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2016
C. Wang, Wang, J., Jia, D., Li, L., Jia, B., Fan, S., Song, J., Hu, X., Wang, Y., and Wang, D., Anti-nociceptive effects of Paecilomyces hepiali via multiple pathways in mouse models, vol. 15, p. -, 2016.
L. Li, Li, M. X., Pan, L. H., Wang, G. M., Guo, M., Fu, L. Q., Guo, J. C., Gao, Y. S., Chen, F., Xie, M. X., Li, L., Li, M. X., Pan, L. H., Wang, G. M., Guo, M., Fu, L. Q., Guo, J. C., Gao, Y. S., Chen, F., and Xie, M. X., Comparative analysis of platelet 5-HT concentrations in Han and Li patients with post-traumatic stress disorder, vol. 15, p. -, 2016.
L. Li, Li, M. X., Pan, L. H., Wang, G. M., Guo, M., Fu, L. Q., Guo, J. C., Gao, Y. S., Chen, F., Xie, M. X., Li, L., Li, M. X., Pan, L. H., Wang, G. M., Guo, M., Fu, L. Q., Guo, J. C., Gao, Y. S., Chen, F., and Xie, M. X., Comparative analysis of platelet 5-HT concentrations in Han and Li patients with post-traumatic stress disorder, vol. 15, p. -, 2016.
F. S. Song, Ni, J. L., Qian, Y. L., Li, L., Ni, D. H., Yang, J. B., Song, F. S., Ni, J. L., Qian, Y. L., Li, L., Ni, D. H., and Yang, J. B., Development of SNP-based dCAPS markers for identifying male sterile gene tms5 in two-line hybrid rice, vol. 15, p. -, 2016.
F. S. Song, Ni, J. L., Qian, Y. L., Li, L., Ni, D. H., Yang, J. B., Song, F. S., Ni, J. L., Qian, Y. L., Li, L., Ni, D. H., and Yang, J. B., Development of SNP-based dCAPS markers for identifying male sterile gene tms5 in two-line hybrid rice, vol. 15, p. -, 2016.
Z. J. Wang, Wang, H. X., Li, L., Wang, L., Dou, H. H., Wang, Z. J., Wang, H. X., Li, L., Wang, L., and Dou, H. H., Influence of different fluid resuscitation techniques on the number of myeloid-derived suppressor cells in rats, vol. 15, p. -, 2016.
Z. J. Wang, Wang, H. X., Li, L., Wang, L., Dou, H. H., Wang, Z. J., Wang, H. X., Li, L., Wang, L., and Dou, H. H., Influence of different fluid resuscitation techniques on the number of myeloid-derived suppressor cells in rats, vol. 15, p. -, 2016.
H. X. Shen, Li, L., Chen, Q., He, Y. Q., Yu, C. H., Chu, C. Q., Lu, X. J., and Chen, J., LECT2 association with macrophage-mediated killing of Helicobacter pylori by activating NF-κB and nitric oxide production, vol. 15, no. 4, p. -, 2016.
Conflicts of interestThe authors declare no conflict of interest.ACKNOWLEDGMENTSResearch supported by the Research Project of Chinese Ministry of Education (#213017A), the Program for the Natural Science Foundation of China (#81400606), the Natural Science Foundation of Ningbo City of China (#2013A610166), and the KC Wong Magna Fund in Ningbo University.REFERENCESAbdullah Z, Knolle PA, et al (2014). Scaling of immune responses against intracellular bacterial infection. EMBO J. 33: 2283-2294. http://dx.doi.org/10.15252/embj.201489055 Ahmed AU, Sarvestani ST, Gantier MP, Williams BR, et al (2014). Integrin-linked kinase modulates lipopolysaccharide- and Helicobacter pylori-induced nuclear factor κB-activated tumor necrosis factor-α production via regulation of p65 serine 536 phosphorylation. J. Biol. Chem. 289: 27776-27793. http://dx.doi.org/10.1074/jbc.M114.574541 Ansari SA, Devi S, Tenguria S, Kumar A, et al (2014). Helicobacter pylori protein HP0986 (TieA) interacts with mouse TNFR1 and triggers proinflammatory