ANALYSES OF SINGLE NUCLEOTIDE POLYMORPHISMS AND HAPLOTYPE LINKAGE OF LOC387715 AND THE HTRA1 GENE IN EXUDATIVE AGE-RELATED MACULAR DEGENERATION IN A CHINESE COHORT

Retina ◽  
2009 ◽  
Vol 29 (7) ◽  
pp. 974-979 ◽  
Author(s):  
HUA JIANG ◽  
YI QU ◽  
GUANGFU DANG ◽  
XIAO ZHANG ◽  
NINGNING YIN ◽  
...  
PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e49905 ◽  
Author(s):  
Akshay Anand ◽  
Neel Kamal Sharma ◽  
Amod Gupta ◽  
Sudesh Prabhakar ◽  
Suresh Kumar Sharma ◽  
...  

2010 ◽  
Vol 74 (3) ◽  
pp. 195-201 ◽  
Author(s):  
Juan A. Ayala-Haedo ◽  
Paul J. Gallins ◽  
Patrice L. Whitehead ◽  
Stephen G. Schwartz ◽  
Jaclyn L. Kovach ◽  
...  

2018 ◽  
Vol 136 (6) ◽  
pp. 682 ◽  
Author(s):  
Lisa Y. Lin ◽  
Qiang Zhou ◽  
Stephanie Hagstrom ◽  
Maureen G. Maguire ◽  
Ebenezer Daniel ◽  
...  

Author(s):  
John Paul SanGiovanni ◽  
Peter M. SanGiovanni ◽  
Przemysław Sapieha ◽  
Vincent De Guire

AbstractAdvanced age-related macular degeneration (AAMD) is a complex sight-threating disease of public health significance. Micro RNAs (miRNAs) have been proposed as biomarkers for AAMD. The presence of certain single nucleotide polymorphisms (SNPs) may influence the explanatory value of these biomarkers. Here we present findings from an integrated approach used to determine whether AAMD-associated SNPs have the capacity to influence miRNA-mRNA pairing and, if so, to what extent such pairing may be manifested in a discrete AAMD transcriptome. Using a panel of 8854 SNPs associated with AAMD at p-values ≤5.0E−7 from a cohort of >30,000 elderly people, we identified SNPs in miRNA target-encoding constituents of: (1) regulator of complement activation (RCA) genes (rs390679,


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