Article citationsMore>>
Kumar, V., Westra, H.J., Karjalainen, J., Zhernakova, D.V., Esko, T., Hrdlickova, B., Almeida, R., Zhernakova, A., Reinmaa, E., Vosa, U., Hofker, M.H., Fehrmann, R.S., Fu, J., Withoff, S., Metspalu, A., Franke, L. and Wijmenga, C. (2013) Human Disease-Associated Genetic Variation Impacts Large Intergenic Non-Coding RNA Expression. PLoS Genetics, 9, e1003201.
http://dx.doi.org/10.1371/journal.pgen.1003201
has been cited by the following article:
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TITLE:
ADRBD1 (GRK2), TBXA2R and VEGFA rSNPs in KLF4 and SP1 TFBS Exhibit Linkage Disequilibrium
AUTHORS:
Norman E. Buroker
KEYWORDS:
ADRBD1 (GRK2), TBXA2R, VEGFA, KLF4, SP1, TFBS, rSNP, LD
JOURNAL NAME:
Open Journal of Genetics,
Vol.4 No.3,
June
4,
2014
ABSTRACT:
The adrenergic
receptor kinase 1 (ADRBK1), thromboxane
A2 receptor (TBXA2R) and vascular endothelial growth
factor (VEGFA) regulatory (r) single
nucleotide polymorphisms (SNPs) found in the potential stimulating protein-1
(SP1) and Kruppel-like factor-4 (KLF4) transcriptional factor binding sites (TFBS)
within these genes are in linkage disequilibrium (LD). The LD may result from
rSNP alleles that create TFBS for the KLF4 and SP1 transcriptional factors (TF)
since the alternate rSNP alleles do not create these TFBS. Consequently,
haplotypes carrying the rSNP alleles that create KLF4 and SP1 TFBS are
essential for ADRBK1, TBXA2R and VEGFA gene
regulation by these TFs.
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