Chen YL - Search Results

1

[ASS1 mutation leading to citrullinemia I in a Chinese Han family].

Hu P, Zhou XY, Ma DY, Sun Y, Zhang XJ, Han SP, Yu ZB, Jiang T, Chen YL, Xu Z. Hu P, et al. Among authors: chen yl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Dec;28(6):630-3. doi: 10.3760/cma.j.issn.1003-9406.2011.06.007. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011. PMID: 22161093 Chinese.

2

Transcutaneous bilirubin nomogram for predicting neonatal hyperbilirubinemia in healthy term and late-preterm Chinese infants.

Yu ZB, Dong XY, Han SP, Chen YL, Qiu YF, Sha L, Sun Q, Guo XR. Yu ZB, et al. Among authors: chen yl. Eur J Pediatr. 2011 Feb;170(2):185-91. doi: 10.1007/s00431-010-1281-9. Epub 2010 Sep 3. Eur J Pediatr. 2011. PMID: 20814696

3

Long-term consequences of the early treatment of children with congenital hypothyroidism detected by neonatal screening in Nanjing, China: a 12-year follow-up study.

Sun Q, Chen YL, Yu ZB, Han SP, Dong XY, Qiu YF, Sha L, Guo XR. Sun Q, et al. Among authors: chen yl. J Trop Pediatr. 2012 Feb;58(1):79-80. doi: 10.1093/tropej/fmr010. Epub 2011 Feb 4. J Trop Pediatr. 2012. PMID: 21296863

4

[Effects of maternal deficiency of folic acid during pregnancy on pulmonary development and SP-A expression in newborn rats].

Qiao LX, Yu ZB, Han SP, Gu XQ, Chen YL, Sha L, Jin JX, Yan LB, Guo XR. Qiao LX, et al. Among authors: chen yl. Zhongguo Dang Dai Er Ke Za Zhi. 2011 Jul;13(7):573-6. Zhongguo Dang Dai Er Ke Za Zhi. 2011. PMID: 21752326 Free article. Chinese.

5

ShRNA-mediated gene silencing of AHR promotes the differentiation of P19 mouse embryonic carcinoma cells into cardiomyocytes.

Zhu C, Chen YL, Wang XJ, Hu XS, Yu ZB, Han SP. Zhu C, et al. Among authors: chen yl. Mol Med Rep. 2012 Sep;6(3):513-8. doi: 10.3892/mmr.2012.941. Epub 2012 Jun 8. Mol Med Rep. 2012. PMID: 22684894

6

Differential expression profile of MicroRNAs during differentiation of cardiomyocytes exposed to polychlorinated biphenyls.

Zhu C, Yu ZB, Zhu JG, Hu XS, Chen YL, Qiu YF, Xu ZF, Qian LM, Han SP. Zhu C, et al. Among authors: chen yl. Int J Mol Sci. 2012 Nov 28;13(12):15955-66. doi: 10.3390/ijms131215955. Int J Mol Sci. 2012. PMID: 23443104 Free PMC article.

7

[Development and application of a method for molecular diagnosis of 21-hydroxylase deficiency].

Ma DY, Sun Y, Chen Y, Yang B, Cheng J, Huang ML, Zhang J, Zhang JJ, Hu P, Lin Y, Jiang T, Xu ZF. Ma DY, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Feb;30(1):49-54. doi: 10.3760/cma.j.issn.1003-9406.2013.01.012. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23450479 Chinese.

8

[Molecular diagnosis of OTC gene mutation in a Chinese family with ornithine transcarbamylase deficiency].

Meng LL, Jiang T, Qin L, Ma DY, Chen YL, Han SP, Yu ZB, Guo XR, Hu P, Xu ZF. Meng LL, et al. Among authors: chen yl. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Apr;30(2):195-8. doi: 10.3760/cma.j.issn.1003-9406.2013.04.016. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013. PMID: 23568734 Chinese.

9

Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency.

Ma D, Chen Y, Sun Y, Yang B, Cheng J, Huang M, Zhang J, Zhang J, Hu P, Lin Y, Jiang T, Xu Z. Ma D, et al. Clin Biochem. 2014 Apr;47(6):455-63. doi: 10.1016/j.clinbiochem.2014.01.019. Epub 2014 Feb 3. Clin Biochem. 2014. PMID: 24503005

10

Neonatal lupus erythematosus with severe persistent pulmonary hypertension.

Zhuang B, Chen Y, Han S. Zhuang B, et al. QJM. 2024 Jul 29:hcae134. doi: 10.1093/qjmed/hcae134. Online ahead of print. QJM. 2024. PMID: 39073906 No abstract available.

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