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1

Skinner, T. L., and B. Peretz. "Age sensitivity of osmoregulation and of its neural correlates in Aplysia." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 256, no. 4 (1989): R989—R996. http://dx.doi.org/10.1152/ajpregu.1989.256.4.r989.

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Osmoregulation was studied in the marine mollusc Aplysia californica in young, mature, and old adults. To monitor volume and osmoregulation, we measured body weight, hemolymph osmolality, and chloride concentration. These parameters were measured at regular intervals with animals in 90% artificial seawater (90% ASW) for up to 36 h. They showed that the rates at which Aplysia osmo- and volume regulate were significantly slowed with increased age. However, no age effect was found in osmoregulation when the hemolymph was diluted to 90% of control in animals without an external stress, i.e., by in
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2

Morgan, JM. "A Gene Controlling Differences in Osmoregulation in Wheat." Functional Plant Biology 18, no. 3 (1991): 249. http://dx.doi.org/10.1071/pp9910249.

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Evidence is presented for a single gene controlling differences in osmoregulation in wheat in response to water stress, confirming earlier results. Analyses of osmoregulation were made on the flag leaves of wheat plants which were grown in pots in the glasshouse and stressed in a controlled environment chamber by withholding water after the flag leaf had fully emerged. Osmoregulation was derived from responses of osmotic potential to relative water content or from responses of relative water content and osmotic potential to water potential. Usable estimates of osmoregulation were obtained for
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3

TAKEUCHI, Nobuo. "Osmoregulation of earthworms." Hikaku seiri seikagaku(Comparative Physiology and Biochemistry) 10, no. 2 (1993): 92–102. http://dx.doi.org/10.3330/hikakuseiriseika.10.92.

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4

Thompson, C. J., and P. H. Baylis. "Osmoregulation of thirst." Journal of Endocrinology 117, no. 2 (1988): 155–57. http://dx.doi.org/10.1677/joe.0.1170155.

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5

MAZZOTTI, FRANK J., and WILLIAM A. DUNSON. "Osmoregulation in Crocodilians." American Zoologist 29, no. 3 (1989): 903–20. http://dx.doi.org/10.1093/icb/29.3.903.

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6

TAPLIN, LAURENCE E. "OSMOREGULATION IN CROCODILIANS." Biological Reviews 63, no. 3 (1988): 333–77. http://dx.doi.org/10.1111/j.1469-185x.1988.tb00721.x.

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7

Diehl, Walter J. "Osmoregulation in echinoderms." Comparative Biochemistry and Physiology Part A: Physiology 84, no. 2 (1986): 199–205. http://dx.doi.org/10.1016/0300-9629(86)90605-5.

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8

Greenwell, Martin G., Johanna Sherrill, and Leigh A. Clayton. "Osmoregulation in fish." Veterinary Clinics of North America: Exotic Animal Practice 6, no. 1 (2003): 169–89. http://dx.doi.org/10.1016/s1094-9194(02)00021-x.

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9

OHWADA, Takuji, and Shonosuke SAGISAKA. "Osmoregulation of bacteria." Kagaku To Seibutsu 28, no. 6 (1990): 360–68. http://dx.doi.org/10.1271/kagakutoseibutsu1962.28.360.

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10

Kasner, Maieli, Jochen Grosse, Martin Krebs, and Gabriele Kaczmarczyk. "Methohexital Impairs Osmoregulation." Anesthesiology 82, no. 6 (1995): 1396–405. http://dx.doi.org/10.1097/00000542-199506000-00011.

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Background Anesthetic agents influence central regulations. This study investigated the effects of methohexital anesthesia on renal and hormonal responses to acute sodium and water loading in dogs in the absence of surgical stress. Methods Fourteen experiments (two in each dog) were performed in seven well-trained, chronically tracheotomized beagle dogs kept in highly standardized environmental and dietary conditions (2.5 mmol sodium and 91 ml water/kg body weight daily). Experiments lasted 3 h, while the dogs were conscious (7 experiments) or, after 1 h control, while they were anesthetized (
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11

Trachtman, Howard. "Taurine and Osmoregulation." American Journal of Diseases of Children 142, no. 11 (1988): 1194. http://dx.doi.org/10.1001/archpedi.1988.02150110072022.

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12

Larsen, Erik Hviid, Lewis E. Deaton, Horst Onken, et al. "Osmoregulation and Excretion." Comprehensive Physiology 4, no. 2 (2014): 405–573. https://doi.org/10.1002/j.2040-4603.2014.tb00553.x.

