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Добірка наукової літератури з теми "Cell adhesion"

Автор: Grafiati

Опубліковано: 4 червня 2021

Оновлено: 25 липня 2025

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Статті в журналах з теми "Cell adhesion"

Lipke, Peter N., Jason M. Rauceo, and Albertus Viljoen. "Cell–Cell Mating Interactions: Overview and Potential of Single-Cell Force Spectroscopy." International Journal of Molecular Sciences 23, no. 3 (2022): 1110. http://dx.doi.org/10.3390/ijms23031110.

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It is an understatement that mating and DNA transfer are key events for living organisms. Among the traits needed to facilitate mating, cell adhesion between gametes is a universal requirement. Thus, there should be specific properties for the adhesion proteins involved in mating. Biochemical and biophysical studies have revealed structural information about mating adhesins, as well as their specificities and affinities, leading to some ideas about these specialized adhesion proteins. Recently, single-cell force spectroscopy (SCFS) has added important findings. In SCFS, mating cells are brough

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Katoh, Kazuo. "FAK-Dependent Cell Motility and Cell Elongation." Cells 9, no. 1 (2020): 192. http://dx.doi.org/10.3390/cells9010192.

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Fibroblastic cells show specific substrate selectivity for typical cell–substrate adhesion. However, focal adhesion kinase (FAK) contributes to controlling the regulation of orientation and polarity. When fibroblasts attach to micropatterns, tyrosine-phosphorylated proteins and FAK are both detected along the inner border between the adhesive micropatterns and the nonadhesive glass surface. FAK likely plays important roles in regulation of cell adhesion to the substrate, as FAK is a tyrosine-phosphorylated protein that acts as a signal transduction molecule at sites of cell–substrate attachmen

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Ventre, Maurizio, Carlo Fortunato Natale, Carmela Rianna, and Paolo Antonio Netti. "Topographic cell instructive patterns to control cell adhesion, polarization and migration." Journal of The Royal Society Interface 11, no. 100 (2014): 20140687. http://dx.doi.org/10.1098/rsif.2014.0687.

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Topographic patterns are known to affect cellular processes such as adhesion, migration and differentiation. However, the optimal way to deliver topographic signals to provide cells with precise instructions has not been defined yet. In this work, we hypothesize that topographic patterns may be able to control the sensing and adhesion machinery of cells when their interval features are tuned on the characteristic lengths of filopodial probing and focal adhesions (FAs). Features separated by distance beyond the length of filopodia cannot be readily perceived; therefore, the formation of new adh

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Young, Katherine A., Laura Biggins, and Hayley J. Sharpe. "Protein tyrosine phosphatases in cell adhesion." Biochemical Journal 478, no. 5 (2021): 1061–83. http://dx.doi.org/10.1042/bcj20200511.

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Adhesive structures between cells and with the surrounding matrix are essential for the development of multicellular organisms. In addition to providing mechanical integrity, they are key signalling centres providing feedback on the extracellular environment to the cell interior, and vice versa. During development, mitosis and repair, cell adhesions must undergo extensive remodelling. Post-translational modifications of proteins within these complexes serve as switches for activity. Tyrosine phosphorylation is an important modification in cell adhesion that is dynamically regulated by the prot

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Nakamura, N., J. Tanaka, and K. Sobue. "Rous sarcoma virus-transformed cells develop peculiar adhesive structures along the cell periphery." Journal of Cell Science 106, no. 4 (1993): 1057–69. http://dx.doi.org/10.1242/jcs.106.4.1057.

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Alteration of the cell/substratum adhesive structures of rat fibroblasts (3Y1 cells) upon transformation by Rous sarcoma virus (RSV) was investigated by immunofluorescence microscopy. In serum-containing culture medium, 3Y1 cells developed focal adhesions as their main adhesive structures, while BY1 cells expressed peculiar close contacts along the cell periphery with the vitronectin receptor integrin, in addition to podosomes. These peripheral close contacts are referred to as the peripheral adhesions. The peripheral adhesions were observed as a darker region than podosomes by interference re

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Simmons, David L. "Dissecting the modes of interactions amongst cell adhesion molecules." Development 119, Supplement (1993): 193–203. http://dx.doi.org/10.1242/dev.119.supplement.193.

