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1

Farlinger, Christopher M. The influence of skeletal muscle cell volume on the regulation of carbohydrate uptake and muscle metabolism. Brock University, Faculty of Applied Health Sciences, 2007.

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2

1943-, Okada Yasunobu, ed. Cell volume regulation: The molecular mechanism and volume sensing machinery : proceedings of the 23rd Taniguichi Foundation Biophysics Symposium held in Okazaki, Japan, 17-21 November 1997. Elsevier, 1998.

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3

Douglas, Ian James. Volume regulation in acinar cells isolated from the rat lacrimal gland. University of Manchester, 1996.

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4

Florian, Lang, ed. Cell volume regulation. Karger, 1998.

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5

W, Beyenbach Klaus, ed. Cell volume regulation. Karger, 1990.

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6

Cell volume regulation. Karger, 1990.

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7

Lang, F., ed. Cell Volume Regulation. S. Karger AG, 1998. http://dx.doi.org/10.1159/isbn.978-3-318-00337-6.

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8

Cell Volume Regulation (Comparative Physiology). S. Karger AG (Switzerland), 1990.

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9

Beyenbach. Cell Volume Regulation (Molecular Comparative Physiology). Hart Associates, 1990.

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10

Lang, F. Mechanisms And Significance of Cell Volume Regulation. S. Karger AG (Switzerland), 2006.

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11

Lang, F., ed. Mechanisms and Significance of Cell Volume Regulation. S. Karger AG, 2006. http://dx.doi.org/10.1159/isbn.978-3-318-01393-1.

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12

1955-, Strange Kevin, ed. Cellular and molecular physiology of cell volume regulation. CRC Press, 1994.

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13

Philippe, Michel, Laurent Meijer, and Silvana Guidet. Progress in Cell Cycle Research: Volume 3. Springer, 2012.

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14

Meijer, Laurent. Progress in Cell Cycle Research: Volume 4. Springer, 2012.

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15

Progress in Cell Cycle Research: Volume 2. Springer, 2011.

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16

(Editor), Laurent Meijer, Silvana Guidet (Editor), and Lee Vogel (Editor), eds. Progress in Cell Cycle Research: Volume 2 (Progress in Cell Cycle Research). Springer, 1996.

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17

(Editor), Earl R. Stadtman, and P. Boon Chock (Editor), eds. Current Topics in Cellular Regulation, Volume 35 (Discontinued(Current Topics in Cellular Regulation)). Academic Press, 1997.

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18

(Editor), A. Columbano, F. Feo (Editor), P. Pani (Editor), and R. Pascale (Editor), eds. Chemical Carcinogenesis, Volume 2: Modulating Factors. Plenum Press, 1991.

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19

III, H. William Detrich (Editor), Monte Westerfield (Editor), and Leonard I. Zon (Editor), eds. The Zebrafish, Volume 1: Biology (A Volume in the Methods in Cell Biology Series) (Methods in Cell Biology, Vol 59). Academic Press, 1998.

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20

(Editor), David W. Deamer, Arnost Kleinzeller (Editor), Douglas M. Fambrough (Editor), and Dale J. Benos (Series Editor), eds. Membrane Permeability, 100 Years Since Ernest Overton (Current Topics in Membranes, Volume 48) (Current Topics in Membranes). Academic Press, 1999.

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21

(Editor), David W. Deamer, Arnost Kleinzeller (Editor), Douglas M. Fambrough (Editor), and Dale J. Benos (Series Editor), eds. Membrane Permeability, 100 Years Since Ernest Overton (Current Topics in Membranes, Volume 48) (Current Topics in Membranes). Academic Press, 1999.

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22

Schönthal, Axel H. Checkpoint Controls and Cancer: Volume 2: Activation and Regulation Protocols (Methods in Molecular Biology). Humana Press, 2004.

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23

Hayat, M. A. Autophagy : Cancer, Other Pathologies, Inflammation, Immunity, Infection, and Aging: Volume 6- Regulation of Autophagy and Selective Autophagy. Elsevier Science & Technology Books, 2015.

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24

Boloorchi, Azadeh. The role of protein kinase C-epsilon (PKCepsilon) in ischemic preconditioning cardioprotection induced by enhancement of cell volume regulation. 2006.

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25

Translation Initiation: Cell Biology, High-throughput and Chemical-based Approaches, Volume 431 (Methods in Enzymology). Academic Press, 2007.

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26

(Editor), W. E. Balch, Channing J. Der (Editor), and Alan Hall (Editor), eds. GTPases Regulating Membrane Targeting and Fusion, Volume 403 (Methods in Enzymology). Academic Press, 2005.

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27

Egan, Brian N. Hyponatremia/Hypernatremia. Edited by Matthew D. McEvoy and Cory M. Furse. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190226459.003.0037.

