Ren X - 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: ren x. 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: ren x. Sheng Wu Gong Cheng Xue Bao. 2012 Oct;28(10):1245-52. Sheng Wu Gong Cheng Xue Bao. 2012. PMID: 23311139 Chinese.

3

A rare case of osteogenesis imperfecta combined with complete tooth loss.

Lu Y, Zhao F, Ren X, Li Z, Yang X, Han J. Lu Y, et al. Among authors: ren x. J Pediatr Endocrinol Metab. 2014 Jan;27(1-2):143-7. doi: 10.1515/jpem-2013-0069. J Pediatr Endocrinol Metab. 2014. PMID: 23934635

4

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: ren x. Clin Endocrinol (Oxf). 2014 Apr;80(4):524-31. doi: 10.1111/cen.12354. Epub 2014 Jan 12. Clin Endocrinol (Oxf). 2014. PMID: 24147872

5

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: ren x. 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.

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: ren x. 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

Effect of Preoperative Growth Status on Clinical Outcomes After Living-Donor Liver Transplantation in Infants.

Lu Y, Xia Q, Yang Y, Wan P, Hou J, Wang Y, Qiu B, Feng M, He K, Huang M, Ren X, Gao L, Zhang J. Lu Y, et al. Among authors: ren x. Transplant Proc. 2017 Oct;49(8):1848-1854. doi: 10.1016/j.transproceed.2017.06.036. Transplant Proc. 2017. PMID: 28923636

8

Circular RNAs and hereditary bone diseases.

Zhai N, Lu Y, Wang Y, Ren X, Han J. Zhai N, et al. Among authors: ren x. 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: ren x. 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: ren x. Mol Pain. 2018 Jan-Dec;14:1744806918781140. doi: 10.1177/1744806918781140. Epub 2018 May 17. Mol Pain. 2018. PMID: 29770739 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

11,184 results

Search Page

Filters