and proapoptotic signaling pathways in cultured macrophage cells (RAW 264.7). Cytokine 68: 110-117. http://dx.doi.org/10.1016/j.cyto.2014.03.006 Baccarini M, et al (2005). Second nature: biological functions of the Raf-1 “kinase”. FEBS Lett. 579: 3271-3277. http://dx.doi.org/10.1016/j.febslet.2005.03.024 Benson MD, James S, Scott K, Liepnieks JJ, et al (2008). Leukocyte chemotactic factor 2: A novel renal amyloid protein. Kidney Int. 74: 218-222. http://dx.doi.org/10.1038/ki.2008.152 Blom N, Gammeltoft S, Brunak S, et al (1999). Sequence and structure-based prediction of eukaryotic protein phosphorylation sites. J. Mol. Biol. 294: 1351-1362. http://dx.doi.org/10.1006/jmbi.1999.3310 Bussière FI, Chaturvedi R, Cheng Y, Gobert AP, et al (2005). Spermine causes loss of innate immune response to Helicobacter pylori by inhibition of inducible nitric-oxide synthase translation. J. Biol. Chem. 280: 2409-2412. http://dx.doi.org/10.1074/jbc.C400498200 Castaño-Rodríguez N, Kaakoush NO, Mitchell HM, et al (2014). Pattern-recognition receptors and gastric cancer. Front. Immunol. 5: 336. Chaturvedi R, Asim M, Lewis ND, Algood HM, et al (2007). L-arginine availability regulates inducible nitric oxide synthase-dependent host defense against Helicobacter pylori. Infect. Immun. 75: 4305-4315. http://dx.doi.org/10.1128/IAI.00578-07 Chaturvedi R, de Sablet T, Coburn LA, Gobert AP, et al (2012). Arginine and polyamines in Helicobacter pylori-induced immune dysregulation and gastric carcinogenesis. Amino Acids 42: 627-640. http://dx.doi.org/10.1007/s00726-011-1038-4 Chen TE, Xu XM, Liu P, Liang SY, et al (2015). Elucidating the function and tolerance mechanism of gamma delta (γ δ) T cells in a Helicobacter pylori infection model. Genet. Mol. Res. 14: 10543-10552. http://dx.doi.org/10.4238/2015.September.8.16 Cid TP, Fernández MC, Benito Martínez S, Jones NL, et al (2013). Pathogenesis of Helicobacter pylori infection. Helicobacter 18 (Suppl 1): 12-17. http://dx.doi.org/10.1111/hel.12076 Dang MH, Kato H, Ueshiba H, Omori-Miyake M, et al (2010). Possible role of LECT2 as an intrinsic regulatory factor in SEA-induced toxicity in d-galactosamine-sensitized mice. Clin. Immunol. 137: 311-321. http://dx.doi.org/10.1016/j.clim.2010.08.002 Dhillon AS, von Kriegsheim A, Grindlay J, Kolch W, et al (2007). Phosphatase and feedback regulation of Raf-1 signaling. Cell Cycle 6: 3-7. http://dx.doi.org/10.4161/cc.6.1.3593 Forbus J, Spratt H, Wiktorowicz J, Wu Z, et al (2006). Functional analysis of the nuclear proteome of human A549 alveolar epithelial cells by HPLC-high resolution 2-D gel electrophoresis. Proteomics 6: 2656-2672. http://dx.doi.org/10.1002/pmic.200500652 Granger DL, Taintor RR, Boockvar KS, HibbsJBJret al. (1996). Measurement of nitrate and nitrite in biological samples using nitrate reductase and Griess reaction. Methods Enzymol. 268: 142-151. http://dx.doi.org/10.1016/S0076-6879(96)68016-1 Gringhuis SI, den Dunnen J, Litjens M, van Het Hof B, et al (2007). C-type lectin DC-SIGN modulates Toll-like receptor signaling via Raf-1 kinase-dependent acetylation of transcription factor NF-kappaB. Immunity 26: 605-616. http://dx.doi.org/10.1016/j.immuni.2007.03.012 Gringhuis SI, den Dunnen J, Litjens M, van der Vlist M, et al (2009). Dectin-1 directs T helper cell differentiation by controlling noncanonical NF-kappaB activation through Raf-1 and Syk. Nat. Immunol. 