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Results: 1 to 20 of 1426

1.

17β-Estradiol up-regulates Nrf2 via PI3K/AKT and estrogen receptor signaling pathways to suppress light-induced degeneration in rat retina.

Zhu C, Wang S, Wang B, Du F, Hu C, Li H, Feng Y, Zhu R, Mo M, Cao Y, Li A, Yu X.

Neuroscience. 2015 Jul 23. pii: S0306-4522(15)00671-5. doi: 10.1016/j.neuroscience.2015.07.057. [Epub ahead of print]

PMID:
26211446
2.

Analysis of Genetic and Environmental Risk Factors and Their Interactions in Korean Patients with Age-Related Macular Degeneration.

Woo SJ, Ahn J, Morrison MA, Ahn SY, Lee J, Kim KW, DeAngelis MM, Park KH.

PLoS One. 2015 Jul 14;10(7):e0132771. doi: 10.1371/journal.pone.0132771. eCollection 2015.

3.

Identification of Genetic Defects in 33 Probands with Stargardt Disease by WES-Based Bioinformatics Gene Panel Analysis.

Xin W, Xiao X, Li S, Jia X, Guo X, Zhang Q.

PLoS One. 2015 Jul 10;10(7):e0132635. doi: 10.1371/journal.pone.0132635. eCollection 2015.

4.

Highly efficient retinal gene delivery with helper-dependent adenoviral vectors.

Lam S, Cao H, Wu J, Duan R, Hu J.

Genes Dis. 2014 Dec;1(2):227-237.

5.

Restoration of mesenchymal retinal pigmented epithelial cells by TGFβ pathway inhibitors: implications for age-related macular degeneration.

Radeke MJ, Radeke CM, Shih YH, Hu J, Bok D, Johnson LV, Coffey PJ.

Genome Med. 2015 Jun 19;7(1):58. doi: 10.1186/s13073-015-0183-x. eCollection 2015.

6.
7.

Rescue of the Stargardt phenotype in Abca4 knockout mice through inhibition of vitamin A dimerization.

Charbel Issa P, Barnard AR, Herrmann P, Washington I, MacLaren RE.

Proc Natl Acad Sci U S A. 2015 Jul 7;112(27):8415-20. doi: 10.1073/pnas.1506960112. Epub 2015 Jun 23.

8.

Association of Genetic Variants with Polypoidal Choroidal Vasculopathy: A Systematic Review and Updated Meta-analysis.

Ma L, Li Z, Liu K, Rong SS, Brelen ME, Young AL, Kumaramanickavel G, Pang CP, Chen H, Chen LJ.

Ophthalmology. 2015 Jun 13. pii: S0161-6420(15)00462-5. doi: 10.1016/j.ophtha.2015.05.012. [Epub ahead of print] Review.

PMID:
26081444
9.

ATF6 Is Mutated in Early Onset Photoreceptor Degeneration With Macular Involvement.

Xu M, Gelowani V, Eblimit A, Wang F, Young MP, Sawyer BL, Zhao L, Jenkins G, Creel DJ, Wang K, Ge Z, Wang H, Li Y, Hartnett ME, Chen R.

Invest Ophthalmol Vis Sci. 2015 Jun;56(6):3889-95. doi: 10.1167/iovs.15-16778.

PMID:
26070061
10.

Differential DNA Methylation Identified in the Blood and Retina of AMD Patients.

Oliver V, Jaffe AE, Song J, Wang G, Zhang P, Branham KE, Swaroop A, Eberhart CG, Zack DJ, Qian J, Merbs SL.

Epigenetics. 2015 Jun 11:0. [Epub ahead of print]

PMID:
26067391
11.

Lipid Nanoparticles for Ocular Gene Delivery.

Wang Y, Rajala A, Rajala RV.

J Funct Biomater. 2015 Jun 8;6(2):379-94. doi: 10.3390/jfb6020379. Review.

12.

Pharmacogenetics and nutritional supplementation in age-related macular degeneration.

Hampton BM, Kovach JL, Schwartz SG.

Clin Ophthalmol. 2015 May 15;9:873-6. doi: 10.2147/OPTH.S84155. eCollection 2015. Review.

13.

Age-related macular degeneration: genome-wide association studies to translation.

Black JR, Clark SJ.

Genet Med. 2015 May 28. doi: 10.1038/gim.2015.70. [Epub ahead of print] Review.

PMID:
26020418
14.

Prioritization of cancer-related genomic variants by SNP association network.

Liu C, Xuan Z.

Cancer Inform. 2015 Apr 1;14(Suppl 2):57-70. doi: 10.4137/CIN.S17288. eCollection 2015.

15.

The genetics of age-related macular degeneration (AMD) - Novel targets for designing treatment options?

Grassmann F, Fauser S, Weber BH.

Eur J Pharm Biopharm. 2015 May 16. pii: S0939-6411(15)00227-1. doi: 10.1016/j.ejpb.2015.04.039. [Epub ahead of print]

PMID:
25986585
16.

The Role of Peptidyl Prolyl Isomerases in Aging and Vascular Diseases.

McClements L, Annett S, Yakkundi A, Robson T.

Curr Mol Pharmacol. 2015 May 19. [Epub ahead of print]

PMID:
25986561
17.

Rare genetic variants in Tunisian Jewish patients suffering from age-related macular degeneration.

Pras E, Kristal D, Shoshany N, Volodarsky D, Vulih I, Celniker G, Isakov O, Shomron N, Pras E.

J Med Genet. 2015 Jul;52(7):484-92. doi: 10.1136/jmedgenet-2015-103130. Epub 2015 May 18.

PMID:
25986072
18.

Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome.

Scheidecker S, Hull S, Perdomo Y, Studer F, Pelletier V, Muller J, Stoetzel C, Schaefer E, Defoort-Dhellemmes S, Drumare I, Holder GE, Hamel CP, Webster AR, Moore AT, Puech B, Dollfus HJ.

Am J Ophthalmol. 2015 Aug;160(2):364-372.e1. doi: 10.1016/j.ajo.2015.05.007. Epub 2015 May 15.

PMID:
25982971
19.

Mitochondrial DNA variants can mediate methylation status of inflammation, angiogenesis and signaling genes.

Atilano SR, Malik D, Chwa M, Cáceres-Del-Carpio J, Nesburn AB, Boyer DS, Kuppermann BD, Jazwinski SM, Miceli MV, Wallace DC, Udar N, Kenney MC.

Hum Mol Genet. 2015 Aug 15;24(16):4491-503. doi: 10.1093/hmg/ddv173. Epub 2015 May 10.

20.

Netrin-1 - DCC Signaling Systems and Age-Related Macular Degeneration.

SanGiovanni JP, Chen J, Gupta AS, Smith LE, Sapieha P, Lee PH.

PLoS One. 2015 May 7;10(5):e0125548. doi: 10.1371/journal.pone.0125548. eCollection 2015.

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