Chen R - Search Results

1

Critical Role of Cytosolic DNA and Its Sensing Adaptor STING in Aortic Degeneration, Dissection, and Rupture.

Luo W, Wang Y, Zhang L, Ren P, Zhang C, Li Y, Azares AR, Zhang M, Guo J, Ghaghada KB, Starosolski ZA, Rajapakshe K, Coarfa C, Li Y, Chen R, Fujiwara K, Abe JI, Coselli JS, Milewicz DM, LeMaire SA, Shen YH. Luo W, et al. Among authors: chen r. Circulation. 2020 Jan 7;141(1):42-66. doi: 10.1161/CIRCULATIONAHA.119.041460. Epub 2019 Dec 30. Circulation. 2020. PMID: 31887080 Free PMC article.

2

Genome-wide identification of direct targets of the Drosophila retinal determination protein Eyeless.

Ostrin EJ, Li Y, Hoffman K, Liu J, Wang K, Zhang L, Mardon G, Chen R. Ostrin EJ, et al. Among authors: chen r. Genome Res. 2006 Apr;16(4):466-76. doi: 10.1101/gr.4673006. Epub 2006 Mar 13. Genome Res. 2006. PMID: 16533912 Free PMC article.

3

Mutation survey of known LCA genes and loci in the Saudi Arabian population.

Li Y, Wang H, Peng J, Gibbs RA, Lewis RA, Lupski JR, Mardon G, Chen R. Li Y, et al. Among authors: chen r. Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1336-43. doi: 10.1167/iovs.08-2589. Epub 2008 Oct 20. Invest Ophthalmol Vis Sci. 2009. PMID: 18936139 Free PMC article.

4

High-throughput multiplex sequencing to discover copy number variants in Drosophila.

Daines B, Wang H, Li Y, Han Y, Gibbs R, Chen R. Daines B, et al. Among authors: chen r. Genetics. 2009 Aug;182(4):935-41. doi: 10.1534/genetics.109.103218. Epub 2009 Jun 15. Genetics. 2009. PMID: 19528327 Free PMC article.

5

optix functions as a link between the retinal determination network and the dpp pathway to control morphogenetic furrow progression in Drosophila.

Li Y, Jiang Y, Chen Y, Karandikar U, Hoffman K, Chattopadhyay A, Mardon G, Chen R. Li Y, et al. Among authors: chen r, chen y. Dev Biol. 2013 Sep 1;381(1):50-61. doi: 10.1016/j.ydbio.2013.06.015. Epub 2013 Jun 20. Dev Biol. 2013. PMID: 23792115 Free PMC article.

6

Comparison and quantitative verification of mapping algorithms for whole-genome bisulfite sequencing.

Kunde-Ramamoorthy G, Coarfa C, Laritsky E, Kessler NJ, Harris RA, Xu M, Chen R, Shen L, Milosavljevic A, Waterland RA. Kunde-Ramamoorthy G, et al. Among authors: chen r. Nucleic Acids Res. 2014 Apr;42(6):e43. doi: 10.1093/nar/gkt1325. Epub 2014 Jan 3. Nucleic Acids Res. 2014. PMID: 24391148 Free PMC article.

7

CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes.

Zhong H, Chen Y, Li Y, Chen R, Mardon G. Zhong H, et al. Among authors: chen r, chen y. Sci Rep. 2015 Feb 10;5:8366. doi: 10.1038/srep08366. Sci Rep. 2015. PMID: 25666713 Free PMC article.

8

IFT81 as a Candidate Gene for Nonsyndromic Retinal Degeneration.

Dharmat R, Liu W, Ge Z, Sun Z, Yang L, Li Y, Wang K, Thomas K, Sui R, Chen R. Dharmat R, et al. Among authors: chen r. Invest Ophthalmol Vis Sci. 2017 May 1;58(5):2483-2490. doi: 10.1167/iovs.16-19133. Invest Ophthalmol Vis Sci. 2017. PMID: 28460050 Free PMC article.

9

REEP6 deficiency leads to retinal degeneration through disruption of ER homeostasis and protein trafficking.

Agrawal SA, Burgoyne T, Eblimit A, Bellingham J, Parfitt DA, Lane A, Nichols R, Asomugha C, Hayes MJ, Munro PM, Xu M, Wang K, Futter CE, Li Y, Chen R, Cheetham ME. Agrawal SA, et al. Among authors: chen r. Hum Mol Genet. 2017 Jul 15;26(14):2667-2677. doi: 10.1093/hmg/ddx149. Hum Mol Genet. 2017. PMID: 28475715 Free PMC article.

10

NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype.

Eblimit A, Zaneveld SA, Liu W, Thomas K, Wang K, Li Y, Mardon G, Chen R. Eblimit A, et al. Among authors: chen r. Exp Eye Res. 2018 Aug;173:32-43. doi: 10.1016/j.exer.2018.04.010. Epub 2018 Apr 17. Exp Eye Res. 2018. PMID: 29674119 Free PMC article.

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