Publications

Found 15 results
Filters: Author is X. Wei  [Clear All Filters]
2016
K. D. Huang, Shen, Y., Wei, X., Zhang, F. Q., Liu, Y. Y., Ma, L., Huang, K. D., Shen, Y., Wei, X., Zhang, F. Q., Liu, Y. Y., and Ma, L., Inhibitory effect of microRNA-27b on interleukin 17 (IL-17)-induced monocyte chemoattractant protein-1 (MCP1) expression, vol. 15, p. -, 2016.
K. D. Huang, Shen, Y., Wei, X., Zhang, F. Q., Liu, Y. Y., Ma, L., Huang, K. D., Shen, Y., Wei, X., Zhang, F. Q., Liu, Y. Y., and Ma, L., Inhibitory effect of microRNA-27b on interleukin 17 (IL-17)-induced monocyte chemoattractant protein-1 (MCP1) expression, vol. 15, p. -, 2016.
L. Hou, Li, W., Wei, X., Zhou, Y., Zhuo, Y., Wu, H., Shen, B., Hou, L., Li, W., Wei, X., Zhou, Y., Zhuo, Y., Wu, H., and Shen, B., RETRACTION of “Immune memory responses to HBV vaccine 13-18 years after primary vaccination” by L. Hou, W. Li, X. Wei, Y. Zhou, Y. Zhuo, H. Wu, B. Shen. Genet. Mol. Res. 14 (3): 8466-8472 (2015), vol. 15. p. -, 2016.
L. Hou, Li, W., Wei, X., Zhou, Y., Zhuo, Y., Wu, H., Shen, B., Hou, L., Li, W., Wei, X., Zhou, Y., Zhuo, Y., Wu, H., and Shen, B., RETRACTION of “Immune memory responses to HBV vaccine 13-18 years after primary vaccination” by L. Hou, W. Li, X. Wei, Y. Zhou, Y. Zhuo, H. Wu, B. Shen. Genet. Mol. Res. 14 (3): 8466-8472 (2015), vol. 15. p. -, 2016.
N. Yu, Dou, L., Li, Y., Deng, L., Wei, X., Guo, Y., Yu, N., Dou, L., Li, Y., Deng, L., Wei, X., and Guo, Y., Roles of ERα and ERβ in estrogen-induced DDP chemoresistance in non-small cell lung cancer, vol. 15, p. -, 2016.
N. Yu, Dou, L., Li, Y., Deng, L., Wei, X., Guo, Y., Yu, N., Dou, L., Li, Y., Deng, L., Wei, X., and Guo, Y., Roles of ERα and ERβ in estrogen-induced DDP chemoresistance in non-small cell lung cancer, vol. 15, p. -, 2016.
2013
J. Ran, Han, T. T., Ding, X. P., Wei, X., Zhang, L. Y., Zhang, Y. P., Li, T. J., Nie, S. S., and Chen, L., Association study between Y-chromosome haplogroups and susceptibility to spermatogenic impairment in Han People from southwest China, vol. 12, pp. 59-66, 2013.
Ferlin A, Arredi B and Foresta C (2006). Genetic causes of male infertility. Reprod. Toxicol. 22: 133-141. http://dx.doi.org/10.1016/j.reprotox.2006.04.016 PMid:16806807   Jin L and Su B (2000). Natives or immigrants: modern human origin in east Asia. Nat. Rev. Genet. 1: 126-133. http://dx.doi.org/10.1038/35038565 PMid:11253652   Karafet TM, Mendez FL, Meilerman MB, Underhill PA, et al. (2008). New binary polymorphisms reshape and increase resolution of the human Y chromosomal haplogroup tree. Genome Res. 18: 830-838. http://dx.doi.org/10.1101/gr.7172008 PMid:18385274 PMCid:2336805   Kent-First M, Muallem A, Shultz J, Pryor J, et al. (1999). Defining regions of the Y-chromosome responsible for male infertility and identification of a fourth AZF region (AZFd) by Y-chromosome microdeletion detection. Mol. Reprod. Dev. 53: 27-41. http://dx.doi.org/10.1002/(SICI)1098-2795(199905)53:1<27::AID-MRD4>3.0.CO;2-W   Krausz C and McElreavey K (1999). Y chromosome and male infertility. Front Biosci. 4: E1-E8. http://dx.doi.org/10.2741/Krausz PMid:9889182   Krausz C and Degl'Innocenti S (2006). Y chromosome and male infertility: update, 2006. Front Biosci. 11: 3049-3061. http://dx.doi.org/10.2741/2032 PMid:16720375   Krausz C, Quintana-Murci L, Rajpert-De ME, Jorgensen N, et al. (2001). Identification of a Y chromosome haplogroup associated with reduced sperm counts. Hum. Mol. Genet. 10: 1873-1877. http://dx.doi.org/10.1093/hmg/10.18.1873 PMid:11555623   Krausz C, Forti G and McElreavey K (2003). The Y chromosome and male fertility and infertility. Int. J. Androl. 26: 70-75. http://dx.doi.org/10.1046/j.1365-2605.2003.00402.x PMid:12641824   Kuroki Y, Iwamoto T, Lee J, Yoshiike M, et al. (1999). Spermatogenic ability is different among males in different Y chromosome lineage. J. Hum. Genet. 