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AbstractThe article discusses advances in osmoregulation and excretion with emphasis on how multicellular animals in different osmotic environments regulate their milieu intérieur. Mechanisms of energy transformations in animal osmoregulation are dealt with in biophysical terms with respect to water and ion exchange across biological membranes and coupling of ion and water fluxes across epithelia. The discussion of functions is based on a comparative approach analyzing mechanisms that have evolved in different taxonomic groups at biochemical, cellular and tissue levels and their integration in
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13

Morgan, JM, RA Hare, and RJ Fletcher. "Genetic variation in osmoregulation in bread and durum wheats and its relationship to grain yield in a range of field environments." Australian Journal of Agricultural Research 37, no. 5 (1986): 449. http://dx.doi.org/10.1071/ar9860449.

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The association between osmoregulation and grain yield was examined using measurements of osmoregulation made on wheat plants grown in pots in a glasshouse and measurements of grain yields made in a wide range of field environments. Osmoregulation was determined from measurements of relative water contents and osmotic potentials made on the flag leaves of plants droughted near anthesis. The genotypes were advanced lines from two distinct breeding programs - one for bread wheats and one for durum wheats. All the genotypes in each program (27 bread and 14 durum) were closely related in having a
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14

Kiilerich, Pia, Sylvain Milla, Armin Sturm, et al. "Implication of the mineralocorticoid axis in rainbow trout osmoregulation during salinity acclimation." Journal of Endocrinology 209, no. 2 (2011): 221–35. http://dx.doi.org/10.1530/joe-10-0371.

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Cortisol and glucocorticoid receptors (GRs) play an important role in fish osmoregulation, whereas the involvement of the mineralocorticoid receptor (MR) and its putative ligand 11-deoxycorticosterone (DOC) is poorly investigated. In this study, we assessed the implication of DOC and MR in rainbow trout (Oncorhynchus mykiss) osmoregulation during hypo- and hypersaline acclimation in parallel with the cortisol–GR system. A RIA for DOC was developed to measure plasma DOC levels, and a MR-specific antibody was developed to localize MR protein in the gill, intestine, and kidney. This is the first
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15

Ortiz, Rudy M. "Osmoregulation in Marine Mammals." Journal of Experimental Biology 204, no. 11 (2001): 1831–44. http://dx.doi.org/10.1242/jeb.204.11.1831.

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SUMMARY Osmoregulation in marine mammals has been investigated for over a century; however, a review of recent advances in our understanding of water and electrolyte balance and of renal function in marine mammals is warranted. The following topics are discussed: (i) kidney structure and urine concentrating ability, (ii) sources of water, (iii) the effects of feeding, fasting and diving, (iv) the renal responses to infusions of varying salinity and (v) hormonal regulation. The kidneys of pinnipeds and cetaceans are reniculate in structure, unlike those of terrestrial mammals (except bears), bu
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16

Herrera, Fabio, Olga Bondarenko, and Sergii Boryshpolets. "Osmoregulation in fish sperm." Fish Physiology and Biochemistry 47, no. 3 (2021): 785–95. http://dx.doi.org/10.1007/s10695-021-00958-1.

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17

Thewissen, J. G. M., L. J. Roe, J. R. O'Neil, S. T. Hussain, A. Sahni, and S. Bajpai. "Evolution of cetacean osmoregulation." Nature 381, no. 6581 (1996): 379–80. http://dx.doi.org/10.1038/381379b0.

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18

Abee, T., R. Palmen, K. J. Hellingwerf, and W. N. Konings. "Osmoregulation in Rhodobacter sphaeroides." Journal of Bacteriology 172, no. 1 (1990): 149–54. http://dx.doi.org/10.1128/jb.172.1.149-154.1990.

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19

Zadunaisky, José A. "Chloride cells and osmoregulation." Kidney International 49, no. 6 (1996): 1563–67. http://dx.doi.org/10.1038/ki.1996.225.

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20

Somero, G. N. "Animal Osmoregulation. Tim Bradley." Integrative and Comparative Biology 49, no. 6 (2009): 717–18. http://dx.doi.org/10.1093/icb/icp083.