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The process of cell adhesion can be mediated by more than SO molecules. Fortunately, most of these can be grouped into a small number of super families. For example, more than half of all leukocyte adhesion molecules are members of the immunoglobulin super-family. The principles of cell-cell adhesion are reviewed including: kinetics and equilibria; on/off rates; affinities/avidities; homotypic/heterotypic interactions; mapping and delineation of binding sites. These principles are illustrated with two CAMs: firstly the interaction of the homotypic epithelial/myeloid adhesins CD66, and the endo

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Lotz, M. M., C. A. Burdsal, H. P. Erickson, and D. R. McClay. "Cell adhesion to fibronectin and tenascin: quantitative measurements of initial binding and subsequent strengthening response." Journal of Cell Biology 109, no. 4 (1989): 1795–805. http://dx.doi.org/10.1083/jcb.109.4.1795.

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Cell-substratum adhesion strengths have been quantified using fibroblasts and glioma cells binding to two extracellular matrix proteins, fibronectin and tenascin. A centrifugal force-based adhesion assay was used for the adhesive strength measurements, and the corresponding morphology of the adhesions was visualized by interference reflection microscopy. The initial adhesions as measured at 4 degrees C were on the order of 10(-5)dynes/cell and did not involve the cytoskeleton. Adhesion to fibronectin after 15 min at 37 degrees C were more than an order of magnitude stronger; the strengthening

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Mentzer, S. J., D. V. Faller, and S. J. Burakoff. "Interferon-gamma induction of LFA-1-mediated homotypic adhesion of human monocytes." Journal of Immunology 137, no. 1 (1986): 108–13. http://dx.doi.org/10.4049/jimmunol.137.1.108.

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Abstract Cell-cell adhesion plays an important role in monocyte function. To investigate the molecular basis for monocyte adhesion, we used recombinant interferon-gamma to induce the formation of homotypic monocyte adhesions. The induction of homotypic adhesions correlated with the increased expression of the LFA-1 membrane molecule. LFA-1 surface expression was increased twofold, whereas expression levels of other monocyte surface molecules including CR3 and p150,95 were unchanged. The direct involvement of LFA-1 in monocyte adhesion was addressed by anti-LFA-1 monoclonal antibody inhibition

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Willaert, Ronnie G., Yeseren Kayacan, and Bart Devreese. "The Flo Adhesin Family." Pathogens 10, no. 11 (2021): 1397. http://dx.doi.org/10.3390/pathogens10111397.

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The first step in the infection of fungal pathogens in humans is the adhesion of the pathogen to host tissue cells or abiotic surfaces such as catheters and implants. One of the main players involved in this are the expressed cell wall adhesins. Here, we review the Flo adhesin family and their involvement in the adhesion of these yeasts during human infections. Firstly, we redefined the Flo adhesin family based on the domain architectures that are present in the Flo adhesins and their functions, and set up a new classification of Flo adhesins. Next, the structure, function, and adhesion mechan

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Murphy-Ullrich, J. E., and M. Höök. "Thrombospondin modulates focal adhesions in endothelial cells." Journal of Cell Biology 109, no. 3 (1989): 1309–19. http://dx.doi.org/10.1083/jcb.109.3.1309.

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We examined the effects of thrombospondin (TSP) in the substrate adhesion of bovine aortic endothelial cells. The protein was tested both as a substrate for cell adhesion and as a modulator of the later stages of the cell adhesive process. TSP substrates supported the attachment of some BAE cells, but not cell spreading or the formation of focal adhesion plaques. In contrast, cells seeded on fibrinogen or fibronectin substrates were able to complete the adhesive process, as indicated by the formation of focal adhesion plaques. Incubation of cells in suspension with soluble TSP before or at the

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Дисертації з теми "Cell adhesion"

Stewart, Alasdair Gwilym. "Studies of focal adhesion kinase in epithelial cells : involvement in cell-cell adhesion." Thesis, University College London (University of London), 2005. http://discovery.ucl.ac.uk/1446839/.

