Yang Y - Search Results

1

Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosa.

Zhang L, Sun Z, Zhao P, Huang L, Xu M, Yang Y, Chen X, Lu F, Zhang X, Wang H, Zhang S, Liu W, Jiang Z, Ma S, Chen R, Zhao C, Yang Z, Sui R, Zhu X. Zhang L, et al. Among authors: yang y, yang z. Hum Mol Genet. 2018 Dec 1;27(23):4157-4168. doi: 10.1093/hmg/ddy281. Hum Mol Genet. 2018. PMID: 30085091 Free PMC article.

2

Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.

Zhang L, Yang Y, Li S, Tai Z, Huang L, Liu Y, Zhu X, Di Y, Qu C, Jiang Z, Li Y, Zhang G, Kim R, Sundaresan P, Yang Z, Zhu X. Zhang L, et al. Among authors: yang y, yang z. Genet Test Mol Biomarkers. 2016 Jul;20(7):346-51. doi: 10.1089/gtmb.2015.0322. Epub 2016 May 26. Genet Test Mol Biomarkers. 2016. PMID: 27228167

3

Whole exome sequencing identified novel CRB1 mutations in Chinese and Indian populations with autosomal recessive retinitis pigmentosa.

Yang Y, Yang Y, Huang L, Zhai Y, Li J, Jiang Z, Gong B, Fang H, Kim R, Yang Z, Sundaresan P, Zhu X, Zhou Y. Yang Y, et al. Among authors: yang z. Sci Rep. 2016 Sep 27;6:33681. doi: 10.1038/srep33681. Sci Rep. 2016. PMID: 27670293 Free PMC article.

4

Candidate Gene Analysis Identifies Mutations in CYP1B1 and LTBP2 in Indian Families with Primary Congenital Glaucoma.

Yang Y, Zhang L, Li S, Zhu X, Sundaresan P. Yang Y, et al. Genet Test Mol Biomarkers. 2017 Apr;21(4):252-258. doi: 10.1089/gtmb.2016.0203. Epub 2017 Feb 27. Genet Test Mol Biomarkers. 2017. PMID: 28384041

5

Identification of LRP5 mutations in families with familial exudative vitreoretinopathy.

Liu YQ, Zhu X, Li SJ, Yang YM, Yang M, Zhao PQ, Zhu XJ. Liu YQ, et al. Yi Chuan. 2017 Mar 20;39(3):241-249. doi: 10.16288/j.yczz.16-339. Yi Chuan. 2017. PMID: 28420620

6

Loss of Tmem30a leads to photoreceptor degeneration.

Zhang L, Yang Y, Li S, Zhang S, Zhu X, Tai Z, Yang M, Liu Y, Guo X, Chen B, Jiang Z, Lu F, Zhu X. Zhang L, et al. Among authors: yang m, yang y. Sci Rep. 2017 Aug 24;7(1):9296. doi: 10.1038/s41598-017-09506-5. Sci Rep. 2017. PMID: 28839191 Free PMC article.

7

Hepatic Tmem30a Deficiency Causes Intrahepatic Cholestasis by Impairing Expression and Localization of Bile Salt Transporters.

Liu L, Zhang L, Zhang L, Yang F, Zhu X, Lu Z, Yang Y, Lu H, Feng L, Wang Z, Chen H, Yan S, Wang L, Ju Z, Jin H, Zhu X. Liu L, et al. Among authors: yang f, yang y. Am J Pathol. 2017 Dec;187(12):2775-2787. doi: 10.1016/j.ajpath.2017.08.011. Epub 2017 Sep 15. Am J Pathol. 2017. PMID: 28919113 Free article.

8

Targeted Next-Generation Sequencing Reveals Novel RP1 Mutations in Autosomal Recessive Retinitis Pigmentosa.

Li S, Yang M, Liu W, Liu Y, Zhang L, Yang Y, Sundaresan P, Yang Z, Zhu X. Li S, et al. Among authors: yang m, yang y, yang z. Genet Test Mol Biomarkers. 2018 Feb;22(2):109-114. doi: 10.1089/gtmb.2017.0223. Genet Test Mol Biomarkers. 2018. PMID: 29425069

9

Targeted Next-Generation Sequencing Reveals a Novel Frameshift Mutation in the MERTK Gene in a Chinese Family with Retinitis Pigmentosa.

Yang M, Li S, Liu W, Yang Y, Zhang L, Zhang S, Jiang Z, Yang Z, Zhu X. Yang M, et al. Among authors: yang y, yang z. Genet Test Mol Biomarkers. 2018 Mar;22(3):165-169. doi: 10.1089/gtmb.2017.0248. Epub 2018 Feb 13. Genet Test Mol Biomarkers. 2018. PMID: 29437494

10

Tmem30a Plays Critical Roles in Ensuring the Survival of Hematopoietic Cells and Leukemia Cells in Mice.

Li N, Yang Y, Liang C, Qiu Q, Pan C, Li M, Yang S, Chen L, Zhu X, Hu Y. Li N, et al. Among authors: yang s, yang y. Am J Pathol. 2018 Jun;188(6):1457-1468. doi: 10.1016/j.ajpath.2018.02.015. Epub 2018 Mar 21. Am J Pathol. 2018. PMID: 29574182 Free article.

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