10: 203-213. http://dx.doi.org/10.1038/ni.1692 Hardbower DM, Asim M, Murray-Stewart T, CaseroRAJret al (2016). Arginase 2 deletion leads to enhanced M1 macrophage activation and upregulated polyamine metabolism in response to Helicobacter pylori infection. Amino Acids 48: 2375-2388. http://dx.doi.org/10.1007/s00726-016-2231-2 Hayden MS, Ghosh S, et al (2011). NF-κB in immunobiology. Cell Res. 21: 223-244. http://dx.doi.org/10.1038/cr.2011.13 Hong JB, Zuo W, Wang AJ, Lu NH, et al (2016). Helicobacter pylori infection synergistic with IL-1β gene polymorphisms potentially contributes to the carcinogenesis of gastric cancer. Int. J. Med. Sci. 13: 298-303. http://dx.doi.org/10.7150/ijms.14239 Huang J, DeGraves FJ, Lenz SD, Gao D, et al (2002). The quantity of nitric oxide released by macrophages regulates Chlamydia-induced disease. Proc. Natl. Acad. Sci. USA 99: 3914-3919. http://dx.doi.org/10.1073/pnas.062578399 Hu Y, Liu JP, Zhu Y, Lu NH, et al (2016). The importance of Toll-like receptors in NF-κB signaling pathway activation by Helicobacter pylori infection and the regulators of this response. Helicobacter, in press. http://dx.doi.org/10.1111/hel.12292 Hughes CE, Sinha U, Pandey A, Eble JA, et al (2013). Critical Role for an acidic amino acid region in platelet signaling by the HemITAM (hemi-immunoreceptor tyrosine-based activation motif) containing receptor CLEC-2 (C-type lectin receptor-2). J. Biol. Chem. 288: 5127-5135. http://dx.doi.org/10.1074/jbc.M112.411462 Jones E, Adcock IM, Ahmed BY, Punchard NA, et al (2007). Modulation of LPS stimulated NF-kappaB mediated Nitric Oxide production by PKCepsilon and JAK2 in RAW macrophages. J. Inflamm. (Lond.) 4: 23. http://dx.doi.org/10.1186/1476-9255-4-23 Kameoka Y, Yamagoe S, Hatano Y, Kasama T, et al (2000). Val58Ile polymorphism of the neutrophil chemoattractant LECT2 and rheumatoid arthritis in the Japanese population. Arthritis Rheum. 43: 1419-1420. http://dx.doi.org/10.1002/1529-0131(200006)43:6<1419::AID-ANR28>3.0.CO;2-I Kim G, Kim TH, Kang MJ, Choi JA, et al (2016). Inhibitory effect of withaferin A on Helicobacter pylori‑induced IL‑8 production and NF‑κB activation in gastric epithelial cells. Mol. Med. Rep. 13: 967-972. Kumar N, Mariappan V, Baddam R, Lankapalli AK, et al (2015). Comparative genomic analysis of Helicobacter pylori from Malaysia identifies three distinct lineages suggestive of differential evolution. Nucleic Acids Res. 43: 324-335. http://dx.doi.org/10.1093/nar/gku1271 Lu DY, Tang CH, Chang CH, Maa MC, et al (2012). Helicobacter pylori attenuates lipopolysaccharide-induced nitric oxide production by murine macrophages. Innate Immun. 18: 406-417. http://dx.doi.org/10.1177/1753425911413164 Lu XJ, Chen J, Yu CH, Shi YH, et al (2013). LECT2 protects mice against bacterial sepsis by activating macrophages via the CD209a receptor. J. Exp. Med. 210: 5-13. http://dx.doi.org/10.1084/jem.20121466 Oeckinghaus A, Hayden MS, Ghosh S, et al (2011). Crosstalk in NF-κB signaling pathways. Nat. Immunol. 