dependent B cell activation induces cell surface changes that correlate with division cycle number. Furthermore, striking stepwise changes are often centered on a single round of cell division.

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Maddox, Amy Shaub, and Jan M. Skotheim. "Cell cycle, cell division, cell death." Molecular Biology of the Cell 30, no. 6 (2019): 732. http://dx.doi.org/10.1091/mbc.e18-12-0819.

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Livanos, Pantelis, Panagiotis Apostolakos, and Basil Galatis. "Plant cell division." Plant Signaling & Behavior 7, no. 7 (2012): 771–78. http://dx.doi.org/10.4161/psb.20530.

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Dissertations / Theses on the topic "Cell division"

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Iqbal, Syed Amir. "Asymmetric Cell Division in Mammalian Cells." Thesis, University of Manchester, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.503635.

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Rabodzey, Aleksandr. "Flow-induced mechanotransduction in cell-cell junctions of endothelial cells." Thesis, Massachusetts Institute of Technology, 2006. http://hdl.handle.net/1721.1/41586.

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Thesis (Ph. D.)--Massachusetts Institute of Technology, Biological Engineering Division, 2006.<br>Includes bibliographical references (leaves 86-92).<br>Endothelial cells show an unexpected behavior shortly after the onset of laminar flow: their crawling speed decreases ~40% within the first 30 min, but only in a confluent monolayer of endothelial cells, not in subconfluent cultures, where cell-cell interactions are limited. This led us to study early shear effects on cell-cell adherens junctions. We found a 30±6% increase in the number of VE-cadherin molecules in the junctions. The strength o

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Dix, Christina Lyn. "Adhesion-dependent cell division." Thesis, University College London (University of London), 2018. http://discovery.ucl.ac.uk/10044469/.

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Animal cells undergo a dramatic series of cell shape changes as they pass through mitosis and divide which depend both on remodelling of the contrac- tile actomyosin cortex and on the release of cell-substrate adhesions. Here, I use the adherent, non-transformed, human RPE1 cell line as a model system in which to explore the dynamics of these shape changes, and the function of mitotic adhesion remodelling. Although these cells are highly motile, and therefore polarised in interphase, many pause migration and elongate to be- come bipolar prior to mitosis. Interestingly, and in contrast to most

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Skoog, Karl. "Cell division in Escherichia coli." Doctoral thesis, Stockholms universitet, Institutionen för biokemi och biofysik, 2011. http://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-62908.

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The Gram-negative bacterium Escherichia coli is a model system to describe the biochemistry and cell biology of cell division in bacteria. This process can be divided into three major steps. The first step involves the replication of the DNA, followed by an elongation step in which the cells become twice as long. In the last step the elongated cell constricts in the middle and the two daughter cells are separated. The cell division process in E. coli has been extensively studied for at least 50 years and a lot is known, however many details are still vague. New proteins involved in the process

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Cheng, Jade. "Regulation of cell division and cell death by GRASP65." Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.544414.

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Spanoudis, Catherine M. "Cell Division Regulation in Staphylococcus aureus." Scholar Commons, 2017. http://scholarcommons.usf.edu/etd/7090.

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Cell division is a fundamental biological process that occurs in all kingdoms of life. Our understanding of cell division in bacteria stems from studies in the rod-shaped model organisms: Gram-negative Escherichia coli and Gram-positive Bacillus subtilis. The molecular underpinnings of cell division regulation in non-rod-shaped bacteria remain to be studied in detail. Rod-shaped bacteria possess many positive and negative regulatory proteins that are essential to the proper placement of the division septa and ultimately the production of two identical daughter cells, many

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Kirby, Melissa Jane. "Regulation of sugar beet cell division." Thesis, De Montfort University, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.391029.

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Dewar, Susan J. "Cell division in Escherichia coli : the expression and regulation of division genes." Thesis, University of Edinburgh, 1988. http://hdl.handle.net/1842/13636.