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Epithelial cell-cell adhesion is mediated by tight junctions, adherens junctions and desmosomes. Epithelial cell-matrix adhesion is mediated by hemidesmosomes and focal contacts. These complexes exhibit great plasticity, and each contains molecular components which are able to participate in one or more of the other adhesive complexes. Focal adhesion kinase (FAK/pl25FAK) is a non-receptor tyrosine kinase which transduces signals from integrins at sites of focal contact to promote adhesion, spreading and migration. FAK possesses a central kinase domain which is flanked by large, non-catalytic,

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Armstrong, Nicola J. "Continuum modelling of cell-cell adhesion." Thesis, Heriot-Watt University, 2008. http://hdl.handle.net/10399/2167.

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Cells adhere to each other through the binding of cell adhesion molecules at the cell surface. This process, known as cell-cell adhesion, is fundamental in many areas of biology, including early embryo development, tissue homeostasis and tumour growth. Here \~e present a new continuum mathematical model of this phenomenon by considering Ã‚Â· the movement of cells in response to the adhesive forces generated through binding. We demonstrate that the model predicts aggregative behaviour, characteristic of an adhesive cell population. Further, when extended to two cell populations, the model predi

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Muniz, Maisonet Maritza. "Topographical Enhancement of Cell Adhesion on Poorly Adhesive Materials." Scholar Commons, 2015. https://scholarcommons.usf.edu/etd/5748.

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The overall thrust of this dissertation is to gain a fundamental understanding of the synergistic effects between surface topography and chemical functionality of poorly adhesive materials on enhancing the adhesion of mouse embryonic fibroblasts. Cellular response to surface topography and chemical functionality have been extensively studied on their own providing valuable information that helps in the design of new and improved biomaterials for tissue engineering applications. However, there is a lack of understanding of the synergistic effect of microscale and nanoscale topography with chemi

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Maghzal, Nadim. "The epithelial cell adhesion molecule (EpCAM) regulates cell motility and cell-cell adhesion by inhibiting PKC signaling." Thesis, McGill University, 2013. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=114215.

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Tissue cohesion is achieved in part by a large family of plasma membrane-bound cell adhesion molecules (CAMs). During morphogenesis, CAM-mediated interactions provide adhesive forces required for cells to aggregate and form tissues. CAM-mediated adhesions in developing cells are highly dynamic, which provides the fluidity required for cellular movements that drive morphogenesis. Xenopus laevis gastrulation is an established model to study morphogenetic movements. During this phase of development, the mesoderm moves inside the embryo through involution, and migrates along the inner surface of t

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Théard, Delphine Francine. "P27Kip1 in cell-cell adhesion and cell polarity." [S.l. : [Groningen : s.n.] ; University Library Groningen] [Host], 2006. http://irs.ub.rug.nl/ppn/291442056.

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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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Pouliot, Yannick 1963. "Study of L6 myoblast cell-cell adhesion." Thesis, McGill University, 1988. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=61797.

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Betson, Martha Elizabeth. "Regulation of cell-cell adhesion in keratinocyes." Thesis, University College London (University of London), 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.274930.

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Zhao, Lee Cheng. "Cell adhesion characterization of adhesive forces and effect of topography /." [Gainesville, Fla.] : University of Florida, 2000. http://etd.fcla.edu/etd/uf/2000/ana7043/LCZhao%5FThesis.pdf.

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Thesis (M.S.)--University of Florida, 2000.<br>Title from first page of PDF file. Document formatted into pages; contains ix, 79 p.; also contains graphics. Vita. Includes bibliographical references (p. 69-77).

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Elineni, Kranthi Kumar. "Regulation of Cell Adhesion Strength by Spatial Organization of Focal Adhesions." Scholar Commons, 2011. http://scholarcommons.usf.edu/etd/3088.

