참고문헌
- Otake M, Schull WJ. Radiation-related brain damage and growth retardation among the prenatally exposed atomic bomb survivors. Int. J. Radiat. Biol. 1998;74(2):159-171. https://doi.org/10.1080/095530098141555
- Schull WJ, Otake M. Cognitive function and prenatal exposure to ionizing radiation. Teratology. 1999;59(4):222-226. https://doi.org/10.1002/(SICI)1096-9926(199904)59:4<222::AID-TERA6>3.0.CO;2-M
- Balentova S, Racekova E, Martoncikova M, Misurova E. Cell proliferation in the adult rat rostral migratory stream following exposure to gamma irradiation. Cell Mol. Neurobiol. 2006;26(7-8):1131-1139.
- Lee WH, Cho HJ, Sonntag WE, Lee YW. Radiation attenuates physiological angiogenesis by differential expression of VEGF, Ang-1, tie-2 and Ang-2 in rat brain. Radiat. Res. 2011;176(6): 753-760. https://doi.org/10.1667/RR2647.1
- Lee WH, Sonntag WE, Lee YW. Aging attenuates radiation-induced expression of pro-inflammatory mediators in rat brain. Neurosci. Lett. 2010;476(2):89-93. https://doi.org/10.1016/j.neulet.2010.04.009
-
Veeraraghavan J, Natarajan M, Herman TS, Aravindan N. Low-dose
${\gamma}$ -radiation-induced oxidative stress response in mouse brain and gut: regulation by NF${\kappa}$ B-MnSOD cross-signaling. Mutat. Res. 2011;718(1-2):44-55. https://doi.org/10.1016/j.mrgentox.2010.10.006 - York JM, Blevins NA, Meling DD, Peterlin MB, Gridley DS, Cengel KA, Freund GG. The biobehavioral and neuroimmune impact of low-dose ionizing radiation. Brain Behav. Immun. 2012;26(2):218-227. https://doi.org/10.1016/j.bbi.2011.09.006
- Huang DW, Sherman BT, Lempicki RA. Systematic and integrative analysis of large gene lists using DAVID Bioinformatics Resources. Nature Protoc. 2009;4(1):44-57.
- Verheyde J, Benotmane MA. Unraveling the fundamental molecular mechanisms of morphological and cognitive defects in the irradiated brain. Brain Research Reviews. 2007;53(2):312-320. https://doi.org/10.1016/j.brainresrev.2006.09.004
- Gavinski S, Woloschak GE. Expression of viral and virus-like elements in DNA repair-deficient/immunodeficient "wasted" mice. J. Immunol. 1989;142(6):1861-1866.
- Tomita M, Morohoshi F, Matsumoto Y, Otsuka K, Sakai K. Role of DNA double-strand break repair genes in cell proliferation under low dose-rate irradiation conditions. J. Radiat. Res. 2008;49(5):557-564. https://doi.org/10.1269/jrr.08036
- Shin SC, Kang YM, Kim HS. Life span and thymic lymphoma incidence in high- and low-dose-rate irradiated AKR/J mice and commonly expressed genes. Radiat. Res. 2010;174(3):341-346. https://doi.org/10.1667/RR1946.1
- Eckert RL, Lee KC. S100A7 (Psoriasin): a story of mice and men. J. Invest. Dermatol. 2006;126(7):1442-1444. https://doi.org/10.1038/sj.jid.5700265
- Lee KC, Eckert RL S100A7 (Psoriasin)--mechanism of antibacterial action in wounds. J. Invest. Dermatol. 2007;127(4):945-957. https://doi.org/10.1038/sj.jid.5700663
- Boniface K, Bernard FX, Garcia M, Gurney, AL, Lecron, JC. Morel F. IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes. J. Immunol. 2005;174(6):3695-3702. https://doi.org/10.4049/jimmunol.174.6.3695
- Boniface K, Diveu C, Morel F, Pedretti N, Froger J, Ravon E, Garcia M, Venereau E, Preisser L, Guignouard E, Guillet G, Dagregorio G, Pene J, Moles JP, Yssel H, Chevalier S, Bernard FX, Gascan H, Lecron JC. Oncostatin M secreted by skin infiltrating T lymphocytes is a potent keratinocyte activator involved in skin inflammation. J. Immunol. 2007;178(7):4615-4622. https://doi.org/10.4049/jimmunol.178.7.4615
- Eckert RL, Broome AM, Ruse M, Robinson N, Ryan D, Lee K. S100 proteins in the epidermis. J. Invest. Dermatol. 2004;123(1):23-33. https://doi.org/10.1111/j.0022-202X.2004.22719.x
- Wolk K, Witte E, Wallace E, Docke WD, Kunz S, Asadullah K, Volk HD, Sterry W, Sabat R. IL-22 regulates the expression of genes responsible for antimicrobial defense, cellular differentiation, and mobility in keratinocytes: a potential role in psoriasis. Eur. J. Immunol. 2006;36(5):1309-1323. https://doi.org/10.1002/eji.200535503
- Zhang H, Wang Y, Chen Y, Sun S, Li N, Lv D, Liu C, Huang L, He D, Xiao X. Identification and validation of S100A7 associated with lung squamous cell carcinoma metastasis to brain. Lung Cancer. 2007;57(1):37-45. https://doi.org/10.1016/j.lungcan.2007.02.020
- Qin W, Ho L, Wang J, Peskind E, Pasinetti GM. S100A7, a novel Alzheimer's disease biomarker with non-amyloidogenic alpha-secretase activity acts via selective promotion of ADAM-10. PLoS One. 2009;4(1):e4183. https://doi.org/10.1371/journal.pone.0004183
- Jansen S, Podschun R, Leib SL, Grotzinger J, Oestern S, Michalek M, Pufe T, Brandenburg LO. Expression and Function of Psoriasin (S100A7) and Koebnerisin (S100A15) in the Brain. Infect Immun. 2013;81(5):1788-1797. https://doi.org/10.1128/IAI.01265-12
- Julius D, Nathans J. Signaling by sensory receptors. Cold Spring Harb Perspect Biol. 2012;4(1):a005991.
- Garcia-Esparcia P, Schluter A, Carmona M, Moreno J, Ansoleaga B, Torrejon-Escribano B, Gustincich S, Pujol A, Ferrer I. Functional Genomics Reveals Dysregulation of Cortical Olfactory Receptors in Parkinson Disease: Novel Putative Chemoreceptors in the Human Brain. J. Neuropathol Exp. Neurol. 2013;72(6):524-539. https://doi.org/10.1097/NEN.0b013e318294fd76
- Zhao W, Ho L, Varghese M, Yemul S, Dams-O'Connor K, Gordon W, Knable L, Freire D, Haroutunian V, Pasinetti GM. Decreased level of olfactory receptors in blood cells following traumatic brain injury and potential association with tauopathy. J. Alzheimers Dis. 2013;34(2):417-429.