12: 695-708. http://dx.doi.org/10.1038/ni.2065 Osorio F, Reis e Sousa C, et al (2011). Myeloid C-type lectin receptors in pathogen recognition and host defense. Immunity 34: 651-664. http://dx.doi.org/10.1016/j.immuni.2011.05.001 Park CG, Takahara K, Umemoto E, Yashima Y, et al (2001). Five mouse homologues of the human dendritic cell C-type lectin, DC-SIGN. Int. Immunol. 13: 1283-1290. http://dx.doi.org/10.1093/intimm/13.10.1283 Polk DB, PeekRMJret al. (2010). Helicobacter pylori: gastric cancer and beyond. Nat. Rev. Cancer 10: 403-414. http://dx.doi.org/10.1038/nrc2857 Saito T, Okumura A, Watanabe H, Asano M, et al (2004). Increase in hepatic NKT cells in leukocyte cell-derived chemotaxin 2-deficient mice contributes to severe concanavalin A-induced hepatitis. J. Immunol. 173: 579-585. http://dx.doi.org/10.4049/jimmunol.173.1.579 Sancho D, Reis e Sousa C, et al (2012). Signaling by myeloid C-type lectin receptors in immunity and homeostasis. Annu. Rev. Immunol. 30: 491-529. http://dx.doi.org/10.1146/annurev-immunol-031210-101352 Suzuki-Inoue K, Fuller GL, García A, Eble JA, et al (2006). A novel Syk-dependent mechanism of platelet activation by the C-type lectin receptor CLEC-2. Blood 107: 542-549. http://dx.doi.org/10.1182/blood-2005-05-1994 Uchida T, Nagai H, Gotoh K, Kanagawa H, et al (1999). Expression pattern of a newly recognized protein, LECT2, in hepatocellular carcinoma and its premalignant lesion. Pathol. Int. 49: 147-151. http://dx.doi.org/10.1046/j.1440-1827.1999.00836.x Yamagoe S, Mizuno S, Suzuki K, et al (1998). Molecular cloning of human and bovine LECT2 having a neutrophil chemotactic activity and its specific expression in the liver. Biochim. Biophys. Acta 1396: 105-113. http://dx.doi.org/10.1016/S0167-4781(97)00181-4 Yamauchi K, Choi IJ, Lu H, Ogiwara H, et al (2008). Regulation of IL-18 in Helicobacter pylori infection. J. Immunol. 180: 1207-1216. http://dx.doi.org/10.4049/jimmunol.180.2.1207    
H. Zhang, Jin, P. F., Niu, L. L., Li, L., Wang, L. J., Chen, Y., Zhang, G. J., Zhang, H. P., Zhong, T., Zhang, H., Jin, P. F., Niu, L. L., Li, L., Wang, L. J., Chen, Y., Zhang, G. J., Zhang, H. P., and Zhong, T., Methylation differences and expression profiles of the caprine DIO3 gene, vol. 15, p. -, 2016.
H. Zhang, Jin, P. F., Niu, L. L., Li, L., Wang, L. J., Chen, Y., Zhang, G. J., Zhang, H. P., Zhong, T., Zhang, H., Jin, P. F., Niu, L. L., Li, L., Wang, L. J., Chen, Y., Zhang, G. J., Zhang, H. P., and Zhong, T., Methylation differences and expression profiles of the caprine DIO3 gene, vol. 15, p. -, 2016.
Q. Song, Han, C. C., Xiong, X. P., He, F., Gan, W., Wei, S. H., Liu, H. H., Li, L., Xu, H. Y., Song, Q., Han, C. C., Xiong, X. P., He, F., Gan, W., Wei, S. H., Liu, H. H., Li, L., and Xu, H. Y., PI3K-Akt-mTOR signal inhibition affects expression of genes related to endoplasmic reticulum stress, vol. 15, p. -, 2016.
Q. Song, Han, C. C., Xiong, X. P., He, F., Gan, W., Wei, S. H., Liu, H. H., Li, L., Xu, H. Y., Song, Q., Han, C. C., Xiong, X. P., He, F., Gan, W., Wei, S. H., Liu, H. H., Li, L., and Xu, H. Y., PI3K-Akt-mTOR signal inhibition affects expression of genes related to endoplasmic reticulum stress, vol. 15, p. -, 2016.
L. Li, Li, Y., Zeng, X. C., Li, J., and Du, X. Y., Role of interleukin-4 genetic polymorphisms and environmental factors in the risk of asthma in children, vol. 15, no. 4, p. -, 2016.
