Chen Y - Search Results

1

Amniotic fluid stem cells provide considerable advantages in epidermal regeneration: B7H4 creates a moderate inflammation microenvironment to promote wound repair.

Sun Q, Li F, Li H, Chen RH, Gu YZ, Chen Y, Liang HS, You XR, Ding SS, Gao L, Wang YL, Qin MD, Zhang XG. Sun Q, et al. Among authors: chen rh, chen y. Sci Rep. 2015 Jun 23;5:11560. doi: 10.1038/srep11560. Sci Rep. 2015. PMID: 26101181 Free PMC article.

2

Direct Reprogramming of Human Amniotic Fluid Stem Cells by OCT4 and Application in Repairing of Cerebral Ischemia Damage.

Qin M, Chen R, Li H, Liang H, Xue Q, Li F, Chen Y, Zhang X. Qin M, et al. Among authors: chen r, chen y. Int J Biol Sci. 2016 Mar 11;12(5):558-68. doi: 10.7150/ijbs.11051. eCollection 2016. Int J Biol Sci. 2016. PMID: 27019637 Free PMC article.

3

Ischemic injury of the liver in a porcine model of cardiac death assessed by in vivo microdialysis.

Yi DH, Liu H, Chen Y, Li H, Xu T, Liu YF. Yi DH, et al. Among authors: chen y. Mol Biol Rep. 2014 Oct;41(10):6611-8. doi: 10.1007/s11033-014-3544-4. Epub 2014 Aug 29. Mol Biol Rep. 2014. PMID: 25167853

4

[A literature review of epidemiological studies on mutation hot spots of Chinese population with non-syndromic hearing loss].

Li H, Li Q, Li H, Chen Y. Li H, et al. Among authors: chen y. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Jul;26(13):589-94. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23002642 Review. Chinese.

5

[SLC26A4 mutations in a Chinese deafness family discovered by next-generation sequencing technology].

Mao J, Wei XM, Li H, Wang SN, Chen Y. Mao J, et al. Among authors: chen y. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012 Nov;47(11):942-5. Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2012. PMID: 23302201 Chinese.

6

Association of SNPs in genes involved in folate metabolism with the risk of congenital heart disease.

Wang B, Liu M, Yan W, Mao J, Jiang D, Li H, Chen Y. Wang B, et al. Among authors: chen y. J Matern Fetal Neonatal Med. 2013 Dec;26(18):1768-77. doi: 10.3109/14767058.2013.799648. Epub 2013 Jun 10. J Matern Fetal Neonatal Med. 2013. PMID: 23701284

7

[A microdeletion of chromosome 9q34.11 may cause suspected cerebral palsy].

Li H, Chen Y, Li Q, Liu M, Mao J, Song D, Li H. Li H, et al. Among authors: chen y. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014 Dec;31(6):725-9. doi: 10.3760/cma.j.issn.1003-9406.2014.06.009. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2014. PMID: 25449075 Chinese.

8

Methylenetetrahydrofolate reductase polymorphisms at 3'-untranslated region are associated with susceptibility to preterm birth.

Zhu Q, Chen Y, Dai J, Wang B, Liu M, Wang Y, Tao J, Li H. Zhu Q, et al. Among authors: chen y. Transl Pediatr. 2015 Jan;4(1):57-62. doi: 10.3978/j.issn.2224-4336.2015.01.02. Transl Pediatr. 2015. PMID: 26835361 Free PMC article.

9

Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy.

Mao J, Wang T, Wang BJ, Liu YH, Li H, Zhang J, Cram D, Chen Y. Mao J, et al. Among authors: chen y. Clin Chim Acta. 2014 Jun 10;433:190-3. doi: 10.1016/j.cca.2014.03.011. Epub 2014 Mar 22. Clin Chim Acta. 2014. PMID: 24667696

10

Association of UGT1A1 variants and hyperbilirubinemia in breast-fed full-term Chinese infants.

Zhou Y, Wang SN, Li H, Zha W, Wang X, Liu Y, Sun J, Peng Q, Li S, Chen Y, Jin L. Zhou Y, et al. Among authors: chen y. PLoS One. 2014 Aug 7;9(8):e104251. doi: 10.1371/journal.pone.0104251. eCollection 2014. PLoS One. 2014. PMID: 25102181 Free PMC article.

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