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The four essential cell division genes <i>ftsQ, ftsA, ftsZ</i>, and <i>envA</i> are arranged sequentially within a large cluster of genes required for cell envelope growth and form. The bacteriophage λJFL100 carries the 1.8 kilobase <i>Eco</i>R1-<i>Hin</i>dIII chromosomal restriction fragment which spans the <i>ftsQ</i> and part of <i>ftsA</i> coding sequences. This fragment contains at least two promoters; one within <i>ftsQ</i> is required for the expression of <i>ftsA</i> and one within <i>ftsA</i> is required for expression of <i>ftsZ</i>. The <i>fts</i> fragment is cloned upstream of a <i

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Yates, Luke Alexander. "Structural studies in cell adhesion and division." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:d66f5602-7e49-4042-8ebf-9457e61d56c3.

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Cell adhesion is a critical process that allows the organisation and functioning of tissues in three-dimensions. However, the replenishing of cells, via cell division, within tissues is equally important for functioning complex life. Both cell adhesion and division are tightly controlled processes and rely on a complex network of signals that, as yet, are not wholly understood. This Thesis presents a structural analysis of several proteins involved in these processes. In the case of cell adhesion, we have made use of high-throughput (HTP) cloning and expression screening technologies in the Ox

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Wongchaowart, Michael B. "Optimization of cell adhesion environments for a liver cell bioreactor." Thesis, Massachusetts Institute of Technology, 2005. http://hdl.handle.net/1721.1/34156.

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Thesis (M. Eng.)--Massachusetts Institute of Technology, Biological Engineering Division, February 2006.<br>Includes bibliographical references (p. 40-44).<br>The MilliF bioreactor offers great potential for the formation of i vivo-like liver tissue outside the body, making it a valuable tool for applications such as drug toxicity models and biosensors. Cell adhesion is an important factor in the maintenance of differentiated hepatocyte functions. Hepatocyte adhesion environments were examined in two settings: spheroid culture prior to seeding in the bioreactor and 2D surface culture methods t

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Books on the topic "Cell division"

1

Snedden, Robert. Cell division & genetics. Heinemann Library, 2008.

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Caillaud, Marie-Cécile, ed. Plant Cell Division. Springer US, 2022. http://dx.doi.org/10.1007/978-1-0716-1744-1.

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Macieira-Coelho, Alvaro, ed. Asymmetric Cell Division. Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-69161-7.

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Caillaud, Marie-Cécile, ed. Plant Cell Division. Springer New York, 2016. http://dx.doi.org/10.1007/978-1-4939-3142-2.

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D, Francis, Dudits Dénes, and Inzé D, eds. Plant cell division. Portland, 1998.

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Renato, Baserga, ed. Cell growth and division: A practical approach. IRL Press at Oxford University Press, 1989.

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Akira, Ishihama, and Yoshikawa Hiroshi 1933-, eds. Control of cell growth and division. Japan Scientific Societies Press, 1991.

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NATO, Advanced Research Workshop on Biomechanics of Cell Division (1986 Istanbul Turkey). Biomechanics of cell division. Plenum Press, 1987.

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Akkas, Nuri, ed. Biomechanics of Cell Division. Springer US, 1987. http://dx.doi.org/10.1007/978-1-4684-1271-0.

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A, Endow Sharyn, and Glover David M, eds. Dynamics of cell division. Oxford University Press, 1998.

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Book chapters on the topic "Cell division"

1

Miyata, Makoto. "Cell Division." In Molecular Biology and Pathogenicity of Mycoplasmas. Springer US, 2002. http://dx.doi.org/10.1007/0-306-47606-1_6.

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Widłak, Wiesława. "Cell Division." In Molecular Biology. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-45361-8_7.

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Rothfield, Lawrence I., and Jorge Garcia-Lara. "Cell Division." In Regulation of Gene Expression in Escherichia coli. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4684-8601-8_26.

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Ryan Arends, S. J., Kyle B. Williams, Ryan J. Kustusch, and David S. Weiss. "Cell Division." In The Periplasm. ASM Press, 2014. http://dx.doi.org/10.1128/9781555815806.ch10.

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Singh, Ram J. "Cell Division." In Practical Manual on Plant Cytogenetics. CRC Press, 2017. http://dx.doi.org/10.4324/9781351228268-7.

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Dye, Frank J. "Cell division." In Human Life Before Birth. CRC Press, 2019. http://dx.doi.org/10.1201/9781351130288-4.

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Lack, Andrew, and David Evans. "Cell division." In Plant Biology, 2nd ed. Taylor & Francis, 2021. http://dx.doi.org/10.1201/9780203002902-13.