Conflicts of interestThe authors declare no conflict of interest.REFERENCESAkinbami LJ, Schoendorf KC, et al (2002). Trends in childhood asthma: prevalence, health care utilization, and mortality. Pediatrics 110: 315-322. http://dx.doi.org/10.1542/peds.110.2.315 Al-Mazam A, Mohamed AG, et al (2001). Risk factors of bronchial asthma in bahrah, saudi arabia. J. Family Community Med. 8: 33-39. Andrews RP, Burrell L, Rosa-Rosa L, Cunningham CM, et al (2001). Analysis of the Ser786Pro interleukin-4 receptor alpha allelic variant in allergic and nonallergic asthma and its functional consequences. Clin. Immunol. 100: 298-304. http://dx.doi.org/10.1006/clim.2001.5082 Antczak A, Domańska-Senderowska D, Górski P, Pastuszak-Lewandoska D, et al (2016). Analysis of changes in expression of IL-4/IL-13/STAT6 pathway and correlation with the selected clinical parameters in patients with atopic asthma. Int. J. Immunopathol. Pharmacol. 29: 195-204. http://dx.doi.org/10.1177/0394632015623794 Bal SM, Bernink JH, Nagasawa M, Groot J, et al (2016). IL-1β, IL-4 and IL-12 control the fate of group 2 innate lymphoid cells in human airway inflammation in the lungs. Nat. Immunol. 17: 636-645. http://dx.doi.org/10.1038/ni.3444 Barner M, Mohrs M, Brombacher F, Kopf M, et al (1998). Differences between IL-4R alpha-deficient and IL-4-deficient mice reveal a role for IL-13 in the regulation of Th2 responses. Curr. Biol. 8: 669-672. http://dx.doi.org/10.1016/S0960-9822(98)70256-8 Borish L, et al (2010). IL-4 and IL-13 dual antagonism: a promising approach to the dilemma of generating effective asthma biotherapeutics. Am. J. Respir. Crit. Care Med. 181: 769-770. http://dx.doi.org/10.1164/rccm.201002-0147ED Boulet LP, FitzGerald JM, Levy ML, Cruz AA, et al (2012). A guide to the translation of the Global Initiative for Asthma (GINA) strategy into improved care. Eur. Respir. J. 39: 1220-1229. http://dx.doi.org/10.1183/09031936.00184511 Chen ZH, Wang PL, Shen HH, et al (2013). Asthma research in China: a five-year review. Respirology 18 (Suppl 3): 10-19. http://dx.doi.org/10.1111/resp.12196 Cook J, Saglani S, et al (2016). Pathogenesis and prevention strategies of severe asthma exacerbations in children. Curr. Opin. Pulm. Med. 22: 25-31. http://dx.doi.org/10.1097/MCP.0000000000000223 Cui T, Wu J, Pan S, Xie J, et al (2003). Polymorphisms in the IL-4 and IL-4R [alpha] genes and allergic asthma. Clin. Chem. Lab. Med. 41: 888-892. http://dx.doi.org/10.1515/CCLM.2003.134 Demirdag YY, Ramadan HH, et al (2016). Direct measurement of upper airway inflammation in children with chronic rhinosinusitis: implications for asthma. Curr. Opin. Allergy Clin. Immunol. 16: 18-23. http://dx.doi.org/10.1097/ACI.0000000000000237 Eaton DK, Kann L, Kinchen S, Shanklin S, Centers for Disease Control and Prevention (CDC)et al (2008). Youth risk behavior surveillance--United States, 2007. MMWR Surveill. Summ. 57: 1-131. Gonzalez-Garcia M, Caballero A, Jaramillo C, Maldonado D, et al (2015). Prevalence, risk factors and underdiagnosis of asthma and wheezing in adults 40 years and older: A population-based study. J. Asthma 52: 823-830. http://dx.doi.org/10.3109/02770903.2015.1010733 Hosseini-Farahabadi S, Tavakkol-Afshari J, Rafatpanah H, Farid Hosseini R, et al (2007). Association between the polymorphisms of IL-4 gene promoter (-590C>T), IL-13 coding region (R130Q) and IL-16 gene promoter (-295T>C) and allergic asthma. Iran. J. Allergy Asthma Immunol. 6: 9-14. Hovland V, Riiser A, Mowinckel P, Carlsen KH, et al (2015). Early risk factors for pubertal asthma. Clin. Exp. Allergy 45: 164-176. http://dx.doi.org/10.1111/cea.12409 Huang ZY, Cheng BJ, Cai GJ, Zhang BF, et al (2015). Association of the IL-4R Q576R polymorphism and asthma in the Chinese Han population: a meta-analysis. Genet. Mol. Res. 14: 2900-2911. http://dx.doi.org/10.4238/2015.March.31.21 Jaakkola MS, Jaakkola JJ, et al (2012). Assessment of public health impact of work-related asthma. BMC Med. Res. Methodol. 12: 22. http://dx.doi.org/10.1186/1471-2288-12-22 Kamali-Sarvestani E, Ghayomi MA, Nekoee A, et al (2007). Association of TNF-alpha -308 G/A and IL-4 -589 C/T gene promoter polymorphisms with asthma susceptibility in the south of Iran. J. Investig. Allergol. Clin. Immunol. 