Guo X - Search Results

1

[Mutation analysis of FBN1 gene in a child with Marfan syndrome].

Jiang L, Zhang D, Xiao Y, Wang Q, Gong B, Guo X, Huang M, Yang Z. Jiang L, et al. Among authors: guo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Jun 10;35(3):414-417. doi: 10.3760/cma.j.issn.1003-9406.2018.03.024. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018. PMID: 29896744 Chinese.

2

A novel FBN1 mutation causes autosomal dominant Marfan syndrome.

Xiao Y, Liu X, Guo X, Liu L, Jiang L, Wang Q, Gong B. Xiao Y, et al. Among authors: guo x. Mol Med Rep. 2017 Nov;16(5):7321-7328. doi: 10.3892/mmr.2017.7544. Epub 2017 Sep 20. Mol Med Rep. 2017. PMID: 28944857 Free PMC article.

3

Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families.

Gong B, Yang L, Wang Q, Ye Z, Guo X, Yang C, Hao F, Shi Y, Huang Y, Qu C, Yang Z. Gong B, et al. Among authors: guo x. Mol Genet Genomic Med. 2019 Apr;7(4):e00594. doi: 10.1002/mgg3.594. Epub 2019 Mar 5. Mol Genet Genomic Med. 2019. PMID: 30838813 Free PMC article.

4

[Analysis of FBN1 gene mutations in two pedigrees affected with Marfan syndrome].

Yang L, Guo X, Jiang L, Gong B, Qu C. Yang L, et al. Among authors: guo x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Jun 10;36(6):566-570. doi: 10.3760/cma.j.issn.1003-9406.2019.06.008. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019. PMID: 31055806 Chinese.

5

A Novel PAX6 Heterozygous Mutation Found in a Chinese Family with Congenital Aniridia.

Xiao Y, Liu X, Yang C, Liu L, Guo X, Wang Q, Gong B. Xiao Y, et al. Among authors: guo x. Genet Test Mol Biomarkers. 2019 Jul;23(7):495-500. doi: 10.1089/gtmb.2018.0334. Epub 2019 Jun 4. Genet Test Mol Biomarkers. 2019. PMID: 31161946

6

Association between hOGG1 polymorphism rs1052133 and gastric cancer.

Zhang D, Guo X, Hu J, Zeng G, Huang M, Qi D, Gong B. Zhang D, et al. Among authors: guo x. Oncotarget. 2017 May 23;8(21):34321-34329. doi: 10.18632/oncotarget.16124. Oncotarget. 2017. PMID: 28415729 Free PMC article. Review.

7

Association of catalase polymorphisms with primary open-angle glaucoma in a Chinese population.

Gong B, Shi Y, Qu C, Ye Z, Yin Y, Tan C, Shuai P, Li J, Guo X, Cheng Y, Yang Z, Lin Y, Liu X. Gong B, et al. Among authors: guo x. Ophthalmic Genet. 2018 Jan-Feb;39(1):35-40. doi: 10.1080/13816810.2017.1342132. Epub 2017 Aug 22. Ophthalmic Genet. 2018. PMID: 28829657

8

Transforming growth factor β induced mutation-associated phenotype in a Chinese family exhibiting lattice corneal dystrophy.

Qu C, Yu M, Guo X, Li J, Liu X, Shi Y, Gong B. Qu C, et al. Among authors: guo x. Biomed Rep. 2017 Oct;7(4):314-318. doi: 10.3892/br.2017.975. Epub 2017 Aug 30. Biomed Rep. 2017. PMID: 29085627 Free PMC article.

9

Mutant RAMP2 causes primary open-angle glaucoma via the CRLR-cAMP axis.

Gong B, Zhang H, Huang L, Chen Y, Shi Y, Tam PO, Zhu X, Huang Y, Lei B, Sundaresan P, Li X, Jiang L, Yang J, Lin Y, Lu F, Chen L, Li Y, Leung CK, Guo X, Zhang S, Huang G, Wu Y, Zhou T, Shuai P, Tham CC, Weisschuh N, Krishnadas SR, Mardin C, Reis A, Yang J, Zhang L, Zhou Y, Wang Z, Qu C, Shaw PX, Pang CP, Sun X, Zhu W, Li DY, Pasutto F, Yang Z. Gong B, et al. Among authors: guo x. Genet Med. 2019 Oct;21(10):2345-2354. doi: 10.1038/s41436-019-0507-0. Epub 2019 Apr 19. Genet Med. 2019. PMID: 31000793 Free article.

10

Identification of CRB1 mutations in two Chinese consanguineous families exhibiting autosomal recessive retinitis pigmentosa.

Guo X, Li J, Wang Q, Shu Y, Wang J, Chen L, Zhang H, Shi Y, Yang J, Lu F, Jiang L, Qu C, Gong B. Guo X, et al. Mol Med Rep. 2019 Sep;20(3):2922-2928. doi: 10.3892/mmr.2019.10495. Epub 2019 Jul 12. Mol Med Rep. 2019. PMID: 31322236

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