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Gupta, Rani, Namita Gupta, and Amuliya Kashyap. "Cell Division." In Fundamentals of Bacterial Physiology and Metabolism. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-0723-3_4.

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Schwab, Manfred. "Asymmetric Cell Division." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27841-9_424-2.

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Enderling, Heiko. "Symmetric Cell Division." In Encyclopedia of Systems Biology. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4419-9863-7_1532.

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Conference papers on the topic "Cell division"

1

Datta, Rupsa, Emmanuel Contreras Guzman, Kiera M. Sapp, Matthew Vander Heiden, and Melissa C. Skala. "Metabolic imaging of cell division." In Multiphoton Microscopy in the Biomedical Sciences XXV, edited by Ammasi Periasamy, Peter T. So, and Karsten König. SPIE, 2025. https://doi.org/10.1117/12.3043455.

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Nieto, César, Sayeh Rezaee, Cesar Augusto Vargas-Garcia, and Abhyudai Singh. "Joint Distribution Dynamics of Cell Cycle Variables in Exponentially-Growing Cells with Stochastic Division." In 2025 33rd Mediterranean Conference on Control and Automation (MED). IEEE, 2025. https://doi.org/10.1109/med64031.2025.11073330.

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Daniyan, Abdullahi, Alessio V. Inchingolo, Andrew McAinsh, and Nigel Burroughs. "Enhanced Kinetochore Detection During Mitotic Human Cell Division using CFAR." In 2024 27th International Conference on Information Fusion (FUSION). IEEE, 2024. http://dx.doi.org/10.23919/fusion59988.2024.10706334.

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Basak, Abhishek, Santanu Mandal, Parnab Das, and Medha Kumari. "Medical Image Cryptosystem using Hyperchaotic Sequence and Scrambling Operations with Sequential Cell-division." In 2024 12th International Conference on Internet of Everything, Microwave, Embedded, Communication and Networks (IEMECON). IEEE, 2024. https://doi.org/10.1109/iemecon62401.2024.10846598.

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Park, Hanmin, and Kiyoung Choi. "Cell division." In ASPDAC '19: 24th Asia and South Pacific Design Automation Conference. ACM, 2019. http://dx.doi.org/10.1145/3287624.3287721.

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Ateshian, Gerard A., Kevin D. Costa, Evren U. Azeloglu, Barclay Morrison, and Clark T. Hung. "Continuum Modeling of Biological Tissue Growth by Cell Division." In ASME 2009 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2009. http://dx.doi.org/10.1115/sbc2009-205495.

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A framework is formulated for continuum modeling of biological tissue growth that explicitly addresses cell division, using a homogenized representation of cells and the extracellular matrix (ECM). The essential elements of this model rely on the description of the cell as containing a solution of water and osmolytes, and having osmotically inactive solid constituents that may be generically described as a porous solid matrix. The division of a cell into two nearly identical daughter cells normally starts with the duplication of cell contents during the synthesis phase, followed by cell divisi

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Hashimoto, Shigehiro, Kiyoshi Yoshinaka, and Hiroki Yonezawa. "Behavior of Cell Under Wall Shear Stress in Flow Field: Comparison Among Cell Types." In ASME 2021 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/fedsm2021-65205.

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Abstract Does the hysteresis effect remain in each cell after division? In the present study, the cell activity has been investigated after division under a shear stress field. To apply the constant shear stress field on cells, a Couette type flow device has been manufactured: between parallel walls (a lower stationary culture disk, and an upper rotating disk) with a constant gap. The wall shear stress was controlled by the rotating speed of the upper disk. Four types of cells were used in the test: C2C12 (mouse myoblast cell line), HUVEC (Human Umbilical Vein Endothelial Cells), 3T3-L1 (mouse

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Hashimoto, Shigehiro, Hiroki Yonezawa, and Ryuya Ono. "Cell Activity Change After Division Under Wall Shear Stress Field." In ASME 2021 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/imece2021-69689.