17: 361-366. Lee JH, Park HS, Park SW, Jang AS, et al (2004). ADAM33 polymorphism: association with bronchial hyper-responsiveness in Korean asthmatics. Clin. Exp. Allergy 34: 860-865. http://dx.doi.org/10.1111/j.1365-2222.2004.01977.x Li Y, Guo B, Zhang L, Han J, et al (2008). Association between C-589T polymorphisms of interleukin-4 gene promoter and asthma: a meta-analysis. Respir. Med. 102: 984-992. http://dx.doi.org/10.1016/j.rmed.2008.02.008 Mak JC, Ko FW, Chu CM, Leung HC, et al (2007). Polymorphisms in the IL-4, IL-4 receptor alpha chain, TNF-alpha, and lymphotoxin-alpha genes and risk of asthma in Hong Kong Chinese adults. Int. Arch. Allergy Immunol. 144: 114-122. http://dx.doi.org/10.1159/000103222 Masoli M, Fabian D, Holt S, Beasley R, Global Initiative for Asthma (GINA) Programet al (2004). The global burden of asthma: executive summary of the GINA Dissemination Committee report. Allergy 59: 469-478. http://dx.doi.org/10.1111/j.1398-9995.2004.00526.x Micheal S, Minhas K, Ishaque M, Ahmed F, et al (2013). IL-4 gene polymorphisms and their association with atopic asthma and allergic rhinitis in Pakistani patients. J. Investig. Allergol. Clin. Immunol. 23: 107-111. Nambu M, Holgate S, et al (2009). Differences in the asthma treatment of children between europe and Japan: a questionnaire-based survey using model cases. World Allergy Organ. J. 2: 54-56. http://dx.doi.org/10.1097/WOX.0b013e31819f20eb Osei-Kumah A, Ammit AJ, Smith R, Ge Q, et al (2006). Inflammatory mediator release in normal bronchial smooth muscle cells is altered by pregnant maternal and fetal plasma independent of asthma. Placenta 27: 847-852. http://dx.doi.org/10.1016/j.placenta.2005.08.007 Pattnaik B, Bodas M, Bhatraju NK, Ahmad T, et al (2016). IL-4 promotes asymmetric dimethylarginine accumulation, oxo-nitrative stress, and hypoxic response-induced mitochondrial loss in airway epithelial cells. J. Allergy Clin. Immunol. 138: 130-141.e9. http://dx.doi.org/10.1016/j.jaci.2015.11.036 Rosa-Rosa L, Zimmermann N, Bernstein JA, Rothenberg ME, et al (1999). The R576 IL-4 receptor alpha allele correlates with asthma severity. J. Allergy Clin. Immunol. 104: 1008-1014. http://dx.doi.org/10.1016/S0091-6749(99)70082-5 Sengler C, Lau S, Wahn U, Nickel R, et al (2002). Interactions between genes and environmental factors in asthma and atopy: new developments. Respir. Res. 3: 7. http://dx.doi.org/10.1186/rr179 Smallwood DT, Apollonio B, Willimott S, Lezina L, et al (2016). Extracellular vesicles released by CD40/IL-4-stimulated CLL cells confer altered functional properties to CD4+ T cells. Blood 128: 542-552. http://dx.doi.org/10.1182/blood-2015-11-682377 Tang L, Lin HG, Chen BF, et al (2014). Association of IL-4 promoter polymorphisms with asthma: a meta-analysis. Genet. Mol. Res. 13: 1383-1394. http://dx.doi.org/10.4238/2014.February.28.11 Toskala E, Kennedy DW, et al (2015). Asthma risk factors. Int. Forum Allergy Rhinol. 5 (Suppl 1): S11-S16. http://dx.doi.org/10.1002/alr.21557 Tulah AS, Holloway JW, Sayers I, et al (2013). Defining the contribution of SNPs identified in asthma GWAS to clinical variables in asthmatic children. BMC Med. Genet. 14: 100. http://dx.doi.org/10.1186/1471-2350-14-100 Wills-Karp M, Luyimbazi J, Xu X, Schofield B, et al (1998). Interleukin-13: central mediator of allergic asthma. Science 282: 2258-2261. http://dx.doi.org/10.1126/science.282.5397.2258 Wongratanacheewin S, et al (2014). Update of cytokines and genes in asthma and allergic rhinitis. Asian Pac. J. Allergy Immunol. 32: 275. Zahran HS, Bailey C, et al (2013). Factors associated with asthma prevalence among racial and ethnic groups--United States, 2009-2010 behavioral risk factor surveillance system. J. Asthma 50: 583-589. http://dx.doi.org/10.3109/02770903.2013.794238  
Q. He, Yao, C. L., Li, L., Xin, Z., Jing, Z. K., Li, L. X., He, Q., Yao, C. L., Li, L., Xin, Z., Jing, Z. K., and Li, L. X., Targeted gene therapy and in vivo bioluminescent imaging for monitoring postsurgical recurrence and metastasis in mouse models of liver cancer, vol. 15, p. -, 2016.
