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1

Kornberg, Roger D. The nucleosome. Preston: Lancashire Polytechnic.Library and Learning Resources Service, 1988.

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2

McQuibban, Angus. Yeast nucleosome and chromatin assembly. Ottawa: National Library of Canada, 1995.

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3

van, Driel Roeland, and Otte Arie P, eds. Nuclear organization, chromatin structure, and gene expression. Oxford: Oxford University Press, 1997.

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4

Zabal, Monique M. Preparation of nucleosome core particles for electron microscopy. Ottawa: National Library of Canada, 1990.

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5

Stone, Graham Robert. Studies of the nucleosome core particle structure in Physarum polycephalum. Portsmouth: Portsmouth Polytechnic, Dept. of Biological Sciences, 1985.

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6

Baudino, Troy A., ed. Cell-Cell Interactions. Totowa, NJ: Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-604-7.

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7

Baluska, Frantisek, Dieter Volkmann, and Peter W. Barlow. Cell-Cell Channels. New York, NY: Springer New York, 2006. http://dx.doi.org/10.1007/978-0-387-46957-7.

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8

J, Nelson W., and Fuchs Elaine, eds. Cell-cell junctions. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory Press, 2010.

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9

J, Nelson W., and Fuchs Elaine, eds. Cell-cell junctions. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory Press, 2010.

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10

Turksen, Kursad, ed. Stem Cell Renewal and Cell-Cell Communication. New York, NY: Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1570-6.

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11

Turksen, Kursad, ed. Stem Cell Renewal and Cell-Cell Communication. New York, NY: Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2590-2.

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12

De Mello, Walmor C., ed. Cell-to-Cell Communication. Boston, MA: Springer US, 1987. http://dx.doi.org/10.1007/978-1-4613-1917-7.

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13

Hsu, C. S. Cell-to-Cell Mapping. New York, NY: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4757-3892-6.

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14

C, De Mello Walmor, ed. Cell-to-cell communication. New York: Plenum Press, 1987.

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15

1927-, Sussex Ian M., ed. Plant cell/cell interactions. Cold Spring Harbor, N.Y: Cold Spring Harbor Laboratory, 1985.

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16

Martin, Dworkin, ed. Microbial cell-cell interactions. Washington, D.C: American Society for Microbiology, 1991.

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17

Mello, Walmor C. Cell-to-Cell Communication. Boston, MA: Springer US, 1987.

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18

Wagoner Johnson, A., and Brendan A. C. Harley, eds. Mechanobiology of Cell-Cell and Cell-Matrix Interactions. Boston, MA: Springer US, 2011. http://dx.doi.org/10.1007/978-1-4419-8083-0.

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19

Johnson, A. Wagoner. Mechanobiology of Cell-Cell and Cell-Matrix Interactions. Boston, MA: Springer Science+Business Media, LLC, 2011.

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20

Moevus, Corentin Jean. Nucleosome Curtains and their application to the study of DNA condensation by condensin. [New York, N.Y.?]: [publisher not identified], 2019.

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21

Brickwood, Sarah-Jane. Nucleosome binding, expression and function of MeCP2 and its Rett Syndrome associated mutations. Portsmouth: University of Portsmouth, 2004.

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22

Smith, Rodney, ed. Cell Technology for Cell Products. Dordrecht: Springer Netherlands, 2007. http://dx.doi.org/10.1007/978-1-4020-5476-1.

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23

Demuth, Donald R., and Richard Lamont, eds. Bacterial Cell-to-Cell Communication. Cambridge: Cambridge University Press, 2006. http://dx.doi.org/10.1017/cbo9780511541506.

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24

Lackie, J. M. Cell Movement and Cell Behaviour. Dordrecht: Springer Netherlands, 1986. http://dx.doi.org/10.1007/978-94-009-4071-0.

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25

Lackie, J. M. Cell movement and cell behaviour. London: Allen & Unwin, 1986.

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26

Cell movement and cell behaviour. London: Allen & Unwin, 1986.

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27

M, Dunny Gary, and Winans Stephen Carlyle, eds. Cell-cell signaling in bacteria. Washington, D.C: ASM Press, 1999.

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28

Phondke, Bal. Life: From cell to cell. 3rd ed. New Delhi: Publications & Information Directorate, 1995.