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Abstract Does cell orientation depend on the cell type in the shear stress field? Does that tendency change after the division? In this study, the behavior of each cell after division was tracked by time-lapse microscopic images through 24 hours of culture under a shear stress field. A constant shear stress field was applied to the cells in the Couette flow between the parallel walls: the lower static culture disc and the upper rotating disc. For comparison, four types of cells were used: C2C12 (mouse myoblast), HUVEC (human umbilical vein endothelial cells), 3T3-L1 (mouse adipose progenitor c

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Cox, Guy C., Teresa Dibbayawan, and Jose Feijo. "Multiphoton microscopy of cell division in plant cells." In BiOS 2001 The International Symposium on Biomedical Optics, edited by Ammasi Periasamy and Peter T. C. So. SPIE, 2001. http://dx.doi.org/10.1117/12.424548.

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Hashimoto, Shigehiro, and Takashi Yokomizo. "Tracings of Interaction Between Myoblasts Under Shear Flow in Vitro." In ASME 2021 Fluids Engineering Division Summer Meeting. American Society of Mechanical Engineers, 2021. http://dx.doi.org/10.1115/fedsm2021-65203.

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Abstract How does the group of cells make orientation perpendicular to the flow direction? How does contact with an adjacent cell affect the orientation of the cell? The orientation of a cell according to the neighbor cell under shear flow fields has been traced in vitro. A Couette type flow device with parallel discs was manufactured for the cell culture under the controlled constant wall shear stress. Cells (C2C12: mouse myoblast cell line) were cultured on the lower disc while applying the shear flow in the medium by the upper rotating disc. After culture for 24 hours without flow for adhes

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Reports on the topic "Cell division"

1

Lifschitz, Eliezer, and Elliot Meyerowitz. The Relations between Cell Division and Cell Type Specification in Floral and Vegetative Meristems of Tomato and Arabidopsis. United States Department of Agriculture, 1996. http://dx.doi.org/10.32747/1996.7613032.bard.

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Meristems were the central issue of our project. Genes that are required for cell division, cell elongation, cell proliferation and cell fate were studied in the tomato system. The analysis of the dUTPase and threonine deaminase genes, along with the dissection of their regulatory regions is completed, while that of the RNR2 and PPO genes is at an advanced stage. All these genes were isolated in our laboratory. In addition, 8 different MADS box genes were studied in transgenic plants and their genetic relevances discovered. We have also shown that a given MADS box gene can modify the polarity

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Jacobs, T. W. Regulation of cell division in higher plants. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/5089653.

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Jacobs, T. W. Regulation of cell division in higher plants. Progress report. Office of Scientific and Technical Information (OSTI), 1992. http://dx.doi.org/10.2172/10151324.

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Jacobs, T. Regulation of cell division in higher plants. Progress report, 1993. Office of Scientific and Technical Information (OSTI), 1993. http://dx.doi.org/10.2172/10178901.

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Jacobs, Thomas W. Regulation of cell division in higher plants. Final technical report. Office of Scientific and Technical Information (OSTI), 2000. http://dx.doi.org/10.2172/765959.

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Arnold, Rebecca S. Reactive Oxygen is a Major Factor Regulating Cell Division and Angiogenesis in Breast Cancer. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada397762.

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Zhongchi Liu. Investigating the Molecular Mechanism of TSO1 Function in Arabidopsis cell division and meristem development. Office of Scientific and Technical Information (OSTI), 2004. http://dx.doi.org/10.2172/832970.

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Gordon, Robert D. Protecting the Force? A Historical Perspective on the Operational Effect of the Division Protection Cell. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada566640.

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Banks, H. T., W. C. Thompson, Cristina Peligero, Sandra Giest, Jordi Argilaguet, and Andreas Meyerhans. A Division-Dependent Compartmental Model for Computing Cell Numbers in CFSE-based Lymphocyte Proliferation Assays. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada556964.

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Barg, Rivka, Erich Grotewold, and Yechiam Salts. Regulation of Tomato Fruit Development by Interacting MYB Proteins. United States Department of Agriculture, 2012. http://dx.doi.org/10.32747/2012.7592647.bard.

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Background to the topic: Early tomato fruit development is executed via extensive cell divisions followed by cell expansion concomitantly with endoreduplication. The signals involved in activating the different modes of growth during fruit development are still inadequately understood. Addressing this developmental process, we identified SlFSM1 as a gene expressed specifically during the cell-division dependent stages of fruit development. SlFSM1 is the founder of a class of small plant specific proteins containing a divergent SANT/MYB domain (Barg et al 2005). Before initiating this project,

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