Q. He, Yao, C. L., Li, L., Xin, Z., Jing, Z. K., Li, L. X., He, Q., Yao, C. L., Li, L., Xin, Z., Jing, Z. K., and Li, L. X., Targeted gene therapy and in vivo bioluminescent imaging for monitoring postsurgical recurrence and metastasis in mouse models of liver cancer, vol. 15, p. -, 2016.
2015
Z. Z. Li, Qin, W. Z., Li, L., Wu, Q., and Wang, Y. J., Accuracy of enzyme-linked immunospot assay for diagnosis of pleural tuberculosis: a meta-analysis, vol. 14, pp. 11672-11680, 2015.
L. Li, Wang, F., Lv, P. W., Zhu, M. Z., He, J. J., Guo, G. C., Gu, Y. T., and Han, M. L., Angiotensin II type 1 receptor gene A1166C polymorphism and breast cancer susceptibility, vol. 14, pp. 15016-15023, 2015.
L. Li, Tian, Y. L., Lv, X. M., Yu, H. F., Xie, Y. Y., Wang, J. D., and Shi, W., Association analysis of IL-17A and IL-17F polymorphisms in Chinese women with cervical cancer, vol. 14, pp. 12178-12183, 2015.
W. Gan, Song, Q., Zhang, N. N., Xiong, X. P., Wang, D. M. C., and Li, L., Association between FTO polymorphism in exon 3 with carcass and meat quality traits in crossbred ducks, vol. 14, pp. 6699-6714, 2015.
R. Yao, Du, Y. Y., Zhang, Y. Z., Chen, Q. H., Zhao, L. S., and Li, L., Association between G-217A polymorphism in the AGT gene and essential hypertension: a meta-analysis, vol. 14, pp. 5527-5534, 2015.
J. Cheng, Cen, J. - M., Cai, M. - Y., Xu, S., Li, L., Li, Z. - C., Yang, X. - L., Chen, C., Liu, X., and Xiong, X. - D., Association between TNFSF4 tagSNPs and myocardial infarction in a Chinese Han population, vol. 14, pp. 6136-6145, 2015.
W. Xu, Liu, S., Li, L., Shen, Z. Y., and Wu, Y. L., Association between XRCC1 Arg280His polymorphism and risk of hepatocellular carcinoma: a systematic review and meta-analysis, vol. 14, pp. 7122-7129, 2015.
Z. Wang, Li, M., Li, L., Sun, H., and Lin, X. Y., Association of single nucleotide polymorphisms in the CYP1B1 gene with the risk of primary open-angle glaucoma: a meta-analysis, vol. 14, pp. 17262-17272, 2015.
P. Wei, Zhang, Z. H., Li, L., Du, X. L., Shan, C. P., and Sheng, X. G., Clinical observational study of conformal radiotherapy combined with topotecan chemotherapy in patients with platinum-resistant recurrent ovarian cancer, vol. 14, pp. 3833-3842, 2015.
H. L. Wu, Li, L., Cheng, Z. C., Ge, W., Gao, J., and Li, X. P., Cloning and stress response analysis of the PeDREB2A and PeDREB1A genes in moso bamboo (Phyllostachys edulis), vol. 14, pp. 10206-10223, 2015.
Y. L. Wen and Li, L., Correlation between matrix metalloproteinase-9 and vascular endothelial growth factor expression in lung adenocarcinoma, vol. 14, pp. 19342-19348, 2015.
Q. M. Chen, Qu, H. D., Qian, W. D., Shen, L., Xu, L., Chen, Y. H., Sang, D. Q., Zhang, L. N., Yin, L., Li, L., and Wang, H., Correlation between neuronal antibodies and limbic encephalitis in Chinese Han subjects, vol. 14, pp. 2312-2321, 2015.