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lSodium is the most abundant cation in the extracellular fluid and is important for regulation of plasma water concentrations and cell volume. Sodium cannot readily cross the blood-brain barrier, and changes in plasma sodium levels by altering free water movement can expand or shrink brain cells. Changes in brain cell volume can cause brain cell dysfunction and apoptosis. Correction of both high and low sodium levels must be done gradually, as rapid correction of dysnatremias can also damage brain cells. In this chapter we review the physiology of sodium regulation, and discuss the clinical im
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28

(Editor), Ravi Iyengar, and John D. Hildebrandt (Editor), eds. G Protein Pathways, Part A: Receptors (Methods in Enzymology, Volume 343) (Methods in Enzymology). Academic Press, 2001.

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29

(Editor), Ravi Iyengar, and John D. Hildebrandt (Editor), eds. G Protein Pathways, Part A: Receptors (Methods in Enzymology, Volume 343) (Methods in Enzymology). Academic Press, 2001.

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30

(Editor), Ravi Iyengar, and John D. Hildebrandt (Editor), eds. G Protein Pathways, Part C: Effector Mechanisms (Methods in Enzymology, Volume 345) (Methods in Enzymology). Academic Press, 2001.

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31

(Editor), Ravi Iyengar, and John D. Hildebrandt (Editor), eds. G Protein Pathways, Part C: Effector Mechanisms (Methods in Enzymology, Volume 345) (Methods in Enzymology). Academic Press, 2001.

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32

Doucet, Alain, and Gilles Crambert. Potassium homeostasis. Edited by Robert Unwin. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0023.

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The equilibrium between the concentration of K+ in the extracellular space (low) and the intracellular compartment (high) is crucial for maintaining the electrical properties of excitable and non-excitable cells, because it determines the membrane resting potential. The high intracellular concentration of K+ (120–140 mmol/L) also contributes to the intracellular osmolarity, a determinant of cell volume. It is therefore crucial to finely tune both extracellular and intracellular K+ concentrations. There is a coordinated regulation between processes/mechanisms that store/release K+ from internal
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33

Mikos, Antonios G., Yoshito Ikada, Robert C. Thomson, David J. Mooney, and Kevin E. Healy. Biomaterials Regulating Cell Function and Tissue Development: Volume 530. University of Cambridge ESOL Examinations, 2014.

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34

(Editor), W. E. Balch, Channing J. Der (Editor), and Alan Hall (Editor), eds. GTPases Regulating Membrane Dynamics, Volume 404 (Methods in Enzymology). Academic Press, 2005.

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35

GTPases Regulating Membrane Dynamics, Volume 404 (Methods in Enzymology). Academic Press, 2005.

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36

(Editor), Ron C. Conaway, and Joan W. Conaway (Editor), eds. Proteins in Eukaryotic Transcription, Volume 67 (Advances in Protein Chemistry). Academic Press, 2004.

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37

(Editor), Ron C. Conaway, and Joan W. Conaway (Editor), eds. Proteins in Eukaryotic Transcription, Volume 67 (Advances in Protein Chemistry). Academic Press, 2004.

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38

Lopez-Arvizu, Carmen, Carmel Bogle, and Harolyn M. E. Belcher. Neurobiology of Fetal Alcohol Spectrum Disorders. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199937837.003.0179.

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Prenatal exposure to ethanol can result in a wide range of clinical presentations that are grouped under the term “Fetal Alcohol Spectrum Disorders” (FASD). The direct cellular teratogenic effects of ethanol on fetal neurodevelopment include damage to cell survival, proliferation, and migration mechanisms. Dysregulation of neurotransmission and alteration of genetic transcription have also been implicated in the neurotoxic effects of prenatal ethanol exposure. These deleterious events lead to brain volume reduction, corpus callosum dysgenesis, cerebellar, and other neuroanatomical anomalies th
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39

(Editor), John N. Abelson, Melvin I. Simon (Editor), Virginia L. Clark (Editor), and Patrik M. Bavoil (Editor), eds. Methods in Enzymology, Volume 235: Bacterial Pathogenesis, Part A: Identification and Regulation of Virulence Factors (Methods in Enzymology). Academic Press, 1994.

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40

Houillier, Pascal. Magnesium homeostasis. Edited by Robert Unwin. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0027.

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Magnesium is critically important in the process of energy release. Although most magnesium is stored outside the extracellular fluid compartment, the regulated concentration appears in blood. Urinary magnesium excretion can decrease rapidly to low values when magnesium entry rate into the extracellular fluid volume is low, which has several important implications: cell and bone magnesium do not play a major role in the defence of blood magnesium concentration; while a major role is played by the kidney and especially the renal tubule, which adapts to match the urinary magnesium excretion and
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