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21

May, Conrad, Michele Haber, Sarah H. Young, Thomas P. Tomai, Gyorgy Csako, and Robert P. Friedland. "Osmoregulation in Alzheimer's Disease." Dementia and Geriatric Cognitive Disorders 1, no. 2 (1990): 90–94. http://dx.doi.org/10.1159/000107125.

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22

Girlich, C., F. Mandraka, and U. Woenckhaus. "St�rungen der Osmoregulation." Intensivmedizin + Notfallmedizin 42, no. 3 (2005): 224–40. http://dx.doi.org/10.1007/s00390-005-0534-8.

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23

Hazon, Neil. "Osmoregulation in elasmobranch fish." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 153, no. 2 (2009): S64. http://dx.doi.org/10.1016/j.cbpa.2009.04.004.

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24

Wegmann, Klaus. "Osmoregulation in eukaryotic algae." FEMS Microbiology Letters 39, no. 1-2 (1986): 37–43. http://dx.doi.org/10.1111/j.1574-6968.1986.tb01840.x.

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25

Bourque, C. W., S. H. R. Oliet, and D. Richard. "Osmoreceptors, Osmoreception, and Osmoregulation." Frontiers in Neuroendocrinology 15, no. 3 (1994): 231–74. http://dx.doi.org/10.1006/frne.1994.1010.

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26

Morgan, JM, and AG Condon. "Water Use, Grain Yield, and Osmoregulation in Wheat." Functional Plant Biology 13, no. 4 (1986): 523. http://dx.doi.org/10.1071/pp9860523.

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Genotypic differences in turgor maintenance in wheat were shown to be associated with differences in grain yield in the field at both high and Low water deficits. High water deficits were produced by growing plants in field plots using water stored in the soil at sowing, and excluding rain with a rain cover. At low water deficits plants received rainfall, and irrigation was supplied before and immediately after sowing, at tillering, at jointing, at ear emergence, and during grain filling. Yield differences were analysed in terms of harvest index, water use, and water use efficiency. Water use
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27

Morgan, J. M. "Changes in rheological properties and endosperm peroxidase activity associated with breeding for an osmoregulation gene in bread wheat." Australian Journal of Agricultural Research 50, no. 6 (1999): 963. http://dx.doi.org/10.1071/ar98132.

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Backcross lines which had been bred for an osmoregulation gene to improve the drought tolerance of 3 commercial bread wheat cultivars were tested for standard grain, dough, and baking characteristics. Three field sites were used to provide a range of protein contents of 10–14%. It was found that backcross lines with high osmoregulation had alterations in dough strength which could only be understood in terms of genetic linkage. Evidence of a linkage effect was found by comparing lines with recurrent parents in a season of low water stress, i.e. where yields and hence protein contents of each g
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28

Aryansyah, Akbar, Sutrisno Anggoro, and Norma Afiati. "Osmoregulation performance, condition factor, and gonad maturity of tilapia (Oreochromis niloticus) in Cengklik reservoir, Boyolali." Acta Aquatica: Aquatic Sciences Journal 10, no. 1 (2023): 53. http://dx.doi.org/10.29103/aa.v10i1.10829.

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Osmoregulation is a physiological adjustment mechanism of fish to environmental conditions. Fish growth performance will reduce when a large amount of energy is redirected for the osmoregulation process. The purpose of this study was to determine the osmotic work level (OWL), osmoregulation pattern, condition factor (K), gonad maturity stages (GMS) and analyze the relationship between OWL with condition factor and GMS of tilapia collected from three floating net cages in Cengklik reservoir, Boyolali. Samples were collected during March – April 2022 followed by some allometric measurements and
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29

Aryansyah, Akbar, Sutrisno Anggoro, and Norma Afiati. "Osmoregulation performance, condition factor, and gonad maturity of tilapia (Oreochromis niloticus) in Cengklik reservoir, Boyolali." Acta Aquatica: Aquatic Sciences Journal 10, no. 2 (2023): 53. http://dx.doi.org/10.29103/aa.v1i2.9356.

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Osmoregulation is a physiological adjustment mechanism of fish to environmental conditions. Fish growth performance will reduce when a large amount of energy is redirected for the osmoregulation process. The purpose of this study was to determine the osmotic work level (OWL), osmoregulation pattern, condition factor (K), gonad maturity stages (GMS) and analyze the relationship between OWL with condition factor and GMS of tilapia collected from three floating net cages in Cengklik reservoir, Boyolali. Samples were collected during March – April 2022 followed by some allometric measurements and
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30

Charmantier, G., C. Haond, J. Lignot, and M. Charmantier-Daures. "Ecophysiological adaptation to salinity throughout a life cycle: a review in homarid lobsters." Journal of Experimental Biology 204, no. 5 (2001): 967–77. http://dx.doi.org/10.1242/jeb.204.5.967.

