Shi C - Search Results

1

Melatonin ameliorates necrotizing enterocolitis by preventing Th17/Treg imbalance through activation of the AMPK/SIRT1 pathway.

Ma F, Hao H, Gao X, Cai Y, Zhou J, Liang P, Lv J, He Q, Shi C, Hu D, Chen B, Zhu L, Xiao X, Li S. Ma F, et al. Among authors: shi c. Theranostics. 2020 Jun 19;10(17):7730-7746. doi: 10.7150/thno.45862. eCollection 2020. Theranostics. 2020. PMID: 32685016 Free PMC article.

2

Metabolic products in urine of preterm infants characterized via gas chromatography-mass spectrometry.

Hao H, Li S, Zhou W, Wang H, Liu M, Shi C, Chen J, Xiao X. Hao H, et al. Among authors: shi c. Int J Clin Exp Med. 2015 Sep 15;8(9):16454-62. eCollection 2015. Int J Clin Exp Med. 2015. PMID: 26629171 Free PMC article.

3

NQDI-1, an inhibitor of ASK1 attenuates acute perinatal hypoxic-ischemic cerebral injury by modulating cell death.

Hao H, Li S, Tang H, Liu B, Cai Y, Shi C, Xiao X. Hao H, et al. Among authors: shi c. Mol Med Rep. 2016 Jun;13(6):4585-92. doi: 10.3892/mmr.2016.5123. Epub 2016 Apr 13. Mol Med Rep. 2016. PMID: 27081917 Free PMC article.

4

Gene Mutation Analysis and Prenatal Diagnosis of the Ornithine Transcarbamylase (OTC) Gene in Two Families with Ornithine Transcarbamylase Deficiency.

Li S, Cai Y, Shi C, Liu M, Liu B, Lin L, Xiao X, Hao H. Li S, et al. Among authors: shi c. Med Sci Monit. 2018 Oct 18;24:7431-7437. doi: 10.12659/MSM.911295. Med Sci Monit. 2018. PMID: 30333473 Free PMC article.

5

[Construction of a mouse model of cblC type methylmalonic acidemia with W203X mutation based on the CRISPR/Cas9 technology].

Ma F, Shi CC, Liang PP, Li ST, Gu X, Xiao X, Hao H. Ma F, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2019 Aug;21(8):824-829. doi: 10.7499/j.issn.1008-8830.2019.08.016. Zhongguo Dang Dai Er Ke Za Zhi. 2019. PMID: 31416510 Free PMC article. Chinese.

6

Segmental uniparental disomy of chromosome 4 in a patient with methylmalonic acidemia.

Chen M, Hao H, Xiong H, Cai Y, Ma F, Shi C, Xiao X, Li S. Chen M, et al. Among authors: shi c. Mol Genet Genomic Med. 2020 Jan;8(1):e1063. doi: 10.1002/mgg3.1063. Epub 2019 Dec 2. Mol Genet Genomic Med. 2020. PMID: 31793236 Free PMC article.

7

[Clinical and variant analysis of 15 patients with methylmalonic acidemia].

Xiong H, Deng W, Guo L, Shi C, Xiao X, Hao H. Xiong H, et al. Among authors: shi c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Dec 10;36(12):1158-1162. doi: 10.3760/cma.j.issn.1003-9406.2019.12.002. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31813137 Chinese.

8

[Tatton-Brown-Rahman syndrome associated with the DNMT3A gene: a case report and literature review].

Chen M, Li ST, Cai Y, Xiao X, Shi CC, Hao H. Chen M, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2020 Oct;22(10):1114-1118. doi: 10.7499/j.issn.1008-8830.2004078. Zhongguo Dang Dai Er Ke Za Zhi. 2020. PMID: 33059810 Free PMC article. Review. Chinese.

9

Prenatal Diagnosis of Two Common Inborn Errors of Metabolism by Genetic and Mass Spectrometric Analysis of Amniotic Fluid.

Shi C, Li S, Gao Y, Deng Z, Hao H, Xiao X. Shi C, et al. Front Pediatr. 2022 Feb 9;10:824399. doi: 10.3389/fped.2022.824399. eCollection 2022. Front Pediatr. 2022. PMID: 35223700 Free PMC article.

10

Serum differential proteomic profiling of patients with isolated methylmalonic acidemia by iTRAQ.

Li S, Shi C, Cai Y, Gu X, Xiong H, Liu X, Zhang Y, Xiao X, Ma F, Hao H. Li S, et al. Among authors: shi c. Front Genet. 2022 Aug 29;13:765637. doi: 10.3389/fgene.2022.765637. eCollection 2022. Front Genet. 2022. PMID: 36105101 Free PMC article.

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