AMD Genetics consortium
The National Eye Institute (NEI) created the International Age Related Macular Degeneration (AMD) Genetics Consortium in 2010 to identify the remaining genetic risk variants for AMD.
Please visit their Web site for more information.
Exploration of Retinal studies
Bibliographic analysis
| KBaSS ViSIOn ID | PubMed ID | Title | Corresponding Author | Acceptation Date |
119  | PMID: 19843539 | The homeobox gene CHX10/VSX2 regulates RdCVF promoter activity in the inner retina. | T. LEVEILLARD | 2009-10 |
| 123 | PMID: 20139892 | The disruption of the rod-derived cone viability gene leads to photoreceptor dysfunction and susceptibility to oxidative stress. | T. LEVEILLARD | 2009-12 |
| 178 | PMID: 22174898 | Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor death. | T. LEVEILLARD | 2011-11 |
| 185 | PMID: 22343139 | Nxnl2 splicing results in dual functions in neuronal cell survival and maintenance of cell integrity. | T. LEVEILLARD | 2012-02 |
| 201 | PMID: 15075390 | A gene atlas of the mouse and human protein-encoding transcriptomes | J.B. HOGENESCH | 2004-03 |
Bioinformatic analysis
All data were extracted from GEO (beginning of April 2013).