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Adaptations to salinity are reviewed throughout development in both species of the genus Homarus. Some populations of homarid lobsters are known to inhabit coastal and estuarine areas where salinity fluctuates. Salinity tolerance varies during development, with 50 % lethal salinities (LS(50)) ranging from approximately 15–17 in larvae to approximately 12 in postlarvae and 10 in adults. Larval and adult lobsters can avoid low-salinity areas using behavioural strategies. When exposed to low salinity, the capacity to osmoregulate varies with development. Embryos are osmoconformers and are osmotic
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31

Lang, M. A. "Correlation between osmoregulation and cell volume regulation." American Journal of Physiology-Regulatory, Integrative and Comparative Physiology 252, no. 4 (1987): R768—R773. http://dx.doi.org/10.1152/ajpregu.1987.252.4.r768.

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The euryhaline crab, Callinectes sapidus, behaves both as an osmoregulator when equilibrated in salines in the range of 800 mosM and below and an osmoconformer when equilibrated in salines above 800 mosM. There exists a close correlation between osmoregulation seen in the whole animal in vivo and cell volume regulation studied in vitro. Hyperregulation of the hemolymph osmotic pressure and cell volume regulation both occurred in salines at approximately 800 mosM and below. During long-term equilibration of the crabs to a wide range of saline environments, the total concentration of hemolymph a
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32

Pierce, V. A., L. D. Mueller, and A. G. Gibbs. "Osmoregulation in Drosophila melanogaster selected for urea tolerance." Journal of Experimental Biology 202, no. 17 (1999): 2349–58. http://dx.doi.org/10.1242/jeb.202.17.2349.

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Animals may adapt to hyperosmolar environments by either osmoregulating or osmoconforming. Osmoconforming animals generally accumulate organic osmolytes including sugars, amino acids or, in a few cases, urea. In the latter case, they also accumulate ‘urea-counteracting’ solutes to mitigate the toxic effects of urea. We examined the osmoregulatory adaptation of Drosophila melanogaster larvae selected to live in 300 mmol l(−)(1) urea. Larvae are strong osmoregulators in environments with high NaCl or sucrose levels, but have increased hemolymph osmolarity on urea food. The increase in osmolarity
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33

Jaafar, Raghad S., and Sumaya M. Ahmed. "Effect of salt stress on osmoregulation and energy consumption in grass carp Ctenopharyngodon idella (Val.,1844)." Iraqi Journal of Aquaculture 8, no. 1 (2022): 15–38. http://dx.doi.org/10.58629/ijaq.v8i1.227.

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This study aims to explain the effect of salt stress on Grass carp Ctenopharyngodon idella. It includes two parts, the first to determine the LC50 during abrupt increase in salinity to 5,10 and 15g/L.While the other part concerned with the physiological effects of the gradual increase in salinity to 5 and 10 g/L on osmoregulation, by measuring ions concentration ( Na+, K+ ) in the blood plasma and muscles, water contents in the muscles , numbers and percentage of chloride cells in the gills epithelia, beside studying the expenditure of osmoregulation by measuring the rate of oxygen consumption
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34

Rasoolzadegan, Y. "OSMOREGULATION IN YOUNG JOJOBA SEEDLINGS." HortScience 25, no. 9 (1990): 1083f—1083. http://dx.doi.org/10.21273/hortsci.25.9.1083f.

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The possibility of osmotic adjustment to salinity in Jojoba was studied in a sand culture system. After being stablished, 2 WKs old seedlings were exposed to 1/2 strength hoagland's solution plus NaCl salt to make up -0.7., -0.4, -0.6, -0.8, & -1 MPa. Shoot & leaf elongation, components of Ψleaf, proline accumulation, & inorganic salts were determined every 24 hour for 9 days. Shoot & leaf length were reduced at -0.8 and -0.4 MPa respectively. Osmotic adjustment occured only above -0.8 MPa at the rate of 0.21 If MPa/day. Total inorganic salts in whole plant increased with a dec
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35

Roberts, Mary, F. "Osmoadaptation and osmoregulation in archaea." Frontiers in Bioscience 5, no. 1 (2000): d796. http://dx.doi.org/10.2741/roberts.