S. - Y. Guo, Ding, Y. - J., Li, L., Zhang, T., Zhang, Z. - Z., and Zhang, E. - S., Correlation of CD4+ CD25+ Foxp3+ Treg with the recovery of joint function after total knee replacement in rats with osteoarthritis, vol. 14, pp. 7290-7296, 2015.
L. Li, Li, J. G., Liu, C. Y., and Ding, Y. J., Effect of CYP1A1 and GSTM1 genetic polymorphisms on bone tumor susceptibility, vol. 14, pp. 16600-16607, 2015.
Y. Wang, Zhang, R. P., Zhao, Y. M., Li, Q. Q., Yan, X. P., Liu, J. Y., Gou, H., and Li, L., Effects of Pax3 and Pax7 expression on muscle mass in the Pekin duck (Anas platyrhynchos domestica), vol. 14, pp. 11495-11504, 2015.
H. Y. Yu, Li, X. Y., Cai, Z. F., Li, L., Shi, X. Z., Song, H. X., and Liu, X. J., Eosinophil cationic protein mRNA expression in children with bronchial asthma, vol. 14, pp. 14279-14285, 2015.
J. Wu, Bai, J. Y., Li, L., Huang, S., Li, C. M., and Wang, G. L., Genetic polymorphisms of the BMAP-28 and MASP-2 genes and their correlation with the somatic cell score in Chinese Holstein cattle, vol. 14, pp. 1-8, 2015.
S. H. Wang, Li, Y., Li, Z. Q., Chang, L., and Li, L., Identification of an SCAR marker related to female phenotype in Idesia polycarpa Maxim., vol. 14, pp. 2015-2022, 2015.
L. Li, Li, E., Zhang, L. H., Jian, L. G., Liu, H. P., and Wang, T., IL-6-174G/C and IL-6-572C/G polymorphisms are associated with increased risk of coronary artery disease, vol. 14, pp. 8451-8457, 2015.
J. M. Li, Hou, J., Li, L., and Wang, Y., Immunohistochemical subtypes of diffuse large B-cell lymphoma in the head and neck region, vol. 14, pp. 3889-3896, 2015.
S. Y. Zhan, Chen, L., Li, L., Wang, L. J., Zhong, T., and Zhang, H. P., Molecular characterization and expression patterns of insulin-like growth factor-binding protein genes in postnatal Nanjiang brown goats, vol. 14, pp. 12547-12560, 2015.
L. Li, Jia, Y. H., Li, P., Yin, S. W., Zhang, G. S., Wang, X. L., Wang, Y. Y., and Wang, X. J., Molecular cloning, characterization, and expression of vacuolar-type-H+-ATPase B1 (VHAB1) gene in the gill of Anguilla marmorata, vol. 14, pp. 8008-8020, 2015.
W. Guo, Gu, H. F., Zhang, H. G., Chen, S. B., Wang, J. Q., Geng, S. X., Li, L., Liu, P., Liu, X., Ji, Y. R., Li, S. W., and Yang, L., An outbreak of Candida parapsilosis fungemia among preterm infants, vol. 14, pp. 18259-18267, 2015.
Y. Dong, Li, L., Wang, L., Zhou, T., Liu, J. W., and Gao, Y. J., Preliminary study of the effects of β-elemene on MCF-7/ADM breast cancer stem cells, vol. 14, pp. 2347-2355, 2015.
Y. Y. Bao, Li, L., Zhang, H., Gao, C. Y., Xiao, C. B., and Li, C. L., Preparation of polyclonal antibody against porcine beta defensin 2 and identification of its distribution in tissues of pig, vol. 14, pp. 18863-18871, 2015.
L. Li, Wei, P., Zhang, M. - H., Zhang, W., Ma, Y., Fang, X., Hao, C. - L., and Zhang, Z. - H., Roles of the AIB1 protein in the proliferation and transformation of human esophageal squamous cell carcinoma, vol. 14, pp. 10376-10383, 2015.
Y. Z. Peng, Zheng, K., Yang, P., Wang, Y., Li, R. J., Li, L., Pan, J. H., and Guo, T., Shock wave treatment enhances endothelial proliferation via autocrine vascular endothelial growth factor, vol. 14, pp. 19203-19210, 2015.
N. N. Zhang, Hu, J. W., Liu, H. H., Xu, H. Y., He, H., and Li, L., SNPs in the 5'-regulatory region of the tyrosinase gene do not affect plumage color in ducks (Anas platyrhynchos), vol. 14, pp. 18623-18628, 2015.

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