Publications

Found 12 results
Filters: Author is G.X. Wang  [Clear All Filters]
2016
S. J. Bi, Hong, X. J., Wang, G. X., Li, Y., Gao, Y. M., Yan, L., Wang, Y. J., Wang, W. D., Bi, S. J., Hong, X. J., Wang, G. X., Li, Y., Gao, Y. M., Yan, L., Wang, Y. J., and Wang, W. D., “Effect of domestication on microorganism diversity and anaerobic digestion of food waste”, vol. 15, p. -, 2016.
S. J. Bi, Hong, X. J., Wang, G. X., Li, Y., Gao, Y. M., Yan, L., Wang, Y. J., Wang, W. D., Bi, S. J., Hong, X. J., Wang, G. X., Li, Y., Gao, Y. M., Yan, L., Wang, Y. J., and Wang, W. D., “Effect of domestication on microorganism diversity and anaerobic digestion of food waste”, vol. 15, p. -, 2016.
Q. Chen, Du, H., Zhang, R., Zhao, J. H., Hu, Q. C., Wang, C., Wang, G. X., Tang, J. L., Wu, R. F., Chen, Q., Du, H., Zhang, R., Zhao, J. H., Hu, Q. C., Wang, C., Wang, G. X., Tang, J. L., and Wu, R. F., “Evaluation of novel assays for the detection of human papilloma virus in self-collected samples for cervical cancer screening”, vol. 15, p. -, 2016.
Q. Chen, Du, H., Zhang, R., Zhao, J. H., Hu, Q. C., Wang, C., Wang, G. X., Tang, J. L., Wu, R. F., Chen, Q., Du, H., Zhang, R., Zhao, J. H., Hu, Q. C., Wang, C., Wang, G. X., Tang, J. L., and Wu, R. F., “Evaluation of novel assays for the detection of human papilloma virus in self-collected samples for cervical cancer screening”, vol. 15, p. -, 2016.
Z. Q. Huang, Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., Zeng, T., Huang, Z. Q., Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., Zeng, T., Huang, Z. Q., Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., and Zeng, T., “Systematic tracking of altered modules identifies disrupted pathways in teratozoospermia”, vol. 15, p. -, 2016.
Z. Q. Huang, Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., Zeng, T., Huang, Z. Q., Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., Zeng, T., Huang, Z. Q., Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., and Zeng, T., “Systematic tracking of altered modules identifies disrupted pathways in teratozoospermia”, vol. 15, p. -, 2016.
Z. Q. Huang, Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., Zeng, T., Huang, Z. Q., Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., Zeng, T., Huang, Z. Q., Wang, G. X., Jiang, X. L., Tian, E. P., Yao, W. L., and Zeng, T., “Systematic tracking of altered modules identifies disrupted pathways in teratozoospermia”, vol. 15, p. -, 2016.
2015
W. Tian, Bi, Y. H., Zeng, W., Jiang, W., Xue, Y. H., Wang, G. X., and Liu, S. P., “Diversity of endophytic fungi of Myricaria laxiflora grown under pre- and post-flooding conditions”, vol. 14, pp. 10849-10862, 2015.
2014
G. X. Wang, Hu, L., Zhang, Z., and Liu, D. P., “Construction of an adenoviral expression vector carrying FLAG and hrGFP-1 genes and its expression in bone marrow mesenchymal stem cells”, vol. 13, pp. 1070-1078, 2014.
G. X. Wang, Hu, L., Hu, H. X., Zhang, Z., and Liu, D. P., “In vivo osteogenic activity of bone marrow stromal stem cells transfected with Ad-GFP-hBMP-2”, vol. 13, pp. 4456-4465, 2014.
C. R. Mi, Wang, H., Jiang, H., Sun, R. P., and Wang, G. X., “Mutation screening of TSC1 and TSC2 genes in Chinese Han children with tuberous sclerosis complex”, vol. 13. pp. 2102-2106, 2014.
2010
G. X. Wang, Sun, R. P., and Song, F. L., “A novel RUNX2 mutation (T420I) in Chinese patients with cleidocranial dysplasia”, vol. 9, pp. 41-47, 2010.
Brooks JK and Nikitakis NG (2008). Multiple unerupted teeth. Cleidocranial dysplasia. Gen. Dent. 56: 393, 395-396. PMid:19284203   Cunningham ML, Seto ML, Hing AV, Bull MJ, et al. (2006). Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations. Birth Defects Res. A Clin. Mol. Teratol. 76: 78-85. http://dx.doi.org/10.1002/bdra.20231 PMid:16463420   Lee B, Thirunavukkarasu K, Zhou L, Pastore L, et al. (1997). Missense mutations abolishing DNA binding of the osteoblast-specific transcription factor OSF2/CBFA1 in cleidocranial dysplasia. Nat. Genet. 16: 307-310. http://dx.doi.org/10.1038/ng0797-307 PMid:9207800   Lee MT, Tsai AC, Chou CH, Sun FM, et al. (2008). Intragenic microdeletion of RUNX2 is a novel mechanism for cleidocranial dysplasia. Genomic Med. 2: 45-49. http://dx.doi.org/10.1007/s11568-008-9024-y PMid:18696259 PMCid:2518658   Lo Muzio L, Tete S, Mastrangelo F, Cazzolla AP, et al. (2007). A novel mutation of gene CBFA1/RUNX2 in cleidocranial dysplasia. Ann. Clin. Lab. Sci. 37: 115-120. PMid:17522365   Mundlos S, Otto F, Mundlos C, Mulliken JB, et al. (1997). Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia. Cell 89: 773-779. http://dx.doi.org/10.1016/S0092-8674(00)80260-3   Otto F, Thornell AP, Crompton T, Denzel A, et al. (1997). Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development. Cell 89: 765-771. http://dx.doi.org/10.1016/S0092-8674(00)80259-7   Quack I, Vonderstrass B, Stock M, Aylsworth AS, et al. (1999). Mutation analysis of core binding factor A1 in patients with cleidocranial dysplasia. Am. J. Hum. Genet. 65: 1268-1278. http://dx.doi.org/10.1086/302622 PMid:10521292 PMCid:1288279   Shen Z, Zou CC, Yang RW and Zhao ZY (2009). Cleidocranial dysplasia: report of 3 cases and literature review. Clin. Pediatr. 48: 194-198. http://dx.doi.org/10.1177/0009922808323107 PMid:18832541   Yoshida T, Kanegane H, Osato M, Yanagida M, et al. (2002). Functional analysis of RUNX2 mutations in Japanese patients with cleidocranial dysplasia demonstrates novel genotype-phenotype correlations. Am. J. Hum. Genet. 71: 724-738. http://dx.doi.org/10.1086/342717 PMid:12196916 PMCid:378531   Zhou G, Chen Y, Zhou L, Thirunavukkarasu K, et al. (1999). CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia. Hum. Mol. Genet. 8: 2311-2316. http://dx.doi.org/10.1093/hmg/8.12.2311 PMid:10545612