Zhou G - Search Results

1

Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte-specific expression in vivo.

Zheng Q, Zhou G, Morello R, Chen Y, Garcia-Rojas X, Lee B. Zheng Q, et al. Among authors: zhou g. J Cell Biol. 2003 Sep 1;162(5):833-42. doi: 10.1083/jcb.200211089. J Cell Biol. 2003. PMID: 12952936 Free PMC article.

2

Dysregulation of chondrogenesis in human cleidocranial dysplasia.

Zheng Q, Sebald E, Zhou G, Chen Y, Wilcox W, Lee B, Krakow D. Zheng Q, et al. Among authors: zhou g. Am J Hum Genet. 2005 Aug;77(2):305-12. doi: 10.1086/432261. Epub 2005 Jun 10. Am J Hum Genet. 2005. PMID: 15952089 Free PMC article.

3

Mutations and promoter SNPs in RUNX2, a transcriptional regulator of bone formation.

Napierala D, Garcia-Rojas X, Sam K, Wakui K, Chen C, Mendoza-Londono R, Zhou G, Zheng Q, Lee B. Napierala D, et al. Among authors: zhou g. Mol Genet Metab. 2005 Sep-Oct;86(1-2):257-68. doi: 10.1016/j.ymgme.2005.07.012. Mol Genet Metab. 2005. PMID: 16140555

4

Dominance of SOX9 function over RUNX2 during skeletogenesis.

Zhou G, Zheng Q, Engin F, Munivez E, Chen Y, Sebald E, Krakow D, Lee B. Zhou G, et al. Proc Natl Acad Sci U S A. 2006 Dec 12;103(50):19004-9. doi: 10.1073/pnas.0605170103. Epub 2006 Dec 1. Proc Natl Acad Sci U S A. 2006. PMID: 17142326 Free PMC article.

5

Localization of the cis-enhancer element for mouse type X collagen expression in hypertrophic chondrocytes in vivo.

Zheng Q, Keller B, Zhou G, Napierala D, Chen Y, Zabel B, Parker AE, Lee B. Zheng Q, et al. Among authors: zhou g. J Bone Miner Res. 2009 Jun;24(6):1022-32. doi: 10.1359/jbmr.081249. J Bone Miner Res. 2009. PMID: 19113928 Free PMC article.

6

Targeted and sustained Sox9 expression in mouse hypertrophic chondrocytes causes severe and spontaneous osteoarthritis by perturbing cartilage homeostasis.

Liang B, Mamidi MK, Samsa WE, Chen Y, Lee B, Zheng Q, Zhou G. Liang B, et al. Among authors: zhou g. Am J Transl Res. 2020 Mar 15;12(3):1056-1069. eCollection 2020. Am J Transl Res. 2020. PMID: 32269734 Free PMC article.

7

CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.

Zhou G, Chen Y, Zhou L, Thirunavukkarasu K, Hecht J, Chitayat D, Gelb BD, Pirinen S, Berry SA, Greenberg CR, Karsenty G, Lee B. Zhou G, et al. Among authors: zhou l. Hum Mol Genet. 1999 Nov;8(12):2311-6. doi: 10.1093/hmg/8.12.2311. Hum Mol Genet. 1999. PMID: 10545612

8

Regulation of glomerular basement membrane collagen expression by LMX1B contributes to renal disease in nail patella syndrome.

Morello R, Zhou G, Dreyer SD, Harvey SJ, Ninomiya Y, Thorner PS, Miner JH, Cole W, Winterpacht A, Zabel B, Oberg KC, Lee B. Morello R, et al. Among authors: zhou g. Nat Genet. 2001 Feb;27(2):205-8. doi: 10.1038/84853. Nat Genet. 2001. PMID: 11175791

9

Dimorphic effects of Notch signaling in bone homeostasis.

Engin F, Yao Z, Yang T, Zhou G, Bertin T, Jiang MM, Chen Y, Wang L, Zheng H, Sutton RE, Boyce BF, Lee B. Engin F, et al. Among authors: zhou g. Nat Med. 2008 Mar;14(3):299-305. doi: 10.1038/nm1712. Epub 2008 Feb 24. Nat Med. 2008. PMID: 18297084 Free PMC article.

10

The transcriptional cofactor Jab1/Cops5 is crucial for BMP-mediated mouse chondrocyte differentiation by repressing p53 activity.

Mamidi MK, Samsa WE, Bashur LA, Chen Y, Chan R, Lee B, Zhou G. Mamidi MK, et al. Among authors: zhou g. J Cell Physiol. 2021 Aug;236(8):5686-5697. doi: 10.1002/jcp.30254. Epub 2021 Jan 3. J Cell Physiol. 2021. PMID: 33393086 Free PMC article.

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