Liu Z - Search Results

1

A Clinical and Molecular Genetic Study in 11 Chinese Children With Peutz-Jeghers Syndrome.

Zheng B, Wang C, Jia Z, Liu Z, Li M, Jin Y, Pan J. Zheng B, et al. Among authors: liu z. J Pediatr Gastroenterol Nutr. 2017 Apr;64(4):559-564. doi: 10.1097/MPG.0000000000001316. J Pediatr Gastroenterol Nutr. 2017. PMID: 27467201

2

[Neonatal intrahepatic cholestasis caused by citrin deficiency: case report].

Liu ZF, Jin Y, Guo HM. Liu ZF, et al. Zhonghua Er Ke Za Zhi. 2010 Nov;48(11):866-7. Zhonghua Er Ke Za Zhi. 2010. PMID: 21215034 Chinese. No abstract available.

3

[Report of a case with Johanson-Blizzard syndrome and literatures review].

Liu ZF, Zhang ZH, Li M, Jin Y, Lian M, Tang WW. Liu ZF, et al. Zhonghua Er Ke Za Zhi. 2011 Jan;49(1):66-9. Zhonghua Er Ke Za Zhi. 2011. PMID: 21429315 Review. Chinese.

4

Association between TGFB1 915G/C polymorphism and susceptibility to chronic hepatitis C virus infection: A meta-analysis.

Hu GR, Zheng BX, Liu ZF. Hu GR, et al. Biomed Rep. 2014 Mar;2(2):239-244. doi: 10.3892/br.2014.230. Epub 2014 Jan 24. Biomed Rep. 2014. PMID: 24649103 Free PMC article.

5

Diagnosis of ABCB11 gene mutations in children with intrahepatic cholestasis using high resolution melting analysis and direct sequencing.

Hu G, He P, Liu Z, Chen Q, Zheng B, Zhang Q. Hu G, et al. Among authors: liu z. Mol Med Rep. 2014 Sep;10(3):1264-74. doi: 10.3892/mmr.2014.2349. Epub 2014 Jun 20. Mol Med Rep. 2014. PMID: 24969679 Free PMC article.

6

Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5'-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis.

Zheng B, Hu G, Yu J, Liu Z. Zheng B, et al. Among authors: liu z. BMC Pediatr. 2014 Oct 15;14:267. doi: 10.1186/1471-2431-14-267. BMC Pediatr. 2014. PMID: 25319636 Free PMC article.

7

Curcumin-induced histone acetylation inhibition improves stress-induced gastric ulcer disease in rats.

He P, Zhou R, Hu G, Liu Z, Jin Y, Yang G, Li M, Lin Q. He P, et al. Among authors: liu z. Mol Med Rep. 2015 Mar;11(3):1911-6. doi: 10.3892/mmr.2014.2958. Epub 2014 Nov 14. Mol Med Rep. 2015. PMID: 25405899

8

Targeted next-generation sequencing identification of a novel missense mutation of the SKIV2L gene in a patient with trichohepatoenteric syndrome.

Zheng B, Pan J, Jin Y, Wang C, Liu Z. Zheng B, et al. Among authors: liu z. Mol Med Rep. 2016 Sep;14(3):2107-10. doi: 10.3892/mmr.2016.5503. Epub 2016 Jul 11. Mol Med Rep. 2016. PMID: 27431780

9

Presumed missense and synonymous mutations in ATP7B gene cause exon skipping in Wilson disease.

Wang C, Zhou W, Huang Y, Yin H, Jin Y, Jia Z, Zhang A, Liu Z, Zheng B. Wang C, et al. Among authors: liu z. Liver Int. 2018 Aug;38(8):1504-1513. doi: 10.1111/liv.13754. Epub 2018 May 2. Liver Int. 2018. PMID: 29637721

10

Eosinophilic colitis in a boy with a novel XIAP mutation: a case report.

Tang J, Zhou X, Wang L, Hu G, Zheng B, Wang C, Lu Y, Jin Y, Guo H, Liu Z. Tang J, et al. Among authors: liu z. BMC Pediatr. 2020 Apr 18;20(1):171. doi: 10.1186/s12887-020-02075-z. BMC Pediatr. 2020. PMID: 32305064 Free PMC article.

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