Publications

Found 18 results
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2015
B. F. Chen, Wang, R., Chen, Y. J., Zhu, Y., Ding, L., and Wen, Y. F., Association between HLA-DRB1 alleles and tuberculosis: a meta-analysis, vol. 14, pp. 15859-15868, 2015.
J. M. Xu, Song, X., Gao, F., and Wang, R., Association between the AGTR1 A1166C polymorphism and risk of IgA nephropathy: a meta-analysis, vol. 14, pp. 19371-19381, 2015.
Y. Dong, Pan, Y., Wang, R., Zhang, Z., Xi, Q., and Liu, R. - Z., Copy number variations in spermatogenic failure patients with chromosomal abnormalities and unexplained azoospermia, vol. 14, pp. 16041-16049, 2015.
X. Q. Yang, Yang, J., Wang, R., Zhang, S., Tan, Q. W., Lv, Q., Meng, W. T., Mo, X. M., and Li, H. J., Effect of specific silencing of EMMPRIN on the growth and cell cycle distribution of MCF-7 breast cancer cells, vol. 14, pp. 15730-15738, 2015.
R. F. Liu, Li, J. Q., Hou, R. X., Wang, R., and Zhang, K. M., Impact of BMMSCs from different sources on proliferation of CD34+ cells, vol. 14, pp. 474-482, 2015.
Z. Y. Chen, Wang, R., Huang, F., Yuan, D. D., and Li, S. R., Inhibition of gap junctions relieves the hepatotoxicity of TNF-α, vol. 14, pp. 11896-11904, 2015.
R. Wang, Jing, G., Lv, J., Song, H., Li, C., Wang, X., Xia, W., Wu, Y., Ren, G., and Guo, W., Interferon-α-2b as an adjuvant therapy prolongs survival of patients with previously resected oral muscosal melanoma, vol. 14, pp. 11944-11954, 2015.
C. F. Sheng, Wang, R., Liu, B. Y., Zhang, H. M., Fang, M., and Zheng, X., Post-surgical treatment of a patient with ectopic pheochromocytoma, vol. 14. pp. 2139-2145, 2015.
L. Zhang, Wang, R., Xiao, C. - S., Wu, Y., and Gao, C. - Q., Relationship between perioperative cardiovascular risk factors and bone marrow cells from patients undergoing coronary artery bypass grafting surgery, vol. 14, pp. 15233-15241, 2015.
R. Wang, Zheng, J., Zhang, D. - S., Yang, Y. - H., and Zhao, Z. - F., Wnt1-induced MAFK expression promotes osteosarcoma cell proliferation, vol. 14, pp. 7315-7325, 2015.
2012
F. - R. Wu, Liu, Y., Shang, M. - B., Yang, X. - X., Ding, B., Gao, J. - G., Wang, R., and Li, W. - Y., Differences in H3K4 trimethylation in in vivo and in vitro fertilization mouse preimplantation embryos, vol. 11, pp. 1099-1108, 2012.
Baqir S, Zhou Q, Renard JP and Smith LC (2002). Aberrant expression profile of imprinted genes in cloned mouse embryos reconstructed with ES cells treated with 5AzaC or TSA. Biol. Reprod. 66: 244-250. Dey SK, Lim H, Das SK, Reese J, et al. (2004). Molecular cues to implantation. Endocr. Rev. 25: 341-373. http://dx.doi.org/10.1210/er.2003-0020 PMid:15180948 Doherty AS, Mann MR, Tremblay KD, Bartolomei MS, et al. (2000). Differential effects of culture on imprinted H19 expression in the preimplantation mouse embryo. Biol. Reprod. 62: 1526-1535. http://dx.doi.org/10.1095/biolreprod62.6.1526 PMid:10819752 Eissenberg JC and Shilatifard A (2010). Histone H3 lysine 4 (H3K4) methylation in development and differentiation. Dev. Biol. 339: 240-249. http://dx.doi.org/10.1016/j.ydbio.2009.08.017 PMid:19703438 Flanagan JF, Mi LZ, Chruszcz M, Cymborowski M, et al. (2005). Double chromodomains cooperate to recognize the methylated histone H3 tail. Nature 438: 1181-1185. http://dx.doi.org/10.1038/nature04290 PMid:16372014 Fleming TP, Kwong WY, Porter R, Ursell E, et al. (2004). The embryo and its future. Biol. Reprod. 71: 1046-1054. http://dx.doi.org/10.1095/biolreprod.104.030957 PMid:15215194 Glaser S, Lubitz S, Loveland KL, Ohbo K, et al. (2009). The histone 3 lysine 4 methyltransferase, Mll2, is only required briefly in development and spermatogenesis. Epigenetics Chromatin 2: 5. http://dx.doi.org/10.1186/1756-8935-2-5 Guillemette B, Drogaris P, Lin HH, Armstrong H, et al. (2011). H3 lysine 4 is acetylated at active gene promoters and is regulated by H3 lysine 4 methylation. PLoS Genet. 