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Cell adhesion to extracellular matrix (ECM) is critical to various cellular processes like cell spreading, migration, growth and apoptosis. At the tissue level, cell adhesion is important in the pathological and physiological processes that regulate the tissue morphogenesis. Cell adhesion to the ECM is primarily mediated by the integrin family of receptors. The receptors that are recruited to the surface are reinforced by structural and signaling proteins at the adhesive sites forming focal adhesions that connect the cytoskeleton to further stabilize the adhesions. The functional roles of thes

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Книги з теми "Cell adhesion"

G, Curtis A. S., Lackie J. M, and Council of Europe, eds. Measuring cell adhesion. Wiley, 1991.

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Behrens, Jürgen, and W. James Nelson, eds. Cell Adhesion. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-540-68170-0.

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C, Beckerle Mary, ed. Cell adhesion. Oxford University Press, 2001.

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Pierre, Bongrand, Claesson P. M, and Curtis A. S. G, eds. Studying cell adhesion. Springer-Verlag, 1994.

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D, Richardson Peter, and Steiner Manfred, eds. Principles of cell adhesion. CRC Press, 1995.

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R, Preedy Victor, ed. Adhesion molecules. Science Publishers, 2010.

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Bongrand, Pierre, Per M. Claesson, and Adam S. G. Curtis, eds. Studying Cell Adhesion. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-662-03008-0.

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Berezin, Vladimir, and Peter S. Walmod, eds. Cell Adhesion Molecules. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4614-8090-7.

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Hemler, Martin E., and Enrico Mihich, eds. Cell Adhesion Molecules. Springer US, 1993. http://dx.doi.org/10.1007/978-1-4615-2830-2.

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Preedy, Victor R. Adhesion molecules. Science Publishers, 2010.

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Частини книг з теми "Cell adhesion"

De Bartolo, Loredana. "Cell Adhesion." In Encyclopedia of Membranes. Springer Berlin Heidelberg, 2016. http://dx.doi.org/10.1007/978-3-662-44324-8_120.

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Peroulis, Dimitrios, Prashant R. Waghmare, Sushanta K. Mitra, et al. "Cell Adhesion." In Encyclopedia of Nanotechnology. Springer Netherlands, 2012. http://dx.doi.org/10.1007/978-90-481-9751-4_100115.

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De Bartolo, Loredana. "Cell Adhesion." In Encyclopedia of Membranes. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-40872-4_120-6.

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Covault, Jonathan. "Cell Adhesion." In Molecular Biology of Membrane Transport Disorders. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-1143-0_2.

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Ofek, Itzhak, Halina Lis, and Nathan Sharon. "Animal Cell Surface Membranes." In Bacterial Adhesion. Springer US, 1985. http://dx.doi.org/10.1007/978-1-4615-6514-7_3.

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Humphries, Martin J. "Cell Adhesion Assays." In Methods in Molecular Biology. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-59745-413-1_14.

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Sedlacek, H. Harald, and Tarik Möröy. "Cell-Adhesion Molecules." In Immune Reactions. Springer Berlin Heidelberg, 1995. http://dx.doi.org/10.1007/978-3-642-79558-9_2.

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Weitz-Schmidt, Gabriele, and Stéphanie Chreng. "Cell Adhesion Assays." In Integrin and Cell Adhesion Molecules. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-166-6_2.

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Vleminckx, Kris. "Cell Adhesion Molecules." In Encyclopedia of Cancer. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-27841-9_989-3.

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Tong, Xiajing, and Yan Zou. "Cell Adhesion Molecules." In Advances in Membrane Proteins. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-9077-7_4.

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Тези доповідей конференцій з теми "Cell adhesion"

Gallant, Nathan D., and Kranthi Kumar Elineni. "Regulation of Adhesion Strength by Focal Adhesion Position and Cell Shape." In ASME 2012 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/sbc2012-80832.

