Ren X - Search Results

1

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

2

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.

3

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.

4

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.

5

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.

6

Novel WNT1 mutations in children with osteogenesis imperfecta: Clinical and functional characterization.

Lu Y, Ren X, Wang Y, Bardai G, Sturm M, Dai Y, Riess O, Zhang Y, Li H, Li T, Zhai N, Zhang J, Rauch F, Han J. Lu Y, et al. Among authors: ren x. Bone. 2018 Sep;114:144-149. doi: 10.1016/j.bone.2018.06.018. Epub 2018 Jun 20. Bone. 2018. PMID: 29935254

7

The impact of the intestinal microbiome on bone health.

Zhang J, Lu Y, Wang Y, Ren X, Han J. Zhang J, et al. Among authors: ren x. Intractable Rare Dis Res. 2018 Aug;7(3):148-155. doi: 10.5582/irdr.2018.01055. Intractable Rare Dis Res. 2018. PMID: 30181933 Free PMC article. Review.

8

Molecular mechanisms and clinical manifestations of rare genetic disorders associated with type I collagen.

Lu Y, Zhang S, Wang Y, Ren X, Han J. Lu Y, et al. Among authors: ren x. Intractable Rare Dis Res. 2019 May;8(2):98-107. doi: 10.5582/irdr.2019.01064. Intractable Rare Dis Res. 2019. PMID: 31218159 Free PMC article. Review.

9

Current diagnosis and management of rare pediatric diseases in China.

Yang D, Ren X, Lu Y, Han J. Yang D, et al. Among authors: ren x. Intractable Rare Dis Res. 2021 Nov;10(4):223-237. doi: 10.5582/irdr.2021.01134. Intractable Rare Dis Res. 2021. PMID: 34877234 Free PMC article. Review.

10

Localization of myocilin to the golgi apparatus in Schlemm's canal cells.

O'Brien ET, Ren X, Wang Y. O'Brien ET, et al. Among authors: ren x. Invest Ophthalmol Vis Sci. 2000 Nov;41(12):3842-9. Invest Ophthalmol Vis Sci. 2000. PMID: 11053284

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