Wang Y - Search Results

1

Osteogenesis imperfecta type III/Ehlers-Danlos overlap syndrome in a Chinese man.

Lu Y, Wang Y, Rauch F, Li H, Zhang Y, Zhai N, Zhang J, Ren X, Han J. Lu Y, et al. Among authors: wang y. Intractable Rare Dis Res. 2018 Feb;7(1):37-41. doi: 10.5582/irdr.2018.01010. Intractable Rare Dis Res. 2018. PMID: 29552444 Free PMC article.

2

[Screening of bone-related microRNAs in serum of patients with osteogenesis imperfect].

Wang Z, Lu Y, Ren X, Wang Y, Li Z, Xu C, Han J. Wang Z, et al. Among authors: wang y. Sheng Wu Gong Cheng Xue Bao. 2012 Oct;28(10):1245-52. Sheng Wu Gong Cheng Xue Bao. 2012. PMID: 23311139 Chinese.

3

Mutational and structural characteristics of four novel heterozygous C-propeptide mutations in the proα1(I) collagen gene in Chinese osteogenesis imperfecta patients.

Lu Y, Ren X, Wang Y, Li T, Li F, Wang S, Xu C, Wu G, Li H, Li G, Zhao F, Wang Z, Mo X, Han J. Lu Y, et al. Among authors: wang z, wang y, wang s. Clin Endocrinol (Oxf). 2014 Apr;80(4):524-31. doi: 10.1111/cen.12354. Epub 2014 Jan 12. Clin Endocrinol (Oxf). 2014. PMID: 24147872

4

Serum microRNA is a promising biomarker for osteogenesis imperfecta.

Wang Z, Lu Y, Zhang X, Ren X, Wang Y, Li Z, Xu C, Han J. Wang Z, et al. Among authors: wang y. Intractable Rare Dis Res. 2012 May;1(2):81-5. doi: 10.5582/irdr.2012.v1.2.81. Intractable Rare Dis Res. 2012. PMID: 25343076 Free PMC article.

5

Low concentrations of zoledronic acid are better at regulating bone formation and repair.

Yang X, Lu Y, Li Z, Wang Y, Zhao F, Han J. Yang X, et al. Among authors: wang y. Intractable Rare Dis Res. 2013 Feb;2(1):18-23. doi: 10.5582/irdr.2013.v2.1.18. Intractable Rare Dis Res. 2013. PMID: 25343096 Free PMC article.

6

Heterozygous mutation of c.3521C>T in COL1A1 may cause mild osteogenesis imperfecta/Ehlers-Danlos syndrome in a Chinese family.

Shi X, Lu Y, Wang Y, Zhang YA, Teng Y, Han W, Han Z, Li T, Chen M, Liu J, Fang F, Dou C, Ren X, Han J. Shi X, et al. Among authors: wang y. Intractable Rare Dis Res. 2015 Feb;4(1):49-53. doi: 10.5582/irdr.2014.01039. Intractable Rare Dis Res. 2015. PMID: 25674388 Free PMC article.

7

The expression profile of IFITM family gene in rats.

Lu Y, Zuo Q, Zhang Y, Wang Y, Li T, Han J. Lu Y, et al. Among authors: wang y. Intractable Rare Dis Res. 2017 Nov;6(4):274-280. doi: 10.5582/irdr.2017.01066. Intractable Rare Dis Res. 2017. PMID: 29259856 Free PMC article.

8

Circular RNAs and hereditary bone diseases.

Zhai N, Lu Y, Wang Y, Ren X, Han J. Zhai N, et al. Among authors: wang y. Intractable Rare Dis Res. 2018 Feb;7(1):1-6. doi: 10.5582/irdr.2018.01013. Intractable Rare Dis Res. 2018. PMID: 29552438 Free PMC article. Review.

9

Complex heterozygous WNT1 mutation in severe recessive osteogenesis imperfecta of a Chinese patient.

Lu Y, Dai Y, Wang Y, Zhai N, Zhang J, Liu J, Yin X, Li T, Ren X, Han J. Lu Y, et al. Among authors: wang y. Intractable Rare Dis Res. 2018 Feb;7(1):19-24. doi: 10.5582/irdr.2018.01014. Intractable Rare Dis Res. 2018. PMID: 29552441 Free PMC article.

10

Novel NTRK1 mutations in Chinese patients with congenital insensitivity to pain with anhidrosis.

Geng X, Liu Y, Ren X, Guan Y, Wang Y, Mao B, Zhao X, Zhang X. Geng X, et al. Among authors: wang y. Mol Pain. 2018 Jan-Dec;14:1744806918781140. doi: 10.1177/1744806918781140. Epub 2018 May 17. Mol Pain. 2018. PMID: 29770739 Free PMC article.

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