7: e1001354. http://dx.doi.org/10.1371/journal.pgen.1001354 PMid:21483810    PMCid:3069113 Hamatani T, Carter MG, Sharov AA and Ko MS (2004). Dynamics of global gene expression changes during mouse preimplantation development. Dev. Cell 6: 117-131. http://dx.doi.org/10.1016/S1534-5807(03)00373-3 Huang JC, Yan LY, Lei ZL, Miao YL, et al. (2007a). Changes in histone acetylation during postovulatory aging of mouse oocyte. Biol. Reprod. 77: 666-670. http://dx.doi.org/10.1095/biolreprod.107.062703 PMid:17582009 Huang JC, Lei ZL, Shi LH, Miao YL, et al. (2007b). Comparison of histone modifications in in vivo and in vitro fertilization mouse embryos. Biochem. Biophys. Res. Commun. 354: 77-83. http://dx.doi.org/10.1016/j.bbrc.2006.12.163 PMid:17210126 Kim JM, Ogura A, Nagata M and Aoki F (2002). Analysis of the mechanism for chromatin remodeling in embryos reconstructed by somatic nuclear transfer. Biol. Reprod. 67: 760-766. http://dx.doi.org/10.1095/biolreprod.101.000612 PMid:12193382 Kim JM, Liu H, Tazaki M, Nagata M, et al. (2003). Changes in histone acetylation during mouse oocyte meiosis. J. Cell Biol. 162: 37-46. http://dx.doi.org/10.1083/jcb.200303047 PMid:12835313    PMCid:2172711 Li L, Zheng P and Dean J (2010). Maternal control of early mouse development. Development 137: 859-870. http://dx.doi.org/10.1242/dev.039487 PMid:20179092    PMCid:2834456 McLaren A (1971). Blastocysts in the mouse uterus: the effect of ovariectomy, progesterone and oestrogen. J. Endocrinol. 50: 515-526. http://dx.doi.org/10.1677/joe.0.0500515 PMid:5558058 Murata K, Kouzarides T, Bannister AJ and Gurdon JB (2010). Histone H3 lysine 4 methylation is associated with the transcriptional reprogramming efficiency of somatic nuclei by oocytes. Epigenetics Chromatin 3: 4. http://dx.doi.org/10.1186/1756-8935-3-4 Murray K (1964). The occurrence of epsilon-n-methyl lysine in histones. Biochemistry 3: 10-15. http://dx.doi.org/10.1021/bi00889a003 PMid:14114491 Nagy A, Gertsenstei M, Vintersten K and Behringer R (2003). Manipulating the Mouse Embryo: A Laboratory Manual. Cold Spring Harbor Laboratory Press, New York, 161-208. Nightingale KP, Gendreizig S, White DA, Bradbury C, et al. (2007). Cross-talk between histone modifications in response to histone deacetylase inhibitors: MLL4 links histone H3 acetylation and histone H3K4 methylation. J. Biol. Chem. 282: 4408-4416. http://dx.doi.org/10.1074/jbc.M606773200 PMid:17166833 Ruthenburg AJ, Allis CD and Wysocka J (2007). Methylation of lysine 4 on histone H3: intricacy of writing and reading a single epigenetic mark. Mol. Cell 25: 15-30. http://dx.doi.org/10.1016/j.molcel.2006.12.014 PMid:17218268 Shi X, Hong T, Walter KL, Ewalt M, et al. (2006). ING2 PHD domain links histone H3 lysine 4 methylation to active gene repression. Nature 442: 96-99. PMid:16728974    PMCid:3089773 Shilatifard A (2008). Molecular implementation and physiological roles for histone H3 lysine 4 (H3K4) methylation. Curr. Opin. Cell Biol. 20: 341-348. http://dx.doi.org/10.1016/j.ceb.2008.03.019 PMid:18508253    PMCid:2504688 Strömstedt M, Keeney DS, Waterman MR, Paria BC, et al. (1996). Preimplantation mouse blastocysts fail to express CYP genes required for estrogen biosynthesis. Mol. Reprod. Dev. 43: 428-436. http://dx.doi.org/10.1002/(SICI)1098-2795(199604)43:4<428::AID-MRD4>3.0.CO;2-R Wysocka J, Swigut T, Xiao H, Milne TA, et al. (2006). A PHD finger of NURF couples histone H3 lysine 4 trimethylation with chromatin remodelling. Nature 442: 86-90. PMid:16728976 Yamanaka K, Sugimura S, Wakai T, Kawahara M, et al. (2009). Acetylation level of histone H3 in early embryonic stages affects subsequent development of miniature pig somatic cell nuclear transfer embryos. J. Reprod. Dev. 55: 638-644. http://dx.doi.org/10.1262/jrd.20245 PMid:19700928 Young LE and Fairburn HR (2000). Improving the safety of embryo technologies: possible role of genomic imprinting. Theriogenology 53: 627-648. http://dx.doi.org/10.1016/S0093-691X(99)00263-0 Zhao Z, Fan L and Frick KM (2010). Epigenetic alterations regulate estradiol-induced enhancement of memory consolidation. Proc. Natl. Acad. Sci. U. S. A. 107: 5605-5610. http://dx.doi.org/10.1073/pnas.0910578107 PMid:20212170    PMCid:2851775