Liu G - Search Results

1

Cancer Cell-derived Exosomes Induce Mitogen-activated Protein Kinase-dependent Monocyte Survival by Transport of Functional Receptor Tyrosine Kinases.

Song X, Ding Y, Liu G, Yang X, Zhao R, Zhang Y, Zhao X, Anderson GJ, Nie G. Song X, et al. Among authors: liu g. J Biol Chem. 2016 Apr 15;291(16):8453-64. doi: 10.1074/jbc.M116.716316. Epub 2016 Feb 19. J Biol Chem. 2016. PMID: 26895960 Free PMC article.

2

Functional Analysis of GLRX5 Mutants Reveals Distinct Functionalities of GLRX5 Protein.

Liu G, Wang Y, Anderson GJ, Camaschella C, Chang Y, Nie G. Liu G, et al. J Cell Biochem. 2016 Jan;117(1):207-17. doi: 10.1002/jcb.25267. J Cell Biochem. 2016. PMID: 26100117

3

5-aza-2'-deoxycytidine activates iron uptake and heme biosynthesis by increasing c-Myc nuclear localization and binding to the E-boxes of transferrin receptor 1 (TfR1) and ferrochelatase (Fech) genes.

Ning B, Liu G, Liu Y, Su X, Anderson GJ, Zheng X, Chang Y, Guo M, Liu Y, Zhao Y, Nie G. Ning B, et al. Among authors: liu y, liu g. J Biol Chem. 2011 Oct 28;286(43):37196-206. doi: 10.1074/jbc.M111.258129. Epub 2011 Sep 7. J Biol Chem. 2011. PMID: 21903580 Free PMC article.

4

Heterozygous missense mutations in the GLRX5 gene cause sideroblastic anemia in a Chinese patient.

Liu G, Guo S, Anderson GJ, Camaschella C, Han B, Nie G. Liu G, et al. Blood. 2014 Oct 23;124(17):2750-1. doi: 10.1182/blood-2014-08-598508. Blood. 2014. PMID: 25342667 Free article. No abstract available.

5

Polymeric Nanoparticles Enhance the Ability of Deferoxamine To Deplete Hepatic and Systemic Iron.

Guo S, Liu G, Frazer DM, Liu T, You L, Xu J, Wang Y, Anderson GJ, Nie G. Guo S, et al. Among authors: liu g, liu t. Nano Lett. 2018 Sep 12;18(9):5782-5790. doi: 10.1021/acs.nanolett.8b02428. Epub 2018 Aug 9. Nano Lett. 2018. PMID: 30085676

6

Correlation of serum hepcidin levels with disease progression in hepatitis B virus-related disease assessed by nanopore film based assay.

Wang J, Dong A, Liu G, Anderson GJ, Hu TY, Shi J, Hu Y, Nie G. Wang J, et al. Among authors: liu g. Sci Rep. 2016 Oct 3;6:34252. doi: 10.1038/srep34252. Sci Rep. 2016. PMID: 27694815 Free PMC article. Clinical Trial.

7

Identification of four SLC19A2 mutations in four Chinese thiamine responsive megaloblastic anemia patients without diabetes.

Liu G, Yang F, Han B, Liu J, Nie G. Liu G, et al. Among authors: liu j. Blood Cells Mol Dis. 2014 Apr;52(4):203-4. doi: 10.1016/j.bcmd.2013.11.002. Epub 2013 Dec 16. Blood Cells Mol Dis. 2014. PMID: 24355766 No abstract available.

8

Identification of FECH gene multiple variations in two Chinese patients with erythropoietic protoporphyria and a review.

Long ZB, Wang YW, Yang C, Liu G, Du YL, Nie GJ, Chang YZ, Han B. Long ZB, et al. Among authors: liu g. J Zhejiang Univ Sci B. 2016 Oct.;17(10):813-820. doi: 10.1631/jzus.B1600085. J Zhejiang Univ Sci B. 2016. PMID: 27704751 Free PMC article. Review.

9

Identification of novel mutations in HFE, HFE2, TfR2, and SLC40A1 genes in Chinese patients affected by hereditary hemochromatosis.

Wang Y, Du Y, Liu G, Guo S, Hou B, Jiang X, Han B, Chang Y, Nie G. Wang Y, et al. Among authors: liu g. Int J Hematol. 2017 Apr;105(4):521-525. doi: 10.1007/s12185-016-2150-8. Epub 2016 Nov 28. Int J Hematol. 2017. PMID: 27896572

10

Identification of CDAN1, C15ORF41 and SEC23B mutations in Chinese patients affected by congenital dyserythropoietic anemia.

Wang Y, Ru Y, Liu G, Dong S, Li Y, Zhu X, Zhang F, Chang YZ, Nie G. Wang Y, et al. Among authors: liu g. Gene. 2018 Jan 15;640:73-78. doi: 10.1016/j.gene.2017.10.027. Epub 2017 Oct 12. Gene. 2018. PMID: 29031773

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