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29

King, Stephen. Cell. Waterville, ME, USA: Thorndike Press, 2006.

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30

King, Stephen. Cell. Barcelona: Plaza & Janés, 2006.

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31

King, Stephen. Cell. London: Hodder & Stoughton, 2006.

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32

Oruba, Agata. Studies of the role of nucleosome-remodeling complexes & activity on cell-type specific gene regulation by RelB. 2013.

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33

Wolffe, A. P. Nucleosome. Elsevier Science & Technology Books, 1996.

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34

The Nucleosome. Elsevier, 1995. http://dx.doi.org/10.1016/b978-1-55938-940-2.x5012-3.

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35

Watkins, John Fredrick. Nucleosome rearrangement in vitro. 1986.

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36

Li, Min, Cizhong Jiang, and Jiannan Lin. Nucleosome Dynamics in Epigenetic Regulation. Taylor & Francis Group, 2019.

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37

Li, Min, Cizhong Jiang, and Jiannan Lin. Nucleosome Dynamics in Epigenetic Regulation. Taylor & Francis Group, 2018.

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38

Chung, Dae-Gyun. Conformations of the core nucleosome. 1986.

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39

Czarnota, Gregory Jan. Structural states of the nucleosome. 1995.

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40

Wolffe, A. P. The Nucleosome (Treatise on the Nucleus). Elsevier Science, 1995.

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41

Weghorn, Donate. Evolution and biophysics of nucleosome positioning. 2012.

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42

van der Vlag, Johan, and Jo H. M. Berden. The patient with systemic lupus erythematosus. Edited by Giuseppe Remuzzi. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0161.

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Systemic lupus erythematosus (SLE) is a systemic autoimmune disease with various clinical manifestations. The hallmark of SLE is the presence of antibodies against nuclear constituents, such as double-stranded (ds)DNA, histones, and nucleosomes. Local deposition of antinuclear antibodies in complex with nuclear autoantigens induces serious inflammatory conditions that can affect several tissues and organs, including the kidney.The levels of antinucleosome and anti-dsDNA antibodies seem to correlate with glomerulonephritis and these autoantibodies can often be detected years before the patient is diagnosed with SLE. Apoptotic debris is present in the extracellular matrix and circulation of patients with SLE due to an aberrant process of apoptosis and/or insufficient clearance of apoptotic cells and apoptotic debris. The non-cleared apoptotic debris in patients with SLE may lead to activation of both the innate (myeloid and plasmacytoid dendritic cells) and adaptive (T and B cells) immune system. In addition to the activation by apoptotic debris and immune complexes, the immune system in SLE may be deregulated at the level of (a) presentation of self-peptides by antigen-presenting cells, (b) selection processes for both B and T cells, and (c) regulatory processes of B- and T-cell responses. Lupus nephritis may be classified in different classes based on histological findings in renal biopsies. The chromatin-containing immune complexes deposit in the capillary filter, most likely due to the interaction of chromatin with the polysaccharide heparan sulphate. A decreased renal expression of the endonuclease DNaseI further contributes to the glomerular persistence of chromatin and the development of glomerulonephritis.Current treatment of lupus nephritis is not specific and aims to reduce the inflammatory response with general immunosuppressive therapies. However, research has revealed novel potential therapeutic candidates at the level of dendritic cells, B cells, and T cells.
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43

Coombs, Neil Alan. A quantitative dark field electron microscopic study of nucleosome structure. 1987.

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44

Kahr, Walter H. A. Histone interactions in nucleosome-like particles determined by photochemical crosslinking. 1994.

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45

Moyer, Richard A. Site-specific aflatoxin B₁ adduction of sequence-positioned nucleosome core particles. 1988.

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46

Moyer, Richard A. Site-specific aflatoxin B₁ adduction of sequence-positioned nucleosome core particles. 1988.

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47

Nicolov, Nicolay. Cell & Cell Division. Akademicno Izdatelstvo, 2002.

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48

Barlow, Peter W., Dieter Volkmann, and Frantisek Baluska. Cell-Cell Channels. Springer, 2008.

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49

Barlow, Peter W., Dieter Volkmann, and Frantisek Baluska. Cell-Cell Channels. Springer London, Limited, 2007.

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50

Barlow, Peter W., Dieter Volkmann, and František Baluška. Cell-Cell Channels. Springer, 2014.

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