Jiang F - Search Results

1

Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1.

Liu F, Li P, Liu Y, Li W, Wong F, Du R, Wang L, Li C, Jiang F, Tang Z, Liu M. Liu F, et al. Among authors: jiang f. Mol Vis. 2013;19:695-701. Epub 2013 Mar 21. Mol Vis. 2013. PMID: 23559863 Free PMC article.

2

Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK. Liu M, et al. Among authors: jiang f. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6. doi: 10.1167/iovs.05-1438. Invest Ophthalmol Vis Sci. 2006. PMID: 16877416

3

A novel de novo frameshift mutation of RPGR ORF15 is associated with X-linked retinitis pigmentosa in a Chinese family.

Chang W, Ding Q, Tang Z, Liu P, Jiang F, Ke T, Ren X, Wang Z, Liu J, Wang QK, Liu M. Chang W, et al. Among authors: jiang f. Mol Vis. 2007 Aug 30;13:1548-54. Mol Vis. 2007. PMID: 17893654

4

Novel USH2A compound heterozygous mutations cause RP/USH2 in a Chinese family.

Liu X, Tang Z, Li C, Yang K, Gan G, Zhang Z, Liu J, Jiang F, Wang Q, Liu M. Liu X, et al. Among authors: jiang f. Mol Vis. 2010 Mar 17;16:454-61. doi: 10.1167/3.9.454. Mol Vis. 2010. PMID: 20309401 Free PMC article.

5

Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa.

Gao M, Zhang S, Liu C, Qin Y, Archacki S, Jin L, Wang Y, Liu F, Chen J, Liu Y, Wang J, Huang M, Liao S, Tang Z, Guo AY, Jiang F, Liu M. Gao M, et al. Among authors: jiang f. Mol Vis. 2016 Mar 18;22:234-42. eCollection 2016. Mol Vis. 2016. PMID: 27081294 Free PMC article.

6

Identification of two novel compound heterozygous mutations of ADGRV1 in a Chinese family with Usher syndrome type IIC.

Zhang N, Wang J, Liu S, Liu M, Jiang F. Zhang N, et al. Among authors: jiang f. Ophthalmic Genet. 2018 Aug;39(4):517-521. doi: 10.1080/13816810.2018.1479430. Epub 2018 Jun 8. Ophthalmic Genet. 2018. PMID: 29883260

7

[Analysis of the CYP1B1 gene mutation in primary congenital glaucoma patients of Hubei Han nationality].

Jiang FG, Liu XW, Hou HP. Jiang FG, et al. Zhonghua Yan Ke Za Zhi. 2007 Sep;43(9):779-83. Zhonghua Yan Ke Za Zhi. 2007. PMID: 18070520 Chinese.

8

Prostaglandin F2α Regulates Adipogenesis by Modulating Extracellular Signal-Regulated Kinase Signaling in Graves' Ophthalmopathy.

Zhu R, Wang XH, Wang BW, Ouyang X, You YY, Xie HT, Zhang MC, Jiang FG. Zhu R, et al. Int J Mol Sci. 2023 Apr 10;24(8):7012. doi: 10.3390/ijms24087012. Int J Mol Sci. 2023. PMID: 37108173 Free PMC article.

9

Investigation of Conjunctival Goblet Cell and Tear MUC5AC Protein in Patients With Graves' Ophthalmopathy.

You Y, Chen J, Chen H, Wang J, Xie H, Pi X, Wang X, Jiang F. You Y, et al. Among authors: jiang f. Transl Vis Sci Technol. 2023 Oct 3;12(10):19. doi: 10.1167/tvst.12.10.19. Transl Vis Sci Technol. 2023. PMID: 37889503 Free PMC article.

10

Genetic variations in the SOCS3 gene in patients with Graves' ophthalmopathy.

Yan R, Yang J, Jiang P, Jin L, Ma J, Huang R, Ma N, Jiang F. Yan R, et al. Among authors: jiang p, jiang f. J Clin Pathol. 2015 Jun;68(6):448-52. doi: 10.1136/jclinpath-2014-202751. Epub 2015 Mar 13. J Clin Pathol. 2015. PMID: 25770161

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