References
- Lee, H. J., Yeo, S. Y. & Jeong, S. H. Antibacterial effect of nanosized silver colloidal solution on textile fabrics. J Mater Sci 38:2199-2204 (2003) https://doi.org/10.1023/A:1023736416361
- Harper, T. Nano Korea. http://www.nanotechweb. org (2003)
- Hamouda, T. et al. A novel surfactant nanoemulsion with broad-spectrum sporicidal activity against Bacillus species. J Infect D 180:2096-2126 (1999) https://doi.org/10.1086/315124
- Sondi, I. & Salopek-Sondi, B. Silver nanoparticles as antimicrobial agent: a case study on E. coli as a model for Gram-negative bacteria. J Colloid Interf Sci 275: 177-182 (2004) https://doi.org/10.1016/j.jcis.2004.02.012
- Yeo, M. K & Kang, K. Effects of nanometer sized silver materials on biological toxicity during zebrafish embryogenesis. Bull Korean Chem Soc 29:1179-1184 (2008) https://doi.org/10.5012/bkcs.2008.29.6.1179
- Rederstorff, M., Krol, A. & Lescure, A. Understanding the importance of selenium and selenoproteins in muscle function. Cell Mol Life Sci 63:52-59 (2006) https://doi.org/10.1007/s00018-005-5313-y
- Radi, A. A. R. & Matkovics, B. Effects of metal ions on the antioxidant enzyme activities, protein contents and lipid peroxidation of carp tissues. Comp Biochem Physiol C 90:69-72 (1988) https://doi.org/10.1016/0742-8413(88)90099-0
- Roche, H. & Boge, G. Effects of Cu, Zn and Cr salts on antioxidant enzyme activities in vitro of red blood cells of a marine fish. Dicentrarchus labrax. Toxicol In Vitro 7:623-629 (1993) https://doi.org/10.1016/0887-2333(93)90096-N
- Berger, T. J., Spadaro J. A., Chapin S. E. & Becker R. O. Electrically generated silver ions: quantitative effects on bacterial and mammalian cells. Antimicrob Agents Ch 9: 357-358 (1976) https://doi.org/10.1128/AAC.9.2.357
- Möller, W., Hofer, T., Ziesenis, A., Karg, E. & Heyder, J. Ultrafine particles cause cytoskeletal dysfunctions in macrophages. Toxicol Appl Pharm 182:197-207 (2002) https://doi.org/10.1006/taap.2002.9430
- Lambert, A. L., Mangum, J. B., Delorme, M. P. & Everitt, J. I. Ultrafine carbon black particles enhance respiratory syncytial virus-induced airway reactivity, pulmonary inflammation, and chemokine expression. Soc Toxicol 72:339-346 (2003) https://doi.org/10.1093/toxsci/kfg032
- Renwick, L. C., Donaldson, K. & Clouter, A. Impairment of alveolar macrophage phagocytosis by ultrafine partic. Toxicol Appl Pharm 172:119-127 (2001) https://doi.org/10.1006/taap.2001.9128
- Yeo, M. K. & Park, S. W. Exposing zebrafish to silver nanoparticles during caudal fin regeneration disrupts caudal fin growth and p53 signaling. Mol Cell Toxicol 4: 311-317(2008)
- Brooker, R. J. & Slayman, C. W. Effects of Mg2+ ions on the plasma membrane [H+]-ATPase of Neurospora crassa. II. Kinetic studies. J Biol Chem 258:8833-8838 (1983)
- Black, C. B., Huang, H. W. & Cowan, J. A. Biological coordination chemistry of magnesium, sodium, and potassium ions. Protein and nucleotide binding sites. Coord Chem Rev 135:165-202 (1994) https://doi.org/10.1016/0010-8545(94)80068-5
- Hossain, Z. & Huq, F. Studies on the interaction between Ag+ and DNA. J Inorg Biochem 91:398-404 (2002) https://doi.org/10.1016/S0162-0134(02)00454-3
- Lee, H. C. et al. Glycogen synthase kinase 3α and 3β have distinct functions during cardiogenesis of zebra-fish embryo. BMC Dev Biol 7:1-15 (2007) https://doi.org/10.1186/1471-213X-7-93
- Woodgett, J. R. cDNA cloning and properties of glycogen synthase kinase-3. Methods Enzymol 200:564-577 (1991) https://doi.org/10.1016/0076-6879(91)00172-S
- Woodgett, J. R. Judging a protein by more than its name: GSK-3. Sci Signal 12:1-11(2001) https://doi.org/10.1126/stke.2001.100.re12
- Ramsdell, A. F. Left-right asymmetry and congenital cardiac defects: getting to the heart of the matter in vertebrate left right axis determination. Dev Biol 288:1-20 (2005) https://doi.org/10.1016/j.ydbio.2005.07.038
- Jia, S., Ren, Z., Li, X., Zheng, Y. & Meng, A. Smad2 and Smad3 are required for mesendoderm induction by transforming growth factor-/nodal signals in Zebrafish. J Biol Chem 283:2418-2426 (2008) https://doi.org/10.1074/jbc.M707578200
- Nagaso, H., Suzuki, A., Tada, M. & Ueno, N. Dual specificity of activin type II receptor ActRIIb in dorsoventral patterning during zebrafish embryogenesis. Develop Growth Differ 41:119-133 (1999) https://doi.org/10.1046/j.1440-169x.1999.00418.x
- Jung, W. K. et al. Antifungal activity of the silver ion against contaminated fabric. Mycoses 50:265-269 (2007) https://doi.org/10.1111/j.1439-0507.2007.01372.x
- Kimmel, W., Ballard, S., Ullman, B. K. & Schilling, T. Stages of embryonic development of the zebrafish. Dev Dynam 203: 253-310 (1995) https://doi.org/10.1002/aja.1002030302