Chen L - Search Results

1

FGF/FGFR signaling in health and disease.

Xie Y, Su N, Yang J, Tan Q, Huang S, Jin M, Ni Z, Zhang B, Zhang D, Luo F, Chen H, Sun X, Feng JQ, Qi H, Chen L. Xie Y, et al. Among authors: chen l, chen h. Signal Transduct Target Ther. 2020 Sep 2;5(1):181. doi: 10.1038/s41392-020-00222-7. Signal Transduct Target Ther. 2020. PMID: 32879300 Free PMC article. Review.

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. Among authors: chen l, chen b. 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

Roles of FGF signaling in skeletal development and human genetic diseases.

Chen L, Deng CX. Chen L, et al. Front Biosci. 2005 May 1;10:1961-76. doi: 10.2741/1671. Front Biosci. 2005. PMID: 15769677 Review.

4

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

Su N, Du X, Chen L. Su N, et al. Among authors: chen l. 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: chen z, chen l. Bone. 2008 Apr;42(4):631-43. doi: 10.1016/j.bone.2007.11.019. Epub 2008 Jan 31. Bone. 2008. PMID: 18242159

6

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: chen l. 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

7

[The change in Toll-like receptor 4 gene expression in skeleton of endotoxemia mice].

Zhao ZY, Yang J, Su N, Lei ZX, Chen MM, Jin M, Li FB, Xie YL, Chen L. Zhao ZY, et al. Among authors: chen mm, chen l. Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2009 Jan;21(1):13-6. Zhongguo Wei Zhong Bing Ji Jiu Yi Xue. 2009. PMID: 19141183 Chinese.

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: chen l, chen b. 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: chen l, chen s, chen d. 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. Among authors: chen z, chen l. 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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