Du X - Search Results

1

Adeno-Associated Virus-Mediated RNAi against Mutant Alleles Attenuates Abnormal Calvarial Phenotypes in an Apert Syndrome Mouse Model.

Luo F, Xie Y, Wang Z, Huang J, Tan Q, Sun X, Li F, Li C, Liu M, Zhang D, Xu M, Su N, Ni Z, Jiang W, Chang J, Chen H, Chen S, Xu X, Deng C, Wang Z, Du X, Chen L. Luo F, et al. Among authors: du x. Mol Ther Nucleic Acids. 2018 Dec 7;13:291-302. doi: 10.1016/j.omtn.2018.09.012. Epub 2018 Sep 22. Mol Ther Nucleic Acids. 2018. PMID: 30321816 Free PMC article.

2

[Gly374Arg mutation in Fgfr3 causes achondroplasia in mice].

Wang JM, Du XL, Li CL, Yin LJ, Chen B, Sun J, Su N, Zhao L, Song RH, Song WW, Chen L, Deng CX. Wang JM, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004 Dec;21(6):537-41. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2004. PMID: 15583977 Chinese.

3

[Effect of p53 on the variation of renal tubular epithelial cells after kidney ischemia/reperfusion injury].

Li KL, Du XL, Song RH, Zhao L, He YN, Zhang JG, Chen L. Li KL, et al. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2007 Jan;23(1):6-10. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2007. PMID: 17210095 Chinese.

4

FGF signaling: its role in bone development and human skeleton diseases.

Su N, Du X, Chen L. Su N, et al. Among authors: du x. Front Biosci. 2008 Jan 1;13:2842-65. doi: 10.2741/2890. Front Biosci. 2008. PMID: 17981758 Review.

5

A Pro253Arg mutation in fibroblast growth factor receptor 2 (Fgfr2) causes skeleton malformation mimicking human Apert syndrome by affecting both chondrogenesis and osteogenesis.

Yin L, Du X, Li C, Xu X, Chen Z, Su N, Zhao L, Qi H, Li F, Xue J, Yang J, Jin M, Deng C, Chen L. Yin L, et al. Among authors: du x. Bone. 2008 Apr;42(4):631-43. doi: 10.1016/j.bone.2007.11.019. Epub 2008 Jan 31. Bone. 2008. PMID: 18242159

6

[Generation of bone morphogenetic protein 4 conditional RNA interference mice].

Li FB, DU XL, Yu Y, Zhao L, He QF, Chen L. Li FB, et al. Yi Chuan. 2008 Mar;30(3):341-6. doi: 10.3724/sp.j.1005.2008.00341. Yi Chuan. 2008. PMID: 18332004 Chinese.

7

Gain-of-function mutation of FGFR3 results in impaired fracture healing due to inhibition of chondrocyte differentiation.

Su N, Yang J, Xie Y, Du X, Lu X, Yin Z, Yin L, Qi H, Zhao L, Feng J, Chen L. Su N, et al. Among authors: du x. Biochem Biophys Res Commun. 2008 Nov 21;376(3):454-9. doi: 10.1016/j.bbrc.2008.08.165. Epub 2008 Sep 24. Biochem Biophys Res Commun. 2008. PMID: 18789890

8

Fibroblast growth factor receptor 1 regulates the differentiation and activation of osteoclasts through Erk1/2 pathway.

Lu X, Su N, Yang J, Huang W, Li C, Zhao L, He Q, Du X, Shen Y, Chen B, Chen L. Lu X, et al. Among authors: du x. Biochem Biophys Res Commun. 2009 Dec 18;390(3):494-9. doi: 10.1016/j.bbrc.2009.09.123. Epub 2009 Oct 1. Biochem Biophys Res Commun. 2009. PMID: 19800312

9

Gain-of-function mutation in FGFR3 in mice leads to decreased bone mass by affecting both osteoblastogenesis and osteoclastogenesis.

Su N, Sun Q, Li C, Lu X, Qi H, Chen S, Yang J, Du X, Zhao L, He Q, Jin M, Shen Y, Chen D, Chen L. Su N, et al. Among authors: du x. Hum Mol Genet. 2010 Apr 1;19(7):1199-210. doi: 10.1093/hmg/ddp590. Epub 2010 Jan 6. Hum Mol Genet. 2010. PMID: 20053668 Free PMC article.

10

Dynamic morphological changes in the skulls of mice mimicking human Apert syndrome resulting from gain-of-function mutation of FGFR2 (P253R).

Du X, Weng T, Sun Q, Su N, Chen Z, Qi H, Jin M, Yin L, He Q, Chen L. Du X, et al. J Anat. 2010 Aug;217(2):97-105. doi: 10.1111/j.1469-7580.2010.01248.x. Epub 2010 Jun 17. J Anat. 2010. PMID: 20557404 Free PMC article.

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