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Paper Details

Sequencing of LRP2 reveals multiple rare variants associated with urinary trefoil factor-3.
J Am Soc Nephrol
6
2014
HAVCR1, LRP2, RASSF8, SNPs, TFF3, exons 16-72, intergenic region, kidney disease, kidney injury, kidney injury molecule-1, locus wer, megalin, participants, patients, rare variants, rs11048230, rs6555820, rs7565788, single-nucleotide polymorphisms, trefoil factor 3, urinary trefoil factor-3, vascular endothelial growth factor, zebrafish
Author NameAffiliation
Gearoid M McMahonand Blood Institute's Framingham Heart Study
Qiong YangBoston University School of Public Health
Shih-Jen Hwangand Blood Institute's Framingham Heart Study
Shih-Jen Hwangand Blood Institute's Framingham Heart Study
Martin G Larsonand Blood Institute's Framingham Heart Study, Boston University School of Public Health
Caroline S Foxand Blood Institute's Framingham Heart Study, Brigham and Women's Hospital
Caroline S Foxand Blood Institute's Framingham Heart Study, Brigham and Women's Hospital
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