44: 289-292. http://dx.doi.org/10.1007/s100380050162 PMid:10496069   Lahn BT, Pearson NM and Jegalian K (2001). The human Y chromosome, in the light of evolution. Nat. Rev. Genet. 2: 207-216. http://dx.doi.org/10.1038/35056058 PMid:11256072   Maurer B, Gromoll J, Simoni M and Nieschlag E (2001). Prevalence of Y chromosome microdeletions in infertile men who consulted a tertiary care medical centre: the Munster experience. Andrologia 33: 27-33. http://dx.doi.org/10.1046/j.1439-0272.2001.00406.x PMid:11167516   Simoni M, Bakker E and Krausz C (2004). EAA/EMQN best practice guidelines for molecular diagnosis of y-chromosomal microdeletions. State of the art 2004. Int. J. Androl. 27: 240-249. http://dx.doi.org/10.1111/j.1365-2605.2004.00495.x PMid:15271204   Su B, Xiao J, Underhill P, Deka R, et al. (1999). Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. Am. J. Hum. Genet. 65: 1718-1724. http://dx.doi.org/10.1086/302680 PMid:10577926 PMCid:1288383   Vogt PH (1998). Human chromosome deletions in Yq11, AZF candidate genes and male infertility: history and update. Mol. Hum. Reprod. 4: 739-744. http://dx.doi.org/10.1093/molehr/4.8.739 PMid:9733430   Vogt PH, Edelmann A, Kirsch S, Henegariu O, et al. (1996). Human Y chromosome azoospermia factors (AZF) mapped to different subregions in Yq11. Hum. Mol. Genet. 5: 933-943. http://dx.doi.org/10.1093/hmg/5.7.933 PMid:8817327   Wu B, Lu NX, Xia YK, Gu AH, et al. (2007). A frequent Y chromosome b2/b3 subdeletion shows strong association with male infertility in Han-Chinese population. Hum. Reprod. 22: 1107-1113. http://dx.doi.org/10.1093/humrep/del499 PMid:17204527   Y Chromosome Consortium (2002). A nomenclature system for the tree of human Y-chromosomal binary haplogroups. Genome Res. 12: 339-348. http://dx.doi.org/10.1101/gr.217602 PMid:11827954 PMCid:155271   Yang Y, Ma M, Li L, Zhang W, et al. (2008). Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment. Hum. Reprod. 23: 2167-2172. http://dx.doi.org/10.1093/humrep/den229 PMid:18579508
2010
D. B. Li, Wei, X., Jiang, L. H., Wang, Y., and Xu, F., Meta-analysis of epidemiological studies of association of P53 codon 72 polymorphism with bladder cancer, vol. 9, pp. 1599-1605, 2010.
Begg CB and Mazumdar M (1994). Operating characteristics of a rank correlation test for publication bias. Biometrics 50: 1088-1101. http://dx.doi.org/10.2307/2533446 PMid:7786990   Chen WC, Tsai FJ, Wu JY, Wu HC, et al. (2000). Distributions of p53 codon 72 polymorphism in bladder cancer-proline form is prominent in invasive tumor. Urol. Res. 28: 293-296. http://dx.doi.org/10.1007/s002400000117 PMid:11127705   Dai S, Mao C, Jiang L, Wang G, et al. (2009). p53 polymorphism and lung cancer susceptibility: a pooled analysis of 32 case-control studies. Hum. Genet. 125: 633-638. http://dx.doi.org/10.1007/s00439-009-0664-3 PMid:19357867   Egger M, Davey SG, Schneider M and Minder C (1997). Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629-634. http://dx.doi.org/10.1136/bmj.315.7109.629 PMid:9310563 PMCid:2127453   Hollstein M, Sidransky D, Vogelstein B and Harris CC (1991). p53 mutations in human cancers. Science 253: 49-53. http://dx.doi.org/10.1126/science.1905840 PMid:1905840   Horikawa Y, Nadaoka J, Saito M, Kumazawa T, et al. (2008). Clinical implications of the MDM2 SNP309 and p53 Arg72Pro polymorphisms in transitional cell carcinoma of the bladder. Oncol. Rep. 20: 49-55. PMid:18575717   Ioannidis JP, Boffetta P, Little J, O'Brien TR, et al. (2008). Assessment of cumulative evidence on genetic associations: interim guidelines. Int. J. Epidemiol. 