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Cell adhesion to extracellular matrices is critical to numerous cellular functions and is primarily mediated by integrin receptors. Binding and aggregation of integrins leads to the formation of focal adhesions (FA) which connect the cytoskeleton to the extracellular matrix in order to reinforce adhesion and transmit signals [1]. Preliminary observations indicated preferential recruitment of FAs to the periphery of the cell spreading area on both uniformly coated and micropatterned fibronectin surfaces (Fig. 1). The current study investigates the biophysical regulation of cell adhesion strengt

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Tuszynski, George P., Vicki L. Rothman, Andrew Murphy, et al. "Thranbospondin Promotes Cell-and Platelet-Substratum Adhesion." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643820.

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Thrombospondin (TSP), isolated from human platelets, promotes the in vitro, calcium-specific adhesion of a variety of cells, including platelets, melanoma cells, muscle cells, endothelial cells, fibroblasts, and epithelial cells. The cell adhesion-promoting activity of TSP is species independent since human, bovine, pig, rat and mouse cells all adhered to TSP. Furthermore, the cell adhesion-promoting activity of TSP is specific and not due to a nonspecific protein effect or to contamination by fibronectin, vitronectin, or laminin. That is, neither bovine serum albumin nor TSP preparations trea

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Chirasatitsin, Somyot, Priyalakshmi Viswanathan, Giuseppe Battaglia, and Adam J. Engler. "Directing Stem Cell Fate in 3D Through Cell Inert and Adhesive Diblock Copolymer Domains." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14442.

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Adhesions are important cell structures required to transduce a variety of chemical and mechanics signals from outside-in and vice versa, all of which regulate cell behaviors, including stem cell differentiation (1). Though most biomaterials are coated with an adhesive ligand to promote adhesion, they do not often have a uniform distribution that does not match the heterogeneously adhesive extracellular matrix (ECM) in vivo (2). We have previously shown that diblock copolymer (DBC) mixtures undergo interface-confined de-mixing to form nanodomins of one copolymer in another (3). Here we demonst

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Lei, Xiaoxiao, Michael B. Lawrence, and Cheng Dong. "Mechanics of Cell Rolling Adhesion in Shear Flow." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-0284.

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Abstract Leukocyte rolling along endothelial cells is a critical step of leukocyte-endothelium interaction, which plays important roles in tissue inflammation and wound healing [1]. The occurrence of rolling results from the dynamic balance of hemodynamic shearing force acting on the cell and adhesive bond force between cell and endothelium, while the balance strongly depends on the leukocyte deformability [2]. The objective of this study is to elucidate the effects of (1) hydrodynamic shear stress, (2) cell deformation, and (3) surface adhesion strength on the rolling adhesion event through i

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Hu, Jia, and Yaling Liu. "Cell Adhesion on a Wavy Surface." In ASME 2013 Summer Bioengineering Conference. American Society of Mechanical Engineers, 2013. http://dx.doi.org/10.1115/sbc2013-14059.

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The ability to control the position of cells in an organized pattern on a substrate has become increasingly important for biosensing and tissue engineering applications [1–3]. With the advent of nanofabrication techniques, a number of researchers have studied the effects of nano-scale grooves on cell spreading, migration, morphology, signaling and orientation [4–6]. Recent studies have shown that cell adhesion/spreading can be influenced by a nanostructured surface [7]. In most current studies, the pattern dimensions are much smaller than the size of a cell. In this paper, we focus on studying

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Dong, Chen. "In Vitro Imaging Technique of Cell Adhesion." In ASME 2002 Pressure Vessels and Piping Conference. ASMEDC, 2002. http://dx.doi.org/10.1115/pvp2002-1630.

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It is the first object of this article to contribute a side-view imaging technique to investigate adhesion to a surface-immobilized ICAM-1 in shear flow, wherein T-leukemic Jurket cells have been used. A side view image has revealed that the cell adhesion on ICAM-1 under flow conditions in vitro is quasistratic. Changes in flow shear stress, cell deformability, or substrate ligand strength resulted in a significant change in the characteristic adhesion binding time and contact length. The elongation of cells in shear flow tempers hydrodynamic shear forces on the cell, which affects the transie

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Slater, John H., Jordan S. Miller, Shann S. Yu, and Jennifer L. West. "Multifaceted Nano- and Micropatterned Surfaces for Cell Adhesion Manipulation." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13177.

