Ou X - Search Results

1

Type 4B hereditary hemochromatosis associated with a novel mutation in the SLC40A1 gene: A case report and a review of the literature.

Zhang W, Lv T, Huang J, Ou X. Zhang W, et al. Among authors: ou x. Medicine (Baltimore). 2017 Sep;96(38):e8064. doi: 10.1097/MD.0000000000008064. Medicine (Baltimore). 2017. PMID: 28930842 Free PMC article. Review.

2

An Analysis of Immunoreactive Signatures in Early Stage Hepatocellular Carcinoma.

Hong Y, Long J, Li H, Chen S, Liu Q, Zhang B, He X, Wang Y, Li H, Li Y, Zhang T, Lu C, Yan H, Zhang M, Li Q, Cao B, Bai Z, Wang J, Zhang Z, Zhu S, Zheng J, Ou X, Ma H, Jia J, You H, Wang S, Huang J. Hong Y, et al. Among authors: ou x. EBioMedicine. 2015 Mar 13;2(5):438-46. doi: 10.1016/j.ebiom.2015.03.010. eCollection 2015 May. EBioMedicine. 2015. PMID: 26137588 Free PMC article.

3

Recent advance in the molecular genetics of Wilson disease and hereditary hemochromatosis.

Lv T, Li X, Zhang W, Zhao X, Ou X, Huang J. Lv T, et al. Among authors: ou x. Eur J Med Genet. 2016 Oct;59(10):532-9. doi: 10.1016/j.ejmg.2016.08.011. Epub 2016 Aug 31. Eur J Med Genet. 2016. PMID: 27592149 Review.

4

Identification and clinical significance of an elevated level of serum aminoacylase-1 autoantibody in patients with hepatitis B virus-related liver cirrhosis.

He X, Hong Y, Wang X, Zhang X, Long J, Li H, Zhang B, Chen S, Liu Q, Li H, Wang X, Ou X, Huang J. He X, et al. Among authors: ou x. Mol Med Rep. 2016 Nov;14(5):4255-4262. doi: 10.3892/mmr.2016.5740. Epub 2016 Sep 14. Mol Med Rep. 2016. PMID: 27633755

5

Development and evaluation of an unlabeled probe high-resolution melting assay for detection of ATP7B mutations in Wilson's disease.

Xu A, Lv T, Zhang B, Zhang W, Ou X, Huang J. Xu A, et al. Among authors: ou x. J Clin Lab Anal. 2017 Jul;31(4):e22064. doi: 10.1002/jcla.22064. Epub 2016 Sep 17. J Clin Lab Anal. 2017. PMID: 27638368 Free PMC article.

6

"Haemochromatotic" characteristics of the human BEL-7402 cell line.

Xu A, Li Y, Chen W, Li X, Zhang W, Li S, Wu L, Wu Z, Zhang B, Ou X, Huang J. Xu A, et al. Among authors: ou x. Br J Haematol. 2018 Oct;183(2):302-306. doi: 10.1111/bjh.14952. Epub 2017 Sep 29. Br J Haematol. 2018. PMID: 28961311 Free article. No abstract available.

7

Effective viral suppression is necessary to reduce hepatocellular carcinoma development in cirrhotic patients with chronic hepatitis B: Results of a 10-year follow up.

Zhang W, Wang X, Wang Y, Zhao X, Duan W, Wang Q, Wu X, Kong Y, Ma H, You H, Ou X, Jia J. Zhang W, et al. Among authors: ou x. Medicine (Baltimore). 2017 Nov;96(44):e8454. doi: 10.1097/MD.0000000000008454. Medicine (Baltimore). 2017. PMID: 29095292 Free PMC article.

8

Molecular alterations of the NF2 gene in hepatocellular carcinoma and intrahepatic cholangiocarcinoma.

Zhang N, Zhao Z, Long J, Li H, Zhang B, Chen G, Li X, Lv T, Zhang W, Ou X, Xu A, Huang J. Zhang N, et al. Among authors: ou x. Oncol Rep. 2017 Dec;38(6):3650-3658. doi: 10.3892/or.2017.6055. Epub 2017 Oct 24. Oncol Rep. 2017. PMID: 29130106

9

Efficacy and safety of fenofibrate add-on therapy for patients with primary biliary cholangitis and a suboptimal response to UDCA.

Duan W, Ou X, Wang X, Wang Y, Zhao X, Wang Q, Wu X, Zhang W, Ma H, You H, Jia J. Duan W, et al. Among authors: ou x. Rev Esp Enferm Dig. 2018 Sep;110(9):557-563. doi: 10.17235/reed.2018.5533/2018. Rev Esp Enferm Dig. 2018. PMID: 29739227 Free article.

10

Non-HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants.

Lv T, Zhang W, Xu A, Li Y, Zhou D, Zhang B, Li X, Zhao X, Wang Y, Wang X, Duan W, Wang Q, Xu H, Zheng J, Zhao R, Zhu L, Dong Y, Lu L, Chen Y, Long J, Zheng S, Wang W, You H, Jia J, Ou X, Huang J. Lv T, et al. Among authors: ou x. J Med Genet. 2018 Oct;55(10):650-660. doi: 10.1136/jmedgenet-2018-105348. Epub 2018 Aug 30. J Med Genet. 2018. PMID: 30166352 Clinical Trial.

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