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36

D'haeseleer, Patrik. "Closing the circle of osmoregulation." Nature Biotechnology 23, no. 8 (2005): 941–42. http://dx.doi.org/10.1038/nbt0805-941.

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37

Csonka, L. N., and A. D. Hanson. "Prokaryotic Osmoregulation: Genetics and Physiology." Annual Review of Microbiology 45, no. 1 (1991): 569–606. http://dx.doi.org/10.1146/annurev.mi.45.100191.003033.

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38

McDonald, M. D. "ACIDIC ABSORBATE INTEGRAL TO OSMOREGULATION." Journal of Experimental Biology 209, no. 21 (2006): vii. http://dx.doi.org/10.1242/jeb.02546.

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39

Lock, R. A. C., and S. E. Wendelaar Bonga. "Toxicants and Osmoregulation in Fish." Netherlands Journal of Zoology 42, no. 2-3 (1991): 478–93. http://dx.doi.org/10.1163/156854291x00469.

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40

Bradley, T. J. "Physiology of Osmoregulation in Mosquitoes." Annual Review of Entomology 32, no. 1 (1987): 439–62. http://dx.doi.org/10.1146/annurev.en.32.010187.002255.

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41

Beck, Franz-X., Adolf Dörge, and Klaus Thurau. "Cellular Osmoregulation in Renal Medulla." Kidney and Blood Pressure Research 11, no. 3-5 (1988): 174–86. http://dx.doi.org/10.1159/000173161.

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42

Kanchanapoom, Kamnoon, and Wendy F. Boss. "Osmoregulation of fusogenic protoplast fusion." Biochimica et Biophysica Acta (BBA) - Biomembranes 861 (1986): 429–39. http://dx.doi.org/10.1016/0005-2736(86)90451-7.

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43

Mayfield, Anderson B., and Ruth D. Gates. "Osmoregulation in anthozoan–dinoflagellate symbiosis." Comparative Biochemistry and Physiology Part A: Molecular & Integrative Physiology 147, no. 1 (2007): 1–10. http://dx.doi.org/10.1016/j.cbpa.2006.12.042.

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44

Roberts, Mary F. "Osmoadaptation and osmoregulation in archaea." Frontiers in Bioscience 5, no. 3 (2000): d796–812. http://dx.doi.org/10.2741/a552.

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45

Laurent, Pierre, and Nadra Hebibi. "Gill morphometry and fish osmoregulation." Canadian Journal of Zoology 67, no. 12 (1989): 3055–63. http://dx.doi.org/10.1139/z89-429.

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Morphofunctional parameters were studied during adaptation of rainbow trout (Oncorhynchus mykiss) to different ionic environments: Strasbourg tap water, ion-poor water, and artificial seawater. The gill lamellae displayed large changes in size. Surface area of individual lamellae increased in trout acclimated to ion-poor water or seawater. Conversely, the harmonic mean thickness of the lamellar epithelium decreased in seawater, and to an even greater extent in ion-poor water. The apical surface area of individual branchial filament chloride cells, the number of these cells, and their apical su
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46

Brown, A. D., Kylie F. Mackenzie, and K. K. Singh. "Selected aspects of microbial osmoregulation." FEMS Microbiology Letters 39, no. 1-2 (1986): 31–36. http://dx.doi.org/10.1111/j.1574-6968.1986.tb01839.x.

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47

Moran, Nava. "Osmoregulation of leaf motor cells." FEBS Letters 581, no. 12 (2007): 2337–47. http://dx.doi.org/10.1016/j.febslet.2007.04.002.

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48

Madea, B., and S. A. Padosch. "Neurogene St�rung der Osmoregulation." Rechtsmedizin 14, no. 5 (2004): 412–16. http://dx.doi.org/10.1007/s00194-004-0284-0.

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49

Beck, Franz, Adolf D�rge, Roger Rick, and Klaus Thurau. "Osmoregulation of renal papillary cells." Pfl�gers Archiv European Journal of Physiology 405, S1 (1985): S28—S32. http://dx.doi.org/10.1007/bf00581776.

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50

Balment, R. J., J. M. Warne, M. Tierney, and N. Hazon. "Arginine vasotocin and fish osmoregulation." Fish Physiology and Biochemistry 11, no. 1-6 (1993): 189–94. http://dx.doi.org/10.1007/bf00004566.

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