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Items: 1 to 20 of 98

1.

Dysfunction of collagen synthesis and secretion in chondrocytes induced by wisp3 mutation.

Wang M, Man XF, Liu YQ, Liao EY, Shen ZF, Luo XH, Guo LJ, Wu XP, Zhou HD.

Int J Endocrinol. 2013;2013:679763. doi: 10.1155/2013/679763. Epub 2013 Mar 19.

3.

[Construction of WISP3 gene's mutants in SEDT-PA and their expression in COS-7 cells].

Wang M, Peng YQ, Zhou HD, Zhai MX, He YL, Xie H.

Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2008 Jan;33(1):8-15. Chinese.

4.

WISP3 suppresses insulin-like growth factor signaling in human chondrocytes.

Cui RR, Huang J, Yi L, Xie H, Zhou HD, Yuan LQ, Wang M, Peng YQ, Luo XH, Liao EY.

Mol Cell Endocrinol. 2007 Dec 15;279(1-2):1-8. Epub 2007 Aug 28.

PMID:
17942216
5.

Novel WISP3 mutations causing spondyloepiphyseal dysplasia tarda with progressive arthropathy in two unrelated Chinese families.

Liu L, Li N, Zhao Z, Li W, Xia W.

Joint Bone Spine. 2015 Mar;82(2):125-8. doi: 10.1016/j.jbspin.2014.10.005. Epub 2014 Dec 29.

PMID:
25553839
6.

WISP3-dependent regulation of type II collagen and aggrecan production in chondrocytes.

Sen M, Cheng YH, Goldring MB, Lotz MK, Carson DA.

Arthritis Rheum. 2004 Feb;50(2):488-97.

7.

[Characterization of biologic behaviors and cDNA expression of articular chondrocytes in spondyloepiphyseal dysplasia tarda with progressive arthropathy].

Zhou HD, Peng YQ, Gu W, Li J, Xie H, Liu M, Luo XH, Huang QX, Guo LJ, Yuan LQ, Ni JD, Zhang XS, Liao EY.

Zhonghua Nei Ke Za Zhi. 2005 Jan;44(1):16-21. Chinese.

PMID:
15769391
8.

[Proliferation, differentiation, and gene expression profile of osteoblast of patient with spondyloepiphyseal dysplasia tarda with progressive arthropathy].

Zhou HD, Huang QX, Xie H, Liu M, Guo LJ, Yuan LQ, Sui GL, Zhai MX, Peng YQ, Gu W, Ni JD, Zhang XS, Liao EY.

Zhonghua Yi Xue Za Zhi. 2005 May 25;85(19):1310-4. Chinese.

PMID:
16029628
9.

WISP3-IGF1 interaction regulates chondrocyte hypertrophy.

Repudi SR, Patra M, Sen M.

J Cell Sci. 2013 Apr 1;126(Pt 7):1650-8. doi: 10.1242/jcs.119859. Epub 2013 Feb 19.

10.

[Pathology and molecular pathogenesis of spondyloepiphyseal dysplasia tarda with progressive arthropathy caused by compound CCN6 heterogeneous gene mutations].

Peng YQ, Liao EY, Gu HM, Wei QY, Zhou HD, Li J, Xie H, Zhai MX, Tan LH, Luo XH, Wu XP, Hu PA, Ni JD, Su X, Jiang Y, Dai RC, Guo LJ, Yuan LQ, Wang M, Wang PF, Liu SP, Yang Y, Wang C, Sui GL, Fang TY.

Zhonghua Yi Xue Za Zhi. 2004 Nov 2;84(21):1796-803. Chinese.

PMID:
15631777
11.

Cellular and molecular responses in progressive pseudorheumatoid dysplasia articular cartilage associated with compound heterozygous WISP3 gene mutation.

Zhou HD, Bu YH, Peng YQ, Xie H, Wang M, Yuan LQ, Jiang Y, Li D, Wei QY, He YL, Xiao T, Ni JD, Liao EY.

J Mol Med (Berl). 2007 Sep;85(9):985-96. Epub 2007 May 5.

PMID:
17483925
12.

Analysis of the WISP3 gene in Indian families with progressive pseudorheumatoid dysplasia.

Dalal A, Bhavani G SL, Togarrati PP, Bierhals T, Nandineni MR, Danda S, Danda D, Shah H, Vijayan S, Gowrishankar K, Phadke SR, Bidchol AM, Rao AP, Nampoothiri S, Kutsche K, Girisha KM.

Am J Med Genet A. 2012 Nov;158A(11):2820-8. doi: 10.1002/ajmg.a.35620. Epub 2012 Sep 17.

PMID:
22987568
13.
14.

Altered synthesis of cartilage-specific proteoglycans by mutant human cartilage oligomeric matrix protein.

Kwak YH, Roh JY, Lee KS, Park HW, Kim HW.

Clin Orthop Surg. 2009 Dec;1(4):181-7. doi: 10.4055/cios.2009.1.4.181. Epub 2009 Nov 25.

15.

[Clinical diagnosis and WISP3 gene mutation analysis for progressive pseudorheumatoid dysplasia].

Ye J, Zhang HW, Wang T, Cao LF, Qiu WJ, Han LS, Zhang YF, Gu XF.

Zhonghua Er Ke Za Zhi. 2010 Mar;48(3):194-8. Chinese.

PMID:
20426955
17.

Role of WISP3 siRNA in proliferation, apoptosis and invasion of bladder cancer cells.

Zeng J, Liao Y, Zhou J, Yang G, Ding K, Zhang X.

Int J Clin Exp Med. 2015 Aug 15;8(8):12792-800. eCollection 2015.

18.

Frameshift mutation of WISP3 gene and its regional heterogeneity in gastric and colorectal cancers.

Lee JH, Choi YJ, Je EM, Kim HS, Yoo NJ, Lee SH.

Hum Pathol. 2016 Apr;50:146-52. doi: 10.1016/j.humpath.2015.12.009. Epub 2015 Dec 30.

PMID:
26997449
19.

The CCN family member Wisp3, mutant in progressive pseudorheumatoid dysplasia, modulates BMP and Wnt signaling.

Nakamura Y, Weidinger G, Liang JO, Aquilina-Beck A, Tamai K, Moon RT, Warman ML.

J Clin Invest. 2007 Oct;117(10):3075-86.

20.

Biochemical consequences of sedlin mutations that cause spondyloepiphyseal dysplasia tarda.

Choi MY, Chan CC, Chan D, Luk KD, Cheah KS, Tanner JA.

Biochem J. 2009 Sep 25;423(2):233-42. doi: 10.1042/BJ20090541.

PMID:
19650763

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