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Προβολή τεκμηρίου 
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • Προβολή τεκμηρίου
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Convergence of linkage, gene expression and association data demonstrates the influence of the RAR-related orphan receptor alpha (RORA) gene on neovascular AMD: A systems biology based approach

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Συγγραφέας
Silveira, A. C.; Morrison, M. A.; Ji, F.; Xu, H.; Reinecke, J. B.; Adams, S. M.; Arneberg, T. M.; Janssian, M.; Lee, J. E.; Yuan, Y.; Schaumberg, D. A.; Kotoula, M. G.; Tsironi, E. E.; Tsiloulis, A. N.; Chatzoulis, D. Z.; Miller, J. W.; Kim, I. K.; Hageman, G. S.; Farrer, L. A.; Haider, N. B.; DeAngelis, M. M.
Ημερομηνία
2010
DOI
10.1016/j.visres.2009.09.016
Λέξη-κλειδί
Haplotypes
Linkage
Microarray
Neovascularization
RORA
Single nucleotide polymorphisms
age related maculopathy susceptibility 2 protein
cell nucleus receptor
cholesterol
gene product
htra serine peptidase 1
peptidase
retinoic acid receptor related orphan receptor alpha
unclassified drug
adult
aged
article
case control study
cohort analysis
controlled study
disease course
female
gene expression
gene interaction
gene locus
genetic association
genetic linkage
genetic risk
genotype
haplotype
human
intron
major clinical study
male
pathophysiology
priority journal
retina macula age related degeneration
retina neovascularization
single nucleotide polymorphism
Aged, 80 and over
Case-Control Studies
Cohort Studies
Family
Gene Expression Profiling
Gene Frequency
Genetic Predisposition to Disease
Humans
Macular Degeneration
Microarray Analysis
Middle Aged
Nuclear Receptor Subfamily 1, Group F, Member 1
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Εμφάνιση Μεταδεδομένων
Επιτομή
To identify novel genes and pathways associated with AMD, we performed microarray gene expression and linkage analysis which implicated the candidate gene, retinoic acid receptor-related orphan receptor alpha (RORA, 15q). Subsequent genotyping of 159 RORA single nucleotide polymorphisms (SNPs) in a family-based cohort, followed by replication in an unrelated case-control cohort, demonstrated that SNPs and haplotypes located in intron 1 were significantly associated with neovascular AMD risk in both cohorts. This is the first report demonstrating a possible role for RORA, a receptor for cholesterol, in the pathophysiology of AMD. Moreover, we found a significant interaction between RORA and the ARMS2/HTRA1 locus suggesting a novel pathway underlying AMD pathophysiology. © 2009 Elsevier Ltd.
URI
http://hdl.handle.net/11615/33021
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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