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Surfaces displaying nano- and micropatterned cell adhesive ligands have led to numerous discoveries in cell biology. Soft lithography techniques such as microcontact printing are well suited for creating surfaces displaying micropatterns of one ligand type in a single arrangement but are difficult to implement for the creation of multifaceted surfaces that present multiple ligand types with each ligand confined to their own pattern. To better understand the influence of extracellular matrix (ECM) composition on adhesion site formation and gross cell behavior (motility, proliferation, different

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Zhao, Yihua, Richard Skalak, and Shu Chien. "Hydrodynamics in Cell Rolling and Adhesion." In ASME 1997 International Mechanical Engineering Congress and Exposition. American Society of Mechanical Engineers, 1997. http://dx.doi.org/10.1115/imece1997-0237.

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Abstract Formulas for the slow viscous motion of a sphere in the presence of a solid wall have been used in analyzing the phenomena of cell rolling and adhesion. The established theories, such as the ones by Brenner and his colleagues [1,2,3], address the ideal situation in which both the sphere and the wall are smooth. However, biological cells such as leukocytes have numerous surface protrusions (microvilli). Therefore, the applicability of the theories of smooth spheres to the problem of cell rolling and adhesion needs to be examined. Also, to facilitate the design and analysis of experimen

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Christ, Kevin V., and Kevin T. Turner. "Hydrodynamically-Confined Microflows for Cell Adhesion Strength Measurement." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13007.

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Cell adhesion plays a fundamental role in numerous physiological and pathological processes, and measurements of the adhesion strength are important in fields ranging from basic cell biology research to the development of implantable biomaterials. Our group and others have recently demonstrated that microfluidic devices offer advantages for characterizing the adhesion of cells to protein-coated surfaces [1,2]. Microfluidic devices offer many advantages over conventional assays, including the ability to apply high shear stresses in the laminar regime and the opportunity to directly observe cell

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Han, Sangyoon J., and Nathan J. Sniadecki. "Traction Forces During Cell Migration Predicted by the Multiphysics Model." In ASME 2011 International Mechanical Engineering Congress and Exposition. ASMEDC, 2011. http://dx.doi.org/10.1115/imece2011-63843.

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Cells rely on traction forces in order to crawl across a substrate. These traction forces come from dynamic changes in focal adhesions, cytoskeletal structures, and chemical and mechanical signals from the extracellular matrix. Several computational models have been developed that help explain the trajectory or accumulation of cells during migration, but little attention has been placed on traction forces during this process. Here, we investigated the spatial and temporal dynamics of traction forces by using a multiphysics model that describes the cycle of steps for a migrating cell on an arra

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Звіти організацій з теми "Cell adhesion"

Byers, Stephen W. Cell-Cell Adhesion and Breast Cancer. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada395237.

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Byers, Stephen W. Cell-Cell Adhesion and Breast Cancer. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada371168.

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Byers, Stephen W. Cell-Cell Adhesion and Breast Cancer. Defense Technical Information Center, 1998. http://dx.doi.org/10.21236/ada345188.

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Surmacz, Eva. IGF-IR, Cell Adhesion and Metastasis. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada400067.

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Surmacz, Eva. IGF-IR, Cell Adhesion and Metastasis. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada420246.

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Surmacz, Ewa. IGF-IR, Cell Adhesion and Metastasis. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada392765.

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Park, Electa R., Alexis L. Bergsma, and Amanda L. Erwin. CD82 and Cell-Cell Adhesion in Metastatic Prostate Cancer. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada588246.

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Bertozzi, Carolyn R. Metabolic Engineering of Reactive Cell Surfaces for Controlled Cell Adhesion. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada421093.

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DaCosta, Stacey. IGF Regulation of Cell Adhesion in Breast Cancer. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada396051.

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DaCosta, Stacey. IGF Regulation of Cell Adhesion in Breast Cancer. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada396635.

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