37: 120-132. http://dx.doi.org/10.1093/ije/dym159 PMid:17898028   Jemal A, Siegel R, Ward E, Hao Y, et al. (2008). Cancer statistics, 2008. CA Cancer J. Clin. 58: 71-96. http://dx.doi.org/10.3322/CA.2007.0010 PMid:18287387   Kaufman DS, Shipley WU and Feldman AS (2009). Bladder cancer. Lancet 374: 239-249. http://dx.doi.org/10.1016/S0140-6736(09)60491-8   Klug SJ, Ressing M, Koenig J, Abba MC, et al. (2009). TP53 codon 72 polymorphism and cervical cancer: a pooled analysis of individual data from 49 studies. Lancet Oncol. 10: 772-784. http://dx.doi.org/10.1016/S1470-2045(09)70187-1   Koushik A, Tranah GJ, Ma J, Stampfer MJ, et al. (2006). p53 Arg72Pro polymorphism and risk of colorectal adenoma and cancer. Int. J. Cancer 119: 1863-1868. http://dx.doi.org/10.1002/ijc.22057 PMid:16721787   Lee JM, Shun CT, Wu MT, Chen YY, et al. (2006). The associations of p53 overexpression with p53 codon 72 genetic polymorphism in esophageal cancer. Mutat. Res. 594: 181-188. http://dx.doi.org/10.1016/j.mrfmmm.2005.09.003 PMid:16318864   Levine AJ (1997). p53, the cellular gatekeeper for growth and division. Cell 88: 323-331. http://dx.doi.org/10.1016/S0092-8674(00)81871-1   Lopez-Beltran A, Escudero AL, Vicioso L, Munoz E, et al. (1996). Human papillomavirus DNA as a factor determining the survival of bladder cancer patients. Br. J. Cancer 73: 124-127. http://dx.doi.org/10.1038/bjc.1996.23 PMid:8554974 PMCid:2074275   Mabrouk I, Baccouche S, El-Abed R, Mokdad-Gargouri R, et al. (2003). No evidence of correlation between p53 codon 72 polymorphism and risk of bladder or breast carcinoma in Tunisian patients. Ann. N. Y. Acad. Sci. 1010: 764-770. http://dx.doi.org/10.1196/annals.1299.137 PMid:15033824   Maloney KE, Wiener JS and Walther PJ (1994). Oncogenic human papillomaviruses are rarely associated with squamous cell carcinoma of the bladder: evaluation by differential polymerase chain reaction. J. Urol. 151: 360-364. PMid:8283525   Matakidou A, Eisen T and Houlston RS (2003). TP53 polymorphisms and lung cancer risk: a systematic review and meta-analysis. Mutagenesis 18: 377-385. http://dx.doi.org/10.1093/mutage/geg008 PMid:12840112   Murgel de Castro Santos LE, Trindade Guilhen AC, Alves de AR, Garcia SL, et al. (2009). The role of TP53 Pro47Ser and Arg72Pro single nucleotide polymorphisms in the susceptibility to bladder cancer. Urol. Oncol. (in press). DOI: 10.1016/j.urolonc.2009.03.026. http://dx.doi.org/10.1016/j.urolonc.2009.03.026   Rubben H, Lutzeyer W, Fischer N, Deutz F, et al. (1988). Natural history and treatment of low and high risk superficial bladder tumors. J. Urol. 139: 283-285. PMid:3339726   Simoneau M, LaRue H and Fradet Y (1999). Low frequency of human papillomavirus infection in initial papillary bladder tumors. Urol. Res. 27: 180-184. http://dx.doi.org/10.1007/s002400050107 PMid:10422819   Soulitzis N, Sourvinos G, Dokianakis DN and Spandidos DA (2002). p53 codon 72 polymorphism and its association with bladder cancer. Cancer Lett. 179: 175-183. http://dx.doi.org/10.1016/S0304-3835(01)00867-9   Sousa H, Santos AM, Pinto D and Medeiros R (2007). Is the p53 codon 72 polymorphism a key biomarker for cervical cancer development? A meta-analysis review within European populations. Int. J. Mol. Med. 20: 731-741. PMid:17912468   Tommiska J, Eerola H, Heinonen M, Salonen L, et al. (2005). Breast cancer patients with p53 Pro72 homozygous genotype have a poorer survival. Clin. Cancer Res. 11: 5098-5103. http://dx.doi.org/10.1158/1078-0432.CCR-05-0173 PMid:16033823   Toruner GA, Ucar A, Tez M, Cetinkaya M, et al. (2001). p53 codon 72 polymorphism in bladder cancer - no evidence of association with increased risk or invasiveness. Urol. Res. 29: 393-395. http://dx.doi.org/10.1007/s002400100218 PMid:11828992   Zhou Y, Li N, Zhuang W, Liu GJ, et al. (2007). p53 codon 72 polymorphism and gastric cancer: a meta-analysis of the literature. Int. J. Cancer 121: 1481-1486. http://dx.doi.org/10.1002/ijc.22833 PMid:17546594